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Global emergency medicine research priorities: a mapping review. 全球急诊医学研究重点:绘图审查。
IF 3.1 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-09-16 DOI: 10.1097/MEJ.0000000000001182
Erin Kim, Prashant Mahajan, Chris Barousse, Vijaya A Kumar, Shu-Ling Chong, Apoorva Belle, Dominik Roth

Recognizing and prioritizing research areas in emergency care is crucial for generating evidence and advancing research programs, aiming to enhance health outcomes for both individuals and populations. The objective of this review is to document global clinical and nonclinical research priorities. The Emergency Medicine Education and Research by Global Experts network, consisting of 22 sites across six continents, conducted a mapping review of publications on emergency medicine research priorities (2000-2022) across seven databases. We included studies with replicable methodologies for determining research priorities, excluding those limited to individual diseases. Three reviewers independently screened, selected, and categorized results into clinical and nonclinical topics. Discrepancies were resolved by an independent investigator and consensus. Outcomes measures and analysis include descriptive analysis of research priorities grouped into clinical and nonclinical topics, characteristics of publications including countries represented in the author list, target audience (such as researchers or policy makers), participants (e.g. patients), and methods (e.g. Delphi) of priority setting. Among 968 screened papers, 57 publications from all WHO regions were included. Most (36, 63%) had authors from only a single country, primarily in North America and Europe. Patient representatives were included in only 10 (18%). Clinical research priorities clustered into resuscitation, cardiology, central nervous system, emergency medical services, infectious disease, mental health, respiratory disease, and trauma. Distribution was broad in North America and Europe but focused on infectious diseases and resuscitation in Africa and Asia. Eleven nonclinical topics included access to care, health policy, screening/triage, social determinants of health, staffing, technology/simulation, shared decision making, cross-sectoral collaboration, education, patient-centered care, and research networks. Nonclinical topics were broad in Europe and America, focused on access to care and health screening in Africa, and mostly absent in other WHO regions. Published research priorities in emergency medicine are heterogeneous and geographically limited, mostly containing groups of authors from the same country. The majority of publications in global research priority setting stem from Western countries, covering a broad spectrum of clinical and nonclinical topics. Research priorities from Africa and Asia tend to focus on specific issues more prevalent in those regions of the world.

