Early reapplication of prone position during venovenous ECMO for acute respiratory distress syndrome: a prospective observational study and propensity-matched analysis.

IF 5.7 1区 医学 Q1 CRITICAL CARE MEDICINE
Rui Wang, Xiao Tang, Xuyan Li, Ying Li, Yalan Liu, Ting Li, Yu Zhao, Li Wang, Haichao Li, Meng Li, Hu Li, Zhaohui Tong, Bing Sun
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引用次数: 0

Abstract

Background: A combination of prone positioning (PP) and venovenous extracorporeal membrane oxygenation (VV-ECMO) is safe, feasible, and associated with potentially improved survival for severe acute respiratory distress syndrome (ARDS). However, whether ARDS patients, especially non-COVID-19 patients, placed in PP before VV-ECMO should continue PP after a VV-ECMO connection is unknown. This study aimed to test the hypothesis that early use of PP during VV-ECMO could increase the proportion of patients successfully weaned from ECMO support in severe ARDS patients who received PP before ECMO.

Methods: In this prospective observational study, patients with severe ARDS who were treated with VV-ECMO were divided into two groups: the prone group and the supine group, based on whether early PP was combined with VV-ECMO. The proportion of patients successfully weaned from VV-ECMO and 60-day mortality were analyzed before and after propensity score matching.

Results: A total of 165 patients were enrolled, 50 in the prone and 115 in the supine group. Thirty-two (64%) and 61 (53%) patients were successfully weaned from ECMO in the prone and the supine groups, respectively. The proportion of patients successfully weaned from VV-ECMO in the prone group tended to be higher, albeit not statistically significant. During PP, there was a significant increase in partial pressure of arterial oxygen (PaO2) without a change in ventilator or ECMO settings. Tidal impedance shifted significantly to the dorsal region, and lung ultrasound scores significantly decreased in the anterior and posterior regions. Forty-five propensity score-matched patients were included in each group. In this matched sample, the prone group had a higher proportion of patients successfully weaned from VV-ECMO (64.4% vs. 42.2%; P = 0.035) and lower 60-day mortality (37.8% vs. 60.0%; P = 0.035).

Conclusions: Patients with severe ARDS placed in PP before VV-ECMO should continue PP after VV-ECMO support. This approach could increase the probability of successful weaning from VV-ECMO.

Trial registration: ClinicalTrials.Gov: NCT04139733. Registered 23 October 2019.

Abstract Image

静脉 ECMO 治疗急性呼吸窘迫综合征期间早期重新采用俯卧位:一项前瞻性观察研究和倾向匹配分析。
背景:俯卧位(PP)与静脉体外膜肺氧合(VV-ECMO)相结合是安全、可行的,而且有可能提高重症急性呼吸窘迫综合征(ARDS)患者的存活率。然而,ARDS 患者,尤其是非 COVID-19 患者,在 VV-ECMO 连接之前接受 PP 治疗,是否应在 VV-ECMO 连接后继续接受 PP 治疗尚不清楚。本研究旨在验证一个假设,即在 VV-ECMO 期间尽早使用 PP 可提高在 ECMO 前接受 PP 的重症 ARDS 患者成功脱离 ECMO 支持的比例:在这项前瞻性观察研究中,根据早期 PP 是否与 VV-ECMO 联合使用,将接受 VV-ECMO 治疗的重度 ARDS 患者分为两组:俯卧组和仰卧组。对倾向评分匹配前后成功脱离 VV-ECMO 的患者比例和 60 天死亡率进行了分析:共有 165 名患者入组,其中俯卧位组 50 人,仰卧位组 115 人。俯卧位组和仰卧位组分别有 32 名(64%)和 61 名(53%)患者成功脱离 ECMO。俯卧位组成功脱离 VV-ECMO 的患者比例往往更高,尽管没有统计学意义。在 PP 期间,动脉血氧分压(PaO2)明显升高,但呼吸机或 ECMO 设置未发生变化。潮气阻抗明显向背侧区域移动,肺部超声评分在前侧和后侧区域明显下降。每组包括 45 名倾向评分匹配的患者。在这个匹配样本中,俯卧位组成功脱离VV-ECMO的患者比例更高(64.4% vs. 42.2%; P = 0.035),60天死亡率更低(37.8% vs. 60.0%; P = 0.035):结论:在 VV-ECMO 支持前使用 PP 的重度 ARDS 患者在 VV-ECMO 支持后应继续使用 PP。试验注册:试验注册:ClinicalTrials.Gov:NCT04139733。注册时间:2019 年 10 月 23 日。
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来源期刊
Annals of Intensive Care
Annals of Intensive Care CRITICAL CARE MEDICINE-
CiteScore
14.20
自引率
3.70%
发文量
107
审稿时长
13 weeks
期刊介绍: Annals of Intensive Care is an online peer-reviewed journal that publishes high-quality review articles and original research papers in the field of intensive care medicine. It targets critical care providers including attending physicians, fellows, residents, nurses, and physiotherapists, who aim to enhance their knowledge and provide optimal care for their patients. The journal's articles are included in various prestigious databases such as CAS, Current contents, DOAJ, Embase, Journal Citation Reports/Science Edition, OCLC, PubMed, PubMed Central, Science Citation Index Expanded, SCOPUS, and Summon by Serial Solutions.
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