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北美德尔塔和奥密克戎疫情期间新冠病毒肺炎的体外膜肺氧合治疗

Extracorporeal Membrane Oxygenation for COVID-19 During the Delta and Omicron Waves in North America.

作者信息

Hickey Andrew J, Greendyk Richard, Cummings Matthew J, Abrams Darryl, O'Donnell Max R, Rackley Craig R, Barbaro Ryan P, Brodie Daniel, Agerstrand Cara

机构信息

From the Division of Pulmonology and Sleep Medicine, Department of Medicine, Atrium Health Pulmonology and Sleep Medicine, Atrium Health, Charlotte, North Carolina.

Division of Pulmonary, Allergy, and Critical Care Medicine, Columbia University Irving Medical Center, New York, New York.

出版信息

ASAIO J. 2025 Apr 1;71(4):325-331. doi: 10.1097/MAT.0000000000002334. Epub 2024 Oct 22.

Abstract

Clinical outcomes for patients with severe acute respiratory failure caused by different variants of the coronavirus disease 2019 (COVID-19) supported with extracorporeal membrane oxygenation (ECMO) are incompletely understood. Clinical characteristics, pre-ECMO management, and hospital mortality at 90 days for adults with COVID-19 who received venovenous ECMO (VV-ECMO) at North American centers during waves predominated by Delta (August 16 to December 12, 2021) and Omicron (January 31 to May 31, 2022) severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants were compared in a competing risks framework. One thousand seven hundred and sixty-six patients (1,580 Delta, 186 Omicron) received VV-ECMO for COVID-19 during the Delta- and Omicron-predominant waves in North American centers. In the unadjusted competing risks model, no significant difference was observed in risk of hospital mortality at 90 days between patients during the Delta- versus Omicron-predominant wave (subhazard ratio [sHR], 0.94; 95% confidence interval [CI], 0.74-1.19), but patients supported with VV-ECMO during the Omicron-predominant wave had a significantly lower adjusted risk of hospital mortality at 90 days (subhazard ratio, 0.71; 95% CI, 0.51-0.99). Patients receiving VV-ECMO during the Omicron-predominant wave had a similar unadjusted risk of hospital mortality at 90 days, but a significantly lower adjusted risk of hospital mortality at 90 days than those receiving VV-ECMO during the Delta-predominant wave.

摘要

对于由2019冠状病毒病(COVID-19)不同变体引起的严重急性呼吸衰竭患者,在体外膜肺氧合(ECMO)支持下的临床结局尚未完全明确。在竞争风险框架下,比较了北美各中心在以德尔塔(2021年8月16日至12月12日)和奥密克戎(2022年1月31日至5月31日)为主的疫情期间,接受静脉-静脉ECMO(VV-ECMO)治疗的COVID-19成年患者的临床特征、ECMO前管理及90天的医院死亡率。在北美各中心,1766例患者(1580例德尔塔变体感染、186例奥密克戎变体感染)在以德尔塔和奥密克戎为主的疫情期间因COVID-19接受了VV-ECMO治疗。在未调整的竞争风险模型中,在以德尔塔为主的疫情期间与以奥密克戎为主的疫情期间的患者之间,90天医院死亡率风险未观察到显著差异(亚风险比[sHR],0.94;95%置信区间[CI],0.74 - 1.19),但在以奥密克戎为主的疫情期间接受VV-ECMO支持的患者90天医院死亡率的调整风险显著更低(亚风险比,0.71;95%CI,0.51 - 0.99)。在以奥密克戎为主的疫情期间接受VV-ECMO治疗的患者90天医院死亡率的未调整风险相似,但90天医院死亡率的调整风险显著低于在以德尔塔为主的疫情期间接受VV-ECMO治疗的患者。

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