确认急诊护理研究领域并确定其优先次序,对于提供证据和推进研究计划至关重要,其目的是提高个人和群体的健康水平。本综述旨在记录全球临床和非临床研究的优先事项。全球专家急诊医学教育与研究网络由横跨六大洲的 22 个站点组成,该网络对七个数据库中有关急诊医学研究重点的出版物(2000-2022 年)进行了绘图审查。我们纳入了采用可复制方法确定研究重点的研究,但不包括仅限于个别疾病的研究。三位审稿人分别独立筛选、选择研究成果,并将其归类为临床和非临床主题。不一致之处由一名独立研究人员解决并达成共识。结果测量和分析包括对临床和非临床主题研究重点的描述性分析、出版物的特点(包括作者名单中的国家代表)、目标受众(如研究人员或政策制定者)、参与者(如患者)以及确定重点的方法(如德尔菲法)。在经过筛选的 968 篇论文中,有 57 篇来自世界卫生组织所有地区。大多数论文(36 篇,占 63%)的作者只来自一个国家,主要是北美和欧洲。仅有 10 篇(18%)包含了患者代表。临床研究重点集中在复苏、心脏病学、中枢神经系统、紧急医疗服务、传染病、心理健康、呼吸系统疾病和创伤。在北美和欧洲分布广泛,但在非洲和亚洲则主要集中在传染病和复苏方面。11 个非临床主题包括:获得护理、卫生政策、筛查/分流、健康的社会决定因素、人员配置、技术/模拟、共同决策、跨部门合作、教育、以患者为中心的护理和研究网络。在欧洲和美洲,非临床主题非常广泛,在非洲则侧重于获得医疗服务和健康筛查,而在世界卫生组织的其他地区则大多没有。已发表的急诊医学优先研究课题各不相同,且受地域限制,大多由来自同一国家的作者共同完成。在确定全球研究重点方面,大多数出版物都来自西方国家,涵盖临床和非临床课题的广泛领域。非洲和亚洲的研究重点往往集中在这些地区更为普遍的特定问题上。
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引用次数: 0
Laryngeal mask vs. laryngeal tube trial in paediatric patients (LaMaTuPe): a single-blinded, open-label, randomised-controlled trial. 儿科患者喉罩与喉管试验(LaMaTuPe):单盲、开放标签、随机对照试验。
IF 4.4 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-09-12 DOI: 10.1097/mej.0000000000001178
Stephan Katzenschlager,Stefan Mohr,Nikolai Kaltschmidt,Franziska Peterstorfer,Frank Weilbacher,Patrick Günther,Markus Ries,Markus A Weigand,Erik Popp
BACKGROUNDIn hypoxemic children with difficult airway, or for minor elective procedures, the use of a supraglottic airway device may be preferred to endotracheal intubation, whether with a laryngeal mask or laryngeal tube. Second-generation laryngeal masks may offer a better safety profile. Whether they should be preferred to laryngeal tubes is unknown. This study aimed to compare the efficacy and safety of second-generation laryngeal masks and laryngeal tubes in children.METHODSThis randomised-controlled trial was conducted in a single university hospital in children <18 years undergoing elective anaesthesia in urology, minor paediatric surgery and gynaecology. Patients were 1 : 1 randomised to the laryngeal mask or laryngeal tube group. Children were allocated a second-generation laryngeal tube or a second-generation laryngeal mask as the primary airway device. The primary endpoint was insertion time. Secondary endpoints included first-attempt success, overall success and complications, which included hypoxia (SpO2 < 90%), laryngospasm, bronchospasm, aspiration and bleeding.RESULTSIn total, 135 patients were randomised, with 61 allocated to the laryngeal tube and 74 to the laryngeal mask group, with a median age of 5.4 and 4.9 years, respectively. Median insertion time was significantly longer in the laryngeal tube group (37 vs. 31 s; difference of medians: 6.0 s; 95% confidence interval: 0.0-13.0). The laryngeal tube had a significantly lower first-attempt (41.0%) and overall success rate (45.9%) than the laryngeal mask (90.5% and 97.3%, respectively). Those allocated to the laryngeal tube group had a higher ratio of complications (27.8%) compared to the laryngeal mask group (2.7%).CONCLUSIONThis randomised-controlled trial reported that in children undergoing elective anaesthesia, the use of a laryngeal tube was associated with a longer insertion time.
背景在低氧血症儿童气道困难或进行小型择期手术时,使用声门上气道装置可能优于气管插管,无论是使用喉罩还是喉管。第二代喉罩可能具有更好的安全性。至于喉罩是否优于喉管还不得而知。这项研究旨在比较第二代喉罩和喉管在儿童中的有效性和安全性。方法这项随机对照试验在一家大学医院进行,对象是接受泌尿科、儿科小手术和妇科择期麻醉的 18 岁以下儿童。患者以 1 :1 的比例随机分配到喉罩组或喉管组。患儿被分配使用第二代喉管或第二代喉罩作为主要气道装置。主要终点是插入时间。次要终点包括首次尝试成功率、总体成功率和并发症,其中并发症包括缺氧(SpO2 < 90%)、喉痉挛、支气管痉挛、吸入和出血。结果共有 135 名患者接受了随机治疗,其中 61 人被分配到喉管组,74 人被分配到喉罩组,中位年龄分别为 5.4 岁和 4.9 岁。喉管组的中位插入时间明显更长(37 秒对 31 秒;中位数差异:6.0 秒;95% 置信区间:0.0-13.0)。喉管首次尝试成功率(41.0%)和总体成功率(45.9%)明显低于喉罩(分别为 90.5% 和 97.3%)。与喉罩组相比,喉管组的并发症发生率(27.8%)更高(2.7%)。
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引用次数: 0
Biomarkers of COVID-19 short-term worsening: a multiparameter analysis within the prospective multicenter COVIDeF cohort. COVID-19 短期恶化的生物标志物:前瞻性多中心 COVIDeF 队列中的多参数分析。
IF 4.4 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-09-12 DOI: 10.1097/mej.0000000000001175
Marta Cancella de Abreu,Jacques Ropers,Nathalie Oueidat,Laurence Pieroni,Corinne Frère,Michaela Fontenay,Krystel Torelino,Anthony Chauvin,Guillaume Hekimian,Anne-Geneviève Marcelin,Beatrice Parfait,Florence Tubach,Pierre Hausfater,
