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ECG monitoring in STREAM Stage 1: can we identify those at increased risk of QT prolongation?
Hughes, G; Bern, H; Chiang, C-Y; Goodall, R L; Nunn, A J; Rusen, I D; Meredith, S K.
Affiliation
  • Hughes G; Medical Research Council Clinical Trials Unit at University College London, Institute of Clinical Trials and Methodology, London, UK.
  • Bern H; Medical Research Council Clinical Trials Unit at University College London, Institute of Clinical Trials and Methodology, London, UK.
  • Chiang CY; Division of Pulmonary Medicine, Department of Internal Medicine, Wanfang Hospital, Taipei Medical University, Taipei, Taiwan, Division of Pulmonary Medicine, Department of Internal Medicine, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan, International Union again
  • Goodall RL; Medical Research Council Clinical Trials Unit at University College London, Institute of Clinical Trials and Methodology, London, UK.
  • Nunn AJ; Medical Research Council Clinical Trials Unit at University College London, Institute of Clinical Trials and Methodology, London, UK.
  • Rusen ID; Research Division, Vital Strategies, New York, NY, USA.
  • Meredith SK; Medical Research Council Clinical Trials Unit at University College London, Institute of Clinical Trials and Methodology, London, UK.
Int J Tuberc Lung Dis ; 26(11): 1065-1070, 2022 Nov 01.
Article de En | MEDLINE | ID: mdl-36281045
ABSTRACT

BACKGROUND:

STREAM (Standardised Treatment Regimen of Anti-tuberculosis Drugs for Patients with Multidrug-resistant Tuberculosis) Stage 1 was a randomised trial of a Short (9-month) regimen for rifampicin-resistant TB (RR-TB). QT or QTcF prolongation ≥500 ms occurred in 31 (11%) of 282 Short regimen participants. The frequent ECG monitoring employed might be challenging for treatment programmes. This analysis aimed to determine whether those at higher risk of severe QT prolongation could be identified early for more targeted monitoring.

METHODS:

Data from the first month of treatment were used to investigate whether participants were at risk of developing QT/QTcF ≥500 ms. QTcF increases from baseline at different time points were examined. Absolute QTcF measurements were categorised in 5 ms increments at each time-point. The most discriminating time points and QTcF cut-offs were combined to optimise sensitivity and specificity.

RESULTS:

Absolute QTcF values were more discriminating than magnitude of increase from baseline. More participants who developed QT/QTcF ≥500 ms had a QTcF of respectively ≥425 ms and ≥430 ms at 4 h and Week 3 (P < 0.05) than those who did not. By combining QTcF values ≥425 ms at 4 h and ≥430 ms at Week 3, we identified high-risk participants with 97% sensitivity and 99% negative predictive value.

CONCLUSION:

Reduced ECG monitoring may be possible for many Short regimen participants.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Syndrome du QT long / Tuberculose multirésistante / Antituberculeux Type d'étude: Clinical_trials / Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limites: Humans Langue: En Journal: Int J Tuberc Lung Dis Année: 2022 Type de document: Article Pays d'affiliation: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Syndrome du QT long / Tuberculose multirésistante / Antituberculeux Type d'étude: Clinical_trials / Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limites: Humans Langue: En Journal: Int J Tuberc Lung Dis Année: 2022 Type de document: Article Pays d'affiliation: Royaume-Uni