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The association between prehospital post-return of spontaneous circulation core temperature and survival after out-of-hospital cardiac arrest. 院前自主循环恢复后核心体温与院外心脏骤停后存活率之间的关系。
IF 3.1 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-10-01 Epub Date: 2024-05-15 DOI: 10.1097/MEJ.0000000000001142
Shadman Aziz, Molly Clough, Emma Butterfield, Zachary Starr, Kate Lachowycz, James Price, Ed B G Barnard, Paul Rees

Background and importance: Following the return of spontaneous circulation (ROSC) after out-of-hospital cardiac arrest (OHCA), a low body temperature on arrival at the hospital and on admission to the ICU is reportedly associated with increased mortality. Whether this association exists in the prehospital setting, however, is unknown.

Objective: The objective of this study was to investigate whether the initial, prehospital core temperature measured post-ROSC is independently associated with survival to hospital discharge in adult patients following OHCA.

Design, setting and participants: This retrospective observational study was conducted at East Anglian Air Ambulance, a physician-paramedic staffed Helicopter Emergency Medical Service in the East of England, UK. Adult OHCA patients attended by East Anglian Air Ambulance from 1 February 2015 to 30 June 2023, who had post-ROSC oesophageal temperature measurements were included.

Outcome measure and analysis: The primary outcome measure was survival to hospital discharge. Core temperature was defined as the first oesophageal temperature recorded following ROSC. Multivariable logistic regression evaluated the adjusted association between core temperature and survival to hospital discharge.

Main results: Resuscitation was attempted in 3990 OHCA patients during the study period, of which 552 patients were included in the final analysis. The mean age was 61 years, and 402 (72.8%) patients were male. Among them, 194 (35.1%) survived to hospital discharge. The mean core temperature was lower in nonsurvivors compared with those who survived hospital discharge; 34.6 and 35.2 °C, respectively (mean difference, -0.66; 95% CI, -0.87 to -0.44; P  < 0.001). The adjusted odds ratio for survival was 1.41 (95% CI, 1.09-1.83; P  = 0.01) for every 1.0 °C increase in core temperature between 32.5 and 36.9 °C.

Conclusion: In adult patients with ROSC following OHCA, early prehospital core temperature is independently associated with survival to hospital discharge.

背景和重要性:据报道,院外心脏骤停(OHCA)后恢复自主循环(ROSC)时,到达医院和进入重症监护室时体温过低与死亡率增加有关。然而,院前环境中是否存在这种关联尚不清楚:本研究的目的是调查院前体温测量是否与OHCA成人患者出院后的存活率有关:这项回顾性观察研究在英国英格兰东部的东安格利亚空中救护中心(East Anglian Air Ambulance)进行。研究对象包括 2015 年 2 月 1 日至 2023 年 6 月 30 日期间由东安格利亚空中救护中心接诊的成人 OHCA 患者,这些患者在手术后接受了食道温度测量:主要结果指标是出院后的存活率。核心温度定义为 ROSC 后记录到的第一个食道温度。多变量逻辑回归评估了核心体温与出院存活率之间的调整关系:主要结果:在研究期间,3990 名 OHCA 患者尝试了复苏,其中 552 名患者纳入了最终分析。平均年龄为 61 岁,402 名(72.8%)患者为男性。其中 194 人(35.1%)存活至出院。与出院后存活的患者相比,未存活患者的平均核心体温较低:分别为 34.6°C 和 35.2°C(平均差,-0.66;95% CI,-0.87 至 -0.44;P 结论:与出院后存活的患者相比,未存活患者的平均核心体温较低(平均差,-0.66;95% CI,-0.87 至 -0.44):在 OHCA 后出现 ROSC 的成人患者中,院前早期核心温度与出院存活率有独立联系。
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引用次数: 0
Artificial intelligence and the future of scientific publication. 人工智能与科学出版的未来。
IF 3.1 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-10-01 Epub Date: 2024-08-27 DOI: 10.1097/MEJ.0000000000001164
Howard Bauchner
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引用次数: 0
Clinician suspicion of unintentional carbon monoxide exposure in emergency department attendees. 临床医生对急诊科就诊者无意接触一氧化碳的怀疑。
IF 3.1 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-10-01 Epub Date: 2024-08-27 DOI: 10.1097/MEJ.0000000000001160
Heather Jarman, Richard W Atkinson, Isabella Myers, Timothy W Gant, Tim Marczylo, Shirley Price
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引用次数: 0
Involvement of relatives during end-of-life care in emergency departments: comparison between the perceptions of physicians and nurses. 急诊科临终关怀中亲属的参与:医生和护士看法的比较。
IF 3.1 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-10-01 Epub Date: 2024-08-27 DOI: 10.1097/MEJ.0000000000001154
Mélanie Roussel, Claire Fourcade, Marion Douplat, Philippe Le Conte, Yonathan Freund, Jennifer Truchot
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引用次数: 0
Providing urgent and emergency care to children and young people: training requirements for emergency medicine specialty trainees. 为儿童和青少年提供紧急和急诊服务:急诊医学专业学员的培训要求。
IF 3.1 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-10-01 Epub Date: 2024-06-03 DOI: 10.1097/MEJ.0000000000001148
Ruud G Nijman, Cornelia Schickerling, Zsolt Bognar, Ruth Brown
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引用次数: 0
Resuscitative endovascular balloon occlusion of the aorta for trauma patients with uncontrolled hemorrhage: a retrospective target trial emulation (the AT-REBOA target trial). 复苏血管内球囊闭塞主动脉创伤患者不受控制的出血:回顾性目标试验模拟(AT-REBOA目标试验)。
IF 3.1 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-09-24 DOI: 10.1097/MEJ.0000000000001183
Barbara Hallmann, Gabriel Honnef, Nicolas Eibinger, Michael Eichlseder, Martin Posch, Paul Puchwein, Philipp Zoidl, Paul Zajic

