Department of Pharmacy, University of Huddersfield, Huddersfield, HD1 3DH, UK.
School of Postgraduate Studies, International Medical University, Kuala Lumpur, 57000, Malaysia.
Am J Cardiovasc Drugs. 2020 Dec;20(6):571-590. doi: 10.1007/s40256-020-00439-5. Epub 2020 Sep 12.
The use of renin-angiotensin system (RAS) inhibitors, including angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs), was alleged to cause a more severe course of novel coronavirus disease 2019 (COVID-19).
We systematically reviewed the published studies to assess the association of RAS inhibitors with mortality as well as disease severity in COVID-19 patients. A systematic literature search was performed to retrieve relevant original studies investigating mortality and severity (severe/critical disease) in COVID-19 patients with and without exposure to RAS inhibitors.
A total of 59 original studies were included for qualitative synthesis. Twenty-four studies that reported adjusted effect sizes (24 studies reported mortality outcomes and 16 studies reported disease severity outcomes), conducted in RAS inhibitor-exposed and unexposed groups, were pooled in random-effects models to estimate overall risk. Quality assessment of studies revealed that most of the studies included were of fair quality. The use of an ACEI/ARB in COVID-19 patients was significantly associated with lower odds (odds ratio [OR] = 0.73, 95% confidence interval [CI] 0.56-0.95; n = 18,749) or hazard (hazard ratio [HR] = 0.75, 95% CI 0.60-0.95; n = 26,598) of mortality compared with non-use of ACEI/ARB. However, the use of an ACEI/ARB was non-significantly associated with lower odds (OR = 0.91, 95% CI 0.75-1.10; n = 7446) or hazard (HR = 0.73, 95% CI 0.33-1.66; n = 6325) of developing severe/critical disease compared with non-use of an ACEI/ARB.
Since there was no increased risk of harm, the use of RAS inhibitors for hypertension and other established clinical indications can be maintained in COVID-19 patients.
有人声称,肾素-血管紧张素系统(RAS)抑制剂的使用,包括血管紧张素转换酶抑制剂(ACEI)和血管紧张素受体阻滞剂(ARB),会导致新型冠状病毒病 2019(COVID-19)的病程更严重。
我们系统地回顾了已发表的研究,以评估 RAS 抑制剂与 COVID-19 患者死亡率以及疾病严重程度的关系。我们进行了系统的文献检索,以检索调查 COVID-19 患者在使用和未使用 RAS 抑制剂情况下的死亡率和严重程度(严重/危重症)的相关原始研究。
共有 59 项原始研究被纳入定性综合分析。共有 24 项研究报告了调整后的效应量(24 项研究报告了死亡率结果,16 项研究报告了疾病严重程度结果),这些研究在暴露于和未暴露于 RAS 抑制剂的组中进行,被汇总在随机效应模型中以估计总体风险。研究质量评估显示,大多数纳入的研究质量为中等。与不使用 ACEI/ARB 相比,COVID-19 患者使用 ACEI/ARB 与较低的死亡风险(比值比 [OR] = 0.73,95%置信区间 [CI] 0.56-0.95;n = 18749)或较低的死亡风险(风险比 [HR] = 0.75,95% CI 0.60-0.95;n = 26598)显著相关。然而,与不使用 ACEI/ARB 相比,使用 ACEI/ARB 与较低的发病风险(OR = 0.91,95% CI 0.75-1.10;n = 7446)或较低的发病风险(HR = 0.73,95% CI 0.33-1.66;n = 6325)无关。
由于没有增加的风险,RAS 抑制剂可用于治疗高血压和其他已确立的临床适应证,在 COVID-19 患者中可以继续使用。