BACKGROUNDDuring a pandemic like COVID-19, hospital resources are constrained and accurate severity triage of the patients is required.OBJECTIVEThe objective of this study is to estimate the predictive performances of candidate biomarkers for short-term worsening (STW) of COVID-19.DESIGNProspective, multicenter (20 hospitals in Paris) cohort study of consecutive COVID-19 patients with systematic biobanking at admission, during the first waves of COVID-19 in France in 2020 (COVIDeF cohort).SETTING AND PARTICIPANTSConsecutive COVID-19 patients were screened for inclusion. They were excluded in presence of severity criteria defined by either an ICU admission, mechanical ventilation (including noninvasive ventilation), acute respiratory distress, or in-hospital death before sampling. Routine blood tests measured during usual care and centralized systematic measurement of creatine kinase, C-reactive protein (CRP), procalcitonin, soluble urokinase plasminogen activator receptor (suPAR), high-sensitive troponin T (TnT-hs), N terminal pro-B natriuretic peptide (NT-proBNP), calprotectin, platelet factor 4, mid-regional pro-adrenomedullin (MR-proADM), and proendothelin were performed.OUTCOME MEASURES AND ANALYSESThe primary outcome was STW, defined by a severity criteria within 7 days. A backward stepwise logistic regression model and a 'best subset' approach were used to identify independent association, and the area under the receiving operator characteristics (AUROC) was computed.RESULTSFive hundred and eleven patients were analyzed, of whom 60 (11.7%) experienced STW. Median time to occurrence of a severity criteria was 3 days. At admission, lower values of eosinophils, lymphocytes, platelets, alanine aminotransferase, and higher values of neutrophils, creatinine, urea, CRP, TnT-hs, suPAR, NT-proBNP, calprotectin, procalcitonin, MR-proADM, and proendothelin were predictive of worsening. Stepwise logistic regression identified three biomarkers significantly associated with worsening: CRP [adjusted odds ratio (aOR): 1.10, 95% confidence interval (95% CI): 1.06-1.15 for a 10-unit increase, AUROC: 0.73 (0.66-0.79)], procalcitonin [aOR: 0.42, 95% CI: 0.22-0.81, AUROC: 0.69 (0.64-0.88)], and MR-proADM [aOR: 2.85, 95% CI: 1.74-4.69, AUROC: 0.75 (0.69-0.81)]. These biomarkers outperformed clinical variables except diabetes and cancer comorbidities.CONCLUSIONIn this multicenter prospective study that assessed a large panel of biomarkers for COVID-19 patients, CRP, procalcitonin, and MR-proADM were independently associated with the risk of STW.TRIAL REGISTRATIONClinicalTrials.gov NCT04352348.
背景在像 COVID-19 这样的大流行期间,医院资源有限,需要对患者进行准确的严重程度分流。目的本研究的目的是评估 COVID-19 短期恶化 (STW) 候选生物标志物的预测性能。设计在 2020 年法国 COVID-19 第一波(COVIDeF 队列)期间,对连续 COVID-19 患者进行入院时系统性生物库收集的前瞻性、多中心(巴黎 20 家医院)队列研究。如果存在严重程度标准,即采样前入住 ICU、机械通气(包括无创通气)、急性呼吸窘迫或院内死亡,则排除这些患者。在常规护理期间进行常规血液检测,并对肌酸激酶、C反应蛋白(CRP)、降钙素原、可溶性尿激酶纤溶酶原激活物受体(suPAR)、高敏肌钙蛋白T(TnT-hs)、N末端前B钠尿肽(NT-proBNP)、calprotectin、血小板因子4、中区域前肾上腺髓质素(MR-proADM)和前内皮素进行集中系统检测。结果测量和分析:主要结果是 STW,以 7 天内的严重程度标准定义。采用后向逐步逻辑回归模型和 "最佳子集 "方法确定独立关联,并计算接受操作者特征下面积(AUROC)。出现严重程度标准的中位时间为 3 天。入院时,嗜酸性粒细胞、淋巴细胞、血小板、丙氨酸氨基转移酶的数值较低,而中性粒细胞、肌酐、尿素、CRP、TnT-hs、suPAR、NT-proBNP、钙蛋白、降钙素原、MR-proADM 和前皮质素的数值较高,这些都是预测病情恶化的指标。逐步逻辑回归确定了三种与病情恶化显著相关的生物标志物:CRP [调整后的几率比(aOR):1.10,95% 置信区间(95% CI):1.06-1.15(增加 10 个单位),AUROC:0.73(0.66-0.79)]、降钙素原[aOR:0.42,95% CI:0.22-0.81,AUROC:0.69(0.64-0.88)]和 MR-proADM [aOR:2.85,95% CI:1.74-4.69,AUROC:0.75(0.69-0.81)]。结论在这项多中心前瞻性研究中,CRP、降钙素原和MR-proADM与STW风险独立相关,该研究评估了COVID-19患者的大量生物标志物。
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引用次数: 0
Videodistraction to reduce agitation in elderly patients in the emergency department: an open label parallel group randomized controlled trial. 通过视频牵引减少急诊科老年患者的躁动:一项开放标签平行分组随机对照试验。
IF 4.4 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-09-12 DOI: 10.1097/mej.0000000000001179
Enver Güvec,Uwe Koedel,Sophia Horster,Vera Pedersen,Stefanie Völk,Michaela Waldow,Florian Weber,Matthias Klein
BACKGROUND AND IMPORTANCEAgitation of elderly patients in the emergency department (ED) often complicates workup and therapy.OBJECTIVEIn this study, we investigated if agitation in the ED can be reduced by showing calming video sequences in elderly agitated patients.DESIGNSProspective randomized intervention study.SETTINGS AND PARTICIPANTSED patients aged ≥65 years were screened for the risk of agitation/delirium using the 4-A's test (4-AT) test. In case of ≥4 4-AT points, patients were scored using the Richmond Agitation-Sedation Scale (RASS) and the Nursing Delirium Screening Scale (Nu-DESC). They were included in the study if RASS was ≥+2 and Nu-DESC ≥ 4 after informed consent of the legal representative. Patients were then randomized to the intervention or control group. A total of n = 57 patients were included in the study.INTERVENTIONPatients in the intervention group were exposed to projections of calming video sequences for 60 min. Patients in the control group received standard care.OUTCOME MEASURES AND ANALYSISChanges in RASS and Nu-DESC were assessed 30 and 60 min after the intervention was started.MAIN RESULTSA total of 57 patients were included in the study, with 30 patients in the intervention group and 27 patients in the control group. Before the intervention, the median (interquartile range) RASS scores were comparable between the intervention group [3 (2-3)] and the control group [3 (2-3)]. After 30 min of exposure to calming video sequences, patients in the intervention group