Relapse rates after short-course (6-month) treatment of tuberculosis in HIV-infected and uninfected persons

TR Sterling, K Alwood, R Gachuhi, W Coggin, D Blazes… - Aids, 1999 - journals.lww.com
TR Sterling, K Alwood, R Gachuhi, W Coggin, D Blazes, WR Bishai, RE Chaisson
Aids, 1999journals.lww.com
Objective: To determine the rate of tuberculosis relapse among HIV-seropositive and-
seronegative persons treated for active tuberculosis with short-course (6-month) therapy.
Design: Consecutive cohort study. Setting: City of Baltimore tuberculosis clinic. Patients:
Tuberculosis patients treated between 1 January 1993 and 31 December 1996. Intervention:
Patients received 2 months of isoniazid, rifampin, pyrazinamide and ethambutol followed by
4 months of isoniazid and rifampin. Main outcome measure: Passive follow-up for …
Abstract
Objective:
To determine the rate of tuberculosis relapse among HIV-seropositive and-seronegative persons treated for active tuberculosis with short-course (6-month) therapy.
Design:
Consecutive cohort study.
Setting:
City of Baltimore tuberculosis clinic.
Patients:
Tuberculosis patients treated between 1 January 1993 and 31 December 1996.
Intervention:
Patients received 2 months of isoniazid, rifampin, pyrazinamide and ethambutol followed by 4 months of isoniazid and rifampin.
Main outcome measure:
Passive follow-up for tuberculosis relapse was performed through September 30, 1998.
Results:
There were 423 cases of tuberculosis during the study period; 280 patients completed a 6-month course of therapy. Therapy was directly-observed for 94% of patients. Of those who completed therapy, 47 (17%) were HIV-seropositive, 127 (45%) were HIV-seronegative, and 106 (38%) had unknown HIV status. HIV-infected patients required more time to complete therapy (median 225 versus 205 days; P= 0.04) but converted sputum culture to negative within the same time period (median 77 versus 72 days; P= 0.43) as HIV-seronegative or unknown patients. Relapse occurred in three out of 47 (6.4%) HIV-infected patients compared to seven out of 127 (5.5%) HIV-seronegative patients (P= 1.0). Relapse rates also did not differ when HIV-seropositive patients were compared with HIV-seronegative and patients with unknown HIV status (6.4% versus 3.0%; P= 0.38). Of the 10 patients with tuberculosis relapse, restriction fragment length polymorphism data were available for five; all five relapse isolates matched the initial isolate.
Conclusions:
These results support current recommendations to treat tuberculosis in HIV-infected patients with short-course (6-month) therapy.
Lippincott Williams & Wilkins