Pub Date : 2026-10-30DOI: 10.1186/s12873-026-01827-x
Rena Isabel Amelung
Background and objective: Patients in the emergency department (ED) are assessed and treated by the ED-Team consisting of nurses and physicians. The clinical assessment (CA) of emergency patients and the clinical reasoning (CR) of both professions play a decisive role in determining the quality of emergency care. This pilot study explores CR in daily routine practice of the ED on a cognitive-individual level, relying on the Dual-process Theory and on a social-interprofessional level, arguing interprofessional collaboration (IPC) as a part of CR. At least, organizational-structural factors influencing CR are analyzed as a third level.
Methods: This is a qualitative study of 13 semi-structured individual interviews with nurses and physicians from three EDs in Germany, analysed using content analysis and methodological fundation.
Results: In the individual-cognitive CR, both physicians and nurses groups identified similar key factors for CA and used Systems 1 and 2 of the Dual-process Theory in their CR. On the social-interprofessional level, IPC was generally described positively, naming characteristics of good IPC and communication barriers were reported as rare. As possible organizational-structural factors influencing CR working experience as a prerequisite, size and region of the ED, age structure of the team and digitization were found.
Conclusion: This pilot study provides insights into the CR of nurses and physicians in the ED and analyzes CR on an individual-cognitive, a social-interprofessional and an organizational-structural level, allowing to conclusions regarding the prerequisites for successful ED-teams.
{"title":"inproTeamED - clinical reasoning in the emergency department as an individual and interprofessional process: a qualitative analysis.","authors":"Rena Isabel Amelung","doi":"10.1186/s12873-026-01827-x","DOIUrl":"https://doi.org/10.1186/s12873-026-01827-x","url":null,"abstract":"<p><strong>Background and objective: </strong>Patients in the emergency department (ED) are assessed and treated by the ED-Team consisting of nurses and physicians. The clinical assessment (CA) of emergency patients and the clinical reasoning (CR) of both professions play a decisive role in determining the quality of emergency care. This pilot study explores CR in daily routine practice of the ED on a cognitive-individual level, relying on the Dual-process Theory and on a social-interprofessional level, arguing interprofessional collaboration (IPC) as a part of CR. At least, organizational-structural factors influencing CR are analyzed as a third level.</p><p><strong>Methods: </strong>This is a qualitative study of 13 semi-structured individual interviews with nurses and physicians from three EDs in Germany, analysed using content analysis and methodological fundation.</p><p><strong>Results: </strong>In the individual-cognitive CR, both physicians and nurses groups identified similar key factors for CA and used Systems 1 and 2 of the Dual-process Theory in their CR. On the social-interprofessional level, IPC was generally described positively, naming characteristics of good IPC and communication barriers were reported as rare. As possible organizational-structural factors influencing CR working experience as a prerequisite, size and region of the ED, age structure of the team and digitization were found.</p><p><strong>Conclusion: </strong>This pilot study provides insights into the CR of nurses and physicians in the ED and analyzes CR on an individual-cognitive, a social-interprofessional and an organizational-structural level, allowing to conclusions regarding the prerequisites for successful ED-teams.</p>","PeriodicalId":9002,"journal":{"name":"BMC Emergency Medicine","volume":"26 1","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-10-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149294069","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-10-21DOI: 10.1186/s12873-026-01822-2
Constantin Maier-Stocker, Rebekka Läng, Jillena Zinsser-Krys, Frank Hanses, Markus Zimmermann, Julian Hupf
Background: Critically ill non-trauma patients treated in the emergency department have a high risk of in-hospital mortality. While point-of-care diagnostics such as blood gas analysis are established tools for urgent management, data on their prognostic value in this specific patient cohort remain limited. This study aimed to evaluate whether initial blood gas parameters are independently associated with in-hospital mortality in critically ill non-trauma patients.
Methods: This retrospective cohort study included adult critically ill non-trauma patients treated in the emergency department of a German university hospital. Initial blood gas parameters and clinical data were analyzed using univariate and multivariable logistic regression to assess their association with in-hospital mortality.
Results: Of 879 screened patients, 542 met the inclusion criteria. In-hospital mortality was 20% (n = 110). In addition to older age and out-of-hospital cardiac arrest, anemia (hemoglobin < 12 g/dL; OR of 2.07, 95% CI 1.20-3.58; p = 0.009), acidosis (pH < 7.35; OR 2.26, 95% CI 1.09-4.95; p = 0.033) and hypobicarbonatemia (< 22 mmol/L; OR 2.79, 95% CI 1.42-5.69; p = 0.004) were independently associated with in-hospital mortality. The association for hyperlactatemia was borderline (> 2.2 mmol/L; OR 1.85, 95% CI 0.93-3.77; p = 0.08). Multivariate analysis did not reveal significant associations between other electrolyte imbalances and in-hospital mortality in this cohort.
Conclusion: In this retrospective cohort, the presence of anemia, acidosis or hypobicarbonatemia on admission to the resuscitation room were independently associated with an elevated risk of in-hospital mortality in critically ill non-trauma patients. These readily available point-of-care parameters may support early risk stratification. Prospective studies are needed to validate these findings.