showed significantly lower RASS and Nu-DESC scores compared to the control group [RASS: 1 (0-1) vs. 2 (1.5-3), P < 0.001; Nu-DESC: 3 (2-4) vs. 5 (4-6), P < 0.001]. This difference persisted at 60 min [RASS: 0 (0-1) vs. 2 (1-2.5), P < 0.001; Nu-DESC: 2 (2-3) vs. 5 (4-6), P < 0.001]. Additionally, fewer patients in the intervention group required additional sedating or antipsychotic medication (1/30) compared to the control group (9/27), with this difference being statistically significant (P = 0.004).CONCLUSIONIn this randomized controlled trial, the use of calming video sequences in elderly patients with agitation in the ED resulted in significant reductions in agitation and the need for additional sedative or antipsychotic medication.
背景和重要性急诊科(ED)中老年患者的躁动通常会使诊疗工作复杂化。目的在这项研究中,我们探讨了是否可以通过播放视频片段来缓解急诊科中老年躁动患者的躁动。如果 4-AT 分数≥4 分,则使用里士满躁动不安量表(RASS)和护理谵妄筛查量表(Nu-DESC)对患者进行评分。经法定代理人知情同意后,RASS≥+2且Nu-DESC≥4的患者被纳入研究。然后,患者被随机分配到干预组或对照组。共有 n = 57 名患者参与了这项研究。干预干预组患者将接受 60 分钟的平静视频投影。结果测量和分析在干预开始 30 分钟和 60 分钟后评估 RASS 和 Nu-DESC 的变化。主要结果共有 57 名患者参与研究,其中干预组 30 人,对照组 27 人。干预前,干预组[3 (2-3)]和对照组[3 (2-3)]的 RASS 评分中位数(四分位数间距)相当。在观看 30 分钟的镇静视频后,干预组患者的 RASS 和 Nu-DESC 分数明显低于对照组[RASS:1 (0-1) vs. 2 (1.5-3),P < 0.001;Nu-DESC:3 (2-4) vs. 5 (1.5-3),P < 0.001]:3 (2-4) vs. 5 (4-6),P < 0.001]。这种差异在 60 分钟后仍然存在[RASS:0 (0-1) vs. 2 (1-2.5),P < 0.001;Nu-DESC:2 (2-3) vs. 5 (4-6),P < 0.001]:2 (2-3) vs. 5 (4-6),P < 0.001]。此外,与对照组(9/27)相比,干预组中需要额外服用镇静剂或抗精神病药物的患者更少(1/30),这一差异具有统计学意义(P = 0.004)。
{"title":"Videodistraction to reduce agitation in elderly patients in the emergency department: an open label parallel group randomized controlled trial.","authors":"Enver Güvec,Uwe Koedel,Sophia Horster,Vera Pedersen,Stefanie Völk,Michaela Waldow,Florian Weber,Matthias Klein","doi":"10.1097/mej.0000000000001179","DOIUrl":"https://doi.org/10.1097/mej.0000000000001179","url":null,"abstract":"BACKGROUND AND IMPORTANCEAgitation of elderly patients in the emergency department (ED) often complicates workup and therapy.OBJECTIVEIn this study, we investigated if agitation in the ED can be reduced by showing calming video sequences in elderly agitated patients.DESIGNSProspective randomized intervention study.SETTINGS AND PARTICIPANTSED patients aged ≥65 years were screened for the risk of agitation/delirium using the 4-A's test (4-AT) test. In case of ≥4 4-AT points, patients were scored using the Richmond Agitation-Sedation Scale (RASS) and the Nursing Delirium Screening Scale (Nu-DESC). They were included in the study if RASS was ≥+2 and Nu-DESC ≥ 4 after informed consent of the legal representative. Patients were then randomized to the intervention or control group. A total of n = 57 patients were included in the study.INTERVENTIONPatients in the intervention group were exposed to projections of calming video sequences for 60 min. Patients in the control group received standard care.OUTCOME MEASURES AND ANALYSISChanges in RASS and Nu-DESC were assessed 30 and 60 min after the intervention was started.MAIN RESULTSA total of 57 patients were included in the study, with 30 patients in the intervention group and 27 patients in the control group. Before the intervention, the median (interquartile range) RASS scores were comparable between the intervention group [3 (2-3)] and the control group [3 (2-3)]. After 30 min of exposure to calming video sequences, patients in the intervention group showed significantly lower RASS and Nu-DESC scores compared to the control group [RASS: 1 (0-1) vs. 2 (1.5-3), P < 0.001; Nu-DESC: 3 (2-4) vs. 5 (4-6), P < 0.001]. This difference persisted at 60 min [RASS: 0 (0-1) vs. 2 (1-2.5), P < 0.001; Nu-DESC: 2 (2-3) vs. 5 (4-6), P < 0.001]. Additionally, fewer patients in the intervention group required additional sedating or antipsychotic medication (1/30) compared to the control group (9/27), with this difference being statistically significant (P = 0.004).CONCLUSIONIn this randomized controlled trial, the use of calming video sequences in elderly patients with agitation in the ED resulted in significant reductions in agitation and the need for additional sedative or antipsychotic medication.","PeriodicalId":11893,"journal":{"name":"European Journal of Emergency Medicine","volume":"45 1","pages":""},"PeriodicalIF":4.4,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142187168","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Testing the validity of three acute care assessment tools for assessing residents' performance during in situ simulation: the ACAT-SimSit study. 测试三种急症护理评估工具的有效性,以评估住院医师在原位模拟中的表现:ACAT-SimSit 研究。
IF 3.1 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-08-01 Epub Date: 2024-03-19 DOI: 10.1097/MEJ.0000000000001133
Anne-Laure Philippon, Antoine Lefevre-Scelles, Xavier Eyer, Carine Zumstein, Aiham Ghazali, Simon Audibert, Pierrick Le Borgne, Emmanuel Triby, Jennifer Truchot

