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Rifampin in the Treatment of Drug-Resistant Mycobacterium tuberculosis Infections

List of authors.
  • A. Vall-Spinosa, M.D.,
  • William Lester, M.D.,
  • Thomas Moulding, M.D.,
  • Paul T. Davidson, M.D.,
  • and J. K. McClatchy, Ph.D.

Abstract

Thirty patients with far advanced, multiple-drug-resistant pulmonary tuberculosis were treated with rifampin for four to 12 months. The regimens included rifampin in a daily dosage of 600 mg combined, whenever possible, with one or more other antituberculosis drugs to which in vitro susceptibility had been demonstrated. Quiescent status was achieved in 21 (70 per cent) of the patients, whereas in nine (30 per cent) cultures remained positive, or the patient relapsed after having initially achieved sputum negativity. The shortest duration of rifampin therapy producing culture conversion was 10 days, and the longest 90 days, with a mean of 40. In seven of the nine failures rifampin resistance developed, and all but one of these patients received rifampin without a satisfactory companion drug because of previously acquired resistance. However, 65 per cent of the patients receiving rifampin as the sole therapy attained quiescent status; to date only two have relapsed. No toxicity attributable to rifampin was noted in this series.

Funding and Disclosures

* From the National Jewish Hospital and Research Center and the Department of Medicine, University of Colorado School of Medicine (address reprint requests to Dr. Lester at the National Jewish Hospital and Research Center, 3800 E. Colfax Ave., Denver, Col. 80206).

Supported in part by a grant (ROI AI 06578–06) from the Public Health Service, U.S. Department of Health, Education, and Welfare.

Presented in part at the 29th Veterans Administration —Armed Forces Pulmonary Disease Research Conference, January 26–29, 1970.

We are indebted to the Pitman-Moore Division of the Dow Chemical Company and to Dr. Robert Nolan, director of clinical pharmacology, for supplying the rifampin, and also to the members of the clinical laboratory staff for doing the bacteriologic studies and the tests needed for monitoring toxicity.

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