Home > Bibliographic references

Swiss Emergency Research collection

2025

  • Schaad, L., Hangartner, E., Berna, C., Nikles, J., Hyvert, L., Anonga Varela, T., Campbell, D., et al. “Healthcare Needs, Expectations And Experiences Of People Experiencing Homelessness In Western Switzerland: A Qualitative And Quantitative Descriptive Study”. Swiss Med Wkly 155, no. 2: 3659. doi:10.57187/s.3659.
    Abstract: AIMS: The literature from Canada, the UK and the USA reports health inequities among people experiencing homelessness; however little is known about this population's health in Switzerland. Our study is the first to comprehensively assess health needs, expectations and experiences of people experiencing homelessness in Switzerland. METHODS: We describe the health needs, expectations and experiences of people experiencing homelessness in French-speaking Switzerland, using both quantitative and qualitative methods. From May to August 2022, 123 people experiencing homelessness completed quantitative questionnaires about health needs, expectations and experiences. Recruitment took place in 10 homeless-serving institutions across four cities in the Canton of Vaud. A total of 18 people experiencing homelessness and 13 professionals involved in the homeless-serving sector completed qualitative interviews. For the qualitative strand, we selected people experiencing homelessness using quota sampling based on health insurance, residency status and sex representativeness according to the study population. For homeless-serving sector professionals, we used quota sampling by professions (i.e. night watcher in shelters; social/healthcare workers) ensuring balance. In addition, we aimed to recruit at least one homeless-serving sector professional from each of the ten institutions included in the parent research project. RESULTS: The most common health issues reported were musculoskeletal, dental and psychiatric. Thirty-one percent of people experiencing homelessness had visited emergency rooms and 27% a community health centre in the prior 6 months. People experiencing homelessness reported low quality of life according to the WHOQOL, especially in social and environmental domains; 33% reported moderate and 17% high grade of psychological distress. Findings indicated that up to 32% of participants reported facing difficulties in reaching out to the healthcare system. In qualitative interviews, people experiencing homelessness described positive perceptions about the Swiss healthcare system. However, people experiencing homelessness reported various barriers encountered while seeking healthcare (e.g., health insurance, financial barriers, appointment delays, hesitancy in accessing care, prioritising other needs). Both groups commonly reported that social situations impacted the health and healthcare use of people experiencing homelessness. CONCLUSION: People experiencing homelessness in Switzerland are not spared by the common health inequities reported in Canada, the USA and the UK. Our results provide interesting foundations on which to build public health actions towards health equity for people experiencing homelessness in Switzerland and suggest that they could benefit from additional medical follow-up and tailored interventions.
    Tags: *Health Services Needs and Demand/statistics & numerical data, *Ill-Housed Persons/psychology/statistics & numerical data, Adult, Female, Health Services Accessibility, Humans, Male, Middle Aged, Qualitative Research, Surveys and Questionnaires, Switzerland.
  • Trachsel, M., Trippolini, M. A., Jermini-Gianinazzi, I., Tochtermann, N., Rimensberger, C., Hubacher, V. N., Blum, M. R., and Wertli, M. M. “Diagnostics And Treatment Of Acute Non-Specific Low Back Pain: Do Physicians Follow The Guidelines?”. Swiss Med Wkly 155, no. 1: 3697. doi:10.57187/s.3697.
    Abstract: BACKGROUND: Clinical guidelines for acute non-specific low back pain recommend avoiding imaging studies, refraining from strong opioids and invasive treatments, and providing information to patients to stay active. Despite these recommendations, many patients undergo diagnostic and therapeutic assessments that are not in line with the current evidence. AIM: To assess the management of acute non-specific low back pain by Swiss general practitioners (GPs) and their adherence to guideline recommendations. METHODS: We performed a survey using two clinical case vignettes of patients with acute non-specific low back pain without red flags or neurological deficits. The main differences between the vignettes were sex, age, profession, pain duration and medical history. GPs were asked about their management of those patients. RESULTS: Of 1253 GPs, 61% reported knowing current clinical guidelines and 76% being aware of "Choosing Wisely" recommendations. Diagnostic evaluations included X-ray (18% for vignette 1, 32% for vignette 2) and magnetic resonance imaging (MRI) (31% and 62%). For pain management, GPs recommended mostly non-steroidal anti-inflammatory drugs, paracetamol and metamizole. Treatments with potential harm included muscle relaxants (78% and 77%), oral steroids (26% and 33%), long-acting opioids (8% and 11%) and spinal injections (28% and 42%). A very high proportion recommended activity restrictions (82% and 71%) and some recommended bed rest (3% and 2%). CONCLUSION: Although GPs reported being aware of current guideline recommendations, management of acute non-specific low back pain was not in line with these recommendations. A substantial proportion of GPs considered imaging, treatments (e.g. muscle relaxants, long-acting strong opioids), and activity and work restrictions with potentially harmful consequences.
    Tags: *General Practitioners/statistics & numerical data, *Guideline Adherence/statistics & numerical data, *Low Back Pain/diagnosis/therapy/drug therapy, *Pain Management/methods, *Practice Patterns, Physicians'/statistics & numerical data, Acetaminophen/therapeutic use, Adult, Anti-Inflammatory Agents, Non-Steroidal/therapeutic use, Dipyrone/therapeutic use, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Practice Guidelines as Topic, Surveys and Questionnaires, Switzerland.
  • Darie, A. M., Grize, L., Jahn, K., Salina, A., Rocken, J., Herrmann, M. J., Pascarella, M., et al. “Preventing Oxygen Desaturation During Bronchoscopy In Copd Patients Using High-Flow Oxygen Versus Standard Management: The Randomised Controlled Prosa 2 Trial”. Eur Respir J 65, no. 5. doi:10.1183/13993003.01586-2024.
    Abstract: BACKGROUND: Patients with COPD are at increased risk for developing additional respiratory comorbidities associated with smoking, and are thus prone to undergo flexible bronchoscopy. However, COPD patients have increased periprocedural complications risk and lower oxygen saturation during bronchoscopy. METHODS: This was an investigator-initiated, single-centre, open-label randomised controlled trial designed to assess the benefits of high-flow nasal oxygen compared to conventional low-flow oxygen by nasal cannula during conscious sedation for bronchoscopy in patients with COPD. Low flow was supplied at a starting rate of 4 L.min(-1) and gradually increased up to 12 L.min(-1) to maintain peripheral oxygen saturation (S (pO(2)) ) >90%. High flow delivered starting at a rate of 60 L.min(-1) and an inspiratory oxygen fraction of 0.6 was increased up to 80 L.min(-1) to preserve S (pO(2)) >90%. The primary end-point was cumulative hypoxaemia time. RESULTS: We randomised 600 COPD cases with a median (interquartile range (IQR)) age of 69.0 (62.0-76.0) years to either high flow (n=295) or low flow (n=305). The cumulative hypoxaemia time was 53% lower in the high-flow group (1.8% (95% CI 1.5-2.2%) versus 3.8% (95% CI 3.2-4.5%) of monitoring time; p<0.001). Additionally, the high-flow group experienced a median (IQR) of 3.0 (1.0-6.0) hypoxaemia events (S (pO(2)) <90%) compared to 6.0 (3.0-10.0) in the low-flow group (p<0.001). The low-flow group had five-fold higher odds of experiencing hypoxaemia during bronchoscopy, (OR 5.1, 95% CI 3.2-8.2; p<0.001). CONCLUSION: High flow is feasible, decreases cumulative hypoxaemia time and reduces hypoxaemia events during bronchoscopy in patients with COPD but does not impact patient comfort.
    Tags: *Bronchoscopy/methods/adverse effects, *Hypoxia/prevention & control, *Oxygen Inhalation Therapy/methods, *Oxygen/blood, *Pulmonary Disease, Chronic Obstructive/therapy/complications, Aged, Berline-Chemie/Menarini, Boehringer Ingelheim, Chiesi, CSL Behring, Curetis AG,, Cannula, D. Stolz is the GOLD representative for Switzerland. The remaining authors have, Female, Foundation, lecture honoraria from AstraZeneca, GSK and Sanofi, travel support, from OrPha Swiss, MSD, Gebro Pharma and Janssen, and advisory board participation, GSK, Merck, MSD, Novartis, Sanofi, Vifor and Roche, and data safety, GSK, Merck, MSD, Roche, Novartis, Sanofi and Vifor, outside the submitted work, Humans, lecture honoraria and travel support from AstraZeneca, outside the submitted, Male, Middle Aged, monitoring/advisory board participation with AstraZeneca,, no potential conflicts of the interest to report., Oxygen Saturation, the submitted work. D. Stolz reports lecture honoraria from AstraZeneca,, University of Basel, Freiwillige Akademische Gesellschaft Basel and Lungitude, with Gebro Pharma, Janssen and MSD, outside the submitted work. J. Rocken reports, work. M.J. Herrmann reports lecture honoraria from Lowenstein Medical, outside.
  • Chiollaz, A. C., Pouillard, V., Seiler, M., Habre, C., Romano, F., Ritter Schenck, C., Spigariol, F., et al. “Evaluating Nfl And Ntprobnp As Predictive Biomarkers Of Intracranial Injuries After Mild Traumatic Brain Injury In Children Presenting To Emergency Departments”. Front Neurol 16: 1518776. doi:10.3389/fneur.2025.1518776.
    Abstract: OBJECTIVE: Blood-biomarkers have the potential to aid clinicians in pediatric emergency departments (PED) in managing children with mild traumatic brain injury (mTBI) acutely. However, studies focusing on pediatric populations remain limited. We aim to assess the performances of two routinely used biomarkers in other fields: the neurofilament light chain protein (NfL), and the N-terminal prohormone of brain natriuretic peptide (NTproBNP), to safely discharge children without intracranial injuries (ICIs). METHODS: A prospective multicenter cohort study was conducted, enrolling children suffering from mTBI, both with and without imaging during their acute management in the PED. A blood sample was collected within 24 h post-trauma for biomarker analysis. Inclusion criteria followed the PECARN (Pediatric Emergency Care Applied Research Network) guidelines for the diagnosis of mTBI and for ICI on CT as the primary outcome (CT+). RESULTS: A total of 302 mTBI patients were analyzed comparing children with ICI (18 CT+) versus all the other children without ICI (54 CT- and 230 in-hospital-observation patients without CT). NfL and NTproBNP were increased in the CT+ group and their performances to safely rule-out patient without ICI reached up to 30% specificity with 100% sensitivity. Equivalent performances were observed whether selecting patients with blood collection within 6 h or 24 h post-trauma. CONCLUSION: NfL and NTproBNP were described for the first time in children suffering mTBI. Their performances were comparable to well-known biomarkers, such as S100b, GFAP, or HFABP, with the benefit of already being used in routine tests for other diseases. Further large-scale studies are necessary to verify and validate these results.
    Tags: blood-biomarkers, commercial or financial relationships that could be construed as a potential, conflict of interest., diagnosis, emergency, mTBI, pediatric.
  • Deglise, A., Guechi, Y., Le Terrier, C., Ribordy, V., Feral-Pierssens, A. L., and Schmutz, T. “Safety Assessment Of A Redirection Process After Triage (Safe Retri) By A Triage Nurse In An Emergency Department: A Monocentric Cohort Study”. Swiss Med Wkly 154, no. 12: 4030. doi:10.57187/s.4030.
    Abstract: AIMS OF THE STUDY: As emergency department consultations rise across Europe, patients must be guided to obtain appropriate care at the right time and place.In Switzerland, the absence of a unique health number that would enable the avoidance of emergency services through telephone medical advice, and the shortage of general practitioners, redirecting low-severity patients from the emergency department before medical consultation to other healthcare facilities could help reduce emergency department overload. This study assessed the safety of a newly implemented redirection process by examining the rate of unexpected returns to any healthcare facility. METHODS: This monocentric cohort study included patients aged 18 or older who presented to the emergency department of a regional hospital in Switzerland between 1 January and 31 May 2023 and who accepted redirection before medical consultation. Patients were identified from our electronic medical registry and retrospectively enrolled after telephone interviews. The primary outcome was the rate of unexpected returns to any healthcare facility within 2 days of redirection. The secondary outcomes were the rate of returns within 7 days, hospital admissions, and patient satisfaction. RESULTS: Among 16,362 patients who came to the emergency department during the study period, 688 (4%) were redirected. A total of 321 patients were included in the final analysis after telephone interviews. The rate of unexpected returns to any healthcare facility after redirection was 4% within 2 days and 16% within 7 days. The rate of returns to any hospital was 1.2% within 2 days and 4.7% within 7 days after redirection. Six patients (2%) required hospitalisation, and no fatalities were reported. The mean satisfaction score was 3.9/5 (standard deviation [SD] = 1.1) for triage experience, 4.4/5 (SD = 1) for care received in partner clinics, and 3.7/5 (SD = 1) for the redirection process. CONCLUSION: The rate of unexpected returns to any healthcare facility after redirection was 4% within 2 days and 16% within 7 days. The implementation of this protocol appeared to provide safe redirection to nearby clinics for redirected low-acuity patients. Satisfaction with care received in partner clinics was high, although it was lower for the redirection process and triage experience.
    Tags: *Emergency Service, Hospital/organization & administration/statistics & numerical, *Patient Safety, *Triage/methods, Adult, Aged, Cohort Studies, data, Female, Humans, Male, Middle Aged, Patient Satisfaction/statistics & numerical data, Referral and Consultation/statistics & numerical data, Retrospective Studies, Switzerland.