Background: The assessment of technical and nontechnical skills in emergency medicine requires reliable and usable tools. Three Acute Care Assessment Tools (ACATs) have been developed to assess medical learners in their management of cardiac arrest (ACAT-CA), coma (ACAT-coma) and acute respiratory failure (ACAT-ARF).

Objective: This study aims to analyze the reliability and usability of the three ACATs when used for in situ (bedside) simulation.

Methods: This prospective multicenter validation study tested ACATs using interprofessional in situ simulations in seven emergency departments and invited training residents to participate in them. Each session was rated by two independent raters using ACAT. Intraclass correlation coefficients (ICC) were used to assess interrater reliability, and Cronbach's alpha coefficient was used to assess internal consistency for each ACAT. The correlation between ACATs' scores and the learners' level of performance was also assessed. Finally, a questionnaire and two focus groups were used to assess the usability of the ACATs.

Results: A total of 104 in situ simulation sessions, including 85 residents, were evaluated by 37 raters. The ICC for ACAT-CA, ACAT-coma and ACAT-ARF were 0.95 [95% confidence interval (CI), 0.93-0.98], 0.89 (95% CI, 0.77-0.95) and 0.92 (95%CI 0.83-0.96), respectively. The Cronbach's alphas were 0.79, 0.80 and 0.73, respectively. The ACAT-CA and ARF showed good construct validity, as third-year residents obtained significantly higher scores than first-year residents ( P  < 0.001; P  < 0.019). The raters supported the usability of the tools, even though they expressed concerns regarding the use of simulations in a summative way.

Conclusion: This study reported that the three ACATs showed good external validity and usability.

