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Esmolol in persistent ventricular fibrillation/tachycardia with de-emphasised adrenaline – Introducing the REVIVE project 艾司洛尔治疗持续性室颤/心动过速,去势肾上腺素--REVIVE 项目介绍。
IF 2.1 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-01-01 DOI: 10.1016/j.resplu.2024.100842
Thomas Gleeson-Hammerton , Julian Hannah , John Pike , Matthew Taylor , James Raitt , Peter Owen , David B. Sidebottom , Adam Watson , David Jeffery , James Plumb
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引用次数: 0
Reply to: Sex-specific health-related quality of life in survivors of cardiac arrest 回复:心脏骤停幸存者性别相关的健康相关生活质量。
IF 2.1 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-01-01 DOI: 10.1016/j.resplu.2024.100852
Matthew Potter, Neil Magee, Eleni Aliki Nikolopoulou, Uzma Sajjad, Thomas R. Keeble, Marco Mion
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引用次数: 0
Challenges during cardiac arrest in pregnancy
IF 2.1 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-01-01 DOI: 10.1016/j.resplu.2024.100855
Korneel Berteloot, Marc Sabbe
A 36-year-old woman at 23 weeks and 3 days of gestation experienced a witnessed cardiopulmonary collapse. Bystander cardiopulmonary resuscitation (CPR) was initiated immediately. After advanced life support, she was transferred under mechanical CPR to a hospital for extracorporeal membrane oxygenation (ECMO). There, a delayed perimortem caesarean section (PMCS) was performed. Consideration to initiate ECMO following the PMCS was ultimately discontinued due to extensive intra-abdominal haemorrhage and the elapsed time of over one hour since the collapse. A full body computed tomography (CT) scan following ROSC revealed bilateral pulmonary embolisms and grade 4 liver laceration with active bleeding due to mechanical CPR. Despite the prolonged duration of cardiac arrest (69 min) and significant metabolic derangements, the patient had a favourable recovery and was discharged after 42 days with a good neurological outcome. This case illustrates the challenges of timely perimortem caesarean section in out-of-hospital cardiac arrest, where guidelines recommend performing the procedure within 4 min of maternal collapse. It also highlights the risks associated with mechanical chest compression devices.
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引用次数: 0
ILCOR World Restart a Heart – Spreading global CPR awareness and empowering communities to save lives since 2018
IF 2.1 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-01-01 DOI: 10.1016/j.resplu.2024.100853
N. Rott , L. Reinsch , B.W. Böttiger , A. Lockey
The International Liaison Committee on Resuscitation (ILCOR) World Restart a Heart (WRAH) Initiative is helping to save countless lives by promoting a culture of preparedness and encouraging widespread lay cardiopulmonary resuscitation (CPR) training. In total from 2018 to 2023 at least 12.6 million people were trained, and 570.7 million people were reached, showing a variety of campaigns adapted to countries current situation and their culture. World Restart a Heart success is based on an annual collaboration between nations, organisations and communities, demonstrating its universal relevance and impact. Because of this it is able to adapt to varies different circumstances and presents an accessible and effective solution to a significant global health problem, saving many lives over the years by promoting bystander CPR.
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引用次数: 0
Prehospital critical care beyond advanced life support for out-of-hospital cardiac arrest: A systematic review 院外心脏骤停高级生命支持之外的院前重症监护:系统综述。
IF 2.1 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-01-01 DOI: 10.1016/j.resplu.2024.100803
Adam J. Boulton , Rachel Edwards , Andrew Gadie , Daniel Clayton , Caroline Leech , Michael A. Smyth , Terry Brown , Joyce Yeung , on behalf of the International Liaison Committee on Resuscitation (ILCOR) Education, Implementation and Team (EIT) taskForce

Aim

To assess the clinical outcomes of patients with out-of-hospital cardiac arrest attended by prehospital critical care teams compared to non-critical care teams.

Methods

This review was prospectively registered with PROSPERO and the eligibility criteria followed a PICOST framework for ILCOR systematic reviews. Prehospital critical care was defined as any provider with enhanced clinical competencies beyond standard advanced life support algorithms and dedicated dispatch to critically ill patients. MEDLINE, Embase and CINAHL databases were searched from inception to 20 April 2024. Risk of bias was assessed using the ROBINS-I tool and the certainty of evidence by the GRADE approach. Meta-analyses of pooled data from studies at moderate risk of bias were performed using a generic inverse-variance with random-effects.

