Vicerrectorado de Investigación, Universidad San Ignacio de Loyola, Lima, Peru.
Programa de Atención Domiciliaria - EsSalud, Lima, Peru.
Pharmacoepidemiol Drug Saf. 2021 Jun;30(6):694-706. doi: 10.1002/pds.5234. Epub 2021 Apr 3.
Hydroxychloroquine, chloroquine, azithromycin, and lopinavir/ritonavir are drugs that were used for the treatment of coronavirus disease 2019 (COVID-19) during the early pandemic period. It is well-known that these agents can prolong the QTc interval and potentially induce Torsades de Pointes (TdP). We aim to assess the prevalence and risk of QTc prolongation and arrhythmic events in COVID-19 patients treated with these drugs.
We searched electronic databases from inception to September 30, 2020 for studies reporting peak QTc ≥500 ms, peak QTc change ≥60 ms, peak QTc interval, peak change of QTc interval, ventricular arrhythmias, TdP, sudden cardiac death, or atrioventricular block (AVB). All meta-analyses were conducted using a random-effects model.
Forty-seven studies (three case series, 35 cohorts, and nine randomized controlled trials [RCTs]) involving 13 087 patients were included. The pooled prevalence of peak QTc ≥500 ms was 9% (95% confidence interval [95%CI], 3%-18%) and 8% (95%CI, 3%-14%) in patients who received hydroxychloroquine/chloroquine alone or in combination with azithromycin, respectively. Likewise, the use of hydroxychloroquine (risk ratio [RR], 2.68; 95%CI, 1.56-4.60) and hydroxychloroquine + azithromycin (RR, 3.28; 95%CI, 1.16-9.30) was associated with an increased risk of QTc prolongation compared to no treatment. Ventricular arrhythmias, TdP, sudden cardiac death, and AVB were reported in <1% of patients across treatment groups. The only two studies that reported individual data of lopinavir/ritonavir found no cases of QTc prolongation.
COVID-19 patients treated with hydroxychloroquine/chloroquine with or without azithromycin had a relatively high prevalence and risk of QTc prolongation. However, the prevalence of arrhythmic events was very low, probably due to underreporting. The limited information about lopinavir/ritonavir showed that it does not prolong the QTc interval.
羟氯喹、氯喹、阿奇霉素和洛匹那韦/利托那韦是在新冠疫情早期用于治疗 2019 冠状病毒病(COVID-19)的药物。众所周知,这些药物可延长 QT 间期,并可能诱发尖端扭转型室性心动过速(TdP)。我们旨在评估这些药物治疗 COVID-19 患者的 QT 间期延长和心律失常事件的发生率和风险。
我们从数据库建立到 2020 年 9 月 30 日检索了电子数据库,以检索报告 QT 间期峰值≥500 ms、QT 间期峰值变化≥60 ms、QT 间期峰值、QT 间期峰值变化、室性心律失常、TdP、心源性猝死或房室传导阻滞(AVB)的研究。所有荟萃分析均采用随机效应模型进行。
共纳入 47 项研究(3 项病例系列、35 项队列研究和 9 项随机对照试验),共涉及 13087 例患者。单独使用羟氯喹/氯喹或联合使用阿奇霉素的患者中,QTc 间期峰值≥500 ms 的总体发生率分别为 9%(95%置信区间[95%CI]:3%-18%)和 8%(95%CI:3%-14%)。同样,与未治疗相比,使用羟氯喹(风险比[RR]:2.68;95%CI:1.56-4.60)和羟氯喹+阿奇霉素(RR:3.28;95%CI:1.16-9.30)与 QT 间期延长的风险增加相关。在治疗组中,报告的室性心律失常、TdP、心源性猝死和 AVB 发生率均<1%。仅两项报告洛匹那韦/利托那韦个体数据的研究均未发现 QT 间期延长的病例。
COVID-19 患者使用羟氯喹/氯喹联合或不联合阿奇霉素治疗,QTc 间期延长的发生率和风险相对较高。然而,心律失常事件的发生率非常低,可能是由于报告不足。关于洛匹那韦/利托那韦的有限信息表明,它不会延长 QT 间期。