thioacetazone and Erythema-Multiforme

Because the number of cases of multiforme skin lesions encountered in the medical department of Yekatit 12 Hospital has increased in recent years, we conducted a retrospective study to identify the likely precipitating factors and the possible relationship of these with HIV infection. Forty-seven patients with Multiforme Skin Lesions (29 males, 18 females) were admitted between 1976 and January 1994, of whom 43 (92%) were admitted in the past 5 years. Most patients were aged 15-49 years. Thirty patients (64%) were discharged improved and 14 (30%) expired in hospital. The outcome of 3 patients are not known. The charts of only 16 patients could be retrieved for review. Fifteen of these (94%) gave a history of intake of streptomycin, isoniazed and thiacetazone prior to developing the skin manifestation. The anti-TB medications were discontinued initially; 14 patients were restarted on STM, INH and ethambutol without recurrence of the rash. All but 1 were discharged improved. HIV screening tests were done on 24 patients with multiforme skin lesion of whom 21 (88%) were seropositive. Our study suggested that the adverse effects of thiacetazone are increased in HIV associated tuberculous patients. We recommend that further studies be conducted in HIV seropositive and seronegative patients.

Topics: Adolescent; Adult; Antitubercular Agents; Erythema Multiforme; Ethiopia; Female; HIV Seropositivity; Hospitalization; Humans; Male; Middle Aged; Precipitating Factors; Prevalence; Retrospective Studies; Thioacetazone; Treatment Outcome; Tuberculosis

The effects of the human immunodeficiency virus (HIV) on tuberculosis management was investigated in 227 patients initially treated with a regimen containing streptomycin, isoniazid, and thiacetazone (STH). 93 of these 227 were HIV-seropositive. 60 patients, of whom 18 were HIV-seropositive, received a regimen consisting of streptomycin, isoniazid, rifampicin, and pyrazinamide (SHRZ) in the initial phase, and thiacetazone and isoniazid (TH) in the continuation phase. Cutaneous hypersensitivity reactions occurred in 22 of 111 (20%) HIV-seropositive patients, and in 2 of 176 (1%) HIV-seronegative patients (RR = 18, 95% CI 4.4-76, p less than 10(-7]. During the first 8 weeks of treatment 18 reactions occurred among the 93 HIV-seropositive patients on STH, whereas no reaction occurred in 17 HIV-seropositive patients during the initial phase of SHRZ/TH (p = 0.04). None of the 18 HIV-seropositive patients with cutaneous reactions who were subsequently challenged with isoniazid reacted, nor did any of the 10 tested with streptomycin, but 6 of the 7 challenged with thiacetazone reacted. 3 patients (all HIV-positive and with toxic epidermal necrolysis) died as a result of the cutaneous reaction. These results have major implications for tuberculosis control programmes in Africa.

Topics: Adult; Antitubercular Agents; Drug Administration Schedule; Drug Eruptions; Erythema Multiforme; Evaluation Studies as Topic; Follow-Up Studies; HIV Seropositivity; Humans; Prospective Studies; Risk Factors; Skin Tests; Stevens-Johnson Syndrome; Thioacetazone; Time Factors; Tuberculosis, Pulmonary

Topics: Drug Eruptions; Erythema Multiforme; Humans; Stevens-Johnson Syndrome; Terminology as Topic; Thioacetazone

Topics: Erythema Multiforme; Humans; Skin; Stevens-Johnson Syndrome; Thioacetazone; Thiosemicarbazones; Tuberculosis, Pulmonary