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体外膜肺氧合与有创通气治疗 COVID-19 急性呼吸窘迫综合征伴纵隔气肿患者的比较:一项队列研究。

Extracorporeal membrane oxygenation versus invasive ventilation in patients with COVID-19 acute respiratory distress syndrome and pneumomediastinum: A cohort trial.

机构信息

Department of Intensive Care, Brugmann University Hospital, Université Libre de Bruxelles, Brussels, Belgium.

Department of Internal Medicine, University Hospital of Patras, Patras, Greece.

出版信息

Artif Organs. 2024 Sep;48(9):1038-1048. doi: 10.1111/aor.14760. Epub 2024 Apr 25.

DOI:10.1111/aor.14760
PMID:38660764
Abstract

BACKGROUND

Patients with severe respiratory failure due to COVID-19 who are not under mechanical ventilation may develop severe hypoxemia when complicated with spontaneous pneumomediastinum (PM). These patients may be harmed by invasive ventilation. Alternatively, veno-venous (V-V) extracorporeal membrane oxygenation (ECMO) may be applied. We report on the efficacy of V-V ECMO and invasive ventilation as initial advanced respiratory support in patients with COVID-19 and acute respiratory failure due to spontaneous PM.

METHODS

This was a retrospective cohort study performed between March 2020 and January 2022. Enrolled patients had COVID-19 and acute respiratory failure due to spontaneous PM and were not invasively ventilated. Patients were treated in the intensive care unit (ICU) with invasive ventilation (invasive ventilation group) or V-V ECMO support (V-V ECMO group) as the main therapeutic option. The primary outcomes were mortality and ICU discharge at 90 days after ICU admission.

RESULTS

Twenty-two patients were included in this study (invasive ventilation group: 13 [59%]; V-V ECMO group: 9 [41%]). The V-V ECMO strategy was significantly associated with lower mortality (hazard ratio [HR] 0.33 [95% CI 0.12-0.97], p = 0.04). Five (38%) patients in the V-V ECMO group were intubated and eight (89%) patients in the invasive ventilation group required V-V ECMO support within 30 days from ICU admission. Three (33%) patients in the V-V ECMO group were discharged from ICU within 90 days compared to one (8%) patient in the invasive ventilation group (HR 4.71 [95% CI 0.48-45.3], p = 0.18).

CONCLUSIONS

Preliminary data suggest that V-V ECMO without invasive ventilation may improve survival in COVID-19-related acute respiratory failure due to spontaneous PM. The study's retrospective design and limited sample size underscore the necessity for additional investigation and warrant caution.

摘要

背景

因 COVID-19 导致严重呼吸衰竭但未行机械通气的患者,并发自发性纵隔气肿时可能会发生严重低氧血症。这些患者可能会因有创通气而受到伤害。或者,可以应用静脉-静脉(V-V)体外膜肺氧合(ECMO)。我们报告了 V-V ECMO 和有创通气作为 COVID-19 患者和自发性 PM 导致的急性呼吸衰竭的初始高级呼吸支持的疗效。

方法

这是一项回顾性队列研究,于 2020 年 3 月至 2022 年 1 月进行。入组患者患有 COVID-19 和自发性 PM 导致的急性呼吸衰竭,且未行有创通气。患者在重症监护病房(ICU)中接受治疗,主要治疗选择为有创通气(有创通气组)或 V-V ECMO 支持(V-V ECMO 组)。主要结局为 ICU 入住后 90 天的死亡率和 ICU 出院率。

结果

本研究共纳入 22 例患者(有创通气组:13 例[59%];V-V ECMO 组:9 例[41%])。V-V ECMO 策略与较低的死亡率显著相关(风险比[HR]0.33[95%CI 0.12-0.97],p=0.04)。V-V ECMO 组中有 5(38%)例患者需要气管插管,而有创通气组中有 8(89%)例患者在 ICU 入住后 30 天内需要 V-V ECMO 支持。V-V ECMO 组中有 3(33%)例患者在 90 天内从 ICU 出院,而有创通气组中只有 1(8%)例患者(HR 4.71[95%CI 0.48-45.3],p=0.18)。

结论

初步数据表明,无有创通气的 V-V ECMO 可能改善 COVID-19 相关自发性 PM 导致的急性呼吸衰竭的生存率。研究的回顾性设计和有限的样本量突出了进一步研究的必要性,并需谨慎对待。

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