Key result
Short-term hydroxychloroquine treatment generates blood concentrations that can persist above the 500 ng/mL safety threshold for up to 16 days after discontinuation, which significantly correlates with QTc prolongation.
Why the study?
Studies on hydroxychloroquine elimination after short-term treatments are lacking, and data regarding its pro-arrhythmic effect via QT interval prolongation in this setting remain inconclusive.
Does short-term hydroxychloroquine therapy cause persistent blood concentrations and QTc prolongation in patients with COVID-19?
Observational (n=91)
No
Does short-term hydroxychloroquine therapy cause persistent blood concentrations and QTc prolongation in patients with COVID-19?
Short-term hydroxychloroquine treatment results in persistent blood concentrations and QTc prolongation, suggesting clinicians should wait 16 days after discontinuation before initiating other QT-prolonging drugs.
May warrant prolonged QTc monitoring after short-term hydroxychloroquine; leaves open arrhythmia risk in prospective cohorts.
Hydroxychloroquine was widely used during the severe acute respiratory syndrome coronavirus 2 pandemic as an antiviral drug. Most previous pharmacokinetic/pharmacodynamic studies on hydroxychloroquine were conducted on healthy volunteers or patients receiving long-term therapy. There are no studies on the elimination of hydroxychloroquine after short-term treatments. Hydroxychloroquine is known to have a pro-arrhythmic effect through QT interval prolongation, but data in this setting are not conclusive. Our aims were to estimate the time needed for hydroxychloroquine concentrations ( C HCQ ) to drop to a safe concentration (500 ng/mL) after a short-term therapeutic cycle and to correlate the corrected QT interval with C HCQ . We collected blood samples and electrocardiograms of patients who underwent short-term therapy with hydroxychloroquine during drug intake and after discontinuation. Hydroxychloroquine concentrations were determined by high-performance liquid chromatography–tandem mass spectrometry and analysed with a linear regression model to estimate the elimination time of the drug after its discontinuation. We conducted a multivariate analysis of the corrected QT interval correlation with C HCQ . Our data suggest that short-term hydroxychloroquine courses can generate significant C HCQ persisting above 500 ng/mL up to 16 days after discontinuation of treatment. Corrected QT interval prolongation significantly correlates with C HCQ . The study confirms the long half-life of hydroxychloroquine and its effect on the corrected QT interval even after short-term courses of the drug. This can inform the clinician using hydroxychloroquine treatments that it would be safer to start or re-initiate treatments with corrected QT interval-prolonging potential 16 days after hydroxychloroquine discontinuation.
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Gregori et al. (2022) conducted an observational in COVID-19 (n=91). Hydroxychloroquine was evaluated on Time for hydroxychloroquine whole blood concentration to drop below the 500 ng/mL safety threshold. Short-term hydroxychloroquine treatment generates blood concentrations that can persist above the 500 ng/mL safety threshold for up to 16 days after discontinuation, which significantly correlates with QTc prolongation.
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