Tuesday 26 September
08:30

"Tuesday 26 September"

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A30
08:30 - 09:00

Herman Delooz Lecture

Moderator: Pr Rick BODY (Professor of Emergency Medicine) (Manchester)
08:30 - 09:00 Do we still need 'Tintinallis' in 2017? Judith TINTINALLI (Professor) (Speaker, Chapel Hill NC, USA)
Trianti Hall
09:10

"Tuesday 26 September"

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A31
09:10 - 10:40

Disaster Medicine III (Cutting Edge)
European Response to Disaster

Moderators: Pr Francesco DELLA CORTE (Head of Emergency Department) (Novara, Italy), Benoît VIVIEN (Adjoint du Chef de Service du SAMU de Paris, Responsable du SAMU Pédiatrique Régional IDF) (Paris, France)
Coordinator: Dr Abdo KHOURY (Coordinator, Besançon, France)
09:10 - 09:40 French Reserve Corps. Sophie MONTAGNON (Praticien hospitalier) (Speaker, New York, France)
09:40 - 10:10 Turkish Response Team. Al BEHCET (faculty speaker) (Speaker, Gaziantep, Turkey)
10:10 - 10:40 Euro Corps: the European Response. Massimo AZZARETTO (Medico Specialista) (Speaker, Lugano, Switzerland)
Trianti Hall

"Tuesday 26 September"

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B31
09:10 - 10:40

Cardiovascular (How To)
Panel discussion

Moderators: Barbra BACKUS (Emergency Physician) (Rotterdam, The Netherlands), Pr Rick BODY (Professor of Emergency Medicine) (Manchester)
Coordinator: Pr Rick BODY (Coordinator, Manchester)
09:10 - 10:40 Panel discussion. Pr Rick BODY (Professor of Emergency Medicine) (Speaker, Manchester), Barbra BACKUS (Emergency Physician) (Speaker, Rotterdam, The Netherlands), Ian STIELL (Physician) (Speaker, Ottawa, Canada), Martin THAN (Speaker, New Zealand), Pr Martin MÖCKEL (Head of Department, Professor) (Speaker, Berlin, Germany)
Mitropoulos

"Tuesday 26 September"

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C31
09:10 - 10:40

Infectious Disease & Sepsis (Game Changers)

Moderators: Laura HOWARD (United Kingdom), Cao YU (emergency) (Chengdu, China)
Coordinator: Christoph DODT (Coordinator, München, Germany)
09:10 - 09:40 Consensus Definitions for Sepsis and Septic Shock Advantages and Disadvantages. Luis GARCIA-CASTRILLO (ED director) (Speaker, ORUNA, Spain)
09:40 - 10:10 Sepsis day and a National Registry of sepsis in Hungary. Peter KANIZSAI (lead emergency physician) (Speaker, Pécs, Hungary)
10:10 - 10:40 Implementation of sepsis guidelines in the ED. Kurt ANSEEUW (Medical doctor) (Speaker, Antwerp, Belgium)
Banqueting Hall

"Tuesday 26 September"

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D31
09:10 - 10:40

YEMD - Eye-opener Quiz

Moderators: Blair GRAHAM (Research Fellow) (Plymouth, United Kingdom), Riccardo LETO (Emergency physician) (Genk, Belgium)
Coordinator: Basak YILMAZ (Coordinator, BURDUR, Turkey)
09:10 - 09:30 Spot Diagnosis. Tony KAMBOURAKIS (Director Medical Services) (Speaker, Melbourne, Australia)
09:30 - 09:50 ECG Conundrum. Blair GRAHAM (Research Fellow) (Speaker, Plymouth, United Kingdom)
09:50 - 10:10 Things you definitely should (not!) know. Basak YILMAZ (Faculty) (Speaker, BURDUR, Turkey)
10:10 - 10:30 For the NERDS. Incifer KANBUR (Assistant doctor) (Speaker, Istanbul, Turkey)
Skalkotas

"Tuesday 26 September"

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E31
09:10 - 10:40

Nursing session 1

Moderators: Marielle DEKKER (The Netherlands), Door LAUWAERT (Manager) (BRUSSELS, Belgium)
09:10 - 09:40 The impact of medical specialist staffing on emergency department patient flow and satisfaction. Christien VAN DER LINDEN (Clinical Epidemiologist) (Speaker, The Hague, The Netherlands)
09:40 - 10:10 Why we should implement a trauma protocol in ED. Georgios PAPAGEORGIOU (Nurse) (Speaker, Nicosia, Cyprus)
10:10 - 10:40 Nonfulfilled needs of the geriatric emergency patient -The role of GEM Nurse in the interprofessional team. Thomas DREHER-HUMMEL (Nurse) (Speaker, Basel, Switzerland)
MC-3

"Tuesday 26 September"

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F31
09:10 - 10:40

Free Papers Session 8

Moderators: Anthony GERASKLIS (Greece), Youri YORDANOV (Médecin) (Paris, France)
09:10 - 09:20 #11171 - OP064 Clinical characteristics of 2013 Haiyan typhoon victims presenting to the Belgian First Aid and Support Team.
OP064 Clinical characteristics of 2013 Haiyan typhoon victims presenting to the Belgian First Aid and Support Team.

Objectives

On November 8, 2013, the central Philippines islands were struck by typhoon Haiyan (Yolanda), damaging many local hospitals and disrupting acute and regular healthcare. The Belgian First Aid and Support Team erected a type 1 field hospital and water purification unit in Palo (south of Tacloban) to temporarily replace the damaged local healthcare. This study aims to describe the diagnoses encountered, and treatment provided by the Belgian team. Hypothesis is that besides disaster-related trauma, medical problems emerge soon, emphasising the importance of an appropriate composition of Emergency Medical Teams and their supplies.

Methods

Using a descriptive observational study design, all patients presenting to the Belgian field hospital were retrospectively reviewed. Each patient had an individual paper medical record that included gender, age, triage chief complaint, all secondary complaints, diagnosis, management and possible referral information. These were compared with a control group of patients from the same area and season, but from another year.

Results

All 1267 patients triaged, examined and treated in the field hospital, were included and analysed. Almost 28% suffered from injury, but the most important part of patients rather presented with medical diseases (64%), particularly respiratory (31%), dermatological (11%) and digestive (8%). The remaining 8% presented for follow-up, mental problems or pregnancy related issues. Most (53%) of the patients did not present with direct disaster-related acute pathology. More than 59% showed signs of infection within two weeks after the event. Most frequently used treatments were wound care (47%), pain relief (33%), vitamins and minerals (31%) and antibiotics (29% of all patients). Procedures were needed for 9%, fluid therapy for 8%, and psychological support for 5%. Logistic regression analysis indicates that children younger than 5 are more at risk for infectious diseases (OR 18.8 CI 10.6-33.3), and for injury (OR 10.3 CI 6.3-16.8), and males are twice more prone to be injured than females (OR 2.1 CI 1.6-2.6).

Conclusions

These results reveal that one week after the acute phase of a typhoon, respiratory, dermatological, and digestive problems emerge to the prejudice of trauma. Most patients did not present with direct disaster-related but with less acute diseases. Young children are more at risk for injury and infectious diseases. These facts should be anticipated when composing Emergency Medical Teams and supplies to be sent to the disaster site. 


Dr Gerlant VAN BERLAER (Brussels - BELGIUM, Belgium), Frank DE JONG, Timothy DAS, Carlos PRIMERO GUNDRAN, Matthijs SAMYN, Geert GIJS, Ronald BUYL, Michel DEBACKER, Ives HUBLOUE
09:20 - 09:30 #11241 - OP065 Bystanders and volunteers in disasters, experience from the Brussels attacks.
OP065 Bystanders and volunteers in disasters, experience from the Brussels attacks.

Purpose: To examine what roles bystanders and volunteers can play during a disaster and to propose an action card for the (medical) incident commander to manage this often unutilised resource of manpower and knowledge.

Relevance: During the terrorist attacks in Brussels on March 22nd 2016 the advantages as well as the problems with bystanders and volunteers during disasters were encountered. Many lives were saved by bystanders by using simple bleeding control techniques and the application of tourniquets. Among the bystanders there were soldiers patrolling the national airport. Their knowledge of lifesaving first aid (e.g. the use of tourniquets), extrication and triage proved pivotal in the first aid rendered to the victims.

However there were also unsolicited medical volunteers arriving with unauthorised private ambulances who became more a liability than a fruitful resource. Drawn to the scene out of curiosity and desire to help, not only were they unfamiliar with the Incident Command System (ICS), but because of the fact they were not registered in the regular EMS system they didn’t have the appropriate means of communication and started freelancing in deciding what to do on site and where to take victims in unregistered ambulances.  

An updated version of a national medical emergency plan was recently published. Being updated with the terrorist attacks in mind, it still fails to recognize bystanders as first aid providers.

Methods: Review of existing literature and unstructured interviews with medical personnel who volunteered during the aftermath of the Brussels Airport attack and the national EMS director.

Results: It is a certainty that (untrained) bystanders are the first providers of help during disasters. During the Brussels attacks we have seen the benefits of bystanders performing lifesaving bleeding control techniques, extrication of entrapped victims, transportation of casualties away from the blast sites and comforting victims.

All too often bystanders and volunteers at a disaster site remain unused and kept outside a perimeter upon arrival of EMS services and police and a clear guideline on how to integrate bystanders and volunteers was and still is lacking in any existing medical emergency plan. However, coordination of highly motivated bystanders and volunteers by professional EMS personnel had a positive effect on reducing morbidity and mortality in the Brussels attacks.  

Conclusion:  Because regular EMS is initially disrupted, bystanders and volunteers can aid in immediate search and rescue and first aid to victims. Instead of discouraging, their desire to help should be encouraged and planned for in emergency plans. To reduce the risk of untrained bystanders and volunteers disrupting the official organised response an action card to aid onsite incident managers is proposed.


Kris SPAEPEN (Brussels, Belgium), Ives HUBLOUE
09:30 - 09:40 #11504 - OP066 Training method in Personal Protective Equipment donning and doffing.
OP066 Training method in Personal Protective Equipment donning and doffing.

Introduction

When working with infectious diseases of high consequences the simple act of donning/doffing Personal Protective Equipment (PPE) becomes a lifesaving procedure not only for the medical staff but for the thousands of people who depend on them. Previous studies have shown that donning and doffing skills may be insufficient even after training. That raises a question on how to properly train staff in PPE donning and doffing to maintain the long term competence of PPE donning and doffing?

This study assessed if there is a performance difference one month after training between a control group that received instructor training and a study group that had access to a video over the month to compare the traditional tutorial based teaching method in teaching PPE donning and doffing.

Methods

This was a randomized controlled trial pilot study of video versus instructor training. 21 medical students and junior doctors where divided into 2 groups by simple randomization. The control group received training with an instructor. This training involved a demonstration of donning and doffing of PPE. Students were then observed donning and doffing of PPE until satisfactory performance had been achieved. There was no other intervention until the day of the assessment. The video group watched a training video demonstrating proper donning and doffing. The video group was given the video to watch at home as many times as they wanted. The training video was made by the same nurse who conducted the instructor training, using the same equipment. After a 1month period, a doctor performed a blind evaluation of all control and study groups using an adjusted Donning and Doffing PPE Competency Validation Checklist 2014.

Results

19 participants attended assessment session after a month with 9 in a control group and 10 in the study group. The mean donning score was 86,5/100.  Mean score was 84,8 for the instructor group, and 88.0 for the video group.There was no statistically significant difference in the donning score between the video and instructor group (95% confidence interval for the effect: -7.7 to 9.5; p-value: 0.54). The mean doffing score was 76,4/100. The mean score for instructor group was 79.1 and 73,9 for the video group. There was no significant difference in the doffing score between the video and instructor group (95% confidence interval for effect: -7,6 to 18,0; p-value: 0.54).

Conclusion

The study results suggests that donning and doffing competencies are similar for those who were trained with an instructor to those who were trained with the video method.


Liva CHRISTENSEN (Køge, Denmark), Thomas BENFIELD, Jeffrey Michael FRANC
09:40 - 09:50 #11653 - OP067 The use of table-top simulation for team training in disaster events.
OP067 The use of table-top simulation for team training in disaster events.

Objective: To find out if a table-top team training program would positively affect perception towards teamwork, and their ability to recognize the presence and quality of team skills in disaster events.

Background: Disaster training involves coordination and communication between various units, which necessitates involvement of the whole chain of response simultaneously. Due to the strict hierarchy culture in Korea, it is not easy to train healthcare providers in teamwork. Hospitals in Korea performs large-scale disaster exercise which takes a lot of preparation and resources. It is also difficult to assess teamwork and communication during a large-scale disaster exercise. Table-top simulation enables you to look at the whole process and the advantage of reflective, repetitive, and safe learning environment, where effective feedback can be provided. Since table-top simulation allows people to go through the thinking process, this could be a good module to train people improving on teamwork competency.

Methods: The educational intervention consisted of a half-day workshop for selected 24 emergency residents and 24 emergency nurses. Participants were given lectures on incident command system and surge capacity. They were randomly mixed into 6 groups (8 participants per group, 4 residents and 4 nurses). Participants were assessed as a group before and after the intervention, which consisted of debriefing session, focusing on the 5 components of teamwork (Team Structure, Communication, Leadership, Situation Monitoring, and Mutual Support). Discussions were focused on breaking the barrier of hierarchy in a crisis situation. The correct number of triage, treatment, and teamwork aspects were assessed. Assessment of teamwork was done in two parts. One was self-assessment of perception of teamwork, the Teamwork Perceptions Questionnaire (TPQ), and the other was assessment of the team performances, the Team Performance Observation Tool (TPOT). Both tools were derived from the TeamSTEPPS® Project (5-point Likert scale). They were modified to fit our culture and translated to Korean. Content validity index was performed (0.94). All pre-to-post differences within subjects were analyzed with paired t tests. The statistical level of significance was set at 0.05.

Results: Correct triaging and treatment improved after training with table-top simulation. Under triaging improved as well, but over triaging seemed to increase. Pre- and post-intervention differences for the 5 sections of the TPQ and TPOT improved. All results were statistically significant (p<0.05).

Conclusion: Teamwork and communication has cultural different aspects. Therefore, carefully planned curriculum tailored to the trainees, and debriefing session including discussion on cultural aspect is important when training for teamwork. Table-top exercise can positively affect perception toward teamwork, and their ability to recognize the presence and quality of team skills in disaster events.


Jiyoung NOH (Seoul, Republic of Korea), Hyun Soo CHUNG
09:50 - 10:00 #11779 - OP068 Evaluation of a training program to professionalize young doctors in humanitarian assistance.
OP068 Evaluation of a training program to professionalize young doctors in humanitarian assistance.

INTRODUCTION

Well-prepared humanitarian workers are now more necessary than ever; simulation-based training and evaluation are essential for the preparation process. This study aimed to assess the efficacy of a training program developed by the Research Center in Emergency and Disaster Medicine (CRIMEDIM) in collaboration with the international organization Médecins Sans Frontières (MSF) to professionalize senior residents in humanitarian assitance.

METHODS

The first three levels of the Kirkpatrick’s evaluation model (Reaction-Learning-Behaviour) were assessed.The 8 participants of the third course edition (4 residents in emergency medicine, 3 in anaesthesia and 1 in pediatrics) were enrolled in the study; the median age was 31. Residents participated in an introductory phase, completed a 3 month e-learning course, attended a residential week and were deployed with MSF in Pakistan (1), Afghanistan (2), Democratic Republic of Congo (1), South Sudan (1), Central African Republic (2) and Yemen (1). Reaction was assessed through a Likert scale questionnaire. The three dimensions of Learning were evaluated separately through a pre and post test as follows: a multiple-choice test was used to assess knowledge, a Likert scale questionnaire was used to evaluate attitudes, and simulation-based performance tests (using the Ottawa Global Rating Scale-GRS) were used to assess skills. Total multiple-choice scores and GRS overall performance scores were considered as primary and secondary outcomes, respectively. Differences were assessed using paired t-­tests. P ­values of less than 0.05 were considered significant. Behaviour was assessed qualitatively at the end of students’ missions by their field supervisors through the MSF standard evaluation module. Supervisors were blind to the students’ participation in the training program.

RESULTS

Reaction: the delivery modality and residential course were highly appreciated. The average median score for the overall course was 5 (excellent). Knowledge: there was a significant improvement in the post-test multiple choice scores when compared to the pre-test scores (p = 0.0011). Skills: there was a significant improvement in the overall performance score (P = 0.000001). No differences were detected in attitudes scores. Behaviour: for most participants the following strengths were highlighted: compliance with MSF standards and principles, flexibility, good team working skills and cross-cultural sensitivity.Their professional competence was never questioned. All residents were recommended for future MSF missions.

CONCLUSIONS

Residents were highly satisfied with this training program and their knowledge and skills in low-resource simulated humanitarian environments improved after participation in the course. The implementation of this project represents a model of how academia can successfully partner with humanitarian aid organizations to increase professionalization within the humanitarian health sector.

 


Alba RIPOLL GALLARDO (Milan, Italy), Luca RAGAZZONI, Ettore MAZZANTI, Grazia MENEGHETTI, Jeffrey Michael FRANC, Francesco DELLA CORTE
10:00 - 10:10 #11824 - OP069 Stampede, or not a stampede – that is the question.
OP069 Stampede, or not a stampede – that is the question.

Study/Objective:

To quantify the frequency and intention with which “stampede” is used to describe types of mass gathering disasters

Background:

Hazard vulnerability analysis would identify “human stampedes” as high probability events at mass gatherings. Over 200 “stampedes” have occurred in the past 30 years. At the 2015 Hajj, at least 2000 pilgrims died in one of the deadliest mass gathering disasters in recent history. News and literature referenced the event as the “Hajj Stampede”, implying abruptly increased speed and mass panic.  At the crux of many of these events, however, is a dense, immobile crowd – not the uncontrolled mindless mass implied.

Methods:

The authors performed a systematic search of peer reviewed literature indexed in PubMed, EMBASE, and Web of Science. Studies were limited to human studies using the keyword stampede. Gray literature using “stampede” in the title or abstract in reference to mass gathering disasters were also reviewed.

 

Results:

Search strategy using the term “stampede” yielded 649 articles. After excluding those using the term 1) apropos computing, 2) as an acronym, or 3) colloquially, 61 remained which used the term in reference to mass gathering disasters. 29 of 61 articles describe a slow-moving, highly dense crowd. 12 articles cite sudden mass movement as the main trigger for the referenced disaster. The remaining 18 described both slow-moving crowds and sudden mass movement. Only three articles distinguished between crowd disasters caused by sudden movement and high density. Overall, “Stampede” was used in the same context as “crowd disaster”, “turbulence”, “quake”, “mass panic”, “crush”, and “trampling”.

Discussion:

It is important to distinguish between stampede and non-stampede events for the benefit of survivors and for mitigation strategies. Few articles describing stampedes actually involve speed anywhere in the description. The generic “stampede”, through suggesting a fast moving, irrational and culpable crowd, focuses on herding the masses rather than improving safe access or egress routes to the gathering site. We must stem the notion that these disasters are a whim of the crowd and work towards evidence-based engineered solutions. 


Sravani ALLURI (Boston, USA), Amalia VOSKANYAN, Ritu SARIN, Michael MOLLOY, Gregory CIOTTONE
10:10 - 10:20 #11965 - OP070 Disaster education in senior Flemish nursing students.
OP070 Disaster education in senior Flemish nursing students.

Introduction: Nurses can be confronted with disasters and the care for the patients resulting from these incidents, be it in - or prehospital or in their own environment. Are they educated to do so? Following worrisome results in a survey on this subject amongst medical students our study hypothesis is that nursing students aren’t educated at all.

Material and methods: To evaluate disaster education in Flemish nursing students an online survey on Disaster Medicine, training and knowledge and willingness to report was sent to students in the last year of basic nursing training. This reported knowledge was tested by a mixed set of 10 theoretical/practical questions. A similar survey was sent to students in the Bachelor-after-Bachelor (BAB) specialisation year of Emergency Medicine and Intensive Care.

 

Results: Preliminary results from the first responding educational basic training centers reveal a M/F ratio of 13/87 with 29% that state that they have had any disaster training what so ever. 25% state to have some knowledge on CBRN incidents. 42% are convinced that a basic training on disaster management should absolutely be included in the basic nursing curriculum. None of the respondents found it useless. Estimated knowledge on several disaster scenarios varied from 1.92/10 (dirty bomb) over 2.24/10 (nuclear) and 3.49/10 (Ebola) to 4.05/10 in highly contagious influenza pandemic. Self-estimated capability to deal with these incidents varied from 2.22/10 (dirty bomb) over 2.59/10 (nuclear) and 3.54/10 (Ebola) to 4.14/10 in mass shooting incidents. Willingness to report to work in these incidents was much higher and varied from 7.19/10 (dirty bomb) over 7.41/10 (Ebola) and 7.56/10 (nuclear) to 7.94/10 in mass shooting incidents. Some topics of the theoretical / practical case mix raise some concern. 64% directs potentially contaminated patients direct into the emergency department. 75% believes that iodine tablets protect against external radiation and 37% would use them as the first step in nuclear decontamination. 37% believes that chemical decontamination consists of a total body antidote spray in a civil defence cabin and only 20% would use a shower with water and soap. Up to 47% would rush unprotected into a traffic accident scene with active leakage from a tanker truck. Self-reported knowledge and capability in the BAB group did not differ from the basic students and also the willingness to report was similar. They had however a better score on the theoretical / practical case mix.

 

Conclusion: Our data support the hypothesis that Flemish nursing students are ill-educated in disaster management. Despite low estimated knowledge and capability there is a high willingness to report.


Luc MORTELMANS (Antwerp, Belgium), Harald DE CAUWER, Marc SABBE
10:20 - 10:30 #10986 - OP071 Comparison of the quality of two speech translators in emergency settings : a case study with standardized Arabic speaking patients with abdominal pain.
OP071 Comparison of the quality of two speech translators in emergency settings : a case study with standardized Arabic speaking patients with abdominal pain.

In the context of the current European refugee crisis, at the Geneva University Hospitals (HUG) the languages which caused most problems were in 2016 Tigrinya, Arabic and Farsi. Several researchers pointed out serious problems of quality, security and equitability when no communication is possible between the doctor and his patient. BabelDr (http://babeldr.unige.ch/) is a common project of Geneva University's Faculty of Translation and Interpreting (FTI) and HUG which aims at facing this problem. The BabelDr application is a flexible speech-enabled phrase-book. The linguistic coverage is organised into domains, centered around body parts (abdomen, chest, head, kidney). Each domains has a limited semantic coverage consisting of 2000-2500 canonical sentences, but users can use a wide variety of surface forms when speaking to the system. The translation is not automatic; the canonical forms are translated into the target languages by translation experts from the FTI, which guarantees the quality of translation. At runtime, the system matches the spoken doctor’s utterance to a canonical sentence and echoes it back to the source-language user, only producing a translation if the source-language user approves. 

We compared BabelDr with the statistical MT system Google Translate (GT) for the anamnesis in emergency settings. French speaking doctors were asked to use both systems to diagnose Arabic speaking patients with abdominal pain, based on two scenarios. For each scenario (appendicitis and cholecystitis), a patient was standardized by the HUG.  Participants were four medical students and five doctors from HUG, who each performed two diagnoses, one with BabelDr and one with GT. 

The translation quality was evaluated in terms of adequacy and comprehensibility by three Arabic advanced translation students. Adequacy was judged on a four point scale (nonsense/mistranslation/ambiguous/correct) and comprehensibility on a four point scale (incomprehensible/syntax errors/non idiomatic/fluent). For the BabelDr translations, 93% of doctor's interactions sent to translation were correct and 94% fluent at the majority judgements. For GT, we respectively obtained 38% and 38%. Inter-annotator agreement for both evaluations was moderate (Light's Kappa for adequacy: 0.483; for comprehensibility: 0.44). With Google Translate 5/9 doctors found the correct diagnosis, against 8/9 with BabelDr. The satisfaction of doctors was also higher with BabelDr than with Google Translate: doctors were more confident in the translation to the target language with BabelDr than Google Translate (1/9 negative opinion with BabelDr vs 8/9 in GT). They also think they could integrate BabelDr in their everyday practice in the emergency room, contrary to GT (1/9 negative opinion with BabelDr vs 5/9 with GT).These results tend to show that BabelDr is a promising tool for the task and that GT translations are insufficiently adequate, accurate and comprehensible for emergency settings. 


Herve SPECHBACH, Sonia HALIMI, Johanna GERLACH, Nikos TSOURAKIS, Pierrette BOUILLON, Herve SPECHBACH (Geneva, Switzerland)
10:30 - 10:40 #11056 - OP072 Predicting Hospital Admission at Emergency Department Triage: a comparison of natural language processing and neural network methodological techniques.
OP072 Predicting Hospital Admission at Emergency Department Triage: a comparison of natural language processing and neural network methodological techniques.

Background

Emergency department (ED) crowding and increasing ED utilization are well-recognized problems for patient care in the United States.  To what degree predictive analytic techniques can improve wait times and patient outcomes when employed early in the ED stay--specifically during the triage process--is not well described.  We created predictive models to compare logistic regression (LR) and multilayer neural network (MLNN) techniques to predict hospital admission/transfer or discharge following initial presentation to ED triage with and without the addition of natural language processing (NLP) to analyze patient-reported free-text information.

