• Int. J. Clin. Pract. · Mar 2021

    Meta Analysis

    High flow nasal cannula versus conventional oxygen therapy in postoperative patients at high risk for pulmonary complications: a systematic review and meta-analysis.

    • Gui-Ling Xiang, Qin-Han Wu, Liang Xie, Jie-Qiong Song, Xu Wu, Sheng-Yu Hao, Ming Zhong, and Shan-Qun Li.
    • Department of Pulmonary Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
    • Int. J. Clin. Pract. 2021 Mar 1; 75 (3): e13828.

    BackgroundThe effects of high flow nasal cannula (HFNC) on postoperative patients at high risk for pulmonary complications(PC) are controversial. We aimed to further determine the effectiveness of HFNC in postoperative patients at high risk for PC by comparison to conventional oxygen therapy (COT).MethodsWe performed a comprehensive search that compared HFNC with COT in postoperative patients at high risk for PC. The main outcomes were length of hospital stay (hospital LOS) and respiratory complications.ResultsSix trials with a total of 733 patients were pooled in our final studies. Except for Hospital LOS (I2  = 53%, χ2  = 8.51, P = .07) and rate of intubation or non-invasive ventilation (NIV) for respiratory failure (RF) (I2  = 49%, χ2  = 1.97, P = .16) between HFNC and COT, no significant heterogeneity was found in outcome measures. Compared with COT, HFNC was associated with a lower rate of intubation or NIV for RF (RR 0.23, 95% CI 0.08-0.66, P = .006) and rate of hypercapnia (RR 0.37, 95% CI 0.20-0.68, P = .002). As for the Hospital LOS, ICU LOS, rate of requirement of O2 after discontinuous and hypoxemia, HFNC did not show any advantage over COT. Trial Sequential Analysis (TSA) for Hospital LOS showed that monitoring boundaries were finally not surpassed and required information size (RIS) was not met.ConclusionsThe available randomised controlled trials (RCTs) suggest that, among the postoperative patients at high risk for PC, HFNC therapy compared with the COT significantly reduces rate of incubation or NIV for RF and rate of hypercapnia, meanwhile is safely administered. Further large-scale, multicenter, randomised and controlled studies are needed to confirm our results.© 2020 John Wiley & Sons Ltd.

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