Key result
Comorbid cardiovascular diseases significantly increased the risk of QT prolongation and related cardiovascular complications in MDR TB patients (OR 4.29; 95% CI 1.46-12.56; p=0.009).
Why the study?
To evaluate predictors of cardiotoxicity when using modern chemotherapy regimens in comorbid patients with multiple drug-resistant tuberculosis to identify those at high risk of cardiovascular events.
What are the predictors of QT prolongation in patients with multiple drug-resistant tuberculosis receiving modern chemotherapy regimens?
Cohort (n=87)
Open-label
No
What are the predictors of QT prolongation in patients with multiple drug-resistant tuberculosis receiving modern chemotherapy regimens?
Odds Ratio: 4.29 (95% CI 1.46–12.56)
p-value: p=0.009
Comorbid cardiovascular disease, family history of CVD, COPD, and female gender are significant predictors of QT prolongation in MDR TB patients undergoing modern chemotherapy.
The objective: to evaluate predictors of cardiotoxicity when using modern chemotherapy regimens in comorbid patients with multiple drug-resistant tuberculosis (MDR TB) to identify a group facing a high risk of cardiovascular events. Subjects and Methods. A single-center, open-label, controlled prospective cohort study was conducted. A total of 87 MDR TB patients were enrolled and divided into 2 groups: Group 1 included 24 patients whose QT interval length exceeded 450 ms at one or more control points; Group 2 included 63 patients whose QT interval duration length was less than 450 ms at all observation periods. Results. In this study, traditional risk factors for QT prolongation, such as: overweight or underweight, smoking, hypokalemia, bradycardia, taking two QT-prolonging anti-tuberculosis drugs (fluoroquinolone and bedaquiline) and in combination with capreomycin, did not provide a significant effect on the development of cardiotoxic reactions during anti-tuberculosis chemotherapy. The risk of QT prolongation and related cardiovascular complications was significantly associated with comorbid cardiovascular diseases (CVD) (OR=4.29, CI 1.46–12.56; p=0.009), a family history of CVD (OR=4, CI 1.26–12.72; p=0.024), chronic obstructive pulmonary disease (OR=2.9, CI 1.1–7.67; p=0.033), and female gender (OR=3.73, CI 1.38–10.07; p=0.015). The identified predictors, even at the stage of compiling an anti-tuberculosis regimen, make it possible to identify a risk group for developing cardiotoxic reactions among MDR TB patients.
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Жукова et al. (2025) conducted a cohort in multiple drug-resistant tuberculosis (MDR TB) (n=87). Comorbid cardiovascular diseases (CVD) vs. No comorbid cardiovascular diseases was evaluated on QT prolongation (>450 ms) and related cardiovascular complications (OR 4.29, 95% CI 1.46-12.56, p=0.009). Comorbid cardiovascular diseases significantly increased the risk of QT prolongation and related cardiovascular complications in MDR TB patients (OR 4.29; 95% CI 1.46-12.56; p=0.009).
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