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Clinical Trial
. 2004 May;8(5):560-7.

Results of a standardised regimen for multidrug-resistant tuberculosis in Bangladesh

Affiliations
  • PMID: 15137531
Clinical Trial

Results of a standardised regimen for multidrug-resistant tuberculosis in Bangladesh

A Van Deun et al. Int J Tuberc Lung Dis. 2004 May.

Abstract

Setting: Individualised regimens based on drug susceptibility test results, generally used to treat multidrug-resistant tuberculosis (MDR-TB), require often unavailable expertise and resources.

Objective: To evaluate a standardised regimen based on the susceptibility profiles of locally prevalent MDR-TB strains.

Design: The activities of a successful DOTS programme in Bangladesh were complemented by offering treatment with a standardised 21-month regimen to patients with laboratory-confirmed MDR-TB disease. The regimen contained kanamycin, ofloxacin, prothionamide, pyrazinamide, ethambutol, isoniazid and clofazimine. Clinical and bacteriological progress was monitored quarterly until treatment completion, then 6 monthly for 2 years.

Results: The status at the end of treatment of this cohort of 58 documented MDR-TB patients was as follows: eight (14%) deaths, seven (12%) defaults, three (5%) failures and 40 (69%) cures. One bacteriologically-confirmed relapse was recognised. Frequent and sometimes serious side effects proved to be the main problem, suggesting the need for a better tolerated but equally effective regimen.

Conclusion: A standardised approach may provide a reasonable alternative to individualised treatment of MDR-TB in resource-poor settings. However, DOTS-plus programmes in resource-poor settings may confront significant difficulties in the enrolment, diagnosis and management of MDR-TB patients.

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