TY - JOUR
T1 - Successful discontinuation of therapy for disseminated Mycobacterium avium complex infection after effective antiretroviral therapy
AU - Shafran, Stephen D.
AU - Mashinter, Laura D.
AU - Phillips, Peter
AU - Lalonde, Richard G.
AU - Gill, M. John
AU - Walmsley, Sharon L.
AU - Toma, Emil
AU - Conway, Brian
AU - Fong, Ignatius W.
AU - Rachlis, Anita R.
AU - Williams, Kurt E.
AU - Garber, Gary E.
AU - Schlech, Walter F.
AU - Smaill, Fiona
PY - 2002/11/5
Y1 - 2002/11/5
N2 - Background: Highly active antiretroviral therapy (HAART) is associated with improvement or resolution of several HIV-associated opportunistic infections. Although prophylaxis against disseminated Mycobacterium avium complex infection may be successfully discontinued after a favorable response to HAART, the 1999 guidelines from the U.S. Public Health Service/Infectious Diseases Society of America recommend continuing therapy for disseminated M. avium complex infection, regardless of the response to HAART. Objective: To examine the outcome among patients with disseminated M. avium complex infection whose antimycobacterial therapy was discontinued after a favorable response to HAART. Design: Retrospective chart review between May 2000 and May 2001. Setting: 13 Canadian HIV clinics. Patients: 52 HIV-infected adults (43 men; mean age, 37.3 years) in whom successful antimycobacterial therapy for disseminated M. avium complex infection was discontinued after a favorable virologic response to HAART. Measurements: Survival, survival free of disseminated M. avium complex infection, and CD4+ cell count responses. Results: At the time of diagnosis of disseminated M. avium complex infection, the median CD4+ cell count was 0.016 × 109 cells/L, and the median plasma HIV RNA level was 90 000 copies/mL (plasma HIV RNA levels were available for only 21 patients). The patients received a median of 32 months of antimycobacterial therapy that included ethambutol plus either clarithromycin or azithromycin. When antimycobacterial therapy was discontinued, the median CD4+ cell count was 0.23 × 109 cells/L and the median plasma HIV RNA level was less than 50 copies/mL. A median of 20 months after discontinuation of antimycobacterial therapy, only 1 patient had developed recurrent M. avium complex disease (37 months after stopping antimycobacterial therapy). This patient had stopped HAART 2 months earlier because of uncontrolled HIV viremia. Twenty months after stopping antimycobacterial therapy, the other 51 patients had a median CD4+ cell count of 0.288 × 109 cells/L; 34 (67%) had undetectable plasma HIV RNA levels, and 8 (15%) had plasma HIV RNA levels of 50 to 1000 copies/mL. Conclusions: Discontinuation of successful disseminated M. avium complex therapy after a successful response to HAART is safe and reduces patients' pill burdens, potential drug adverse effects, drug interactions, and costs of therapy.
AB - Background: Highly active antiretroviral therapy (HAART) is associated with improvement or resolution of several HIV-associated opportunistic infections. Although prophylaxis against disseminated Mycobacterium avium complex infection may be successfully discontinued after a favorable response to HAART, the 1999 guidelines from the U.S. Public Health Service/Infectious Diseases Society of America recommend continuing therapy for disseminated M. avium complex infection, regardless of the response to HAART. Objective: To examine the outcome among patients with disseminated M. avium complex infection whose antimycobacterial therapy was discontinued after a favorable response to HAART. Design: Retrospective chart review between May 2000 and May 2001. Setting: 13 Canadian HIV clinics. Patients: 52 HIV-infected adults (43 men; mean age, 37.3 years) in whom successful antimycobacterial therapy for disseminated M. avium complex infection was discontinued after a favorable virologic response to HAART. Measurements: Survival, survival free of disseminated M. avium complex infection, and CD4+ cell count responses. Results: At the time of diagnosis of disseminated M. avium complex infection, the median CD4+ cell count was 0.016 × 109 cells/L, and the median plasma HIV RNA level was 90 000 copies/mL (plasma HIV RNA levels were available for only 21 patients). The patients received a median of 32 months of antimycobacterial therapy that included ethambutol plus either clarithromycin or azithromycin. When antimycobacterial therapy was discontinued, the median CD4+ cell count was 0.23 × 109 cells/L and the median plasma HIV RNA level was less than 50 copies/mL. A median of 20 months after discontinuation of antimycobacterial therapy, only 1 patient had developed recurrent M. avium complex disease (37 months after stopping antimycobacterial therapy). This patient had stopped HAART 2 months earlier because of uncontrolled HIV viremia. Twenty months after stopping antimycobacterial therapy, the other 51 patients had a median CD4+ cell count of 0.288 × 109 cells/L; 34 (67%) had undetectable plasma HIV RNA levels, and 8 (15%) had plasma HIV RNA levels of 50 to 1000 copies/mL. Conclusions: Discontinuation of successful disseminated M. avium complex therapy after a successful response to HAART is safe and reduces patients' pill burdens, potential drug adverse effects, drug interactions, and costs of therapy.
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U2 - 10.7326/0003-4819-137-9-200211050-00008
DO - 10.7326/0003-4819-137-9-200211050-00008
M3 - Article
C2 - 12416943
AN - SCOPUS:0037027459
SN - 0003-4819
VL - 137
SP - 734
EP - 737
JO - Annals of Internal Medicine
JF - Annals of Internal Medicine
IS - 9
ER -