住院呼吸系统疾病患者的高流量鼻氧疗法与传统氧疗的比较:系统综述和荟萃分析。

IF 3.6 3区 医学 Q1 RESPIRATORY SYSTEM
Daniel Seow, Yet H Khor, Su-Wei Khung, David M Smallwood, Yvonne Ng, Amy Pascoe, Natasha Smallwood
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引用次数: 0

摘要

背景:高流量鼻氧疗法(HFNO)被广泛用于治疗急性呼吸衰竭(ARF)患者。本系统综述旨在总结有关高流量鼻氧疗法与传统氧疗(COT)相比对急性呼吸衰竭患者的益处的证据:于 2023 年 3 月 22 日检索了三个数据库(Embase、Medline 和 CENTRAL),以评估高频硝化氧治疗与传统氧疗相比在治疗 ARF 方面的效果,主要结果为住院死亡率,次要结果包括(但不限于)升级为有创机械通气(IMV)或无创通气(NIV)。偏倚风险采用 Cochrane 偏倚风险工具(随机对照试验 (RCT))、ROBINS-I(非随机对照试验)或纽卡斯尔-渥太华量表(观察性研究)进行评估。在进行主要分析时,将随机对照试验和观察性研究集中在一起;在进行次要分析时,仅使用随机对照试验数据。采用随机效应模型对治疗效果进行汇总:共纳入 63 项研究(26 项研究性临床试验、13 项交叉研究和 24 项观察性研究),共有 10 230 名参与者。对于所有原因引起的急性心力衰竭,HFNO 和 COT 在住院死亡率这一主要结果上没有明显差异(风险比 RR 1.08,95% CI 0.93 至 1.26;P=0.29;17 项研究,n=5887)。然而,与COT相比,HFNO显著降低了升级至IMV的总体需求(RR 0.85,95% CI 0.76至0.95;P=0.003;39项研究,n=8932);以及升级至NIV的总体需求(RR 0.70,95% CI 0.50至0.98;P=0.04;16项研究,n=3076)。在亚组分析中,当考虑到患者的疾病类型时,与COT相比,接受HFNO治疗的急性-慢性呼吸衰竭患者的院内死亡率显著降低(RR为0.58,95% CI为0.37至0.91;P=0.02):讨论:HFNO在减少对IMV和NIV的升级需求方面优于COT,但对住院死亡率这一主要结果没有影响。这些研究结果支持将 HFNO 作为 ARF 一线疗法的建议:CRD42021264837。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-flow nasal oxygen therapy compared with conventional oxygen therapy in hospitalised patients with respiratory illness: a systematic review and meta-analysis.

Background: High-flow nasal oxygen therapy (HFNO) is used in diverse hospital settings to treat patients with acute respiratory failure (ARF). This systematic review aims to summarise the evidence regarding any benefits HFNO therapy has compared with conventional oxygen therapy (COT) for patients with ARF.

Methods: Three databases (Embase, Medline and CENTRAL) were searched on 22 March 2023 for studies evaluating HFNO compared with COT for the treatment of ARF, with the primary outcome being hospital mortality and secondary outcomes including (but not limited to) escalation to invasive mechanical ventilation (IMV) or non-invasive ventilation (NIV). Risk of bias was assessed using the Cochrane risk-of-bias tool (randomised controlled trials (RCTs)), ROBINS-I (non-randomised trials) or Newcastle-Ottawa Scale (observational studies). RCTs and observational studies were pooled together for primary analyses, and secondary analyses used RCT data only. Treatment effects were pooled using the random effects model.

Results: 63 studies (26 RCTs, 13 cross-over and 24 observational studies) were included, with 10 230 participants. There was no significant difference in the primary outcome of hospital mortality (risk ratio, RR 1.08, 95% CI 0.93 to 1.26; p=0.29; 17 studies, n=5887) between HFNO and COT for all causes ARF. However, compared with COT, HFNO significantly reduced the overall need for escalation to IMV (RR 0.85, 95% CI 0.76 to 0.95 p=0.003; 39 studies, n=8932); and overall need for escalation to NIV (RR 0.70, 95% CI 0.50 to 0.98; p=0.04; 16 studies, n=3076). In subgroup analyses, when considering patients by illness types, those with acute-on-chronic respiratory failure who received HFNO compared with COT had a significant reduction in-hospital mortality (RR 0.58, 95% CI 0.37 to 0.91; p=0.02).

Discussion: HFNO was superior to COT in reducing the need for escalation to both IMV and NIV but had no impact on the primary outcome of hospital mortality. These findings support recommendations that HFNO may be considered as first-line therapy for ARF.

Prospero registration number: CRD42021264837.

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来源期刊
BMJ Open Respiratory Research
BMJ Open Respiratory Research RESPIRATORY SYSTEM-
CiteScore
6.60
自引率
2.40%
发文量
95
审稿时长
12 weeks
期刊介绍: BMJ Open Respiratory Research is a peer-reviewed, open access journal publishing respiratory and critical care medicine. It is the sister journal to Thorax and co-owned by the British Thoracic Society and BMJ. The journal focuses on robustness of methodology and scientific rigour with less emphasis on novelty or perceived impact. BMJ Open Respiratory Research operates a rapid review process, with continuous publication online, ensuring timely, up-to-date research is available worldwide. The journal publishes review articles and all research study types: Basic science including laboratory based experiments and animal models, Pilot studies or proof of concept, Observational studies, Study protocols, Registries, Clinical trials from phase I to multicentre randomised clinical trials, Systematic reviews and meta-analyses.
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