Successful discontinuation of therapy for disseminated Mycobacterium avium complex infection after effective antiretroviral therapy

被引:29
作者
Shafran, SD
Mashinter, LD
Phillips, P
Lalonde, RG
Gill, MJ
Walmsley, SL
Toma, E
Conway, B
Fong, IW
Rachlis, AR
Williams, KE
Garber, GE
Schlech, WF
Smaill, F
机构
[1] Univ Alberta, Edmonton, AB, Canada
[2] Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
[3] McGill Univ, Montreal, PQ, Canada
[4] Univ Montreal, Montreal, PQ, Canada
[5] Univ Calgary, Calgary, AB, Canada
[6] Univ Toronto, Toronto, ON, Canada
[7] Univ Saskatchewan, Saskatoon, SK, Canada
[8] Univ Ottawa, Ottawa, ON, Canada
[9] Dalhousie Univ, Halifax, NS, Canada
[10] McMaster Univ, Hamilton, ON, Canada
关键词
D O I
10.7326/0003-4819-137-9-200211050-00008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 anti mycobacterial 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 x 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 anti mycobacterial therapy was discontinued, the median CD4(+) cell count was 0.23 x 10(9) 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 anti mycobacterial therapy, the other 51 patients had a median CD4(+) cell count of 0.288 x 10(9) 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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收藏
页码:734 / 737
页数:4
相关论文
共 20 条
[1]   Eradication of AIDS-related disseminated Mycobacterium avium complex infection after 12 months of antimycobacterial therapy combined with highly active antiretroviral therapy [J].
Aberg, JA ;
Yajko, DN ;
Jacobson, MA .
JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (05) :1446-1449
[2]   Treatment of HIV-1-associated microsporidiosis and cryptosporidiosis with combination antiretroviral therapy [J].
Carr, A ;
Marriott, D ;
Field, A ;
Vasak, E ;
Cooper, DA .
LANCET, 1998, 351 (9098) :256-261
[3]   Recurrence of Mycobacterium avium infection in patients receiving highly active antiretroviral therapy and antimycobacterial agents [J].
Cinti, SK ;
Kaul, DR ;
Sax, PE ;
Crane, LR ;
Kazanjian, PH .
CLINICAL INFECTIOUS DISEASES, 2000, 30 (03) :511-514
[4]   Discontinuation of Mycobacterium avium complex prophylaxis in patients with antiretroviral therapy-induced increases in CD4+ cell count -: A randomized, double-blind, placebo-controlled trial [J].
Currier, JS ;
Williams, PL ;
Koletar, SL ;
Cohn, SE ;
Murphy, RL ;
Heald, AE ;
Hafner, R ;
Bassily, EL ;
Lederman, HM ;
Knirsch, C ;
Benson, CA ;
Valdez, H ;
Aberg, JA ;
McCutchan, JA .
ANNALS OF INTERNAL MEDICINE, 2000, 133 (07) :493-503
[5]   A randomized trial of the discontinuation of primary and secondary prophylaxis against Pneumocystis carinii pneumonia after highly active antiretroviral therapy in patients with HIV infection. [J].
de Quiros, JCLB ;
Miro, JM ;
Pena, JM ;
Podzamczer, D ;
Alberdi, JC ;
Martínez, E ;
Cosin, J ;
Claramonte, X ;
Gonzalez, J ;
Domingo, P ;
Casado, JL ;
Ribera, E .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (03) :159-167
[6]   Discontinuation of prophylaxis against Mycobacterium avium complex disease in HIV-infected patients who have a response to antiretroviral therapy. [J].
El-Sadr, WM ;
Burman, WJ ;
Grant, LB ;
Matts, JP ;
Hafner, R ;
Crane, L ;
Zeh, D ;
Gallagher, B ;
Mannheimer, SB ;
Martinez, A ;
Gordin, F .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (15) :1085-1092
[7]   Discontinuation of secondary prophylaxis for toxoplasmic encephalitis in human immunodeficiency virus infection after immune restoration with highly active antiretroviral therapy [J].
Guex, AC ;
Radziwill, AJ ;
Bucher, HC .
CLINICAL INFECTIOUS DISEASES, 2000, 30 (03) :602-603
[8]   Resolution of Mycobacterium avium complex bacteremia following highly active antiretroviral therapy [J].
Hadad, DJ ;
Lewi, DS ;
Pignatari, ACC ;
Martins, MC ;
Vitti, W ;
Arbeit, RD .
CLINICAL INFECTIOUS DISEASES, 1998, 26 (03) :758-759
[9]   Resolution of intractable molluscum contagiosum in a human immunodeficiency virus-infected patient after institution of antiretroviral therapy with ritonavir [J].
Hicks, CB ;
Myers, SA ;
Giner, J .
CLINICAL INFECTIOUS DISEASES, 1997, 24 (05) :1023-1025
[10]  
KAPLAN JE, 1995, CLIN INFECT DIS S, V1, pS1