Columbia University Vagelos College of Physicians and Surgeons, Columbia University, New York City, NY, United States of America.
Massachusetts General Hospital, Harvard Medical School, Harvard University, Boston, MA, United States of America.
PLoS One. 2021 Nov 4;16(11):e0259514. doi: 10.1371/journal.pone.0259514. eCollection 2021.
Famotidine is a competitive histamine H2-receptor antagonist most commonly used for gastric acid suppression but thought to have potential efficacy in treating patients with Coronavirus disease 2019 (COVID-19). The aims of this systematic review and meta-analysis are to summarize the current literature and report clinical outcomes on the use of famotidine for treatment of hospitalized patients with COVID-19.
Five databases were searched through February 12, 2021 to identify observational studies that reported on associations of famotidine use with outcomes in COVID-19. Meta-analysis was conducted for composite primary clinical outcome (e.g. rate of death, intubation, or intensive care unit admissions) and death separately, where either aggregate odds ratio (OR) or hazard ratio (HR) was calculated.
Four studies, reporting on 46,435 total patients and 3,110 patients treated with famotidine, were included in this meta-analysis. There was no significant association between famotidine use and composite outcomes in patients with COVID-19: HR 0.63 (95% CI: 0.35, 1.16). Across the three studies that reported mortality separated from other endpoints, there was no association between famotidine use during hospitalization and risk of death-HR 0.67 (95% CI: 0.26, 1.73) and OR 0.79 (95% CI: 0.19, 3.34). Heterogeneity ranged from 83.69% to 88.07%.
Based on the existing observational studies, famotidine use is not associated with a reduced risk of mortality or combined outcome of mortality, intubation, and/or intensive care services in hospitalized individuals with COVID-19, though heterogeneity was high, and point estimates suggested a possible protective effect for the composite outcome that may not have been observed due to lack of power. Further randomized controlled trials (RCTs) may help determine the efficacy and safety of famotidine as a treatment for COVID-19 patients in various care settings of the disease.
法莫替丁是一种竞争性的组胺 H2 受体拮抗剂,最常用于抑制胃酸,但被认为对治疗 2019 年冠状病毒病(COVID-19)患者具有潜在疗效。本系统评价和荟萃分析的目的是总结目前的文献,并报告使用法莫替丁治疗 COVID-19 住院患者的临床结果。
通过 2021 年 2 月 12 日检索了 5 个数据库,以确定报告法莫替丁使用与 COVID-19 患者结局相关性的观察性研究。对复合主要临床结局(例如死亡率、插管或重症监护病房入院率)和死亡率分别进行荟萃分析,其中计算了总比值比(OR)或风险比(HR)。
共有 4 项研究,涉及 46435 名总患者和 3110 名接受法莫替丁治疗的患者,纳入了本荟萃分析。法莫替丁的使用与 COVID-19 患者的复合结局之间无显著相关性:HR 0.63(95%CI:0.35,1.16)。在报告死亡率与其他结局分开的三项研究中,住院期间使用法莫替丁与死亡风险无相关性:HR 0.67(95%CI:0.26,1.73)和 OR 0.79(95%CI:0.19,3.34)。异质性范围为 83.69%至 88.07%。
根据现有的观察性研究,法莫替丁的使用与 COVID-19 住院患者的死亡率或死亡率、插管和/或重症监护服务的复合结局降低风险无关,尽管异质性较高,且点估计值表明对复合结局可能存在保护作用,但由于缺乏效力,可能未观察到。进一步的随机对照试验(RCT)可能有助于确定法莫替丁在 COVID-19 患者各种疾病治疗环境中的疗效和安全性。