Prevention of disseminated Mycobacterium avium complex infection with reduced dose clarithromycin in patients with advanced HIV disease

Citation
Rg. Hewitt et al., Prevention of disseminated Mycobacterium avium complex infection with reduced dose clarithromycin in patients with advanced HIV disease, AIDS, 13(11), 1999, pp. 1367-1372
Citations number
26
Categorie Soggetti
Immunology
Journal title
AIDS
ISSN journal
02699370 → ACNP
Volume
13
Issue
11
Year of publication
1999
Pages
1367 - 1372
Database
ISI
SICI code
0269-9370(19990730)13:11<1367:PODMAC>2.0.ZU;2-T
Abstract
Objective: To evaluate the ability of once daily reduced dose clarithromyci n to prevent disseminated Mycobacterium avium complex (dMAC) infection in p atients with advanced HIV disease. Design: Non-randomized, retrospective study. Setting: Outpatient clinic of an urban university-affiliated municipal hosp ital. Patients: A group of 192 HIV-infected patients with a CD4 count < 100 x 10( 6) cells/l who were followed for at least 90 days during a 6-year period (1 991-1996) before the use of protease inhibitors. Interventions: Clarithromycin 500 mg orally once daily (n = 84), rifabutin 300 mg orally once daily (n = 47) or no prophylaxis (n = 61). Main outcome measures: Positive blood culture for M. avium complex (MAC), t ime to development of dMAC, and time to death. Results: When compared with no prophylaxis or rifabutin, the incidence of d MAC and time to development of dMAC were improved among those patients rece iving clarithromycin (P < 0.001). Prolonged survival was associated with bo th clarithromycin and rifabutin use when compared with no prophylaxis (P < 0.002). In patients who failed prophylaxis, resistance to clarithromycin an d rifabutin was observed. Conclusions: In the era prior to protease inhibitor use, once daily clarith romycin at a dose of 500 mg was associated with a reduction in the incidenc e of dMAC, appeared to be superior to rifabutin, and was associated with pr olonged survival in patients with advanced HIV disease. (C) 1999 Lippincott Williams & Wilkins.