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Swiss Emergency Research collection

2025

  • Brabrand, M., Flojstrup, M., Bogh, S. B., Cooksley, T., and Nickel, C. H. “Utilizing D-Dimer Levels For Predicting Survival Probability In Unplanned Hospital Admissions: Insights From A 5-Year Nationwide Population-Based Register Study”. Eur J Intern Med 137: 149-151. doi:10.1016/j.ejim.2025.02.026.
    Tags: Admission, D-dimer, Emergency medicine, Mortality, Prognosis, Survival.
  • Randegger, S., Wunderle, C., Johansen, O. E., Tribolet, P., Pavlicek, V., Braendle, M., Henzen, C., et al. “Low Plasma Pancreatic Lipase As A Novel Predictor Of Nutritional Target Achievement And Response To Nutritional Interventions In Malnourished Inpatients: Secondary Analysis Of A Randomized Clinical Trial”. Clin Nutr 47: 196-203. doi:10.1016/j.clnu.2025.02.029.
    Abstract: BACKGROUND & AIMS: Pancreatic lipase plays an essential role in digesting dietary fats in the intestine, facilitating nutrient absorption. Plasma lipase serves as a surrogate for pancreatic exocrine function, which decreases with age and potentially leads to inadequate nutrient digestion and gastrointestinal symptoms. We investigated clinical implications of plasma lipase among medical inpatients at nutritional risk. METHODS: This secondary analysis investigated admission plasma lipase concentrations among patients at risk for malnutrition regarding clinical outcomes and treatment response in patients included in the Effect of Early Nutritional Support on Frailty Outcomes, and Recovery of Malnourished Medical Inpatients Trial (EFFORT), a randomized controlled trial comparing individualized nutritional support to usual care. RESULTS: Of 810 patients with available admission plasma lipase concentrations, 158 (19.5 %) had concentrations below the reference range. Patients with low concentrations had a 1.6-fold higher risk of not reaching energy or protein targets during hospitalization (adjusted odds ratio 1.62 [95 % confidence interval 1.07 to 2.45], p = 0.022 and 1.61 [95 % confidence interval 1.07 to 2.44], p = 0.023, respectively). They also tended to have a more pronounced benefit from nutritional interventions in terms of reduced mortality (adjusted hazard ratio for patients with low lipase 0.48 [95 % confidence interval 0.18 to 1.26] compared to 0.99 [95 % confidence interval 0.60 to 1.63] in patients with normal lipase concentrations, p for interaction = 0.224). CONCLUSION: Findings from this multicenter trial indicate that around 20 % of polymorbid older patients had plasma lipase concentrations below the reference range, suggesting exocrine pancreatic insufficiency, which placed them at a greater risk for failing to meet nutritional targets; however, they also demonstrated a pronounced improvement from nutritional support. Further studies should assess the impact of pancreatic enzyme replacement therapy in this population. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02517476.
    Tags: *Lipase/blood, *Malnutrition/blood/therapy/diet therapy, *Nutritional Support/methods, Aged, Aged, 80 and over, Biomarkers/blood, Diagnostics, not related to this project. Zeno Stanga reports consulting fees, Disease-related malnutrition, Female, from Nestle Health Science, Abbott Nutrition, Fresenius Kabi and B. Braun, not, Health Science, Thermo Fisher, bioMerieux, Abbott Nutrition and Roche, Hospitalization, Humans, Inpatients, Lipase, Male, Middle Aged, Nutritional Status, Nutritional support, Pancreas/enzymology, Pancreatic insufficiency, Polymorbid medical inpatient, related to this project. Odd Erik Johansen reports employment by Nestle Health, Science. No other disclosures are reported., Treatment Outcome, Treatment response.
  • Wespi, R., Neher, A. N., Birrenbach, T., Schauber, S. K., Frenkel, M. O., Schrom-Feiertag, H., Sauter, T. C., and Kammer, J. E. “Physiological Team Dynamics Explored: Physiological Synchrony In Medical Simulation Training”. Adv Simul (Lond) 10, no. 1: 5. doi:10.1186/s41077-025-00335-5.
    Abstract: INTRODUCTION: For researchers and medical simulation trainers, measuring team dynamics is vital for providing targeted feedback that can lead to improved patient outcomes. It is also valuable for research, such as investigating which dynamics benefit team performance. Traditional assessment methods, such as questionnaires and observations, are often subjective and static, lacking the ability to capture team dynamics. To address these shortcomings, this study explores the use of physiological synchrony (PS) measured through electrocardiogram (ECG) data to evaluate team dynamics automated and in high-resolution. METHODS: A multicentre observational field study was conducted involving 214 medical first responders during mixed reality (MR) mass casualty training sessions. Participants were equipped with electrocardiogram (ECG) sensors and MR gear. The study measured dyadic PS using heart rate (HR), root mean square of successive differences (RMSSD), and standard deviation of NN intervals (SDNN). Data were collected at high frequency and analysed using dynamic time warping (dtw) to assess fluctuations in PS. RESULTS: Findings indicate that PS varies significantly by task nature, with higher synchrony during cooperative tasks compared to baseline. Different ECG metrics offered unique insights into team dynamics. Proximity and scenario conditions influenced PS, with closer teamwork leading to higher PS. Smaller sampling intervals (e.g. 5 s) provided a detailed view of PS fluctuations over time. DISCUSSION: The results demonstrate the potential of PS as an indicator of team performance and cohesion. High-resolution monitoring provides detailed insights into team dynamics, offering high-resolution feedback that traditional methods cannot provide. The integration of physiological measures into training programmes can enhance team performance by providing objective, high-resolution data. CONCLUSION: This study shows that PS, measured by ECG data, is sensitive to medical team activities, offering insights into team dynamics. Different ECG metrics highlight various aspects of team performance, and high-resolution monitoring captures detailed dynamics. Further research is needed to validate these findings across diverse scenarios. This approach could improve training methodologies, resulting in better-prepared medical teams and improved patient care outcomes.
  • Jachmann, A., Loser, A., Mettler, A., Exadaktylos, A., Muller, M., and Klingberg, K. “Burnout, Depression, And Stress In Emergency Department Nurses And Physicians And The Impact On Private And Work Life: A Systematic Review”. J Am Coll Emerg Physicians Open 6, no. 2: 100046. doi:10.1016/j.acepjo.2025.100046.
    Abstract: OBJECTIVES: In today's fast-paced world, work-related stress is a prevalent problem, particularly among health care professionals in high-pressure environments such as emergency departments (EDs). This stress can lead to mental health disorders, such as depression and burnout, affecting job performance, patient care, and the quality of professional and private life. This systematic review aimed to investigate the prevalence of burnout, depression, and stress among ED nurses and physicians and the impact of these conditions on personal and professional quality of life (QoL). METHODS: The systematic literature search covered PubMed, PsycINFO, Embase, and grey literature databases. Articles were included if they were published in English or German by 31 January 2020, focused on ED physicians or nurses, and examined burnout, depression, or stress and its impact on professional or personal QoL. Quality assessment of the included studies was performed using a modified version of the Newcastle-Ottawa Scale. RESULTS: The systematic search resulted in 893 articles, of which 11 met the inclusion criteria. All reviewed studies had a cross-sectional study design and were of low to moderate quality. Depression, burnout, and stress were prevalent among ED physicians, ranging from 15.5% to 19.3%, 18% to 71.4%, and 19.5% to 22.7%, respectively. These were associated with lower job satisfaction in ED physicians, while findings in ED nurses also showed a considerable rate of burnout with an inverse association with compassion satisfaction. Burnout and stress were significantly associated with intentions to quit emergency medicine in ED physicians, whereas no association was found for depression. In addition, burnout showed a negative relationship to work-life balance and QoL, while higher stress levels were associated with lower life satisfaction in ED physicians. CONCLUSION: Our review underlines the high prevalence of stress, depression, and burnout among ED health care professionals and their potential negative impact on private and professional life, emphasizing the need for targeted support and interventions to enhance resilience, reduce stress, and prevent the onset or deterioration of mental health diseases. This, in turn, can contribute to maintaining and strengthening the already limited human resources in EDs, ensuring the quality of patient care, and strengthening health care systems.
