2)增加值[SMD=1.87,95% CI(1.73,2.02),P<0.01]、二氧化碳分壓(pCO2)下降值[SMD=-0.91,95% CI(-1.03,-0.78),P<0.01]、第1秒用力呼氣量(FEV1)增加值[SMD=1.06,95% CI(0.87,1.25),P<0.01]均優(yōu)于對照組,且未增加藥物不良反應(yīng)發(fā)生率 [RR=1.50,95% CI(0.55,4.08),P>0.05]。結(jié)論 納美芬能顯著改善COPD并發(fā)Ⅱ型呼吸衰竭患者呼吸衰竭癥狀,改善肺功能。;Objective To systematically evaluate the efficacy and safety of nalmefene in the treatment of chronic obstructive pulmonary disease (COPD) complicated with type Ⅱ respiratory failure. Methods Data was retrieved from CNKI, VIP, Wanfang Data, CBM, PubMed, Web of Science, The Cochrane Library, Embase, Wiley Online Library until the 30 th January 2021. Screening a randomized controlled trial (RCT) of nalmefene (experimental group) vs naloxone or blank control (control group) in the treatment of COPD complicated with type Ⅱ respiratory failure. Two reviewers conducted independent quality evaluations for the included studies. After data extraction, RevMan 5.3 software was used for Meta-analysis. Results A total of 13 RCTs and 1 122 patients were included. Meta-analysis results showed that the nalmefene group in the clinical effective rate [RR= 1.22, 95%CI (1.15, 1.29), P<0.01], pH arise [SMD= 1.01, 95%CI (0.67, 1.34), P<0.01], pO2 arise [SMD= 1.87, 95%CI (1.73, 2.02), P<0.01], pCO2 decline [SMD= -0.91, 95%CI (-1.03, -0.78), P<0.01], FEV1 arise [SMD= 1.06, 95%CI (0.87, 1.25), P<0.01] were better than those of the control group, and the incidence of adverse drug reactions was not increased [RR= 1.50, 95%CI (0.55, 4.08), P>0.05]. Conclusion Nalmefene can significantly improve the respiratory symptoms of COPD patients with type Ⅱ respiratory failure, improve lung function."/>