Bedaquiline for multidrug-resistant tuberculosis and QTc prolongation in California.

Adverse event Bedaquiline Multidrug-resistant Safety Treatment Tuberculosis

Journal

Journal of clinical tuberculosis and other mycobacterial diseases
ISSN: 2405-5794
Titre abrégé: J Clin Tuberc Other Mycobact Dis
Pays: England
ID NLM: 101682877

Informations de publication

Date de publication:
May 2021
Historique:
entrez: 18 2 2021
pubmed: 19 2 2021
medline: 19 2 2021
Statut: epublish

Résumé

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. 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. 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. 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.

Sections du résumé

BACKGROUND 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 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 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 CONCLUSIONS
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.

Identifiants

pubmed: 33598568
doi: 10.1016/j.jctube.2021.100216
pii: S2405-5794(21)00005-X
pmc: PMC7868725
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100216

Informations de copyright

© 2021 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Shereen Katrak (S)

Tuberculosis Control Branch, California Department of Public Health, Richmond, CA, United States.
Division of Infectious Diseases, University of California, San Francisco, CA, United States.

Phil Lowenthal (P)

Tuberculosis Control Branch, California Department of Public Health, Richmond, CA, United States.

Richard Shen (R)

Division of Infectious Diseases, Maine Medical Center, Portland, ME, United States.

Lisa True (L)

Tuberculosis Control Branch, California Department of Public Health, Richmond, CA, United States.

Leslie Henry (L)

Tuberculosis Control Branch, California Department of Public Health, Richmond, CA, United States.

Pennan Barry (P)

Tuberculosis Control Branch, California Department of Public Health, Richmond, CA, United States.
Division of Infectious Diseases, University of California, San Francisco, CA, United States.

Classifications MeSH