Results

The search returned 6,444 results and 17 articles were included, reporting 1,192,158 patients. Three studies reported traumatic patients and one reported paediatric patients. All studies were non-randomised and 15 were at moderate risk of bias. Most studies included prehospital physicians (n = 16). For adult non-traumatic patients, the certainty of evidence was low and prehospital critical care was associated with improved survival to hospital admission (OR 1.95, 95% CI 1.35–2.82), survival to hospital discharge (OR 1.34, 95% CI 1.10–1.63), survival at 30 days (OR 1.56, 95% CI 1.38–1.75), and favourable neurological outcome at 30 days (OR 1.48, 95% CI 1.19–1.84). Prehospital critical care was also associated with improved outcomes for traumatic and paediatric patients and the certainty of evidence was very low.

Conclusion

Attendance of prehospital critical care teams to patients with out-of-hospital cardiac arrest is associated with improved outcomes.
目的:评估院前重症监护小组与非重症监护小组对院外心脏骤停患者的临床结果。方法:本综述在PROSPERO前瞻性注册,入选标准遵循PICOST框架进行ILCOR系统评价。院前重症监护被定义为任何具有增强临床能力的提供者,超出标准的高级生命支持算法,并专门派遣重症患者。检索自成立至2024年4月20日的MEDLINE、Embase和CINAHL数据库。偏倚风险采用ROBINS-I工具评估,证据确定性采用GRADE方法评估。对来自中等偏倚风险研究的汇总数据进行荟萃分析,采用随机效应的通用反方差法。结果:检索结果为6444条,包括17篇文章,报告1192158例患者。三项研究报告了创伤患者,一项研究报告了儿科患者。所有的研究都是非随机的,其中15项具有中等偏倚风险。大多数研究包括院前医生(n = 16)。对于成人非创伤性患者,证据的确定性较低,院前重症监护与入院前生存率(OR 1.95, 95% CI 1.35-2.82)、出院前生存率(OR 1.34, 95% CI 1.10-1.63)、30天生存率(OR 1.56, 95% CI 1.38-1.75)和30天良好的神经预后(OR 1.48, 95% CI 1.19-1.84)相关。院前重症监护也与创伤和儿科患者预后的改善有关,证据的确定性非常低。结论:院前重症监护小组对院外心脏骤停患者的护理与改善预后相关。
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引用次数: 0
Respiratory metrics of neonatal positive pressure ventilation on different ventilatory rates: A simulation study
IF 2.1 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-01-01 DOI: 10.1016/j.resplu.2024.100860
Ming Zhou , Xiaohong Xi , Pu Zhao , Silu Wang , Fangfang Tao , Xiaoying Gu , Po-Yin Cheung , Jiang-Qin Liu

Background

Effective ventilation is the core of neonatal resuscitation (NR). T-piece resuscitators (TPR) and self-inflating bags (SIB) are the two most widely utilized resuscitation devices. Nevertheless, limited information is available regarding the respiratory metrics during NR with these devices.

Objectives

This study aimed to evaluate the respiratory metrics at different ventilatory rates (VR) using a TPR or SIB during NR training.

Methods

An observational, simulation study was conducted during a NR training course. The participants were instructed to perform positive pressure ventilation at predetermined pressures and varying rates using TPR and SIB. They were subsequently grouped into three categories based on their actual VR: 20–40 breaths per minute (bpm) (SlowVR), 40–60 bpm (StdVR), and 60–80 bpm (FastVR). Respiratory metrics were recorded and analyzed using a neonatal active lung model (NALM).

Results

Of the 71 participants in the training course, data from 66 were validated by analyzing 198 ventilations. In general, the participants manipulated the TPR slightly slower than the SIB. Notably, the positive end-expiratory pressure (PEEP) detected via TPR in the NALM was substantially higher, whereas the tidal volume (Tv) and minute volume (MV) with TPR were significantly smaller than those with SIB (p < 0.05). A significant decrease in the peak alveolar pressure (palva) was observed with faster TPR ventilation (p < 0.001), whereas no such reduction was observed with SIB (p = 0.103). Additionally, faster VR correlated positively with higher PEEP levels for both TPR (F = 7.543, p = 0.002) and SIB (F = 7.720, p = 0.002) and inversely with smaller Tv for both TPR (F = 19.239, p < 0.001) and SIB (F = 14.937, p < 0.001). However, no significant differences in MV were observed across the different VR for either TPR or SIB (both p > 0.05).

