Feasibility and accuracy of mobile QT interval monitoring strategies in bedaquiline-enhanced prophylactic leprosy treatment.


Journal

Clinical and translational science
ISSN: 1752-8062
Titre abrégé: Clin Transl Sci
Pays: United States
ID NLM: 101474067

Informations de publication

Date de publication:
Aug 2024
Historique:
revised: 30 05 2024
received: 02 04 2024
accepted: 02 06 2024
medline: 30 7 2024
pubmed: 30 7 2024
entrez: 30 7 2024
Statut: ppublish

Résumé

Some anti-mycobacterial drugs are known to cause QT interval prolongation, potentially leading to life-threatening ventricular arrhythmia. However, the highest leprosy and tuberculosis burden occurs in settings where electrocardiographic monitoring is challenging. The feasibility and accuracy of alternative strategies, such as the use of automated measurements or a mobile electrocardiogram (mECG) device, have not been evaluated in this context. As part of the phase II randomized controlled BE-PEOPLE trial evaluating the safety of bedaquiline-enhanced post-exposure prophylaxis (bedaquiline and rifampicin, BE-PEP, versus rifampicin, SDR-PEP) for leprosy, all participants had corrected QT intervals (QTc) measured at baseline and on the day after receiving post-exposure prophylaxis. The accuracy of mECG measurements as well as automated 12L-ECG measurements was evaluated. In total, 635 mECGs from 323 participants were recorded, of which 616 (97%) were of sufficient quality for QTc measurement. Mean manually read QTc on 12L-ECG and mECG were 394 ± 19 and 385 ± 18 ms, respectively (p < 0.001), with a strong correlation (r = 0.793). The mean absolute QTc difference between both modalities was 11 ± 10 ms. Mean manual and automated 12L-ECG QTc were 394 ± 19 and 409 ± 19 ms, respectively (n = 636; p < 0.001), corresponding to moderate agreement (r = 0.655). The use of a mECG device for QT interval monitoring was feasible and yielded a median absolute QTc error of 8 ms. Automated QTc measurements were less accurate, yielding longer QTc intervals.

Identifiants

pubmed: 39075882
doi: 10.1111/cts.13861
doi:

Substances chimiques

bedaquiline 78846I289Y
Diarylquinolines 0
Rifampin VJT6J7R4TR
Leprostatic Agents 0

Types de publication

Journal Article Randomized Controlled Trial Clinical Trial, Phase II

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13861

Informations de copyright

© 2024 The Author(s). Clinical and Translational Science published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.

Références

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Auteurs

Auke T Bergeman (AT)

Department of Cardiology, Heart Centre, Amsterdam UMC location AMC, University of Amsterdam, Amsterdam, The Netherlands.

Said Nourdine (S)

National Tuberculosis and Leprosy Control Program, Moroni, Comoros.

Alberto Piubello (A)

Damien Foundation, Brussels, Belgium.

Zahara Salim (Z)

National Tuberculosis and Leprosy Control Program, Moroni, Comoros.

Sofie M Braet (SM)

Institute of Tropical Medicine, Antwerp, Belgium.

Abdallah Baco (A)

National Tuberculosis and Leprosy Control Program, Moroni, Comoros.

Silahi H Grillone (SH)

National Tuberculosis and Leprosy Control Program, Moroni, Comoros.

Rian Snijders (R)

Institute of Tropical Medicine, Antwerp, Belgium.

Carolien Hoof (C)

Institute of Tropical Medicine, Antwerp, Belgium.

Achilleas Tsoumanis (A)

Institute of Tropical Medicine, Antwerp, Belgium.

Harry van Loen (H)

Institute of Tropical Medicine, Antwerp, Belgium.

Younoussa Assoumani (Y)

National Tuberculosis and Leprosy Control Program, Moroni, Comoros.

Aboubacar Mzembaba (A)

National Tuberculosis and Leprosy Control Program, Moroni, Comoros.

Nimer Ortuño-Gutiérrez (N)

Damien Foundation, Brussels, Belgium.

Epco Hasker (E)

Institute of Tropical Medicine, Antwerp, Belgium.

Christian van der Werf (C)

Department of Cardiology, Heart Centre, Amsterdam UMC location AMC, University of Amsterdam, Amsterdam, The Netherlands.

Bouke C de Jong (BC)

Institute of Tropical Medicine, Antwerp, Belgium.

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