背景:急诊医学技术和非技术技能的评估需要可靠和可用的工具。目前已开发出三种急性护理评估工具(ACAT),用于评估医学学习者对心脏骤停(ACAT-CA)、昏迷(ACAT-coma)和急性呼吸衰竭(ACAT-ARF)的处理能力:本研究旨在分析三种 ACAT 在用于原位(床旁)模拟时的可靠性和可用性:这项前瞻性多中心验证研究在七个急诊科使用跨专业原位模拟对 ACAT 进行了测试,并邀请接受培训的住院医师参与其中。每节课都由两名独立评分员使用 ACAT 进行评分。类内相关系数(ICC)用于评估评分者之间的可靠性,克朗巴赫α系数用于评估每个 ACAT 的内部一致性。此外,还评估了 ACAT 分数与学习者成绩水平之间的相关性。最后,还通过问卷调查和两个焦点小组来评估 ACAT 的可用性:37名评分员对包括85名住院医师在内的104个原位模拟课程进行了评估。ACAT-CA、ACAT-coma 和 ACAT-ARF 的 ICC 分别为 0.95 [95% 置信区间 (CI),0.93-0.98]、0.89 (95% CI,0.77-0.95) 和 0.92 (95%CI 0.83-0.96)。Cronbach's alphas 分别为 0.79、0.80 和 0.73。ACAT-CA和ARF显示出良好的建构效度,因为三年级住院医师的得分明显高于一年级住院医师(P 结论:ACAT-CA和ARF显示出良好的建构效度:本研究表明,三种 ACAT 具有良好的外部效度和可用性。
{"title":"Testing the validity of three acute care assessment tools for assessing residents' performance during in situ simulation: the ACAT-SimSit study.","authors":"Anne-Laure Philippon, Antoine Lefevre-Scelles, Xavier Eyer, Carine Zumstein, Aiham Ghazali, Simon Audibert, Pierrick Le Borgne, Emmanuel Triby, Jennifer Truchot","doi":"10.1097/MEJ.0000000000001133","DOIUrl":"10.1097/MEJ.0000000000001133","url":null,"abstract":"<p><strong>Background: </strong>The assessment of technical and nontechnical skills in emergency medicine requires reliable and usable tools. Three Acute Care Assessment Tools (ACATs) have been developed to assess medical learners in their management of cardiac arrest (ACAT-CA), coma (ACAT-coma) and acute respiratory failure (ACAT-ARF).</p><p><strong>Objective: </strong>This study aims to analyze the reliability and usability of the three ACATs when used for in situ (bedside) simulation.</p><p><strong>Methods: </strong>This prospective multicenter validation study tested ACATs using interprofessional in situ simulations in seven emergency departments and invited training residents to participate in them. Each session was rated by two independent raters using ACAT. Intraclass correlation coefficients (ICC) were used to assess interrater reliability, and Cronbach's alpha coefficient was used to assess internal consistency for each ACAT. The correlation between ACATs' scores and the learners' level of performance was also assessed. Finally, a questionnaire and two focus groups were used to assess the usability of the ACATs.</p><p><strong>Results: </strong>A total of 104 in situ simulation sessions, including 85 residents, were evaluated by 37 raters. The ICC for ACAT-CA, ACAT-coma and ACAT-ARF were 0.95 [95% confidence interval (CI), 0.93-0.98], 0.89 (95% CI, 0.77-0.95) and 0.92 (95%CI 0.83-0.96), respectively. The Cronbach's alphas were 0.79, 0.80 and 0.73, respectively. The ACAT-CA and ARF showed good construct validity, as third-year residents obtained significantly higher scores than first-year residents ( P  < 0.001; P  < 0.019). The raters supported the usability of the tools, even though they expressed concerns regarding the use of simulations in a summative way.</p><p><strong>Conclusion: </strong>This study reported that the three ACATs showed good external validity and usability.</p>","PeriodicalId":11893,"journal":{"name":"European Journal of Emergency Medicine","volume":" ","pages":"281-286"},"PeriodicalIF":3.1,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140179472","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Using case vignettes to study the presence of outcome, hindsight, and implicit bias in acute unplanned medical care: a cross-sectional study. 利用病例小故事研究急性计划外医疗护理中存在的结果、后见之明和隐性偏见:一项横断面研究。
IF 3.1 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-08-01 Epub Date: 2024-02-16 DOI: 10.1097/MEJ.0000000000001127
Patricia Plaum, Laura N Visser, Bas de Groot, Marlies E B Morsink, Wilma L J M Duijst, Bart G J Candel

Background and importance: Various biases can impact decision-making and judgment of case quality in the Emergency Department (ED). Outcome and hindsight bias can lead to wrong retrospective judgment of care quality, and implicit bias can result in unjust treatment differences in the ED based on irrelevant patient characteristics.

Objectives: First, to evaluate the extent to which knowledge of an outcome influences physicians' quality of care assessment. Secondly, to examine whether patients with functional disorders receive different treatment compared to patients with a somatic past medical history.

Design: A web-based cross-sectional study in which physicians received case vignettes with a case description and care provided. Physicians were informed about vignette outcomes in a randomized way (no, good, or bad outcome). Physicians rated quality of care for four case vignettes with different outcomes. Subsequently, they received two more case vignettes. Physicians were informed about the past medical history of the patient in a randomized way (somatic or functional). Physicians made treatment and diagnostic decisions for both cases.

Setting and participants: One hundred ninety-one Dutch emergency physicians (EPs) and general practitioners (GPs) participated.

Outcome measures and analysis: Quality of care was rated on a Likert scale (0-5) and dichotomized as adequate (yes/no). Physicians estimated the likelihood of patients experiencing a bad outcome for hindsight bias. For the second objective, physicians decided on prescribing analgesics and additional diagnostic tests.

