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QT prolongation in the STREAM Stage 1 Trial

BACKGROUND : STREAM (Standardized Treatment Regimen of Anti-TB Drugs for Patients with MDR-TB) Stage 1 demonstrated non-inferior efficacy of a shortened regimen (the Short regimen) for rifampicinresistant TB (RR-TB) compared to the contemporaneous WHO-recommended regimen. This regimen included moxif...

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Autores principales: Hughes, G., Bern, H., Chiang, C-Y., Goodall, R. L., Nunn, A. J., Rusen, I. D., Meredith, S. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Union 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8982645/
https://www.ncbi.nlm.nih.gov/pubmed/35351238
http://dx.doi.org/10.5588/ijtld.21.0403
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author Hughes, G.
Bern, H.
Chiang, C-Y.
Goodall, R. L.
Nunn, A. J.
Rusen, I. D.
Meredith, S. K.
author_facet Hughes, G.
Bern, H.
Chiang, C-Y.
Goodall, R. L.
Nunn, A. J.
Rusen, I. D.
Meredith, S. K.
author_sort Hughes, G.
collection PubMed
description BACKGROUND : STREAM (Standardized Treatment Regimen of Anti-TB Drugs for Patients with MDR-TB) Stage 1 demonstrated non-inferior efficacy of a shortened regimen (the Short regimen) for rifampicinresistant TB (RR-TB) compared to the contemporaneous WHO-recommended regimen. This regimen included moxifloxacin and clofazimine, known to cause QT prolongation, and severe prolongation was more common on the Short regimen. Here we investigate risk factors for QT prolongation with the Short regimen. METHODS : Data from patients prescribed the Short regimen (n = 282) were analysed to identify risk factors for severe QT prolongation (QT/QTcF ≥500 ms or ≥60 ms increase in QTcF from baseline). RESULTS : Of the 282 patients on the Short regimen, 94 (33.3%) developed severe QT prolongation: 31 QT/QTcF ≥500 ms; 92 experienced ≥60 ms QTcF increase from baseline. The median time to QT/QTcF ≥500 ms was 20 weeks (IQR 8–28), and the time to ≥60 ms increase from baseline was 18 weeks (IQR 8–28). Prolongation ≥500 ms was most frequent in patients from Mongolia (10/22, 45.5%) compared with 3.5–11.9% at other sites, P < 0.001. Higher baseline QTcF increased risk of prolongation to ≥500 ms (QTcF ≥400 ms: OR 5.99, 95% CI 2.04–17.62). CONCLUSION : One third of patients on the Short regimen developed severe QT prolongation. QT/QTcF ≥500 ms was more common in patients from Mongolia and in those with a higher baseline QTcF, which may have implications for implementation of treatment.
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spelling pubmed-89826452022-04-08 QT prolongation in the STREAM Stage 1 Trial Hughes, G. Bern, H. Chiang, C-Y. Goodall, R. L. Nunn, A. J. Rusen, I. D. Meredith, S. K. Int J Tuberc Lung Dis Original Articles BACKGROUND : STREAM (Standardized Treatment Regimen of Anti-TB Drugs for Patients with MDR-TB) Stage 1 demonstrated non-inferior efficacy of a shortened regimen (the Short regimen) for rifampicinresistant TB (RR-TB) compared to the contemporaneous WHO-recommended regimen. This regimen included moxifloxacin and clofazimine, known to cause QT prolongation, and severe prolongation was more common on the Short regimen. Here we investigate risk factors for QT prolongation with the Short regimen. METHODS : Data from patients prescribed the Short regimen (n = 282) were analysed to identify risk factors for severe QT prolongation (QT/QTcF ≥500 ms or ≥60 ms increase in QTcF from baseline). RESULTS : Of the 282 patients on the Short regimen, 94 (33.3%) developed severe QT prolongation: 31 QT/QTcF ≥500 ms; 92 experienced ≥60 ms QTcF increase from baseline. The median time to QT/QTcF ≥500 ms was 20 weeks (IQR 8–28), and the time to ≥60 ms increase from baseline was 18 weeks (IQR 8–28). Prolongation ≥500 ms was most frequent in patients from Mongolia (10/22, 45.5%) compared with 3.5–11.9% at other sites, P < 0.001. Higher baseline QTcF increased risk of prolongation to ≥500 ms (QTcF ≥400 ms: OR 5.99, 95% CI 2.04–17.62). CONCLUSION : One third of patients on the Short regimen developed severe QT prolongation. QT/QTcF ≥500 ms was more common in patients from Mongolia and in those with a higher baseline QTcF, which may have implications for implementation of treatment. The Union 2022-04 2022-04-01 /pmc/articles/PMC8982645/ /pubmed/35351238 http://dx.doi.org/10.5588/ijtld.21.0403 Text en © 2022 The Union https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Original Articles
Hughes, G.
Bern, H.
Chiang, C-Y.
Goodall, R. L.
Nunn, A. J.
Rusen, I. D.
Meredith, S. K.
QT prolongation in the STREAM Stage 1 Trial
title QT prolongation in the STREAM Stage 1 Trial
title_full QT prolongation in the STREAM Stage 1 Trial
title_fullStr QT prolongation in the STREAM Stage 1 Trial
title_full_unstemmed QT prolongation in the STREAM Stage 1 Trial
title_short QT prolongation in the STREAM Stage 1 Trial
title_sort qt prolongation in the stream stage 1 trial
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8982645/
https://www.ncbi.nlm.nih.gov/pubmed/35351238
http://dx.doi.org/10.5588/ijtld.21.0403
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