Key result
Bedaquiline therapy for multidrug-resistant tuberculosis was associated with a non-transient QTc elevation >500 ms in 11% of patients, with no episodes of cardiac arrhythmia.
Why the study?
Bedaquiline is recommended for multidrug-resistant tuberculosis but has the potential to prolong the QTc interval, warranting assessment of the frequency and severity of QTc prolongation.
Does bedaquiline therapy cause significant QTc prolongation in patients with multidrug-resistant tuberculosis?
Cohort (n=37)
Does bedaquiline therapy cause significant QTc prolongation in patients with multidrug-resistant tuberculosis?
Answers are grounded in this paper and cite their sources.
Bedaquiline therapy for MDR TB is associated with a risk of QTc prolongation >500 ms in 11% of patients, highlighting the need for ECG monitoring, though no clinical arrhythmias were observed.
BACKGROUND: Bedaquiline (BDQ) is recommended for the treatment of multidrug-resistant tuberculosis (MDR TB), however, it has the potential to prolong QTc interval. We assessed the frequency and severity of QTc prolongation in patients receiving BDQ in California. METHODS: Based on chart review for patients receiving BDQ as part of MDR TB therapy from January 2013-May 2019, we analyzed QTc values at six pre-specified time points during BDQ therapy (baseline, 2, 4, 8, 12, and 24 weeks), as well as peak QTc, time to peak QTc, and the clinical characteristics of patients who had QTc elevation >500 milliseconds (ms) during therapy. RESULTS: A total of 37 patients were treated with BDQ during the analysis period, with a total of 449 QTc measurements available for analysis. Most patients (89%) received at least one QTc-prolonging drug in addition to BDQ. Median QTc values at all pre-specified time points were <450 ms. Median peak QTc was 455 ms (interquartile range [IQR]: 437-486) and median time to peak was 57 days (IQR: 19-156). Four patients (11%) had a non-transient elevation in QTc to >500 ms, including one patient with profound hypokalemia and one receiving concurrent chemotherapy, but none had cardiac arrhythmia. Less than 10% of patient in our cohort had ECGs performed at all six pre-specified time points. DISCUSSION: BDQ was generally well-tolerated in a cohort of patients treated for MDR TB in California, with 11% of patients experiencing a non-transient QTc elevation >500 ms, and no episodes of arrhythmia. Frequent ECG monitoring during BDQ therapy presents a challenge for TB clinicians, even in well-resourced countries.
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Katrak et al. (2021) conducted a cohort in multidrug-resistant tuberculosis (n=37). Bedaquiline was evaluated on non-transient elevation in QTc to >500 ms. Bedaquiline therapy for multidrug-resistant tuberculosis was associated with a non-transient QTc elevation >500 ms in 11% of patients, with no episodes of cardiac arrhythmia.
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