Methods

Using data from the National Hospital Ambulatory Medical Care Survey (NHAMCS), a cross-sectional probability sample of United States EDs from 2012 and 2013 survey years, we developed several models to predict patients’ disposition: hospital admission or transfer vs. discharge. We included patient characteristics which are immediately available after the patient presents to the ED following ED triage. We used this information to construct logistic regression and multilayer neural network models which included NLP and principal component analysis to incorporate the patient-reported reason for visit.  Ten-fold cross validation was used to test the predictive capacity of each model and c-statistics / receiver operating curves (AUC) were calculated to compare these predictive models.

Results

Of the 47,200 ED visits from 642 hospitals, 6,335 (13.4%) resulted in hospital admission (or transfer). A total of 48 principal components were extracted by NLP from patient’s reason for visit, which explained 75% of the overall variance for hospitalization. In the model excluding patient’s free-text reason for visit, the AUC was 0.824 (95% CI 0.818-0.830) for LR and 0.823 (95% CI 0.817-0.829) for MLNN. When patients’ free text reasons for visit were included, the AUC increased to 0.846 (95% CI 0.839-0.853) for LR and 0.844 (95% CI 0.836-0.852) for MLNN.

Conclusions

The predictive accuracy of hospital admission/transfer or discharge for patients who presented to ED triage improved with the inclusion of free text data from patients’ reason for visit regardless of modeling approach.  The predictive ability of these models was generally quite good at predicting disposition with the limited information immediately available during the triage process. Natural language processing and multilayer neural networks provide ways to incorporate patient-reported free-text information when predicting various outcomes that are important in providers’ clinical decision-making. 


Justin SCHRAGER, Rachel PATZER, Xingyu ZHANG, Joyce KIM, Justin SCHRAGER (Atlanta, USA)
Kokkali
10:45

"Tuesday 26 September"

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PH4 - S1
10:45 - 11:05

E-Poster Highlight Session 4 - Screen 1

Moderators: Yonathan FREUND (PUPH) (Paris, France), Dr George NOTAS (DOCTOR) (HERAKLION, Greece)
10:45 - 10:50 #11217 - Risk factors associated with difficult venous access in adult emergency department patients.
Risk factors associated with difficult venous access in adult emergency department patients.

Background:

Establishing vascular access is one of the most common procedures carried out in the emergency department (ED) and a high priority for the care of a critically ill and unstable patients.

It is generally easy to realize, nevertheless, the difficulty or the impossibility of this access is a challenge of any emergency physician. Difficult venous access (DVA) can cause delays in diagnosis and treatment implementation in critically ill patients.

Methods:
This was a prospective, observational study conducted in the ED and in prehospital care which enroll adult patients undergoing intravenous (IV) placement. The primary outcome was DVA, defined as 2 or more IV attempts to establish IV access. Univariate analyze for factors predicting DVA was performed using Pearson's chi-squared test.

Results:

A total of 500 patients were enrolled, of which 90 (18%) met the criteria for DVA. In the univariate analysis, 5  conditions were significantly associated with DVA: elderly (p=0.015), history of chemotherapy (p=0.008), women (p=0.006), obesity (p=0.001), and cardiac arrest (p=0.006).

The most common alternative approach to DVA were: changing the operator (66 patients), change of site's puncture (85 patients), smaller IV catheter size (19 patients).

Discussion:
Difficult venous access is a common problem in the ED that can be frustrating for both patients and providers.  The prevalence of DVA was 18%, which is similar  to previous studies reporting a range of  from 10 to 40%.

Patients who are likely to present with challenges to peripheral intravenous line insertion often can be identified by certain risk factor (elderly, women, chemotherapy, obesity, cardiac arrest status). Several factors previously thought to be associated with DVA such as diabetes, IV drug abuse, sickle cell disease, dialysis, history of frequent  admissions in ED were not found to be significant in the current study. One issue with this finding is that these other conditions typically associated with DVA were not significant in our study. Future research is needed to confirm and expand these findings and to develop interventions to improve IV insertion skills and outcomes.


Majdi OMRI, Hajer KRAIEM (Sousse, Tunisia), Amal BACCARI, Nizar NAOUAR, Sami BEN AHMED, Mohamed Aymen JAOUADI, Mounir NAIJA, Naoufel CHEBILI
10:50 - 10:55 #11242 - Headaches and post-traumatic stress disorder: a 3-year prospective monocentric survey.
Headaches and post-traumatic stress disorder: a 3-year prospective monocentric survey.

INTRODUCTION: Post-traumatic stress disorder (PTSD) is an adjustment disorder that can occur after exposure to potentially traumatic event. Joint headaches are often observed in the accompanying painful complaints. Since the relation between the association of headaches and a PTSD has not been insufficiently studied, our primary objective was to study the incidence and the impact of headaches in a PTSD; the secondary objective was to analyze the influence of the PTSD's treatment on these headaches.

MATERIALS: Prospective observational monocentric survey conducted between January 2013 and December 2015. Inclusion criteria: patients suffering from PTSD after exposure to situations with high traumatic potential (armed attacks, road accidents, etc.) and voluntary for the self-administered questionnaire. Study variables: epidemiological data, headaches and their type before and after the diagnosis of PTSD (ICHD scale), impact on the quality of life (HIT6 score), on mood (POMS scale), severity of the PTSD (PCLS scale) and treatments received. Statistics: Fisher's exact test and Chi2 tests (qualitative variables), Mann-Whitney U-test (quantitative variables), Spearmans correlation (score comparison), all significant if p<0.05.

RESULTS: Over a period of 3 years, 101 patients (90% men) were included in 437 questionnaires sent (23.1%). The median age was 32 [27;39] years. The overall incidence of headaches was 54.5% (N=55) and the post-PTSD incidence was 36.6% (N=18). The HIT-6 score was 58.8 +- 8,3 with a major impact in 56.4% (N=31) of the cases. The severity of PTSD was correlated to PCLS scale same as the intensity of headaches on HIT-6 score (Spearman’s rho=0.35, p=0.009). In the post-PTSD time, tension headaches were predominantly found (45.5%, N=25). Associated head trauma was not an aggravating factor (p=0.3). Patients suffering from headaches were more often treated for PTSD (p=0.02). The pattern of mood, particularly anger and depression, showed a higher average score in headache patients (p=0.039).

DISCUSSION: Headaches should be recognized in the cohort of painful complaints that may accompany PTSD, as a potential indicator of its severity. Wartime’s pathology inviting itself particularly in the French territory after the attacks of 2015, the training and  multidisciplinary care approach by the health care givers are more than ever important and relevant.


Julie DEFRANCE, Stéphane FOUCHER, Jean-Pierre SIMSON, Marion TROUSSELARD, Eric RAMDANI, Dr Abdo KHOURY (Besançon), Christophe LABLANCHE, Hugues LEFORT, Laurent GUILLOTON
10:55 - 11:00 #11512 - Sensitivity of SOFA and qSOFA scores for critical illness among ED infected patients.
Sensitivity of SOFA and qSOFA scores for critical illness among ED infected patients.

Background: We designed this study to assess the validity of the Sequential ( sepsis - related) Organ Failure Assessment (SOFA) score of 2 points or more and quick SOFA (qSOFA) ≥ 2 for identifying emergency department (ED) infected patients with critical illness.

Methods: This prospective observational study will be performed in the ED university -affiliated tertiary care hospital. Adults patients will be included in this study if they had the following criteria: older than 18 years, present in our ED with infection probable or documented, are competent to give informed consent, and to be admitted to the hospital's service. Collected data includes age, sex, vital signs, origin of infection, SOFA and qSOFA score, and outcome. The primary outcome was the incidence of a critical illness defined as a stay in the intensive care unit of 72 hours or longer or hospital mortality. The ability of SOFA score ≥ 2 and qSOFA score ≥ 2 in predicting critical illness was evaluated by determining the sensitivity, specificity, positive and negative predictive values, and the area under the Receiver Operating Characteristics (ROC) curves. 

Results: We included 255 patients with a median age of 68 years (25 - 75% IQR: 59-79) who were admitted for infection. Pulmonary and urinary tracts were the most frequently infection. The frequency of patients with SOFA ≥ 2 AND qSOFA ≥ 2 were respectively 76% and 23%. The sensitivity of SOFA ≥ 2 for predicting critical illness was 93% (95% confidence interval (CI), 83% -98%) and the area under the ROC curve was 0.78 (95% CI, 0.71 - 0.85). The sensitivity of qSOFA was 49% (95% CI, 36% - 62%) and the area under the ROC curve was 0.76 (95% CI, 0.69- 0.83).

Conclusion: In ED the SOFA score was more sensitive than qSOFA for predicting critical illness.


Wiem KERKENI, Wiem KERKENI (DAX), Samia BETOUT, Nahla JERBI, Insaf DLALA, Yosra YAHYIA, Ahlam BAKHROUF, Maroua BEN ABDALLAH, Hajer SAID, Ikram FETHALLAH, Soudani MARGHLI
11:00 - 11:05 #11575 - qSOFA, SIRS and early warning scores for predicting sepsis outcomes in emergency room.
qSOFA, SIRS and early warning scores for predicting sepsis outcomes in emergency room.

Background. Sepsis is a life-threatening organ dysfunction caused by a dysregulated host response to infection. Sepsis contributes to up to half of hospital deaths and is responsible for the utilization of a significant proportion of healthcare resources. Early diagnosis and quick interventions are associated with better outcomes. Early warning scores (EWS) are physiological monitoring systems that are used for detection of acutely deteriorating patients. The recently updated definitions of sepsis proposed the Quick Sequential (Sepsis-related) Organ Failure Assessment (qSOFA) score in order to consider diagnosis of sepsis in the emergency department and on the wards. Physiological EWS including the National Early Warning Score (NEWS) and the Modified Early Warning Scores (MEWS) have been shown to predict mortality and escalation of care in patients admitted to hospital. SIRS criteria are usually criticized for their poor specificity. MEWS and the NEWS are commonly implemented in clinical practice outside the ICU. Our study sought to compare qSOFA, SIRS, NEWS and MEWS scores to identify high-risk septic patients in the Emergency Room (ER).

Methods. All patients admitted to the ER meeting criteria for suspicion of sepsis during 2016 September-December were included in the retrospective single-centre study. qSOFA, SIRS, MEWS and NEWS scores were compared for predicting death and ICU-stay.

Results. In total, 64 patients (38 male (59.4%), 26 female (40.6%) were admitted due to suspected sepsis during September – December of 2016. The mean age was 64.05 ± 18.63 years. 20.3% (n=13) patients died. Discrimination for in-hospital mortality or ICU-stay was highest for NEWS (AUC 0.738 [95% CI 0.612-0.841], p=0.001), followed by qSOFA ( AUC 0.686 [ 95% CI 0.557-0.797], p=0.003),  MEWS (AUC 0.654 [95% CI 0.523-0.769], p=0.027) and  SIRS (AUC 0.635 [95% CI 0.504-0.752], p=0.035) (p >0.05 for all pairwise comparisons). Using a patient’s highest non-ICU score, ≥2 SIRS had a sensitivity of 15.38% and specificity of 100% for the composite outcome compared to 7.69% and 96% for NEWS ≥8 and 0% and 98% for MEWS ≥5. And these results are in contrary to most of the studies. Highest sensitivity and specificity of MEWS was for >2 scores (38.46% and 76%), for NEWS - >4 scores (69.23% and 70%), for SIRS - >1 (84.62% and 40%). The mean time spent in ER was 287 min (IQR 188-403). The median hospitalization time was 12.5 days (IQR 8-18).

Discussion. Our study showed, that even though qSOFA showed higher discrimination for in-hospital mortality or ICU-stay than MEWS and SIRS criteria, NEWS criteria showed better one. On the other hand, the diagnostic test value is still poor, same as SIRS. Study needs further investigation in behalf of objection to other studies on this matter.


Ruseckaitė RENATA, Smiltė KOLEVINSKAITĖ (Vilnius, Lithuania)
E-Poster Area

"Tuesday 26 September"

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PH4 - S4
10:45 - 11:05

E-Poster Highlight Session 4 - Screen 4

10:45 - 10:50 #9857 - Value of physiological scoring systems in prediction of long-term mortality in traumatic brain injury patients.
Value of physiological scoring systems in prediction of long-term mortality in traumatic brain injury patients.

Background: Rapid acute physiological score (RAPS) and Worthing physiological scoring system(WPSS) models have received much attention in recent years. Yet, the value of these systems in outcome prediction of traumatic brain injury (TBI) patients has not been assessed. Therefore, the present study was designed aiming to compare the value of the 2 mentioned models in prediction of 6-month mortality of head trauma patients.
Methods: The present study is a diagnostic accuracy one evaluating head trauma patients presenting to emergency department. Each patient had a WPSS score and a RAPS score, and then the discriminatory powers of the 2 models with 95% confidence interval (95% CI) were compared.
Results: Data of 735 head trauma patients was assessed. During the 6-month follow-up, 48 (6.53%) patients died. Area under the curve of RAPS and WPSS in prediction of 6-month mortality were 0.93 (95% CI: 0.88-0.98) and 0.97 (95% CI: 0.96-0.98), respectively. The 2 evaluation models had similarvalue in prediction of mortality in head trauma patients (p=0.10). The best cut off point for RAPS and WPSS in prediction of trauma patients’ mortality was 5 and 2, respectively. RAPS had sensitivity and specificity of 89.58 (95% CI: 76.56-96.10) and 85.15 (95% CI: 82.22-87.68), respectively. Sensitivity and specificity of WPSS model were 100.0 (95% CI: 90.77-100.0) and 87.92 (95% CI: 85.19-90.21), respectively.
Conclusion: Findings show that there is a significant correlation between physiological factors on admission and mortality of head trauma patients. In addition, it was determined that RAPS and WPSS physiological scoring systems have high value in prediction of mortality following TBI.

Sahar MIRBAHA, Alireza BARATLOO, Alaleh ROOHIPOUR, Hamidreza HATAMABADI (Tehran, Islamic Republic of Iran)
10:50 - 10:55 #10508 - Door-to-Balloon in patients with ST Elevation Myocardial Infarction: Minding the gap.
Door-to-Balloon in patients with ST Elevation Myocardial Infarction: Minding the gap.

Mor Saban,  Efrat Dagan,  Aziz Darawsha, Rabia Salama

Background. A fast and correct identification of ST Elevation Myocardial Infarction (STEMI) in the Emergency Department (ED) significantly correlates to decrease morbidity, mortality and related complications in patients with chest pain. Yet, delayed diagnosis in patients with STEMI still represented a blind spot in the assessment of quality health care indicators.

Aim. To evaluate a 'fast-track' intervention intended to shorten Door-to-Balloon waiting times in patients presenting to the ED triage with STEMI.

Methods. In 2016, a 'fast track' intervention program for patients with chest pain was implemented in the ED at Rambam Health Care Campus. We determined a set of clinical guidelines for patients' assessment as follows: 15’ to triage, 10’ to ECG, 40’ for physician assessment, 60’ waiting time for decision and 90’ to catheterization lab (Door-To-Balloon-Time). The program was comprised of four steps: 1. Laying the patient immediately. 2. Marking the chart with a dedicated sticker 3. Assessing time-lags according defined clinical guidelines. 4. Signing the ECG and the dedicated sticker by a physician.
A retrospective-archive study was conducted between January 2015 and December 2016, to evaluate the intervention program achievements. We compared the adherence to clinical guidelines between all STEMI patients (n=140) who were attending to ED before (i.e during 2015, n=60) and after (i.e during 2016, n=80) implementing the intervention.  A lift chart and receiver operating characteristic
(ROC) curve were used to determine the optimal time lags in ED for achieving the objective of 60 minutes for evaluating the patients in ED.
Results. After implementing the intervention more patients have reached ECG evaluation within 10’ (57.5%) compared to pre- intervention (40%) (p=0.04); and more patients were stayed at ED less than 60’ (87.5% and 63.3%, respectively, p=0.01).
It clearly appears that post- compared to pre- intervention, less time lags (in minutes) were measured in patients who their clinical guidelines were not achieved before the program. This was found for physician assessment (70.25±30.24 vs. 52.86±13.51, respectively, p=0.05), for total waiting time in ED (126.18±59.63 vs. 72±9.67, respectively, p<0.001) and time to balloon (164.61±53.89 vs. 125±32.25, respectively, p<0.01). Interestingly, The ROC curve show that patients who were treated at ED according to the three clinical guidelines (15' for the nurse, 10' for E.C.G and 40'  for the Physician), had the largest probability to uphold the 60 minute waiting time in ED (AUC=0.98).
Conclusions. A ‘fast-track’ management for patients with chest pain providing early diagnosis of STEMI and shortened the waiting time for catheterization. The findings call for implementing programs for identifying patients at risk for STEMI in ED triage and programs’ interventions to reduce time lags for reperfusion for these patients at risk as fast as possible.


Saban MOR (Zychron Yaakov, Israel)
10:55 - 11:00 #11167 - The simplified Pulmonary Embolism Severity Index and HESTIA rule to identify eligible patients with pulmonary embolism for outpatient management.
The simplified Pulmonary Embolism Severity Index and HESTIA rule to identify eligible patients with pulmonary embolism for outpatient management.

Background: The management of pulmonary embolism (PE) has evolved over the past decade. Henceforth, outpatient treatment is an option for selected patients at low risk of complications. To assist clinician in identifying those patients, several rules have been proposed. The most validated to date are the Pulmonary Embolism Severity Index (PESI) or its simplified version (sPESI) stratifying patients according to their mortality risk and the the HESTIA rule based on a list of exclusion criteria, each one requiring inhospital care. Both strategies are used in clinical practice, but very few studies confront them.

Aim: To compare the proportion of patients eligible for outpatient management according to the sPESI and HESTIA rule.

Methods: This is a retrospective monocentric study. All patients with confirmed PE through CT scan or V/Q scan within 48 hours after Emergency Department admission were included. Medical records were retrieved to determine the sPESI score and HESTIA criteria at admission. Patients were considered suitable for outpatient management according to the sPESI if it was equal to 0, or if none of the criteria were met for HESTIA rule.

Results: 105 patients were included. HESTIA rule and the sPESI did not significantly differ on the proportion of patients suitable for outpatient management, respectively 45.7% [36.5-55.2] and 39.1% [30.3-48.6], p = 0.328. However, taking into account medical conditions not allowing outpatient management (severe comorbidities, social condition…) in addition to the sPESI score, the HESTIA rule significantly overtook the sPESI, with respectively 45.7% [36.5-55.2] and 26.7% [19.1-35.8], p = 0.004. Of note, the number of discordant results (suitable or not for outpatient management) between the two rules was 33.3% [25.1-42.8]. These conclusions were unchanged using the original version of the PESI.

Conclusion: sPESI score or HESTIA rule both identify a relevant proportion of PE patients suitable for outpatient care, but with a high level of discordance between the two rules. The HESTIA rule may select a higher proportion of patients when considering medical conditions requiring inpatient management despite a low-risk of death according to sPESI.


Thomas MOUMNEH (Tours), Julie LECHEVAILLIER, Delphine DOUILLET, Pierre-Marie ROY
11:00 - 11:05 #11666 - Cbrn preparedness of Dutch ambulance teams: the impact of research.
Cbrn preparedness of Dutch ambulance teams: the impact of research.

Introduction: The Netherlands is a densely populated country in Northern Europe. With several nuclear installations, a heavy petrochemical industry, transport of related products by road, rail or water and possible terrorist targets, the risk for CBRN incidents is eminent. In case of such an incident, ambulance personnel will be first to be confronted with victims but are they really prepared?  The Dutch Ambulance Academy shared this concern and organised an introductory day course on working in CBRN circumstances as pilot project in cooperation with the Defence CBRN Centre. A previous study revealed the gaps in preparedness. The course enhanced the scores of the participants but the practical knowledge however seemed to remain limited. Following this conclusions a 2-day course was designed with emphasis on practical training.

Material and methods: Participants of this new course completed an online survey on demographics, perceived knowledge, capability, willingness to work and training.  The reported answers were controlled with a set of theoretical/practical questions on the subject. Scores were compared with those of the pilot course and untrained ambulance personnel.

Results: Preliminary results reveal a mean age of 49 years, 44% has had any disaster training before. Eighty per cent works in the vicinity of a chemical risk installation and 20% near a nuclear installation. There was a higher estimated knowledge, ranging from 4.8/10 (vs. 2.9 in the untrained group and 3.6 in the pilot group) for nuclear incidents to 5.53/10 (vs. 4.46 and 4.59) in chemical incidents. Self estimated capability to deal with these incidents also scored higher, from 3.93/10 (vs. 2.28 and 3.59) in nuclear incidents to 4.67/10 (vs. 4.06 and 4.63) in chemical incidents. Up to 100% stated to be practically trained to use personal protective equipment (vs. 24 and 26%) with a clearly higher score on self estimated practical knowledge on this subject (7.53/10 vs. 3.35 and  4.22). A good practical training in decontamination was reported in 93.33% (vs. 27% and 43%) with also a higher score on practical knowledge (6.87/10 vs. 3.22 and 4.48).  The end score on the theoretical/practical test was also higher in the study group (7.47/10 vs. 4.65 and 5.98).  There was however no higher willingness to work, nor in nuclear nor in chemical incidents.

Conclusion: The preliminary data of this study illustrate how research has an impact on the evolution in training and enhances CBRN preparedness of Dutch ambulance teams. Further evaluation of participants of following training sessions seems mandatory.


Luc MORTELMANS (Antwerp, Belgium), Greet DIELTIENS, Marc SABBE
E-Poster Area

"Tuesday 26 September"

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PH4 - S2
10:45 - 11:05

E-Poster Highlight Session 4 - Screen 2

10:45 - 10:50 #11069 - Impact of a stroke information campaign on the number of emergency medical services calls between September 2014 and October 2015, in the Rhône area, France.
Impact of a stroke information campaign on the number of emergency medical services calls between September 2014 and October 2015, in the Rhône area, France.

BACKGROUND :

Approximately 150,000 strokes occur each year in France, but only 5 to 10% of patients have access to thrombolysis, mainly due to poor knowledge of stroke symptoms by the population. The main objective of our study was to evaluate the impact of a local information campaign on emergency medical services (EMS) call, for suspected stroke, in the Rhône area between September 2014 and October 2015, compared to a control area.

METHODS :

We carried out a controlled before and after study on 3 time-periods of 2 months to evaluate a multifaceted stroke awareness program deployed in the Rhône area (France), from October to December 2014. Key messages of the campaign were the recognition of stroke warning signs and the need to call EMS urgently, using multiple information media. We analysed all the calls to EMS for stroke suspicion, using databases of emergency health centers in the Rhône area and control area. To determine the impact of the campaign, we assessed the evolution of the number of EMS calls for stroke suspicions before the launch of the campaign (T0), at 3 months (T1) and 12 months (T2), compared to control area. We also studied the impact on the time between onset of symptoms and EMS calls and on the evolution of thrombolysis number.

RESULTS & DISCUSSION :

During these periods, we studied 707 calls (214 at T0, 234 at T1 and 259 at T2) to EMS in the Rhône area for stroke suspicion, compared with 519 (186 at T0, 174 at T1 and 159 at T2) in the control area. We found a 21% significant increase of EMS calls in the intervention area over the period studied (p <0.05). No significant effect was found on the secondary criteria.

CONCLUSION :

Our information campaign had an impact on the population, improving EMS call, but it remains limited and to be confirmed by other studies. The goal will be to develop better information campaign to improve access to reperfusion strategies.


Caroline LAUDE (LYON), Anne TERMOZ, François LOIZZO, Norbert NIGHOGHOSSIAN, Anne Marie SCHOTT, Julie HAESEBAERT
10:50 - 10:55 #11235 - Effect of low doses of ketamine in nephritic colic.
Effect of low doses of ketamine in nephritic colic.

Background:
Renal colic is a frequent reason for consultation in emergency department (ED). Its adequate analgesic treatment remains a preoccupation of the clinician. The aim of our study is to evaluate the tolerability and efficiency of the association of low doses of ketamine with morphine in the management of renal colic in ED.

Methods:

Prospective, randomized, double-blind study conducted at the ED in university hospital over a six-month period, including 62 patients admitted for renal colic with numerical pain rating scale (NRS)>5, randomized into three groups: standard group: receiving morphine 0.1mg / kg associated with placebo, group1: receiving morphine 0.1mg / kg associated with 0.15mg / kg ketamine and group 2: receiving morphine 0.1mg / kg associated with 0.3 Mg / kg ketamine.

Results:The demographic characteristics were comparable for the three groups with an average age at 38 ± 12 years, a sex ratio at 1.13.   51.6% of the patients didn't have previous diseases and 27.4% were known carriers of renal lithiasis. 53.2% of patients used analgesics prior to initiation of the protocol. The three groups were also clinically comparable with an initial mean NRS of 9.4. A significant decrease in NRS within 30mn is observed in the ketamine0.3 group compared to the other two groups (p= 0.01).  The analgesic effect, judged by the SPID, was better in group 2 compared to the 2 other groups with p <0.05.  The total dose of morphine consumed decreased significantly in the two ketamine groups with an average of 9.59 mg for group 1 and 7.55 mg for group 2 compared to the standard group which showed an average of 11.95 mg with p <0.01. Total patient satisfaction assessed via TOTPAR was better in group 1 compared to placebo (p = 0.22) and in group 2 compared to group 1 (p = 0.013) in group 2 compared to placebo (p < 0.01). Ketamine was globally well tolerated. There was no statistically significant difference in adverse events among the three groups (p = 0.806) with predominance of gastrointestinal adverse events in the placebo morphine group (p = 0.01) and neuropsychic adverse effects in the 2 ketamine groups compared to the morphine group alone (p = 0.04).

Discussion:The association of low doses of ketamine (at a dose of 0.3 mg / kg) to morphine is well tolerated and allowed a better analgesia, with greater patient satisfaction compared to morphine alone in patients suffering from nephritic colic.


