Antituberculosis treatment containing
thiacetazone is associated with a high incidence of life-threatening cutaneous
drug reactions in patients infected with the human immunodeficiency virus (HIV). In order to develop a local policy concerning the use of this
drug, a study was undertaken to determine the incidence of such reactions in a total of 1063 Ghanaian adult patients treated for
pulmonary tuberculosis (PTB) with
thiacetazone-containing regimens. The incidence was retrospectively determined in 3 different treatment groups, comparing: (A) unselected use of
thiacetazone; (B) exclusion of
thiacetazone from all patients with positive HIV serology; (C) selective exclusion of
thiacetazone from patients with clinical criteria suggesting
HIV infection plus education of health workers and patients. Of the 408 patients in group A receiving
thiacetazone, 9 (2.2%) developed life-threatening cutaneous reactions and 7 of these were HIV-positive. Overall, 6.8% of HIV-positive patients compared to 0.65% of HIV-negative patients developed severe reactions (P < 0.01; relative risk = 10.5). Six of the 9 patients with reactions died. All 379 patients in group B were screened for
HIV antibodies and positive cases (23%) received a regimen in which
thiacetazone was substituted by
ethambutol. In contrast to Group A, only one HIV-negative patient (0.26%) developed a severe cutaneous reaction (P = 0.02). Among 276 patients in group C,
thiacetazone was substituted with
ethambutol only in those with clinical evidence of
HIV infection (8%) and staff and patients were educated about early recognition of the side-effect. With this policy, these were no admissions with severe cutaneous reactions compared to 2.2% of those in group A (P = 0.01). In conclusion, a policy of selective use of
thiacetazone in the treatment of PTB based on clinical criteria combined with patient and staff education was found to be a practical and cost-effective strategy combating severe cutaneous reactions to
thiacetazone.