  • Vallelian, M., Juillerat, A., Sunic, M., Schneider, C., and Boet, S. “Two Cases Of Highly Concentrated Hydrogen Peroxide Poisoning With Portal Venous Gas Treated Using Hyperbaric Oxygen Therapy”. Bmj Case Rep 18, no. 2. doi:10.1136/bcr-2024-261916.
    Abstract: Hydrogen peroxide poisoning is a rare but potentially severe poisoning that can cause digestive tract irritation and/or gas embolism when ingested. The clinical presentation varies from asymptomatic patients to severe embolic consequences or even death. There is little evidence on the treatment of such poisoning to guide physicians in caring for these patients. This paper reports on two cases of highly concentrated hydrogen peroxide poisoning after accidental ingestion. Both patients showed evidence of portal venous gas, with one patient exhibiting significant symptoms while the other did not. Both were treated with hyperbaric oxygen therapy (HBOT), with a follow-up CT scan revealing a complete resolution of the portal venous gas. This suggests that HBOT is effective for both symptomatic and asymptomatic patients with portal venous gas and should be considered as an effective treatment option in cases of highly concentrated hydrogen peroxide poisoning.
    Tags: *Embolism, Air/therapy/chemically induced/diagnostic imaging, *Hydrogen Peroxide/poisoning, *Hyperbaric Oxygenation/methods, *Portal Vein/diagnostic imaging, Adult, Female, Gas/Free Gas, Humans, Male, Middle Aged, Poisoning, Tomography, X-Ray Computed, Treatment Outcome.
  • Saxena, S., Barreto Chang, O. L., Suppan, M., Meco, B. C., Vacas, S., Radtke, F., Matot, I., et al. “A Comparison Of Large Language Model-Generated And Published Perioperative Neurocognitive Disorder Recommendations: A Cross-Sectional Web-Based Analysis”. Br J Anaesth. doi:10.1016/j.bja.2025.01.001.
    Abstract: BACKGROUND: Perioperative neurocognitive disorders (PNDs) are common complications after surgery and anaesthesia, particularly in older adults, leading to increased morbidity, mortality, and healthcare costs. Therefore, major medical societies have developed recommendations for the prevention and treatment of PNDs. Our study evaluated the reliability of large language models, specifically ChatGPT-4 and Gemini, in generating recommendations for PND management and comparing them with published guidelines. METHODS: We conducted an online cross-sectional web-based analysis over 48 h in June 2024. Artificial intelligence (AI)-generated recommendations were produced in six different locations across five countries (Switzerland, Belgium, Turkey, Canada, and the East and West Coasts of the USA). The English prompt 'a table of a bundle of care for perioperative neurocognitive disorders' was entered into ChatGPT-4 and Gemini, generating tables evaluated by independent reviewers. The primary outcomes were the Total Disagreement Score (TDS) and Quality Assessment of Medical Artificial Intelligence (QAMAI), which compared AI-generated recommendations with published guidelines. RESULTS: The study generated 14 tables, with TDS and QAMAI scores showing similar results for ChatGPT-4 and Gemini (2 [1-3] vs 2 [2-3], P=0.636 and 4 [4-4] vs 4 [3-4], P=0.424, respectively). AI-generated recommendations aligned well with published guidelines, with the highest alignment observed in ChatGPT-4-generated recommendations. No complete agreement with guidelines was achieved, and lack of cited sources was a noted limitation. CONCLUSIONS: Large language models can generate perioperative neurocognitive disorder recommendations that align closely with published guidelines. However, further validation and integration of clinician feedback are required before clinical application.
    Tags: Anesthesiology and Intensive Care (ESAIC) and has received speaker's fees from, artificial intelligence (AI), ChatGPT-4, clinical guidelines, Gemini, JBE is a member of the Board of Directors of the European Society of, large language models (LLM), Medtronic., patient outcomes, perioperative neurocognitive disorders (PND), trial OLIVER from Medtronic. SS has received speaker's fees from Medtronic/Merck..
  • Taleb, C., Gouvea Bogossian, E., Bittencour Rynkowski, C., Moller, K., Lormans, P., Quintana Diaz, M., Caricato, A., et al. “Liberal Versus Restrictive Transfusion Strategies In Subarachnoid Hemorrhage: A Secondary Analysis Of The Train Study”. Crit Care 29, no. 1: 67. doi:10.1186/s13054-025-05270-5.
    Abstract: BACKGROUND: The optimal hemoglobin (Hb) threshold to trigger red blood cell transfusions (RBCT) in subarachnoid hemorrhage (SAH) patients is unclear. This study evaluated the impact of liberal versus restrictive transfusion strategies on neurological outcome in patients with SAH. METHODS: This is a pre-planned secondary analysis of the "TRansfusion Strategies in Acute brain INjured Patients" (TRAIN) study. We included all SAH patients from the original study that were randomized to receive RBCT when Hb levels dropped below 9 g/dL (liberal group) or 7 g/dL (restrictive group). The primary outcome was an unfavorable neurological outcome at 180 days, defined by a Glasgow Outcome Scale Extended score of 1-5. RESULTS: Of the 190 SAH patients in the trial, 188 (98.9%) had data available for the primary outcome, with 86 (45.3%) in the liberal group and 102 (53.6%) in the restrictive group. Patients in the liberal group were older than in the restrictive group, but otherwise had similar baseline characteristics. Patients in the liberal group received more RBCT and showed higher Hb levels over time. At 180 days, 57 (66.3%) patients in the liberal group and 78 (76.4%) in the restrictive group had unfavorable outcomes (risk ratio, RR 0.87; 95% confidence intervals, 95% CI 0.71-1.04). Patients in the liberal group had a significantly lower risk of cerebral ischemia (RR 0.63; 95% CI 0.41-0.97). In a multivariate analysis, randomization to the liberal group was associated with a lower risk of unfavorable outcome (RR 0.83, 95% CI 0.70-0.99). CONCLUSIONS: A liberal transfusion strategy was not associated with a lower incidence of unfavorable outcome after SAH when compared to a restrictive strategy. However, in a multivariable analysis adjusted for confounders randomization to the liberal group was associated with lower risk of unfavorable outcome. The occurrence of cerebral ischemia was significantly lower in the liberal transfusion strategy group. TRIAL REGISTRATION: ClinicalTrials.gov number-NCT02968654 registered on November 16th, 2016.
    Tags: (P2015/327). Written informed consent was obtained from a legal surrogate before, *Blood Transfusion/methods, *Erythrocyte Transfusion/methods/standards, *Subarachnoid Hemorrhage/therapy, Acute brain injury, Aged, analysis of the TRAIN study. The TRAIN study was approved by the ethics, Anemia, Blood, committees in each hospital. The primary ethics committee, "Comite d'Ethique, Competing interests: Jean Louis Vincent is editor in chief of critical care. No, enrollment. Whenever possible, deferred consent was also obtained from the, Erasme-ULB", approved this multicentric study on the 14th of March 2016, Female, Glasgow Outcome Scale, Hemoglobins/analysis, Humans, Male, Middle Aged, other authors have reported competing interests., patients who regained mental capacity. Consent for publication: Not applicable., Stroke, Treatment Outcome.
  • Haaf, P., Mansella, G., Gherca, S., Zellweger, M. J., and Boeddinghaus, J. “Heatstroke-Induced Thromboembolic Myocardial Infarction”. Eur Heart J Cardiovasc Imaging 26, no. 6: 1079. doi:10.1093/ehjci/jeaf053.
    Tags: cardiac imaging, Heatstroke, invasive coronary angiography, magnetic resonance imaging, multi organ failure, thromboembolic myocardial infarction, thrombus.
  • Stephan, F. P., Riede, F. N., Unlu, L., Capoferri, G., Bosia, T., Regeniter, A., Bingisser, R., and Nickel, C. H. “Hyperkalemia Or Not? A Diagnostic Pitfall In The Emergency Department”. West J Emerg Med 26, no. 1: 176-179. doi:10.5811/westjem.35286.
    Abstract: INTRODUCTION: Hyperkalemia, a potentially life-threatening electrolyte disturbance, is commonly encountered in the Emergency Department (ED). However, the frequency of factitious hyperkalemia, an artificially elevated potassium level in hyperkalemic ED patients, is unknown. This study aims to detect the rate of factitious hyperkalemia among patients with a potassium concentration of >/=5.0 mmol/l in an all-comer ED population. METHODS: This retrospective, monocentric chart review analyzed data of 2,440 ED patients who presented with a potassium concentration of >/=5.0 mmol/L in their initial whole blood or plasma sample, who also underwent a repeat potassium measurement on the same day. Two groups were established based on potassium levels in the initial and repeat blood tests: 1) True hyperkalemia, characterized by consistently elevated potassium levels in both the initial and repeat samples; and 2) Factitious hyperkalemia, defined by an elevated initial potassium level while the repeat blood test showed a normal potassium level. A subset of factitious hyperkalemia was spurious hyperkalemia. In spurious hyperkalemia, the initial blood sample showed an elevated potassium level with evidence of hemolysis, but a repeat test revealed a normal potassium level without evidence of hemolysis. RESULTS: Of the 2,440 patients, 1,576 (65%) had true hyperkalemia and 864 (35%) factitious hyperkalemia. Among the 864 patients with factitious hyperkalemia, 597 (69%) displayed hemolysis in their initial blood sample, indicating spurious hyperkalemia due to in-vitro hemolysis. CONCLUSION: These data show that about one third of all hyperkalemic blood samples drawn in the ED were due to factitious hyperkalemia. The leading cause of factitious hyperkalemia was spurious hyperkalemia due to in-vitro hemolysis.
    Tags: *Diagnostic Errors/statistics & numerical data, *Emergency Service, Hospital, *Factitious Disorders/diagnosis/blood, *Hyperkalemia/diagnosis/blood, *Potassium/blood, Adult, Aged, Female, Humans, Male, Middle Aged, Retrospective Studies.
  • Larribau, R., and Sigaux, A. “There May Be More To This Than Meets The Eye: Hospital Performance And Racial Disparities In Neurological Outcome After Out-Of-Hospital Cardiac Arrest”. Resuscitation 208: 110527. doi:10.1016/j.resuscitation.2025.110527.
  • Dunser, M. W., Leach, R., Al-Haddad, M., Arafat, R., Baker, T., Balik, M., Brown, R., et al. “Emergency Critical Care - Life-Saving Critical Care Before Icu Admission: A Consensus Statement Of A Group Of European Experts”. J Crit Care 87: 155035. doi:10.1016/j.jcrc.2025.155035.
    Tags: Critical illness, Emergency department, Hospital wards, Intensive care, Inter-hospital, of techniques, methods, or drugs discussed in this manuscript., Pre-hospital, Survival.
  • Bonhomme, V., Putensen, C., Bottiger, B. W., Stevens, M. F., Marczin, N., Arnal, D., Brotfain, E., et al. “Brain Health: A Concern For Anaesthesiologists And Intensivists”. Eur J Anaesthesiol Intensive Care 3, no. 6: e0063. doi:10.1097/EA9.0000000000000063.
    Abstract: Damage to the brain can have disastrous and long-lasting consequences. The European Society of Anaesthesiology and Intensive Care (ESAIC) is aware of the importance of taking good care of the brain, both of patients and of anaesthesia and intensive care unit (ICU) caregivers, and has organised a complete learning track on brain health to bring this concern to the attention of practitioners. This learning track included an online Focus Meeting on Brain Health (November 25, 2023). We here provide readers with a digest of the information that was delivered during that meeting in an opinion paper driven by the authors' own reading of the literature. It is divided according to the meeting's sessions, including how to improve the health of an injured brain, how to keep a young or old brain healthy, how to keep a healthy adult brain unimpaired, how monitoring can impact brain health in the operating room and in the intensive care unit, and how to keep the anaesthesia and ICU caregivers' brain healthy. Each part is a brief and focused summary. The main delivered messages are that the management of injured brain patients involves an adequate choice of sedation, adequate brain monitoring, and focused attention to specific points depending on the underlying pathology; that several measures can be undertaken to protect the brain of the very young needing anaesthesia; that it is possible to detect older patients at risk of postoperative neurocognitive disorders, and that dedicated perioperative management by a multidisciplinary expert team may improve their outcomes; that apparently healthy adult brains may suffer during anaesthesia; that the electroencephalogram may track peri-operative brain dysfunction, and that female patients should be given special care in this respect; that multimodal brain monitoring helps to detect pathological processes and to maintain brain homeostasis; and that burnout in anaesthesiologists can be effectively fought using personal, organisational, managerial and legal approaches.
  • Beysard, N., Agudo, T., Serfozo, P., Zingg, T., Truong, P., Albrecht, R., Darioli, V., and Pasquier, M. “Adherence To Prehospital Thoracostomy Practice Guidelines For Traumatic Cardiac Arrest: A Retrospective Study”. Resusc Plus 22: 100870. doi:10.1016/j.resplu.2025.100870.