Khaoula RAMMEH, Hajer KRAIEM (Sousse, Tunisia), Dorsaf ADALA, Majdi OMRI, Mariem KHROUF, Mehdi METHAMEM
10:55 - 11:00 #11441 - Unexpected situations in a medical dispatch center: added-value of a training session.
Unexpected situations in a medical dispatch center: added-value of a training session.

Introduction

Managing unexpected situations such as mass casualties, disaster relief, and failure of dispatch software or equipment breakdown requires specific knowledge from both Emergency Medical Dispatcher (EMD) and dispatching physicians.

Both EMDs and physicians handle all incoming medical emergency calls in France and they need to work in close cooperation. Training sessions were performed in a pre-hospital emergency medical service for all professionals working at a dispatch center in order to reinforce this teamwork in unexpected situations. These half-day sessions consisted in different scenarios split in 2 situations: 1) mass casualty events (flood, building fire and mass shooting); 2) technical breakdown (computer aided dispatch system breakdown). Each session was composed of 2-persons teams: 3 EMDs working in partnership with 3 physicians. Each training session started with an evaluation of knowledge followed by evaluation after training.

The objective of this survey was to evaluate the added value of a training session that concerned unexpected situations in a medical dispatch center.

Method

5 training sessions from May 2016 to February 2017 were organized. 24 people (10 EMD and 14 physicians) answered a 26-item questionnaire that included 9 technical questions and 16 mass casualties’ questions before the training session and immediately after training. They answered to each assertion as true, false or did not know. A mark of 1 was assigned for each correct answer. Age, gender and seniority in the profession were also collected.

Analyses were presented as means and percentages. Each 26-item score was analyzed as a score, with 2 sub-scores concerning technical breakdown and mass casualty. Comparisons were performed with Ttests.

Results

2/3 of participants were female. 46% were younger than 40 years old and 12% older than 50 years old. 79% of them did work 5 years or less in a dispatch center.

Mean global scores were 11.66 (4.67 Standard Deviation – SD) out of 26 before the evaluation and 19.83 after the evaluation (SD: 3.34) (p<10-3). The mean scores for mass casualty were 7.42 (SD: 3.10) out of 16 at first evaluation and 12.83 (SD: 1.90) after the session. The mean scores for technical breakdown were 4.13 (SD: 2.66) out of 9 at first evaluation and 6.54 (SD: 1.44) after the session. There were no differences in scores when comparing EMDs and physicians, but there were significant differences in the scores between first and second evaluation.

Discussion

These training sessions were very positive, with significant improvement of scores after the half-day sessions. Organizing training sessions for all professionals working in a dispatch center is essential, specifically concerning events that happen very rarely. Teamwork brought cohesion, which is critical in the first minutes of such unexpected events.


Isabelle LAFFRAT (GARCHES), Jérémie BOUTET, Cecile URSAT, Céline FENIOUX, Jonathan FOURNÉE, Mathias HUITOREL, Céline VINTEZOU, Anna OZGULER, Michel BAER, Thomas LOEB
11:00 - 11:05 #11539 - Nine years (2008-2017) in-hospital Basic Life Support Training for all nurses: We keep going!
Nine years (2008-2017) in-hospital Basic Life Support Training for all nurses: We keep going!

Objective

The first 2 links in the “Chain of survival”, and thus cardiopulmonary resuscitation training, are mandatory for a good patient outcome. Poor knowledge and skill retention following resuscitation training has been documented over the past 25 years.

We developed a basic life support training program for clinical nurses and we composed a six-stage plan based on the ERC algorithm for in-hospital resuscitation.

We defined two quality standards (which we had to modify, as the guidelines changed in 2010) to measure if there was an improvement in the resuscitation skills after four sessions.

Methods

The whole nursing staff (ca. 400 individuals) in our hospital had to register for a fourth obligatory basic life support session, with the consent of the Board of Directors.

The performance of the nurses was recorded on an Ambuman manikin (with Ambu CPR software version 2.3.9), lying in a hospital bed.

Several variables were recorded, e.a. the correct execution of the sequence of the six-stage-plan, the compression rate, the compression depth and the ventilation volume. Using two quality ‘standards’, we compared the results session.

Results

The attendance to those sessions is significantly lower when the nursing staff had to enrole themselves.

For the first two sessions (2005 guidelines), we saw a compression depth between 40mm and 50mm was achieved by 120 or 37% (vs 95 or 31% in first session) (p=0,09) (fig. 2); a compression rate between 80/min and 120/min was achieved by 254 or 79% (vs 221 or 72% in first session) (p=0,03) (fig. 3); a ventilation volume between 400ml and 700ml was achieved by 148 or 46% (vs 97 or 31% in first session) (p<0,001) (fig. 4).

Optimal resuscitation (defined as a combination of those three determinants) was achieved by 44 or 14% (vs 25 or 8% in first session) (p=0,03). Satisfying resuscitation (defined as a combination of a compression rate between 70/min and 130/min, a compression depth more than 35mm and a ventilation volume more than 300ml) was achieved by 228 or 71% (vs 98 or 32% in first session) (p<0,001) (fig 5.)

For the third, fourth, fifth, sixth, seventh and eighth session, we defined  optimal resuscitation as a compression depth >50mm, compression rate 100-120/min and ventilation volume between 400ml and 700ml. We defined satisfying resuscitation as a compression depth >45mm, compression rate 90-130/min and a ventilation volume more than 300ml. The 2017 session showed that 73% achieved a satisfying compression depth, 96% achieved a satisfying compression rate and 96% achieved a satisfying ventilation volume. This is, so far, our best result in 9 years.

Using Fisher exact test, we found a significant improvement (p<0,001) for ventilation volume and for satisfying resuscitation.

 

Conclusion & perspectives

We need to thank the team of BLS instructors for their efforts to keep the resuscitation knowledge of the whole nursing staff at this level. We will continue to support this project on director’s level.


Thierry SCHISSLER, Fien DEWULF (jabbeke, Belgium), Dr Bart LESAFFRE
E-Poster Area

"Tuesday 26 September"

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PH4 - S3
10:45 - 11:05

E-Poster Highlight Session 4 - Screen 3

10:45 - 10:50 #11135 - Out-of-hospital cardiac arrest and pregnancy: observational study.
Out-of-hospital cardiac arrest and pregnancy: observational study.

Introduction: There is very little data in scientific literature regarding out-of-hospital cardiac arrest (OHCA) in pregnant women. This study aims to describe a group of pregnant women who experienced an OHCA and were treated by a pre-hospital Advanced Life Support (ALS) team, and to report the short-term outcome.

Materials and Methods: Retrospective observational study. Approval of the Ethics Committee. Inclusion criteria: pregnant woman > 18 years of age experiencing an OHCA, regardless of the stage of the pregnancy, treated by an ALS Team. Collected variables: age, term of pregnancy (weeks of gestation), location, presence of a witness, first documented rhythm, number of external electric shocks (EES) administered by an automatic external defibrillator (AED), use of an automated chest compression device (ACD), administration of drugs, and outcome (dead in the field, transport to hospital). Statistics: qualitative variables were expressed as a percentage, quantitative variables as a median [interquartile range, IQR]. The description was univariate.

Results: Over a period of 5 years, among 19,515 OHCAs, 17 concerned pregnant women. These 17 (100%) patients had a median age of 31 years (IQR [28-34]) and a median term of 20 weeks of gestation (IQR [9-32]) (6 missing data). Three (18%) OHCAs occurred in a public area and 14 (82%) took place at home. A witness was present in 12 (70%) cases, of which 6 bystanders initiated chest compressions (CC). The no-flow median time was 4.5 min (IQR [1-9]) and the low-flow median time was 42 min (IQR [30-70]). The cause of the OHCA was identified in 11 cases/17: 4 injuries (2 stab wounds, 1 hanging, 1 defenestration) and 7 medical causes (3 pulmonary embolisms, 2 myocardial infarctions, 1 hypoxia, 1 hypertrophic cardiomyopathy). Two patients (12%) received an EES by the first aid worker’s AED. Nine (53%) benefited from ACD. The median quantity of adrenaline injected was 10 mg (IQR [5-15]). One patient underwent thrombolysis and 6 were transported alive to hospital. Two patients were alive on day 30 following the OHCA.

Discussion : This is the first series of cases documented in medical literature. The diverse causes of OHCA were most often not related to the pregnancy. The rate of Ventricular Fibrillation was lower than for the general population. Of the 3 OHCA≥20 weeks of gestation, none survived. The recommendations for the treatment of OHCA in pregnant women are currently not applicable to the pre-hospital setting and are the subject of local consensus meetings aimed at producing a protocol adapted to these specific pre-hospital situations.

 


Olga MAURIN (Marseille), Sabine LEMOINE, Daniel JOST, Olivier YAVARI, Clément DERKENNE, Michel BIGNAND, Jean-Pierre TOURTIER
10:50 - 10:55 #11256 - Acute Decompensated Heart Failure - Are we failing?
Acute Decompensated Heart Failure - Are we failing?

INTRODUCTION

Acute Dyspnoea is a common presenting complaint to the Emergency Department (ED). Studies have shown that acute decompensated heart failure (ADHF) is difficult to diagnose with standard modalities in the ED. The primary objective of this study is to estimate the accuracy of ADHF diagnosis in two Irish tertiary EDs.

METHODS

This is a retrospective multi-center study conducted in two tertiary university hospitals in Dublin. All patients who were discharged from the hospitals between 1st January 2016 to 30th June 2016 with a HIPE diagnosis of ADHF were included.

RESULTS

280 patients were found in the HIPE search. 61 elective patients were excluded leaving a total of 219 study patients. Of these, 95 (43.4%) were accurately diagnosed with ADHF by the Emergency Physician.  Of those who were not diagnosed in the ED (n=124, 56.6%) . 65 (52.4%) had a CXR which was normal or suggested an alternative pathology compared to 21 (22.1%) p<0.0001 in the accurate group. In the missed group, 57 (46%) had no previous history of CCF compared to the accurate group 43 (45.3%). Length of stay for the missed group was 13.2 days compared to 13.6 days (p=0.896) for the accurate group. Time to X-ray for both groups 

CONCLUSION 

With the currently available diagnostic strategies, our study suggests that the diagnosis of ADHF is difficult in the ED. Recent studies suggest that basic bedside lung ultrasound would improve the early diagnosis of ADHF by emergency physicians.


Dr Nicolas LIM (Singapore, Singapore), Arthur HENNESSY, Andrew PATTON, Geraldine MCMAHON, John CRONIN
10:55 - 11:00 #11350 - Similar clinical performance of a novel point-of-care cardiac troponin assay with central laboratory high-sensitivity cardiac troponin I testing for diagnosis of acute myocardial infarction.
Similar clinical performance of a novel point-of-care cardiac troponin assay with central laboratory high-sensitivity cardiac troponin I testing for diagnosis of acute myocardial infarction.

Rapid diagnosis of acute myocardial infarction (AMI) facilitates early disposition of chest pain patients presenting to the emergency department (ED). Point-of-care (POC) cardiac troponin testing may improve patient throughput but is currently discussed due to limited diagnostic accuracy. We compared the diagnostic accuracy of a novel cTnI test (Minicare cTnI, Philips), with a currently available POC cTnI (i-Stat cTnI, Abbott) and high-sensitivity central laboratory cTnI assay (Architect Stat High Sensitive Troponin-I assay, Abbott).

Methods: The clinical performances of these assays were compared in samples from 450 patients from an adjudicated outcome of AMI. The blood samples were drawn on ED admission and 3 h later. Bassink-Bablok regression analysis was used for comparisons between assays.

Results: Minicare cTnI correlated with Architect hs-cTnI (r2=0.85, p<0.0001) and I-Stat cTnI (r2=0.93, p<0.0001). Areas under the receiver operating characteristics curves were 0.87-0.91 at admission (p=ns) and 0.96-0.97 3h after admission (p=ns). The negative predictive value (NPV) at admission were 95% (92-97%, 95% CI) for Minicare cTnI and increased to 99% (97-100%) at follow-up testing, and were comparable to Architect hs-cTnI (98%, 96-100%), but higher than I-Stat cTnI (95%, 92-97%; p<0.01). Negative likelihood ratios (LR-) after 2-4h were 0.06 (0.02-0.17, 95% CI) for Minicare cTnI, 0.11 (0.05-0.24) for Architect hs-cTnI (p=0.02) and 0.28 (0.18-0.43) for I-Stat cTnI (p<0.0001). The clinical concordances between Minicare cTnI and Architect hs-cTnI were 92% (admission) and 95% (2-4h), with lower concordances among Minicare cTnI and i-Stat cTnI testing (83% and 78%, respectively; p=0.007).

Conclusion: The Minicare cTnI POC assay tested on fresh whole blood samples demonstrated similar clinical performances to a current, high-sensitivite cTnI assay fort he diagnosis of AMI 3h after presentation. Minicare cTnI POC assay may be useful to aid in ruling-out of AMI in ED patients with suspicion of acute coronary syndrome using a guideline supported 0/3h testing protocol.


Christ MICHAEL (Lucerne, Switzerland), Per VENGE, Van Lippen LIAN, Blaschke SABINE, Geier FELICITAS, Giannitsis EVANGELOS, Emil HAGSTRÖM, Pierre HAUSFATER, Khellaf MEHDI, Johannes MAIR, David PARIENTE, Volkher SCHARNHORST, Veronique SEMJONOW
11:00 - 11:05 #11599 - Optimizing the ISAR-HP to screen efficiently for functional decline in older patients.
Optimizing the ISAR-HP to screen efficiently for functional decline in older patients.

Introduction: The Identification of Seniors At Risk-Hospitalized Patients (ISAR-HP) has recently been included in guidelines as a frailty indicator to identify patients for comprehensive geriatric assessment. Previous studies showed that the conventional cut-off score classifies a high percentage of patients as high risk incorrectly. We aimed to optimize the predictive value of ISAR-HP by using different cut-offs in older acutely hospitalized patients.

Methods: A prospective follow-up study was performed in two Dutch hospitals. Acutely hospitalized patients aged ≥70 years were included. Demographics, illness severity parameters, geriatric measurements and the ISAR-HP scores were obtained at baseline. The primary outcome was a combined end point of functional decline or mortality during ninety day follow-up.

Results: In total 861 acutely hospitalized older patients were included, with a median age of 79 years, of whom 276 (36.1%) experienced functional decline or mortality. The conventional ISAR-HP cut-off of ≥2 assigned 432/765 patients (56.5%) as high risk, with a positive predictive value (PPV) of 0.49 (95%CI 0.45-0.54) and a negative predictive value of 0.81 (95%CI 0.76-0.85). Thus, 51% of those whom the ISAR-HP denoted as high risk did not experience the outcome of interest.  Raising the cut-off to ≥4 assigned 205/765 patients (26.8%) as high risk, with a marginally increased PPV to 0.55 (95%CI 0.48-0.62).

Conclusion: The ISAR-HP with the conventional cut-off of ≥2 incorrectly identifies a large group of  patients at high risk for functional decline or mortality and raising the cut-off to 4 only marginally improved performance. Caution is warranted to ensure efficient screening and follow-up interventions. 


J. DE GELDER, J.a. LUCKE (Haarlem, The Netherlands), L.c. BLOMAARD, E HAENEN, R.a.j. SMIT, H.g. KLOP, K. MESRI, B. DE GROOT, A.j. FOGTELOO, S ANTEN, G.j. BLAUW, S.p. MOOIJAART
E-Poster Area

"Tuesday 26 September"

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PH4 - S5
10:45 - 11:05

E-Poster Highlight Session 4 - Screen 5

10:45 - 10:50 #10841 - How often does troponin elevation identify acute myocardial infarction in the Emergency Department in the United States?
How often does troponin elevation identify acute myocardial infarction in the Emergency Department in the United States?

Background: Cardiac troponin I (cTnI) is widely measured in Emergency Department (ED) patients (up to14% of all) having any suspicion of possible Acute Myocardial Infarction (AMI). However cTnI can be elevated in a multitude of clinical scenarios other than the thrombotic occlusion of a coronary artery, such as tachycardia, heart failure, sepsis, pulmonary embolism, renal failure, stroke and others. The objective of this study was to determine how often elevated cTnI, at various levels, is associated with a final diagnosis of AMI.

Methods: Adult ED patients being evaluated for possible AMI were prospectively enrolled (from May, 2013 through April 2015) in a single urban center study in the United States (US). Exclusion criteria included acute trauma, distress requiring immediate life-saving intervention, cardioversion or defibrillation or receiving thrombolytic therapy within 24 hours, STEMI requiring immediate reperfusion, pregnancy or breast feeding, and if previously enrolled in the study. Serial cTnI (Siemens Ultra cTnI) measurements were obtained with values > 0.04 ng/ml (99th %) considered to be elevated. The diagnosis of AMI was adjudicated by a cardiologist and an emergency medicine physician (with a 3rd cardiologist available if there was diagnosis disagreement) in accordance with the 3rd universal definition of AMI using all available clinical information obtained over the 30 days after the ED visit. The highest individual patient cTnI was utilized for the analysis and the cTnI values were divided into interquartile ranges.

Results: Of the 569 patients enrolled 116 (20.4 %) had at least one cTnI > 0.04 ng/ml. Of these 72 (62.1%) had a non-AMI diagnosis while 44 (37.9 %) had a final AMI diagnosis. Baseline characteristics of these 2 groups showed no significant differences with the exception of higher medical history of prior revascularization, congestive heart failure and emphysema in those with AMI. Patients with lower cTnI levels (0.05-0.06 ng/ml) were unlikely to have AMI and the incidence of AMI increased with higher cTnI values (p< 0.001). The highest individual patient cTnI values were divided into interquartile ranges. The number of individuals in each quartile with AMI were: 0.05-0.06; 1 AMI (2.3%), 28 non-AMI; 0.07-0.10; 7 AMI (15.9%), 21 non-AMI: 0.11-0.67; 12 AMI (27.3%), 18 non-AMI:  and >0.68 ng/ml; 24 AMI (54.5%), 5 non-AMI. There were very few 30-day deaths (4/569, 0.7%) out of which 3 were non-cardiac in etiology.

Conclusions: cTnI is a highly sensitive biomarker aiding in the detection of myocardial cell damage. However, the majority (62.1%) of ED patients being evaluated for possible AMI and having at least one elevated cTnI (> 99th %) value did not have a final AMI diagnosis. However the incidence of adjudicated AMI diagnosis significantly increased with higher cTnI interquartile ranges. This trend will likely increase in the US with the current introduction of high sensitivity cardiac troponin assays.

 


Richard NOWAK (Detroit, USA), Tarun JAIN, Michele MOYER, Michael HUDSON, Gordon JACOBSEN, James MCCORD
10:50 - 10:55 #11091 - Patterns of ultrasound diaphragm function in infants with bronchiolitis: a prospective study.
Patterns of ultrasound diaphragm function in infants with bronchiolitis: a prospective study.

BACKGROUND

Ultrasonography allows direct observation of the diaphragm. Its thickness variation has been recently used to assess work of breathing in ventilated patients. In children, only one study describing diaphragm ultrasound findings in healthy children have been performed. We aimed to assess the diaphragmatic function in infants with bronchiolitis.

 

METHODS:

Prospective study of infants with bronchiolitis (first episode, aged 1-12 months) evaluated in a tertiary level pediatric emergency room. Infants with life threatening disease requiring immediate intervention, preterms, infants with with cardiac diseases or comorbidities or genetical disorders or disability were excluded. Diaphragm thickness was measured in the zone of apposition and the thickening fraction (TF) was calculated as (thickness at inspiration - thickness at expiration)/thickness at expiration per 100 (therefore expressed as percentage); the higher the values, the higher the respiratory effort of the child, while values ≤ 20% indicated diaphragm dysfunction. Diaphragm excursion (DE), Ti/Ttot (time of inspiration divided by total respiratory act time – the lower the value the longer the expiration time)  were calculated.

 

RESULTS:

61 infants were enrolled (mean age 83 days, IQR 60.5 – 180, males 50.1%). Bronchiolitis score was mild in 43.1%, moderate in 48.3%, severe in 8.6% cases. 19.7 % children were discharged, 80.3 % were admitted for a median length of 4 days (IQR 2-6.5). Respiratory Syncitial Virus was the most common etiological agent (47.4% cases). 27 children required no oxygen delivery, HFNC were started in 25 cases, among these 7 required CPAP, of these 2 required mechanical ventilation.

Mean TF was 47% (IQR 28.6-64.7), mean Ti/Ttot was 0.47 (± 0.15), mean DE was 10.39 mm (± 4)

Infants with severe bronchiolitis had lower TF than moderate (P 0.03), indicating diaphragm dysfunction, while those with moderate bronchiolitis showed the highest respiratory effort (highest TF). All children with lower values of TF required HFNC and one of them required CPAP. There was a linear correlation between TF and oxygen saturation (P 0.013).

Children with severe bronchiolitis had higher DE and lower Ti/Ttot compared with those with mild bronchiolitis, even though statistically significant differences were not reached probably due to low numbers of patients evaluated.

The higher the eco score the higher DE (P < 0.05).

These parameters did not significantly correlate with length of admission and type of respiratory support, while correlated with length of HFNC support.

 

CONCLUSIONS:

For the first time to our knowledge, this study provides reference values for DE, TF and Ti/Ttot in otherwise healthy infants with bronchiolitis. TF seems a promising parameter to predict those infants that might require respiratory support. Further studies are needed to understand which one of these parameters may predict need of respiratory support and admission.


Danilo BUONSENSO, Maria Chiara SUPINO, Antonino REALE, Emanuele GIGLIONI, Massimo BATTAGLIA, Simona SCATENI, Alessia MESTURINO, Barbara SCIALANGA, Nicola PIROZZI, Anna Maria Caterina MUSOLINO (rome, Italy)
10:55 - 11:00 #11623 - The Diagnostic Value of Novamed’s Sens-a-Heart Rapid Assay in Patients with Definite and Possible ACS.
The Diagnostic Value of Novamed’s Sens-a-Heart Rapid Assay in Patients with Definite and Possible ACS.

Background:

Sensitivity, specificity, and precision of the various commercially available troponin assays vary considerably. Sens-a-Heart is a novel rapid test using a combination of biomarkers, which provides a yes/no answer within 15 minutes using a single droplet of blood.

 

Aims:

The purpose of this study was to evaluate diagnostic accuracy of rapid Sens-a-Heart testing in patients with definite or possible ACS.

 

Methods:

The Sens-a-Heart test was performed in 191consecutive pts with definite or possible ACS admitted to departments of Hadassah Medical Center (Jerusalem) from 01.09.2015 till 31.03.2017. Initial troponin evaluation and simultaneous Sens-a-Heart testing were done under the ESC and ACC consensus guidelines.

 

Results:

Final diagnosis of ACS was established in 124 (65%), nonischemic heart disease documented in 3 (1.5%) and noncardiac disease in 64 (33.5%) of patients.

 

The Sens-a-Heart test was highly sensitive to coronary events. (77% of cases vs standard Hadassah troponin test which revealed 67% of cases).

 

The Sens-a-Heart test is also has high specificity for ACS. (96% vs 94% in Hadassah troponin test). Upon combining of both test results a higher sensitivity is achieved (86% sensitivity with specificity of 90%).

 

Table 1.

 

Roche ultra-sensitive troponin T test (Hadassah)

Sens-a-Heart Rapid Assay (Novamed)

Combined results (Sens-a-Heart + Hadassah’s Troponin)

Sensitivity

67%

77%

86%

Specificity

94%

96%

90%

 

 

Roche ultra-sensitive troponin T test (Hadassah)

Sens-a-Heart Rapid Assay (Novamed)

Combined results (Sens-a-Heart + Hadassah’s Troponin)

Sensitivity

67%

77%

86%

Specificity

94%

96%

90%

 

Conclusion: Novamed’s Sens-a-Heart Rapid Assay has prominent diagnostic sensitivity and specificity in patients with ACS in a very short time.

 


Ahmad NAMA (Jerusalem, Israel)
11:00 - 11:05 #11665 - Quick SOFA scores predict mortality in adult emergency department patients with and without suspected infection.
Quick SOFA scores predict mortality in adult emergency department patients with and without suspected infection.

Introduction :

The quick sequential Organ Failure Assessment scores (q SOFA) may identify patients with infection who are at risk of complications .We determined the correlation between q SOFA scores and mortality in adult emergency department (ED) patients with and without infection.

Methods:

We performed a prospective and descriptive study of all adult patients admitted to the ED between February 2017 to March 2017. We calculated the qSOFA for all patients on admission .We study the correlation between q SOFA scores and inpatient mortality (intra hospital and 2 weeks mortality )

Results:

We included 153 patients. Mean age was 60±7 years old. 34 % were female and 66% were male. Hypertension and diabetes are the frequent associated disease (46, 2% and 37, 8% respectively) Different diagnosis are defined, the most frequent are coronary disease (35 %) and pneumonia (27%).  Septic patients are representing 43 % of patients .We studied the correlation between q SOFA scores and mortality. We find that when the q SOFA is less than 2 we have 1, 6% of mortality. and  when the q SOFA more than 2 the  mortality rate is  13% .We concluded a significant positive correlation between the Q sofa score and 2 weeks mortality ( p=0.04)

Conclusion:

QSOFA scores were associated with inpatient mortality, in adult ED patients likely to be admitted both with and without suspected infection and may be useful in predicting outcomes.


