Gallo M E, Alvim M F, Nery J A, Albuquerque E C, Sarno E N
National Coordination Sanitary, Dermatology of the Ministry of Health.
Indian J Lepr. 1996 Jul-Sep;68(3):235-45.
This study compares the clinical, bacilloscopic, and histopathological evolution of 140 patients classified as having multibacillary leprosy with no previous specific treatment who were submitted to two multidrug treatment regimens with a fixed dose. Regimen I-Group 1: 70 cases received 600 mg rifampicin (RMP) + 100 mg dapsone (DDS) daily for three consecutive months followed by 100 mg DDS daily, self-administered doses for 21 months. Regimen II-Group II: 70 cases received 600 mg RMP + 300 mg clofazimine (CLO) once a month under supervision plus self-administered doses of 50 mg CLO + 100 mg DDS daily for 24 months. The bacilloscopic, histopathological and neuromotor evaluation parameters showed no statistically meaningful differences (P > 0.05) between the two groups except for reaction frequency (P < 0.05) in that group II patients presented the least number of reactional episodes during the treatment and in the dermatological examination at discharge. Follow-up after treatment was carried out for a consecutive four year period. During routine clinical examination one case submitted to regimen I developed nodular skin lesion over the right arm. Skin biopsy was done for histopathological examination and mouse foot-pad experiment by Shepard technique. The drug susceptibility test with DDS and RPM showed that M. leprae strain isolated was susceptible to both the drugs.
本研究比较了140例确诊为多菌型麻风且此前未接受过特异性治疗的患者的临床、细菌学及组织病理学演变情况,这些患者接受了两种固定剂量的联合化疗方案。方案I - 第1组:70例患者连续三个月每日服用600毫克利福平(RMP)+ 100毫克氨苯砜(DDS),随后每日自行服用100毫克DDS,持续21个月。方案II - 第2组:70例患者在监督下每月服用一次600毫克RMP + 300毫克氯法齐明(CLO),并每日自行服用50毫克CLO + 100毫克DDS,持续24个月。细菌学、组织病理学及神经运动评估参数显示,两组之间除反应频率(P < 0.05)外无统计学意义上的显著差异(P > 0.05),即第2组患者在治疗期间及出院时的皮肤科检查中出现的反应性发作次数最少。治疗后进行了连续四年的随访。在常规临床检查期间,接受方案I治疗的1例患者右臂出现结节性皮肤病变。进行了皮肤活检以进行组织病理学检查,并采用谢泼德技术进行小鼠足垫实验。对DDS和RPM的药敏试验表明,分离出的麻风杆菌菌株对这两种药物均敏感。