    Abstract: OBJECTIVES: The management of traumatic cardiac arrest (TCA) focuses on the immediate treatment of reversible causes, including bilateral thoracostomy. In our prehospital emergency service, bilateral thoracostomy has been recommended since 2012 for the management of TCA. We sought to analyse the prehospital management and clinical course of patients with TCA, focusing on changes over time in the use of thoracostomy. METHODS: In this single-centre retrospective observational study, we included patients with TCA managed by physicians of the prehospital service of Lausanne University Hospital from 2012 to 2024. The primary outcome was the annual rate of bilateral thoracostomy. Secondary outcomes included the rate of additional on-site measures, such as pelvic binder placement and airway management, and follow-up at 48 h. RESULTS: Among 3206 cardiac arrests during the study period, 473 (15%) were TCAs. Among the 247 patients with resuscitation attempts, thoracostomy was judged as indicated in 223 (90%) and performed in 148 (66%). Twenty-seven (18%) patients who had a thoracostomy were alive on arrival at hospital, with 9 (6.1%) still alive at 48 h. The mean annual proportion of patients in whom a thoracostomy was performed was 68% (range 0-100%) and increased significantly over the years (p < 0.001). CONCLUSIONS: The annual rate of thoracostomy in TCA patients increased significantly in the period 2012 to 2024. Larger studies are required to determine the impact of thoracostomy on survival.
    Tags: Adherence, Guidelines, personal relationships that could have appeared to influence the work reported in, Prehospital, this paper., Thoracostomy, Traumatic cardiac arrest.
  • Abramovich, I., Crisan, I., Scudellari, A., and Bilotta, F. “Recent Educational Tools In Anaesthesiology Residency Training Programs Aligned With The European Training Requirements”. Eur J Anaesthesiol Intensive Care 3, no. 5: e0058. doi:10.1097/EA9.0000000000000058.
  • Holtmann, J. A., Kipfer, B., Lehmann, B., Galanis, M., Hautz, W., and Exadaktylos, A. “Iatrogenic Stemi In A Male Trauma Patient Due To Coronary Artery Compression By A Left Sided Chest Tube”. Am J Emerg Med 90: 253 e5-253 e6. doi:10.1016/j.ajem.2025.01.040.
    Abstract: Iatrogenic ST segment elevation myocardial infarction (STEMI) after insertion of a left sided thoracic tube is a rare insertional complication. We present a case of coronary artery compression of the left anterior descending artery (LAD) caused by a left sided chest tube placed after blunt thoracic trauma with pneumothorax resulting in a STEMI. A 53-year-old male patient with severe blunt thoracic trauma presented in the emergency department. After diagnosing a left sided pneumothorax in the primary survey according to ATLS, a chest drain was inserted. Shortly after insertion of the chest tube, a STEMI pattern appeared on the ECG (electrocardiogram). CT scans showed proximity of the chest tube to the LAD. Immediate pullback of the chest tube led to resolution of the electrocardiographic abnormalities. Complications after chest tube insertion can occur in up to 30 % of patients. However, no similar case with iatrogenic ST segment elevation myocardial infarction due to compression of a coronary artery has been reported in the literature so far. Knowledge of the possible complications of an intervention is important and a 'high level of suspicion' is required in order to recognize and resolve them quickly.
    Tags: *Chest Tubes/adverse effects, *Pneumothorax/therapy/etiology, *ST Elevation Myocardial Infarction/etiology/diagnosis, *Thoracic Injuries/therapy/complications, *Wounds, Nonpenetrating/complications/therapy, Blunt thoracic trauma, Complication, Coronary Vessels/injuries, Electrocardiography, Humans, Iatrogenic Disease, Male, Middle Aged, Stemi, Thoracic drain, Thoracic tube, Tomography, X-Ray Computed.
  • Poletto, S., Diaper, J., Montanarini, A., Merighi, G., Fontao, F., Belin, X., Zannin, E., Habre, W., and Dellaca, R. L. “Experimental Validation Of A Novel Portable Device Integrating An Oxygen Concentrator And A Ventilation Module For Patients With Ali/Ards In Low Resource Countries: A Cross-Over Non-Inferiority Trial”. Pediatr Res 98, no. 1: 100-106. doi:10.1038/s41390-024-03792-2.
    Abstract: BACKGROUND: This non-inferiority, cross-over study aims to evaluate a novel proof-of-concept portable respiratory support device specifically designed for low-resource settings. The device integrates a ventilation module and an oxygen concentrator. METHODS: We studied twelve 4-week-old piglets with a mean weight of 8.4 kg before and after oleic acid-induced acute respiratory distress syndrome (ARDS). In each condition, animals received 1-h pressure control ventilation using a conventional ventilator (Servo-i, Getinge, SE) and the experimental ventilator in random sequence. Arterial blood gas analysis was performed every half-hour to adjust the ventilator settings. The primary outcome was partial pressure of oxygen to FiO(2) ratio (P/F) with a non-inferiority margin of 50 mmHg. RESULTS: P/F did not differ significantly between the experimental and the control ventilation at baseline (459.6(30.9) vs 454.4(28.6) mmHg) and during ARDS condition (165.1(36.9) vs 182.5(48.4) mmHg). The upper 95% CI of the difference between P/F after ventilation using the control and the experimental ventilator was 37.3 and 44.1 mmHg during baseline and ARDS, respectively. CONCLUSIONS: The experimental device was not inferior to a conventional ventilator during both baseline and ARDS conditions, suggesting that it can provide adequate treatment to infants with mild to moderate hypoxemic lung disease in resource-limited care settings. IMPACT STATEMENT: This manuscript provides the results of a non-inferiority study that compared a novel proof-of-concept respiratory support device, integrating a ventilation module and an oxygen concentrator, specifically designed for respiratory support in low-resource settings, with a conventional pediatric intensive care ventilator in an oleic-acid model of acute lung injury. Our results showed that the experimental device was non-inferior to a conventional ventilator, suggesting that it can provide adequate treatment to infants with mild to moderate hypoxemic lung disease in resource-limited care settings. The developed solution can also be relevant for other applications, including home mechanical ventilation.
    Tags: *Acute Lung Injury/therapy/chemically induced, *Oxygen Inhalation Therapy/instrumentation, *Oxygen/blood, *Respiration, Artificial/instrumentation, *Respiratory Distress Syndrome/therapy/chemically induced, animal protection laws (LPA, RS455)., Animals, Blood Gas Analysis, Canton of Geneva (GE184). Animals were cared for in accordance with current Swiss, Cross-Over Studies, Developing Countries, Disease Models, Animal, Equipment Design, Humans, Oleic Acid, Swine, The study was approved by the University of Geneva Animal Ethics Committee of the, Ventilators, Mechanical.
  • Gaechter, P., Ebrahimi, F., Kutz, A., and Szinnai, G. “Hospitalizations In People With Down Syndrome Across Age Groups: A Population-Based Cohort Study In Switzerland”. Eclinicalmedicine 80: 103062. doi:10.1016/j.eclinm.2024.103062.
    Abstract: BACKGROUND: People with Down syndrome suffer from multiple associated diseases. However, knowledge on rates and causes of hospitalizations is limited. METHODS: This population-based cohort study used national hospital claims data in Switzerland between January 1, 2012 and December 31, 2020. Included were hospitalizations of people aged 0-90 years. People with Down syndrome were identified using ICD-10-GM code Q90 and were compared to the general population. The primary outcome was the hospitalization rate. Secondary outcomes were the primary reasons for hospitalizations, secondary diagnoses, and in-hospital outcomes. Analyses were stratified by three age groups: neonates and infants (0-12 months), children and adolescents (1-17 years), and adults (18-90 years). We calculated incidence rates, risk ratios (RR), and regression coefficients with corresponding 95% confidence intervals (CI). FINDINGS: Among 9,992,538 hospitalizations, 5697 were identified for people with Down syndrome. Hospitalization rate for people with Down syndrome was highest in the first two years of life. In the total general population, it was highest in adults beyond 60 years. Primary reasons for hospitalization among people with Down syndrome were classified as diagnoses of the circulatory system (neonates and infants: RR 13.3 [95% CI 12.0-14.6], children and adolescents: RR 3.3 [95% CI 2.7-3.9]), and infectious diseases (adults: RR 4.0 [95% CI 3.7-4.2]). At birth, individuals with Down syndrome typically had an average of six diagnoses, a number that the general population reaches, on average, by the age of 69. People with Down syndrome experienced worse in-hospital outcomes, including longer stays in both the hospital and intensive care unit by a factor of 1.7 and a higher all-cause in-hospital mortality by an overall rate difference of 1.9%. INTERPRETATION: The findings underscore the medical complexity of hospitalized people with Down syndrome and emphasize the need for a comprehensive, age-inclusive approach to improve in-hospital outcomes and anticipate emergency hospitalizations across age groups. FUNDING: Kantonsspital Aarau AG.
    Tags: Down syndrome, Down's syndrome, Hospitalization rate, In-hospital outcome, Mortality, Trisomy 21.
  • Hautz, W. E., Marcin, T., Hautz, S. C., Schauber, S. K., Krummrey, G., Muller, M., Sauter, T. C., et al. “Diagnoses Supported By A Computerised Diagnostic Decision Support System Versus Conventional Diagnoses In Emergency Patients (Ddx-Bro): A Multicentre, Multiple-Period, Double-Blind, Cluster-Randomised, Crossover Superiority Trial”. Lancet Digit Health 7, no. 2: e136-e144. doi:10.1016/S2589-7500(24)00250-4.
    Abstract: BACKGROUND: Diagnostic error is a frequent and clinically relevant health-care problem. Whether computerised diagnostic decision support systems (CDDSSs) improve diagnoses is controversial, and prospective randomised trials investigating their effectiveness in routine clinical practice are scarce. We hypothesised that diagnoses made with a CDDSS in the emergency department setting would be superior to unsupported diagnoses. METHODS: This multicentre, multiple-period, double-blind, cluster-randomised, crossover superiority trial was done in four emergency departments in Switzerland. Eligible patients were adults (aged >/=18 years) presenting with abdominal pain, fever of unknown origin, syncope, or non-specific symptoms. Emergency departments were randomly assigned (1:1) to one of two predefined sequences of six alternating periods of intervention or control. Patients presenting during an intervention period were diagnosed with the aid of a CDDSS, whereas patients presenting during a control period were diagnosed without a CDDSS (usual care). Patients and personnel assessing outcomes were masked to group allocation; treating physicians were not. The primary binary outcome (false or true) was a composite score indicating a risk of reduced diagnostic quality, which was deemed to be present if any of the following occurred within 14 days: unscheduled medical care, a change in diagnosis, an unexpected intensive care unit admission within 24 h if initially admitted to hospital, or death. We assessed superiority of supported versus unsupported diagnoses in all consenting patients using a generalised linear mixed effects model. All participants who received any study treatment (including control) and completed the study were included in the safety analysis. This trial is registered with ClinicalTrials.gov (NCT05346523) and is closed to accrual. FINDINGS: Between June 9, 2022, and June 23, 2023, 15 845 patients were screened and 1204 (591 [49.1%] female and 613 [50.9%] male) were included in the primary efficacy analysis. The median age of participants was 53 years (IQR 34-69). Diagnostic quality risk was observed in 100 (18%) of 559 patients with CDDSS-supported diagnoses and 119 (18%) of 645 with unsupported diagnoses (adjusted odds ratio 0.96 [95% CI 0.71-1.3]). 94 (7.8%) patients suffered a serious adverse event, none related to the study. INTERPRETATION: Use of a CDDSS did not reduce the occurrence of diagnostic quality risk compared with the usual diagnostic process in adults presenting to emergency departments. Future research should aim to identify specific contexts in which CDDSSs are effective and how existing CDDSSs can be adapted to improve patient outcomes. FUNDING: Swiss National Science Foundation and University Hospital Bern.
    Tags: *Decision Support Systems, Clinical, *Diagnostic Errors/prevention & control, *Emergency Service, Hospital, Adult, Aged, and support for attending meetings or travel, authors declare no competing interests., Centre for Health Education Scholarship at the University of Vancouver. AKE, DS,, consulting fees, Cross-Over Studies, Double-Blind Method, EU, Drager Medical Switzerland, and Roche Diagnostics Germany, Female, for Postgraduate Education SIWF, from AO Foundation Switzerland, MDI Medical Australia, and the Swiss Institute, from Mundipharma Switzerland. SCH reports research grants from BELearn and a, Hospital of Bern, Humans, Male, Middle Aged, MN, and HS report financial support for the present study from the Swiss National, research grants from the Swiss National Science Foundation, the, Science Foundation and intramural funding from the Inselspital, University, Science Foundation. MM reports research grants from the Swiss Heart Foundation,, Switzerland, the International Emergency Care Foundation, and Burgergemeinde. All other.
  • Da Costa Rodrigues, J., Gazarian, C., Maillard, J., Albu, G., Assouline, B., Lador, F., and Schiffer, E. “Emergency Ecmo Deployment During Liver Transplantation In Portopulmonary Hypertension Patients”. Am J Case Rep 26: e946268. doi:10.12659/AJCR.946268.