Background: Noncompressible truncal hemorrhage is a major contributor to preventable deaths in trauma patients and, despite advances in emergency care, still poses a big challenge.

Objectives: This study aimed to assess the clinical efficacy of trauma resuscitation care incorporating Resuscitative Endovascular Balloon Occlusion of the Aorta (REBOA) compared to standard care for managing uncontrolled torso or lower body hemorrhage.

Methods: This study utilized a target trial design with a matched case-control methodology, emulating randomized 1 : 1 allocation for patients receiving trauma resuscitation care with or without the use of REBOA. The study was conducted at a high-volume trauma center in Southern Austria, including trauma patients treated between January 2019 and October 2023, aged 16 and above, with suspected severe non-compressible torso hemorrhage. The primary outcome was 30-day in-hospital mortality. Secondary outcomes were in-hospital mortality rates at 3, 6, 24 h, and 90 days, need for damage control procedures, time to these procedures, computed tomography (CT) scan rates during resuscitation, complications, length of intensive care and in-hospital stay, and causes of death.

Results: Median age was 55 [interquartile range (IQR) 42-64] years. Median total injury severity, assessed by Injury Severity Score, was 46.5 (IQR: 43-57). There was no significant difference in 30-day in-hospital mortality between groups [9/11 (41%) vs. 9/11 (41%), odds ratio: 1.00, 95% confidence interval (CI): 0.3-3.36, P > 0.999]. Lower mortality rates within 3, 6, and 24 h were observed in the REBOA group; in a Cox proportional hazards model, hazard ratio (95% CI) for mortality in the REBOA group was 0.87 (0.35-2.15). Timing to damage control procedures did not significantly differ between groups, although patients in the REBOA group underwent significantly more CT scans. Bleeding was cited as the main cause of death less frequently in the REBOA group.

Conclusion: In severely injured patients presenting with possible major non-compressible torso hemorrhage, a systematically implemented resuscitation strategy including REBOA during the initial hospital phase, is not associated with significant changes in mortality.

背景:不可压缩性截骨出血是创伤患者可预防死亡的主要原因,尽管急诊护理取得了进展,但仍然面临着巨大的挑战。目的:本研究旨在评估创伤复苏护理结合复苏血管内球囊阻断主动脉(REBOA)的临床疗效,与标准护理相比,治疗不受控制的躯干或下体出血。方法:本研究采用匹配病例对照方法的目标试验设计,模拟使用REBOA或不使用REBOA接受创伤复苏护理的患者随机1:1分配。该研究是在奥地利南部的一个大容量创伤中心进行的,包括2019年1月至2023年10月期间接受治疗的16岁及以上的创伤患者,怀疑严重的不可压缩性躯干出血。主要终点是30天住院死亡率。次要结局是3、6、24小时和90天的住院死亡率、损害控制程序的需要、这些程序的时间、复苏期间的计算机断层扫描(CT)扫描率、并发症、重症监护和住院时间的长度以及死亡原因。结果:中位年龄为55岁[四分位间距42 ~ 64]岁。损伤严重程度评分中位数为46.5 (IQR: 43-57)。两组间30天住院死亡率无显著差异[9/11 (41%)vs. 9/11(41%),优势比:1.00,95%可信区间(CI): 0.3-3.36, P < 0 0.999]。REBOA组在3、6和24小时内的死亡率较低;在Cox比例风险模型中,REBOA组死亡率的风险比(95% CI)为0.87(0.35-2.15)。尽管REBOA组患者接受了更多的CT扫描,但两组之间进行损伤控制程序的时间没有显著差异。在REBOA组中,出血被列为主要死亡原因的频率较低。结论:在可能出现严重不可压缩性躯干出血的严重受伤患者中,在住院初期系统实施包括REBOA在内的复苏策略与死亡率的显着变化无关。
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引用次数: 0
Association between pre-arrest left ventricular ejection fraction and survival in nontraumatic out-of-hospital cardiac arrest. 非创伤性院外心脏骤停患者骤停前左心室射血分数与存活率之间的关系。
IF 3.1 4区 医学 Q1 EMERGENCY MEDICINE Pub Date : 2024-09-16 DOI: 10.1097/MEJ.0000000000001181
Yi-Ju Ho, Chun-Ju Lien, Ren-Jie Tsai, Cheng-Yi Fan, Chi-Hsin Chen, Chien-Tai Huang, Ching-Yu Chen, Yun-Chang Chen, Chun-Hsiang Huang, Wen-Chu Chiang, Chien-Hua Huang, Chih-Wei Sung, Edward Pei-Chuan Huang