Main results: Large differences existed in rated quality of care for three out of four vignettes based on different case outcomes. For example, physicians rated the quality of care as adequate in 44% (95% CI 33-57%) for an abdominal pain case with a bad outcome, compared to 88% (95% CI 78-94%) for a good outcome, and 84% (95% CI 73-91%) for no outcome ( P  < 0.01). The estimated likelihood of a bad outcome was higher if physicians received a vignette with a bad patient outcome. Fewer diagnostic tests were performed and fewer opioids were prescribed for patients with a functional disorder.

Conclusion: Outcome, hindsight, and implicit bias significantly influence decision-making and care quality assessment by Dutch EPs and GPs.

背景和重要性:各种偏见会影响急诊科(ED)的决策和对病例质量的判断。结果偏差和事后偏差会导致对护理质量做出错误的回顾性判断,而内隐偏差则会导致在急诊科根据无关的患者特征进行不公正的治疗:首先,评估对结果的了解在多大程度上影响了医生对护理质量的评估。其次,研究功能性障碍患者与有躯体性既往病史的患者相比,是否接受了不同的治疗:设计:一项基于网络的横断面研究,医生会收到包含病例描述和所提供护理的病例小故事。医生以随机方式获知小故事的结果(无结果、好结果或坏结果)。医生对四个不同结果的病例小故事的护理质量进行评分。随后,他们又收到了两个病例小故事。医生以随机方式(躯体或功能)了解病人的既往病史。医生对两个病例做出治疗和诊断决定:结果测量与分析:以李克特量表(0-5)对医疗质量进行评分,并将其二分为适当(是/否)。医生会估计患者出现不良后果的可能性,以防事后诸葛亮。对于第二个目标,医生决定是否开具镇痛药和进行额外的诊断检测:主要结果:根据不同的病例结果,在四个小故事中,有三个小故事的护理质量评分存在很大差异。例如,对于结果不佳的腹痛病例,44%(95% CI 33-57%)的医生将护理质量评为适当,而对于结果良好的病例,88%(95% CI 78-94%)的医生将护理质量评为适当,而对于无结果的病例,84%(95% CI 73-91%)的医生将护理质量评为适当:结果、后见之明和隐性偏见对荷兰急诊医生和全科医生的决策和护理质量评估有重大影响。
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引用次数: 0
High-flow nasal cannula oxygen versus noninvasive ventilation for the management of acute cardiogenic pulmonary edema: a randomized controlled pilot study. 高流量鼻插管供氧与无创通气治疗急性心源性肺水肿:随机对照试验研究。
IF 3.1 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-08-01 Epub Date: 2024-02-16 DOI: 10.1097/MEJ.0000000000001128
Nicolas Marjanovic, Melyne Piton, Jennifer Lamarre, Camille Alleyrat, Raphael Couvreur, Jérémy Guenezan, Olivier Mimoz, Jean-Pierre Frat

Background: Whether high-flow nasal oxygen can improve clinical signs of acute respiratory failure in acute heart failure (AHF) is uncertain.

Objective: To compare the effect of high-flow oxygen with noninvasive ventilation (NIV) on respiratory rate in patients admitted to an emergency department (ED) for AHF-related acute respiratory failure.

Design, settings and participants: Multicenter, randomized pilot study in three French EDs. Adult patients with acute respiratory failure due to suspected AHF were included. Key exclusion criteria were urgent need for intubation, Glasgow Coma Scale <13 points or hemodynamic instability.

Intervention: Patients were randomly assigned to receive high-flow oxygen (minimum 50 l/min) or noninvasive bilevel positive pressure ventilation.

Outcomes measure: The primary outcome was change in respiratory rate within the first hour of treatment and was analyzed with a linear mixed model. Secondary outcomes included changes in pulse oximetry, heart rate, blood pressure, blood gas samples, comfort, treatment failure and mortality.

Main results: Among the 145 eligible patients in the three participating centers, 60 patients were included in the analysis [median age 86 (interquartile range (IQR), 90; 92) years]. There was a median respiratory rate of 30.5 (IQR, 28; 33) and 29.5 (IQR, 27; 35) breaths/min in the high-flow oxygen and NIV groups respectively, with a median change of -10 (IQR, -12; -8) with high-flow nasal oxygen and -7 (IQR, -11; -5) breaths/min with NIV [estimated difference -2.6 breaths/min (95% confidence interval (CI), -0.5-5.7), P  = 0.052] at 60 min. There was a median SpO 2 of 95 (IQR, 92; 97) and 96 (IQR, 93; 97) in the high-flow oxygen and NIV groups respectively, with a median change at 60 min of 2 (IQR, 0; 5) with high-flow nasal oxygen and 2 (IQR, -1; 5) % with NIV [estimated difference 0.8% (95% CI, -1.1-2.8), P  = 0.60]. PaO 2 , PaCO 2 and pH did not differ at 1 h between groups, nor did treatment failure, intubation and mortality rates.

