Division of Electrophysiology, Department of Cardiology, North Shore University Hospital, Northwell Health, Manhasset, NY (M.S., J.G., D.C., B.S.K., A.M., E.M., P.M., J.W., S.B., R.M., R.J., L.M.E.).
Division of Electrophysiology, Department of Cardiology, Lenox Hill Hospital, Northwell Health, New York, NY (M.S., P.M., N.S., S.M.).
Circ Arrhythm Electrophysiol. 2020 Jun;13(6):e008662. doi: 10.1161/CIRCEP.120.008662. Epub 2020 Apr 29.
The novel SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) is responsible for the global coronavirus disease 2019 pandemic. Small studies have shown a potential benefit of chloroquine/hydroxychloroquine±azithromycin for the treatment of coronavirus disease 2019. Use of these medications alone, or in combination, can lead to a prolongation of the QT interval, possibly increasing the risk of Torsade de pointes and sudden cardiac death.
Hospitalized patients treated with chloroquine/hydroxychloroquine±azithromycin from March 1 to the 23 at 3 hospitals within the Northwell Health system were included in this prospective, observational study. Serial assessments of the QT interval were performed. The primary outcome was QT prolongation resulting in Torsade de pointes. Secondary outcomes included QT prolongation, the need to prematurely discontinue any of the medications due to QT prolongation, and arrhythmogenic death.
Two hundred one patients were treated for coronavirus disease 2019 with chloroquine/hydroxychloroquine. Ten patients (5.0%) received chloroquine, 191 (95.0%) received hydroxychloroquine, and 119 (59.2%) also received azithromycin. The primary outcome of torsade de pointes was not observed in the entire population. Baseline corrected QT interval intervals did not differ between patients treated with chloroquine/hydroxychloroquine (monotherapy group) versus those treated with combination group (chloroquine/hydroxychloroquine and azithromycin; 440.6±24.9 versus 439.9±24.7 ms, =0.834). The maximum corrected QT interval during treatment was significantly longer in the combination group versus the monotherapy group (470.4±45.0 ms versus 453.3±37.0 ms, =0.004). Seven patients (3.5%) required discontinuation of these medications due to corrected QT interval prolongation. No arrhythmogenic deaths were reported.
In the largest reported cohort of coronavirus disease 2019 patients to date treated with chloroquine/hydroxychloroquine±azithromycin, no instances of Torsade de pointes, or arrhythmogenic death were reported. Although use of these medications resulted in QT prolongation, clinicians seldomly needed to discontinue therapy. Further study of the need for QT interval monitoring is needed before final recommendations can be made.
新型严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)是导致全球 2019 年冠状病毒病(COVID-19)大流行的病原体。一些小型研究表明,氯喹/羟氯喹联合或不联合阿奇霉素治疗 COVID-19 可能有益。这些药物单独或联合使用可导致 QT 间期延长,可能增加尖端扭转型室性心动过速(TdP)和心源性猝死的风险。
本前瞻性观察性研究纳入了 3 家 Northwell Health 系统医院于 2020 年 3 月 1 日至 23 日期间接受氯喹/羟氯喹联合或不联合阿奇霉素治疗的 COVID-19 住院患者。对 QT 间期进行了连续评估。主要结局为导致尖端扭转型室性心动过速的 QT 间期延长。次要结局包括 QT 间期延长、因 QT 间期延长而提前停用任何一种药物以及心律失常性死亡。
共有 201 例患者因 COVID-19 接受氯喹/羟氯喹治疗。10 例(5.0%)患者接受氯喹治疗,191 例(95.0%)患者接受羟氯喹治疗,119 例(59.2%)患者还接受了阿奇霉素治疗。在整个人群中均未观察到尖端扭转型室性心动过速的主要结局。接受氯喹/羟氯喹(单药治疗组)与接受联合治疗组(氯喹/羟氯喹联合阿奇霉素)的患者的校正 QT 间期(QTc)基础值无差异(440.6±24.9 毫秒比 439.9±24.7 毫秒,=0.834)。与单药治疗组相比,联合治疗组在治疗期间的最大校正 QT 间期显著延长(470.4±45.0 毫秒比 453.3±37.0 毫秒,=0.004)。7 例(3.5%)患者因 QTc 延长而需要停用这些药物。未报告心律失常性死亡。
在迄今报告的最大 COVID-19 患者氯喹/羟氯喹联合或不联合阿奇霉素治疗队列中,未报告尖端扭转型室性心动过速或心律失常性死亡。尽管这些药物的使用导致了 QT 间期延长,但临床医生很少需要停止治疗。在做出最终建议之前,还需要进一步研究是否需要监测 QT 间期。