Background and importance: Out-of-hospital cardiac arrest (OHCA) poses major public health issues. Pre-arrest heart function is a prognostic factor, but the specific contribution of pre-arrest echocardiographic evaluation in predicting OHCA outcome remains limited.

Objective: The primary objective was to investigate the association between left ventricular ejection fraction (LVEF) measured in echocardiography prior to OHCA and survival to hospital discharge.

Design, settings, and participants: This multicenter retrospective cohort study analyzed data from the National Taiwan University Hospital and its affiliated hospitals. We included adult nontraumatic OHCA patients who were treated by the emergency medical services (EMS) and underwent echocardiography within 6 months prior to the OHCA event from January 2016 to December 2022. Data included demographics, preexisting diseases, resuscitation events, and echocardiographic reports.

Outcomes measure and analysis: The primary outcome was the survival to hospital discharge after post-arrest care. Statistical analysis involved multivariable logistic regression to modify potential confounders, reported as adjusted odds ratio (aOR) and 95% confidence interval (CI), and evaluate the association between echocardiographic findings and survival to hospital discharge.

Main results: This study analyzed 950 patients, with 33.6% surviving to discharge. A higher pre-arrest LVEF was independently associated with increased survival. Compared to patients with LVEF < 40%, those with LVEF between 40% and 60% had significantly higher odds of survival (aOR = 3.68, 95% CI = 2.14-6.35, P < 0.001), and those with LVEF > 60% had even greater odds of survival (aOR = 5.46, 95% CI = 3.09-9.66, P < 0.001). There was also an association between lower tricuspid regurgitation pressure gradient and survival (aOR = 0.98, 95% CI = 0.97-1.00, P = 0.015). Younger age, male gender, dyslipidemia, stroke, cancer, witnessed arrest, initial shockable rhythm, and shorter low-flow time are other significant predictors of survival.

Conclusion: In adult, nontraumatic, EMS-treated OHCA patients, a higher LVEF 6 months prior to OHCA was associated with improved survival at hospital discharge.

