Gosling, Roly D., Uiso, Leonard O., Sam, Noel E., Bongard, Emily ![]() |
Abstract
Patients in whom acid-fast bacilli smear-positive pulmonary tuberculosis was newly diagnosed were randomized to receive 400 mg moxifloxacin, 300 mg isonaizid, or 600 mg rifampin daily for 5 days. Sixteen-hour overnight sputa collections were made for the 2 days before and for 5 days of monotherapy. Bactericidal activity was estimated by the time taken to kill 50% of viable bacilli (vt50) and the fall in sputum viable count during the first 2 days designated as the early bactericidal activity (EBA). The mean vt50 of moxifloxacin was 0.88 days (95% confidence interval [CI], 0.43–1.33 days) and the mean EBA was 0.53 (95% CI 0.28–0.79). For the isoniazid group, the mean vt50 was 0.46 days (95% CI, 0.31–0.61 days) and the mean EBA was 0.77 (95% CI, 0.54–1.00). For rifampin, the mean vt50 was 0.71 days (95% CI, 0.48–0.95 days) and the mean EBA was 0.28 (95% CI, 0.15–0.41). Using the EBA method, isoniazid was significantly more active than rifampin (p < 0.01) but not moxifloxacin. Using the vt50 method, isoniazid was more active than both rifampin and moxifloxacin (p = 0.03). Moxifloxacin has an activity similar to rifampin in human subjects with pulmonary tuberculosis, suggesting that it should undergo further assessment as part of a short course regimen for the treatment of drug-susceptible tuberculosis.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Medicine |
Subjects: | Q Science > QR Microbiology R Medicine > R Medicine (General) |
Uncontrolled Keywords: | clinical trials; Africa; tuberculosis; quinolone |
Publisher: | American Thoracic Society |
ISSN: | 1073-449X |
Last Modified: | 25 Oct 2022 08:43 |
URI: | https://orca.cardiff.ac.uk/id/eprint/54067 |
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