背景:在急诊科治疗的危重非创伤患者有很高的院内死亡风险。虽然即时诊断(如血气分析)是紧急管理的既定工具,但关于其在这一特定患者群体中的预后价值的数据仍然有限。本研究旨在评估初始血气参数是否与危重非创伤患者的住院死亡率独立相关。方法:本回顾性队列研究纳入了在德国一所大学医院急诊科接受治疗的成人非创伤重症患者。采用单变量和多变量logistic回归分析初始血气参数和临床数据,以评估其与住院死亡率的关系。结果:879例筛查患者中,542例符合纳入标准。住院死亡率为20% (n = 110)。除了年龄较大和院外心脏骤停,贫血(血红蛋白2.2 mmol/L; OR 1.85, 95% CI 0.93-3.77; p = 0.08)。多变量分析未显示该队列中其他电解质失衡与住院死亡率之间的显著关联。结论:在这一回顾性队列研究中,进入复苏室时出现贫血、酸中毒或低碳酸盐血症与危重症非创伤患者院内死亡风险升高独立相关。这些现成的护理点参数可能支持早期风险分层。需要前瞻性研究来验证这些发现。
{"title":"Prognostic value of early point-of-care blood gas analysis in critically ill non-trauma patients.","authors":"Constantin Maier-Stocker, Rebekka Läng, Jillena Zinsser-Krys, Frank Hanses, Markus Zimmermann, Julian Hupf","doi":"10.1186/s12873-026-01822-2","DOIUrl":"10.1186/s12873-026-01822-2","url":null,"abstract":"<p><strong>Background: </strong>Critically ill non-trauma patients treated in the emergency department have a high risk of in-hospital mortality. While point-of-care diagnostics such as blood gas analysis are established tools for urgent management, data on their prognostic value in this specific patient cohort remain limited. This study aimed to evaluate whether initial blood gas parameters are independently associated with in-hospital mortality in critically ill non-trauma patients.</p><p><strong>Methods: </strong>This retrospective cohort study included adult critically ill non-trauma patients treated in the emergency department of a German university hospital. Initial blood gas parameters and clinical data were analyzed using univariate and multivariable logistic regression to assess their association with in-hospital mortality.</p><p><strong>Results: </strong>Of 879 screened patients, 542 met the inclusion criteria. In-hospital mortality was 20% (n = 110). In addition to older age and out-of-hospital cardiac arrest, anemia (hemoglobin < 12 g/dL; OR of 2.07, 95% CI 1.20-3.58; p = 0.009), acidosis (pH < 7.35; OR 2.26, 95% CI 1.09-4.95; p = 0.033) and hypobicarbonatemia (< 22 mmol/L; OR 2.79, 95% CI 1.42-5.69; p = 0.004) were independently associated with in-hospital mortality. The association for hyperlactatemia was borderline (> 2.2 mmol/L; OR 1.85, 95% CI 0.93-3.77; p = 0.08). Multivariate analysis did not reveal significant associations between other electrolyte imbalances and in-hospital mortality in this cohort.</p><p><strong>Conclusion: </strong>In this retrospective cohort, the presence of anemia, acidosis or hypobicarbonatemia on admission to the resuscitation room were independently associated with an elevated risk of in-hospital mortality in critically ill non-trauma patients. These readily available point-of-care parameters may support early risk stratification. Prospective studies are needed to validate these findings.</p>","PeriodicalId":9002,"journal":{"name":"BMC Emergency Medicine","volume":"26 1","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13689306/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149236762","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-10-20DOI: 10.1186/s12873-026-01818-y
Florian Breuer, Stefan K Beckers, Bastian Brune, Marcel Dudda, Thomas Franke, Rolf Lefering, Andre Nohl
Background: Mass casualty incidents (MCIs) pose substantial challenges to prehospital emergency medical systems due to limited resources and the need for rapid prioritization. Evidence regarding the impact of routine civilian MCIs on the management and outcomes of severely injured patients remains limited. This study aimed to evaluate the influence of MCIs on prehospital care, transport strategies, and clinical outcomes compared with routine individual care.
Methods: Data from the TraumaRegister DGU® were analysed for patients treated in Germany between mid-2020 and 2023. Patients with severe trauma (Maximum Abbreviated Injury Scale; MAIS ≥ 3) were included. Mass casualty incident cases were identified based on registry documentation. A 1:4 matched cohort was performed using age group, injury pattern and traffic involvement as matching criteria. The primary endpoint was in-hospital mortality; secondary endpoints included prehospital time intervals, performed interventions, and transport strategies. An additional multivariable logistic regression was performed as a sensitivity analysis of the primary endpoint.
Results: A total of 65,152 patients were included, of whom 430 were treated during mass casualty incidents (MCIs). After matching, 423 MCI patients were compared with 1,692 controls. Patients treated during MCIs had slightly higher injury severity (Injury Severity Score (ISS) 24.8 vs. 20.3). Median total prehospital time was significantly longer in the MCI group (85 [IQR 67-100] vs. 67 [IQR 53-83] minutes; p < 0.001). Invasive interventions, including prehospital intubation (33.6% vs. 20.9%) and administration of tranexamic acid (32.1% vs. 15.0%) were more frequently performed in the MCI group. Helicopter emergency medical services (HEMS) transport was used more frequently (34.5% vs. 20.7%). In the matched cohort, in-hospital mortality did not differ significantly between groups (13.5% vs. 11.7%; p = 0.317). In an additional multivariable sensitivity analysis, MCI status was not significantly associated with in-hospital mortality (adjusted OR 1.19, 95% CI 0.77-1.85).
Conclusion: Mass casualty incidents (MCIs) were associated with prolonged prehospital care and modified transport strategies. No statistically significant difference in in-hospital mortality was observed between MCI patients and matched controls. These findings describe outcomes among severely injured patients captured by the TraumaRegister DGU® but should be interpreted in light of residual confounding and the observational study design.
背景:由于资源有限和需要快速优先处理,大规模伤亡事件(MCIs)对院前急救医疗系统构成了重大挑战。关于常规民用MCIs对严重受伤患者的管理和预后的影响的证据仍然有限。本研究旨在评估MCIs与常规个体护理相比对院前护理、转运策略和临床结果的影响。方法:分析2020年中期至2023年期间在德国接受治疗的创伤登记DGU®患者的数据。纳入严重创伤患者(最大简略损伤量表;MAIS≥3)。根据登记文件确定大规模伤亡事件病例。以年龄组、损伤类型和交通事故为匹配标准,进行1:4匹配队列。主要终点是住院死亡率;次要终点包括院前时间间隔、实施的干预措施和运输策略。另外进行多变量逻辑回归作为主要终点的敏感性分析。结果:共纳入65,152例患者,其中430例在大规模伤亡事件(MCIs)中接受治疗。匹配后,423名MCI患者与1,692名对照。在MCIs期间接受治疗的患者损伤严重程度略高(损伤严重程度评分(ISS) 24.8比20.3)。MCI组的院前总时间中位数明显更长(85 [IQR 67-100] vs. 67 [IQR 53-83]分钟);p结论:大规模伤亡事件(MCIs)与院前护理时间延长和运输策略改变有关。在MCI患者和匹配的对照组之间,住院死亡率没有统计学上的显著差异。这些发现描述了创伤登记DGU®记录的严重受伤患者的结局,但应根据残留混杂因素和观察性研究设计来解释。
