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T-wave morphology abnormalities in the STREAM stage 1 trial.
Hughes, Gareth; Young, William J; Bern, Henry; Crook, Angela; Lambiase, Pier D; Goodall, Ruth L; Nunn, Andrew J; Meredith, Sarah K.
Affiliation
  • Hughes G; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, London, UK.
  • Young WJ; Centre for Clinical Pharmacology and Precision Medicine, William Harvey Research Institute, Queen Mary University of London, London, UK.
  • Bern H; Barts Heart Centre, St Bartholomews Hospital, Barts Health NHS Trust, London, UK.
  • Crook A; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, London, UK.
  • Lambiase PD; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, London, UK.
  • Goodall RL; Institute of Cardiovascular Science, University College London, London, UK.
  • Nunn AJ; NIHR Barts Biomedical Research Centre, London, UK.
  • Meredith SK; MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, London, UK.
Expert Opin Drug Saf ; 23(4): 469-476, 2024 Apr.
Article in En | MEDLINE | ID: mdl-38462751
ABSTRACT

BACKGROUND:

Shorter regimens for drug-resistant tuberculosis (DR-TB) have non-inferior efficacy compared with longer regimens, but QT prolongation is a concern. T-wave morphology abnormalities may be a predictor of QT prolongation. RESEARCH DESIGN AND

METHODS:

STREAM Stage 1 was a randomized controlled trial in rifampicin-resistant TB, comparing short and long regimens. All participants had regular ECGs. QT/QTcF prolongation (≥500 ms or increase in ≥60 ms from baseline) was more common on the short regimen which contained high-dose moxifloxacin and clofazimine. Blinded ECGs were selected from the baseline, early (weeks 1-4), and late (weeks 12-36) time points. T-wave morphology was categorized as normal or abnormal (notched, asymmetric, flat-wave, flat peak, or broad). Differences between groups were assessed using Chi-Square tests (paired/unpaired, as appropriate).

RESULTS:

Two-hundred participants with available ECGs at relevant times were analyzed (QT prolongation group n = 82; non-prolongation group n = 118). At baseline, 23% (45/200) of participants displayed abnormal T-waves, increasing to 45% (90/200, p < 0.001) at the late time point. Abnormalities were more common in participants allocated the Short regimen (75/117, 64%) than the Long (14/38, 36.8%, p = 0.003); these occurred prior to QT/QTcF ≥500 ms in 53% of the participants (Long 2/5; Short 14/25).

CONCLUSIONS:

T-wave abnormalities may help identify patients at risk of QT prolongation on DR-TB treatment. TRIAL REGISTRATION The trial is registered at ClinicalTrials.gov (CT.gov identifier NCT02409290). Current Controlled Trial number, ISRCTN78372190.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Long QT Syndrome / Tuberculosis, Multidrug-Resistant Limits: Humans Language: En Journal: Expert Opin Drug Saf Journal subject: FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Year: 2024 Document type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Long QT Syndrome / Tuberculosis, Multidrug-Resistant Limits: Humans Language: En Journal: Expert Opin Drug Saf Journal subject: FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Year: 2024 Document type: Article Affiliation country: United kingdom
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