Conclusion: In this pilot study, we did not observe a statistically significant difference in changes in respiratory rate among patients with acute respiratory failure due to AHF and managed with high-flow oxygen or NIV. However, the point estimate and its large confidence interval may suggest a benefit of high-flow oxygen.

Trial registration: NCT04971213 ( https://clinicaltrials.gov ).

背景:高流量鼻氧能否改善急性心力衰竭(AHF)患者急性呼吸衰竭的临床症状尚不确定:比较高流量吸氧与无创通气(NIV)对急诊科(ED)收治的急性心力衰竭相关急性呼吸衰竭患者呼吸频率的影响:法国三家急诊室的多中心随机试验研究。研究对象包括疑因 AHF 导致急性呼吸衰竭的成人患者。主要排除标准为急需插管、格拉斯哥昏迷量表干预:结果测量:主要结果是治疗后一小时内呼吸频率的变化,并采用线性混合模型进行分析。次要结果包括脉搏血氧饱和度、心率、血压、血气样本、舒适度、治疗失败和死亡率的变化:在三个参与中心的 145 名符合条件的患者中,有 60 名患者被纳入分析[中位年龄为 86(四分位数间距(IQR),90;92)岁]。60 分钟时,高流量鼻氧组和 NIV 组的中位呼吸频率分别为 30.5(IQR,28;33)次/分钟和 29.5(IQR,27;35)次/分钟,中位变化分别为:高流量鼻氧-10(IQR,-12;-8)次/分钟,NIV-7(IQR,-11;-5)次/分钟[估计差异为-2.6 次/分钟(95% 置信区间 (CI),-0.5-5.7),P = 0.052]。高流量吸氧组和 NIV 组的 SpO2 中位数分别为 95(IQR,92;97)和 96(IQR,93;97),60 分钟时的中位数变化为:高流量鼻氧为 2(IQR,0;5)%,NIV 为 2(IQR,-1;5)%[估计差异为 0.8%(95% CI,-1.1-2.8),P = 0.60]。1小时后各组的PaO2、PaCO2和pH值没有差异,治疗失败率、插管率和死亡率也没有差异:在这项试验性研究中,我们没有观察到因 AHF 导致急性呼吸衰竭并接受高流量供氧或 NIV 治疗的患者的呼吸频率变化有显著的统计学差异。然而,点估计值及其较大的置信区间可能表明高流量供氧有一定的益处:NCT04971213 (https://clinicaltrials.gov)。
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引用次数: 0
Increased mortality in elderly patients who spent the night in the emergency department: lessons from the 'No Bed Night' study? 在急诊科过夜的老年患者死亡率增加:"无床之夜 "研究的启示?
IF 3.1 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-08-01 Epub Date: 2024-04-30 DOI: 10.1097/MEJ.0000000000001139
Mélanie Roussel
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引用次数: 0
Drug users coming to European emergency departments: general basic approach and recommendations for safe discharge. 前往欧洲急诊科就诊的吸毒者:一般基本方法和安全出院建议。
IF 3.1 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-08-01 Epub Date: 2024-05-20 DOI: 10.1097/MEJ.0000000000001145
Guillermo Burillo-Putze, Òscar Miró
{"title":"Drug users coming to European emergency departments: general basic approach and recommendations for safe discharge.","authors":"Guillermo Burillo-Putze, Òscar Miró","doi":"10.1097/MEJ.0000000000001145","DOIUrl":"10.1097/MEJ.0000000000001145","url":null,"abstract":"","PeriodicalId":11893,"journal":{"name":"European Journal of Emergency Medicine","volume":" ","pages":"236-239"},"PeriodicalIF":3.1,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141070783","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Authors' response to comment on 'Acute heart failure in elderly patients admitted to the emergency department with acute dyspnea: a multimarker approach diagnostic study'. 作者对 "急诊科收治的急性呼吸困难老年患者的急性心力衰竭:多标志物诊断研究 "评论的回复。
IF 3.1 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-08-01 Epub Date: 2024-06-25 DOI: 10.1097/MEJ.0000000000001125
Omide Taheri, Frédéric Mauny, Patrick Ray, Thibaut Desmettre
{"title":"Authors' response to comment on 'Acute heart failure in elderly patients admitted to the emergency department with acute dyspnea: a multimarker approach diagnostic study'.","authors":"Omide Taheri, Frédéric Mauny, Patrick Ray, Thibaut Desmettre","doi":"10.1097/MEJ.0000000000001125","DOIUrl":"https://doi.org/10.1097/MEJ.0000000000001125","url":null,"abstract":"","PeriodicalId":11893,"journal":{"name":"European Journal of Emergency Medicine","volume":"31 4","pages":"297-298"},"PeriodicalIF":3.1,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141456057","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
European Journal of Emergency Medicine
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