{"title":"Prehospital management and hospital outcomes of severely injured patients during routine civilian mass casualty incidents: a 1:4 matched cohort analysis of the TraumaRegister DGU<sup>®</sup>.","authors":"Florian Breuer, Stefan K Beckers, Bastian Brune, Marcel Dudda, Thomas Franke, Rolf Lefering, Andre Nohl","doi":"10.1186/s12873-026-01818-y","DOIUrl":"10.1186/s12873-026-01818-y","url":null,"abstract":"<p><strong>Background: </strong>Mass casualty incidents (MCIs) pose substantial challenges to prehospital emergency medical systems due to limited resources and the need for rapid prioritization. Evidence regarding the impact of routine civilian MCIs on the management and outcomes of severely injured patients remains limited. This study aimed to evaluate the influence of MCIs on prehospital care, transport strategies, and clinical outcomes compared with routine individual care.</p><p><strong>Methods: </strong>Data from the TraumaRegister DGU<sup>®</sup> were analysed for patients treated in Germany between mid-2020 and 2023. Patients with severe trauma (Maximum Abbreviated Injury Scale; MAIS ≥ 3) were included. Mass casualty incident cases were identified based on registry documentation. A 1:4 matched cohort was performed using age group, injury pattern and traffic involvement as matching criteria. The primary endpoint was in-hospital mortality; secondary endpoints included prehospital time intervals, performed interventions, and transport strategies. An additional multivariable logistic regression was performed as a sensitivity analysis of the primary endpoint.</p><p><strong>Results: </strong>A total of 65,152 patients were included, of whom 430 were treated during mass casualty incidents (MCIs). After matching, 423 MCI patients were compared with 1,692 controls. Patients treated during MCIs had slightly higher injury severity (Injury Severity Score (ISS) 24.8 vs. 20.3). Median total prehospital time was significantly longer in the MCI group (85 [IQR 67-100] vs. 67 [IQR 53-83] minutes; p < 0.001). Invasive interventions, including prehospital intubation (33.6% vs. 20.9%) and administration of tranexamic acid (32.1% vs. 15.0%) were more frequently performed in the MCI group. Helicopter emergency medical services (HEMS) transport was used more frequently (34.5% vs. 20.7%). In the matched cohort, in-hospital mortality did not differ significantly between groups (13.5% vs. 11.7%; p = 0.317). In an additional multivariable sensitivity analysis, MCI status was not significantly associated with in-hospital mortality (adjusted OR 1.19, 95% CI 0.77-1.85).</p><p><strong>Conclusion: </strong>Mass casualty incidents (MCIs) were associated with prolonged prehospital care and modified transport strategies. No statistically significant difference in in-hospital mortality was observed between MCI patients and matched controls. These findings describe outcomes among severely injured patients captured by the TraumaRegister DGU<sup>®</sup> but should be interpreted in light of residual confounding and the observational study design.</p>","PeriodicalId":9002,"journal":{"name":"BMC Emergency Medicine","volume":"26 1","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13689070/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149236749","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-10-20DOI: 10.1186/s12873-026-01821-3
Michael Alfertshofer, Cosima C Hoch, Dirk Nolte, Hans-Günther Machens, Leonard Knoedler, Shady Abu-Sirhan, Siti Rahmayanti, Deise Caldas Kühlman, Jeffrey E Janis, Zachary S Peacock, Steffen Koerdt, Sarina Bucher, Max Heiland, Nicholas Moellhoff, Samuel Knoedler
Background: Head, face, and neck injuries impose a substantial burden for emergency departments (ED); the mechanisms driving them across the life course however remain poorly understood at the population level. Large-scale, integrated analysis spanning anatomical regions, injury mechanisms, age groups, settings, and associated products or environmental surfaces offers an opportunity to identify the patterns and vulnerable populations that smaller or shorter-term studies cannot resolve.
Methods: We queried National Electronic Injury Surveillance System (NEISS) records from 2006 to 2025 for injuries to the head, face, eyes, mouth, neck, or ears. Demographics, anatomical region, injury setting, associated products or environmental surfaces, and ED disposition were extracted, and a rule-based narrative classifier assigned 1 of 17 injury mechanisms from free-text descriptions. Non-routine ED disposition was defined as admission, transfer, observation, or fatality. Analyses were descriptive and based on unweighted NEISS case records.
Results: Among 2,345,287 ED presentations, representing 31.8% of all NEISS-coded visits, the head was most often injured (51.2%), followed by the face (28.2%). Annual volume rose 35.2% (105,727 in 2006 to 142,918 in 2025), driven mainly by head injuries (+ 83.4%). Median age was 14 years and 56.4% of patients were male, but among older adults (≥ 65 years), females predominated (60.6%). Falls were the leading mechanism (53.0% across subcategories). Most patients were treated and discharged (89.4%) and admission rate rose roughly 18-fold from toddlers (1.3%) to older adults (23.3%). Non-routine ED disposition increased with age, and syncope- or medical-related falls had the highest non-routine ED disposition rate (33.9%). The home was the most common injury setting (63.1%). Injury exposures varied by age group, with beds most common in infants, tables in toddlers, sports equipment in children and adolescents, and floors in older adults.
Conclusions: Head, face, and neck injuries represent a large and growing share of NEISS-coded ED presentations, with distinct patterns by age, sex, injury mechanism, setting, and clinical outcome. These findings may assist in the planning of targeted prevention strategies and future research on risk stratification for vulnerable age groups and injury mechanisms.
{"title":"Head, face, and neck injury patterns across the life course: a 20-year NEISS analysis of 2,345,287 emergency department visits in the U.S.","authors":"Michael Alfertshofer, Cosima C Hoch, Dirk Nolte, Hans-Günther Machens, Leonard Knoedler, Shady Abu-Sirhan, Siti Rahmayanti, Deise Caldas Kühlman, Jeffrey E Janis, Zachary S Peacock, Steffen Koerdt, Sarina Bucher, Max Heiland, Nicholas Moellhoff, Samuel Knoedler","doi":"10.1186/s12873-026-01821-3","DOIUrl":"10.1186/s12873-026-01821-3","url":null,"abstract":"<p><strong>Background: </strong>Head, face, and neck injuries impose a substantial burden for emergency departments (ED); the mechanisms driving them across the life course however remain poorly understood at the population level. Large-scale, integrated analysis spanning anatomical regions, injury mechanisms, age groups, settings, and associated products or environmental surfaces offers an opportunity to identify the patterns and vulnerable populations that smaller or shorter-term studies cannot resolve.</p><p><strong>Methods: </strong>We queried National Electronic Injury Surveillance System (NEISS) records from 2006 to 2025 for injuries to the head, face, eyes, mouth, neck, or ears. Demographics, anatomical region, injury setting, associated products or environmental surfaces, and ED disposition were extracted, and a rule-based narrative classifier assigned 1 of 17 injury mechanisms from free-text descriptions. Non-routine ED disposition was defined as admission, transfer, observation, or fatality. Analyses were descriptive and based on unweighted NEISS case records.