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Substitution of Rifapentine for Rifampin During Intensive Phase Treatment of Pulmonary Tuberculosis: Study 29 of the Tuberculosis Trials Consortium

Dorman, Susan E. ; Goldberg, Stefan ; Stout, Jason E. ; Muzanyi, Grace ; Johnson, John L. ; Weiner, Marc ; Bozeman, Lorna ; Heilig, Charles M. ; Feng, Pei-Jean ; Moro, Ruth ; Narita, Masahiro ; Nahid, Payam ; Ray, Susan ; Bates, Edward ; Haile, Betial ; Nuermberger, Eric L. ; Vernon, Andrew ; Schluger, Neil W.

The Journal of infectious diseases, 2012-10, Vol.206 (7), p.1030-1040 [Periódico revisado por pares]

Oxford: Oxford University Press

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Título:
Substitution of Rifapentine for Rifampin During Intensive Phase Treatment of Pulmonary Tuberculosis: Study 29 of the Tuberculosis Trials Consortium
Autor: Dorman, Susan E. ; Goldberg, Stefan ; Stout, Jason E. ; Muzanyi, Grace ; Johnson, John L. ; Weiner, Marc ; Bozeman, Lorna ; Heilig, Charles M. ; Feng, Pei-Jean ; Moro, Ruth ; Narita, Masahiro ; Nahid, Payam ; Ray, Susan ; Bates, Edward ; Haile, Betial ; Nuermberger, Eric L. ; Vernon, Andrew ; Schluger, Neil W.
Assuntos: Adult ; Antibiotics, Antitubercular - adverse effects ; Antibiotics, Antitubercular - therapeutic use ; BACTERIA ; Bacterial diseases ; Bacterial diseases of the respiratory system ; Biological and medical sciences ; Cultural groups ; Dosage ; Drug Substitution ; Female ; Fundamental and applied biological sciences. Psychology ; Health care administration ; Human bacterial diseases ; Humans ; Infectious diseases ; Liquids ; Logistic Models ; Male ; Medical sciences ; Microbiology ; Middle Aged ; Multivariate Analysis ; Mycobacterium tuberculosis ; Mycobacterium tuberculosis - drug effects ; Mycobacterium tuberculosis - growth & development ; Pulmonary tuberculosis ; Registered nurses ; Rifampin - adverse effects ; Rifampin - analogs & derivatives ; Rifampin - therapeutic use ; Solids ; Sputum ; Treatment Outcome ; Tuberculosis ; Tuberculosis, Pulmonary - drug therapy ; Tuberculosis, Pulmonary - microbiology
É parte de: The Journal of infectious diseases, 2012-10, Vol.206 (7), p.1030-1040
Notas: ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
ObjectType-News-3
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Descrição: Background. Rifapentine administered 5 days per week has potent activity in mouse models of antituberculosis chemotherapy, but efficacy and safety data are limited in humans. We compared the antimicrobial activity and safety of rifapentine vs rifampin during the first 8 weeks of pulmonary tuberculosis treatment. Methods. In total, 531 adults with sputum smear-positive pulmonary tuberculosis were randomized to rifapentine 10 mg/kg/dose or rifampin 10 mg/kg/dose, administered 5 days per week for 8 weeks (intensive phase), with isoniazid, pyrazinamide, and ethambutol. Coprimary outcomes were negative sputum culture on liquid and on solid media at completion of intensive phase. Results. Negative cultures on solid media occurred in 145 of 174 participants (83.3%) in the rifampin group and 171 of 198 participants (86.4%) in the rifapentine group (difference, 3.0%; 95% confidence interval [CI]: −4.3, 10.5); negative cultures in liquid media occurred in 110 of 169 (65.1%) in the rifampin group and 133 of 196 (67.9%) in the rifapentine group (difference, 2.8%; 95% CI: −6.9, 12.4). Among 529 participants who received study therapy, 40 of 254 participants (15.7%) in the rifampin group and 40 of 275 participants (14.5%) in the rifapentine group prematurely discontinued treatment (P= .79). Conclusions. The rifapentine regimen was safe but not significantly more active than a standard rifampin regimen, by the surrogate endpoint of culture status at completion of intensive phase. Assessment of higher exposures to rifapentine for tuberculosis treatment is warranted.
Editor: Oxford: Oxford University Press
Idioma: Inglês

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Substitution of Rifapentine for Rifampin During Intensive Phase Treatment of Pulmonary Tuberculosis: Study 29 of the Tuberculosis Trials Consortium

Oxford: Oxford University Press

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