    Tags: burnout, depression, emergency service, health personnel, mental health, quality of life, stress.
  • von During, S., Chevalley, B., Wozniak, H., Desmettre, T., Quintard, H., Suppan, L., and Fehlmann, C. A. “Clinical Factors Associated With The Use Of Niv In The Pre-Hospital Setting In Adult Patients Treated For Acute Copd Exacerbation: A Single-Center Retrospective Cohort Study”. Bmc Emerg Med 25, no. 1: 32. doi:10.1186/s12873-025-01193-0.
    Abstract: BACKGROUND: Non-invasive ventilation (NIV) is a cornerstone in the management of acute chronic obstructive pulmonary disease (COPD) exacerbations with respiratory failure. While extensively studied in hospital settings, limited data exist on its use in the pre-hospital setting and clinical factors influencing its application. This study aimed to identify predictors of NIV use in the pre-hospital setting and to assess its association with patient-centered outcomes. METHODS: This single-center retrospective cohort study analyzed data from a pre-hospital emergency medical service registry in Geneva, Switzerland. Adult patients with a presumptive diagnosis of acute COPD exacerbation were included, spanning a control period (2007-2010, before NIV implementation) and an intervention period (2013-2017, after NIV implementation). For the primary analysis, multivariable logistic regression was used to identify predictors of NIV use during the intervention period. For the secondary analysis, coarsened exact matching balanced patients treated with NIV during the intervention period with those from the control period, followed by conditional regression analyses to assess patient-centered outcomes. RESULTS: Among 270 included patients, 84 (46%) received NIV during the intervention period. Age >/= 70 years (aOR 2.49, 95% CI 1.11, 5.76), female sex (aOR 2.48, 95% CI 1.13, 5.60), and systolic blood pressure (SBP) >/= 140 mmHg (aOR 2.75, 95% CI 1.19, 6.62) were independent predictors associated with receiving NIV in the pre-hospital setting. In the matched cohort, pre-hospital NIV use was significantly associated with increased ICU admission rates, but was not associated with transport time, emergency department length of stay, hospital length of stay, or 28-day mortality. Sensitivity analyses demonstrated consistent results across different modeling approaches. CONCLUSIONS: Age >/= 70 years, female sex, and SBP >/= 140 mmHg were independent predictors associated with receiving NIV in the pre-hospital management of acute COPD exacerbation. The association between NIV use and increased ICU admissions may reflect its application in more severely ill patients. Pre-hospital NIV was not associated with short- or long-term outcomes beyond ICU admission. These findings underscore the need for prospective studies to clarify the role of pre-hospital NIV in patient outcomes.
    Tags: *Emergency Medical Services/methods, *Noninvasive Ventilation/statistics & numerical data, *Pulmonary Disease, Chronic Obstructive/therapy, Acute disease, Aged, Aged, 80 and over, All data were collected without personal identity information. Consent for, approval from the Research Ethics Board of the Geneva University Hospitals in, Chronic obstructive, competing interests., Disease Progression, Emergency medical services, Female, Humans, January 2019 (Project ID 2018-22-45), with a waiver of written informed consent., Male, Middle Aged, Noninvasive, Prehospital care, publication: Not applicable. Competing interests: The authors declare no, Pulmonary disease, Respiratory insufficiency, Retrospective Studies, Switzerland, Ventilation.
  • Collaborators, G. B. D. Epilepsy. “Global, Regional, And National Burden Of Epilepsy, 1990-2021: A Systematic Analysis For The Global Burden Of Disease Study 2021”. Lancet Public Health 10, no. 3: e203-e227. doi:10.1016/S2468-2667(24)00302-5.
    Abstract: BACKGROUND: Epilepsy is one of the most common serious neurological disorders and affects individuals of all ages across the globe. The aim of this study is to provide estimates of the epilepsy burden on the global, regional, and national levels for 1990-2021. METHODS: Using well established Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) methodology, we quantified the prevalence of active idiopathic (epilepsy of genetic or unknown origin) and secondary epilepsy (epilepsy due to an underlying abnormality of the brain structure or chemistry), as well as incidence, death, and disability-adjusted life-years (DALYs) by age, sex, and location (globally, 21 GBD regions and seven super-regions, World Bank country income levels, Socio-demographic Index [SDI], and 204 countries) and their trends from 1990 to 2021. Vital registrations and verbal autopsies provided information about deaths, and data on the prevalence and severity of epilepsy, largely came from population representative surveys. All estimates were calculated with 95% uncertainty intervals (UIs). FINDINGS: In 2021, there were 51.7 million (95% UI 44.9-58.9) people with epilepsy (idiopathic and secondary combined) globally, with an age-standardised prevalence of 658 per 100 000 (569-748). Idiopathic epilepsy had an age-standardised prevalence of 307 per 100 000 (235-389) globally, with 24.2 million (18.5-30.7) prevalent cases, and secondary epilepsy had a global age-standardised prevalence of 350 per 100 000 (322-380). In 2021, 0.7% of the population had active epilepsy (0.3% attributed to idiopathic epilepsy and 0.4% to secondary epilepsy), and the age-standardised global prevalence of epilepsy from idiopathic and secondary epilepsy combined increased from 1990 to 2021 by 10.8% (1.1-21.3), mainly due to corresponding changes in secondary epilepsy. However, age-standardised death and DALY rates of idiopathic epilepsy reduced from 1990 to 2021 (decline of 15.8% [8.8-22.8] and 14.5% [4.2-24.2], respectively). There were three-fold to four-fold geographical differences in the burden of active idiopathic epilepsy, with the bulk of the burden residing in low-income to middle-income countries: 82.1% (81.1-83.4) of incident, 80.4% prevalent (79.7-82.7), 84.7% (83.7-85.1) fatal epilepsy, and 87.9% (86.2-89.2) epilepsy DALYs. INTERPRETATION: Although the global trends in idiopathic epilepsy deaths and DALY rates have improved in the preceding decades, in 2021 there were almost 52 million people with active epilepsy (24 million from idiopathic epilepsy and 28 million from secondary epilepsy), with the bulk of the burden (>80%) residing in low-income to middle-income countries. Better treatment and prevention of epilepsy are required, along with further research on risk factors of idiopathic epilepsy, good-quality long-term epilepsy surveillance studies, and exploration of the possible effect of stigma and cultural differences in seeking medical attention for epilepsy. FUNDING: Bill and Melinda Gates Foundation.
    Tags: *Epilepsy/epidemiology/mortality, *Global Burden of Disease/trends, *Global Health/statistics & numerical data, Adolescent, Adult, Aged, Child, Child, Preschool, Disability-Adjusted Life Years, Female, Humans, Incidence, Infant, Infant, Newborn, Male, Middle Aged, Prevalence, Young Adult.