</p><p><strong>Results: </strong>Among 2,345,287 ED presentations, representing 31.8% of all NEISS-coded visits, the head was most often injured (51.2%), followed by the face (28.2%). Annual volume rose 35.2% (105,727 in 2006 to 142,918 in 2025), driven mainly by head injuries (+ 83.4%). Median age was 14 years and 56.4% of patients were male, but among older adults (≥ 65 years), females predominated (60.6%). Falls were the leading mechanism (53.0% across subcategories). Most patients were treated and discharged (89.4%) and admission rate rose roughly 18-fold from toddlers (1.3%) to older adults (23.3%). Non-routine ED disposition increased with age, and syncope- or medical-related falls had the highest non-routine ED disposition rate (33.9%). The home was the most common injury setting (63.1%). Injury exposures varied by age group, with beds most common in infants, tables in toddlers, sports equipment in children and adolescents, and floors in older adults.</p><p><strong>Conclusions: </strong>Head, face, and neck injuries represent a large and growing share of NEISS-coded ED presentations, with distinct patterns by age, sex, injury mechanism, setting, and clinical outcome. These findings may assist in the planning of targeted prevention strategies and future research on risk stratification for vulnerable age groups and injury mechanisms.</p>","PeriodicalId":9002,"journal":{"name":"BMC Emergency Medicine","volume":"26 1","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13685241/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149227135","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-10-12DOI: 10.1186/s12873-026-01784-5
Raif Kaan Bas, Sumeyye Cakmak
<p><strong>Background: </strong>Emergency department (ED) utilization continues to rise globally, and a disproportionate share of visits is attributable to a small subgroup of patients. This subgroup is referred to throughout the present report by the single term high-frequency users (HFUs), defined as patients with four or more ED visits within a 12-month period. Characterizing the clinical profile, utilization patterns and cost structure of HFUs is relevant to emergency care planning and resource allocation.</p><p><strong>Methods: </strong>This retrospective, single-center observational study analyzed all adult ED presentations at a high-volume urban tertiary hospital over a 12-month period. HFU status was defined at the patient level as four or more ED visits within the study period. The unit of analysis was specified for every comparison: age, sex, the ICD-10 diagnostic spectrum and all logistic regression models were analyzed at the patient level (one observation per unique patient), whereas triage category, timing of presentation, mode of arrival, resource utilization and per-visit costs were analyzed at the visit level. For the regression models, visit attributes and diagnostic categories were aggregated to the patient level as ever/history indicators. Groups were compared using the Mann-Whitney U and Pearson chi-square tests, with effect sizes reported alongside p values.</p><p><strong>Results: </strong>Among 466,884 unique adult patients accounting for 726,696 ED presentations, 26,871 patients (5.8%) were HFUs. HFUs represented 5.8% of adult patients but accounted for 148,322 of 726,696 presentations (20.4%) and approximately one-fifth (21.0%) of cumulative laboratory, imaging and medication costs. Total cost per visit was similar between groups (median 6.39 USD in both; p = 0.647), and differences in individual cost components, although statistically significant, were small in practical terms (rank-biserial correlations +0.03 for laboratory, -0.05 for radiology and +0.08 for medication cost). A higher proportion of HFU than non-HFU presentations involved any laboratory test (29.3% vs 26.7%) and any medication order (57.8% vs 51.4%), whereas any radiologic imaging was less frequent among HFUs (40.5% vs 44.7%). HFUs were marginally younger, presented more often during the night shift and were less likely to arrive by ambulance (3.5% vs 5.0%). Yellow-triage presentations predominated among HFUs, and symptom-based and pain-related diagnoses were over-represented. In the patient-level multivariable model, male sex, a history of yellow- or red-triage presentation, a history of evening- or night-shift presentation and multiple symptom-based diagnostic groups were associated with HFU status, whereas a history of ambulance arrival was associated with lower odds.</p><p><strong>Conclusions: </strong>HFUs constitute a small proportion of adult ED patients but account for a disproportionate share of presentations and of cumulative diagnostic and pha
背景:急诊科(ED)的使用率继续在全球范围内上升,并且不成比例的访问份额可归因于一小部分患者。该亚组在本报告中被称为单术语高频使用者(HFUs),定义为在12个月内就诊4次或以上的患者。表征hfu的临床概况、利用模式和成本结构与急诊护理计划和资源分配有关。方法:这项回顾性、单中心观察性研究分析了一家大型城市三级医院12个月期间的所有成人急诊科病例。在患者层面,HFU状态定义为在研究期间有4次或4次以上ED就诊。为每个比较指定了分析单位:年龄、性别、ICD-10诊断谱和所有逻辑回归模型在患者水平上进行分析(每个独特患者一次观察),而分诊类别、就诊时间、到达方式、资源利用和每次就诊费用在就诊水平上进行分析。对于回归模型,访问属性和诊断类别作为既往/历史指标汇总到患者水平。使用Mann-Whitney U和Pearson卡方检验对各组进行比较,并在p值旁边报告效应量。结果:在726,696例ED表现的466,884例独特成年患者中,26,871例(5.8%)为hfu。hfu占成年患者的5.8%,但在726,696例病例中占148,322例(20.4%),约占累积实验室、成像和药物费用的五分之一(21.0%)。两组间每次就诊的总费用相似(两组的中位数为6.39美元,p = 0.647),个别费用组成部分的差异虽然具有统计学意义,但在实际应用中却很小(实验室的秩双相关为+0.03,放射学为-0.05,药物费用为+0.08)。HFU的比例高于非HFU,包括任何实验室检查(29.3%对26.7%)和任何药物处方(57.8%对51.4%),而HFU中任何放射成像的频率较低(40.5%对44.7%)。hfu患者年龄偏小,更常出现在夜班,不太可能被救护车到达(3.5% vs 5.0%)。黄色分类表现在hfu中占主导地位,基于症状和疼痛相关的诊断被过度代表。在患者水平的多变量模型中,男性、黄色或红色分类表现史、夜班或夜班表现史以及基于多种症状的诊断组与HFU状态相关,而救护车到达史与HFU状态的相关性较低。结论:hfu在成人ED患者中所占比例很小,但在临床表现和累积诊断和药物资源使用中所占比例不成比例。由于两组之间每次就诊的总费用相似,而个别费用组成部分的差异实际上很小,因此主要发现是与重复就诊相关的累积资源负担,而不是个别就诊的较高费用。这种模式与非工作时间访问和症状驱动的呈现相一致;然而,目前的观察数据无法建立这些机制或确定哪些干预措施可以减少ED的频繁使用。
{"title":"Impact of frequent emergency department visits on resource utilization.","authors":"Raif Kaan Bas, Sumeyye Cakmak","doi":"10.1186/s12873-026-01784-5","DOIUrl":"https://doi.org/10.1186/s12873-026-01784-5","url":null,"abstract":"<p><strong>Background: </strong>Emergency department (ED) utilization continues to rise globally, and a disproportionate share of visits is attributable to a small subgroup of patients. This subgroup is referred to throughout the present report by the single term high-frequency users (HFUs), defined as patients with four or more ED visits within a 12-month period. Characterizing the clinical profile, utilization patterns and cost structure of HFUs is relevant to emergency care planning and resource allocation.</p><p><strong>Methods: </strong>This retrospective, single-center observational study analyzed all adult ED presentations at a high-volume urban tertiary hospital over a 12-month period. HFU status was defined at the patient level as four or more ED visits within the study period. The unit of analysis was specified for every comparison: age, sex, the ICD-10 diagnostic spectrum and all logistic regression models were analyzed at the patient level (one observation per unique patient), whereas triage category, timing of presentation, mode of arrival, resource utilization and per-visit costs were analyzed at the visit level. For the regression models, visit attributes and diagnostic categories were aggregated to the patient level as ever/history indicators. Groups were compared using the Mann-Whitney U and Pearson chi-square tests, with effect sizes reported alongside p values.