Houda NASRI (CHARTRES), Olfa DJEBBI, Rim HAMAMI, Yosra GUETARI, Dkhera HAMDI, Saloua MANSOURI, Khaled LAMINE
E-Poster Area
11:10

"Tuesday 26 September"

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A32
11:10 - 12:40

Cardiovascular (Cutting Edge)

Moderators: Barbra BACKUS (Emergency Physician) (Rotterdam, The Netherlands), Szabolcs GAAL (Deputy head) (Budapest, Hungary)
Coordinator: Pr Rick BODY (Coordinator, Manchester)
11:10 - 11:40 What is the future of chest pain assessment? Moving beyond single biomarkers and dichotomous test results. Martin THAN (Speaker, New Zealand)
11:40 - 12:10 Make Endocarditis Great Again. Dr David CARR (Associate Professor of Emergency Medicine) (Speaker, Toronto Canada, Canada)
12:10 - 12:40 Management of Recent-onset Atrial Fibrillation and Flutter (RAFF): Time for the ED to take Control. Ian STIELL (Physician) (Speaker, Ottawa, Canada)
Trianti Hall

"Tuesday 26 September"

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B32
11:10 - 12:40

SonoOlympics-Ultrasound in the cradle of civilization
The ultimative and interactive ultrasound competition

Moderators: James CONNOLLY (Consultant) (Newcastle-Upon-Tyne), Riccardo LETO (Emergency physician) (Genk, Belgium), Senad TABAKOVIC (Medical director emergency department) (Zürich, Switzerland)
Coordinator: Senad TABAKOVIC (Coordinator, Zürich, Switzerland)
Keynote Speaker: Hein LAMPRECHT (Keynote Speaker, South Africa)
Mitropoulos

"Tuesday 26 September"

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C32
11:10 - 12:40

Neurological (How To)

Moderators: Vassilios GROSSOMANIDES (Greece), Christian HOHENSTEIN (PHYSICIAN) (BAD BERKA, Germany)
Coordinator: Christian HOHENSTEIN (Coordinator, BAD BERKA, Germany)
11:10 - 11:40 Stroke. Carsten KLINGNER (Speaker, Germany)
11:40 - 12:10 SAH. Jeff PERRY (Physician) (Speaker, Ottawa, Canada)
12:10 - 12:40 Damned If you do, damned If you don’t – Malpractice in stroke care. Greg HENRY (Speaker, USA)
Banqueting Hall

"Tuesday 26 September"

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D32
11:10 - 12:40

YEMD - WLB
Health & Wellbeing

Moderators: Alice HUTIN (PH) (Paris, France), Judith TINTINALLI (Professor) (Chapel Hill NC, USA)
Coordinator: Basak YILMAZ (Coordinator, BURDUR, Turkey)
11:10 - 11:30 Sleep deprivation and physical issues in emergency physicians. Laura HOWARD (Speaker, United Kingdom)
11:30 - 11:50 Is Emergency Medicine a job good for a lifetime? Roberta PETRINO (Head of department) (Speaker, Italie, Italy)
11:50 - 12:10 How to make an ED attractive to young doctors. Judith TINTINALLI (Professor) (Speaker, Chapel Hill NC, USA)
12:10 - 12:30 Can we get over the sadness in Emergency Medicine? Tatjana RAJKOVIC (Speaker, NIS, Serbia)
Skalkotas

"Tuesday 26 September"

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E32
11:10 - 12:40

Nursing session 2
Detection of Family Maltreatment at the Emergency Department

Moderators: Thomas DREHER-HUMMEL (Nurse) (Basel, Switzerland), Door LAUWAERT (Manager) (BRUSSELS, Belgium)
11:10 - 11:30 Detection of child maltreatment: screening in the Emergency Departments. Henriette MOLL (paediatrician) (Speaker, rotterdam, The Netherlands)
11:30 - 11:50 A new successful method for detecting child maltreatment based on parental characteristics. Hester DIDERICH-LOLKES DE BEER (policy officer family maltreatment) (Speaker, THE HAGUE, The Netherlands)
11:50 - 12:10 Implementation with the help of mandated training and e-learning. Marielle DEKKER (Speaker, The Netherlands)
12:10 - 12:30 Detection of Elderly maltreatment. Sivera BERBEN (research coordinator) (Speaker, Nijmegen, The Netherlands)
MC-3

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F32
11:10 - 12:40

Free Papers Session 9

Moderators: Anthony GERASKLIS (Greece), Felix LORANG (Consultant) (Erfurt, Germany)
11:10 - 11:20 #10724 - OP073 Management of Coronary Artery Disease in Emergency Phase: Experiences of Iranian Patients.
OP073 Management of Coronary Artery Disease in Emergency Phase: Experiences of Iranian Patients.

Background:

Coronary Artery Disease (CAD) is one of the major causes of death. Evidence suggests that some preventive measures by patients in emergency phase can reduce the rate and risk of mortality. Thus, understanding the signs and risk factors of CAD from the patients’ perspective and their ways of dealing with this disease is of vital importance.

Objectives: This qualitative study aimed to explore the Iranian patients’ experiences about CAD and how they manage it in their first encounter.

Patients and Methods: This study was a grounded theory study conducted on 18 patients with CAD. The data were collected through semi-structured interviews. Initially, purposeful sampling was performed followed by maximum variety. Sampling continued until data saturation. Then, all the interviews were recorded and transcribed verbatim. After all, the data were analyzed by constant comparative analysis using MAXQUDA2010 software.

Results:

The themes manifested in this phase of disease included 1- "Invasion of Disease"  with subthemes of "warning signs" and "risk factors", 2- "Patients’ Primary Challenges" with subthemes of "doubting primary diagnosis and treatment", and feeling of being different from others", 3- "Psychological Issues" with subthemes of "mental preoccupation", "fear of death and surgical intervention", "stress due to recurrence",  and "anxiety and depression", 4- "Management Strategies" with subthemes of "seeking for information", "follow-up' , and "control measures".

Conclusions: Based on the results, physicians and nurses should focus on empowerment of patients by facilitating this process as well as by educating them with regards to dealing with CAD. Further, it is also essential for the mass media to educate the public on how to treat patients with CAD.

Key words: Management, Coronary Artery Disease, Emergency Phase, Grounded theory, Iran 


Hossein KARIMI MOONAGHI (Mashhad, Islamic Republic of Iran), Mohammad MOJALLI
11:20 - 11:30 #10853 - OP074 Positive feedback with Human Factors - Does it matter in an Emergency Department ?
OP074 Positive feedback with Human Factors - Does it matter in an Emergency Department ?

Background: Our Emergency department at New Queen Elizabeth Hospital in Birmingham is one of the busiest Major Trauma Centres in UK with around 250 staff with annual attendances of more than 100,000 patients. The issues of work load, space, staffing level and performance makes it a challenging environment. A multidisciplinary teams are more likely to perform better if they are made to feel appreciated and their good practices are acknowledged. 

Learning from excellence is a new concept. The positive feedbacks are widely used in education for children and by corporate non- medical institutions. We wanted to explore its role in adult education and behaviour in the medical background. It’s very rare we recognise, celebrate and learn from good practice in the current working climate. The feedback had to timely, genuine, reflective, meaningful, specific and consistent. A template of a positive feedback along with specific local human factors framework (modification of NOTECHS II system) was developed based on the previous work on Favourable Event Reporting Form (FERF). The Human factors were analysed under the following topics- Leadership & management, Team building & cooperation, Problem solving and decision making, Situational awareness and environment. 

The new initiative of positive feedback forms were introduced to the entire medical, Nursing and managerial staff in the emergency department. We organised few educational sessions for all the staff. The project went live three months ago in January 2017. We chose the option of hard copies rather than the online version to capture more data.

Analysis and results: We had sixty positive feedback forms form last three months. The returned forms were reviewed and analysed by Non-Emergency department staff to minimise the bias. The common theme was that the staff felt more appreciated and acknowledged. The newly appointed staff felt more welcome and seemed to understand the expectation of their new working environment. Interestingly we also found that the staff would highlight the issues such as staff shortages and process on a feedback form. This has enabled the senior management to respond immediately to appoint more staff and emphasise/encourage on process to improve performance. It also shared the exemplary practice of certain staff highlighting their leadership skills, situational awareness and decision making process in a high pressure environment. The forms also were beneficial for all the staff as a part of their yearly appraisal. The staff felt supported during difficult times regardless of role or grade.A short staff survey is also planned following the implementation. The feedbacks are now a regular part of clinical governance structure .

In summary, the positive feedback forms are a valuable tool in adult education, behaviour and performance of a multidisciplinary team. The positive feedback reinforces good practice and encourages positive self- esteem among the various members of the team. 


Umesh SALANKE (Birmingham, United Kingdom), June SARGEANT, Tracey CLATWORTHY, Fran IVES
11:30 - 11:40 #10891 - OP075 Fast Track in the Emergency Department: an effective measure?
OP075 Fast Track in the Emergency Department: an effective measure?

Introduction: The increase in attendance of Emergency Department is responsible of a real problem of flow management. The implementation of a Fast Track (FT) is one of the organizational measures to improve this flow and thus to reduce the length of stay of daily patients. The aim of this study was to evaluate the effectiveness of implementation of a non-traumatologic FT (a trauma FT already existing) in our ED, and also to evaluate the staff’s satisfaction with the establishment of this procedure and the number of orientation errors.

Methods: We present here a prospective and observationnal study over a period of three months (winter 2015-2016) in an academic French ED. A total of 258 patients who received in FT were included in the study. This cohort was compared with a control group that consulted a year previously during the same period and who could have been eligible for care in the FT.

Results: Our study showed a significant reduction of ED length of stay of patients referred to FT (95.5 min for the FT group versus 141 min for the control group, p<0.0001) and a significant decrease in patients left without care by 6,1% (1.1% for FT group versus 2.8% for the control group, p=0.01). The rate of errors of orientation in patients initially referred to FT who had to be reoriented to the standard care system was 3,3% (95%CI: [3.2-3.4]). The implantation of this Fast Track was a measure deemed satisfactory by the paramedical ED teams with a score of 3.65 ±0.57 out of a total of 4 and in a more nuanced way by the medical teams with a satisfaction noted at 2.58 ±1.24 out of 4. In spite of the relative satisfaction of both paramedical and medical teams, our study also highlights the problem of ED utilization by patients with minor complaints.

Conclusion: Establishing a Fast Track in the ED could be one of the answer to reduce the length of stay of patients present with minor complaints. Organizational measures such as adequacy between the working hours of the FT and those of the physician responsible for it or the improvement of the computer tool (DxCare®) would make it possible to improve its functioning. The establishment of a FT was a satisfactory measure by paramedical and medical ED teams and significantly reduced the time taken to manage patients with non-urgent complaints.


Fanny SCHWEITZER, Claire KAM, Carmen HAMMANN, Céline RENFER, Sarah UGÉ (Strasbourg), Gabriella PINTEA, Pierrick LE BORGNE, Pascal BILBAULT
11:40 - 11:50 #11184 - OP076 Moderate to high complexity patients use the majority of resources in the emergency department - a modified TDABC analysis of ED utilization by RETTS category.
OP076 Moderate to high complexity patients use the majority of resources in the emergency department - a modified TDABC analysis of ED utilization by RETTS category.

Background Emergency department crowding and poor flow has been shown to lead to both poor clinical outcomes and poor patient experience.  As such, improving ED care is usually important to policymakers, but which visits should be highest priority to address is often controversial.  Many interventions to improve ED flow are focused on low-acuity, “fast-track” or primary care type patients, but it is not clear that these patients are the biggest drivers of ED crowding. Using a previously-developed Patient Encounter Costing (PEC) system, we show that simple triage level (RETTS in Sweden) can identify which patients drive ED utilization, and should be the key targets of improvement efforts.

Methods We used data from Region Halland, Sweden, a county of 300,000 people over 5,500 km2. We analyzed all 88,132 ED visits across 2 hospital-based ED sites in 2015.  These visits incurred total costs of 255 million Swedish Crowns (SEK), or approximately 26 million EUR. Time spent per visit was determined from prospectively recorded ED records, and resource adjusted by published weighting factors for nursing care by triage acuity level. We used PEC methods to determine unit-time costs for ED care, which were then used to determine total ED patient-care costs for each visit. These data were aggregated at the triage (RETTS) level, showing the variation by triage score.

Results In 2015, Region Halland spent 255 million SEK on its emergency departments, incurring unit costs of 1,645 SEK per nursing hour. This represents approximately 4% of total healthcare expenses in the region.  Patients were receiving care in a designated care space for a total of 262,705 hours.  The average ED visit service cost 2,886 SEK (95%CI 2,264-2,299). Average costs by RETTS level were: 650 SEK for triage level 5, 1 696 SEK for level 4, 2 824 SEK for level 3, 4 551 SEK for level 2, and 4 534 SEK for level 1.  In terms of total costs, 4% of total ED costs were spend on level 5 or uncoded visits, 9% on level 4, 47% on level 3, 34% on level 2, and 6% on level 1 patients.  ED treatment space utilization followed a similar pattern.

Conclusion 81% of ED costs, and 80% of total treatment-space utilization time, is spent on RETTS level 2 and 3 patients.  Interventions to improve ED throughput and resource utilization will be most effective if they focus on moderate to high-acuity and complexity patients, who often have multiple comorbidities and are at a higher risk of being admitted.  Low acuity and primary care oriented interventions are likely to have a more limited effect potential.


Zayed YASIN (Boston, USA), Jonathan SLUTZMAN, Magnus ROMELL, Jonas HULTGREN, Japneet KWATRA, Philip ANDERSON
11:50 - 12:00 #11270 - OP077 Nurse-led, physician-led or teamwork instead of triage: A longitudinal study of different triage processes and their impacts on patient flow at a busy emergency department.
OP077 Nurse-led, physician-led or teamwork instead of triage: A longitudinal study of different triage processes and their impacts on patient flow at a busy emergency department.

Objectives - To evaluate the impacts of two triage interventions compared to protocol-based comprehensive nurse-led triage on emergency department (ED) waiting times: senior physician-led triage and triage replaced by inter-professional teamwork in modules.

Design - A single center before-and-after study.

Setting – Conducted 2012.05.09 to 2015.11.11 at the adult ED of an urban county teaching hospital in Sweden, with 110 000 annual visits.

Participants – Registry data of patients arriving on weekdays 8 am to 9 pm during one year prior to the first intervention and one year immediately following each intervention.

Interventions - Senior physicians were reassigned to replace the triage nurses 8 am to 9 pm in the first intervention. In the second intervention, the triage section was abolished and replaced by inter-professional teamwork in modules.

Main outcome measures – Primary outcomes were the median total length-of-stay (LOS) and time to physician (TTP). Secondary outcome was the proportion of patients who left before treatment completed (LBTC).

Results – When senior physicians replaced the triage nurses, the median TTP plunged from 119 (95% CI; 117 to 120) to 57 min (95 % CI; 56 to 58). However, the median LOS increased from 236 (95% CI; 235 to 238) to 258 min (95 % CI; 256 to 260). When triage was abolished during teamwork in modules, the median LOS decreased to 229 min (95 % CI; 227 to 231). The median TTP was increased to 74 min (95 % CI; 73 to 76), yet 45 min shorter than during nurse-led triage. The LBTC rate increased over time: 2.5 % for nurse-led, 2.7 % for physician-led and 4.0 % for no triage during teamwork in modules. All differences in outcome measures were statistically significant with p-values < 0.001, except the non-significant difference in LBTC rate between nurse-led and physician-led triage.

Conclusions - Inter-professional teamwork in modules replacing triage performed the shortest LOS and may be an approach to cut waiting times in large busy EDs.


Jenny LIU (Stockholm, Sweden), Sari PONZER, Italo MASIELLO, Nasim FARROKHNIA
12:00 - 12:10 #11289 - OP078 "I am the Boss“ – Leading ad hoc teams in the shock room.
OP078 "I am the Boss“ – Leading ad hoc teams in the shock room.

Background

Teams in the shock room (SR) usually are so-called „ad hoc teams”: They randomly convene to fulfill an ambitious task under time pressure with limited information and usually leave the scene as soon as this task is completed. What are the essential requirements to lead such a team? What can help to reach excellence as team leader in the SR?

Methods

We searched in the medical literature for the expressions team leading / team leader / team coordinator and emergency medicine. Moreover we conducted a survey with experienced consultants in our Emergency Department, who regularly work as team leaders, asking them to tell us their challenges, but also tips and tricks for reaching high performance in the SR.

Results

Structure is often mentioned as important factor for high performance in the SR in the literature. This includes a briefing before the patient arrives, hands-off during handover, standards like the ABCDE and CRM (crisis research management) criteria or non-technical skills, and team debriefing after completion of the task. Additionally team resilience or high-performance teams can be found  in the literature as important factors for high-quality teamwork. These terms primarily stem from other highly dynamic industries outside of healthcare like nuclear power plants or aviation.

In interviews with experienced emergency physicians who regularly work as team leaders in the shock rooms, they stressed the importance of pre-existing structures and standards, which should be implemented by an experienced emergency physician as team leader. As examples the “ABCDE” and CRM principles are mentioned. Many of the emergency physicians expressed being challenged by their colleagues from anaesthesiology or surgery. “Risk factors” for losing the lead in the SR are being inexperienced, junior, short or female, having a low voice or the wrong position in the room. In order to clarify their role and responsibility, ED consultants mention good visibility by wearing a coloured jacket defining them as team leader, using a footstool, developing a strong voice or knowing the names and functions of all involved team members. They emphasize the importance of Interdisciplinary and interprofessional in-situ simulation training for developing standards of collaboration and shared mental models.

Discussion

Team leading in the shock room is extremely challenging: an ad-hoc team must collaborate in a highly dynamic situation with many uncertainties. Excellence as team leader not only depends on the team leader who must be highly competent in content, coordination and communication, but also on clear structures and standards. In order toe be prepared for often “unpreparable” situations, simulation training with all team members helps to reach excellence of care for patients whose survival often depends on high team performance.


Dr Monika BRODMANN MAEDER (Bern, Switzerland), Thomas SAUTER, Wolf HAUTZ, Aristomenis EXADAKTYLOS
12:10 - 12:20 #11968 - OP079 IMMIGRATION PROBLEM IN GREECE, Emergency Medical System Management.
OP079 IMMIGRATION PROBLEM IN GREECE, Emergency Medical System Management.

INTRODUCTION

Over 10,000 refugees lost their lives in the Mediterranean since 2016 in their endeavor to reach the European Union (EU), first half of 2016 there were 2809 deaths

Immigration, most important problem in the world today & a purely human challenge for all stakeholders, especially the EMS in GREECE, as national first responder.

The large flow of refugees into our country, through the Aegean islands, has created great challenges, in the field of health.

SCOPE-METHOD

In 2015, Greece, the main point of entry into the EU for refugees and immigrants from Turkey. It is estimated that 850,000 people attempted the dangerous passage of the Aegean Sea.

47,000 refs remained in Greece. Most of them (90%), originate from Syria, Iraq, Afghanistan. Among them people with severe health problems, pregnant women, infants.

The management of the severely ill amongst refugees based on a survival chain starting at the pre-hospital level, often at the site of arrival, and ends at the definitive care.

The role of EKAB, especially in the specific geographical relief of Greece, is particularly critical for the survival of people in distress.

Refugee-related diseases are unexpectedly severe, complex due to the difficulties of their situation: the extreme events of war; long-distance travel; lack of available medication for chronic pathologies; malnutrition; or the existence of past injuries. This vulnerable population, often consisting of infants and elderly, have reduced reserves in injury & sickness

CHARACTERISTICS

Children, 48% of the refugee population; men 30% & 22% women. 10% of refugees in Greece are 2 to 4 years old, 14% are aged between 5 and 9 years, 11% are aged 10 to 14 years old

MD in  small islands deal with an emergency patient among POPULATIONS ON THE MOVE in remote areas, in the absence of proper medical equipment in a small regional clinic on a border island and is able only to offer Initial stabilization and nothing  more. Afterwards the EKAB system ensures the transfer of the patient to a definitive care Centre.

 DATA

 Aeromedical Department of EKAB archives:

2016: Emergency Transfers by the Aeromedical Department numbered 46, involving newly arrived seriously-ill refugees. Of these 46 patients, 17 were infants with res/ry distress; another 7 were children (1.5 to 12 ys ) suffering from various infections, burns, choking, swallowing of foreign bodies. 72% male & 28% female. Syrians comprised 64% of the pts; Afghans 20%; Iraqis 12%; and Kurds, Iranians etc. Athens was the destination for 34 patients; 5 were sent to Crete; 7 to peripheral hospitals. AIRBORNE TRANSPORT was carried out in cooperation with the Greek Air Force C27 and C130 planes H/Ps: Chinook, Super Puma. The choice was based on geographic distances, availability of appropriate landing facilities, and local meteorological conditions.

The experience of air transport provides the opportunity for prompt intervention and better management of vulnerable patients involved in a mass migration event.


Jimi JIANNOUSI (ATHENS, Greece), Spyros PAPANIKOLAOU, Spiros DIMITROPOULOS, George PERDIKOGIANNIS, Dionysios KOUSKOUS
12:20 - 12:30 #10980 - OP080 Non-specific abdominal pain and readmissions in a high-volume emergency department.
OP080 Non-specific abdominal pain and readmissions in a high-volume emergency department.

Background

Acute abdominal pain is among the most common reasons for emergency department (ED) admissions. As abdominal symptoms are often vague, intermittent and non-specific, it may be difficult to distinguish non-specific conditions from specific and possibly severe conditions. Consequently, second admission to ED may be required to reach a diagnosis. As delay in diagnostics may lead to poor outcomes (including higher morbidity, mortality, prolonged hospitalization and higher costs of care), readmission rate has been one of the parameters used to evaluate the quality of care. While it has been well recorded and studied in elective surgery, the studies are few in the field of emergency medicine.

During the recent years in Finland, the emergency services have been reorganized and a new specialty of emergency medicine has been established. Emergency physicians have obtained a major role in EDs. Our aim was to evaluate the care, diagnostic accuracy and rate of readmissions in patients admitted to ED due to non-specific abdominal pain (NSAP) during the era of former and new ED organization.

Materials and Methods

All patients discharged with the diagnosis of NSAP during 2015 (former ED organization) and 2016 (new ED organization) in Tampere University Hospital were registered. Out of these, all patients readmitted to ED within 48 hours from the index admission with the diagnosis of NSAP or pelvic pain (ICD-10 codes R10.0, R10.1, R10.3 and R10.4) were included in the study. Planned readmissions were excluded. The number and reasons for readmissions, diagnostic accuracy and examinations performed were registered, and the findings between the two time periods were compared.

Results

Out of a total of 173,630 ED admissions, 10,609 patients (6%) were discharged with the diagnosis of NSAP. Median age was 32 years (range 0-98) and 60% were female. 313 of these (1.2%; median age 32 years (range 0-98), 59.8% female) were readmitted to ED within 48 hours. The readmission rate was highest (4.1%) among patients aged 18 years or less. Non-specific diagnoses were significantly less common in 2016 than in 2015 (n=7.1% vs. 5.2%, p<0.001). However, the rate of readmissions remained similar (3.0% vs. 2.9%, p=0.975). Again, the rate of computed tomography and ultrasonography remained equal. An improvement in the diagnostic accuracy was noted especially in patients with acute cholecystitis, which was the single most important reason (n=16; 9.4%) for ED readmissions during 2015.

Conclusions

Readmission rate among patients discharged from ED with the diagnosis of NSAP was surprisingly low. After the ED organizational change in our hospital the diagnostic accuracy during the index admission has improved, but no reduction in the rate of readmissions has been observed. Better availability of radiological imaging may have reduced the misdiagnoses of some conditions, such as acute cholecystitis.


Leena SAARISTO (Tampere, Finland), Mika UKKONEN, Johanna LAUKKARINEN, Satu-Liisa PAUNIAHO
12:30 - 12:40 #11029 - OP081 What are the factors that affect the institution of ceilings of treatment in the emergency department?
OP081 What are the factors that affect the institution of ceilings of treatment in the emergency department?

BACKGROUND: Ceilings of treatment are crucial early decisions aimed at improving the quality of care for patients in whom they are deemed appropriate. Decision making concerning limitation of potentially life prolonging treatments is often challenging. Knowledge of end of life issues and decision making involved is lacking, and no research into ED ceiling of treatment decision making has been conducted in the UK. A qualitative approach is needed to expand the limited literature and validate transferability of research to current UK practice. AIMS: To determine the factors that influence the institution of ceilings of treatment for patients presenting critically ill to the Emergency Department. METHODS: This qualitative study used a phenomenological approach to explore attitudes and factors considered important in driving end-of-life decision making by ED consultants. Semi-structured interviews were conducted until data saturation was achieved (n=15). Participants were recruited via convenience sampling and represented 5 EDs in the West of Scotland. Interviews were audio recorded, transcribed verbatim, and thematic analysis was carried out using NVivo. A reflexive diary was kept throughout the data collection and analysis process, and emergent themes were returned to participants to validate findings. RESULTS: We present a model of factors that influence ceiling of treatment decisions making. It was found that acute clinical factors and patient specific factors lay the foundations of ceiling of treatment decisions. Such case-specific information is heavily contextualised by patient and family wishes, collateral information, anticipated outcome and whether the patient is accepted for higher care. This process flows through a ‘filter’ of cultural and environmental factors. The overarching nature of patient benefit was found to be of key importance, framing all aspects of ceiling of treatment institution. Ultimately, all decisions determining an appropriate ceiling of treatment for a given patient resulted in one of three common patient pathways: full escalation, ward-based care or palliative care initiation. CONCLUSIONS: To our knowledge, this is the first investigation of factors that affect ED ceiling-of-treatment decision making in the UK. Key factors identified included acute clinical factors, patient specific factors, patient and family wishes, anticipated outcome and eligibility for higher care. Together with cultural factors, environmental factors and collateral information factors, these key themes are framed by patient benefit to establish an appropriate level of treatment. This may have importance as an educational tool and can act as a guide for physicians making end-of-life decisions in the E.D. How different factors are combined, their weighting and influence on the decision to institute ceilings of treatment is variable. Clinicians should be cognizant of these factors and their associated biases when making these challenging decisions.


