Association of vasopressors with mortality in critically ill patients with COVID-19: a systematic review and meta-analysis

Maria Mermiri, Georgios Mavrovounis, Eleni Laou, Nikolaos Papagiannakis, Ioannis Pantazopoulos, Athanasios Chalkias
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Abstract

Exogenous catecholamines may have pronounced side effects and affect physiological cascades. The aim of this study was to investigate the effect of vasopressors on mortality of critically ill patients with coronavirus disease 2019 (COVID-19). A systematic search of PubMed, Scopus, and ClinicalTrials.gov was conducted for relevant articles until December 2022. Eligibility criteria were randomized controlled and non-randomized trials. The primary outcome was in-hospital and 30-day mortality. The quality of studies was assessed using the Methodological Index for Non-Randomized Studies (MINORS) tool, while paired meta-analysis was used to estimate the pooled risk ratios (RR) along with their 95% Confidence Interval (95% CI). Analyses of 22 studies (n = 8034) revealed that vasopressor use is associated with mortality compared to no vasopressor therapy [RR (95%CI): 4.30 (3.21, 5.75); p < 0.001]. In-hospital and 30-day mortality are significantly higher in patients who receive vasopressors [RR (95%CI): 4.60 (2.47, 8.55); p < 0.001 and RR (95%CI): 2.97 (1.72, 5.14); p < 0.001, respectively]. Also, analyses of data from 10 studies (n = 3519) revealed that vasopressor use is associated with acute kidney injury [RR (95%CI): 3.17 (2.21, 4.54); p < 0.001]. In conclusion, current use of vasopressors in critically ill patients with COVID-19 may be associated with higher in-hospital mortality, 30-day mortality, and incidence rate of acute kidney injury. Further research is required to estimate the correlation of specific vasopressor characteristics (type, timing, dose, combination) with adverse effects and mortality in this population.

Graphical Abstract

血管加压药与 COVID-19 重症患者死亡率的关系:系统回顾与荟萃分析
外源性儿茶酚胺可能会产生明显的副作用并影响生理级联。本研究旨在探讨血管加压剂对 2019 年冠状病毒病(COVID-19)重症患者死亡率的影响。在PubMed、Scopus和ClinicalTrials.gov上系统检索了截至2022年12月的相关文章。资格标准为随机对照试验和非随机试验。主要结果为住院和 30 天死亡率。研究质量采用非随机研究方法学指数(MINORS)工具进行评估,同时采用配对荟萃分析法估算汇总风险比(RR)及其 95% 置信区间(95% CI)。对 22 项研究(n = 8034)的分析表明,与不使用血管加压疗法相比,使用血管加压疗法与死亡率相关[RR (95%CI): 4.30 (3.21, 5.75); p < 0.001]。接受血管加压疗法的患者的院内死亡率和 30 天死亡率明显更高[RR (95%CI): 4.60 (2.47, 8.55); p <0.001,RR (95%CI): 2.97 (1.72, 5.14); p <0.001]。此外,对 10 项研究(n = 3519)的数据进行分析后发现,使用血管加压素与急性肾损伤有关[RR (95%CI): 3.17 (2.21, 4.54); p <0.001]。总之,目前 COVID-19 重症患者使用血管加压药可能与较高的院内死亡率、30 天死亡率和急性肾损伤发病率有关。需要进一步开展研究,以估计血管加压剂的具体特征(类型、时间、剂量、组合)与该人群的不良反应和死亡率之间的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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