03045nas a2200457 4500000000100000008004100001260004900042653002900091653001000120653000900130653002400139653003000163653001100193653002200204653001100226653001000237653002300247653001200270653000900282653001600291653001600307653001400323653001500337653003000352653001300382653001700395653000900412653001700421653002200438653001600460100001400476700001300490700001300503700001000516245016500526856005000691300001100741490000700752520181400759022001402573 2011 d c2011 SepbLEPRA Health in ActionaColchester10aAcademies and institutes10aAdult10aAged10aBiomedical Research10aDrug Therapy, Combination10aFemale10aFollow-Up Studies10aHumans10aIndia10aLeprostatic Agents10aleprosy10aMale10aMiddle Aged10aMinocycline10aOfloxacin10aRecurrence10aReferral and Consultation10aRifampin10aRisk Factors10aSkin10aTime Factors10aTreatment Outcome10aYoung Adult1 aShetty VP1 aWakade A1 aGhate SD1 aPai V00aClinical, bacteriological and histopathological study of 62 referral relapse cases between Jan 2004 and Dec 2009 at the Foundation for Medical Research, Mumbai. uhttps://leprosyreview.org/article/82/3/01-622 a235-430 v823 a
UNLABELLED: Sixty two patients with relapsed leprosy seen between Jan 2004 and Dec 2009 were studied using clinical, bacteriological and histopathological parameters. The findings thus obtained were correlated to parameters such as trend and source of referral, clinical characteristics at diagnosis, treatment received, other events during or after RFT and duration between cessation of treatment and relapse.
FINDINGS: Referrals per year have doubled since 2006. Most patients were referred by NGOs (58%), followed by Govt. hospitals (16%) and then by GPs (25%); 76% had received one of the WHO - MDT regimens including 16 treated with 24 months or more MB - MDT, 23 with 12 months MB - MDT and eight with 6 months PB - MDT. Of the remaining 14 cases, four had received DDS mono-therapy, seven had single dose of Rifampicin, Ofloxacin and Minocycline (ROM) and four Rifampicin and Ofloxacin (RO) daily for 28 days. The average incubation time of relapse, defined as duration between cessation of treatment and relapse was (SD) + 6-4 years. 59% of patients had positive slit skin smears on relapse. Relapse for the second time occurred in six BL cases including five from group 2 and one RO treated patient and 11/23 cases from group 2 conferred to BT-BB leprosy. Clinical features at diagnosis and on relapse were comparable in 47% of cases.
CONCLUSION: All leprosy patients, regardless of their type and MDT regime, carry 'risk of relapse'. A shorter treatment duration reduces the incubation time to relapse. In group 2 (treated with 12 months MB-MDT regime) 11/23 were BT-BB cases and 5/23 (21%) were relapse for the second time, which further supports our earlier documented findings and maybe the efficacy of WHO-MDT regime is poor in a small subset of patients.
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