  • Espejo, T., Nieves-Ortega, R., Amsler, L., Riedel, H. B., Balestra, G., Rosin, C., Becker, C., Lippay, K., Nickel, C. H., and Bingisser, R. “Clinical Gestalt To Predict Bacterial Infection And Mortality In Emergency Department Patients: A Prospective Observational Study”. J Gen Intern Med. doi:10.1007/s11606-025-09440-7.
    Abstract: BACKGROUND: Time to treatment is a significant predictor of mortality in emergency department (ED) patients with bacterial sepsis. Strategies for the early detection of bacterial infection and sepsis are lacking. Clinical gestalt is a tool for assessing and synthesizing the entire clinical picture, focusing on the first clinical impression at presentation. OBJECTIVE: This study aimed to assess ED physicians' clinical gestalt for the prediction of bacterial infection and mortality in ED patients presenting with signs and symptoms of infection. DESIGN: Prospective, observational study with a 30-day follow-up. PARTICIPANTS: Patients aged 18 or older presenting to the ED with signs and symptoms compatible with an infection and abnormal vital signs were included. MAIN MEASURES: ED physicians recorded their clinical gestalt using a visual analog scale (VAS) to assess the likelihood of bacterial infection and responded to a dichotomous question regarding the probability of a patient's death. The main outcome was the confirmed diagnosis of an acute bacterial infection. Final diagnoses, based on laboratory and follow-up information, were adjudicated by an expert panel. KEY RESULTS: In total, 444 patients were included. Median age was 68 years [IQR 51, 80] and median National Early Warning Score (NEWS) was 5 [IQR 3, 7]. Median VAS for physicians' clinical gestalt regarding bacterial infection likelihood was 8.2 [IQR 6.7, 9.0] of 10 in patients with bacterial infection, 2.3 [IQR 1.2, 4.3] in patients with viral infection, 4.6 [IQR 4.0, 7.3] in patients with an infection due to another pathogen, and 2.3 [IQR 1.1 6.2] in patients with no acute infection (p-value = <0.001). Clinical gestalt's sensitivity regarding 30-day mortality was 57.1% [95%CI 37.2 to 75.5] with a specificity of 83.4% [95%CI 79.7 to 86.9]. CONCLUSION: In this study of ED patients presenting with signs and symptoms of infection, clinical gestalt was shown to be useful differentiating between bacterial and infections of other causes. Antibiotic prescription rate increased with the likelihood of bacterial infection according to physician gestalt. Lastly, simple heuristic prognostication of mortality (likely vs. unlikely) carried some, but limited, prognostic value.
    Tags: Antibiotics, Clinical gestalt, conflict of interest., Emergency department, Infection, Sepsis.
  • Schoenmaekers, B., Derraz, I., Tahhan, N., and Metrailler, P. “Spontaneous Spinal Epidural Hematoma Under Rivaroxaban And Clopidogrel: A Case Report And Literature Review”. Open Access Emerg Med 17: 129-135. doi:10.2147/OAEM.S489072.
    Abstract: Spontaneous spinal epidural hematoma (SSEH) is a rare pathology with potentially severe consequences for the patient. Given its uncommon incidence and frequent atypical presentation, SSEH can easily be misdiagnosed. The association between anticoagulation or antiplatelet therapy and SSEH has been described in multiple case reports and literature reviews. We present a case of a 61-year-old man on anticoagulation and antiplatelet therapy (Rivaroxaban and Clopidogrel respectively), diagnosed with spinal SSEH with good recovery after laminectomy and hematoma evacuation. However, treatment guidelines for SSEH are difficult to find and there is no clear strategy about management of anticoagulation and antiplatelet therapy. The aim of this report is to highlight the importance of rapid diagnosis and surgical therapy in selected cases and to give an insight on the anticoagulation and antiplatelet management in these patients and their prognosis.
    Tags: anticoagulation, neurosurgery, platelet inhibitors, prognosis, treatment.
  • Ryser, B., Merz, S., Flueckiger, S., Exadaktylos, A., and Lindner, G. “Gender Disparities In Diagnostic Procedures Of Primary Hyperventilation”. Eur J Emerg Med 32, no. 2: 147-148. doi:10.1097/MEJ.0000000000001201.
    Tags: article, diagnosis, diagnostic procedure, gender inequality, human, hyperventilation, male.
  • Roth, E., Cattaneo, M., Hollenstein, Y., Weisser, M., Bassetti, S., Tschudin Sutter, S., Bingisser, R., Nickel, C. H., and Egli, A. “The Impact Of Rapid Molecular Diagnostics For Influenza On Antibiotic Stewardship In The Emergency Department-An Observational Retrospective Study”. Antibiotics (Basel) 14, no. 2. doi:10.3390/antibiotics14020120.
    Abstract: OBJECTIVE: The clinical diagnosis of respiratory tract infections (RTIs) may result in unnecessary antibiotic treatment due to clinical exams' low sensitivity and specificity to differentiate viral from bacterial infections and costly diagnostic work-ups. Unnecessary antibiotic consumption drives antibiotic resistance. We explored whether a rapid influenza-specific polymerase chain reaction (PCR) assay reduced antibiotic use in an emergency room before the COVID-19 pandemic. METHODS: We conducted an observational retrospective study of patients with RTI symptoms treated in the ER of the University Hospital Basel from September 2014 to June 2015. We evaluated the impact of rapid diagnostic results, such as an influenza-specific PCR, blood sample results, and radiological imaging, on antibiotic prescription rates. Patient-related confounding factors were included since a patient's clinical condition affects doctors' clinical decision-making. RESULTS: We included 607 patients with RTIs, tested with PCR for influenza A or B. Logistic regression showed that the odds ratio (OR) of being treated with antibiotics was significantly reduced by more than two-thirds in patients with a positive influenza PCR result (OR = 0.37; 95% CI, 0.22-0.59; p < 0.001). Increasing C-reactive protein (CRP) levels by tenfold (OR = 5.14; 95% CI, 3.34-8.12; p < 0.001) or suspected chest infection on a radiograph (OR = 5.81; 95% CI, 3.23-10.89; p < 0.001) increased the OR of antibiotic treatment by fivefold. The highest OR for antibiotic prescription was due to increased procalcitonin level by tenfold (OR = 10.13; 95% CI, 4.79-23.4; p < 0.001). CONCLUSIONS: Our study provides real-world evidence from a pre-COVID-19 ER setting of diagnostic tools used for RTI evaluation and their impact on antibiotic prescriptions. Rapid influenza-specific PCR results may affect the prescription rate of antibiotics but should be seen as part of a comprehensive diagnostic approach to guide clinical decision-making.
    Tags: antibiotic stewardship, diagnostics, influenza, management, molecular diagnostics, rapid PCR, respiratory tract infection.
  • Klukowska-Rotzler, J., Graber, F., Exadaktylos, A. K., Ziaka, M., and Jakob, D. A. “Gender-Specific Patterns Of Injury In Older Adults After A Fall From A Four-Wheeled Walker (Rollator): Retrospective Study From A Swiss Level 1 Trauma Centre”. Int J Environ Res Public Health 22, no. 2. doi:10.3390/ijerph22020143.
