Mermiri Maria, Mavrovounis Georgios, Laou Eleni, Papagiannakis Nikolaos, Pantazopoulos Ioannis, Chalkias Athanasios
Department of Anesthesiology, Faculty of Medicine, University of Thessaly, 41110 Larisa, Biopolis Greece.
Department of Emergency Medicine, Faculty of Medicine, University of Thessaly, Larisa, Greece.
Anesthesiol Perioper Sci. 2023;1(2):10. doi: 10.1007/s44254-023-00013-7. Epub 2023 Apr 23.
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 ( = 8034) revealed that vasopressor use is associated with mortality compared to no vasopressor therapy [RR (95%CI): 4.30 (3.21, 5.75); < 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); < 0.001 and RR (95%CI): 2.97 (1.72, 5.14); < 0.001, respectively]. Also, analyses of data from 10 studies ( = 3519) revealed that vasopressor use is associated with acute kidney injury [RR (95%CI): 3.17 (2.21, 4.54); < 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.
The online version contains supplementary material available at 10.1007/s44254-023-00013-7.
外源性儿茶酚胺可能有明显的副作用并影响生理级联反应。本研究的目的是调查血管升压药对2019冠状病毒病(COVID-19)危重症患者死亡率的影响。截至2022年12月,对PubMed、Scopus和ClinicalTrials.gov进行了系统检索以查找相关文章。纳入标准为随机对照试验和非随机试验。主要结局是住院死亡率和30天死亡率。使用非随机研究方法学指数(MINORS)工具评估研究质量,同时采用配对荟萃分析来估计合并风险比(RR)及其95%置信区间(95%CI)。对22项研究(n = 8034)的分析显示,与未使用血管升压药治疗相比,使用血管升压药与死亡率相关[RR(95%CI):4.30(3.21,5.75);P < 0.001]。接受血管升压药治疗的患者住院死亡率和30天死亡率显著更高[RR(95%CI):4.60(2.47,8.55);P < 0.001和RR(95%CI):2.97(1.72,5.14);P < 0.001,分别]。此外,对10项研究(n = 3519)的数据分析显示,使用血管升压药与急性肾损伤相关[RR(95%CI):3.17(2.21,4.54);P < 0.001]。总之,目前在COVID-19危重症患者中使用血管升压药可能与更高的住院死亡率、30天死亡率以及急性肾损伤发生率相关。需要进一步研究来评估特定血管升压药特征(类型、时机、剂量、联合使用)与该人群不良反应和死亡率之间的相关性。
在线版本包含可在10.1007/s44254-023-00013-7获取的补充材料。