</p><p><strong>Results: </strong>Among 466,884 unique adult patients accounting for 726,696 ED presentations, 26,871 patients (5.8%) were HFUs. HFUs represented 5.8% of adult patients but accounted for 148,322 of 726,696 presentations (20.4%) and approximately one-fifth (21.0%) of cumulative laboratory, imaging and medication costs. Total cost per visit was similar between groups (median 6.39 USD in both; p = 0.647), and differences in individual cost components, although statistically significant, were small in practical terms (rank-biserial correlations +0.03 for laboratory, -0.05 for radiology and +0.08 for medication cost). A higher proportion of HFU than non-HFU presentations involved any laboratory test (29.3% vs 26.7%) and any medication order (57.8% vs 51.4%), whereas any radiologic imaging was less frequent among HFUs (40.5% vs 44.7%). HFUs were marginally younger, presented more often during the night shift and were less likely to arrive by ambulance (3.5% vs 5.0%). Yellow-triage presentations predominated among HFUs, and symptom-based and pain-related diagnoses were over-represented. In the patient-level multivariable model, male sex, a history of yellow- or red-triage presentation, a history of evening- or night-shift presentation and multiple symptom-based diagnostic groups were associated with HFU status, whereas a history of ambulance arrival was associated with lower odds.</p><p><strong>Conclusions: </strong>HFUs constitute a small proportion of adult ED patients but account for a disproportionate share of presentations and of cumulative diagnostic and pha","PeriodicalId":9002,"journal":{"name":"BMC Emergency Medicine","volume":"26 1","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149294135","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-10-06DOI: 10.1186/s12873-026-01785-4
Wilhelm Flatz, Dominik Hinzmann, Philip Kampmann, Leonhard Poehlmann, Paul Reidler, Jenny Schlichtiger, Karl-Georg Kanz, Jeffrey Bazarian, Jens Ricke, Viktoria Bogner-Flatz
Background: Mass gatherings such as the Munich Oktoberfest increase demand on Emergency Medical Services (EMS), particularly for trauma patients requiring imaging. Suspected mild traumatic brain injury (mTBI) often necessitates hospital referral and diagnostic imaging, placing strain on prehospital and hospital resources.
Methods: This retrospective observational before-after study evaluated the impact of an on-site mobile computed tomography (CT) scanner deployed during the Oktoberfest in 2022 and 2023. Patients with suspected head, facial, or cervical spine trauma requiring CT imaging were included. EMS hospital transport data during these events (with mobile CT) were compared with a historical reference period from 2015 to 2019 (without mobile CT) and with matched pre- and post-event periods. Standardized prehospital protocols guided patient assessment and imaging decisions.
Results: A total of 498 patients underwent on-site CT imaging. Of these, 429 (86%) were treated on-site and discharged after imaging and clinical evaluation, while 52 (10%) required hospital transport based on CT findings. Additional transports occurred for unrelated medical issues. On-site CT availability prevented 429 EMS transports, corresponding to an estimated 22,737 min of EMS deployment time. Trauma-related hospital admissions during Oktoberfest were lower in 2022-2023 than in 2015-2019, and the relative increase in admissions during the event was reduced.
Conclusion: This retrospective analysis of the use of a mobile CT scanner in a prehospital setting during a mass gathering found that its implementation was associated with improved patient triage, fewer hospital transports, and more efficient EMS resource utilization. While the retrospective before-after study design does not permit direct causal inference, on-site imaging may have contributed to more targeted patient management and reduced demand on hospital resources. These findings suggest that mobile CT could represent a useful model for supporting medical services at large-scale public events and warrant further prospective evaluation.
{"title":"Impact of on-site mobile CT imaging on prehospital patient management during the Munich Oktoberfest: a retrospective observational before-after study at a mass gathering.","authors":"Wilhelm Flatz, Dominik Hinzmann, Philip Kampmann, Leonhard Poehlmann, Paul Reidler, Jenny Schlichtiger, Karl-Georg Kanz, Jeffrey Bazarian, Jens Ricke, Viktoria Bogner-Flatz","doi":"10.1186/s12873-026-01785-4","DOIUrl":"10.1186/s12873-026-01785-4","url":null,"abstract":"<p><strong>Background: </strong>Mass gatherings such as the Munich Oktoberfest increase demand on Emergency Medical Services (EMS), particularly for trauma patients requiring imaging. Suspected mild traumatic brain injury (mTBI) often necessitates hospital referral and diagnostic imaging, placing strain on prehospital and hospital resources.</p><p><strong>Methods: </strong>This retrospective observational before-after study evaluated the impact of an on-site mobile computed tomography (CT) scanner deployed during the Oktoberfest in 2022 and 2023. Patients with suspected head, facial, or cervical spine trauma requiring CT imaging were included. EMS hospital transport data during these events (with mobile CT) were compared with a historical reference period from 2015 to 2019 (without mobile CT) and with matched pre- and post-event periods. Standardized prehospital protocols guided patient assessment and imaging decisions.</p><p><strong>Results: </strong>A total of 498 patients underwent on-site CT imaging. Of these, 429 (86%) were treated on-site and discharged after imaging and clinical evaluation, while 52 (10%) required hospital transport based on CT findings. Additional transports occurred for unrelated medical issues. On-site CT availability prevented 429 EMS transports, corresponding to an estimated 22,737 min of EMS deployment time. Trauma-related hospital admissions during Oktoberfest were lower in 2022-2023 than in 2015-2019, and the relative increase in admissions during the event was reduced.</p><p><strong>Conclusion: </strong>This retrospective analysis of the use of a mobile CT scanner in a prehospital setting during a mass gathering found that its implementation was associated with improved patient triage, fewer hospital transports, and more efficient EMS resource utilization. While the retrospective before-after study design does not permit direct causal inference, on-site imaging may have contributed to more targeted patient management and reduced demand on hospital resources. These findings suggest that mobile CT could represent a useful model for supporting medical services at large-scale public events and warrant further prospective evaluation.</p>","PeriodicalId":9002,"journal":{"name":"BMC Emergency Medicine","volume":"26 1","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13644297/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149126812","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Although continuous noradrenaline infusion (CNI) is standard vasopressor therapy during the initial resuscitation of patients with septic shock, hemodynamic stabilization may not be immediate. Push-dose noradrenaline (PDNA) has been proposed as a temporary measure while CNI is being established. However, its clinical use, dosing, early hemodynamic response, and short-term safety in the emergency department (ED) are not well described.