    Abstract: AIM: As the population is aging, falls by older people, in particular falls from four-wheeled walkers ("rollators"), are a growing problem. These falls must be examined by targeted research and interventions that incorporate gender differences. Therefore, this study examined the injury patterns of elderly patients admitted to a tertiary trauma centre in Switzerland after falls from rollators and focussed on gender differences. METHODS: This was a retrospective single-centre study for the period from May 2012 to December 2019 which included elderly patients (>/=65 years) who had suffered a fall from a rollator. Injury history, patient data, demographic information, and patient outcomes were compared between males and females, with the data sourced from the Ecare patient database, which contains all information related to patient visits and treatment procedures. RESULTS: A total of 152 eligible patients were included in the analysis, with 56.6% hospitalised at our facility and 14.5% transferred to another hospital. The cohort comprised 50 (32.9%) males and 102 (67.1%) females. Males were more prevalent in the 75-84 age group, while females predominated in the 85 and older group, and this difference was statistically significant (p = 0.043). Osteoporosis was significantly more common in females (37.3% vs. 10%, p </= 0.001). Consequently, treatment with vitamin D and/or calcium was also significantly more prevalent among women (29.4% vs. 8%, p = 0.003). Most falls occurred at home (22.4%) or in nursing care facilities and rehabilitation centres (22.4%), without gender-based differences (p = 0.570). Men were six times more likely than women to sustain injuries when under the influence of alcohol (p = 0.002). Fractures to the lower extremities were the most common injuries, accounting for 34.2% of all injuries, with no statistically significant differences between groups (p = 0.063). Head injuries occurred in 34.9% of patients, with a trend towards more injuries in males (44% vs. 30.4%, p = 0.098). The cumulative rates of fractures to the pelvis, upper extremities, and lower extremities were significantly higher in females (59.8%) than in males (38%), p = 0.011. In-hospital mortality was significantly higher in men than in women (12.9% vs. 2.9%, p = 0.026). Operative procedures were significantly more common in women (33% vs. 16.3%; p < 0.001). CONCLUSION: Women were more frequently affected by falls related to rollators than men. Most falls occurred at home, in nursing care facilities, or rehabilitation centres, with no significant gender-based differences. There was a trend toward more head injuries in males, while the cumulative fracture rate of the pelvis, upper extremities, and lower extremities was significantly higher in females. In-hospital mortality was more than four times higher in men. These findings may guide the development of gender-specific interventions to reduce rollator-related injuries in the vulnerable elderly population.
    Tags: *Accidental Falls/statistics & numerical data, *Wounds and Injuries/epidemiology/etiology, Aged, Aged, 80 and over, falls, Female, four-wheeled walker, geriatric patients, Humans, Male, Retrospective Studies, rollator, Sex Factors, Switzerland/epidemiology, trauma, Trauma Centers/statistics & numerical data.
  • Moeckel, J., Wenzel, V., Angerer, V., Albrecht, R., and Pietsch, U. “Droplet Formation In Drugs During Extreme Temperature Conditions In The Emergency Medical Service, A Problem?”. Air Med J 44, no. 1: 114-116. doi:10.1016/j.amj.2024.10.007.
    Abstract: OBJECTIVE: Because of high-altitude operations, cold exposure is common for helicopter emergency medical services. However, drug emulsions such as propofol and etomidate are prone to degradation and the formation of lipid droplets, possibly large enough to cause pulmonary embolism, when frozen. Amiodarone may be prone to crystallization, possibly causing phlebitis, when exposed to cold temperatures. The aim of this study was to microscopically identify physical changes in common emergency drugs under cold exposure. METHODS: Exposure time frames and temperature ranges were chosen according to real-world data collected on a rescue helicopter in Switzerland. Samples were stored in a laboratory freezer with a temperature range of -2.3 degrees C (27.7 degrees F) for 1 hour, 0.6 degrees C to -3.6 degrees C (33.1 degrees F-25.5 degrees F) for 12 hours, and -22 degrees C (-7.6 degrees F) for 1 hour and 12 hours. Analysis was performed under a light microscope. RESULTS: No physical changes in the form of large lipid droplets or crystallization were found in the samples stored at -2.3 degrees C (27.7 degrees F). Lipid droplets were found in the propofol samples stored at 0.6 degrees C to -3.4 degrees C (33.1 degrees F-25.5 degrees F) and -22 degrees C (-7.6 degrees F) over 12 hours. CONCLUSION: There was no observation of physical changes under temperature conditions commonly found in helicopter emergency medical services. However, lipid droplets could be observed in the propofol samples with long exposure times or under deep frozen temperature conditions. These findings highlight the need to establish a safe threshold for cold exposure of medications in the prehospital environment.
    Tags: *Air Ambulances, *Cold Temperature, *Emergency Medical Services, *Lipid Droplets, Amiodarone/chemistry, Humans, Propofol/chemistry, Switzerland, There was no grant funding or financial support for this manuscript..
  • Makowska, A., Ananthakrishnan, G., Christ, M., and Dehmer, M. “Screening For Left Ventricular Hypertrophy Using Artificial Intelligence Algorithms Based On 12 Leads Of The Electrocardiogram-Applicable In Clinical Practice?-Critical Literature Review With Meta-Analysis”. Healthcare (Basel) 13, no. 4. doi:10.3390/healthcare13040408.
    Abstract: Background/Objectives: The increasing utilization of artificial intelligence (AI) in the medical field holds the potential to address the global shortage of doctors. However, various challenges, such as usability, privacy, inequality, and misdiagnosis, complicate its application. This literature review focuses on AI's role in cardiology, specifically its impact on the diagnostic accuracy of AI algorithms analyzing 12-lead electrocardiograms (ECGs) to detect left ventricular hypertrophy (LVH). Methods: Following PRISMA 2020 guidelines, we conducted a comprehensive search of PubMed, CENTRAL, Google Scholar, Web of Science, and Cochrane Library. Eligible studies included randomized controlled trials (RCTs), observational studies, and case-control studies across various settings. This review is registered in the PROSPERO database (registration number 531468). Results: Seven significant studies were selected and included in our review. Meta-analysis was performed using RevMan. Co-CNN (with incorporated demographic data and clinical variables) demonstrated the highest weighted average sensitivity at 0.84. 2D-CNN models (with demographic features) showed a balanced performance with good sensitivity (0.62) and high specificity (0.82); Co-CNN models excelled in sensitivity (0.84) but had lower specificity (0.71). Traditional ECG criteria (SLV and CV) maintained high specificities but low sensitivities. Scatter plots revealed trends between demographic factors and performance metrics. Conclusions: AI algorithms can rapidly analyze ECG data with high sensitivity. The diagnostic accuracy of AI models is variable but generally comparable to classical criteria. Clinical data and the training population of AI algorithms play a critical role in their efficacy. Future research should focus on collecting diverse ECG data across different populations to improve the generalizability of AI algorithms.
    Tags: artificial intelligence, deep learning, electrocardiogram, left ventricle hypertrophy, machine learning.
  • Ageron, F. X., Evain, J. N., Chifflet, J., Vallot, C., Greze, J., Mortamet, G., Bouzat, P., Gauss, T., and Group, Trenau. “Improving Paediatric Undertriage In A Regional Trauma Network - A Registry Cohort Study”. Anaesth Crit Care Pain Med 44, no. 2: 101497. doi:10.1016/j.accpm.2025.101497.