Nathan WALZL (Glasgow, United Kingdom), Jessica JAMESON, John KINSELLA, David LOWE
Kokkali
14:10

"Tuesday 26 September"

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A33
14:10 - 15:40

Infectious Disease & Sepsis (Cutting Edge)

Moderators: Kurt ANSEEUW (Medical doctor) (Antwerp, Belgium), Christoph DODT (Head of the Department) (München, Germany)
Coordinator: Christoph DODT (Coordinator, München, Germany)
14:10 - 14:40 The septic patient with meningitis. Jeff PERRY (Physician) (Speaker, Ottawa, Canada)
14:40 - 15:10 Most effective strategies to detect sepsis early. Pr Lisa KURLAND (speaker) (Speaker, Örebro, Sweden)
15:10 - 15:40 Septic arthritis and osteomyelitis in the ED. Dr Thomas BEATTIE (Senior lecturer) (Speaker, Edinburgh, United Kingdom)
Trianti Hall

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B33
14:10 - 15:40

Leadership (The Boss' Office)

Moderators: Raed ARAFAT (Romania), Robert LEACH (Head of Dept.) (BRUXELLES, Belgium)
Coordinator: Christoph DODT (Coordinator, München, Germany)
14:10 - 14:40 The value of team work. Michael RADEOS (Speaker, USA)
14:40 - 15:10 Effective & creative views of administrative power. Greg HENRY (Speaker, USA)
15:10 - 15:40 How to make the big jump forward -Tips & Tricks. Jan STROOBANTS (Head of the Emergency Department) (Speaker, Brecht, Belgium)
Mitropoulos

"Tuesday 26 September"

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C33
14:10 - 15:40

Cardiovascular (Game Changers)

Moderators: Basar CANDER (Turkey), Pr Martin MÖCKEL (Head of Department, Professor) (Berlin, Germany)
Coordinator: Pr Rick BODY (Coordinator, Manchester)
14:10 - 14:40 Development of a national care system for cardiac syncope. Szabolcs GAAL (Deputy head) (Speaker, Budapest, Hungary)
14:40 - 15:10 Troponins and point of care troponins: what every emergency physician needs to know. Martin THAN (Speaker, New Zealand)
15:10 - 15:40 Cardiovascular Killers: Aortic Dissection. Dr David CARR (Associate Professor of Emergency Medicine) (Speaker, Toronto Canada, Canada)
Banqueting Hall

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D33
14:10 - 15:40

YEMD - Current Issues

Moderators: Dean DE MEIRSMAN (Emergency medicine resident) (Geel, Belgium), Basak YILMAZ (Faculty) (BURDUR, Turkey)
Coordinator: Basak YILMAZ (Coordinator, BURDUR, Turkey)
14:10 - 14:40 Working in the ED of a Small Hospital: A Survival Guide. Eleni SALAKIDOU (Delegate) (Speaker, Heraklion, Greece)
14:40 - 15:10 Working in the ED of a Large Hospital: A Survival Guide. Incifer KANBUR (Assistant doctor) (Speaker, Istanbul, Turkey)
15:10 - 15:40 Working in the ED of a Hospital in war settings: A Survival Guide. Alba RIPOLL GALLARDO (Physician) (Speaker, Milan, Italy)
Skalkotas

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E33
14:10 - 15:40

Nursing session 3

Moderators: Stamatina IORDANOPOULOU (Greece), Door LAUWAERT (Manager) (BRUSSELS, Belgium)
14:10 - 14:40 A patient with malaria at the emergency department: a practice story. Christien VAN DER LINDEN (Clinical Epidemiologist) (Speaker, The Hague, The Netherlands)
14:40 - 15:10 Echoing away sepsis 2, welcoming sepsis 3. Georgios PAPAGEORGIOU (Nurse) (Speaker, Nicosia, Cyprus)
15:10 - 15:40 Hellenic Regulatory Body of Nurses: Project, "Health Education and Training in First Aids through the School, the Family, and the Community", 2014-2017. Tzannis POLYKANDRIOTIS (Speaker, Greece)
MC-3

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F33
14:10 - 15:40

Free Papers Session 10

Moderators: Pr Cem OKTAY (FACULTY) (ANTALYA, Turkey), Pr Riccardo PINI (Director, E.D. High Dependency Unit) (Florence, Italy)
14:10 - 14:20 #10835 - OP082 Acute kidney injury and mortality among patients with rhabdomyolysis.
OP082 Acute kidney injury and mortality among patients with rhabdomyolysis.

Acute kidney injury and mortality among patients with rhabdomyolysis

 Nielsen FE1,2, Cordtz J1,3, Rasmussen TB4, Christiansen CF4.

1Department of Emergency Medicine, Slagelse Hospital, Denmark. 2Institute of Regional Health Services Research, University of Southern Denmark. 3Department of Emergency Medicine, University Hospital of Zealand, Denmark. 4Department of Clinical Epidemiology, Aarhus University Hospital, Denmark.

 

Background

Acute kidney injury (AKI) is a life-threatening complication of rhabdomyolysis (RM). There is controversy if the degree of the initial creatine phosphokinase (CK) elevation is associated with the risk of AKI and death.

Purpose

To examine the risk of AKI, renal replacement therapy (RRT) and mortality among patients with RM and to evaluate the association between CK level and the risk of AKI, RRT and death.

Methods

Register-based study of adult patients admitted to hospitals in the region Zealand during November 1, 2011 to March 1, 2014 with CK levels higher than 1,000 U/L within 72 hours of admission. Information about CK and other laboratory data was obtained from a regional laboratory database. Data on medical history, medical treatment and survival were obtained from the Danish National Registry of Patients, the National Health Service Prescription Database and the Danish Civil Registration System. Patients with preexisting end-stage renal disease or acute myocardial infarction were excluded. AKI was defined according to Kidney Disease Improving Global Outcome. Logistic regression was used to compute odds-ratios (OR) with 95% confidence intervals (CI) comparing the risk of AKI, RRT and all-cause mortality according to CK-level adjusting for confounding.

Results

The study included 1,024 patients with a median age of 72.9 years. Median CK was 2,226 U/L, 831 (81.2%) patients with CK 1,000-5,000 U/L, 154 (15.0%) with CK 5,001-15,000 U/L and 39 (3.8%) with CK 15,001+ U/L. A total of 442 (43.2%) patients developed AKI within 30 days, and 42 (4.1%) required RRT during the first year. A total of 170 (16.7%) patients had died within 30 days and 277 (27.1%) had died within 365 days.  Twenty-seven (69.2%) patients with CK > 15,000 U/L developed AKI within 30 days compared to 62 patients (40.3%) patients with CK 5,000-15,000 U/L and 353 (42.5%) patients with CK < 5,000 U/L. Five (12.8%) patients with CK > 15,000 U/L required RRT within a year compared to 7 (4.6%) patients with CK 5,000-15,000 U/L and 30 (3.6%) patients with CK < 5,000 U/L. In multivariate analyses it was found that OR of AKI within 30 days was 2.6 (95% CI 0.9-7.3) and the OR of RRT within one year was 3.0 (95% CI 0.8-10.9) among patients with CK +15,000 U/L (CK < 5,000 U/L as reference). The CK level was not associated with the risk of death.

Conclusion

Our initial analyses showed that elevated initial CK values was not associated with death. However, elevated CK values was associated with increased risk of AKI and RRT, although estimates were statistically imprecise.


Finn Erland NIELSEN (Aarhus, Denmark), Cordtz JOAKIM, Rasmussen THOMAS, Christian CHRISTIANSEN
14:20 - 14:30 #10907 - OP083 Emergency Department Utilization among Kidney Transplant Recipients in the United States.
OP083 Emergency Department Utilization among Kidney Transplant Recipients in the United States.

Introduction: Patients with End Stage Renal Disease (ESRD) use the emergency department (ED) at a 6-fold higher rate than U.S. adults.  No national studies have described ED utilization rates among kidney transplant (KTx) recipients, and the factors associated with higher ED utilization. A more definitive understanding of the trends, causes, and outcomes of ED utilization among KTx patients is necessary to identify the potentially modifiable factors and to identify opportunities for better care coordination, lower resource utilization, and improved quality of care. 

Methods: We examined a cohort of 132,725 incident adult KTx recipients in the United States Renal Data System, a comprehensive national database of ESRD patients in the US, from 2005-2013.  ED use, hospital admission, and diagnoses were obtained from the Medicare Physician/Supplier and Inpatient databases.  Multivariable Poisson regression was conducted to assess the association of relevant patient variables with each of the primary and secondary endpoints where appropriate. 

Results: Nearly half (46.1%) of KTx patients had at least one ED visit within the first post-transplant year (1.61 ED visits/patient year); 39.7% of ED utilizers were hospitalized in the first year post-transplant. ED visit rate was high in the first 30 days (5.26 visits/person year), but declined substantially thereafter (1.81 visits/person year (PY) in months 1-3; 1.13 visits/PY in months 3-12 post-transplant) (Figure 1). In multivariable analysis, factors associated with a lower ED utilization rate included preemptive transplantation (RR: 0.770, 95% CI: 0.751-0.790), peritoneal dialysis (RR: 0.859, 95% CI:  0.843-0.875), private insurance coverage, and transplant at high-volume centers (>200 transplants/year). Predictors of higher ED utilization rate included older age (RR: 1.010, 95% CI: 1.005-1.015 per 10 years), female sex (RR: 1.173, 95% CI: 1.159-1.187), comorbid medical conditions, Medicaid or Medicare insurance coverage, higher proportion of neighborhood poverty (RR: 1.002, 95% CI 1.001-1.002), longer dialysis vintage (RR: 1.302, 95% CI: 1.271-1.333 per 10 years), older donor age (RR: 1.002, 95% CI: 1.002-1.003, greater degree of HLA mismatch, longer index hospitalization (RR: 1.004, (%% CI: 1.004-1.004), delayed graft function (RR: 1.268, 95% CI: 1.251-1.285).  

Conclusions: ED utilization for KTx patients is three-fold higher than the general population, but less than half the rate for ESRD patients on dialysis. Policies and strategies addressing preventable ED visits have high potential for improvement and savings


Brendan LOVASIK, Justin SCHRAGER (Atlanta, USA), Rachel PATZER
14:30 - 14:40 #11548 - OP084 Short-term exposure to breathable particulate matter and stroke incidence.
OP084 Short-term exposure to breathable particulate matter and stroke incidence.

Introduction and objective:

Particulate matter (PM) with particle sizes less than 10 microns, which are known as breathable suspended particulates, can get deep into the lungs and cause a broad range of health effects, respiratory and cardiovascular particularly. Studies confirmed a strong association between air concentrations of PM and cardiovascular disease. On the other hand, it is still unclear if exposure to breathable (size 10 microns or less) PM leads to stroke events and whether the timing of exposure is associated with stroke risk. In this study we examined the association between occurrence of stroke and respirable PM air concentration.

Methods:

We retrospectively studied Emergency Department (ED) admission of acute stroke patients from Jan 2011 to Dec 2016. We registered occurrence of stroke compared to breathable PM (PM 10 and PM2.5) concentrations. Incidence of events was associated with PM levels on the day of onset and on the 3 days following PM elevation. PM concentrations were provided from local monitoring data from the Veneto Regional Agency for Prevention and Environmental Protection (ARPAV), classified accordingly with EU health based standards for pollutants in air (25 µg/m3 for PM2.5 and 50µg/m3 for PM10).

Results:

During the study period 2,590 stroke patients referred to our ED: 1,721 (66.4%) were ischemic and 869 (33.5%) were hemorrhagic. Gender (ischemic stroke: M: 49.3%; F: 51.7%; hemorrhagic stroke: M 51.6%; F: 48.4%) and age (ischemic stroke: 74 years, range: 18-102; hemorrhagic stroke: 68 years, range: 18-99) distribution were similar in the two groups. We did not observe any difference in stroke incidence with PM10 levels within or over the EU standards. PM2.5 air concentration over the EU standards revealed to be associated, acutely and on 3 following 3 days, with a higher incidence of ischemic stroke (+38.4%) and hemorrhagic stroke (+12.5%), compared to stroke events occurred on the within the EU standards PM2.5 levels days. Also in this case no age and gender differences were observed between the two study groups.

Conclusions:

Medical researches show that the risk for various health impacts increases with air particulate matter exposure but there is little evidence to suggest a threshold below which no adverse health effects would be anticipated. It has also been shown that the health risks would be higher for those particles with particle sizes of 2.5 microns or less, which are commonly referred to as fine suspended particles or PM2.5. Our study suggests that short-term exposure to elevated PM 2.5 is associate with a higher incidence of ischemic stroke whereas the association with hemorrhagic stroke is less clear.


Massimo ZANNONI (VERONA, Italy), Manuel CAPPELLARI, Gianni TURCATO, Lucia ANTOLINI, Alberto RIGATELLI, Giorgio RICCI
14:40 - 14:50 #11741 - OP085 Thrombolysis for Acute Ischemic Stroke in the Emergency Department(ED) is safe. comparative study : ED versus stroke unit.
OP085 Thrombolysis for Acute Ischemic Stroke in the Emergency Department(ED) is safe. comparative study : ED versus stroke unit.

Introduction : Stroke has a major impact on individual lives and the nation's health and economy. It is the third  cause of death in the world, and a major cause of adult disability. The therapeutic revolution has completely changed the functional and vital prognosis of patients with stroke due to reperfusion, and particular intravenous stroke thrombolysis with rt-PA. Because «  time is brain  », thrombolysis should be performed as early as possible. Istablishing specific neurovascular units may improve  the management of acute ischemic stroke. However, initiation of thrombolysis in the emergency room is still controversed.

Objective : The objective of this study is to compare the results of intravenous stroke thrombolysis performed in the ED versus that performed in the department of neurology in terms of delays, prognosis and complications .    

Methods : we made a  transversal analytical study in our ED during 2 years  . In this study we analysed all the patients alerted for thrombolysis. We made two groups (group 1 = thrombolysis performed in the ED and group 2 = thrombolysis performed in the neurology department). All patients underwent brain CT in the ED. All delays were noted, in particular the delay "door to needle". The NIHSS score before thrombolysis, H1, H6 and H24 post thrombolysis and the occurrence of hemorrhagic transformation were noted too.

Results : 520  patients were included, only 188 patients were alerted for thrombolysis protocol. 60 patients underwent thrombolysis divided into 2 groups : group 1 in the ED and group 2 in the neurology department. The mean age was 64±12 years in group 1 vs 67±13 years in group 2. There wis no great gender predominance in the 2 groups.The time onset to needle was 2h50±30mn in group1 and 4h10±20mn in group2( p=0.007). There is a significant difference in the mean door-to-needle time between 2 groups : 80±33mn in groupe 1 vs 173±39 in group2 (p=0.0001). There is no significant difference between 2 groups in NIHSS score (at admission,at H1 and H6 post thrombolysis) and  in good early outcome. The risk of intracerebral hemorrahge is more important in group 2than group 1 (10% vs 3% respectively with a significant difference p=0.004).

Conclusion : the beneficial effect of thrombolysis on mortality and functional outcome  in patients with acute ischemic stroke may be improved  when it is performed early and within the recommended delays.


Rabaa SABBEGH, Asma ZORGATI, Rim YOUSSEF, Chawki JEBALI, Riadh BOUKEF, Ali OUSJI (Sousse, Tunisia)
14:50 - 15:00 #10975 - OP086 Oligoanalgesia in the emergency department waiting room: predictive factors.
OP086 Oligoanalgesia in the emergency department waiting room: predictive factors.

Background

 

Pain is the leading symptom in emergency departments (ED). Due to overcrowding, some patients are oriented to the waiting room and their medical evaluation deferred.  In order to ease analgesia in the waiting room, we have enforced a dedicated pain management protocol allowing nurses to administer analgesia when indicated. The objectives of this study were: (1) to measure treatment administration to patients with documented pain upon arrival; (2) to identify predictors of non administration of pain treatment (oligoanalgesia) ; (3) to evaluate pain protocol adherence by nurses.

 

Methods

Prospective observational study in the ED of a primary and tertiary urban teaching hospital with an annual census of 68‘000 patients.  All patients with a pain score documented on arrival and oriented to the waiting room were eligible.  Demographic characteristics, pain severity scores (0 to 10), time delays, triage complaint and emergency level as well as medication use were extracted from the electronic patient records.  Univariate and multivariate analyses were performed to identify predictors of oligoanalgesia.

Results

During a three months period, 2’371 patients were included. Their mean age was 49 years and the majority were male (51%). The leading triage complaint was abdominal pain (30.3%). Pain treatment was given to 734 patients (31%). Treatment was more frequently administered (43%) for pain severity scores > 5 than for lower acuity scores (16%, p <.0001). Time to treatment was 60 minutes (IQR 20-121) and 16 minutes (IQR 7-40) for pain scores < 5 and > 5 respectively (p =.01). Patients with an initial pain score < 5 were treated in accordance to the nurses’ protocol in 73.1% of the cases. This rate dropped to 32% in patients with initial pain scores ≥ 5.

In multivariate analyses, risk predictors for non treatment of pain in the waiting room were:

age > 80 y (OR 2.32 ; 95% CI 1.49-3.60), admission by ambulance (OR 1.50 ; 95% CI 1.12-2.01), higher triage severity level (OR 1.67 ; 95% CI 1.32-2.11), initial pain score < 5 (OR 3.78 ; 95% CI 2.99-4.76), waiting room LOS < 30 minutes (OR 2.79 ; 95% CI 2.06-3.78). When compared to pain suggestive of renal colic, pain associated with a neurological complaint (OR 6.54; 95% CI 2.88-14.84) was the most important predictor for oligoanalgesia. In the multivariate model neither waiting room occupancy nor ED’s patients’ load were significantly associated with non treatment.

 

Conclusion

 

In the waiting room of our ED, the proportion of patients receiving pain medication is low.  Adherence to our pain protocol is insufficient. Older patients, patients with low intensity pain scores and presenting complaints other than renal colic are at higher risk of treatment abstention independently of emergency room workload. These patients should be targeted by specific interventions.


Mio GOBET (Geneva, Switzerland), Olivier RUTSCHMANN, Francois SARASIN, Villar ADOLFO, Bernard MUGNIER, Majd RAMLAWI
15:00 - 15:10 #11074 - OP087 Midazolam or haloperidol premedication in prevention of ketamine induced agitation in emergency department: A randomized double blind clinical trial.
OP087 Midazolam or haloperidol premedication in prevention of ketamine induced agitation in emergency department: A randomized double blind clinical trial.

Introduction: The effective and safe sedation for painful procedures in the emergency department is one of the principal concerns of emergency physicians. The sedative agent must be one with rapid onset, steady effects, quick recovery, and acceptable side-effects. Ketamine is an ideal sedative agent but emergency physicians are reluctant to use it due to fear of recovery agitation. It has been proposed to use other drugs specifically benzodiazepines as premedication to reduce the agitation.The goal of our study was to evaluate the effect of midazolam and haloperidol premedication on ketamine induced agitation, and also the emergency physician satisfaction with the procedure.

Method: This was a randomized double-blind placebo-controlled trial to assess the efficacy of ketamine premedication by midazolam or haloperidol, in reducing agitation incidence and severity. The study was approved by the university ethics committee. The samples were chosen from patients older than 18 of either sex who needed sedation in emergency department at Sina Hospital. Patients who had any contraindication to ketamine, midazolam or haloperidol were excluded.

Patients randomly allocated in 3 groups, Arm 1: patients received 2 intravenous injections of distilled water (1cc and 0.05 cc/kg) 5 minutes prior to receiving a sedative dose of 1 mg/kg IV ketamine.  Arm 2: patients received 2 intravenous injections, 1cc of distilled water and 0.05 mg/kg midazolam, 5 minutes prior to ketamine. Arm 3: patients received 2 intravenous injections, 0.05 cc/kg of distilled water and 5mg of haloperidol, 5 minutes prior to ketamine.

Level of sedation and agitation were assessed using RASS score (after 5, 15 and 30 minutes of ketamine injection) and Pittsburgh Agitation Scale. Also, physician satisfaction with the sedation procedure was evaluated using Clinician Sedation Satisfaction Index(CSSI).

 Results: 180 sample enrolled from July 2016 to March 2017.The incidence of Recovery Agitation, was 66% in the group that received no premedication and 20% in both groups that received premedication, whether midazolam or haloperidol (p<0.001). Also, agitation severity (mean PAS score of 3.37) in the group which only received ketamine was much higher in comparison to the other two groups (mean PAS score of 0.65 and .063) (p<0.001). The comparison between the two intervention groups (midazolam versus haloperidol) showed no significant difference in agitation severity (mean PAS score of 0.65 versus .063).The score of physician satisfaction was significantly higher in the field of reduced agitation in premedicated group (p<0.001).

Discussion: We found a significant reduction in recovery agitation of ketamine by using midazolam or haloperidol as premedication. Our results were similar to most previous studies about the effect of BZDs. However, few studies have been done about the effect of haloperidol on reducing ketamine induced agitation.

Trial registration: ClinicalTrials.gov NCT02909465


Narges AKHLAGHI (Tehran, Islamic Republic of Iran), Pooya PAYANDEMEHR, Mehdi YASERI, Ali ABDORAZAGH NEZHAD
15:10 - 15:20 #11098 - OP088 Retrospective chart review exploring safety profile of ketamine-propofol in the pediatric emergency room.
OP088 Retrospective chart review exploring safety profile of ketamine-propofol in the pediatric emergency room.

Background

Procedural sedation and analgesia (PSA) is routinely used in pediatric patients for painful procedures. The use of IV ketamine and propofol (‘ketofol’) for PSA is established in adult patients and has been shown to be safe and effective. The purpose of this study was to analyze the safety of ketofol in pediatric patients. 

Methods

This was a single-center retrospective study at a Canadian pediatric tertiary care centre. Patients were included if they were less than 18 years old at time of PSA, and received ketofol within the period January 1, 2011 to December 31, 2016. Adverse events, interventions and recovery times were captured.

Results

233 charts were analyzed, of which 163 met the inclusion criteria. 65% of the patients were male. 9% had an underlying medical condition, with 6% of all patients having asthma. The average age was 9.5 years (range 2 months to 18 years).

The indications for PSA using ketofol were usually fracture or joint reduction (63%) and laceration repair (18%). Other indications included plastics procedures (6%), lumbar puncture (4%), abscess incision and drainage (4%), burn/wound debridement (3%), and CT sedation (1%). The median procedure time was 13 minutes (interquartile range 8-22 minutes) and median time to recovery was 30 minutes (IQR 21-46 minutes).

The major adverse reaction experienced was hypoxia (10%) with resolution by conservative measures (stimulation, airway positioning and supplemental oxygen). Two cases with hypoxia required bag mask ventilation and none required intubation. Only one case had a severe adverse reaction (laryngospasm and hypotension), which resolved with supplemental oxygen, bag mask ventilation, and fluid bolus. 3% of cases had nausea or vomiting. No cases had hypersalivation, bradycardia, emergence reaction, or seizure. There was no relation to the dose of either ketamine or propofol to the observed adverse reactions. Three cases required re-sedation due to failure of previous sedation. Two of these cases failed intranasal sedation or local block and then received ketofol. Only one sedation failure was due to inadequate sedation from ketofol with repeat sedation requiring additional adjunct of midazolam.

Subgroup analysis on patients less than 24 months yielded no additional risk for adverse events or failed sedation.

Discussion

This is the largest study to date analyzing the safety profile of ketofol in the pediatric population. Overall, ketofol is a safe and effective combination for pediatric PSA. Major adverse effects were lower than previous smaller studies. Additionally, mean recovery time was similar to published literature.


Vidushi KHATRI, Mohammed ALROWAYSHED (Hamilton, Canada), Leanne PATEL, Angelica RIVAS, Patrick TANG, Rahim VALANI
15:20 - 15:30 #11233 - OP089 Low-dose Ketamine in association with IV morpnine for acute pain in emergency department.
OP089 Low-dose Ketamine in association with IV morpnine for acute pain in emergency department.

Background:

Acute pain is the most frequent complaint in emergency department (ED), but its management is often  complex, placing patients at risk of oligoanalgesia. Emergency physicians are considering alternative, complimentary medications, such as ketamine, combined with traditional drugs such as opioids to achieve multimodal analgesia in the acute setting.

The aim of this study was to determine the effectiveness of low-dose ketamine as an adjunct to morphine versus standard care with morphine alone for the treatment of acute moderate to severe pain among ED patients.

Methods:

We conducted a double-blind, randomized, placebo-controlled trial at the ED, over a six-month period. Eligibility criteria were: age between 18 and 65, acute moderate or severe pain (the numerical pain rating scale (NRS)>5) who require morphine. Patients were randomized on three study groups: standard group receiving morphine and normal saline placebo; group1 receiving morphine and 0.15 mg/kg ketamine and group2 receiving morphine and 0.3 mg/kg ketamine. Pain was assessed at 30, 60 and 120 minutes after drug administration; rescue analgesia consisting on 0.5mg/kg morphine was prescribed if the reduction of pain was lower than 50%. The occurrence of adverse events was also measured.