Methods: To address this gap, we conducted a single-center retrospective descriptive study at a tertiary care hospital in Japan in 2019. Adults with Sepsis-3 septic shock who received PDNA in the ED and were admitted to the intensive care unit were included. We assessed the context and dosing of PDNA administration, CNI use, mean arterial pressure (MAP) within 15 min after PDNA administration, and adverse events.
Results: Of 91 patients with septic shock, 50 (55%) received PDNA. PDNA was administered at CNI initiation in 25 patients, during CNI dose escalation in 6, and as rescue administration before CNI initiation in 19. The median (interquartile range [IQR]) initial PDNA dose was 20 (20-30) µg. During the 15-minute observation window, 32 (64%) patients received one bolus, 14 (28%) received two, 3 (6%) received three, and 1 (2%) received four. The directly observed median (IQR) MAP was 52 (44-61) mmHg at initial PDNA administration (n = 30) and 62 (50-68) mmHg 1 min later (n = 25). One of 36 patients evaluable for prespecified physiological adverse events experienced an adverse event; however, no serious adverse events were documented.
Conclusions: In this single-center retrospective descriptive study, PDNA was most commonly administered at CNI initiation, and administration was followed by an early increase in median MAP. However, the noncomparative design and concurrent resuscitative interventions preclude attribution of this change solely to PDNA administration. No serious adverse events were documented; however, safety assessment was limited owing to missing data and retrospective ascertainment. These findings do not establish the effectiveness or safety of PDNA. Prospective comparative studies with standardized monitoring are required.
{"title":"Early hemodynamic changes after the use of push-dose noradrenaline in patients presenting to the emergency department with septic shock: a descriptive study.","authors":"Atsushi Yamamoto, Tomoyuki Akita, Aya Sugiyama, Sayaka Nakahara, Yuhei Urakami, Soichiro Mae, Tetsunori Ikegami, Junko Tanaka","doi":"10.1186/s12873-026-01773-8","DOIUrl":"10.1186/s12873-026-01773-8","url":null,"abstract":"<p><strong>Background: </strong>Although continuous noradrenaline infusion (CNI) is standard vasopressor therapy during the initial resuscitation of patients with septic shock, hemodynamic stabilization may not be immediate. Push-dose noradrenaline (PDNA) has been proposed as a temporary measure while CNI is being established. However, its clinical use, dosing, early hemodynamic response, and short-term safety in the emergency department (ED) are not well described.</p><p><strong>Methods: </strong>To address this gap, we conducted a single-center retrospective descriptive study at a tertiary care hospital in Japan in 2019. Adults with Sepsis-3 septic shock who received PDNA in the ED and were admitted to the intensive care unit were included. We assessed the context and dosing of PDNA administration, CNI use, mean arterial pressure (MAP) within 15 min after PDNA administration, and adverse events.</p><p><strong>Results: </strong>Of 91 patients with septic shock, 50 (55%) received PDNA. PDNA was administered at CNI initiation in 25 patients, during CNI dose escalation in 6, and as rescue administration before CNI initiation in 19. The median (interquartile range [IQR]) initial PDNA dose was 20 (20-30) µg. During the 15-minute observation window, 32 (64%) patients received one bolus, 14 (28%) received two, 3 (6%) received three, and 1 (2%) received four. The directly observed median (IQR) MAP was 52 (44-61) mmHg at initial PDNA administration (n = 30) and 62 (50-68) mmHg 1 min later (n = 25). One of 36 patients evaluable for prespecified physiological adverse events experienced an adverse event; however, no serious adverse events were documented.</p><p><strong>Conclusions: </strong>In this single-center retrospective descriptive study, PDNA was most commonly administered at CNI initiation, and administration was followed by an early increase in median MAP. However, the noncomparative design and concurrent resuscitative interventions preclude attribution of this change solely to PDNA administration. No serious adverse events were documented; however, safety assessment was limited owing to missing data and retrospective ascertainment. These findings do not establish the effectiveness or safety of PDNA. Prospective comparative studies with standardized monitoring are required.</p>","PeriodicalId":9002,"journal":{"name":"BMC Emergency Medicine","volume":"26 1","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13685283/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149227061","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-09-11DOI: 10.1186/s12873-026-01766-7
Eva Mishuris, Alexander Wallraff, Rüdger Kopp, Jan Larmann, Lasse J Strudthoff, Christian Bleilevens, Patrick Winnersbach
Background: Extracorporeal cardiopulmonary resuscitation (ECPR) is a time-critical intervention for selected patients with refractory cardiac arrest. Survival depends on minimizing low-flow duration before ECPR initiation. Timely deployment requires organizational preparedness, trained personnel, and rapid extracorporeal membrane oxygenation (ECMO) circuit readiness. However, data on ECPR organization in centers operating without dedicated perfusionist support are limited.
Methods: A nationwide cross-sectional online survey was conducted among German ECMO centers operating without perfusionist support. The questionnaire assessed circuit readiness, responsible personnel, training frequency, and the availability of standard operating procedures (SOPs).
Results: Responses from 42 centers were evaluated, of which 64% reported performing ECPR (n = 27). Most centers (90%, n = 38) had low annual ECMO volumes (< 50 cases). ECMO use was largely limited to the Cardiohelp and iLA activve/Xenios Console systems. Setup times were significantly shorter for ECPR than for non-ECPR ECMO: median 15 min (IQR 12-18; range 5-30) versus 30 min (IQR 20-40; range 15-105) (Mann-Whitney U = 46, p < 0.0001; Cliff's delta = 0.77; 95% CI 0.54-0.94). Nurses were more frequently involved in ECMO deployment in ECPR than in non-ECPR settings (59% (16/27 centers) vs. 20% (3/15 centers)). Within ECPR programs, regular training was reported more frequently for nurses than for physicians (87.5% (14/16 centers) vs. 60% (6/10 centers)). Overall, 76% (n = 32) of centers reported regular training (at least annually) for responsible personnel, 86% (n = 36) had internal SOPs in place, and 69% (n = 29) expressed the need for a universally applicable evidence-based SOP. All centers that reported a pre-defined maximum storage duration (n = 28) adhered to the Extracorporeal Life Support Organization guidelines regarding maximum storage duration of pre-assembled ECMO systems (30 days).
Conclusions: German ECMO centers without perfusionist support reported substantial heterogeneity in ECPR readiness and operational workflows. ECPR-performing centers were associated with shorter setup times and more frequently reported interdisciplinary team structures and recurrent team training. These findings describe current organizational practices and perceived needs and support the value of interdisciplinary teamwork, structured training, and standardized protocols as organizational components that may facilitate timely, standardized ECPR deployment.
