Can chemoprophylaxis against opportunistic infections be discontinued after an increase in CD4 cells induced by highly active antiretroviral therapy?

被引:66
作者
Kirk, O [1 ]
Lundgren, JD
Pedersen, C
Nielsen, H
Gerstoft, J
机构
[1] Univ Copenhagen, Hvidovre Hosp, Dept Infect Dis 144, DK-2650 Hvidovre, Denmark
[2] Odense Univ Hosp, Dept Infect Dis, DK-5000 Odense, Denmark
[3] Aalborg Hosp, Dept Infect Dis, Aalborg, Denmark
[4] Univ Copenhagen, Rigshosp, Dept Infect Dis, DK-2100 Copenhagen, Denmark
关键词
chemoprophylaxis; combination therapy; immune reconstitution; opportunistic infections;
D O I
10.1097/00002030-199909100-00007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: In the 'USPHS/IDSA Guidelines for Prevention of Opportunistic Infections in Persons Infected with Human Immunodeficiency Virus', the indications for chemoprophylaxis are based on nadir CD4 cell count. Many patients have, however, experienced an increase in CD4 cell count after the introduction of highly active antiretroviral therapy (HAART). Objectives: To assess incidences of opportunistic infections after discontinuation of chemoprophylaxis in HIV-infected patients, who have experienced a HAART-induced increase in CD4 cell count. Methods: The Danish guidelines for chemoprophylaxis against opportunistic infections in HIV-infected patients were revised in late 1997, allowing discontinuation of chemoprophylaxis after initiation of HAART if the CD4 cell count remained above a specified limit for more than 6 months. Consecutive patients were followed, and incidences of opportunistic infections after discontinuation of chemoprophylaxis were assessed. Results: A total of 219 patients discontinued Pneumocystis carinii pneumonia (PCP)chemoprophylaxis (12% maintenance therapy). One case of PCP was diagnosed within 174 person-years (PY) of follow-up, resulting in an incidence of 0.6 cases/100 PY follow-up (95% confidence interval, 0.0-3.2). No cases of cerebral toxoplasmosis, cytomegalovirus chorioretinitis, or disseminated Mycobacterium avium infection were observed. Follow-up time for these was, however, limited. Conclusion: PCP-chemoprophylaxis can be safely discontinued after HAART-induced increase in CD4 cell count to more than 200 x 10(6) cells/l. Among consecutive patients who discontinue chemoprophylaxis according to well-defined guidelines, the observed incidence of PCP is below those reported earlier in patients with similar CD4 cell count. (C) 1999 Lippincott Williams & Wilkins.
引用
收藏
页码:1647 / 1651
页数:5
相关论文
共 23 条
  • [1] Eradication of AIDS-related disseminated Mycobacterium avium complex infection after 12 months of antimycobacterial therapy combined with highly active antiretroviral therapy
    Aberg, JA
    Yajko, DN
    Jacobson, MA
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (05) : 1446 - 1449
  • [2] Positive effects of combined antiretroviral therapy on CD4(+) T cell homeostasis and function in advanced HIV disease
    Autran, B
    Carcelain, G
    Li, TS
    Blanc, C
    Mathez, D
    Tubiana, R
    Katlama, C
    Debre, P
    Leibowitch, J
    [J]. SCIENCE, 1997, 277 (5322) : 112 - 116
  • [3] Discontinuation of primary prophylaxis against Pneumocystis carinii pneumonia in HIV-1-infected adults treated with combination antiretroviral therapy
    Furrer, H
    Egger, M
    Opravil, M
    Bernasconi, E
    Hirschel, B
    Battegay, M
    Telenti, A
    Vernazza, PL
    Rickenbach, M
    Flepp, M
    Malinverni, R
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (17) : 1301 - 1306
  • [4] Gill J, 1998, AIDS, V12, P680
  • [5] GULICK RM, 1997, NEW ENGL J MED, V337, P743
  • [6] A controlled trial of two nucleoside analogues plus indinavir in persons with human immunodeficiency virus infection and CD4 cell counts of 200 per cubic millimeter or less
    Hammer, SM
    Squires, KE
    Hughes, MD
    Grimes, JM
    Demeter, LM
    Currier, JS
    Eron, JJ
    Feinberg, JE
    Balfour, HH
    Dayton, LR
    Chodakewitz, JA
    Fischl, MA
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (11) : 725 - 733
  • [7] Hartung T, 1998, Curr Opin Hematol, V5, P221, DOI 10.1097/00062752-199805000-00013
  • [8] Cytomegalovirus retinitis after initiation of highly active antiretroviral therapy
    Jacobson, MA
    Zegans, M
    Pavan, PR
    ODonnell, JJ
    Sattler, F
    Rao, N
    Owens, S
    Pollard, R
    [J]. LANCET, 1997, 349 (9063) : 1443 - 1445
  • [9] Risk factors for primary Pneumocystis carinii pneumonia in human immunodeficiency virus-infected adolescents and adults in the United States:: Reassessment of indications for chemoprophylaxis
    Kaplan, JE
    Hanson, DL
    Navin, TR
    Jones, JL
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (04) : 1126 - 1132
  • [10] Long-lasting recovery in CD4 T-cell function and viral-load reduction after highly active antiretroviral therapy in advanced HIV-1 disease
    Li, TS
    Tubiana, R
    Katlama, C
    Calvez, V
    Ait Mohand, H
    Autran, B
    [J]. LANCET, 1998, 351 (9117) : 1682 - 1686