    Abstract: BACKGROUND: Trauma remains a leading cause of death in children worldwide. Management in dedicated paediatric trauma centres is beneficial, making accurate prehospital triage crucial. We assessed undertriage in a regional trauma system after implementing a revised paediatric triage rule. METHODS: This retrospective, multicentre registry study included all injured children <15 years admitted to hospitals in the Northern French Alps with suspected major trauma and/or an Abbreviated Injury Scale >/=3. Triage performance was assessed before and after implementation of a revised paediatric triage rule. Multivariate logistic regression identified predictors of undertriage defined as a child with major trauma (need for trauma intervention) not directly transported to the paediatric trauma centre. RESULTS: All 1524 injured children from January 2009 to December 2020 were included. Of these, 725/1524 (47.6%) presented with major trauma; 593/1524 (38.9%) were referred to a non-paediatric trauma centre, and 220/1524 (15%) were considered undertriaged. Over the years, undertriage decreased from 15% to 9%, after the implementation of a revised triage rule. After adjustment, revised paediatric triage rules decreased undertriage, OR = 0.5; 95% CI: 0.3-0.9; P < 0.02. The multivariate regression model identified the following risk factors of undertriage: children >10 years, two-wheel vehicle road traffic accident, girls after a fall, for boys after a winter ski accident, and infants with severe limb and pelvic injuries. CONCLUSION: The implementation of regional revised triage rule contributed to a reduction in the paediatric undertriage rate to 9%; several clinical factors were associated with undertriage.
    Tags: *Trauma Centers/statistics & numerical data, *Triage/standards/methods/statistics & numerical data, *Wounds and Injuries/therapy/diagnosis, Adolescent, Child, Child, Preschool, Cohort Studies, Female, France, Humans, Infant, Infant, Newborn, Male, Paediatric trauma, Registries, Retrospective Studies, Trauma system, Triage, Undertriage.
  • Neher, A. N., Buhlmann, F., Muller, M., Berendonk, C., Sauter, T. C., and Birrenbach, T. “Virtual Reality For Assessment In Undergraduate Nursing And Medical Education - A Systematic Review”. Bmc Med Educ 25, no. 1: 292. doi:10.1186/s12909-025-06867-8.
    Abstract: BACKGROUND: Virtual reality (VR) is increasingly used in healthcare education, offering immersive training experiences that are as effective as conventional methods, with benefits like cost-effectiveness, replicating complex scenarios, and reduced need for physical resources. However, the use of VR as an assessment tool is still emerging, particularly in nursing and medical education. The aim of this systematic review was to examine how immersive VR is used as an assessment tool for nursing and medical students. METHODS: Embase, PubMed, PsycINFO, Cochrane, CINAHL, and ERIC were searched for articles that assessed nursing and/or medical students using immersive/HMD VR. The data was extracted, and content analysis was performed. RESULTS: Twenty-six studies met the inclusion criteria, investigating VR assessments in various settings mostly emergencies. Assessments focused on core competencies Patient Care such as first triage, Interpersonal and Communication Skills (e.g., interprofessional communication), and Medical Knowledge (e.g., about coma), utilizing a range of assessment methods from knowledge to performance levels. VR was used either as an automated or supporting assessment tool. Practical considerations in VR implementation were also examined, such as hardware and software. CONCLUSION: The use of VR in medical education assessment shows promise, particularly for emergency scenarios and performance-based tasks related to core competencies such as Patient Care, Interpersonal and Communication Skills, and Medical Knowledge. While this technology offers opportunities to automate assessments and reduce examiner workload, challenges related to software, costs, and feasibility must be addressed. Additionally, aligning learning objectives, teaching methods, and VR assessments through constructive alignment is essential to ensure effective implementation as both a teaching and evaluation tool.
    Tags: *Education, Medical, Undergraduate/methods, *Education, Nursing, Baccalaureate/methods, *Education, Nursing/methods, *Educational Measurement/methods, *Virtual Reality, and utilized the MERSQI Tool instead of the Cochrane Risk-of-Bias-Tool (as, applicable. Consent for publication: Not applicable. Competing interests: TCS, Bern sponsored by the Touring Club Switzerland. The sponsor has no influence on, Clinical Competence, holds the endowed professorship of emergency telemedicine at the University of, Humans, initially registered) for assessing data quality due to the inclusion of a wide, Medical education, Nursing, Performance assessment, range of study designs. Ethics approval and consent to participate: Not, Students, Medical, the research or decision to publish. All other authors have nothing to disclose., Virtual reality.
  • G. B. D. Suicide Collaborators,. “Global, Regional, And National Burden Of Suicide, 1990-2021: A Systematic Analysis For The Global Burden Of Disease Study 2021”. Lancet Public Health 10, no. 3: e189-e202. doi:10.1016/S2468-2667(25)00006-4.
    Abstract: BACKGROUND: Deaths from suicide are a tragic yet preventable cause of mortality. Quantifying the burden of suicide to understand its geographical distribution, temporal trends, and variation by age and sex is an essential step in suicide prevention. We aimed to present a comprehensive set of global, regional, and national estimates of suicide burden. METHODS: We produced estimates of the number of deaths and age-standardised mortality rates of suicide globally, regionally, and for 204 countries and territories from 1990 to 2021, and disaggregated these results by age and sex. The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2021 estimates of deaths attributable to suicide were broken down into two comprehensive categories: those by firearms and those by other specified means. For this analysis, we also produced estimates of mean age at the time of death from suicide, incidence of suicide attempts compared with deaths, and age-standardised rates of suicide by firearm. We acquired data from vital registration, verbal autopsy, and mortality surveillance that included 23 782 study-location-years of data from GBD 2021. Point estimates were calculated from the average of 1000 randomly selected possible values of deaths from suicide by age, sex, and geographical location. 95% uncertainty intervals (UIs) were derived from the 2.5th and 97.5th percentiles from a 1000-draw distribution. FINDINGS: Globally, 746 000 deaths (95% UI 692 000-800 000) from suicide occurred in 2021, including 519 000 deaths (485 000-556 000) among males and 227 000 (200 000-255 000) among females. The age-standardised mortality rate has declined over time, from 14.9 deaths (12.8-15.7) per 100 000 population in 1990 to 9.0 (8.3-9.6) per 100 000 in 2021. Regionally, mortality rates due to suicide were highest in eastern Europe (19.2 [17.5-20.8] per 100 000), southern sub-Saharan Africa (16.1 [14.0-18.3] per 100 000), and central sub-Saharan Africa (14.4 [11.0-19.1] per 100 000). The mean age at which individuals died from suicide progressively increased during the study period. For males, the mean age at death by suicide in 1990 was 43.0 years (38.0-45.8), increasing to 47.0 years (43.5-50.6) in 2021. For females, it was 41.9 years (30.9-46.7) in 1990 and 46.9 years (41.2-52.8) in 2021. The incidence of suicide attempts requiring medical care was consistently higher at the regional level for females than for males. The number of deaths by suicide using firearms was higher for males than for females, and substantially varied by country and region. The countries with the highest age-standardised rate of suicides attributable to firearms in 2021 were the USA, Uruguay, and Venezuela. INTERPRETATION: Deaths from suicide remain variable by age and sex and across geographical locations, although population mortality rates have continued to improve globally since the 1990s. This study presents, for the first time in GBD, a quantification of the mean age at the time of suicide death, alongside comprehensive estimates of the burden of suicide throughout the world. These analyses will help guide future approaches to reduce suicide mortality that consider a public health framework for prevention. FUNDING: Bill & Melinda Gates Foundation.
