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Observational Study
. 2020 Jun;13(6):e008662.
doi: 10.1161/CIRCEP.120.008662. Epub 2020 Apr 29.

Effect of Chloroquine, Hydroxychloroquine, and Azithromycin on the Corrected QT Interval in Patients With SARS-CoV-2 Infection

Affiliations
Observational Study

Effect of Chloroquine, Hydroxychloroquine, and Azithromycin on the Corrected QT Interval in Patients With SARS-CoV-2 Infection

Moussa Saleh et al. Circ Arrhythm Electrophysiol. 2020 Jun.

Abstract

Background: 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.

Methods: 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.

Results: 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, P=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, P=0.004). Seven patients (3.5%) required discontinuation of these medications due to corrected QT interval prolongation. No arrhythmogenic deaths were reported.

Conclusions: 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.

Keywords: COVID-19; QT prolongation; azithromycin; chloroquine; hydroxychloroquine; pandemic.

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Figures

Figure 1.
Figure 1.
Trajectory of corrected QT interval (QTc) change in 201 patients receiving hydroxychloroquine±azithromycin. Change in QTc was seen starting on day 2 of therapy with max QTc being reached on day 4 by the majority of patients.
Figure 2.
Figure 2.
Percentage of patients with increase in corrected QT interval (QTc) for HCQ monotherapy vs hydroxychloroquine and azithromycin combination therapy. The majority of patients in both groups had an increase in QTc of 0–20 ms. Higher percentage of patients treated with the combination therapy had an increase in QTc of 40–60 ms and >60 ms.
Figure 3.
Figure 3.
Trajectory of corrected QT interval (QTc) changes for patients whose hydroxychloroquine (HCQ)±azithromycin (AZM) was discontinued due to QT prolongation (n=7). The majority of the patients that had their HCQ±AZM therapy discontinued reached a max QTc >500 ms. Decision to discontinue therapy was based on clinician preference.

References

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