{"title":"ECPR readiness without perfusionist support: a cross-sectional national survey on circuit preparation, team structure, and training.","authors":"Eva Mishuris, Alexander Wallraff, Rüdger Kopp, Jan Larmann, Lasse J Strudthoff, Christian Bleilevens, Patrick Winnersbach","doi":"10.1186/s12873-026-01766-7","DOIUrl":"10.1186/s12873-026-01766-7","url":null,"abstract":"<p><strong>Background: </strong>Extracorporeal cardiopulmonary resuscitation (ECPR) is a time-critical intervention for selected patients with refractory cardiac arrest. Survival depends on minimizing low-flow duration before ECPR initiation. Timely deployment requires organizational preparedness, trained personnel, and rapid extracorporeal membrane oxygenation (ECMO) circuit readiness. However, data on ECPR organization in centers operating without dedicated perfusionist support are limited.</p><p><strong>Methods: </strong>A nationwide cross-sectional online survey was conducted among German ECMO centers operating without perfusionist support. The questionnaire assessed circuit readiness, responsible personnel, training frequency, and the availability of standard operating procedures (SOPs).</p><p><strong>Results: </strong>Responses from 42 centers were evaluated, of which 64% reported performing ECPR (n = 27). Most centers (90%, n = 38) had low annual ECMO volumes (< 50 cases). ECMO use was largely limited to the Cardiohelp and iLA activve/Xenios Console systems. Setup times were significantly shorter for ECPR than for non-ECPR ECMO: median 15 min (IQR 12-18; range 5-30) versus 30 min (IQR 20-40; range 15-105) (Mann-Whitney U = 46, p < 0.0001; Cliff's delta = 0.77; 95% CI 0.54-0.94). Nurses were more frequently involved in ECMO deployment in ECPR than in non-ECPR settings (59% (16/27 centers) vs. 20% (3/15 centers)). Within ECPR programs, regular training was reported more frequently for nurses than for physicians (87.5% (14/16 centers) vs. 60% (6/10 centers)). Overall, 76% (n = 32) of centers reported regular training (at least annually) for responsible personnel, 86% (n = 36) had internal SOPs in place, and 69% (n = 29) expressed the need for a universally applicable evidence-based SOP. All centers that reported a pre-defined maximum storage duration (n = 28) adhered to the Extracorporeal Life Support Organization guidelines regarding maximum storage duration of pre-assembled ECMO systems (30 days).</p><p><strong>Conclusions: </strong>German ECMO centers without perfusionist support reported substantial heterogeneity in ECPR readiness and operational workflows. ECPR-performing centers were associated with shorter setup times and more frequently reported interdisciplinary team structures and recurrent team training. These findings describe current organizational practices and perceived needs and support the value of interdisciplinary teamwork, structured training, and standardized protocols as organizational components that may facilitate timely, standardized ECPR deployment.</p>","PeriodicalId":9002,"journal":{"name":"BMC Emergency Medicine","volume":"26 1","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13587460/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148988012","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-09-07DOI: 10.1186/s12873-026-01764-9
Muhammed Emin Zora, Ömer Sert
<p><strong>Background: </strong>The Fibrosis-4 (FIB-4) index combines age, aminotransferase levels, and platelet count. Although developed for chronic liver fibrosis, its components may reflect acute hepatic and systemic injury after cardiac arrest. The primary aim of this study was to characterize early changes in FIB-4 from admission to an approximately 72-hour repeat assessment after out-of-hospital cardiac arrest (OHCA). Secondarily, we evaluated the association of FIB-4 values with 28-day mortality and whether repeat measurement provided additional prognostic information.</p><p><strong>Methods: </strong>This single-center retrospective cohort study included adults admitted to the intensive care unit after sustained return of spontaneous circulation between May 1, 2023, and May 1, 2026. After a record-level eligibility audit, 188 patients were included; 28-day vital status was available for 182. FIB-4 was calculated from the first laboratory set obtained at intensive care unit admission and from the complete laboratory set closest to 72 h after the admission laboratory sample within a 48-96-hour window. The primary analysis assessed paired change in FIB-4. Secondary analyses examined the association of admission FIB-4 with 28-day mortality and, using a 72-hour landmark approach, the association of repeat FIB-4 with subsequent mortality through day 28 and its incremental contribution beyond the admission value.</p><p><strong>Results: </strong>A valid repeat FIB-4 measurement was available in 122 patients. In paired analysis, median FIB-4 decreased from 5.21 at admission to 3.16 at approximately 72 h (p < 0.001). Of the 182 patients with known 28-day vital status, 82 died (45.1%). Admission FIB-4 was higher in patients who died than in survivors (6.84 [3.25-10.75] vs. 4.14 [2.32-8.16]; p = 0.019). Each doubling of admission FIB-4 was associated with higher odds of mortality in the unadjusted analysis (OR, 1.26; 95% CI, 1.02-1.55; p = 0.029); however, in the OHCA-specific complete-case model, the adjusted association was not statistically significant (OR, 1.16; 95% CI, 0.91-1.46; p = 0.227), and adding FIB-4 to the clinical model increased the AUC only from 0.647 to 0.648 (difference, 0.001). In the 72-hour landmark cohort, 56 patients had an available pre-landmark repeat measurement and known 28-day vital status; 29 died after the landmark. Repeat FIB-4 showed weak discrimination for subsequent mortality (AUC, 0.585), and the OR per doubling was 1.23 (95% CI, 0.86-1.76; p = 0.255). Adding repeat FIB-4 to the admission value increased the AUC from 0.575 to 0.581 (difference, 0.006; 95% CI, - 0.053 to 0.205; likelihood-ratio p = 0.294).</p><p><strong>Conclusions: </strong>Among patients with available paired measurements, FIB-4 decreased from admission to the approximately 72-hour repeat assessment; however, the magnitude of change showed little discriminatory ability for subsequent mortality in the landmark cohort. Higher admission FIB-4 was ass