    Tags: *Global Burden of Disease/trends, *Global Health/statistics & numerical data, *Suicide/statistics & numerical data/trends, Adolescent, Adult, Aged, Child, Female, Humans, Male, Middle Aged, Young Adult.
  • Weaver, N. D., Bertolacci, G. J., Rosenblad, E., Ghoba, S., Cunningham, M., Ikuta, K. S., Moberg, M. E., et al. “Global, Regional, And National Burden Of Suicide, 1990-2021: A Systematic Analysis For The Global Burden Of Disease Study 2021”. The Lancet Public Health 10, no. 3: e189-e202. doi:10.1016/S2468-2667(25)00006-4.
    Abstract: Background: Deaths from suicide are a tragic yet preventable cause of mortality. Quantifying the burden of suicide to understand its geographical distribution, temporal trends, and variation by age and sex is an essential step in suicide prevention. We aimed to present a comprehensive set of global, regional, and national estimates of suicide burden. Methods: We produced estimates of the number of deaths and age-standardised mortality rates of suicide globally, regionally, and for 204 countries and territories from 1990 to 2021, and disaggregated these results by age and sex. The Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2021 estimates of deaths attributable to suicide were broken down into two comprehensive categories: those by firearms and those by other specified means. For this analysis, we also produced estimates of mean age at the time of death from suicide, incidence of suicide attempts compared with deaths, and age-standardised rates of suicide by firearm. We acquired data from vital registration, verbal autopsy, and mortality surveillance that included 23 782 study-location-years of data from GBD 2021. Point estimates were calculated from the average of 1000 randomly selected possible values of deaths from suicide by age, sex, and geographical location. 95% uncertainty intervals (UIs) were derived from the 2·5th and 97·5th percentiles from a 1000-draw distribution. Findings: Globally, 746 000 deaths (95% UI 692 000-800 000) from suicide occurred in 2021, including 519 000 deaths (485 000-556 000) among males and 227 000 (200 000-255 000) among females. The age-standardised mortality rate has declined over time, from 14·9 deaths (12·8-15·7) per 100 000 population in 1990 to 9·0 (8·3-9·6) per 100 000 in 2021. Regionally, mortality rates due to suicide were highest in eastern Europe (19·2 [17·5-20·8] per 100 000), southern sub-Saharan Africa (16·1 [14·0-18·3] per 100 000), and central sub-Saharan Africa (14·4 [11·0-19·1] per 100 000). The mean age at which individuals died from suicide progressively increased during the study period. For males, the mean age at death by suicide in 1990 was 43·0 years (38·0-45·8), increasing to 47·0 years (43·5-50·6) in 2021. For females, it was 41·9 years (30·9-46·7) in 1990 and 46·9 years (41·2-52·8) in 2021. The incidence of suicide attempts requiring medical care was consistently higher at the regional level for females than for males. The number of deaths by suicide using firearms was higher for males than for females, and substantially varied by country and region. The countries with the highest age-standardised rate of suicides attributable to firearms in 2021 were the USA, Uruguay, and Venezuela. Interpretation: Deaths from suicide remain variable by age and sex and across geographical locations, although population mortality rates have continued to improve globally since the 1990s. This study presents, for the first time in GBD, a quantification of the mean age at the time of suicide death, alongside comprehensive estimates of the burden of suicide throughout the world. These analyses will help guide future approaches to reduce suicide mortality that consider a public health framework for prevention. Funding: Bill & Melinda Gates Foundation. © 2025 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license
    Tags: adolescent, adult, Africa south of the Sahara, age standardised mortality rate, aged, Article, child, Eastern Europe, epidemiological data, female, firearm, geographic distribution, Global Burden of Disease, global disease burden, global health, human, Humans, ICD-10, incidence, male, middle aged, mortality rate, preschool child, school child, suicide, suicide mortality, time of death, Uruguay, Venezuela, verbal autopsy, young adult.
  • Collaborators, G. B. D. Europe Life Expectancy. “Changing Life Expectancy In European Countries 1990-2021: A Subanalysis Of Causes And Risk Factors From The Global Burden Of Disease Study 2021”. Lancet Public Health 10, no. 3: e172-e188. doi:10.1016/S2468-2667(25)00009-X.
    Abstract: BACKGROUND: Decades of steady improvements in life expectancy in Europe slowed down from around 2011, well before the COVID-19 pandemic, for reasons which remain disputed. We aimed to assess how changes in risk factors and cause-specific death rates in different European countries related to changes in life expectancy in those countries before and during the COVID-19 pandemic. METHODS: We used data and methods from the Global Burden of Diseases, Injuries, and Risk Factors Study 2021 to compare changes in life expectancy at birth, causes of death, and population exposure to risk factors in 16 European Economic Area countries (Austria, Belgium, Denmark, Finland, France, Germany, Greece, Iceland, Ireland, Italy, Luxembourg, the Netherlands, Norway, Portugal, Spain, and Sweden) and the four UK nations (England, Northern Ireland, Scotland, and Wales) for three time periods: 1990-2011, 2011-19, and 2019-21. Changes in life expectancy and causes of death were estimated with an established life expectancy cause-specific decomposition method, and compared with summary exposure values of risk factors for the major causes of death influencing life expectancy. FINDINGS: All countries showed mean annual improvements in life expectancy in both 1990-2011 (overall mean 0.23 years [95% uncertainty interval [UI] 0.23 to 0.24]) and 2011-19 (overall mean 0.15 years [0.13 to 0.16]). The rate of improvement was lower in 2011-19 than in 1990-2011 in all countries except for Norway, where the mean annual increase in life expectancy rose from 0.21 years (95% UI 0.20 to 0.22) in 1990-2011 to 0.23 years (0.21 to 0.26) in 2011-19 (difference of 0.03 years). In other countries, the difference in mean annual improvement between these periods ranged from -0.01 years in Iceland (0.19 years [95% UI 0.16 to 0.21] vs 0.18 years [0.09 to 0.26]), to -0.18 years in England (0.25 years [0.24 to 0.25] vs 0.07 years [0.06 to 0.08]). In 2019-21, there was an overall decrease in mean annual life expectancy across all countries (overall mean -0.18 years [95% UI -0.22 to -0.13]), with all countries having an absolute fall in life expectancy except for Ireland, Iceland, Sweden, Norway, and Denmark, which showed marginal improvement in life expectancy, and Belgium, which showed no change in life expectancy. Across countries, the causes of death responsible for the largest improvements in life expectancy from 1990 to 2011 were cardiovascular diseases and neoplasms. Deaths from cardiovascular diseases were the primary driver of reductions in life expectancy improvements during 2011-19, and deaths from respiratory infections and other COVID-19 pandemic-related outcomes were responsible for the decreases in life expectancy during 2019-21. Deaths from cardiovascular diseases and neoplasms in 2019 were attributable to high systolic blood pressure, dietary risks, tobacco smoke, high LDL cholesterol, high BMI, occupational risks, high alcohol use, and other risks including low physical activity. Exposure to these major risk factors differed by country, with trends of increasing exposure to high BMI and decreasing exposure to tobacco smoke observed in all countries during 1990-2021. INTERPRETATION: The countries that best maintained improvements in life expectancy after 2011 (Norway, Iceland, Belgium, Denmark, and Sweden) did so through better maintenance of reductions in mortality from cardiovascular diseases and neoplasms, underpinned by decreased exposures to major risks, possibly mitigated by government policies. The continued improvements in life expectancy in five countries during 2019-21 indicate that these countries were better prepared to withstand the COVID-19 pandemic. By contrast, countries with the greatest slowdown in life expectancy improvements after 2011 went on to have some of the largest decreases in life expectancy in 2019-21. These findings suggest that government policies that improve population health also build resilience to future shocks. Such policies include reducing population exposure to major upstream risks for cardiovascular diseases and neoplasms, such as harmful diets and low physical activity, tackling the commercial determinants of poor health, and ensuring access to affordable health services. FUNDING: Gates Foundation.