Conclusions

Faster VR were inversely associated with smaller Tv but increased PEEP in both devices. Despite the guidelines of NR, VR exceeding 60 bpm with TPR might sometimes be used, was associated with excessive PEEP in TPR, which may not be a safe in clinical practice. The effect of varying VR on MV was relatively minor for both TPR and SIB.
背景:有效通气是新生儿复苏(NR)的核心。T型复苏器(TPR)和自充气袋(SIB)是目前使用最广泛的两种复苏设备。然而,有关使用这些设备进行新生儿复苏时的呼吸指标的信息却很有限:本研究旨在评估 NR 培训期间使用 TPR 或 SIB 在不同通气速率 (VR) 下的呼吸指标:方法: 在 NR 培训课程中进行了一项观察性模拟研究。参与者在指导下使用 TPR 和 SIB 以预定压力和不同通气速率进行正压通气。随后根据他们的实际 VR 将他们分为三类:每分钟 20-40 次呼吸(bpm)(慢速 VR)、40-60 bpm(标准 VR)和 60-80 bpm(快速 VR)。使用新生儿主动肺模型(NALM)记录和分析呼吸指标:在参加培训课程的 71 名学员中,通过分析 198 次通气验证了 66 名学员的数据。总体而言,学员对 TPR 的操作略慢于对 SIB 的操作。值得注意的是,在 NALM 中通过 TPR 检测到的呼气末正压(PEEP)要高得多,而使用 TPR 时的潮气量(Tv)和分钟容量(MV)明显小于使用 SIB 时的潮气量和分钟容量(P 0.05):在两种设备中,较快的 VR 与较小的 Tv 成反比,但增加了 PEEP。尽管有 NR 指南,TPR 有时也可使用超过 60 bpm 的 VR,但这与 TPR 的 PEEP 过高有关,在临床实践中可能并不安全。对 TPR 和 SIB 而言,改变 VR 对 MV 的影响相对较小。
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引用次数: 0
The association between the type of bystander and survival after an out-of-hospital cardiac arrest: A French nationwide study
IF 2.1 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-01-01 DOI: 10.1016/j.resplu.2024.100858
Hizia Benkerrou , Marguerite Lockhart , Matthieu Heidet , Ramy Azzouz , Christian Vilhelm , Hervé Hubert , Morgan Recher , Valentine Baert , GR-RéAC

Background

Early bystander interventions are associated with more favorable outcomes after out-of-hospital cardiac arrest (OHCA). The objective of the present study was to determine whether the type of bystander-patient relationship was associated with survival and neurological outcomes after OHCA in France.

Methods

We analyzed data registered in the French National Cardiac Arrest Registry (RéAC) between July 1st, 2011, and April 30th, 2023. The study population comprised bystander-attended cases of OHCA managed by the emergency medical services. Bystanders were categorized as family members, other laypersons, off-duty professional first responders, or off-duty healthcare professionals. The primary outcome was 30-day survival with a favorable neurological outcome (Cerebral Performance Category 1 or 2). The secondary outcomes included the bystander cardiopulmonary resuscitation (CPR) initiation rate, return of spontaneous circulation, and survival upon admission to the hospital. Our statistical analyses were based on bivariate and multivariable logistic regressions analyses.

Results

Among the 89,861 OHCA cases analyzed, family members constituted the largest group of bystanders (69.2%). Compared with non-family-member bystanders, family bystander status was associated with a lower CPR initiation rate, a longer no-flow time, and lower 30-day survival rates. Specifically, cases of OHCA with non-family-member bystanders were 32% more likely to survive with a CPC of 1–2 at day 30 than cases with family member bystanders. Medically trained bystander status (off-duty professional first responders and healthcare professionals) was associated with higher CPR initiation and 30-day survival rates, relative to nontrained laypersons.