    Abstract: BACKGROUND Portopulmonary hypertension (POPH) is part of Group 1 of the clinical classification of pulmonary hypertension and represents 5-15% of patients with pulmonary hypertension, with a 5-year mortality rate of 40%. The implementation of preoperative pulmonary antihypertensive treatment allows liver transplantation depending on clinical response, which constitutes potential curative treatment. Uncontrolled pulmonary hypertension is a major risk factor of perioperative morbimortality in the context of liver transplantation. In case of major hemodynamic instability, extracorporeal membrane oxygenation (ECMO) can be placed to manage circulatory failure. We describe a case of a patient with POPH in whom an emergency ECMO was implanted during liver transplantation complicated by an intraoperative worsening of pulmonary vascular resistances leading to cardiac arrest. CASE REPORT A 16-year-old patient with POPH had an orthotopic liver transplantation (OLT) after management of pulmonary hypertension with a triple antihypertensive therapy, which was complicated by hemorrhagic shock. Management of hemorrhagic shock led to greatly increased pulmonary vascular resistances, which led to a perioperative cardiac arrest, necessitating the implantation of a veno-arterial ECMO, allowing the completion of critical surgical steps before admission to the intensive care unit. CONCLUSIONS POPH is a challenge in the perioperative setting. OLT is a therapeutic option in that setting. ECMO may be necessary for patients with POPH in the perioperative hemodynamic management during OLT. In highly selected cases, VA-ECMO implantation and timing should be discussed by a multidisciplinary team before induction. The emergency perioperative implantation of ECMO is a realistic alternative.
    Tags: *Extracorporeal Membrane Oxygenation/methods, *Hypertension, Portal/complications/therapy, *Hypertension, Pulmonary/therapy/complications, *Liver Transplantation, Adolescent, Heart Arrest/etiology/therapy, Humans, Male.
  • Mackert, S., Walker, M., Pirlich, N., Schauble, J. C., Cardenas Marban, A., Ganter, M. T., Eichenberger, U., Nubling, M., and Heidegger, T. “Current Airway Management Practice Among Swiss Anesthesiologists : Results Of A National Survey”. Anaesthesiologie 74, no. 2: 89-96. doi:10.1007/s00101-024-01499-x.
    Abstract: BACKGROUND: While limited data on the impact of implementing guidelines in airway management on outcomes exist, there is a consensus that the implementation and the adherence to guidelines enhance patient safety. Recently, the Swiss Society for Anesthesiology and Perioperative Medicine (SSAPM) endorsed the guidelines of The Fondation Latine des Voies Aeriennes (FLAVA) as the official guidelines for airway management in Switzerland. This study aimed to determine current practice of airway management in Switzerland. OBJECTIVE: To determine the available equipment, the differences between institutions and between specialists and residents in dealing with airway management. METHODS: In collaboration with the SSAPM, a covering letter with a survey link to the questionnaire used in the online airway management survey among German anesthesiologists was sent to all heads of departments of anesthesia and members of the SSAPM in August 2023. The participants (residents and specialists) were asked about their personal and institutional backgrounds, access to airway management devices, awareness of recognized airway management guidelines and the importance and application of airway management techniques. RESULTS: Overall, 555 anesthesiologists participated in the survey (response rate 21%). The main findings were: in general, Swiss anesthesia departments are well-equipped and adhere to airway management guidelines. The guidelines of FLAVA are only known by just over 50%. The vast majority used the traditional screening tests to identify an airway that might be potentially difficult to manage. Of the respondents, 25% still adhere to the myth that a mask ventilation check is necessary before the administration of a muscle relaxant and 14% said that their institution used video laryngoscopy as the primary intubation device. More than 80% think that the expertise to perform awake fiberoptic intubation is important for their daily practice; however, 31% consider their expertise in this technique to be insufficient. In other words, there is a big safety gap. CONCLUSION: Swiss anesthesia departments are well-equipped and adhere to airway management guidelines. The need for regular training to gain and maintain expertise in managing difficult airways, especially to future specialists, still prevails. Thus, developing and establishing a nationwide educational program in airway management and its continuous evaluation would be a milestone for patient safety.
    Tags: *Airway Management/methods/statistics & numerical data/standards, *Anesthesiologists/statistics & numerical data, *Anesthesiology, *Practice Patterns, Physicians'/statistics & numerical data, Airway guidelines, article no studies with human participants or animals were performed by any of, declare that they have no competing interests. T. Heidegger has received research, Difficult airway, Female, Fiberoptic intubation, grants from the Foundation of Natural Science and Technological Research and from, Guideline Adherence/statistics & numerical data, Humans, indicated in each case., J.C. Schauble, A. Cardenas Marban, M.T. Ganter, U. Eichenberger and M. Nubling, Male, Middle Aged, Practice Guidelines as Topic, Safety, Surveys and Questionnaires, Switzerland, the authors. All studies mentioned were in accordance with the ethical standards, the Maiores Foundation, both in Vaduz, Principality of Liechtenstein. For this, Video laryngoscopy.
  • Renggli, L., Burri, A., Ehrhard, S., Gasser, M., Kronenberg, A., and Swiss Centre for Antibiotic, Resistance. “Incidence And Resistance Rates Of Pseudomonas Aeruginosa Bloodstream Infections In Switzerland: A Nationwide Surveillance Study (2010-2022)”. Infection 53, no. 4: 1373-1381. doi:10.1007/s15010-024-02452-1.
    Abstract: PURPOSE: Bloodstream infections (BSIs) cause significant morbidity and mortality worldwide. Pseudomonas aeruginosa is an important microorganism in BSIs. The aim of this study was to analyze recent trends in the incidence and resistance rates of P. aeruginosa BSIs in Switzerland and its different linguistic regions. METHODS: This retrospective, nationwide observational study analyzed the incidence (using Poisson regression models) and antimicrobial resistance (using logistic regression models) of P. aeruginosa BSIs in Switzerland from 2010 to 2022. RESULTS: The annual incidence of P. aeruginosa BSIs in Switzerland increased from 5.5 BSIs per 100,000 inhabitants in 2010 to 7.6 BSIs per 100,000 inhabitants in 2022 (p < 0.001). The incidence was higher in the French-speaking region than in the German-speaking region. The resistance rates increased significantly for cefepime (2.4% in 2010, 8.8% in 2022; p < 0.001), ceftazidime (5.6% in 2010, 9.4% in 2022; p = 0.014), ciprofloxacin (3.3% in 2010, 6.5% in 2022; p = 0.014), and piperacillin-tazobactam (6.4% in 2010, 11.2% in 2022; p = 0.002). No significant trends were observed for carbapenem-, aminoglycoside-, or multidrug-resistant P. aeruginosa. A high incidence was observed in patients >/= 80 years, whereas resistance rates were high in young patients. CONCLUSION: The increase in the incidence of P. aeruginosa BSIs emphasizes the importance of monitoring resistant and susceptible P. aeruginosa BSIs. Compared to the population-weighted mean resistance rates in Europe in 2022, those in Switzerland were lower, but an increase was observed for most antibiotics. The high resistance rates in young patients require further investigation.
    Tags: *Bacteremia/epidemiology/microbiology, *Drug Resistance, Bacterial, *Pseudomonas aeruginosa/drug effects, *Pseudomonas Infections/epidemiology/microbiology, Adolescent, Adult, Aged, Aged, 80 and over, Anti-Bacterial Agents/pharmacology/therapeutic use, Bacteremia, Bloodstream infections, Child, Child, Preschool, Epidemiological Monitoring, Female, Humans, Incidence, Infant, Male, Microbial Sensitivity Tests, Middle Aged, nature of the data, neither ethical approval nor written informed consent was, needed. Competing interests: The authors declare no competing interests., Pseudomonas aeruginosa, Resistance rate, Retrospective Studies, Switzerland, Switzerland/epidemiology, the Swiss Centre for Antibiotic Resistance ANRESIS. Because of the anonymous, Young Adult.
  • Eidenbenz, D., Gauss, T., Zingg, T., Darioli, V., Vallot, C., Carron, P. N., Bouzat, P., and Ageron, F. X. “Identification Of Major Trauma Using The Simplified Abbreviated Injury Scale To Estimate The Injury Severity Score: A Diagnostic Accuracy And Validation Study”. Scand J Trauma Resusc Emerg Med 33, no. 1: 13. doi:10.1186/s13049-025-01320-7.
    Abstract: BACKGROUND: The Abbreviated Injury Scale (AIS) and Injury Severity Score (ISS) grade the severity of injuries and are useful for trauma audit and benchmarking. However, AIS coding is complex and requires specifically trained staff. A simple yet reliable scoring system is needed. The aim of this study was two-fold. First, to develop and validate a simplified AIS (sAIS) chart centred on the most frequent injuries for use by non-trained healthcare professionals. Second, to evaluate the diagnostic accuracy of the sAIS (index test) to calculate the simplified ISS (sISS) to identify major trauma, compared with the reference AIS (rAIS) to calculate the reference ISS (rISS). METHODS: This retrospective study used data (2013-2014) from the Northern French Alps Trauma Registry to develop and internally validate the sAIS. External validation was performed with data from the Trauma Registry of Acute Care of Lausanne University Hospital, Switzerland (2019-2021). Both datasets comprised a random sample of 100 injured patients. Following the Standards for Reporting of Diagnostic Accuracy Studies 2015 guidelines, all patients completed the rAIS and the sAIS. The sISS and the rISS were calculated using the sAIS and the rAIS, respectively. Accuracy was evaluated with the mean difference between the sISS and the rISS and the Pearson correlation coefficient. A clinically relevant equivalence limit was set at +/- 4 ISS points. Precision was analyzed using Bland-Altmann plots with 95% limits of agreement. RESULTS: Accuracy was good. The mean ISS difference of 0.97 (95% CI, -0.03 to 1.97) in the internal validation dataset and - 1.77 (95% CI, - 3.04 to 0.50) in the external validation dataset remained within the equivalence limit. The Pearson correlation coefficient was 0.93 in the internal validation dataset (95% CI, 0.90-0.95) and 0.82 in the external validation dataset (95% CI, 0.75-0.88). The limits of agreement were wider than the predetermined relevant range. CONCLUSIONS: The sAIS is accurate, but slightly imprecise in calculating the ISS. The development of this scale increases the possibilities to use a scoring system for severely injured patients in settings with a reduced availability of the AIS. TRIAL REGISTRATION: Retrospectively registered.
    Tags: *Abbreviated Injury Scale, *Wounds and Injuries/diagnosis, Abbreviated injury scale, Adult, Aged, by the human research ethics committees responsible for each participating site,, Canton of Vaud (project ID 2022-01180), Switzerland. Consent for publication: We, Clermont-Ferrand (no. 5891), France, and the cantonal ethics committee of the, consent). Competing interests: The authors declare no competing interests., Female, Humans, i.e., the Institutional Review Board of the University Hospital of, included exclusively patients with written informed consent (institutional, Injury Severity Score, Major traumatic injury, Male, Middle Aged, Registries, Reproducibility of Results, Retrospective Studies, Switzerland, Trauma, Wounds and injuries.
  • Brunkert, T., Pfundstein, I., Nickel, C. H., Lampert, M. L., Trutschel, D., and Mauthner, O. “Advantage: Implementation And Evaluation Of An Interprofessional Transitional Care Model For Frail Older Adults-Protocol Of An Effectiveness-Implementation Hybrid Study”. J Adv Nurs 81, no. 8: 5130-5142. doi:10.1111/jan.16745.
    Abstract: AIM: To implement and evaluate an Advanced Practice Nurse-led transitional care model (AdvantAGE) to reduce rehospitalisation rates in frail older adults discharged from a Swiss geriatric hospital. DESIGN: The study adopts an effectiveness-implementation hybrid design (Type 1) to simultaneously evaluate the effectiveness of the care model and explore the implementation process. METHODS: The primary outcome, the 90-day rehospitalisation rate, will be evaluated using a matched-cohort design with a prospective intervention group and a retrospective control group. Secondary outcomes include the number of emergency department visits, health-related quality of life and intervention costs. The care model was developed through comprehensive contextual analysis and pilot testing in an iterative approach. It comprises five core elements: continuous support, care coordination, comprehensive health management at home, medication and self-management and advance care planning. Data collection includes both quantitative and qualitative methods, utilising routine hospital data, structured and semi-structured interviews and observations. Qualitative data will provide insights into implementation outcomes, potential barriers and facilitators. Additionally, a process evaluation will offer an in-depth understanding of individual intervention effects and reasons for rehospitalisation. DISCUSSION: The AdvantAGE project, grounded in implementation science methodology, aims to significantly improve transitional care outcomes for frail older adults. The results are expected to provide essential recommendations for scaling up the model to other settings. IMPACT: The study addresses the issue of frequent rehospitalisations in older adults, which carry risks of functional and cognitive decline. By implementing a comprehensive transitional care model, the study aims to improve continuity of care, reduce readmissions and enable frail older adults to remain in the community longer. The project highlights the importance of contextually adapted intervention and implementation strategies to bridge the gap between research and real-world healthcare practice. PATIENT OR PUBLIC INVOLVEMENT: The project employs a participatory approach, engaging representatives from the hospital and primary care settings, the cantonal health department and older people and their caregivers. TRIAL REGISTRATION: This study has been registered at clinicaltrials.gov on 5 January 2024 (Identifier: NCT06190288).
    Tags: *Advanced Practice Nursing, *Frail Elderly, *Patient Readmission/statistics & numerical data, *Transitional Care/organization & administration/standards, advanced practice nurses, Aged, Aged, 80 and over, Female, Humans, implementation science, Male, mixed-methods, nurse-led care model, Prospective Studies, quantitative and qualitative methods, readmission, Retrospective Studies, Switzerland, transitional care.
  • Baetzner, A. S., Hill, Y., Roszipal, B., Gerwann, S., Beutel, M., Birrenbach, T., Karlseder, M., et al. “Mass Casualty Incident Training In Immersive Virtual Reality: Quasi-Experimental Evaluation Of Multimethod Performance Indicators”. J Med Internet Res 27: e63241. doi:10.2196/63241.
