Yamamoto Ryohei, Sugimura Sosuke, Kikuyama Kazuki, Takayama Chihiro, Fujimoto Junichi, Yamashita Koichi, Norisue Yasuhiro, Narita Chihiro
Department of Healthcare Epidemiology, School of Public Health, Graduate School of Medicine, Kyoto University, Kyoto, JPN.
Department of Medical Engineering, Faculty of Health Care Science, Himeji Dokkyo University, Hyogo, JPN.
Cureus. 2022 Jul 18;14(7):e26957. doi: 10.7759/cureus.26957. eCollection 2022 Jul.
Previous systematic reviews and meta-analyses assessing the pooled effects of higher positive end-expiratory pressure (PEEP) failed to show significantly reduced mortality in patients with acute respiratory distress syndrome (ARDS). Some new randomized controlled trials (RCTs) have been reported and an updated systematic review is needed to evaluate the use of higher PEEP in patients with ARDS. We searched MEDLINE, Cochrane Central Register of Controlled Trials (CENTRAL), EMBASE, Cumulative Index to Nursing and Allied Health Literature (CINAHL), Igaku-Chuo-Zasshi, ICTRP, the National Institute of Health Clinical Trials Register, and the reference list of recent guidelines. We included RCTs to compare the higher PEEP ventilation strategy with the lower strategy in patients with ARDS. Two authors independently assessed the eligibility of the studies and extracted the data. The primary outcomes were 28-day mortality. The GRADE (Grading of Recommendations, Assessment, Development, and Evaluations) methodology was used to evaluate the certainty of the evidence. Among the 6530 screened records, 16 randomized trials involving 4150 patients were included in our meta-analysis. When comparing higher PEEP versus lower PEEP, the pooled risk ratio (RR) for 28-day mortality was 0.85 (15 studies, n=4108, 95% CI 0.72 to 1.00, I=58%, low certainty of evidence). Subgroup analysis by study participants with a low tidal volume (LTV) strategy showed an interaction (P for interaction, 0.001). Our study showed that in patients with ARDS, the use of higher PEEP did not significantly reduce 28-day mortality compared to the use of lower PEEP.
以往评估较高呼气末正压(PEEP)综合效应的系统评价和荟萃分析未能显示急性呼吸窘迫综合征(ARDS)患者的死亡率显著降低。已有一些新的随机对照试验(RCT)报告,因此需要进行更新的系统评价来评估在ARDS患者中使用较高PEEP的情况。我们检索了MEDLINE、Cochrane对照试验中心注册库(CENTRAL)、EMBASE、护理学与健康相关文献累积索引(CINAHL)、《医学中央杂志》、国际临床试验注册平台(ICTRP)、美国国立卫生研究院临床试验注册库以及近期指南的参考文献列表。我们纳入了比较ARDS患者较高PEEP通气策略与较低PEEP通气策略的RCT。两位作者独立评估研究的纳入资格并提取数据。主要结局为28天死亡率。采用GRADE(推荐分级、评估、制定和评价)方法评估证据的确定性。在筛查的6530条记录中,我们的荟萃分析纳入了16项涉及4150例患者的随机试验。比较较高PEEP与较低PEEP时,28天死亡率的合并风险比(RR)为0.85(15项研究,n = 4108,95%CI 0.72至1.00,I² = 58%,证据确定性低)。对采用低潮气量(LTV)策略的研究参与者进行的亚组分析显示存在交互作用(交互作用P值为0.001)。我们的研究表明,在ARDS患者中,与使用较低PEEP相比,使用较高PEEP并不能显著降低28天死亡率。