Conclusions

Survival after an OHCA appears to be associated with the type of bystander. Although family members were the most common bystanders, they were less likely to initiate CPR and less likely to see the OHCA patient survive. Efforts to increase the post-OHCA survival rate should include targeted interventions (such as public education and training programs) that emphasize the importance of early CPR and automated external defibrillator use by family members.
背景:院外心脏骤停(OHCA)后,旁观者的早期干预与更有利的预后有关。本研究旨在确定旁观者与患者关系的类型是否与法国院外心脏骤停患者的存活率和神经系统预后有关:我们分析了 2011 年 7 月 1 日至 2023 年 4 月 30 日期间在法国国家心脏骤停登记处 (RéAC) 登记的数据。研究对象包括由急救医疗服务部门处理的旁观者参与的 OHCA 病例。旁观者分为家庭成员、其他非专业人员、休班专业急救人员或休班医护人员。主要结果是 30 天存活率和良好的神经功能结果(脑功能 1 类或 2 类)。次要结果包括旁观者心肺复苏(CPR)启动率、自主循环恢复率和入院后存活率。我们的统计分析基于双变量和多变量逻辑回归分析:在分析的 89,861 例 OHCA 病例中,旁观者的最大群体是家庭成员(69.2%)。与非家属旁观者相比,家属旁观者身份与较低的心肺复苏启动率、较长的无血流时间和较低的 30 天存活率有关。具体来说,与有家庭成员旁观的 OHCA 病例相比,有非家庭成员旁观的 OHCA 病例在第 30 天 CPC 为 1-2 的存活率要高出 32%。接受过医疗培训的旁观者身份(非当班专业急救人员和医疗保健专业人员)与更高的心肺复苏启动率和30天存活率相关,而未接受过培训的非专业人员则与更高的心肺复苏启动率和30天存活率相关:结论:心脏骤停后的存活率似乎与旁观者的类型有关。尽管家人是最常见的旁观者,但他们启动心肺复苏术的可能性较低,看到心外HCA 患者存活的可能性也较低。要提高心外HCA后的存活率,应采取有针对性的干预措施(如公共教育和培训计划),强调家庭成员尽早实施心肺复苏术和使用自动体外除颤器的重要性。
{"title":"The association between the type of bystander and survival after an out-of-hospital cardiac arrest: A French nationwide study","authors":"Hizia Benkerrou ,&nbsp;Marguerite Lockhart ,&nbsp;Matthieu Heidet ,&nbsp;Ramy Azzouz ,&nbsp;Christian Vilhelm ,&nbsp;Hervé Hubert ,&nbsp;Morgan Recher ,&nbsp;Valentine Baert ,&nbsp;GR-RéAC","doi":"10.1016/j.resplu.2024.100858","DOIUrl":"10.1016/j.resplu.2024.100858","url":null,"abstract":"<div><h3>Background</h3><div>Early bystander interventions are associated with more favorable outcomes after out-of-hospital cardiac arrest (OHCA). The objective of the present study was to determine whether the type of bystander-patient relationship was associated with survival and neurological outcomes after OHCA in France.</div></div><div><h3>Methods</h3><div>We analyzed data registered in the French National Cardiac Arrest Registry (RéAC) between July 1st, 2011, and April 30th, 2023. The study population comprised bystander-attended cases of OHCA managed by the emergency medical services. Bystanders were categorized as family members, other laypersons, off-duty professional first responders, or off-duty healthcare professionals. The primary outcome was 30-day survival with a favorable neurological outcome (Cerebral Performance Category 1 or 2). The secondary outcomes included the bystander cardiopulmonary resuscitation (CPR) initiation rate, return of spontaneous circulation, and survival upon admission to the hospital. Our statistical analyses were based on bivariate and multivariable logistic regressions analyses.</div></div><div><h3>Results</h3><div>Among the 89,861 OHCA cases analyzed, family members constituted the largest group of bystanders (69.2%). Compared with non-family-member bystanders, family bystander status was associated with a lower CPR initiation rate, a longer no-flow time, and lower 30-day survival rates. Specifically, cases of OHCA with non-family-member bystanders were 32% more likely to survive with a CPC of 1–2 at day 30 than cases with family member bystanders. Medically trained bystander status (off-duty professional first responders and healthcare professionals) was associated with higher CPR initiation and 30-day survival rates, relative to nontrained laypersons.</div></div><div><h3>Conclusions</h3><div>Survival after an OHCA appears to be associated with the type of bystander. Although family members were the most common bystanders, they were less likely to initiate CPR and less likely to see the OHCA patient survive. Efforts to increase the post-OHCA survival rate should include targeted interventions (such as public education and training programs) that emphasize the importance of early CPR and automated external defibrillator use by family members.</div></div>","PeriodicalId":94192,"journal":{"name":"Resuscitation plus","volume":"21 ","pages":"Article 100858"},"PeriodicalIF":2.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11780125/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143070624","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
In situ simulation for cardiopulmonary resuscitation training: A systematic review
IF 2.1 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-01-01 DOI: 10.1016/j.resplu.2024.100863
Andrea Cortegiani , Mariachiara Ippolito , Cristian Abelairas-Gómez , Sabine Nabecker , Alexander Olaussen , Kasper G. Lauridsen , Yiqun Lin , Taylor Sawyer , Joyce Yeung , Andrew S. Lockey , Adam Cheng , Robert Greif

