02450nas a2200373 4500000000100000008004100001260001300042653001200055653001200067653003100079653001100110653001100121653001200132653000900144653000900153653002400162653002500186653001300211100001700224700001600241700001600257700001600273700001200289700001300301700001900314700001700333245006800350856005900418300001100477490000700488050003200495520153500527022001402062 1993 d c1993 Jun10aAnimals10aDapsone10aDrug Resistance, Microbial10aFemale10aHumans10aleprosy10aMale10aMice10aMice, Inbred BALB C10aMycobacterium leprae10aRifampin1 aGonzalez A B1 aMaestre J L1 aHernandez O1 aColumbié Y1 aAtrio N1 aMartin M1 aFernández A M1 aRodríguez J00aSurvey for secondary dapsone and rifampicin resistance in Cuba. uhttp://leprev.ilsl.br/pdfs/1993/v64n2/pdf/v64n2a06.pdf a128-350 v64 aInfolep Library - available3 a
A total of 1211 Cuban multibacillary leprosy patients treated for at least 5 years were clinically and bacteriologically examined. They were being treated according to a 2-phase monotherapy regimen with RMP first and DADDS afterwards. On skin-smear examination 50 patients were found positive, of which 9 showed a BI of 3+ or higher at any site. With regard to the clinical status the only cases found with clinical signs of relapse were 5 out of 7 long-standing patients with BI of 4+ and 5+. A 6th patient of this high BI group who showed a good clinical condition, except for a heavy infiltration of both earlobes, was receiving a second RMP course when examined and biopsied for this research. These 9 patients were biopsied and susceptibility tests to RMP and DDS performed. The results showed that in 1 case the Mycobacterium leprae were resistant to both drugs; the organisms from 2 other patients were susceptible to RMP but low-grade resistant to DDS. Those from another patient were susceptible to RMP and fully resistant to DDS. In 3 other cases the bacilli did not multiply in any of the mice but 1 of these strains was from the patient taking a second RMP course, therefore this strain might also be susceptible to RMP and resistant to DDS. In the last 2 cases multiplication was only observed in 2 of the controls and in 1 of the 0.0001% DDS treated mice; therefore, these experiments were not conclusive, and the AFB recovered were inoculated into fresh mice to repeat the tests but these failed to multiply.
a0305-7518