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非插管 COVID-19 急性低氧性呼吸衰竭患者清醒俯卧位治疗效果的系统评价和荟萃分析。

Effect of Awake Prone Positioning in non-Intubated COVID-19 Patients with Acute Hypoxemic Respiratory Failure: A Systematic Review and Meta-Analysis.

机构信息

Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine, 74639Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.

出版信息

J Intensive Care Med. 2022 Nov;37(11):1493-1503. doi: 10.1177/08850666221121593. Epub 2022 Aug 25.

Abstract

BACKGROUND

Awake prone positioning (APP) has been considered as a feasible treatment for patients with acute hypoxemic respiratory failure in non-intubated coronavirus disease 2019 (COVID-19). However, the efficacy and safety of APP remain uncertain. This meta-analysis aims to assess the effect of APP on intubation rate and mortality in COVID-19 patients with acute respiratory failure.

METHODS

Relevant studies published from January 1, 2020, to June 17, 2022, were systematically searched. The primary outcomes were the intubation rate and mortality; the secondary outcome was the incidence of adverse events.

RESULTS

Of 5746 identified publications, 22 were eligible for inclusion in the meta-analysis (N = 5146 patients). In comparison to the non-APP group, APP could decrease the intubation rates (OR 0.64; 95% CI 0.48-0.83;  = .001), particularly in the subgroup of the daily median duration of APP > 8 h and in the subgroup of receiving high flow nasal cannula (HFNC) or non-invasive ventilation (NIV). Patients treated with APP were associated with lower mortality rates (OR 0.61; 95% CI 0.45-0.81;  = .0008), but no mortality benefit was found in the APP group in the subgroup of randomized controlled trials (RCTs). No significant difference was found in the incidence of adverse events between the groups (OR 1.13; 95% CI 0.75-1.71;  = .56).

CONCLUSION

Our results demonstrated that APP could be an effective strategy to avoid intubation without detrimental effects in non-intubated patients with COVID-19, especially for patients requiring HFNC or NIV, and the daily APP duration with the target of minimally eight hours was suggested. In the subgroup of RCTs, the pooled results did not demonstrate any benefit of APP on mortality. Given the limited number of RCTs, further high-quality RCTs are needed to confirm the results.

INPLASY REGISTRATION NUMBER

INPLASY2021110037.

摘要

背景

清醒俯卧位(APP)已被认为是一种可行的治疗方法,用于非插管的 2019 年冠状病毒病(COVID-19)急性低氧性呼吸衰竭患者。然而,APP 的疗效和安全性仍不确定。本荟萃分析旨在评估 APP 对 COVID-19 急性呼吸衰竭患者插管率和死亡率的影响。

方法

系统检索了 2020 年 1 月 1 日至 2022 年 6 月 17 日发表的相关研究。主要结局是插管率和死亡率;次要结局是不良事件的发生率。

结果

在 5746 篇鉴定文献中,22 篇符合纳入荟萃分析的条件(N=5146 例患者)。与非 APP 组相比,APP 可降低插管率(OR 0.64;95%CI 0.48-0.83;=0.001),特别是在 APP 每日中位持续时间>8 小时的亚组和接受高流量鼻导管(HFNC)或无创通气(NIV)的亚组。接受 APP 治疗的患者死亡率较低(OR 0.61;95%CI 0.45-0.81;=0.0008),但在随机对照试验(RCT)亚组中,APP 组并未发现死亡率获益。两组不良事件发生率无显著差异(OR 1.13;95%CI 0.75-1.71;=0.56)。

结论

我们的结果表明,APP 可能是一种有效的策略,可以避免非插管 COVID-19 患者插管,且不会产生有害影响,尤其是对于需要 HFNC 或 NIV 的患者,建议 APP 每日持续时间达到 8 小时的目标。在 RCT 亚组中,汇总结果并未显示 APP 对死亡率有任何益处。鉴于 RCT 数量有限,需要进一步开展高质量的 RCT 来证实这些结果。

INPLASY 注册号:INPLASY2021110037。

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