Objectives

To evaluate the effectiveness of in situ simulation for cardiopulmonary resuscitation (CPR) training on clinical and educational outcomes.

Methods

Randomised controlled trials (RCT) and non-randomised studies evaluating in situ simulation for cardiopulmonary resuscitation CPR training of healthcare workers in any setting compared to traditional training and reporting data on patients’ survival, patients’ outcomes, clinical performance and teamwork in actual or simulated resuscitation and resources needed were included. PubMed, Embase and Cochrane were searches from inception to October 28th 2024 (PROSPERO CRD42024521780). The assessment of risk of bias was done using RoB2 or ROBINS-I and the certainty of evidence was assessed by the GRADE approach. Meta-analysis was not possible due to significant heterogeneity in setting, interventions, control, and outcome definitions. The evidence was summarised according to the Synthesis Without Meta-Analysis (SwiM) reporting guidelines. No funding has been obtained.

Results

From 1062 records, 10 articles were included after full-text review (4 RCTs, 6 non-randomised). The risk of bias was judged as high or some concerns for RCTs and critical or serious for non-randomised studies. The certainty of evidence was very low for all the evaluated outcomes mainly due to risk of bias, inconsistency and imprecision. Two non-randomised studies reported data on patient survival, while two other non-randomized studies provided data on the review outcome of ’patient outcomes’, suggesting a potential benefit of in situ simulation or no difference. Four non-randomised studies reported improving or no difference in clinical performance in actual resuscitation. One study reported improved teamwork in actual resuscitation while another reported no difference. Most included studies reported improved clinical performance, teamwork and CPR skill in simulated resuscitation after in situ simulation training vs. traditional training. No study evaluated the resources needed.