    Tags: *COVID-19/epidemiology, *Global Burden of Disease/trends, *Life Expectancy/trends, Adult, Aged, Aged, 80 and over, Cause of Death/trends, Europe/epidemiology, Female, Humans, Infant, Male, Middle Aged, Risk Factors.
  • G. B. D. Europe Life Expectancy Collaborators,. “Changing Life Expectancy In European Countries 1990-2021: A Subanalysis Of Causes And Risk Factors From The Global Burden Of Disease Study 2021”. Lancet Public Health 10, no. 3: e172-e188. doi:10.1016/S2468-2667(25)00009-X.
    Abstract: BACKGROUND: Decades of steady improvements in life expectancy in Europe slowed down from around 2011, well before the COVID-19 pandemic, for reasons which remain disputed. We aimed to assess how changes in risk factors and cause-specific death rates in different European countries related to changes in life expectancy in those countries before and during the COVID-19 pandemic. METHODS: We used data and methods from the Global Burden of Diseases, Injuries, and Risk Factors Study 2021 to compare changes in life expectancy at birth, causes of death, and population exposure to risk factors in 16 European Economic Area countries (Austria, Belgium, Denmark, Finland, France, Germany, Greece, Iceland, Ireland, Italy, Luxembourg, the Netherlands, Norway, Portugal, Spain, and Sweden) and the four UK nations (England, Northern Ireland, Scotland, and Wales) for three time periods: 1990-2011, 2011-19, and 2019-21. Changes in life expectancy and causes of death were estimated with an established life expectancy cause-specific decomposition method, and compared with summary exposure values of risk factors for the major causes of death influencing life expectancy. FINDINGS: All countries showed mean annual improvements in life expectancy in both 1990-2011 (overall mean 0.23 years [95% uncertainty interval [UI] 0.23 to 0.24]) and 2011-19 (overall mean 0.15 years [0.13 to 0.16]). The rate of improvement was lower in 2011-19 than in 1990-2011 in all countries except for Norway, where the mean annual increase in life expectancy rose from 0.21 years (95% UI 0.20 to 0.22) in 1990-2011 to 0.23 years (0.21 to 0.26) in 2011-19 (difference of 0.03 years). In other countries, the difference in mean annual improvement between these periods ranged from -0.01 years in Iceland (0.19 years [95% UI 0.16 to 0.21] vs 0.18 years [0.09 to 0.26]), to -0.18 years in England (0.25 years [0.24 to 0.25] vs 0.07 years [0.06 to 0.08]). In 2019-21, there was an overall decrease in mean annual life expectancy across all countries (overall mean -0.18 years [95% UI -0.22 to -0.13]), with all countries having an absolute fall in life expectancy except for Ireland, Iceland, Sweden, Norway, and Denmark, which showed marginal improvement in life expectancy, and Belgium, which showed no change in life expectancy. Across countries, the causes of death responsible for the largest improvements in life expectancy from 1990 to 2011 were cardiovascular diseases and neoplasms. Deaths from cardiovascular diseases were the primary driver of reductions in life expectancy improvements during 2011-19, and deaths from respiratory infections and other COVID-19 pandemic-related outcomes were responsible for the decreases in life expectancy during 2019-21. Deaths from cardiovascular diseases and neoplasms in 2019 were attributable to high systolic blood pressure, dietary risks, tobacco smoke, high LDL cholesterol, high BMI, occupational risks, high alcohol use, and other risks including low physical activity. Exposure to these major risk factors differed by country, with trends of increasing exposure to high BMI and decreasing exposure to tobacco smoke observed in all countries during 1990-2021. INTERPRETATION: The countries that best maintained improvements in life expectancy after 2011 (Norway, Iceland, Belgium, Denmark, and Sweden) did so through better maintenance of reductions in mortality from cardiovascular diseases and neoplasms, underpinned by decreased exposures to major risks, possibly mitigated by government policies. The continued improvements in life expectancy in five countries during 2019-21 indicate that these countries were better prepared to withstand the COVID-19 pandemic. By contrast, countries with the greatest slowdown in life expectancy improvements after 2011 went on to have some of the largest decreases in life expectancy in 2019-21. These findings suggest that government policies that improve population health also build resilience to future shocks. Such policies include reducing population exposure to major upstream risks for cardiovascular diseases and neoplasms, such as harmful diets and low physical activity, tackling the commercial determinants of poor health, and ensuring access to affordable health services. FUNDING: Gates Foundation.
    Tags: *COVID-19/epidemiology, *Global Burden of Disease/trends, *Life Expectancy/trends, Adult, Aged, Aged, 80 and over, Cause of Death/trends, Europe/epidemiology, Female, Humans, Infant, Male, Middle Aged, Risk Factors.
  • Raess, L., Staubli, G., and Seiler, M. “Assessing Guideline Adherence And Child Abuse Evaluation In Infants With Fractures: A Retrospective Quality Control Study”. Swiss Med Wkly 154, no. 9: 3781. doi:10.57187/s.3781.
    Abstract: AIMS OF THE STUDY: To standardise the assessment of infants with fractures at University Children's Hospital Zurich, a guideline was implemented in February 2021. The aim of this study was to assess adherence to this guideline and to assess changes in management before and after guideline implementation. The primary outcome was the overall adherence rate to the guideline. Additionally, we evaluated specific omissions of guideline steps by clinicians and investigated differences in adherence for infants younger vs older than six months, as well as variations between in- and outpatient care. Secondary outcomes focused on changes in the frequency of involvement of the child protection team, skeletal survey rates and child abuse detection, comparing these rates before and after guideline implementation. METHODS: We conducted a retrospective single-centre quality control study. We included infants younger than 12 months diagnosed with fractures at the emergency department between 1 February 2021 and 31 August 2022. We excluded children with prior bone disease diagnoses and those whose parents did not consent to their children's data being used for research. RESULTS: A total of 61 emergency department visits of infants with fractures were included in the study. The overall adherence rate to the guideline was 39%. Notably, in 68% of cases where clinicians deviated from the guideline, the primary reason was a missing consultation of the paediatrician or family doctor. Adherence levels were consistent across age groups (under and over six months), but there was a notable discrepancy between inpatient (53%) and outpatient (26%) care settings. Child protection team involvement increased to 54%, twice the rate observed before guideline implementation. CONCLUSIONS: Overall adherence to the guideline was poor, emphasising the necessity for continuous training of clinicians to raise awareness regarding the differential diagnosis of child abuse. Despite the guideline's implementation leading to a doubled rate of child protection team involvement, there remains a need for improvement. Notably, outpatient care exhibited lower guideline adherence, signalling an area requiring focused attention.