{"title":"Early serial changes in FIB-4 after out-of-hospital cardiac arrest and short-term clinical outcomes: a retrospective cohort study.","authors":"Muhammed Emin Zora, Ömer Sert","doi":"10.1186/s12873-026-01764-9","DOIUrl":"10.1186/s12873-026-01764-9","url":null,"abstract":"<p><strong>Background: </strong>The Fibrosis-4 (FIB-4) index combines age, aminotransferase levels, and platelet count. Although developed for chronic liver fibrosis, its components may reflect acute hepatic and systemic injury after cardiac arrest. The primary aim of this study was to characterize early changes in FIB-4 from admission to an approximately 72-hour repeat assessment after out-of-hospital cardiac arrest (OHCA). Secondarily, we evaluated the association of FIB-4 values with 28-day mortality and whether repeat measurement provided additional prognostic information.</p><p><strong>Methods: </strong>This single-center retrospective cohort study included adults admitted to the intensive care unit after sustained return of spontaneous circulation between May 1, 2023, and May 1, 2026. After a record-level eligibility audit, 188 patients were included; 28-day vital status was available for 182. FIB-4 was calculated from the first laboratory set obtained at intensive care unit admission and from the complete laboratory set closest to 72 h after the admission laboratory sample within a 48-96-hour window. The primary analysis assessed paired change in FIB-4. Secondary analyses examined the association of admission FIB-4 with 28-day mortality and, using a 72-hour landmark approach, the association of repeat FIB-4 with subsequent mortality through day 28 and its incremental contribution beyond the admission value.</p><p><strong>Results: </strong>A valid repeat FIB-4 measurement was available in 122 patients. In paired analysis, median FIB-4 decreased from 5.21 at admission to 3.16 at approximately 72 h (p < 0.001). Of the 182 patients with known 28-day vital status, 82 died (45.1%). Admission FIB-4 was higher in patients who died than in survivors (6.84 [3.25-10.75] vs. 4.14 [2.32-8.16]; p = 0.019). Each doubling of admission FIB-4 was associated with higher odds of mortality in the unadjusted analysis (OR, 1.26; 95% CI, 1.02-1.55; p = 0.029); however, in the OHCA-specific complete-case model, the adjusted association was not statistically significant (OR, 1.16; 95% CI, 0.91-1.46; p = 0.227), and adding FIB-4 to the clinical model increased the AUC only from 0.647 to 0.648 (difference, 0.001). In the 72-hour landmark cohort, 56 patients had an available pre-landmark repeat measurement and known 28-day vital status; 29 died after the landmark. Repeat FIB-4 showed weak discrimination for subsequent mortality (AUC, 0.585), and the OR per doubling was 1.23 (95% CI, 0.86-1.76; p = 0.255). Adding repeat FIB-4 to the admission value increased the AUC from 0.575 to 0.581 (difference, 0.006; 95% CI, - 0.053 to 0.205; likelihood-ratio p = 0.294).</p><p><strong>Conclusions: </strong>Among patients with available paired measurements, FIB-4 decreased from admission to the approximately 72-hour repeat assessment; however, the magnitude of change showed little discriminatory ability for subsequent mortality in the landmark cohort. Higher admission FIB-4 was ass","PeriodicalId":9002,"journal":{"name":"BMC Emergency Medicine","volume":"26 1","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13673793/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"149191317","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: The 2021 European Society of Cardiology (ESC) guidelines classify acute heart failure (AHF) into four phenotypes: acute decompensated heart failure (ADHF), acute pulmonary oedema (APO), isolated right ventricular failure (IRVF), and cardiogenic shock (CS). However, differences in clinical characteristics and long-term outcomes among these phenotypes in the emergency department (ED) remain unclear. This study aimed to evaluate their characteristics and prognostic implications in the ED setting.
Methods: In this prospective-retrospective observational real-world study, adults presenting with AHF in the ED were consecutively enrolled and categorized according to ESC-defined phenotypes. The study endpoints were 1-year all-cause and cardiovascular mortality. Associations between phenotypes and mortality were assessed using Cox regression models with progressive adjustment.
Results: A total of 2,960 patients were included. Clinical characteristics and treatment patterns differed substantially across phenotypes. The 1-year all-cause mortality rates were 10.3% in ADHF, 11.0% in APO, 24.5% in IRVF, and 58.7% in CS (P < 0.001). In multivariable Cox analyses adjusting for clinical variables and treatments, IRVF remained independently associated with increased risks of all-cause mortality (HR 1.92, 95% CI 1.02-3.63; P = 0.044) and cardiovascular mortality (HR 2.22, 95% CI 1.10-4.48; P = 0.027). CS was also independently associated with higher risks of all-cause mortality (HR 2.22, 95% CI 1.34-3.67; P = 0.002) and cardiovascular mortality (HR 2.71, 95% CI 1.57-4.66; P < 0.001).
Conclusions: In this ED-based AHF cohort, IRVF and CS were independently associated with worse 1-year outcomes, supporting phenotype-based risk stratification in the ED.
{"title":"Clinical characteristics and prognostic differences among acute heart failure phenotypes in the emergency department: a real-world study.","authors":"Hanyang Liang, Yimeng Wang, Yijing Xin, Yulong Li, Chujie Zhang, Yanmin Yang","doi":"10.1186/s12873-026-01628-2","DOIUrl":"10.1186/s12873-026-01628-2","url":null,"abstract":"<p><strong>Background: </strong>The 2021 European Society of Cardiology (ESC) guidelines classify acute heart failure (AHF) into four phenotypes: acute decompensated heart failure (ADHF), acute pulmonary oedema (APO), isolated right ventricular failure (IRVF), and cardiogenic shock (CS). However, differences in clinical characteristics and long-term outcomes among these phenotypes in the emergency department (ED) remain unclear. This study aimed to evaluate their characteristics and prognostic implications in the ED setting.</p><p><strong>Methods: </strong>In this prospective-retrospective observational real-world study, adults presenting with AHF in the ED were consecutively enrolled and categorized according to ESC-defined phenotypes. The study endpoints were 1-year all-cause and cardiovascular mortality. Associations between phenotypes and mortality were assessed using Cox regression models with progressive adjustment.</p><p><strong>Results: </strong>A total of 2,960 patients were included. Clinical characteristics and treatment patterns differed substantially across phenotypes. The 1-year all-cause mortality rates were 10.3% in ADHF, 11.0% in APO, 24.5% in IRVF, and 58.7% in CS (P < 0.001). In multivariable Cox analyses adjusting for clinical variables and treatments, IRVF remained independently associated with increased risks of all-cause mortality (HR 1.92, 95% CI 1.02-3.63; P = 0.044) and cardiovascular mortality (HR 2.22, 95% CI 1.10-4.48; P = 0.027). CS was also independently associated with higher risks of all-cause mortality (HR 2.22, 95% CI 1.34-3.67; P = 0.002) and cardiovascular mortality (HR 2.71, 95% CI 1.57-4.66; P < 0.001).</p><p><strong>Conclusions: </strong>In this ED-based AHF cohort, IRVF and CS were independently associated with worse 1-year outcomes, supporting phenotype-based risk stratification in the ED.</p>","PeriodicalId":9002,"journal":{"name":"BMC Emergency Medicine","volume":"26 1","pages":""},"PeriodicalIF":3.1,"publicationDate":"2026-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13536624/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"148872951","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}