Conclusion

The heterogenous evidence suggests that in situ simulation should be considered as an option for CPR training. The certainty of evidence is very low and cost-benefit balance is uncertain due to lack of data about resource needed.
{"title":"In situ simulation for cardiopulmonary resuscitation training: A systematic review","authors":"Andrea Cortegiani ,&nbsp;Mariachiara Ippolito ,&nbsp;Cristian Abelairas-Gómez ,&nbsp;Sabine Nabecker ,&nbsp;Alexander Olaussen ,&nbsp;Kasper G. Lauridsen ,&nbsp;Yiqun Lin ,&nbsp;Taylor Sawyer ,&nbsp;Joyce Yeung ,&nbsp;Andrew S. Lockey ,&nbsp;Adam Cheng ,&nbsp;Robert Greif","doi":"10.1016/j.resplu.2024.100863","DOIUrl":"10.1016/j.resplu.2024.100863","url":null,"abstract":"<div><h3>Objectives</h3><div>To evaluate the effectiveness of in situ simulation for cardiopulmonary resuscitation (CPR) training on clinical and educational outcomes.</div></div><div><h3>Methods</h3><div>Randomised controlled trials (RCT) and non-randomised studies evaluating in situ simulation for cardiopulmonary resuscitation CPR training of healthcare workers in any setting compared to traditional training and reporting data on patients’ survival, patients’ outcomes, clinical performance and teamwork in actual or simulated resuscitation and resources needed were included. PubMed, Embase and Cochrane were searches from inception to October 28th 2024 (PROSPERO CRD42024521780). The assessment of risk of bias was done using RoB2 or ROBINS-I and the certainty of evidence was assessed by the GRADE approach. Meta-analysis was not possible due to significant heterogeneity in setting, interventions, control, and outcome definitions. The evidence was summarised according to the Synthesis Without Meta-Analysis (SwiM) reporting guidelines. No funding has been obtained.</div></div><div><h3>Results</h3><div>From 1062 records, 10 articles were included after full-text review (4 RCTs, 6 non-randomised). The risk of bias was judged as high or some concerns for RCTs and critical or serious for non-randomised studies. The certainty of evidence was very low for all the evaluated outcomes mainly due to risk of bias, inconsistency and imprecision. Two non-randomised studies reported data on patient survival, while two other non-randomized studies provided data on the review outcome of ’patient outcomes’, suggesting a potential benefit of in situ simulation or no difference. Four non-randomised studies reported improving or no difference in clinical performance in actual resuscitation. One study reported improved teamwork in actual resuscitation while another reported no difference. Most included studies reported improved clinical performance, teamwork and CPR skill in simulated resuscitation after in situ simulation training vs. traditional training. No study evaluated the resources needed.</div></div><div><h3>Conclusion</h3><div>The heterogenous evidence suggests that in situ simulation should be considered as an option for CPR training. The certainty of evidence is very low and cost-benefit balance is uncertain due to lack of data about resource needed.</div></div>","PeriodicalId":94192,"journal":{"name":"Resuscitation plus","volume":"21 ","pages":"Article 100863"},"PeriodicalIF":2.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11787034/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143082736","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Not all shockable initial rhythms have the similar clinical outcome in cardiac arrest victims
IF 2.1 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-01-01 DOI: 10.1016/j.resplu.2024.100832
Ali Çoner, Can Ramazan Öncel, Cemal Köseoğlu
{"title":"Not all shockable initial rhythms have the similar clinical outcome in cardiac arrest victims","authors":"Ali Çoner,&nbsp;Can Ramazan Öncel,&nbsp;Cemal Köseoğlu","doi":"10.1016/j.resplu.2024.100832","DOIUrl":"10.1016/j.resplu.2024.100832","url":null,"abstract":"","PeriodicalId":94192,"journal":{"name":"Resuscitation plus","volume":"21 ","pages":"Article 100832"},"PeriodicalIF":2.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143098594","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Team resuscitation for paediatrics (TRAP); application and validation of a paediatric resuscitation quality instrument in non-simulated resuscitations 儿科团队复苏(TRAP);一种儿科复苏质量仪器在非模拟复苏中的应用与验证。
IF 2.1 Q3 CRITICAL CARE MEDICINE Pub Date : 2025-01-01 DOI: 10.1016/j.resplu.2024.100844
Shannon Flood , Michelle Alletag , Beth D’Amico , Sarah Halstead , Patrick Mahar , Laura Rochford , Geoffrey Markowitz , Jan Leonard , Lilliam Ambroggio , Tara Neubrand

Background

Resuscitation of paediatric cardiac and respiratory arrest is a high-stakes and low frequency event in the paediatric emergency department. Resuscitation team performance assessment tools have been developed and validated for use in the simulation environment, but no tool currently exists to evaluate clinical performance in non-simulated, live paediatric resuscitations.

Methods

This is a validation study assessing inter-rater reliability of a novel assessment tool of clinical performance of non-simulated resuscitations, the Team Resuscitation for Paediatrics tool. Videos of medical resuscitations at a tertiary care paediatric emergency department were collected and analysed over a 6-month period. Four paediatric emergency medicine attending physicians reviewed the videos and scored team performance based on the tool. Percent agreement and Fleiss’ Kappa were calculated in 3 subcategories: team communication, cardiac arrest and respiratory arrest. Percent agreement ranges were established a priori as > 80 % considered good and < 60 % poor.

Results

Of 51 resuscitations occurring during the study period, 24 met inclusion criteria. All subcategories demonstrated overall moderate agreement however individual items showed a wide range of agreement. Kappa scores were low on both individual items and overall. Three of four items on the team communication tool met criteria for good agreement, 12/34 items on the cardiac arrest tool met good agreement and 9/27 items on the respiratory arrest tool met good agreement.