    Abstract: BACKGROUND: Immersive virtual reality (iVR) has emerged as a training method to prepare medical first responders (MFRs) for mass casualty incidents (MCIs) and disasters in a resource-efficient, flexible, and safe manner. However, systematic evaluations and validations of potential performance indicators for virtual MCI training are still lacking. OBJECTIVE: This study aimed to investigate whether different performance indicators based on visual attention, triage performance, and information transmission can be effectively extended to MCI training in iVR by testing if they can discriminate between different levels of expertise. Furthermore, the study examined the extent to which such objective indicators correlate with subjective performance assessments. METHODS: A total of 76 participants (mean age 25.54, SD 6.01 y; 45/76, 59% male) with different medical expertise (MFRs: paramedics and emergency physicians; non-MFRs: medical students, in-hospital nurses, and other physicians) participated in 5 virtual MCI scenarios of varying complexity in a randomized order. Tasks involved assessing the situation, triaging virtual patients, and transmitting relevant information to a control center. Performance indicators included eye-tracking-based visual attention, triage accuracy, triage speed, information transmission efficiency, and self-assessment of performance. Expertise was determined based on the occupational group (39/76, 51% MFRs vs 37/76, 49% non-MFRs) and a knowledge test with patient vignettes. RESULTS: Triage accuracy (d=0.48), triage speed (d=0.42), and information transmission efficiency (d=1.13) differentiated significantly between MFRs and non-MFRs. In addition, higher triage accuracy was significantly associated with higher triage knowledge test scores (Spearman rho=0.40). Visual attention was not significantly associated with expertise. Furthermore, subjective performance was not correlated with any other performance indicator. CONCLUSIONS: iVR-based MCI scenarios proved to be a valuable tool for assessing the performance of MFRs. The results suggest that iVR could be integrated into current MCI training curricula to provide frequent, objective, and potentially (partly) automated performance assessments in a controlled environment. In particular, performance indicators, such as triage accuracy, triage speed, and information transmission efficiency, capture multiple aspects of performance and are recommended for integration. While the examined visual attention indicators did not function as valid performance indicators in this study, future research could further explore visual attention in MCI training and examine other indicators, such as holistic gaze patterns. Overall, the results underscore the importance of integrating objective indicators to enhance trainers' feedback and provide trainees with guidance on evaluating and reflecting on their own performance.
    Tags: *Emergency Responders/education, *Mass Casualty Incidents, *Virtual Reality, Adult, disaster medicine, emergency medicine, emergency simulation, eye tracking, Female, Humans, Male, mass casualty incident, medical education, prehospital decision-making, Triage, virtual reality.
  • Yamaguchi, K., Takahashi, K., Jakob, D. A., Abe, T., Matsushima, K., and Demetriades, D. “Pre-Injury Narcotic Drug Use In Isolated Severe Traumatic Brain Injury: Effect On Outcomes”. Eur J Trauma Emerg Surg 51, no. 1: 50. doi:10.1007/s00068-024-02743-0.
    Abstract: PURPOSE: The aim of this study was to explore the association between pre-injury narcotic drug use (opioids, methadone, and/or oxycodone) and outcomes in isolated severe traumatic brain injury (TBI) patients. METHODS: ACS TQIP study included adult trauma patients (>/= 16 years) with complete drug and alcohol screening. Isolated severe TBI was defined as head trauma with AIS 3-5 and without significant extracranial trauma. Exact matching was used to compare patients with isolated pre-injury narcotic drug use to those with no illicit drug or alcohol use. Patients were matched 1:1 based on the following matching criteria: age, gender, mechanism of injury, Injury Severity Score, systolic blood pressure, head AIS, and comorbidities. RESULTS: Of 1,846,630 patients, 141,058 had isolated severe head injuries with complete drug and alcohol screenings. After exact matching, 1,560 patients in each group were analyzed. There were no significant differences in hospital mortality, craniectomy rates, complication rates, or length of hospital stay. Patients that tested positive for narcotics had lower rates of mechanical ventilation (16.5% vs. 25.3%, p < 0.01) and shorter ICU stays [3 (2-4) days vs. 3 (2-6) days; p < 0.01]. CONCLUSION: Pre-injury narcotic drug use in isolated severe TBI is not associates with adverse outcomes. Further research is needed to understand the biochemical and physiological effects of narcotic drugs on TBI outcomes.
    Tags: *Brain Injuries, Traumatic/mortality/epidemiology, *Narcotics/adverse effects, *Opioid-Related Disorders/epidemiology, *Substance-Related Disorders/complications/epidemiology, Adult, Analgesics, Opioid, California. Competing interests: The authors declare no competing interests., Female, Hospital Mortality, Humans, Injury Severity Score, Length of Stay/statistics & numerical data, Male, Methadone/adverse effects, Middle Aged, Narcotic use, Outcomes, performed in line with the principles of the Declaration of Helsinki. Approval, Respiration, Artificial/statistics & numerical data, Severe traumatic head injury, Trauma, was granted by Institutional Review board of the University of Southern.
  • Brandenberger, J., Stedman, I., Stancati, N., Sappleton, K., Kanathasan, S., Fayyaz, J., and Singh, D. “Using Artificial Intelligence Based Language Interpretation In Non-Urgent Paediatric Emergency Consultations: A Clinical Performance Test And Legal Evaluation”. Bmc Health Serv Res 25, no. 1: 138. doi:10.1186/s12913-025-12263-1.
    Abstract: OBJECTIVE: To evaluate the accuracy of Google Translate (GT) in translating low-acuity paediatric emergency consultations involving respiratory symptoms and fever, and to examine legal and policy implications of using AI-based language interpretation in healthcare. METHODS: Based on the methodology used for conducting language performance testing routinely at the Interpreter Services Department of the Hospital for Sick Children, clinical performance testing was completed using a paediatric emergency scenario (child with respiratory illness and fever) on five languages: Spanish, French, Urdu, Arabic, and Mandarin. The study focused on GT's translation accuracy and a legal and policy evaluation regarding AI-based interpretation in healthcare was conducted by legal scholars. RESULTS: GT demonstrated strong translation performance, with accuracy rates from 83.5% in Urdu to 95.4% in French. Challenges included dialect sensitivity and pronoun misinterpretations. Legal evaluation indicated inconsistent access to language interpretation services across healthcare jurisdictions and potential risks involving data privacy, consent, and malpractice when using AI-based translation tools. CONCLUSIONS: Google Translate can effectively support communication in specific non-critical paediatric emergency scenarios. However, its use necessitates careful monitoring, understanding of its limitations, and attention to dialect and literal translation risks along with equity considerations. Establishing legal and policy frameworks for language interpretation in healthcare is crucial, alongside addressing funding and data security concerns, to optimize the use of AI-based translation tools in healthcare contexts.
    Tags: *Artificial Intelligence/legislation & jurisprudence, *Language, *Pediatrics, *Referral and Consultation/legislation & jurisprudence, *Translating, applicable. Competing interests: The authors declare no competing interests., Artificial intelligence, Child, Humans, Minor health visits, Non-urgent health visits, Pediatric emergency medicine, Pediatric migrant health, Pediatrics, Standard operating procedures, paragraph 5.3.2). Consent for publication: Not, study is not involving patients but is a quality performance test conducted at, the interpreter department (according to the SickKids Research Ethics Board.
  • Schranc, A., Sudy, R., Daniels, J., Fontao, F., Petak, F., Habre, W., and Albu, G. “Effects Of Variable Ventilation On Gas Exchange In An Experimental Model Of Capnoperitoneum: A Randomized Crossover Study”. Anesth Analg. doi:10.1213/ANE.0000000000007418.
    Abstract: BACKGROUND: The rapid advancement of minimally invasive surgical techniques has made laparoscopy a preferred alternative because it reduces postoperative complications. However, inflating the peritoneum with CO2 causes a cranial shift of the diaphragm decreasing lung volume and impairing gas exchange. Additionally, CO2 absorption increases blood CO2 levels, further complicating mechanical ventilation when the lung function is already compromised. Standard interventions such as lung recruitment maneuvers or increasing positive end-expiratory pressures can counteract these effects but also increase lung parenchymal strain and intrathoracic pressure, negatively impacting cardiac output. The application of variability in tidal volume and respiratory rate during mechanical ventilation to mimic natural breathing has shown benefits in various respiratory conditions. Therefore, we aimed to evaluate the short-term benefits of variable ventilation (VV) on gas exchange, respiratory mechanics, and hemodynamics during and after capnoperitoneum, compared to conventional pressure-controlled ventilation (PCV). METHODS: Eleven anaesthetized rabbits were randomly assigned to PCV or VV. Oxygenation index (Pao2/FiO2), arterial partial pressure of carbon dioxide (Paco2), and respiratory mechanical parameters were assessed after a 15-minute-long ventilation period before, during, and after capnoperitoneum. According to a crossover design, after measurements at the 3 different stages, the ventilation mode was changed, and the entire sequence was repeated. RESULTS: Capnoperitoneum compromised respiratory mechanics, decreased oxygenation, and caused CO2-retention compared to baseline measurements under both ventilation modalities (P < .05, for all). Application of VV resulted in lower Pao2/FiO2 (405. 5 +/- 34.1 (mean +/- standard deviation [SD]) vs 370. 5 +/- 44.9, P < .001) and higher Paco2 (48. 4 +/- 5.1 vs 52. 8 +/- 6.0 mm Hg, P = .009) values during capnoperitoneum compared to PCV. After abdominal deflation and a lung recruitment maneuver, VV proved more beneficial for CO2 removal than PCV (41. 0 +/- 2.3 vs 44. 6 +/- 4.3mmHg, P = .027). No significant difference was observed in the respiratory mechanical or hemodynamic parameters between the ventilation modalities under the same conditions. CONCLUSIONS: The detrimental effects of capnoperitoneum on gas exchange were more pronounced with VV. However, after the release of capnoperitoneum, VV significantly improved CO2 clearance. Therefore, VV could possibly be considered as an alternative ventilation modality to restore physiological gas exchange after, but not during, capnoperitoneum.
  • Lengeler, N., Starvaggi, C. A., Jaboyedoff, M., Affentranger, S., and Keitel, K. “Caregiver Alignment With Triage Acuity Levels And Drivers For Discrepancy Between Caregiver Assessment And Triage Acuity Levels: A Cross-Sectional Questionnaire Based Study”. Bmc Health Serv Res 25, no. 1: 96. doi:10.1186/s12913-024-12163-w.
    Abstract: BACKGROUND: Caregiver concern is the main driver to paediatric emergency departments visits. Understanding caregiver worries is crucial to guide patients to the most appropriate healthcare setting. Previous research shows mixed findings on the accordance between caregiver assessment and professional triage. METHODS: We assessed data from two questionnaire-based studies conducted over 27 months in two tertiary paediatric emergency departments in Switzerland to compare caregiver perception of their child's medical acuity and standard nurse triage. Furthermore, we examined socioeconomic factors associated with caregiver perception. RESULTS: Our study of 2,126 children seen in the two paediatric emergency departments showed that caregiver assessment aligned well with the acuity assigned by professional triage in 89% (1,901/2,126) of cases. In 142 cases (7%, 142/2,126), caregivers rating their child's severity higher than nurse's triage while in 83 cases (4%, 83/2,126), they rated it lower. In an univariable analysis, we found that family's difficulties paying bills (20% vs. 12%) and low maternal education (19% vs. 10%) were associated with a higher percentage of caregiver rating their child's severity higher than nurse's triage. Fever as the main complaint was associated with caregiver rating their child's severity lower than nurse's triage. CONCLUSIONS: This questionnaire-based study shows that caregiver's assessment of the severity of the child and nurse triage are concordant in most situations. Our study sheds light on the association between caregiver assessment and professional triage in two paediatric emergency departments in Switzerland, revealing some of the factors leading to discordance. These factors most probably reflect health illiteracy. It is important that healthcare professionals recognize and address factors influencing caregiver assessments to facilitate accurate decision-making and enhanced paediatric emergency care outcomes.
    Tags: *Caregivers/psychology, *Patient Acuity, *Triage/standards, accordance with the ethical standards of both Ethics Committees and with the, Adult, Bern (project number 2019-00538 and 2019-02280). They were conducted in, Caregiver assessment, Child, Child, Preschool, Cross-Sectional Studies, Emergency Service, Hospital, Female, Humans, Infant, Male, Not applicable. Competing interests: The authors declare no competing interests., Paediatric emergency medicine, parent at the time of PED visit for all participants. Consent for publication:, principles of the Declaration of Helsinki. Informed consent was obtained from the, Severity of Illness Index, Sociodemographic factors, Surveys and Questionnaires, Switzerland, Triage, were approved by the Cantonal Research Ethics Committees of Cantons of Vaud and.
  • Van Kerkhove, M. D. “Don't Pretend Covid-19 Didn't Happen”. Science 387, no. 6731: 229. doi:10.1126/science.adv8836.
    Abstract: Just over 5 years ago, on New Year's Eve 2019, the World Health Organization (WHO) became aware of the first cases of pneumonia of unknown etiology in Wuhan, China. A massive global infectious disease storm was already brewing-one that would shut down the world, with profound economic, social, and political impacts that still reverberate today. It's understandable that governments and individuals may want to forget that the COVID-19 pandemic ever happened, but such collective amnesia prevents humanity from being ready for the next pandemic. The world did the same in the 1920s, eager to move on from the devastation of the 1918 influenza pandemic. A repeat of this behavior squanders opportunities right now to institutionalize and embed best practices for current and future threats.