Results:

One hundred twenty patients were enrolled: 41 patients in standard group, 42 patients in both groups 1 and 2. There were no difference between the three groups in baseline NRS, as well as in the demographic and clinical characteristics. The most common cause of pain was nephritic colic in 50.4% of patients. NRS improvement was more important and rapid in group 2 compared to the other groups with a statistically significant difference at 120 minutes. The SPID was higher in ketamine’s groups compared to standard group. Among patients receiving rescue analgesia, 28 were in standard group, 24 in group1 and 5 in group2 (p<0.001). The total  dose of morphine was significantly greater in morphine group comparing to the ketamine groups. There was no difference in side effects between the three groups. More participants in the ketamine groups reported minor neuropsychiatric adverse effects  such as dysphoria and dizziness. Patients from placebo group developed more digestive events such as nausea and vomiting.

Conclusion:

Low doses of ketamine are well tolerated and present efficient analgesic effect in adjunction to morphine compared to morphine alone for pain management in ED. The dose of 0.3mg/kg seems more effective than 0.15 mg/kg but might cause more adverse neuropsychiatric events.


Khaoula RAMMEH, Hajer KRAIEM (Sousse, Tunisia), Sana MABSOUT, Majdi OMRI, Mariem KHROUF, Mehdi METHAMEM
15:30 - 15:40 #11234 - OP090 Low-dose Ketamine in association with IV morpnine for acute pain in emergency department.
OP090 Low-dose Ketamine in association with IV morpnine for acute pain in emergency department.

Background:

Acute pain is the most frequent complaint in emergency department (ED), but its management is often  complex, placing patients at risk of oligoanalgesia. Emergency physicians are considering alternative, complimentary medications, such as ketamine, combined with traditional drugs such as opioids to achieve multimodal analgesia in the acute setting.

The aim of this study was to determine the effectiveness of low-dose ketamine as an adjunct to morphine versus standard care with morphine alone for the treatment of acute moderate to severe pain among ED patients.

Methods:

We conducted a double-blind, randomized, placebo-controlled trial at the ED, over a six-month period. Eligibility criteria were: age between 18 and 65, acute moderate or severe pain (the numerical pain rating scale (NRS)>5) who require morphine. Patients were randomized on three study groups: standard group receiving morphine and normal saline placebo; group1 receiving morphine and 0.15 mg/kg ketamine and group2 receiving morphine and 0.3 mg/kg ketamine. Pain was assessed at 30, 60 and 120 minutes after drug administration; rescue analgesia consisting on 0.5mg/kg morphine was prescribed if the reduction of pain was lower than 50%. The occurrence of adverse events was also measured.

Results:

One hundred twenty five patients were enrolled: 41 patients in standard group, 42 patients in both groups 1 and 2. There were no difference between the three groups in baseline NRS, as well as in the demographic and clinical characteristics. The most common cause of pain was nephritic colic in 50.4% of patients. NRS improvement was more important and rapid in group 2 compared to the other groups with a statistically significant difference at 120 minutes. The SPID was higher in ketamine’s groups compared to standard group. Among patients receiving rescue analgesia, 28 were in standard group, 24 in group1 and 5 in group2 (p<0.001). The total  dose of morphine was significantly greater in morphine group comparing to the ketamine groups. There was no difference in side effects between the three groups. More participants in the ketamine groups reported minor neuropsychiatric adverse effects  such as dysphoria and dizziness. Patients from placebo group developed more digestive events such as nausea and vomiting.

Conclusion:

Low doses of ketamine are well tolerated and present efficient analgesic effect in adjunction to morphine compared to morphine alone for pain management in ED. The dose of 0.3mg/kg seems more effective than 0.15 mg/kg but might cause more adverse neuropsychiatric events.


Khaoula RAMMEH, Hajer KRAIEM (Sousse, Tunisia), Sana MABSOUT, Majdi OMRI, Mariem KHROUF, Mehdi METHAMEM
Kokkali
15:45

"Tuesday 26 September"

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PH5 - S1
15:45 - 16:05

E-Poster Highlight Session 5 - Screen 1

Moderators: Felix LORANG (Consultant) (Erfurt, Germany), Judith TINTINALLI (Professor) (Chapel Hill NC, USA)
15:45 - 15:50 #9803 - COPEPTIN, MYELOPEROXIDASE AND PRO-ADRENOMEDULLIN FOR CHEST PAIN IN CHRONIC RENAL FAILURE PATIENTS.
COPEPTIN, MYELOPEROXIDASE AND PRO-ADRENOMEDULLIN FOR CHEST PAIN IN CHRONIC RENAL FAILURE PATIENTS.

Objectives: Copeptin, Myeloperoxidase and Pro-adrenomedullin have emerged as potential biomarkers for diagnosis and prognosis of acute coronary syndrome. However, their applicability with chronic renal failures remains unknown as these patients were excluded from the previous studies. Our objective was to determine the superior novel cardiac marker to predict 30-day and 6-month adverse cardiac event (ACE) as defined as cardiac related death, myocardial infarction and ventricular fibrillation.

Methods: A prospective observational study was carried out. Patients were included if they presented to the ED with a chief complaint of chest pain and had chronic renal failure as defined as a serum creatinine of more than 130umol/L. Copeptin, Myeloperoxidase and Pro-adrenomedulin assays were performed. Occurrence of ACE was traced from review of the patients’ case records and checking of the registry of deaths.

Results: Seven hundred and twenty four patients were recruited with a median age of 67. 60.6% of the study population were male. 88.3% of the population had CKD stage 4 and 5, with 33.5% on dialysis. The rates of ACE at 30-day and 6-month were 15.1% and 21.7% respectively. All readings of the 3 biomarkers were not significantly different in patients with ACE compared to those without at both 30-day and 6-month. The AUCs for Copeptin, Myeloperoxidase and Pro-adrenomedullin are 0.53, 0.50 and 0.45 respectively (p all >0.05).

Conclusions: The performance the biomarkers was poor attributable to the lack of specificity for acute coronary syndrome as elevated levels could be due to other causes in patients with chronic renal disease. Routine testing cannot be recommended.


Jen Heng PEK (Singapore, Singapore), Swee Han LIM
15:50 - 15:55 #11138 - Finnish Prehospital Stroke Scale – a simple tool for paramedics for rapid detection of both thrombectomy and thrombolysis candidates.
Finnish Prehospital Stroke Scale – a simple tool for paramedics for rapid detection of both thrombectomy and thrombolysis candidates.

Background:
 
In ischemic stroke caused by a thrombosis of a large brain artery, IV-thrombolysis (IV-tPA) appears ineffective, while mechanical thrombectomy (MT) is reported to be a powerful tool to open the occlusion (1). However, the favorable effect of recanalization is highly time-dependent (2). Previously validated and generally used stroke signs (face-arm-leg-speech-visual disturbance) recognize stroke in general. Furthermore, conjugate eye deviation (CED) is highly related to large vessel occlusion (LVO). Currently, patients with suspected stroke are transported to the nearest hospital with facilities for IV-tPA but not necessarily for MT. Hence, this can cause significant treatment delay.  We hypothesized that combining general stroke signs with CED will produce an easy-to-use prehospital stroke scale for prehospital use by emergency medical services (EMS), recognizing both stroke in general and LVO separately.  Thus, unnecessary visits to non-tertiary hospitals could be avoided.
Methods: We retrospectively analyzed n=856 consecutive patients with prehospital Code Stroke (thrombolysis candidate). National Institutes of Health Stroke Scale (NIHSS) was executed on patient arrival. Computed tomography (CT) was performed for all patients and CT angiography based on clinical decision. With random forest analysis and deviance analysis of the general linear model we confirmed superiority of NIHSS ‘Best Gaze’ over other NIHSS items in LVO detection.

Results: NIHSS ‘Best Gaze’ had the best predictive value of NIHSS items in detecting LVO of the anterior circulation. Based on this and generally used stroke signs we presented Finnish Prehospital Stroke Scale (FPSS) including dichotomized face drooping, extremity weakness, speech difficulty, visual disturbance and CED.  “Face droop”, “extremity weakness”, “disturbed speech” and “disturbance of vision” give each one point while “forged or partial conjugated gaze deviation to one side” gives four points. FPSS with combined score values of 1-4 indicates a thrombolysis candidate whereas values 5-8 indicate a thrombectomy candidate.   FPSS detected LVO with a sensitivity of 54%, specificity of 91%, PPV 48%, NPV 93%, and LR of 6.2 which are comparable to previous scales aimed to detect LVO only.
Conclusions: FPSS is simple to use and with dichotomized items, easily implementable for emergency medical services and emergency response centers. Furthermore, the high specificity of FPSS for LVO enables direct transfer of candidates for endovascular treatment to tertiary stroke centers. Containing a clear cut off point FPSS is convenient regardless of operational environment. Based on CED, FPSS can recognize LVO and on general stroke signs (face-arm-leg-speech-visual disturbance) stroke in general, thus aiding patient logistics in stroke management.


Jyrki OLLIKAINEN (Tampere, Finland), Heikki JANHUNEN, Juho TYNKKYNEN, Kalle MATTILA, Minna HÄLINEN, Niku OKSALA, Satu-Liisa PAUNIAHO
15:55 - 16:00 #11251 - Conditions for laryngeal mask airway placement: a comparison of blind insertion and insertion with the use of a laryngoscope.
Conditions for laryngeal mask airway placement: a comparison of blind insertion and insertion with the use of a laryngoscope.

In emergent airway management, the laryngeal mask airway (LMA) have served as a bridge between endotracheal intubation and the face mask. For achieving the ideal anatomical position of the LMA, various trails, including insertion with the use of laryngoscope, have been described. Yet, except fiberoptic assessment, reliable tests for this technique of correct placement of LMA are not established.

Recently, oropharyngeal leak pressures are commonly performed with the LMA to indicate the degree of airway protection, the feasibility for positive pressure ventilation and the likelihood for successful supraglottic airway placement

The objective of this randomized prospective study was to assess the efficacy of insertion techniques, blind insertion and insertion with laryngoscope. The primary outcome was the measurement of oropharyngeal leak pressure with the two techniques. The secondary outcomes were the success rate on first attempt.

Method

Approval was obtained from the IRB, a prospective comparison of 100 patients divided into 2 groups (50 with blind technique and 50 with the laryngoscope technique) were evaluated. A standard anesthetic protocol without muscle relaxant was followed. After loss of consciousness, a LMA was inserted using the blind approach in blind insertion group or using laryngoscopy in laryngoscope group.

The oropharyngeal leak pressure was performed by closing the expiratory valve of the circuit at a fixed gas flow of 6 L/min and noting the airway pressure at which gas leaked into the mouth. The failure of first attempt insertion was recorded. Failed insertion was defined by any of the following criteria: failed passage into the pharynx; malposition; ineffective ventilation (maximum expired tidal volume < 6 ml/kg). We analyzed the data with SPSS version 17 (SPSS Inc., Chicago, Illinois, USA). Continous data were analyzed using Student’s t-test. Nonminal data were analyzed with x2 test. A p value less than 0.05 was considered significant.

Result

There was no significant difference between two groups on oropharyngeal leak pressure (18.4 ± 5.4 mmHg in blind group vs 20.6 ± 7.1 mmHg in laryngoscope group, p=0.16) and success rate on first attempt (89.2 % in blind group vs 94.5% in laryngoscope group, p=0.46).

Conclusion

In terms of oropharyngeal leak pressure, insertion with laryngoscope did not show any superiority compared to blind insertion. Blind insertion technique is easier and simpler method for insertion of LMA and has a reasonable success rate, so it is recommended to be used.


Sung Yong PARK (Suwon, Republic of Korea), Jong Yeop KIM, Sook Young LEE, Bong Ki MOON, Sang Ki MIN
16:00 - 16:05 #11340 - Evaluation of the practice of lumbar puncture in the resuscitation of emergencies.
Evaluation of the practice of lumbar puncture in the resuscitation of emergencies.

Introduction: Lumbar puncture (PL) is a common diagnostic procedure in the management of patients admitted to emergency departments. Its main indication is the search for an infection of the Central nervous system. Few epidemiological data are available in the literature concerning the use of PL, its efficiency and the populations benefiting from this review.

Purpose of Work: The objective of our work is to study the profiles of the patients benefiting from the lumbar puncture and to evaluate the predictive factors of its positivity, in order to propose a decision algorithm of the realization of the lumbar puncture in the emergencies.

Materials and methods: We carried out a retrospective study over a period of 4 years (between January 1, 2013 and December 31, 2016), within the adult emergency resuscitation department of the Ibn Rochd University Hospital Center. The inclusion criteria: Patient benefiting from a PL at the time of his/her management in the emergencies, taking into account the first effective PL carried out for the same patient during the same passage.  Excluded:   Patients who had CSF analysis by a technique other than lumbar puncture,Patients who had CSF analysis by PL without passing through the adultSAU.Epidemiological, clinical, biological, radiological and evolutionary characteristics were analyzed, according to a global descriptive study and a multivariate analysis and a univariate analytical study aiming at assessing the association between two variables.

Results: 590 patients received a PL after admission to the emergency room, representing 4.11% of patients admitted to emergency departments during study periods. Nearly 34.2% of the PLs performed were contributory and confirmed a diagnosis of meningitis (174 cases), meningeal haemorrhage (16 cases) or polyradiculoneuritis (12 cases). These contributory PLs were mainly related to infectious meningitis. The main diagnoses found in the presence of non-contributory PLs were related to neurological pathologies (convulsions and strokes) and infectious pathologies outside the central nervous system. In this work, it was found that a history of head trauma, presence of obliteration, clinical association of fever-headache, fever-meningitis stiffness, and fever-headache-meningeal stiffness are predictive factors, A positive lumbar puncture. Concerning cerebral imaging, 83.73% of patients with lumbar puncture had a CT scan. The importance of using the brain scan seems to be excessive, and the expectation of the result may be the cause of a delay in diagnosis and management leading to a situation prejudicial to the patient.

 Conclusion: A decision algorithm for performing lumbar puncture in emergency departments is proposed, based on the existence of factors predictive of CSF positivity, whether signs of gravity are present or not. And the key message is not to delay the administration of antibiotics to any suspected cases of community meningitis.


Mezgui OTHMAN (CASABLANCA, Morocco), Khaleq KHALED, En_Noqobi JAMAL
E-Poster Area

"Tuesday 26 September"

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PH5 - S2
15:45 - 16:05

E-Poster Highlight Session 5 - Screen 2

15:45 - 15:50 #10089 - Evaluating the Implementation of a Sepsis Pathway in the Emergency Department.
Evaluating the Implementation of a Sepsis Pathway in the Emergency Department.

 

Background: The importance of early management of sepsis is well known and has led to increased efforts in improving the recognition of and response to septic patients in emergency departments    

Objectives: To evaluate the impact of utilising a Sepsis Pathway Program, aimed at improving recognition of and response to septic patients, in a metropolitan Emergency Department 

Method: Following the introduction of a Sepsis Pathway Program in June 2015, a review of patients presenting to the emergency department of Casey Hospital, Victoria from June to December 2015 with sepsis was conducted. Main outcome measures were: time to antibiotic administration and to lactate measurement; rate and duration of intensive care admission; in-hospital mortality, and total duration of hospital admission. Outcomes were compared to a retrospective review of septic patients presenting to emergency from June to December 2014.

Results: The review included 171 patients in 2014 and 130 patients in 2015. The median time to antibiotic administration was significantly shorter in the post-intervention group (102 minutes vs. 190 minutes, p<0.05. The time to lactate measurement, number and duration of intensive care admissions, in-hospital mortality and total length of stay was not significantly different between the two groups.  

Conclusion: Implementation of the Sepsis Pathway Program resulted in earlier administration of antibiotics in septic patients presenting to the emergency department. Although a significant difference in secondary outcomes were not observed in this study, further evaluation in a larger multi-centre study may be warranted.


Dr Pourya POURYAHYA (Melbourne, Australia), Judy CHOW, Alastair MEYER, Neil GOLDIE
15:50 - 15:55 #11037 - Can differences in the management of children with shortness of breath be explained by disease severity alone?
Can differences in the management of children with shortness of breath be explained by disease severity alone?

Introduction

The aim of this study was to assess differences in population, management and outcome of children with respiratory complaints in 5 different European emergency departments

Methods

This study was part of the TrIAGE project, a prospective observational study consisting of a large cohort of children visiting the emergency department (ED) in 5 different hospitals in 4 European countries (UK, Austria, Portugal, the Netherlands). Data collection consisted of routinely recorded patient data, automatically extracted from electronic medical records. Data harmonization and quality checks were performed.  We included all children aged The associations between population (age, hospital, triage urgency, vital signs) and management (lab, imaging, inhalation medication and hospital admission) were assessed using a logistic regression model.

Results

In total, 13.552 children with shortness of breath were included. Of those, 55% (8.560) were categorized as urgent. This ranged from 13% in a low-urgency setting to 80% in a high-urgency setting.
The majority of children was below the age of 5 years (77%, range 73-84%).

Regarding vital signs, 41% of the total population had an abnormal respiratory rate according to APLS normal values, 9% had an abnormal oxygen saturation and 53% showed increased work of breathing.
Lab tests were performed in 16% of children (range between hospitals: 8-32%, adjusted odds ratio 5.6, 95% CI 4.0-7.9) and an X-ray was performed in 19% (range: 8-33%, adjusted odds ratio 8.6, 95% CI 6.4-11.6).
Forty-six procent of all children were treated with inhalation medication (range: 21-61%, adjusted odds ratio 0.5, 95% CI 0.3-0.7) and 19% was admitted (range 8-47%, adjusted odds ratio 0.1, 95% CI 0.1-0.2). Two hundred and five children (1.5%) were admitted to the ICU (range: 0.1-9%, adjusted odds ratio 43.4, 95% CI 13.4-140.7).

Patient characteristics (age, gender, urgency, presence of fever, abnormal vital signs) could explain part of the observed differences in management. However, after correcting for these population characteristics, we still observed substantial differences between hospitals concerning the management of these children.

Conclusion & discussion

European EDs differ substantially regarding the management of children with respiratory complaints, even when correcting for triage urgency or age. Possible explanations might be other aspects of patient characteristics such as underlying problem or comorbidity, or differences in local practice and use of different guidelines. 


Dorine BORENSZTAJN (Rotterdam, The Netherlands), Joany M ZACHARIASSE, Susanne GREBER-PLATZER, Claudio F ALVES, Paulo FREITAS, Frank J SMIT, Johan VAN DER LEI, Ewout W STEYERBERG,, Ian MACONOCHIE,, Henriëtte A MOLL
16:00 - 16:05 #11395 - Prospective study of the association of coagulopathy and isolated traumatic brain injury.
Prospective study of the association of coagulopathy and isolated traumatic brain injury.

The complex pathophysiological mechanisms behind coagulopathy that occurs after traumatic brain injury are multifactorial and remains poorly defined  , but many studies have shown the progression of parenchymal lesions particularly in patients with coagulopathy . Disorders of coagulation may be amenable to treatment  , adequate and prompt intervention may prevent secondary complications and poorer outcome.

Objectives : The purpose of this study is to evalute the association of coagulopathy and isolated traumatic brain injury as regard its frequency and outcome for patients who developed coagulopathy .

Patients : this prospective study was conducted to include 60 patients with isolated traumatic brain injury admitted to the emergency department of Alexandria main university hospital within 24 hours of trauma . Patients with known coagulopathy , on anticoagulants therapy , or those with intra abdominal collection , hemothorax or other injuries that affect coagulation were excluded from the study.

Methods : Primary survey and secondary survey were done for those patients . Radiological investigations were done including CT brain to exclude other sources of bleeding which can lead to coagulopathy . This also includes laboratory tests to asses coagulation as INR , platelet count , PTT and FDP for those who showed abnormality with the previous three tests .

Results : The frequency  of coagulopathy among those 60 patients was  8.3% . In this study 80% of cases who developed coagulopathy had severe traumatic brain injury and 20% had moderate TBI , but non of the  cases who developed coagulopathy had mild TBI .  Brain edema was the most common CT finding in patients with coagulopathy following TBI as it was present in 80% of cases . Acute Subdural hematoma is the second most common CT  finding in those who developed coagulopathy occured in 60% of those patients . Intra ventricular hemorrhage and hemorrhagic contusion occured in 40% of cases .All patients with coagulopathy had FDP > 10 mic/ ml and INR >1.3 , while PTT> 34 seconds in 80% of cases who developed coagulopathy.  Platelets count  < 100,000 cell/mm3 was present only in 40% of patients who developed coagulopathy . As regard outcome in ED  80% of cases who developed coagulopathy had deterioration of their GCS, while only 40 % of those who developed coagulopathy had disseminated intravascular coagulopathy .Also 80% of those had progressive hemorrhagic lesion on follow up CT  brain .

 Conclusion : coagulopathy occurs frequently after TBI . Coagulopathy is much more pronounced in patients with severe TBI than in patients with mild or moderate TBI .  Brain edema and acute subdural hematoma ate the most common CT finding in patients with coagulopathy after TBI . Not all cases of TBI  that had high levels of FDP had disseminated intravascular coagulopathy. 


Asmaa RAMADAN (Alexandria, Egypt), Ahmed FARHOUD, Eman TAYAE, Ahmed MARIE
E-Poster Area

"Tuesday 26 September"

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PH5 - S3
15:45 - 16:05

E-Poster Highlight Session 5 - Screen 3

15:45 - 15:50 #10506 - Prognostic analysis of pulmonary contusion in severe head trauma patients.
Prognostic analysis of pulmonary contusion in severe head trauma patients.

Introduction:

Severe head trauma is a common reason for patient’s admission to the intensive care unit and it is the leading cause of death in young adults. The outcome of these patients depends on many factors such as cerebral hypoxia. Pulmonary contusion can cause an acute respiratory failure that aggravates head trauma.

Study objective:

To evaluate the impact on morbidity and mortality of pulmonary contusion in patients admitted for severe head trauma.

Patients and methods:

This was a retrospective study performed in the emergency and intensive care department in the regional hospital of Zaghouan. The patients were recruited during 3 years, from January 2013 to December 2015. All adult patients admitted for severe head trauma (Glasgow coma score (GCS) 8) were included and evaluated by quantified injury severity scores including APACHE2, GCS, ISS, TISS. The diagnosis of pulmonary contusion was based on the history of blunt chest trauma and the appearance of four types of lesions on chest CT scans. Hospital length of stay, mortality rate, incidence of adverse events including pneumonia, ARDS and shock were recorder and compared into the tow groups (with or without pulmonary contusion).

 Results:

During the study period, 104 patients were included. The diagnosis of pulmonary contusion was retained in 34 patients (32.7%). The two groups were compared for age, genre, APACHE 2 and GCS. There was a significant difference in the ISS and TISS (p <0.001). Patients with pulmonary contusion had significantly lower PaO2/FiO2 ratio (240 [range, 160-380]) vs. 430 [range, 210-590]; p = 0.009); and significantly higher PaCO2 levels (43.5 mmHg [range, 38-52 mmHg] vs. 38 mmHg [range, 32-40 mmHg], p < 0.001). The number of cases of pneumothorax and hemothorax were significantly higher in the group of pulmonary contusion (p = 0.003, p = 0.021; respectively). Likewise, The occurrence of pneumonia and ARDS was significantly higher in the group of pulmonary contusion (p = 0.031, p = 0.023; respectively) with a shorter length of time between ICU admission and the occurrence of such complications; (6 days [range, 6-10 days]) vs. 13 days [range, 8-16 days]; p = 0.024) and (6 days [range, 2-8 days]) vs. 10 days [range, 8-10 days]; p = 0.016), respectively. No significant difference was observed with regard to the number of cases of shock (p = 0.174). The length of hospital stay was significantly higher in the group of pulmonary contusion (13.44 ± 6 days vs. 12.44 ± 4 days; p < 0.001). The overall mortality rate was 11.5% in pulmonary contusion group and 7.7% in the other group (Odds ratio, 4.22; 95% confidence interval, 1.527 to 11.703; p = 0.004).

Conclusion:

In this study, pulmonary contusion alters gas exchange and appears to increase the morbidity and mortality in patients with severe head trauma.


Snouda SALAH (Zaghouan, Tunisia), Hebaieb FATMA, Abbes MOHAMED FEHMI, Kaddour MOEZ, Ben Ghezala HASSEN
15:50 - 15:55 #11155 - Prognostic value of anatomic, physiologic and combined trauma scores to predict mortality.
Prognostic value of anatomic, physiologic and combined trauma scores to predict mortality.

Background: Trauma is a leading cause of mortality in young people aged under 40 years. Early assessment of prognosis is a cornerstone in the management of severe trauma. Several prognostic scores have been proposed in the literature during last decade. The aim of this study was to evaluate the prognostic value and to compare five trauma scores in terms of mortality at day 30 in severe trauma patients admitted to the emergency department.     

Methods: This was a prospective, observational study with inclusion of severe trauma admitted to the emergency department during a 20-month period. We focused on the predictive value of 5 specific trauma scores in terms of mortality in severe trauma admitted to the resuscitation room. Five scores were included: The Injury Severity Score (ISS), the New NISS, The Emergency Trauma Score (EMTRAS) and the GAP and M-GAP scores. Multivariate analysis of mortality at day 30 post-trauma was conducted with comparison of ROC curves.

Results: We included 298 patients. Median age was 40 (15-80) years. Sex ratio was 4,5. Clinical characteristics: n (%): GCS ≤ 8: 62 (21); PAS <90 mm Hg: 32 (11) and pulse oximetry <90%: 44 (15). The median ISS was 17 (0-75) and 176 (59%) trauma patients had a score ISS ≥ 16. The global mortality  was 21.5%. Independent predictors of mortality after multivariate analysis were respectively : EMTRAS score ≥ 3 (adjusted OR 1.80, 95% CI [1.05-3.08], p = 0.0033), ISS ≥ 16 (adjusted OR 2.05; 95% CI [1.26-3.46],p = 0.002),GAP <20 (adjusted OR 1.92, 95% CI [1.268-2.92], p = 0.002) 1.74, 95% CI [1.17-2.592], p = 0.005). After comparison of the 5 scoring tools, the GAP score showed the best AUC= 0.811 followed by the EMTRAS with an AUC of 0.789.

