Key result
Treatment with Hydroxychloroquine and Azithromycin under an arrhythmia risk management plan in COVID-19 patients resulted in an 8.6% incidence of QTc ≥ 500 ms and no ventricular tachycardia.
Why the study?
The study was conducted to assess cardiac safety in COVID-19 patients treated with hydroxychloroquine and azithromycin using an arrhythmia risk management plan.
Does an arrhythmia risk management plan prevent severe QTc prolongation and ventricular tachycardia in COVID-19 patients treated with Hydroxychloroquine and Azithromycin?
Observational (n=81)
Does an arrhythmia risk management plan prevent severe QTc prolongation and ventricular tachycardia in COVID-19 patients treated with Hydroxychloroquine and Azithromycin?
Implementation of a pre-defined arrhythmia risk management plan is associated with a low incidence of severe QTc prolongation and no ventricular tachycardia in COVID-19 patients receiving hydroxychloroquine and azithromycin.
Supports arrhythmia monitoring protocols for hydroxychloroquine-azithromycin in COVID-19; leaves open need for randomized safety confirmation.
AIMS: To assess cardiac safety in COVID-19 patients treated with the combination of Hydroxychloroquine and Azithromycin using arrhythmia risk management plan. METHODS AND RESULTS: We retrospectively examined arrhythmia safety of treatment with Hydroxychloroquine and Azithromycin in the setting of pre-defined arrhythmia risk management plan. The data was analyzed using R statistical package version 4.0.0. A two-tailed p-value<0.05 was considered significant. 81 patients were included from March 23rd to May 10th 2020. The median age was 59 years, 58.0% were female. The majority of the study population (82.7%) had comorbidities, 98.8% had radiological signs of pneumonia. Fourteen patients (17.3%) experienced QTc ≥ 480 ms and 16 patients (19.8%) had an increase of QTc ≥ 60 ms. Seven patients (8.6%) had QTc prolongation of ≥ 500 ms. The treatment was discontinued in 4 patients (4.9%). None of the patients developed ventricular tachycardia. The risk factors significantly associated with QTc ≥ 500 ms were hypokalemia (p = 0.032) and use of diuretics during the treatment (p = 0.020). Three patients (3.7%) died, the cause of death was bacterial superinfection with septic shock in two patients, and disseminated intravascular coagulation with multiple organ failure in one patient. None of these deaths were associated with cardiac arrhythmias. CONCLUSION: We recorded a low incidence of QTc prolongation ≥ 500 ms and no ventricular tachycardia events in COVID-19 patients treated with Hydroxychloroquine and Azithromycin using cardiac arrhythmia risk management plan.
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Maneikis et al. (2020) conducted an observational in COVID-19 (n=81). Hydroxychloroquine and Azithromycin was evaluated on QTc prolongation ≥ 500 ms. Treatment with Hydroxychloroquine and Azithromycin under an arrhythmia risk management plan in COVID-19 patients resulted in an 8.6% incidence of QTc ≥ 500 ms and no ventricular tachycardia.
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