    Tags: *COVID-19/epidemiology/prevention & control, *Pandemic Preparedness, *Pandemics/prevention & control, China/epidemiology, Humans, SARS-CoV-2, World Health Organization.
  • Jossein, T., and Hugli, O. “In Reply To: Reevaluating The Pulmonary Embolism Rule-Out Criteria In Younger Adults-Insights From The Riete Registry”. Acad Emerg Med 32, no. 4: 480. doi:10.1111/acem.15110.
  • Backes, C., Godot, C., Gujer, C. Y., Obegi, N., Perez, A., Gervaix, A., and Schneider, M. P. “Digital Healthcare Services In Community Pharmacies In Switzerland: Pharmacist And Patient Acceptability, And Pharmacist Readiness-The Pneumoscope Pilot Study”. Digit Health 11: 20552076241313164. doi:10.1177/20552076241313164.
    Abstract: BACKGROUND: The integration of artificial intelligence (AI)-based pharmaceutical services in community pharmacy (CP) settings has the potential to enhance point-of-care services and improve informed patient access to healthcare. The Pneumoscope, an innovative AI-powered digital stethoscope that analyses lung sounds to detect specific respiratory pathologies, could be a valuable tool for pharmacists in conducting respiratory screening. To understand how this device can be implemented in the healthcare system, this exploratory research aims to assess the acceptability of pharmacists and patients, and the pharmacists' readiness to use the Pneumoscope in CPs for respiratory disease management. METHODS: A 2-stage exploratory approach was conducted using mixed methods: 1) a qualitative analysis of pharmacists' acceptability and readiness was developed using semi-structured interviews and focus groups ; 2) followed by a quantitative cross-sectional survey of patients' acceptability of the device in CPs. RESULTS: Pharmacists were generally positive about the integration of e-health services into their daily clinical practice, recognizing their potential to improve advanced pharmaceutical triage and collaboration with physicians. Most patients were satisfied with the care provided by CPs, and their acceptability to use the Pneumoscope was significantly associated with their level of confidence in AI (p = 0.0092) and with the location of their CP (p = 0.0276). CONCLUSIONS: Digital devices such as the Pneumoscope have the potential to reinforce the pharmacists' clinical roles within an interprofessional team and improve patient care, but further scientific evaluation and implementation are necessary to support its integration and ensure its reimbursement by health insurers.
    Tags: artificial intelligence, community pharmacist, Covid-19, digital healthcare, interprofessionality, Pneumoscope, primary care, research, authorship, and/or publication of this article., respiratory symptoms, Triage.
  • Baum, E., Bernhardsgrutter, D., Engst, R., Maurer, C., Ebneter, J., Zenklusen, A., Wartlsteiner, B., et al. “The Meaning Of Trust Along The Treatment Pathway Of Women With Breast Cancer: A Mixed-Methods Study Among Cancer Survivors”. Bmc Womens Health 25, no. 1: 25. doi:10.1186/s12905-024-03540-y.
    Abstract: PURPOSE: Women with breast cancer face a high degree of uncertainty. Trust between health providers and patients has been shown to improve patient quality of life and may enhance clinical outcomes. This study aimed to explore the meaning of trust along the treatment pathway. METHODS: The study followed a convergent mixed-methods design. We collected qualitative data longitudinally from diagnosis to follow-up using unstructured digital diaries and 45 semi-structured interviews with twelve women with breast cancer. To measure symptom burden and trust, we collected quantitative data by means of 57 questionnaires. Data analysis was based on phenomenology according to van Manen and on descriptive statistics. Data synthesis resulted in a conceptual model of trust. RESULTS: The women experienced trust as a dynamic phenomenon within the biomedical cancer care "machinery". Their trust was strongly influenced by contextual factors, professionals' expertise, and person-centeredness. The relevance of trust differed according to treatment phases. CONCLUSIONS: Due to a high degree of uncertainty, trust was particularly important. Professionals positively influenced the women's trust to a certain extent through a patient-centered approach and by demonstrating expertise within the biomedical cancer care "machinery". The conceptual model of trust should receive attention to bring care closer to the women's lived experience so that their care experience can be improved.
    Tags: (reg. number 2021 - 00730) and carried out in accordance with the Declaration of, *Breast Neoplasms/psychology/therapy, *Cancer Survivors/psychology, *Trust/psychology, Adult, Advanced practice nursing, Aged, Breast neoplasms, by the responsible ethical committee of Northwest and Central Switzerland (EKNZ), Female, Helsinki. Women interested in participation received an information letter from, Humans, identifying information of participants that compromises anonymity. The patient, interests., Middle Aged, names are pseudonyms. Competing interests: The authors declare no competing, Physician-Patient Relations, Qualitative Research, Quality of Life, Surveys and Questionnaires, their treating APN-GO and provided written informed consent prior to commencing, Trust, Uncertainty, with the study. Consent for publication: Not applicable. The paper contains no.
  • Pontiero, A., Bulgarelli, C., Ciuffoli, E., Buzzurra, F., Villani, A., Troia, R., and Giunti, M. “Triage Body Temperature Predicts Outcome In Cats At Emergency Department Admission: A Retrospective Study Of 1440 Cases (January 2018 To December 2021)”. J Feline Med Surg 27, no. 1: 1098612X241291295. doi:10.1177/1098612X241291295.
    Abstract: OBJECTIVES: The aim of the study was to evaluate the association between triage body temperature (BT) and outcome in cats presenting to the emergency department (ED). METHODS: A retrospective observational study was conducted on cats presented to the ED. BT, clinical diagnosis and outcome were recorded. BT was categorised as follows: normothermia (37.8-39.7 degrees C); hyperthermia (⩾39.8 degrees C); mild hypothermia (36.8-37.7 degrees C); moderate hypothermia (35.6-36.7 degrees C); severe hypothermia (33.1-35.5 degrees C); and critical hypothermia (⩽33 degrees C). Outcome in the ED was categorised as death, euthanasia, hospital admission and discharge. Outcome at hospital discharge was evaluated in patients admitted to the intensive care unit (ICU). Systemic inflammatory response syndrome (SIRS) was identified in patients. No-SIRS cats were divided into three disease categories (urinary system, cardiovascular and miscellanea) and SIRS cats into four categories (urinary system, cardiovascular, trauma and miscellanea). The presence of sepsis was evaluated. Non-parametric statistics were used. RESULTS: A total of 1440 cats were included. The hospital mortality rate was 21.9%. Hypothermia in the ED was reported in 510 (35.4%) cats, normothermia in 849 (59%) cats and hyperthermia in 81 (5.6%) cats. In the ED, the median temperature in non-survivors (35.4 degrees C, 95% confidence interval [CI] 34.6-36.3) was significantly lower than in survivors (38.2 degrees C, 95% CI 38.1-38.3; P <0.0001). The risk of non-survival in the ED was significantly higher in cats with a decreased BT, progressively increasing with the severity of hypothermia (P <0.0001). Furthermore, BT was significantly associated with a higher risk of mortality in the ICU (P <0.0001). A diagnosis of sepsis was associated with a high prevalence of hypothermia (79/124 cats, 63.7%) and a higher risk of non-survival (odds ratio [OR] 2.62, 95% CI 1.52-4.54; P = 0.0006). The mortality risk significantly increased in SIRS cats with a cardiovascular disease (OR 8.27, 95% CI 4.09-16.68; P <0.0001). CONCLUSIONS AND RELEVANCE: Hypothermia is common in cats at ED admission and is significantly associated with outcome. Triage hypothermia might identify patients with sepsis or SIRS complicated by comorbidities, such as cardiovascular and urinary diseases.
    Tags: *Body Temperature, *Cat Diseases/mortality/diagnosis/therapy, *Hypothermia/veterinary/diagnosis/mortality, *Triage/methods/statistics & numerical data, Animals, cardiovascular, Cats, Emergency Service, Hospital/statistics & numerical data, Female, Hospitals, Animal/statistics & numerical data, Hypothermia, Male, respect to the research, authorship, and/or publication of this article., Retrospective Studies, sepsis, shock, Sirs, Systemic Inflammatory Response Syndrome/diagnosis/mortality/veterinary.
  • Vecchia, M., Sacchi, P., Marvulli, L. N., Ragazzoni, L., Muzzi, A., Polo, L., Bruno, R., and Salio, F. “Healthcare Application Of Failure Mode And Effect Analysis (Fmea): Is There Room In The Infectious Disease Setting? A Scoping Review”. Healthcare (Basel) 13, no. 1. doi:10.3390/healthcare13010082.
    Abstract: Background: Failure mode and effect analysis (FMEA) is a valuable risk analysis tool aimed at predicting the potential failures of a system and preventing them from occurring. Since its initial use, it has also recently been applied to the healthcare setting, which has been made progressively more complex by technological developments and new challenges. Infection prevention and control (IPC) is an area that requires effective strategies. The aim of this study is to review the literature on the employment of FMEA in the healthcare environment, with special consideration for its application in the infectious disease setting. Methods: An extensive search was carried out in two international and public databases, PUBMED and EMBASE; we included all studies regarding the use of FMEA in hospital settings and human patient care processes. Results: A total of 163 studies published over the period from 2003 to 2023 were included for data extraction. These studies were analyzed regarding bibliometric data (publication year and country of origin), the healthcare issues to be addressed, the application fields, and the utilized FMEA methods. Among these, 13 studies were found that took an interest in infectious diseases. Conclusions: FMEA can be effectively used for healthcare risk assessment. Its implementation as a standard tool in healthcare settings, though demanding, may serve as an important tool for preventing the risk of biohazard incidents, epidemics, and environmental contamination, thereby improving safety for both patients and healthcare workers.
    Tags: Fmea, healthcare, infection control, infectious diseases, risk analysis, risk management.
  • Morello, E., Bosio, S., and Salvadeo, S. A. T. “Kounis Syndrome Following Moxifloxacin And Deflazacort Administration”. Eur J Case Rep Intern Med 11, no. 12: 004971. doi:10.12890/2024_004971.
    Abstract: Kounis syndrome (KS), characterized by the simultaneous occurrence of acute coronary syndrome (ACS) and allergic reactions, can be triggered by a range of factors and drugs. We report on the case of a patient who arrived at our emergency department (ED) with symptoms of an allergic reaction after taking moxifloxacin and deflazacort orally. In the ED, the patient experienced a 5-minute episode of oppressive chest pain. A 12-lead electrocardiogram (ECG) was registered, and elevated troponin levels were detected in the blood, suggesting myocardial damage. The patient was admitted to the internal medicine department for observation, and a second 12-lead ECG demonstrated a significant variation in the repolarization pattern. The day after, a coronary angiography revealed no significant stenosis, thus supporting, along with elevated serum tryptase levels, the diagnosis of KS. This case report highlights two potential triggers for KS and emphasizes the critical importance of early recognition and prompt treatment of KS. LEARNING POINTS: Kounis syndrome can be triggered by moxifloxacin and/or deflazacort. This case report documents the onset of Kounis syndrome following the administration of moxifloxacin and deflazacort.Diagnosing and treating Kounis syndrome can be challenging. Its diverse triggers and clinical manifestations complicate accurate diagnosis. Effective treatment involves addressing both cardiac and allergic symptoms, with the understanding that medications used for cardiac issues may exacerbate allergic reactions, and vice versa.Nonspecific electrocardiogram (ECG) alterations should not be underestimated. In the context of an allergic reaction, ECG alterations, including nonspecific ones, might be an early warning sign.
    Tags: allergic reaction, coronary disease, interests., Kounis syndrome.
  • Ponthus, S., Odiakosa, M., Gautier, B., and Dumont, L. “Successful Awake Intubation Using Airtraq((R)) In A Low-Resource Setting For A Patient With Severe Post-Burn Contractures”. Bmc Anesthesiol 25, no. 1: 12. doi:10.1186/s12871-024-02887-x.
    Abstract: BACKGROUND: In resource-limited settings, advanced airway management tools like fiberoptic bronchoscopes are often unavailable, creating challenges for managing difficult airways. We present the case of a 25-year-old male with post-burn contractures of the face, neck, and thorax in Nigeria, who had been repeatedly denied surgery due to the high risk of airway management complications. This case highlights how an awake intubation was safely performed using an Airtraq((R)) laryngoscope, the only device available, as fiberoptic intubation was not an option. The patient had a mouth opening of 3.5 cm, a Mallampati score of 4, and no neck extension, making intubation challenging. Pre-procedural counseling was provided, and after explaining the risks, the patient gave informed consent. CASE PRESENTATION: Preoxygenation was performed, followed by topical anesthesia using lidocaine gargles and incremental spraying of lidocaine to the vocal cords via a feeding tube. The Airtraq((R)) laryngoscope enabled glottic visualization despite limited neck mobility and challenging anatomy. Procedural challenges included managing aspiration during gargling, precise lidocaine application without advanced tools, and maintaining patient cooperation. The procedure was successfully completed, allowing surgery for contracture release. CONCLUSIONS: This case emphasizes that safe awake intubation with an Airtraq((R)) laryngoscope is feasible in low-resource environments when key principles-oxygenation, topical anesthesia, and careful procedural steps-are followed. The reuse of a single-use device like the Airtraq((R)) laryngoscope extends its utility in resource-constrained settings, enabling complex airway management when alternatives are unavailable. The patient tolerated the procedure well and reported minimal discomfort. This experience underscores the critical importance of innovation, resourcefulness, and patient cooperation in managing difficult airways when standard tools are unavailable, offering valuable lessons for similar resource-constrained environments.