Conclusion:  Severe trauma is a dynamic process with high rate of morbidity and mortality. The need to an accurate evaluation of the prognosis remains a challenge for the emergency physician. Many scoring tools were proposed. In our study, all scores were able to predict mortality but physiological GAP score showed the higher AUC and so that could be proposed as safe to be used at the early stage for evaluation in the ED.


Hamed RYM (Tunis, Tunisia), Maaref AMEL, Ahmed SOUYAH, Bellili SARRA, Alaa ZAMMITI, Badra BAHRI, Wided DEROUICHE, Chokri HAMOUDA
15:55 - 16:00 #11606 - Lactate at admission versus Injury Severity Score in trauma patients for predicting mortality.
Lactate at admission versus Injury Severity Score in trauma patients for predicting mortality.

Introduction :

Early detection of at-risk trauma patients remains a challenge for emergency physicians and guides both triage and making decision. In this context, biological tools were proposed within the last decades such as lactate – rapidly available in the emergency department (ED) and widely correlated with severity and mortality. This study aimed to compare the lactate prognostic value in terms of early and delayed mortality with the anatomical Injury Severity Score (ISS), a reference score proposed worldwide in the litterature but obtained after completing explorations in trauma patients.

Methods:

It was a single-center prospective study (12 months). Inclusion of severe trauma patients over 18 years admitted to the emergency resuscitation room at the ED. Arterial lactate at admission was drawn on a point-of-care sample gaz before any resuscitation attempts. ISS were calculated after completed explorations and assessment. Mortality at day 7 and 30 was colliged with comparison of the ROC curve’s characteristics of both lactate and ISS towards mortality.

Results:

We enrolled 190 trauma patients with median age (min, max) = 34 years (18,85) and sex-ration= 4. Road traffic accident was the predominant cause of trauma in 140 cases (74%). Average ISS (SD)= 20 (12) with ISS >= 16 in 122 patients (22%). Mortality rate was respectively 26% at day-7 and 29,5% at day-30. Median lactate (IQR) =2,4 mmol/l (0,4- 10,9) and lactate >=2,5 mmol/l was found in 118 patients (62%). ISS and lactate were significantly higher in non-survivors than in survivors; p<0,001. Moreover, ISS was superior to lactate in predicting mortality. The ROC curves characteristics were respectively :  Mortality at Day-7  (ISS: AUC = 0,930; CI95% [0,895-0,964]; p<0,001) vs (Lactate: AUC =0,704; CI95% [0,622- 0,786]; p<0,001) and mortality at Day-30 ( ISS: AUC 0,951; CI95% [0,924- 0,978]; p<0,001) vs (lactate: AUC 0,700 ; CI95% [0,621-0,779]; p<0,001).

Conclusion :

In this study, indeed ISS remains a higher tool for predicting mortality but is difficult to calculate and is late to obtain with the need of exhaustive morphologic injury assessment. Lactate showed a good predictive value for both early and delayed mortality with strong significative AUC. Moreover, lactate is  rapidly available in few minutes after admission at the ED and so that can be proposed for early  accurate assessment in severe injured patients. Our study was single-center with a limitation of small size sample. Enlargement of the size and conducting multi-centric study in the future could improve sensitivity and predictive value of lactate biomarker.


Hamed RYM (Tunis, Tunisia), Aymen ZOUBLI, Hana HEDHLI, Alaa ZAMMITI, Badra BAHRI, Wided DEROUICHE, Héla BEN TURKIA, Chokri HAMOUDA
16:00 - 16:05 #11826 - Systematic review of interventional studies carried out in emergency medical call centres.
Systematic review of interventional studies carried out in emergency medical call centres.

Introduction

Methodological evaluation of interventional studies conducted via emergency medical call centres has not previously been performed.

Objective

To describe in both quantitative and qualitative terms interventional research performed in medical call centres.

Methods

Study: Systematic review.

Search engines: PubMed, World of Science, Cochrane Methodological Register, OMS Register and ClinicalTrials.

Inclusion criteria: Studies evaluating therapeutic or organisational interventions, directed by call centres, enacted by responding physicians, paramedical teams or bystanders, in the context of situations judged to be emergencies by callers.

Exclusion criteria: Studies focussed on call management for general practice or non-healthcare agencies.

Parameters collected: Delay to publication, general characteristics of the study, study population (patients, mannequin based training, experimental modelling), number of patients included, theme or pathology targeted by the study, primary and secondary outcome measure(s), funding, ethical approval, quality criteria evaluated according to the risk of bias scale (ROB) or the Newcastle-Ottawa scale (NOS). For NOS, scores of 0-3, 4-6, and 7-9 are regarded as low, moderate, and high quality respectively.

Methodology: Extraction of parameters by two independent investigators. In cases of disagreement, a third expert investigator was consulted.

Results

Our search terms yielded 3896 articles. After examining abstracts, 47 articles were retained. The median delay to publication was 36 weeks (IQR: 30-48). Thirty-three of the studies were clinical trials (70%) and 14 (30%) were before-after trials. Studies were monocentric in 33 (70%) of cases and 32 (70%) used randomisation. The models used were simulation training, patient based or experimental studies in 26 (55%), 17 (38%), and 3 (6%) of articles respectively. The median number of subjects included was 147 (IQR: 74-1271). The theme most commonly targeted was cardiac arrests (n=36, 77%), with outcome measures of CPR quality and dispatch assistance. Other themes included triage in the call centre, management of pathologies such as myocardial infarct, severe trauma, cerebrovascular accidents, and analysis of the transmission of information. Ethical committee approval was declared in 38 (81%) of cases. Funding was reported by 26 (55%) of studies. Among the randomised-trials, selective reporting was high for 24 (75%) studies, blinding of outcome was low for 28 (88%) and incomplete outcome was low for 23 (72%) studies. Regarding non-randomised studies, quality was high, intermediate and low respectively in 7 (50%), 6 (43%) and 1 (7%) of cases.

Conclusion

Few interventional studies have been carried out in call centres. Those that exist principally describe simulation studies, and often focus on cardiac arrest. The quality of studies needs improvement in order to allow a better recognition and understanding of emergency medical call control.


Paul-Georges REUTER (Rennes), Anthony CHAUVIN, Frédéric ADNET, Frédéric LAPOSTOLLE, Youri YORDANOV
E-Poster Area

"Tuesday 26 September"

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PH5 - S4
15:45 - 16:05

E-Poster Highlight Session 5 - Screen 4

15:45 - 15:50 #11008 - Sesamin Ameliorates Mucosal Tissue Injury of Mesenteric Ischemia and Reperfusion in an Experimental Rat Model.
Sesamin Ameliorates Mucosal Tissue Injury of Mesenteric Ischemia and Reperfusion in an Experimental Rat Model.

Introduction

Mesenteric ischemia/reperfusion (I/R) injury is a serious clinical condition. There were a lot of experimental studies performed in the treatment of I/R injury. In our knowledge, this is the first experimental study with effects of sesamin on I/R injury model. We aimed to investigate the protective effect of sesamine on mesenteric I/R injury model.

Materials and methods

A total of 32 male Sprague-Dawley rats were divided into four groups. Control group: superior mesenteric artery (SMA) exposed without clamping. I/R group: SMA was clamped for 60 minutes and then reperfused for 2 hours. Sesamin group (S): 30 mg/kg sesamin were given for 5 days, and SMA exposed without clamping. I/R+S group: 30 mg/kg sesamin were given for 5 days, SMA was clamped for 60 minutes and then reperfused for 2 hours. We studied plasma and tissue oxidant parameters and histopathological evaluation was performed.

Result

Plasma and tissue TAS levels were significantly higher in I/R+S group compared to the rest (p<0.005). The plasma TAS levels in I/R group was significantly low. The highest tissue TAS levels were detected in I/R+S group. The high levels of plasma and tissue TOS were found in I/R+S group. Plasma and tissue OSI levels were significantly higher in I/R group. Histopathologic evaluation showed that; the mean level of intestinal tissue injury score in I/R group was 2,75 and was 1.38 in I/R+S group. 

Conclusion

Sesamin helps to protect the intestinal tissue at the cellular level by reducing the oxidative stress and inflamation at both the plasma and tissue levels in the experimental I/R model.

 


Mustafa SAYHAN, Serhat OGUZ, Ömer SALT (EDIRNE, Turkey), Nuray CAN, Taner OZGURTAS, Tulin YALTA
15:50 - 15:55 #11193 - Emergency EEG: actual indications and clinical practice.
Emergency EEG: actual indications and clinical practice.

Introduction

Electroencephalography is regularly used in the emergency department, but its relevance and value are actually difficult to assess, despite clear guidelines from the Société de Neurophysiologie Clinique de la Langue Française (SNCLF). The purpose of this study was to evaluate the relevance of EEGs in the emergency department by comparing actual indications and clinical practice.

Method

Monocentric, retrospective study over a 6 months period, from 01/01/2014 to 31/06/2014 at the emergency department. The EEGs performed were classified as recommended and non-recommended, as regards to the guidelines from the SNCLF.

Results

476 EEGs were performed over this period. 389 were used for statistical analysis. Mean age was 62.6 +/- 20.3 years, with a sex ratio of 1.2 (M:F). 30.8% of EEGs were recommended. The clinical symptoms that led to an EEG were varied and often linked. We noted 57.5% of confusion and 50.8% for generalized tonic-clonic seizures in the recommended group. In the non-recommended group, 40.9% of EEGs were performed for funny turns and 28.3% for altered mental states. The recommended EEGs lead to the final diagnosis in 24.4% of the generalized tonic-clonic seizures and 6.2% of altered mental states. For the non-recommended group, rates were 4.8% and 9% for these clinical presentations. 19.2% of recommended EEGs had a therapeutic impact VS 5.9% for non-recommended. The duration of hospitalization was 4.54 days for the group of recommended EEG VS 8.45 days for the non-recommended.

Discussion

Our study demonstrates that the EEG has a greater diagnostic and therapeutic contribution when the guidelines of the SNCLF are followed. Concerning altered mental states, diagnostic value of the EEG is weak and almost equivalent in both groups. This suggests that EEGs should not be performed in this indication. Half of the hospital stay for patients with recommended EEG was also reduced.

Conclusions

Although the indications of the EEG in the emergency department are clearly established, its relevance remains uncertain. Indeed, our study shows that non-recommended EEGs are equivalent in diagnostic value regarding altered mental states, reaffirming the premise that any paraclinic examination should be requested after a thorough clinical examination. 


Amish SEERUTTUN (STRASBOURG), Hakim SLIMANI, Thibault DESMETTRE, Marianne-Claire LABOUREYRAS, Vinh Phuc LUU, Thibault SCHILLIG
15:55 - 16:00 #11466 - Potential of novel biomarkers in prehospital management of traumatic brain injury: the pre-tbi study.
Potential of novel biomarkers in prehospital management of traumatic brain injury: the pre-tbi study.

Background: Traumatic brain injury (TBI) is the leading cause of death and disability among young adults worldwide. Difficulties in clinical assessment and triage of TBI patients in the prehospital phase results in numerous precautionary hospital admissions of mild TBI patients and treatment delay due to mis-triage of moderate and severe TBI patients. Early knowledge on biomarker values is suggested key to improvement of patient outcome as it may guide clinical-decision-making already in the prehospital phase.

Aim: To investigate the potential of early biomarker measurements in prehospital management of TBI patients.

Methods: 3 Prospective, observational studies were designed to investigate ROC characteristics of S100B, GFAP and NSE in relation to clinically relevant endpoints. 690 adult patients suffering mild, moderate and severe TBI in Central Denmark Region will be included from February 15 2017 - June 15 2018. Blood samples are drawn in the ambulance, on admission and repeatedly during the first 12 hours past trauma. Blood samples are stores in a biological bank and batch analysis will be done after 6, 12 and 18 months during the period og inclusion. An endpoint adjutication comittee of senior researchers will review patient causes blinded to biomarker values in relation to endpoint of the relevant study:

PreTBI I:Diagnostic Potential of S100B and GFAP in Prehospital Rule-Out of Intracranial Lesions in Patients suffering Mild TBI.

PreTBI II:S100B and GFAP in Prehospital Prediction of Need for Neurosurgical Observation or Intervention in Patients suffering Moderate TBI.

PreTBI III: Prognostic Potential of S100B, GFAP and NSE in Patients suffering Severe TBI.

Perspectives: To underline the potential of prehospital biomarker measurements for effective rule-out of low risk patients and rule-in of high-risk patients in order to minimize treatment delay, secure optimal resource consumption and streamline patient courses for patients suffering neurotrauma. Ultimately to elucidate the need for development of a point-of-care analysis.


Sophie-Charlott SEIDENFADEN (Aarhus N, Denmark), Morten Thingemann BØTKER, Niels JUUL, Hans KIRKEGAARD, Ingunn Skogstad RIDDERVOLD
16:00 - 16:05 #11714 - Pediatric cardiac arrest: Is outcome related to the time of admission?
Pediatric cardiac arrest: Is outcome related to the time of admission?

Background and Objectives: Nights and weekends represent a potentially high-risk time for pediatric cardiac arrest (CA) patients in emergency departments (EDs). Data regarding night or weekend arrest and its impact on outcomes is controversial. This study performed to determine the relationship between cardiopulmonary resuscitation (CPR) during the various ED shifts and survival to discharge.

Methods: We conducted a retrospective, observational study in which patients who had visited our ED for cardiac arrest from January, 2013 to December 2015. We examined survival from cardiac arrest in hourly time segments, defining within working hours as 8:00 AM to 17:00 PM, out of working hours as 17:00 PM to 7:59 AM and weekend as 17:00 PM on Friday to 7:59 AM on Monday. Medical records and patient characteristics of 54 children with cardiac arrest were retrieved from patient admission files.

Results: The median age was 3 years, 59% were male and 17 patients were younger than 12 months. A total of 26 cases of cardiac arrest admitted at working hours to ED and 28 cases admitted at out of working hours. Rates of survival to discharge 30.8% (n=8) within working hours vs out of working hours 3.6% (n=1). Among in cardiac arrests presenting to ED, survival was higher on working hours than out of working hours (p=0.01). Rate of return of spontaneous circulation within working hours was higher than out of working hours (54% vs.18%) (p=0.009).  Patients older than 5 years had poor outcome, whereas better outcome was associated with in-hospital cardiac arrest (p<0.05). The first documented rhythm at our group was more frequently to be asystole (92%).

Conclusion: Survival rates from pediatric cardiac arrest are lower during out of working hours.  The outcome has also been related to duration of CPR, age and location of CA.


Eylem Ulas SAZ (IZMIR, Turkey), Dr Ali YURTSEVEN, Caner TURAN
E-Poster Area

"Tuesday 26 September"

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PH5 - S5
15:45 - 16:05

E-Poster Highlight Session 5 - Screen 5

15:45 - 15:50 #9948 - Neuroprotection and reduced gliosis by pre- and post-treatments of hydroquinone in a gerbil model of transient cerebral ischemia.
Neuroprotection and reduced gliosis by pre- and post-treatments of hydroquinone in a gerbil model of transient cerebral ischemia.

Purpose: Hydroquinone (HQ), a major metabolite of benzene, exists in many plant-derived food and products. Although many studies have addressed biological properties of HQ including the regulation of immune responses and antioxidant activity, neuroprotective effects of HQ following ischemic insults have not yet been considered. Therefore, in this study, we examined neuroprotective effects of HQ against ischemic damage in the gerbil hippocampal cornu ammonis 1 (CA1) region following 5 min of transient cerebral ischemia.

Methods: To elucidate the neuroprotective effects of HQ against ischemic damage, the gerbils were divided into 8 groups (n = 7 in each group), as follows: 1) vehicle-treated sham-operated group (vehicle-sham-group), 2) vehicle-treated ischemia-operated groups (vehicle-ischemia-group), 3) and 4) 50 and 100 mg/kg HQ-pre-treated sham-operated groups (pre-HQ-sham-groups), 5) and 6) 50 and 100 mg/kg HQ-post-treated sham-operated groups (post-HQ-sham-groups) 7 and 8) 50 and 100 mg/kg HQ-pretreated ischemia-operated groups (pre-HQ-ischemia-groups), 9 and 10) 50 and 100 mg/kg HQ-post-treated ischemia-operated groups (post-HQ-ischemia-groups). HQ was purchased from Sigma (St. Louis, MO, USA) and dissolved in saline. For pre- and post-treatment, HQ or saline was intraperitoneally administered once at 30 min before or after ischemic surgery, respectively. Sham-operated animals were subjected to the same surgical procedures except that the common carotid arteries were not occluded.

Results: We found that pre- and post-treatments with 50 and 100 mg/kg of HQ protected CA1 pyramidal neurons from ischemic insult. Especially, pre- and post-treatments with 100 mg/kg of HQ showed strong neuroprotective effects against ischemic damage. In addition, pre- and post-treatments with 100 mg/kg of HQ significantly attenuated activations of astrocytes and microglia in the ischemic CA1 region compared to the vehicle-treated-ischemia-operated group.

Conclusion: Briefly, these results show that pre- and post-treatments with HQ can protect neurons from transient cerebral ischemia and strongly attenuate ischemia-induced glial activation in the hippocampal CA1 region, and indicate that HQ can be used for both prevention and therapy of ischemic injury.


Jun Hwi CHO, Joong Bum MOON, Myoung Chul SHIN (Chuncheonsi, Republic of Korea), Taek Geun OHK, Chan Woo PARK, Moo Ho WON
15:50 - 15:55 #11095 - Applying a modified time-driven activity based costing method to emergency department care in Sweden.
Applying a modified time-driven activity based costing method to emergency department care in Sweden.

Background Costs of healthcare services are difficult to determine. Accurately allocating costs of healthcare services to activities would enable better policy decisions on subjects such as optimal care venues, spending priorities, and staffing. Current cost-per-patient systems (kostnad-per-patient, KPP) consolidate Emergency Department costs for some patient encounters with inpatient costs, obscuring the true costs of ED care. Standard cost accounting allocates all costs to current patients, creating the appearance of cost increases with decreased utilization. We developed the Patient Encounter Cost (PEC), a method for more accurately assigning costs within a regional emergency department (ED) care system to account for excess capacity.

Methods We used data from Region Halland, Sweden, a county of 300,000 people over 5,500 km2. We analyzed 2015 records of the entire population of 88,132 ED visits across 2 ED sites in the region.  We calculated total costs incurred of 212 million Swedish Crowns (SEK), or approximately 25 million USD. Time spent per visit was determined from prospectively recorded ED records and adjusted by published weighting factors for nursing care by triage acuity level. Total capacity was determined based on available nursing and physician staff time. We developed the PEC using time-driven activity based costing (TDABC) methods to determine unit-time costs for ED care. Unit-time costs were then used to determine total ED patient-care costs for the year 2015.

Results In 2015, Region Halland spent 212 million SEK on its emergency departments, incurring unit costs of 1,787 SEK per nursing hour. The average ED visit service cost 2,363 SEK (95%CI 2,273-2,453), ranging from 460 SEK (454-466 SEK) for triage level 5 patients to 4,507 SEK (4,505-4,509 SEK) for triage level 1 patients. Total costs spent on direct patient care accounted for 191 million SEK, showing a utilization of 81% of available capacity. The average ED visit service cost 2,363 SEK using PEC techniques compared to 2,865 SEK using traditional health care cost accounting techniques.

Conclusion PEC can be used to allocate costs down to the individual patient encounter level within a regional emergency care system using readily-available data. This method has the potential to contribute to policy decisions regarding appropriate excess capacity and allocation of scarce healthcare resources, as well as more closely aligning costs with prices in systems without a single payer. Next steps include refining the model for greater granularity of cost assignment to patient care visits.


Jonathan SLUTZMAN, Zayed YASIN (Boston, USA), Jonny ERIKSSON, Jonas HULTGREN, Philip ANDERSON
15:55 - 16:00 #11593 - Can Serum S100B be a predictor of neuronal damage and clinical poor outcomes associated with the use of synthetic cannabinoids?
Can Serum S100B be a predictor of neuronal damage and clinical poor outcomes associated with the use of synthetic cannabinoids?

Background: There has been an increasing number of emergency department visits due to synthetic cannabinoid use. There is little information about the structural and functional damage caused by the use of synthetic cannabinoids. This study aims to evaluate the serum S100B levels to predict neuronal damage and clinical poor outcomes associated with the use of synthetic cannabinoids.

Method: Thirty patients with synthetic cannabinoid user and 30 healthy controls were included in the study. The S100B levels were measured with a Human ELISA kit. Serum S100B levels were compared to healthy controls with synthetic cannabinoid users. Among the users of synthetic cannabinoids, patients with the following outcomes were considered to have a composite outcome: the need for endotracheal intubation due to hypoventilation and decreased GCS; seizures; the need for intensive care unit admission; and in-hospital mortality. Clinical and laboratory findings associated with composite clinical outcomes were examined.

Results: We found significantly increased S100B levels in patients with synthetic cannabinoid use. The mean serum S100B level was 19.32 ± 4.92 pg/mL in patients with synthetic Cannabinoid user, and 15.94 ± 2.43 pg/mL in the control group (p = 0.001).  In patients with and without composite clinical outcomes, the mean serum S100B level was measured as 24.13 ± 5.48 pg/mL, and 17.58 ± 3.38 pg/mL, respectively (p = 0.001). With the cut-off value for S100B set at 20 pg/mL based on the highest sensitivity; the sensitivity, specificity, positive predictive value, and negative predictive value for S100B were 89.9%, 52.0%, 44.4% and 91.9%, respectively.

Conclusion: Our data suggest that serum S100B levels are elevated in patients using synthetic cannabinoids. But the role of high S100B level in determining neuronal damage and clinical poor outcomes was limited. These results show that S100B can help clinicians to exclude neuronal damage and possible poor outcomes. 


Yilmaz SERKAN (İstanbul, Turkey), Karakayalı ONUR, Kale EBRU, Akdogan AHMET
16:00 - 16:05 #11467 - Traumatic brain injury - how do we dispatch ?
Traumatic brain injury - how do we dispatch ?

Background: Severe traumatic brain injury (TBI) is considered a time-critical condition. Relevant emergency medical response must be commenced, which makes dispatch key. Danish ambulance dispatch is criteria-based depending on main symptom or incident, but no separate dispatch criteria exist for head trauma or suspected TBI. Dispatch are graded level A to E according to severity of emergency call.

Aim: To investigate which dispatch criteria are assigned patients with severe TBI (confirmed intracranial lesion), if the highest level (A) of emergency response are commenced and to examine related 30-day mortality.

Methods: Population-based follow-up study of emergency medical calls in the Central Denmark Region from October 1 2011 - December 31 2014 concerning patients subsequently diagnosed with severe TBI according to ICD-10 codes from Danish National Patient Registry. For patients with confirmed intracranial lesion odds of receiving the highest level of emergency response was investigated in a logistic regression model.

Results: Of 76,009 emergency medical calls, 1382 patients were subsequently diagnosed with TBI (1.8%) of which 216 patients suffered severe TBI with intracranial lesion. Patients were assigned 14 different dispatch criteria. Level of emergency response was dependent on assigned dispatch criteria: 11 of the 216 severe TBI patients were assigned the lowest level of emergency response (telemedical advice). 30-day mortality was 1.5% (95% CI 1.0-2.0%) for overall TBI and 8.8% (95% CI 5.7-13.3%) in severe TBI.

Conclusion: Severe TBI patients are assigned different dispatch criteria. Highest level of emergency response varies within subgroups of dispatch criteria. Patients suffering intracranial lesions have a high 30-day mortality.