背景和重要性:院外心脏骤停(OHCA)是重大的公共卫生问题。心跳骤停前的心脏功能是一个预后因素,但心跳骤停前超声心动图评估在预测 OHCA 结果方面的具体作用仍然有限:主要目的是研究 OHCA 发生前超声心动图测量的左心室射血分数(LVEF)与出院后存活率之间的关系:这项多中心回顾性队列研究分析了台湾大学医院及其附属医院的数据。我们纳入了2016年1月至2022年12月期间接受紧急医疗服务(EMS)治疗并在OHCA事件发生前6个月内接受超声心动图检查的成人非创伤性OHCA患者。数据包括人口统计学、既往疾病、复苏事件和超声心动图报告:主要结果是患者在急救后出院的存活率。统计分析包括多变量逻辑回归,以改变潜在的混杂因素,报告为调整后的几率比(aOR)和95%置信区间(CI),并评估超声心动图结果与出院后存活率之间的关联:这项研究分析了950名患者,其中33.6%的患者存活至出院。入院前 LVEF 越高,存活率越高。与 LVEF < 40% 的患者相比,LVEF 在 40% 到 60% 之间的患者生存几率明显更高(aOR = 3.68,95% CI = 2.14-6.35,P < 0.001),而 LVEF > 60% 的患者生存几率更高(aOR = 5.46,95% CI = 3.09-9.66,P < 0.001)。较低的三尖瓣反流压力梯度也与存活率有关(aOR = 0.98,95% CI = 0.97-1.00,P = 0.015)。年龄较小、男性、血脂异常、中风、癌症、目击停搏、初始可电击心律和较短的低流量时间也是预测存活率的重要因素:结论:在非创伤性、经急救服务处理的成人 OHCA 患者中,OHCA 发生前 6 个月 LVEF 越高,出院时的存活率越高。
{"title":"Association between pre-arrest left ventricular ejection fraction and survival in nontraumatic out-of-hospital cardiac arrest.","authors":"Yi-Ju Ho, Chun-Ju Lien, Ren-Jie Tsai, Cheng-Yi Fan, Chi-Hsin Chen, Chien-Tai Huang, Ching-Yu Chen, Yun-Chang Chen, Chun-Hsiang Huang, Wen-Chu Chiang, Chien-Hua Huang, Chih-Wei Sung, Edward Pei-Chuan Huang","doi":"10.1097/MEJ.0000000000001181","DOIUrl":"https://doi.org/10.1097/MEJ.0000000000001181","url":null,"abstract":"<p><strong>Background and importance: </strong>Out-of-hospital cardiac arrest (OHCA) poses major public health issues. Pre-arrest heart function is a prognostic factor, but the specific contribution of pre-arrest echocardiographic evaluation in predicting OHCA outcome remains limited.</p><p><strong>Objective: </strong>The primary objective was to investigate the association between left ventricular ejection fraction (LVEF) measured in echocardiography prior to OHCA and survival to hospital discharge.</p><p><strong>Design, settings, and participants: </strong>This multicenter retrospective cohort study analyzed data from the National Taiwan University Hospital and its affiliated hospitals. We included adult nontraumatic OHCA patients who were treated by the emergency medical services (EMS) and underwent echocardiography within 6 months prior to the OHCA event from January 2016 to December 2022. Data included demographics, preexisting diseases, resuscitation events, and echocardiographic reports.</p><p><strong>Outcomes measure and analysis: </strong>The primary outcome was the survival to hospital discharge after post-arrest care. Statistical analysis involved multivariable logistic regression to modify potential confounders, reported as adjusted odds ratio (aOR) and 95% confidence interval (CI), and evaluate the association between echocardiographic findings and survival to hospital discharge.</p><p><strong>Main results: </strong>This study analyzed 950 patients, with 33.6% surviving to discharge. A higher pre-arrest LVEF was independently associated with increased survival. Compared to patients with LVEF < 40%, those with LVEF between 40% and 60% had significantly higher odds of survival (aOR = 3.68, 95% CI = 2.14-6.35, P < 0.001), and those with LVEF > 60% had even greater odds of survival (aOR = 5.46, 95% CI = 3.09-9.66, P < 0.001). There was also an association between lower tricuspid regurgitation pressure gradient and survival (aOR = 0.98, 95% CI = 0.97-1.00, P = 0.015). Younger age, male gender, dyslipidemia, stroke, cancer, witnessed arrest, initial shockable rhythm, and shorter low-flow time are other significant predictors of survival.</p><p><strong>Conclusion: </strong>In adult, nontraumatic, EMS-treated OHCA patients, a higher LVEF 6 months prior to OHCA was associated with improved survival at hospital discharge.</p>","PeriodicalId":11893,"journal":{"name":"European Journal of Emergency Medicine","volume":" ","pages":""},"PeriodicalIF":3.1,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142282365","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
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%)。
{"title":"Laryngeal mask vs. laryngeal tube trial in paediatric patients (LaMaTuPe): a single-blinded, open-label, randomised-controlled trial.","authors":"Stephan Katzenschlager,Stefan Mohr,Nikolai Kaltschmidt,Franziska Peterstorfer,Frank Weilbacher,Patrick Günther,Markus Ries,Markus A Weigand,Erik Popp","doi":"10.1097/mej.0000000000001178","DOIUrl":"https://doi.org/10.1097/mej.0000000000001178","url":null,"abstract":"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.","PeriodicalId":11893,"journal":{"name":"European Journal of Emergency Medicine","volume":"44 1","pages":""},"PeriodicalIF":4.4,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142187171","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
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。
{"title":"Biomarkers of COVID-19 short-term worsening: a multiparameter analysis within the prospective multicenter COVIDeF cohort.","authors":"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,","doi":"10.1097/mej.0000000000001175","DOIUrl":"https://doi.org/10.1097/mej.0000000000001175","url":null,"abstract":"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.","PeriodicalId":11893,"journal":{"name":"European Journal of Emergency Medicine","volume":"37 1","pages":""},"PeriodicalIF":4.4,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142263971","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
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)。
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European Journal of Emergency Medicine
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