Conclusion

This study demonstrated that development, application and testing of clinical tools to assess resuscitation team performance of non-simulated, video-recorded resuscitations is feasible, however, the Team Resuscitation for Paediatrics tool did not demonstrate adequate inter-rater reliability suggesting that further tool development may be necessary to better evaluate clinical resuscitation performance.
背景:小儿心脏和呼吸骤停的复苏是儿科急诊科高风险和低频率的事件。已经开发并验证了在模拟环境中使用的复苏团队绩效评估工具,但目前还没有工具用于评估非模拟的儿科活体复苏的临床绩效。方法:这是一项验证性研究,评估非模拟复苏临床表现的新型评估工具-儿科团队复苏工具的评级间可靠性。在6个月的时间里,收集和分析了三级护理儿科急诊科的医疗复苏录像。四名儿科急诊主治医生审查了视频,并根据该工具对团队绩效进行评分。在团队沟通、心脏骤停和呼吸骤停三个子类中计算一致性百分比和Fleiss’Kappa。结果:在研究期间发生的51例复苏中,24例符合纳入标准。所有子类别均表现出总体上的中等一致性,但个别项目表现出广泛的一致性。Kappa在单项和总体上的得分都很低。团队沟通工具的4个项目中有3个符合良好一致性标准,12/34的心脏骤停工具项目符合良好一致性,9/27的呼吸骤停工具项目符合良好一致性。结论:本研究表明,开发、应用和测试临床工具来评估非模拟、视频复苏团队的表现是可行的,然而,儿科团队复苏工具没有表现出足够的评级间可靠性,这表明进一步的工具开发可能是必要的,以更好地评估临床复苏表现。
{"title":"Team resuscitation for paediatrics (TRAP); application and validation of a paediatric resuscitation quality instrument in non-simulated resuscitations","authors":"Shannon Flood ,&nbsp;Michelle Alletag ,&nbsp;Beth D’Amico ,&nbsp;Sarah Halstead ,&nbsp;Patrick Mahar ,&nbsp;Laura Rochford ,&nbsp;Geoffrey Markowitz ,&nbsp;Jan Leonard ,&nbsp;Lilliam Ambroggio ,&nbsp;Tara Neubrand","doi":"10.1016/j.resplu.2024.100844","DOIUrl":"10.1016/j.resplu.2024.100844","url":null,"abstract":"<div><h3>Background</h3><div>Resuscitation of paediatric cardiac and respiratory arrest is a high-stakes and low frequency event in the paediatric emergency department. Resuscitation team performance assessment tools have been developed and validated for use in the simulation environment, but no tool currently exists to evaluate clinical performance in non-simulated, live paediatric resuscitations.</div></div><div><h3>Methods</h3><div>This is a validation study assessing inter-rater reliability of a novel assessment tool of clinical performance of non-simulated resuscitations, the Team Resuscitation for Paediatrics tool. Videos of medical resuscitations at a tertiary care paediatric emergency department were collected and analysed over a 6-month period. Four paediatric emergency medicine attending physicians reviewed the videos and scored team performance based on the tool. Percent agreement and Fleiss’ Kappa were calculated in 3 subcategories: team communication, cardiac arrest and respiratory arrest. Percent agreement ranges were established a priori as &gt; 80 % considered good and &lt; 60 % poor.</div></div><div><h3>Results</h3><div>Of 51 resuscitations occurring during the study period, 24 met inclusion criteria. All subcategories demonstrated overall moderate agreement however individual items showed a wide range of agreement. Kappa scores were low on both individual items and overall. Three of four items on the team communication tool met criteria for good agreement, 12/34 items on the cardiac arrest tool met good agreement and 9/27 items on the respiratory arrest tool met good agreement.</div></div><div><h3>Conclusion</h3><div>This study demonstrated that development, application and testing of clinical tools to assess resuscitation team performance of non-simulated, video-recorded resuscitations is feasible, however, the Team Resuscitation for Paediatrics tool did not demonstrate adequate inter-rater reliability suggesting that further tool development may be necessary to better evaluate clinical resuscitation performance.</div></div>","PeriodicalId":94192,"journal":{"name":"Resuscitation plus","volume":"21 ","pages":"Article 100844"},"PeriodicalIF":2.1,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11729005/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142981090","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Resuscitation plus
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