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The efficacy of a four-week, ofloxacin-containing regimen compared with standard WHO-MDT in PB leprosy
Author(s) -
Marivic Balagon,
Roland V. Cellona,
Rodolfo M. Abalos,
R H Gelber,
Paul Saunderson
Publication year - 2010
Publication title -
leprosy review
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 43
eISSN - 2162-8807
pISSN - 0305-7518
DOI - 10.47276/lr.81.1.27
Subject(s) - medicine , regimen , ofloxacin , leprosy , rifampicin , placebo , surgery , antibiotics , tuberculosis , dermatology , ciprofloxacin , pathology , alternative medicine , microbiology and biotechnology , biology
OBJECTIVESTo compare the efficacy of a 4-week ofloxacin-containing regimen and the standard WHO-MDT regimen for PB leprosy, in terms of the rate and timing of relapse after treatment completion.DESIGN124 PB patients were enrolled in a randomised, double-blind trial. Of these, 66 received the standard 6-month WHO-MDT regimen, whereas 58 received 28 daily supervised doses of rifampicin 600mg + ofloxacin 400 mg, plus 5 months of placebo. Patients were regularly monitored for clinical response and for signs of relapse after treatment completion.RESULTSPatients enrolled in the ofloxacin group had a mean follow-up of 10.8 years (628 patient-years) with 1 early relapse at 3 years after treatment completion. On relapse, this patient remained smear negative but was reclassified by current WHO criteria (> or =6 skin lesions) as multibacillary (MB). Patients on the WHO-MDT regimen had a mean follow-up of 11.3 years (749 patient-years) with two late relapses at 8 and 12 years, both still classified as PB on relapse.CONCLUSIONIn conclusion, both regimens appeared generally efficacious, and, in particular, resulted in few relapses.

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