    Tags: *Burns/complications, *Contracture/surgery, *Intubation, Intratracheal/methods/instrumentation, *Laryngoscopes, Adult, Airtraq(R) laryngoscope, Anesthetics, Local/administration & dosage, Anticipated difficult airway, authorization form the patient was provided for submission of a case report., Awake intubation, Competing interests: The authors declare no competing interests., Humans, informed consent for the procedure. Consent for publication: Written, Lidocaine/administration & dosage, Low-resource setting, Male, Nigeria, Patient safety, Wakefulness.
  • Sekhavati, P., Wild, T., Martinez, Idpc, Dion, P. M., Woo, M., Ramlogan, R., Boet, S., Shorr, R., and Gu, Y. “Instructional Design Features In Ultrasound-Guided Regional Anaesthesia Simulation-Based Training: A Systematic Review”. Anaesthesia 80, no. 5: 572-581. doi:10.1111/anae.16527.
    Abstract: INTRODUCTION: Ultrasound-guided regional anaesthesia enhances pain control, patient outcomes and lowers healthcare costs. However, teaching this skill effectively presents challenges with current training methods. Simulation-based medical education offers advantages over traditional methods. However, the use of instructional design features in ultrasound-guided regional anaesthesia simulation training has not been defined. This systematic review aimed to identify and evaluate the prevalence of various instructional design features in ultrasound-guided regional anaesthesia simulation training and their correlation with learning outcomes using a modified Kirkpatrick model. METHODS: A comprehensive literature search was conducted including studies from inception to August 2024. Eligibility criteria included randomised controlled trials; controlled before-and-after studies; and other experimental designs focusing on ultrasound-guided regional anaesthesia simulation training. Data extraction included study characteristics; simulation modalities; instructional design features; and outcomes. RESULTS: Of the 2023 articles identified, 62 met inclusion criteria. Common simulation modalities included live-model scanning and gel phantom models. Instructional design features such as the presence of expert instructors, repetitive practice and multiple learning strategies were prevalent, showing significant improvements across multiple outcome levels. However, fewer studies assessed behaviour (Kirkpatrick level 3) and patient outcomes (Kirkpatrick level 4). DISCUSSION: Ultrasound-guided regional anaesthesia simulation training incorporating specific instructional design features enhances educational outcome; this was particularly evident at lower Kirkpatrick levels. Optimal combinations of instructional design features for higher-level outcomes (Kirkpatrick levels 3 and 4) remain unclear. Future research should standardise outcome measurements and isolate individual instructional design features to better understand their impact on clinical practice and patient safety.
    Tags: *Anesthesia, Conduction/methods, *Anesthesiology/education, *Simulation Training/methods, *Ultrasonography, Interventional/methods, Clinical Competence, Humans, instructional design features, Randomized Controlled Trials as Topic, simulation, systematic review, ultrasound-guided regional anaesthesia.
  • Gray, D., Pasquier, M., Brugger, H., Musi, M., and Paal, P. “Correction: A Regional Modification To The Revised Swiss System For Clinical Staging Of Hypothermia Including Confusion”. Scand J Trauma Resusc Emerg Med 33, no. 1: 2. doi:10.1186/s13049-024-01303-0.
    Abstract: Following the publication of the original article, the authors reported that Fig. 1 was incomplete, and the legend was missing. The authors have provided the correct figure and legend, as well as updated the reference list. Two additional references cited in Fig. 1 are: [6] Pasquier M, Hugli O, Paal P, Darocha T, Blancher M, Husby P, et al. Hypothermia outcome prediction after extracorporeal life support for hypothermic cardiac arrest patients: the HOPE score Resuscitation. 2018;126:58–64 [7] Lott C, Truhlar A, Alfonzo A, Barelli A, Gonzalez-Salvado V, Hinkelbein J, et al. European Resuscitation Council Guidelines 2021: Cardiac arrest in special circumstances Resuscitation. 2021;161:152–219 aIn this regional modification to the Revised Swiss System, “Alert” corresponds to a GCS score of 15; “Confused” corresponds to a GCS score of 14, “Verbal” corresponds to a GCS score of 9–13; “Pain” and “Unresponsive” correspond to a GCS score < 9. While shivering is not used as a stage-defining sign in this regional modification to the Revised Swiss System, its presence usually means that the temperature is > 30 °C, a temperature at which hypothermic CA is unlikely to occur [6]. bNo respiration, no palpable carotid or femoral pulse, no measurable blood pressure. Check for signs of life (pulse and, especially, respiration) for up to 1 min [7]. cThe transition of colours between stages represents the overlap of patients within groups. The estimated risk of cardiac arrest is based on accidental hypothermia being the only cause of the clinical findings. If other conditions impair consciousness, such as asphyxia, intoxication, high altitude cerebral oedema or trauma, this regional modification to the Revised Swiss System may falsely predict a higher risk of cardiac arrest due to hypothermia. Caution should be taken if a patient remains “alert”, “confused” or “verbal” while showing signs of haemodynamic or respiratory instability such as bradycardia, bradypnoea, or hypotension because this may suggest transition to a stage with higher risk of cardiac arrest. The reference list has been updated. The Original Article has been corrected. © The Author(s) 2024.
    Tags: erratum, human.
  • Schmucki, R., Rust, C. A., and Filipovic, M. “Intra-Operative Norepinephrine Via Peripheral Venous Catheter Is Safe: A Short Scientific Report”. Eur J Anaesthesiol 42, no. 2: 172-173. doi:10.1097/EJA.0000000000002080.
  • Wiemker, V., Nijman, R. G., and Brandenberger, J. “Imagine Every Child Healthy: Transforming Paediatric Migrant Health Through Participation And Collaboration In Europe”. Acta Paediatr 114, no. 3: 475-478. doi:10.1111/apa.17561.

2024

  • Greiter, B. M., Sidorov, S., Osuna, E., Seiler, M., Relly, C., Hackenberg, A., Luchsinger, I., et al. “Clinical Characteristics And Serological Profiles Of Lyme Disease In Children: A 15-Year Retrospective Cohort Study In Switzerland”. Lancet Reg Health Eur 48: 101143. doi:10.1016/j.lanepe.2024.101143.
    Abstract: BACKGROUND: Lyme disease (LD) is caused by Borrelia burgdorferi and is the most common tickborne disease in the northern hemisphere. Although classical characteristics of LD are well-known, the diagnosis and treatment are often delayed. Laboratory diagnosis by serological testing is recommended for most LD manifestations. The objective of this study was to describe clinical characteristics and associated serological profiles in children with LD. METHODS: This retrospective cohort study included children aged 0-18 years, diagnosed with LD according to current guidelines at University Children's Hospital Zurich between January 1, 2006 and December 31, 2020. Two-tier serological testing with the recomWell enzyme-linked immunosorbent assay and recomLine Western blot (MIKROGEN Diagnostik, MIKROGEN GmbH, Neuried, Germany) was performed at the Institute of Medical Microbiology, University of Zurich. FINDINGS: In total, 469 children diagnosed with LD were included (median age, 7.9 years); 190 patients (40.5%) with Lyme neuroborreliosis (LNB), 171 (36.5%) patients with skin manifestations (erythema migrans, n = 121; multiple erythema migrans, n = 11; borrelial lymphocytoma, n = 37; and acrodermatitis chronica atrophicans, n = 2), and 108 (23.0%) patients with Lyme arthritis. We observed seasonal variations for patients with skin manifestations and LNB, with high prevalence in May-October, but not for patients with Lyme arthritis. Significant differences between LD manifestation groups were found for age, inflammatory parameters, and specificity and concentration of B. burgdorferi-specific serum antibody responses. We observed distinct patterns of pronounced serum antibody responses against B. burgdorferi antigens in LNB (IgM against VlsE, p41, and OspC) and Lyme arthritis (IgG against p100, VlsE, p58, p41, p39, and p18). INTERPRETATION: Our study is one of the largest and most detailed for children with LD. We present unique findings regarding the differences in clinical characteristics and immune responses between various manifestations of LD in children. FUNDING: No specific funding to disclose for this study.
    Tags: AstraZeneca) and given presentations (Fomf, FPH Forum, ZAIM MediDays, Insight, authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of, Borrelia burgdorferi, Erythema migrans, Facial nerve palsy, industry sponsored symposia (lllumina, Copan, Bruker), and support from the, Interest., Laboratory Medicine Society of Korea for attendance at and travel to the annual, Lyme arthritis, meeting of the Laboratory Medicine Society of Korea in the past 36 months. All, Meningitis, Neuroborreliosis, Paediatrics) with payments to the institution (University Children's Hospital, to start-up companies), honoraria for presentations at various conferences at, Zurich). A.E. has received consultancy fees from Sefunda and Phast (advisory role.
  • Fusi, C., and Bulleri, E. “Current Insights Oesophageal Pressure Monitoring: A Real Advanced Tool For Icu Nurses”. Intensive Crit Care Nurs 87: 103923. doi:10.1016/j.iccn.2024.103923.
  • Nutbeam, T., Stassen, W., Foote, E., and Ageron, F. X. “Derivation And Validation Of The Simplified Bleedingaudit Triage Trauma (Sbatt) Score: A Simplified Trauma Score For Major Trauma Patients Injured In Motor Vehicle Collisions”. Bmj Open 14, no. 12: e090517. doi:10.1136/bmjopen-2024-090517.
    Abstract: OBJECTIVES: To develop and validate a simplified Bleeding Audit Triage Trauma (sBATT) score for use by lay persons, or in areas and environments where physiological monitoring equipment may be unavailable or inappropriate. DESIGN: The sBATT was derived from the original BATT, which included prehospital systolic blood pressure (SBP), heart rate, respiratory rate, Glasgow Coma Scale (GCS), age and trauma mechanism. Variables suitable for lay interpretation without monitoring equipment were included (age, level of consciousness, absence of radial pulse, tachycardia and trapped status). The sBATT was validated using data from the UK Trauma Audit Research Network (TARN) registry. SETTING: Data sourced from prehospital observations from multiple trauma systems in the UK. PARTICIPANTS: 70 027 motor vehicle collision (MVC) patients from the TARN registry (2012-2019). Participants included were those involved in MVCs, with exclusion criteria being incomplete data or non-trauma-related admissions. INTERVENTIONS: Not applicable. PRIMARY AND SECONDARY OUTCOME MEASURES: Death within 24 hours of MVC. Secondary: need for trauma intervention. RESULTS: In a cohort of 70 027 MVC patients, 1976 (3%) died within 24 hours. The sBATT showed an area under receiver operating characteristic curve of 0.90 (95% CI: 0.90 to 0.91) for predicting 24-hour mortality, surpassing other trauma scores such as the Shock Index and Assessment of Blood Consumption score. Sensitivity was 96% and specificity 72%, with a negative likelihood ratio below 0.1, indicating strong rule-out capability. Sensitivity analyses confirmed consistent performance across varying SBP and GCS thresholds. The sBATT was equally effective across sexes with no significant predictive discrepancies. CONCLUSIONS: The sBATT is a novel, simplified tool that performs well at predicting early death in the TARN dataset. It demonstrates high predictive accuracy for 24-hour mortality and need for trauma intervention. Further research should validate sBATT in diverse populations and real-world scenarios to confirm its utility and applicability.
    Tags: *Accidents, Traffic, *Triage/methods/standards, Accident & emergency medicine, Adult, Aged, Blood Pressure, Female, Glasgow Coma Scale, Hemorrhage/diagnosis/etiology, Humans, Male, Middle Aged, Registries, ROC Curve, Trauma management, Trauma Severity Indices, Triage, United Kingdom, Wounds and Injuries/complications/mortality, Young Adult.
  • Buyck, M., Desaulniers, P., Chenier, C., and Moussa, A. “Experiential Faculty Development To Increase The Number Of Entrustable Professional Activity Assessments”. Clin Teach 22, no. 1: e70006. doi:10.1111/tct.70006.
    Abstract: BACKGROUND: Emergency medicine (EM) residents must complete both adult and paediatric entrustable professional activities (EPAs). During their paediatric emergency medicine rotation at a university paediatric hospital, EM residents struggled to receive EPA assessments because preceptors had not yet been trained due to the stepwise implementation of EPAs. This study aimed to evaluate the impact of a workshop on behaviour change by measuring the number of EPA assessments. METHODS: A comparative pretraining and posttraining study involving 27 invited faculty members was conducted to assess the impact of a faculty development programme. The training was delivered via videoconference with experiential learning techniques to practise every aspect of the supervision of an EPA, including selecting the appropriate EPA according to mirroring real-world situations, giving feedback, evaluating autonomy and recording the EPA in the resident's logbook. RESULTS/FINDINGS: In total, 20 out of 27 eligible faculty members (74%) agreed to participate in the study. Their main challenges reported were a lack of trainee initiative, preceptor training and competence in supervising EPAs. Over the 12-month analysis period, the enrolled faculty assessed 125 EPAs for 38 EM residents, including 52 pre-intervention EPAs and 73 post-intervention EPAs. Calculation of data points above the median showed a 1-point difference in the EPAs assessments to resident ratio between the pre- and post-intervention periods (3/7 vs. 4/7). CONCLUSION: Our findings suggest that faculty training using multiple educational strategies may enable EM residents to receive more EPA assessments during their paediatric emergency medicine rotation.