    Tags: *Child Abuse/diagnosis/statistics & numerical data, *Fractures, Bone/diagnosis, *Guideline Adherence/statistics & numerical data, Emergency Service, Hospital/statistics & numerical data, Female, Humans, Infant, Infant, Newborn, Male, Practice Guidelines as Topic, Quality Control, Retrospective Studies, Switzerland.
  • Dirren, E., Escribano Paredes, J. B., Klug, J., Barthoulot, M., Fluss, J., Fracasso, T., Kurian, G. K., et al. “Stroke Incidence, Case Fatality, And Mortality Using The Who International Classification Of Diseases 11: The Geneva Stroke Study”. Neurology 104, no. 5: e213353. doi:10.1212/WNL.0000000000213353.
    Abstract: BACKGROUND AND OBJECTIVES: In the field of stroke epidemiology, one of the major advances in the recently implemented International Classification of Diseases, 11th revision (ICD-11) relates to the definition of ischemic stroke, which now includes events shorter than 24 hours when ischemia can be proven on brain imaging. However, data are scarce to ascertain the incidence of strokes of short duration with tissue evidence of ischemia. In this study, we determined the incidence, 30-day case fatality, and mortality rate of stroke in the Geneva population using the new ICD-11 criteria, taking advantage of the organization of stroke service in the area. METHODS: In this population-based observational cohort study, we used data from the Swiss Stroke Registry, supplemented by hospital records, outpatient medical files, and autopsy, to identify residents of the canton of Geneva, Switzerland, meeting the ICD-11 criteria for first-ever stroke, including ischemic strokes, nontraumatic intracerebral hemorrhage (ICH), or subarachnoid hemorrhage (SAH), from January 1, 2018, to December 31, 2019. RESULTS: We identified 1,186 first-ever strokes (75.8 years [interquartile range 63.4-84.5]; 571 women [48.1%]). MRI was performed in 90.9% of patients with ischemic strokes. The annual incidence of first-ever stroke, age-adjusted to the European Standard Population, was 127.0/100,000 (95% CI 119.8-134.3) (107.3 [100.7-114.0] for ischemic stroke, 13.2 [10.9-15.5] for ICH, and 6.0 [4.4-7.5] for SAH [3.1 2.0-4.2 for aneurysmal SAH]). Overall, the 30-day case fatality was higher in ICH (32.5% [95% CI 19.7-38.8], compared with SAH (17.2% [6.6-27.9] and ischemic strokes 10.8% [8.4-12.4]). The incidence of ischemic stroke was 107.3 (100.7-114.0) according to ICD-11 and 90.4 (84.3-96.5) according to ICD-10 (excluding patients with radiologic infarct and symptoms lasting <24 hours). Compared with ICD-10, ICD-11 increased the number of ischemic stroke cases by 18.3%. Patients with ischemic strokes identified with ICD-11 but not under ICD-10 (i.e., patients with symptoms lasting <24 hours and a brain lesion) were younger and presented with a lower National Institutes of Health Stroke Scale (NIHSS) score on admission compared with those identified by ICD-10 and ICD-11. DISCUSSION: The new ICD-11 clinicoradiologic definition of ischemic stroke increased the number of ischemic stroke cases by 18.3% in our Western European population. Future studies will evaluate the impact of ICD-11 on the human, organizational, and economic needs allocated to the management of the disease.
    Tags: *International Classification of Diseases, *Ischemic Stroke/mortality/epidemiology, *Registries/statistics & numerical data, *Stroke/mortality/epidemiology, Aged, Aged, 80 and over, Cohort Studies, Female, Humans, Incidence, Male, Middle Aged, Subarachnoid Hemorrhage/mortality/epidemiology, Switzerland/epidemiology, World Health Organization.
  • Beil, M., Alberto, L., Bourne, R. S., Brummel, N. E., de Groot, B., de Lange, D. W., Elbers, P., et al. “Esicm Consensus-Based Recommendations For The Management Of Very Old Patients In Intensive Care”. Intensive Care Med 51, no. 2: 287-301. doi:10.1007/s00134-025-07794-4.
    Abstract: PURPOSE: The heterogeneity of very old patients (age >/= 80 years) and the prevalence of complex geriatric syndromes in this cohort constitute major challenges for the classical methods of evidence-based medicine to inform clinical practice. The lack of robust guidance for the management of critical conditions in these patients contributes to considerable uncertainty among practitioners and unwarranted variations of care. The European Society of Intensive Care Medicine (ESICM) initiated a Delphi study to translate the empirical knowledge of experts in this field into consensus-based recommendations for clinical practice. METHODS: A multi-national group of specialists in intensive care, emergency, and geriatric medicine provided opinions on managing very old patients with critical conditions. Strong or moderate consensus was defined as having at least 90% or 80% of experts, respectively, expressing agreement or disagreement on the three highest or lowest levels of a 9-points Likert scale. RESULTS: Twenty-eight members of the expert steering group and 82 additional experts completed two Delphi rounds. After discussing the results, the steering group issued recommendations for 48 statements and 2 checklists for which consensus was achieved. In addition to determining fundamental principles, they include advice on goals of care and the decision-making about admission to and treatment of patients in intensive care and the management after discharge. CONCLUSION: A multi-disciplinary group of experts achieved consensus on recommendations concerning intensive care for very old patients, which were approved and endorsed by ESICM. The implementation requires a careful analysis of available healthcare resources and should proceed in a stepwise fashion.
    Tags: *Critical Care/standards/methods, *Geriatrics/standards, Aged, 80 and over, BD, and Integra. ML received fees as consultants from Edwards, AOP Pharma, and, Consensus, Critical care, Delphi study, Delphi Technique, Emergency medicine, Europe, Geriatric medicine, Heinrich-Heine-University in Dusseldorf, Germany, granted ethical approval for, Humans, Intensive care, the study (No. 2023-2680)., Viatris. Ethical approval: The Ethics Committee at the Medical School of the.
  • Zagalioti, S. C., Ziaka, M., Exadaktylos, A., and Fyntanidou, B. “An Effective Triage Education Method For Triage Nurses: An Overview And Update”. Open Access Emerg Med 17: 105-112. doi:10.2147/OAEM.S498085.
    Abstract: BACKGROUND: Accurate decision-making in triage largely determines the amount of time required for a patient to be evaluated and treated while in the emergency department. Nursing staff worldwide have similar learning characteristics with similar working hours and common goals, despite the fact that different triage scales are used globally. The aim of this mini review is to present the different educational methods and identify the most effective for triage training of triage nurses. MATERIALS AND METHODS: We screened studies concerning triage education for nurses in Emergency Department, in databases including PubMed, CENTRAL and CINAHL. From November 12, 2023 to February 15, 2024, databases were searched for relevant literature. "Triage education" OR "triage training" AND "emergency nurses" OR "triage nurses" were the MeSH terms. RESULTS: There are various educational methods, including traditional, web-based, audiovisual, simulation-based, blended learning, and other specialized approaches. Almost all of the studies that are currently available demonstrate how effectively an educational intervention might improve nurses' comprehension of triage. Except for one, every study concluded that the educational intervention significantly improved nurses' triage knowledge. Comparing the included studies is challenging due to their heterogeneity, and applying the results in practice requires caution. CONCLUSION: The majority of studies reported that educational interventions effectively increased nurses' triage knowledge. Blended learning in conjunction with refresher courses enhanced triage-related knowledge and decision-making; however, additional research is required to ascertain whether this approach is superior to the others and whether these improvements will last.
    Tags: educational method, emergency department, triage education.
  • 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.
  • 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.
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