Sophie-Charlott SEIDENFADEN (Aarhus N, Denmark), Ingunn Skogstad RIDDERVOLD, Niels JUUL, Hans KIRKEGAARD, Morten Thingemann BØTKER
E-Poster Area
16:10

"Tuesday 26 September"

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A34
16:10 - 17:40

Neurological (Cutting Edge)

Moderators: Dr David CARR (Associate Professor of Emergency Medicine) (Toronto Canada, Canada), Pr Jim DUCHARME (Immediate Past President) (Mississauga, Canada)
Coordinator: Christian HOHENSTEIN (Coordinator, BAD BERKA, Germany)
16:10 - 16:40 TIA. Jeff PERRY (Physician) (Speaker, Ottawa, Canada)
16:40 - 17:10 Thunderclap headache - not just an SAH. Pr Jim DUCHARME (Immediate Past President) (Speaker, Mississauga, Canada)
17:10 - 17:40 Turning a zebra into a horse. Dr David CARR (Associate Professor of Emergency Medicine) (Speaker, Toronto Canada, Canada)
Trianti Hall

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B34
16:10 - 17:40

Infectious Disease & Sepsis (How To)

Moderators: Christoph DODT (Head of the Department) (München, Germany), Marc SABBE (Medical staff member) (Leuven, Belgium)
Coordinator: Christoph DODT (Coordinator, München, Germany)
16:10 - 16:40 Sepsis treatment: in the ED or ICU? Christoph DODT (Head of the Department) (Speaker, München, Germany)
16:40 - 17:10 Evaluation of the effect of improved qSOFA score on the severity and prognosis of emergency adult sepsis patients. Cao YU (emergency) (Speaker, Chengdu, China)
17:10 - 17:40 Ultrasound in the ED in patients with sepsis. Cornelia HÄRTEL (Medical Director of the ED, Consultant in EM, Director of Medical Education in EM) (Speaker, STOCKHOLM, Sweden)
Mitropoulos

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C34
16:10 - 17:40

Work-life balance (The Boss' Office)

Moderators: Pr Pinchas HALPERN (department chair) (Tel Aviv, Israel, Israel), Katrin HRUSKA (Emergency Physician) (Stockholm, Sweden)
Coordinator: Pr Rick BODY (Coordinator, Manchester)
16:10 - 16:40 The myth of gender gaps in EM. Adela GOLEA (Associate Professor) (Speaker, Cluj Napoca, Romania)
16:40 - 17:10 Physician, Parent, Ironman: How to Have it All. Gayle GALLETTA (Emergency medicine physician) (Speaker, USA/Norway, USA)
17:10 - 17:40 The challenge to be the man in the ED. Robert LEACH (Head of Dept.) (Speaker, BRUXELLES, Belgium)
Banqueting Hall

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D34
16:10 - 17:40

YEMD - Simulation

Moderators: Dr Anastasia SFAKIOTAKI (Emergency Physician) (Melbourne, Australia), Jennifer TRUCHOT (MEDECIN) (Paris, France)
Coordinator: Basak YILMAZ (Coordinator, BURDUR, Turkey)
16:10 - 16:40 Building simulation "on the cheap": full scale simulation for less than 10.000€. Mohammed MOUHAOUI (Professeur) (Speaker, Casablanca, Morocco)
16:40 - 17:10 Research in simulation: 2017 update. Luca CARENZO (SIMULATION COMPETITION ONLY) (Speaker, NOVARA, Italy)
17:10 - 17:40 Communication in a crisis: how to become a confident (young) team leader. Jennifer TRUCHOT (MEDECIN) (Speaker, Paris, France)
Skalkotas

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E34
16:10 - 17:40

Nursing session 4

Moderators: Sivera BERBEN (research coordinator) (Nijmegen, The Netherlands), Door LAUWAERT (Manager) (BRUSSELS, Belgium)
16:10 - 16:40 BLS/AED training of deaf and hard-hearing citizens under the ERC guidelines. Tzannis POLYKANDRIOTIS (Speaker, Greece)
16:40 - 17:10 Managing delirium in the ED. Thomas DREHER-HUMMEL (Nurse) (Speaker, Basel, Switzerland)
17:10 - 17:40 EARLY WARNING SCORE-The need for inclusion in Greek hospitals. Stamatina IORDANOPOULOU (Speaker, Greece)
MC-3

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F34
16:10 - 17:40

Free Papers Session 11

Moderators: Pr Cem OKTAY (FACULTY) (ANTALYA, Turkey), Pr Riccardo PINI (Director, E.D. High Dependency Unit) (Florence, Italy)
16:10 - 16:20 #10843 - OP091 Diagnostic Value of New Sepsis Criteria in the Emergency Department (DISC study).
Diagnostic Value of New Sepsis Criteria in the Emergency Department (DISC study).

In February 2016 a new definition of the sepsis was introduced, redefining sepsis as a life-threatening organ dysfunction caused by a dysregulated host response to infection (.Sepsis-3). A shortened sequential Sepsis-related Organ Failure Assessment score (Q- SOFA score) is used to identify sepsis according to Sepsis-3 criteria. However, these new criteria have not yet been validated in a general emergency department (ED) patient population.

Methods

This is a multi-center, non-interventional observational pilotstudy. During this pilotstudy all adult patients who visit the ED with a suspected or proven systemic infection were included. In all included patients the SIRS criteria and the qSOFA criteria were collected. In addition to routine diagnostic tests such as blood cultures, the PCT levels will be determined.

Results from the first 100 inclusions

In this pilot of 100 patients 61 were male. Median age was 65.5 years (range 18 to 94). The q-SOFA was positive in 4 patients, while SIRS was positive in 44. The mortality in the total study population was 6%. 5 critically ill patients were not identified by qSOFA, while SIRS missed 2. 2 of the SIRS positive patients and none of the qSOFA positive patients were admitted to the intensive care unit. 

Conclusion

This pilot study showed the implementation of q-SOFA as a screening tool in suspected systemic infection, did not identify all patients who needed intensive care or those with bad outcome after visiting an emergency department. More research needs to be done in a larger study to compare validity and usefulness of this scores in the ED population.


Kaoutar AZIJLI (Amsterdam, The Netherlands), Tanca MINDERHOUD, Nicole HES, Rishi NANNA PANDAY, Susanne GIJSBERG, Nieke MULLAART, Tom BOEIJE, Bas HUISMAN, Prabath NANAYAKKARA
16:20 - 16:30 #11022 - OP092 Predictive factors of mortality in patients admitted to the emergency department for sepsis.
Predictive factors of mortality in patients admitted to the emergency department for sepsis.

Introduction: Despite major efforts to identify and treat sepsis early, this disease remains a major cause of mortality in hospitalized patients in the emergency department (ED).

Objective: To identify factors associated with intra-hospital mortality in patients admitted to ED for sepsis.

Methods: Prospective, observational, monocentric study, over 12 months in ED. Inclusion: patients (age ≥ 18 years) with a suspected infection associated with two or more criteria of the systemic inflammatory response syndrome (temperature ≥ 38 ° or ≤ 36 °C, heart rate> 90 bpm, respiratory rate> 20 / min, or Blood pressure in CO2 <32 mmHg or White blood cells> 12,000 cel / mm3, or <4,000 / mm3). Epidemiological, clinical, therapeutic and outcome criteria were collected. APACHE 2, SOFA and quickSOFA (qSOFA) scores were calculated. Prognosis was evaluated in intra-hospital mortality. Multivariate regression analysis to identify factors associated with mortality was performed.

Results: Inclusion of 185 patients (169 in sepsis and 16 in septic shock). Mean age = 61 ± 17 years. Sex ratio = 0.46. Comorbidities n (%): diabetes 88 (48), hypertension 87 (47), dyslipidemia 23 (12), chronic obstructive pulmonary disease 14 (7). Clinical manifestations (%): fever (76), altered general state (41), respiratory signs (39), digestive signs (35), neurological signs (9). Site of Infection (%): renal (39), pulmonary (30), cutaneous (15), digestive (12). Organ failure (%): renal (20), cardiac (15), respiratory (12), hepatic (8) and haematological (7) events. Median APACHE 2 score = 9. Median SOFA score = 6. Median qSOFA score = 1.Intra-hospital mortality = 5%.  

In adjusted multiple regression models, age >75 years (adjusted OR = 2.8, 95% CI [1.72- 3,25], p<0.001), renal failure (adjusted OR = 4.6, 95% CI [1.4-14.6], p=0.009), septic shock (adjusted OR= 2.7, 95% CI [1.9 -8.32], p=0.05), and HCO3- level<18mmol/l (adjusted OR= 2.9, 95% CI [1.1-7.6], p=0.03) were independently associated with intra-hospital mortality. 

Conclusion: In this study, age of 75 years, HCO3- level <18 mmol /, renal failure and septic shock were predictive factors for in-hospital mortality for patients admitted to ED for sepsis.

 


Hanen GHAZALI (Ben Arous, Tunisia), Soumaya MAHDHAOUI, Ines CHERMITI, Aymen ZOUBLI, Ihsen HNEN, Sawsen CHIBOUB, Mohamed MGUIDICH, Sami SOUISSI
16:30 - 16:40 #11113 - OP093 Using Support Vector Machine to develop of a Mortality Prediction Model for Septic Patients in the Emergency Department.
Using Support Vector Machine to develop of a Mortality Prediction Model for Septic Patients in the Emergency Department.

Background: Many studies in the past have reported that sepsis is one of the leading causes of mortality in hospitalized patients. However, information regarding factors for early predictive mortality is limited.

Objective: The aim of this present study was to develop a 28-day mortality prediction model and assess the validity of it for the septic patient population in the emergency department by a machine-learning algorithm, Support Vector Machine and to compare with the Sequential Organ Failure Assessment (SOFA) Score.

Methods: This prospective observational study conducted in the emergency department in the Chang Gung Memorial Hospital in Linkou. Consecutive patients meeting the criteria for sepsis during the first 24 hours of ED admission were included. The 28-day mortality collected prospectively by inpatient database or telephone follow-up. We made use of the demographic and laboratory variables that used to diagnosis sepsis as the candidate variables, and applied the recursive feature elimination method to select the significant ones to build the prediction models. Data were divided into training (75%) and testing (25%) sets, and repeated 30 times to avoid selection bias. To assess the performance of the build prediction model, we calculated the area under the Receiver Operating Characteristic curve (AUC), sensitivity, specificity, and accuracy for either individual variable but also the combination of selected variables.

Results: 379 patients were prospectively recruited from the emergency department with sepsis (SIRS and infection, 42.22%), severe sepsis (or Sepsis 3.0, 56.2%), and septic shock (1.58%) with a 28-day mortality rate of 10.03%. The selected variables for prediction model were respiratory rate, albumin, C-reactive protein, D-dimer, and fibrin-degradation products. The analysis results summarized in Table illustrates that the method of Support Vector Machine had promising performance of accuracy, specificity, and AUC in training (0.842, 0.853, and 0.879, respectively) and testing (0.821, 0.890, and 0.754, respectively) sets where better than SOFA score (AUC: 0.711, accuracy: 0.835).

Conclusion: Our results revealed that using the combination of several laboratory variables is promising for early prediction of mortality in sepsis. However, further efforts still need to improve and increase the reliability of early predict mortality of sepsis such as the technique of machine learning.


Pr Kuan-Fu CHEN (Taipei, Taiwan), Chin-Chien WU
16:40 - 16:50 #11147 - OP094 Eosinopenia: an interesting biological marker for the diagnosis of different infections in the ED.
Eosinopenia: an interesting biological marker for the diagnosis of different infections in the ED.

Introduction: The relevance of eosinopenia, as marker of infection, has been described in internal medicine, intensive care, and more recently in Emergency Departement (ED), for all infections combined. We aimed to specify the contribution of this biomarker in different common infections in ED, alone or in association with other inflammatory markers.

Methods: We present here a retrospective mono-centric study carried out in the Emergency Department of a teaching hospital in France for a  6 months period (September 2015-February 2016). All patients with one of the following diagnosis were eligible: appendicitis, cholecystitis, sigmoiditis, acute pyelonephritis, male urinary tract infection, pneumonia. Uninfected patients were randomly selected to form a control group of equivalent size to the cohort of infected patients collected for the study.

Results: We included a total of 466 infected patients and 466 controls. The sex-ratio in the infected group was 0.94, the mean age was 57.9 years (SD: 24.7 years). The eosinophil count in the infected patients was significantly reduced compared to controls (59/mm3 versus 129/ mm3, p <0.001). Deep eosinopenia (3) had a specificity of 94.4% for the diagnosis of infection (all combined) with a positive likelihood ratio (LR +) of 6.3 and an area under the curve (AUC ) of 75.9%. Eosinopenia was more effective in pyelonephritis, male urinary tract infections and acute cholecystitis (AUC > 80%), but had lower diagnostic performance in pneumonia (AUC =75%), appendicitis or sigmoiditis (AUC < 70%). The AUC of eosinopenia was higher than those of leucoccytosis in pyelonephritis and cholecystis. The association of eosinopenia with an increase of C-reactive Protein (> 40mg/l) or simply with the presence of fever (Temperature >38.5 ° C) showed a specificity greater than 99% and an LR + of 61 and 45 respectively.

Conclusion:  Eosinopenia is an interesting biological marker to consider in the ED, alone or in combination with other clinical or biological parameters in order to diagnose an infection. It is particularly interesting in urinary or biliary infections in which it is a better marker than leukocytosis.


Charles-Eric LAVOIGNET, Joffrey BIDOIRE, Sylvie CHABRIER, Sarah UGÉ (Strasbourg), Mickaël FORATO, Fanny SCHWEITZER, Pierrick LE BORGNE, Pascal BILBAULT
16:50 - 17:00 #11383 - OP095 Validation of qSOFA in the emergency department - a prospective study.
Validation of qSOFA in the emergency department - a prospective study.

Background

Sepsis is the primary cause of death from infection worldwide. Recently, the 2016 Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3) defined sepsis as “life-threatening organ dysfunction caused by a dysregulated host response to infection.” Together with the updated definition of sepsis, a new clinical concept termed ‘Quick Sepsis-Related Organ Failure Assessment’ (qSOFA) was introduced to identify high-risk patients with suspected infection outside of intensive care settings. The previous criteria- Systemic Inflammatory Response Syndrome (SIRS) - were removed from the current sepsis definition. qSOFA has not been validated in Hong Kong (HK). In the current study, we aimed to validate qSOFA in an emergency department in HK. Furthermore, we sought to compare the prognostic value of qSOFA and SIRS as well as another commonly used early warning score, the National Early Warning Score (NEWS).

 

Methods

This is a single-centre, prospective study conducted in the ED of Prince of Wales Hospital, HK between Jul 2016 and Feb 2017. 665 patients presenting to the ED triaged as category 2 (Emergency) and 3 (Urgent) were recruited. All variables for calculating qSOFA, SIRS and NEWS were collected. The outcome measure was 30-day mortality. Venous lactate was also measured to investigate whether lactate level provide additional value for the prediction of 30-day mortality. The prognostic value of qSOFA, SIRS and NEWS to predict 30-day mortality was studied. Receiver Operating Characteristic analysis were performed to determine the Area Under the Curve (AUC), sensitivity, specificity, positive and negative predictive value, positive and negative likelihood ratio for qSOFA≥2, SIRS≥2 and NEWS>5.

 

Results

Of 665 patients recruited, median age was 73 years (IQR: 58-84); 313 (47%) were male. Overall 30-day mortality was 4.8%. The prognostic value for prediction of 30-day mortality, with AUC of for qSOFA≥2, SIRS≥2 and NEWS>5 were 0.54 (95%CI 0.51-0.58), 0.65 (95%CI 0.61-0.69) and 0.65 (95%CI 0.61-0.68) respectively. Using pairwise comparison of ROC curves, the difference between NEWS>5 and qSOFA≥2 in predicting 30-day mortality in ED patients was significant (p=0.0168). The AUC of lactate level ≥ 2 mmol/l of predicting 30-day mortality was 0.66 (95%CI 0.62-0.69). The combination of lactate level ≥ 2 mmol/l with qSOFA≥2, SIRS≥2 and NEWS>5, AUC were 0.53 (95%CI 0.49-0.57), 0.65 (95%CI 0.61-0.69) and 0.60 (95%CI 0.56 to 0.64) respectively. In addition, positive likelihood ratio of qSOFA≥2, SIRS≥2 and NEWS>5 to predict 30-day mortality were 19.69 (95%CI 4.14-93.73), 2.53 (95%CI 1.73-3.70) and 3.55 (95%CI 2.22-5.70).

 

Discussion

Among emergency and urgent patients presenting to the ED, the prognostic value for using NEWS was greater than qSOFA, while there was no difference between qSOFA and SIRS. Combinations of lactate level with qSOFA, SIRS or NEWS did not improve the prognostic value in predicting 30-day mortality for ED patients.


Ling Yan LEUNG, Dr Kevin Kei Ching HUNG (Hong Kong, Hong Kong), Ronson Sze Long LO, Yuk Ki LEUNG, Catherine Siu King CHEUNG, Chun Yu YEUNG, Suet Yi CHAN, Colin GRAHAM
17:00 - 17:10 #11486 - OP096 Early lactate clearance and short-term mortality in severe sepsis and septic shock patients.
Early lactate clearance and short-term mortality in severe sepsis and septic shock patients.

Introduction: The sensitivity and specificity of single lactate concentrations as markers of tissue hypoperfusion in sepsis have been debated. However, serial measurements or lactate clearance over time may be better prognosticators of organ failure and mortality.

Objective: Examine the clinical utility of the lactate clearance (or the percent decrease in lactate) as early as after 6 hours as an indicator of outcome in severe sepsis and septic shock.

Methods: Prospective observational study over one year. Inclusion of adult patients presenting to the emergency department (ED) with severe sepsis or septic shock. Inclusion criteria consisted of a suspected sepsis source and the following: a) two or more criteria of the systemic inflammatory response syndrome (SIRS) (temperature ≥38 ° C or ≤36 ° C, heart rate> 90 beats/min, respiratory rate > 20 / min or PaCO2 <32 mm Hg or WBC > 12,000 cel / mm3 or <4,000 / mm3) associated with organ failure (defining severe sepsis) or b) two of the SIRS criteria and a persistent hypotension (SBP <90 mmHg) despite fluid resuscitation or signs of hypoperfusion (lactate ≥4 mmol / l) (defining septic shock). Serial lactate levels in ED admission and 6 hours (h) later were measured. Lactate clearance, percent decrease in lactate level in 6 h ((lactate admission – lactate 6 h) x 100/lactate admission) was calculated. The main outcome measure was 7-day mortality.

Results: Inclusion of 253 patients. Mean age was 61 ± 17 years. Sex-ratio = 0.84. The overall mortality at the seven day was 10%. Baseline APACHE II score was 12 ± 78 and the median admission lactate was 1.1 mmol/L [0.6, 2.27]. Survivors compared with nonsurvivors had a median lactate clearance of 25 vs. 19, respectively (p=0.05). Based on Area Under the Curve in receiver operating characteristic analysis, lactate clearance have a significant inverse relationship with short-term mortality (0.63, 95% CI [0.45 to 0.80]), with a cut-off at 25%. The sensitivity, specificity, positive predictive value and negative predictive value of this cut-off were   56, 47, 25 and 81% respectively.

Conclusions: Lactate clearance in the most proximal presentation of severe sepsis and septic shock is associated with improved mortality rates. This is consistent with current efforts that emphasize the importance of identifying and treating tissue hypoperfusion during the first 6 hours of resuscitation. 


Hanen GHAZALI (Ben Arous, Tunisia), Ihsen HNEN, Soumaya MAHDHAOUI, Ines CHERMITI, Aymen ZOUBLI, Ahlem AZOUZI, Sawsen CHIBOUB, Sami SOUISSI
17:10 - 17:20 #11543 - OP097 An e-learning program to attempt to decrease the use of Third-generation cephalosporin for pneumonia in the Emergency Department.
An e-learning program to attempt to decrease the use of Third-generation cephalosporin for pneumonia in the Emergency Department.

Background: Third-generation cephalosporins are particularly prone to promote bacterial resistance. Their use for pneumonia increased between 2002 and 2012 in our Emergency Department, and 80% of these prescriptions may have been avoided, i.e. third-generation cephalosporin may have been replaced by a penicillin. In 2013, we implemented an e-learning program that encouraged treating pneumonia with a penicillin rather than a Third-generation cephalosporin, when possible. The e-learning was completed by 65% of physicians in 2013 and by every Emergency Department resident since 2013. 

Objectives: to assess if the e-learning implementation was associated with a decreased proportion of patients treated with a Third-generation cephalosporin and with a decreased proportion of avoidable Third-generation cephalosporin prescriptions.

Methods: Retrospective study of a random sample of patients treated for community-acquired pneumonia in an emergency department between 2002 and 2015, and subsequently hospitalized in non-Intensive Care Units. Third-generation cephalosporin prescriptions were presumed unavoidable if they met both criteria: (i) age ≥ 65 year’s old or a comorbid condition; and (ii) allergy or intolerance to penicillin, or failure of penicillin first-line therapy, or treatment with penicillin in three previous months. Prescriptions were otherwise deemed avoidable. Percentages are shown with 95% confidence interval.

Results: 956 patients were included. The proportion of patients treated with a Third-generation cephalosporin increased significantly from 14% [7%–24%] in 2002 to 30% [20% – 42%] in 2012 (Chi-scare for trend, P=0,02). This proportion was stable between 2013 (26% [18%-36%]) and 2015 (29% [19%-40%]; Chi-scare for trend, P=0,78). Treatment with a Third-generation cephalosporin was avoidable in 165 out of 212 patients (78% [72% – 84%]) during the whole study period. The proportion of avoidable prescriptions tended to decrease after the e-learning implementation, but the difference was not statistically significant (before e-learning, 79% [72%– 85%]; after e-learning, 74 % [62% – 84%]; P=0,6). 

Conclusion: The implementation of an e-learning program seemed to stop the yearly increase of the proportion of patients treated with a Third-generation cephalosporin for pneumonia in the Emergency Department, but it failed to decrease the proportion of avoidable prescriptions of Third-generation cephalosporin. Other interventions are necessary to decrease the use of Third-generation cephalosporin for pneumonia in the Emergency Department.


Nicolas GOFFINET (Nantes), Loan THUONG, François JAVAUDIN, Emmanuel MONTASSIER, Philippe LE CONTE, Eric BATARD
17:20 - 17:30 #11576 - OP098 QuickSOFA is an independent predictor of 30-day mortality among patients admitted to an emergency department with suspected or documented infection.
QuickSOFA is an independent predictor of 30-day mortality among patients admitted to an emergency department with suspected or documented infection.

QuickSOFA is an independent predictor of 30-day mortality among patients admitted to an emergency department with suspected or documented infection

Osama Bin Abdullah1, Johannes Grand1, Astha Sijapati1, Petrine Nimskov1 , Finn Erland Nielsen1,2
1. Department of Emergency Medicine, Slagelse Hospital, Slagelse, DENMARK
2. Institute of Regional Health Services Research, University of Southern Denmark, DENMARK.

Background. Definitions and clinical criteria for sepsis have been revised in 2016. A simple bedside score (‘qSOFA’, for quick Sequential [Sepsis-Related] Organ Failure Assessment) has been proposed, which incorporates hypotension (systolic blood pressure ≤100mmHg), altered mental status and respiratory rate ≥ 22/min: the presence of at least two of these criteria has been associated with poor outcomes typical of sepsis.

Purpose. To evaluate qSOFA as a predictor of 30-day mortality in a model with other predictors of death among patients admitted to a single-centre emergency department (ED) with either suspected or documented infection on admission.

Methods. A historical cohort study among prospectively registered patients with suspected or documented infection. The patients were having at least two Systemic Inflammatory Response Syndrome (SIRS) criteria on admission and all the patients were treated with intravenous antibiotics in the ED. The admission period was from 1 November 2013 to 31 October 2014. Baseline clinical data and data for survival were obtained from a standard sepsis admission form, the patient records and The Danish Civil Registration System. Logistic regression analysis was used to adjust for potential confounders and to determine whether the predictive factors for death in the crude analyses were independently associated with 30-day mortality.

Results. A total of 434 patients with a median age of 70 years were included in the study, 246 (56.7%) were men. Fifty seven (13.1%; 95% confidence interval [CI] 9.9-16.3%) patients died during the first 30 days. Among several potential confounders tested in the model we found that age (odds ratio [OR] 1.29; 95% CI 1.03-1.61), Charlson Comorbidity Score ≥ 3 (OR 3.83; 95% CI 1.41-10.37), qSOFA score ≥2 (OR 4.78; 95% CI 2.09-10.91) and lactate values (lactate values < 2.0 as reference) in the interval 2.00-3.99 (OR 2.21; 95% CI 1.06-4.62) and lactate values ≥ 4.0 (OR 3.97; 95% CI 1.44-2,92) were associated with 30-day mortality.

Conclusion. This study shows that a new simple clinical bedside index, qSOFA, can be helpful to identify infectious patients in an ED with an increased risk of 30-day mortality.


Dr Osama Bin ABDULLAH (Copenhagen, Denmark), Johannes GRAND, Astha SIJAPATI, Petrine NIMSKOV, Finn Erland NIELSEN
17:30 - 17:40 #11719 - OP099 A predictive score of acute appendicitis for practice in emergency department.
A predictive score of acute appendicitis for practice in emergency department.

Introduction :

Acute appendicitis is the most surgical emergency. Its diagnosis is not already evident. So we need a predictive score as simple and effective  to avoid  unnecessary investigations.Objective :To establish a predictive score of acute appendicitis more adapted  to our population and more practical.Methods :      A prospective study carried out in our  emergency department) over a period  of 2 years, involving patients presenting with acute abdominal pain in the right iliac fossa (FID). Datas interesting medical caracteristics , biologic and imaging were collected at baseline. diagnosis of acute appendicitis is confirmed by positive histological exam. Results :400 patients were enrolled and completed follow-up .the mean age of the study population was  33 +/-7 years. The sex ratio was 1.4 . Among these patients , for only 240 ( 60%) the diagnosis of appendicitis was comfirmed histologically  . The most common reason for consultation in this series is FID pain,this sign is present in 77.5% in the confirmed group group with p = 0.016. Univariate analysis identified other signs as  significantly predictifs ( p = 0.001 ) : radiation of pain from epigastrum to the umbilicus ,  positive rovsing sign and sensitive abdomen in palpation.In  multivariate analysis, our score was estabished, containing 7 variables : Vomiting>=2 épisode =1 point) , pain project From the epigastrium to the umbilicus =  2 point ,  positive  Rovsing sign =1 point , positive Blumberg sign = 1 point, sensitive abdomen =2 point , défense de la FID=  2 point and  White blood cells >10000 (hyperleucocytosis) =2 point .

The descrimination power is represented by the ROC curve. Area under the ROC curve of the appendicitis score was 0.874.This score can have a sensitivity of 99% and a specifity of 80%.

Conclusion :  many  scores have been developed (Alvarado, Andersson, François, ...), but are not common practice. A model based on variables easily available at ED, like our appendicitis score , can help ED physicians to diagnosis the acute appendicitis.


Houda BEN SALAH, Asma ZORGATI, Lotfi BOUKADIDA, Ali OUSJI (Sousse, Tunisia), Ikhlass BEN AICHA, Riadh BOUKEF
Kokkali
17:40

"Tuesday 26 September"

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AGM
17:40 - 18:40

EUSEM Annual General Assembly
for Members only

Mitropoulos