    Tags: *Clinical Competence, *Faculty, Medical, *Internship and Residency/standards, Educational Measurement/methods, emergency medicine, Emergency Medicine/education, entrustable professional activities, faculty development, Humans, Preceptorship/organization & administration/standards, Problem-Based Learning, Staff Development/organization & administration.
  • Tan, R., Kavishe, G., Kulinkina, A. V., Renggli, S., Luwanda, L. B., Mangu, C., Ashery, G., et al. “A Cluster Randomized Trial Assessing The Effect Of A Digital Health Algorithm On Quality Of Care In Tanzania (Dynamic Study)”. Plos Digit Health 3, no. 12: e0000694. doi:10.1371/journal.pdig.0000694.
    Abstract: Digital clinical decision support tools have contributed to improved quality of care at primary care level health facilities. However, data from real-world randomized trials are lacking. We conducted a cluster randomized, open-label trial in Tanzania evaluating the use of a digital clinical decision support algorithm (CDSA), enhanced by point-of-care tests, training and mentorship, compared with usual care, among sick children 2 to 59 months old presenting to primary care facilities for an acute illness in Tanzania (ClinicalTrials.gov NCT05144763). The primary outcome was the mean proportion of 14 major Integrated Management of Childhood Illness (IMCI) symptoms and signs assessed by clinicians. Secondary outcomes included antibiotic prescription, counseling provided, and the appropriateness of antimalarial and antibiotic prescriptions. A total of 450 consultations were observed in 9 intervention and 9 control health facilities. The mean proportion of major symptoms and signs assessed in intervention health facilities was 46.4% (range 7.7% to 91.7%) compared to 26.3% (range 0% to 66.7%) in control health facilities, an adjusted difference of 15.1% (95% confidence interval [CI] 4.8% to 25.4%). Only weight, height, and pallor were assessed statistically more often when using the digital CDSA compared to controls. Observed antibiotic prescription was 37.3% in intervention facilities, and 76.4% in control facilities (adjusted risk ratio 0.5; 95% CI 0.4 to 0.7; p<0.001). Appropriate antibiotic prescription was 81.9% in intervention facilities and 51.4% in control facilities (adjusted risk ratio 1.5; 95% CI 1.2 to 1.8; p = 0.003). The implementation of a digital CDSA improved the mean proportion of IMCI symptoms and signs assessed in consultations with sick children, however most symptoms and signs were assessed infrequently. Nonetheless, antibiotics were prescribed less often, and more appropriately. Innovative approaches to overcome barriers related to clinicians' motivation and work environment are needed.
  • Misirocchi, F., Quintard, H., Rossetti, A. O., Florindo, I., Sarbu, O. E., Kleinschmidt, A., Schaller, K., Seeck, M., and De Stefano, P. “Hypoalbuminemia In Status Epilepticus Is A Biomarker Of Short- And Long-Term Mortality: A 9-Year Cohort Study”. Eur J Neurol 32, no. 1: e16573. doi:10.1111/ene.16573.
    Abstract: BACKGROUND: Outcome prediction in Status epilepticus (SE) aids in clinical decision-making, yet existing scores have limitations due to SE heterogeneity. Serum albumin is emerging as a readily available prognostic biomarker in various clinical conditions. This study evaluates hypoalbuminemia in predicting short- and long-term mortality. METHODS: Observational cohort study including non-hypoxic SE adult patients admitted to the University Hospital of Geneva (Switzerland) between 2015 and 2023. Primary outcomes were in-hospital and 6-month mortality. RESULTS: Four hundred and ninety-six patients were included, 46 (9.3%) died in hospital; 6-month outcome was available for 364 patients, 86 (23.6%) were not alive at follow-up. Hypoalbuminemia was associated with older age and patients' comorbidities. Binomial regression showed an independent correlation between hypoalbuminemia and short- (p = 0.005, OR = 3.35, 95% CI = 1.43-7.86) and long-term mortality (p = 0.001, OR = 3.59,95% CI = 1.75-7.35). The Status Epilepticus Severity Score (STESS) had an overall AUC of 0.754 (95% CI = 0.656-0.836) for predicting in-hospital mortality and of 0.684 (95% CI = 0.613-0.755) for 6-month mortality. Through an exploratory analysis, we replaced age with hypoalbuminemia in the STESS, creating the Albumin-STESS (A-STESS) score (0-6). The global A-STESS AUC significantly improved for both in-hospital (0.837, 95% CI = 0.760-0.916, p = 0.002) and 6-month (0.739, 95% CI = 0.688-0.826; p = 0.033) mortality prediction. A-STESS-3 cutoff demonstrated a strong sensitivity-specificity balance for both in-hospital (sensitivity = 0.88, specificity = 0.68, accuracy = 0.70) and 6-month (sensitivity = 0.67, specificity = 0.73, accuracy = 0.72) mortality. CONCLUSIONS: Hypoalbuminemia is an easily measurable biomarker reflecting the overall patient's condition and is independently related to short- and long-term SE mortality. Integrating hypoalbuminemia into the STESS (A-STESS) significantly enhances mortality prediction. Future studies are needed to externally validate the A-STESS and evaluate the benefits of albumin supplementation in SE patient prognosis.
    Tags: (163,398, CRS115-180365) and is supported by the 2022 Swiss League Against, (IFCN) Research Fellowship Grant. HQ declares no competing interests. AOR, *Biomarkers/blood, *Hypoalbuminemia/blood/mortality, *Status Epilepticus/mortality/blood, Adult, Aged, Aged, 80 and over, albumin, Cohort Studies, competing interests. MS is a shareholder of Epilog NV (Ghent, Belgium). She, compliance with the Declaration of Helsinki first published in 1964 and its, CRS115-180365). PDS was supported by the Swiss National Science Foundation, declares no competing interests. IF declares no competing interests. OES declares, EliLilly, Lundbeck, Mitsubishi Tanabe, Novartis, and TEVA that were paid to a, Epilepsy Research Support Prize. The study protocol was reviewed and approved by, Female, following amendments., Hospital Mortality, Humans, Icu, Male, Middle Aged, no competing interests. AK has received honoraria for consulting from Abbvie,, outcome, Prognosis, received grants from the Swiss National Science Foundation (163,398,, Severity of Illness Index, status epilepticus, Stess, teaching and research fund at the University Hospital Geneva. KS declares no, the local ethic committee (CCER 2019-00836), and patient's consent was waived in.
  • Stebler, K., Elia, N., Zaccaria, I., and Fournier, R. M. “Popliteal Plexus Block In Total Knee Arthroplasty: A Single-Center Randomized Controlled Double-Blinded Trial”. Reg Anesth Pain Med. doi:10.1136/rapm-2024-105782.
    Abstract: INTRODUCTION: Whether a popliteal plexus block improves postoperative pain following total knee arthroplasty remains debated. This randomized trial tested if adding a popliteal plexus block to a continuous femoral nerve block decreases postoperative opioid requirement. METHODS: We included 66 patients undergoing total knee arthroplasty. 32 received continuous femoral nerve block and popliteal plexus block (intervention), and 34 received continuous femoral nerve block alone (control). The primary endpoint was the 12-hour postoperative morphine-equivalent consumption (mg). Secondary outcomes included opioid consumption, Visual Analog Pain Score (0-10), and sensorimotor extension of the block in postanesthesia care unit, at 12 hours, 24 hours and 48 hours postoperatively. RESULTS: 66 patients with a median body mass index of 28.7 (IQR 26.3-33.8) were included in the study. In an intention-to-treat analysis, the median 12-hour morphine-equivalent consumption was lower in the intervention group (6.1 mg (0.5-14.5) vs 10 mg (5.0-17.3); one-sided Wilcoxon test (p=0.04)). The average pain intensity experienced in postanesthesia care unit was lower in the intervention group (median: 3.0 (3.0-5.0) vs 2.0 (1.0-4.0), two-sided Wilcoxon p=0.01) and fewer patients reported lateroposterior pain of the knee (11 (34.4%) vs 21 (61.8%) p=0.03). These benefits disappeared after 24 hours. The median duration of the popliteal plexus block procedure was 5.0 min (2.0-5.0). CONCLUSIONS: Adding a popliteal plexus block to a continuous femoral nerve block decreases 12-hour opioid utilization, but the effect size is small, calling into question its clinical relevance. TRIAL REGISTRATION NUMBER: NCT04048889.
    Tags: Anesthesia, Local, Lower Extremity, Nerve Block, Pain, Postoperative.
  • Lee, C. C., Porta, L., Liu, Y., Chen, P. T., Pan, H. H., Lee, Y. T., Chen, K. F., et al. “Grade-Based Procalcitonin Guideline For Emergency Departments”. Am J Emerg Med 89: 109-123. doi:10.1016/j.ajem.2024.11.093.
    Abstract: Procalcitonin is a useful biomarker for infection. Over the past two decades, there has been much research on the clinical applications of procalcitonin, yet the majority of these studies have been conducted in the intensive care setting. Despite the extensive use of procalcitonin in emergency departments, there have been no guidelines focusing specifically on these clinical settings. Additionally, previous guidelines were predominantly shaped by expert consensus and rarely incorporate evidence-based medicine concepts. To address these shortcomings, the current guideline adopts a novel approach. Initially, we identified the most critical questions regarding the use of procalcitonin in emergency settings through expert voting. This was followed by a systematic literature review and the evaluation of evidence levels using the GRADE (Grading of Recommendations, Assessment, Development, and Evaluation) methodology. Key characteristics of individual studies will be summarized and evaluated by the guideline development group to determine the overall quality of evidence. The GRADE working group's categorization system will be employed to rate evidence quality into four levels. Recommendations will be formulated based on explicit consideration of established criteria. This structured approach ensures that guideline recommendations are founded on robust evidence and transparently assessed for strength and potential caveats. This is the first guideline on the use of procalcitonin to be applied in emergency departments that adopts the principles of evidence-based medicine and encompasses the up-to-date literatures, and it marks an advancement in providing guidance on the utilization of procalcitonin in emergency departments.
    Tags: *Emergency Service, Hospital/standards, *Practice Guidelines as Topic, *Procalcitonin/blood, Antibiotic stewardship, Biomarkers/blood, declare., Diagnostic performance, Evidence-Based Medicine, Guideline, Humans, Molecular testing, Procalcitonin, Septic patients.
  • Le Terrier, C., Bouvier, M., Kerbol, A., Dell'Acqua, C., Nara Network, members, Nordmann, P., and Poirel, L. “In-Vitro Activity Of The Novel Beta-Lactam/Beta-Lactamase Inhibitor Combinations And Cefiderocol Against Carbapenem-Resistant Pseudomonas Spp. Clinical Isolates Collected In Switzerland In 2022”. Eur J Clin Microbiol Infect Dis 44, no. 3: 571-585. doi:10.1007/s10096-024-04994-6.
    Abstract: To evaluate the in-vitro activity of the novel commercially-available drugs, including meropenem-vaborbactam (MEV), ceftazidime-avibactam (CZA), ceftolozane-tazobactam (C/T), imipenem-relebactam (IPR) as well as cefiderocol (FDC), against carbapenem-resistant Pseudomonas spp. (CRP) isolates. All CRP isolates collected at the Swiss National Reference Laboratory (NARA) over the year 2022 (n = 170) have been included. Most of these isolates (n = 121) were non-carbapenemase producers. Among the 49 carbapenemase producers, 47 isolates produced metallo-beta-lactamases (MBL) including NDM-1 (n = 11), VIM-like (n = 28), IMP-like (n = 7), and both NDM-1 and VIM-2 (n = 1) and two isolates produced the class A carbapenemase GES-5. Susceptibility testing was determined by broth microdilution method (BMD), or disk diffusion test, and results interpreted following EUCAST guidelines. The susceptibility rates for MEV, CZA, C/T and IPR were found to be 41%, 45%, 59% and 58%, respectively, for the whole set of isolates tested. Among non-carbapenemase producers, susceptibility rates for these beta-lactam/beta-lactamase inhibitors (BL/BLI) combinations were higher, determined at 55%, 61%, 83%, and 82%, respectively. The overall susceptibility of carbapenemase-producing Pseudomonas spp. to novel BL/BLI was relatively low, while 80% of these isolates demonstrated susceptibility to FDC, with a similar proportion (79%) observed among MBL producers. A total of 10 MBL-producing isolates (6%), mainly NDM-1, were found to exhibit resistance to all drugs tested, with the exception of colistin. FDC exhibited an excellent in-vitro activity against this collection of CRP recovered from Switzerland in 2022, including MBL producers. The new BL/BLI combinations displayed significant activity against non-carbapenemase CRP, with IPR and C/T showing the highest susceptibility rates.
    Tags: *Anti-Bacterial Agents/pharmacology, *beta-Lactamase Inhibitors/pharmacology, *Cephalosporins/pharmacology, *Pseudomonas Infections/microbiology/drug therapy, *Pseudomonas/drug effects/isolation & purification, Avibactam, Azabicyclo Compounds/pharmacology, Bacterial Proteins, Beta-lactamase, beta-Lactamases/metabolism, Carbapenemase, Carbapenems/pharmacology, Cefiderocol, Cefiderocol/pharmacology, Ceftazidime, Ceftolozane, declare no competing interests., Drug Combinations, Humans, Imipenem, Meropenem, Microbial Sensitivity Tests, Relebactam, Switzerland, Tazobactam, Vaborbactam.
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