Interruption of prophylaxis for major opportunistic infections in HIV-infected patients receiving triple combination antiretroviral therapy

被引:0
|
作者
Jubault, V [1 ]
Pacanowski, J [1 ]
Rabian, C [1 ]
Viard, JP [1 ]
机构
[1] Hop Necker Enfants Malad, Serv Immunol Clin, F-75743 Paris 15, France
来源
ANNALES DE MEDECINE INTERNE | 2000年 / 151卷 / 03期
关键词
antiretroviral therapy; CD4; cellular immunity; opportunistic infections; infectious diseases; Pneumocystis carinii pneumonia; viral load;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To determine whether HIV-infected patients receiving highly active antiretroviral therapy (HAART) and recovering a CD4 cell number above 200x10(6)/l may safely discontinue primary and secondary prophylaxes for major opportunistic infections. Design: Retrospective study of a single-center, prospectively constituted cohort of 223 patients receiving HAART with a protease inhibitor, of whom 137 received at least one prophylaxis. Methods: Exhaustive informations on prophylaxis use, clinical and laboratory data were used to produce descriptive statistics on infectious events, duration of HIV infection, time on HAART, time to prophylaxis interruption, length of follow-up and biological values at relevant time points. Results: Fifty-one patients with a history of severe immunodepression (median CD4 nadir: 62x10(6)/l), including 16 patients with CDC stage C infection, discontinued at least one prophylaxis. Primary or secondary P. carinii pneumonia prophylaxis was discontinued in 43 patients: 1 first episode of PCP occurred after 2 months but no other episode was recorded after a median follow-up of 16 months. Toxoplasmosis primary or secondary prophylaxis, secondary cytomegalovirus prophylaxis and primary or secondary M. avium complex prophylaxes were discontinued in respectively 37, 5 and 5 bpatients, and no event was recorded after respective follow-ups of 16, 7 and 15 months. Nine secondary and 2 primary acyclovir prophglaxes were discontinued, and two events were observed after 1 and 19 months; no other event was noted after a follow-up of 22 months. Conclusion: Prophylaxis for opportunistic infections could be safely interrupted in most of these severely immunodeficient patients recovering a CD4 cell count above 200x10(6)/l on HAART. This confirms the efficiency of immune restoration and is beneficial to patients but, since 3 infectious events were recorded, caution should be taken before making a decision based on immunological and virological considerations.
引用
收藏
页码:163 / 168
页数:6
相关论文
共 50 条
  • [1] Discontinuation of secondary prophylaxis for opportunistic infections in HIV-infected patients receiving highly active antiretroviral therapy
    Soriano, V
    Dona, C
    Rodríguez-Rosado, R
    Barreiro, P
    González-Lahoz, J
    AIDS, 2000, 14 (04) : 383 - 386
  • [2] Prophylaxis for opportunistic infections among HIV-infected patients receiving medical care
    Sackoff, J
    McFarland, J
    Su, S
    Bryan, E
    JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES AND HUMAN RETROVIROLOGY, 1998, 19 (04): : 387 - 392
  • [3] DRUG-THERAPY OF MAJOR OPPORTUNISTIC INFECTIONS IN HIV-INFECTED PATIENTS
    STEIN, M
    MAYER, K
    HOSPITAL FORMULARY, 1991, 26 (09): : 706 - 713
  • [4] Interruption of antiretroviral therapy in chronically HIV-infected patients
    Amador, C
    Pasquau, F
    Ena, J
    Benito, C
    de Apodaca, RFR
    MEDICINA CLINICA, 2005, 125 (02): : 41 - 45
  • [5] Prophylaxis of opportunistic infections in HIV-Infected patients in the HAART era
    Vasa, CV
    Tang, I
    Glatt, AE
    INFECTIONS IN MEDICINE, 2002, 19 (10) : 452 - +
  • [6] CURRENT STATUS OF PROPHYLAXIS FOR OPPORTUNISTIC INFECTIONS IN HIV-INFECTED PATIENTS
    DECKER, CF
    MASUR, H
    AIDS, 1994, 8 (01) : 11 - 20
  • [7] Optimum Timing of Antiretroviral Therapy for HIV-Infected Patients with Concurrent Serious Opportunistic Infections
    Meintjes, Graeme
    Wilkinson, Robert J.
    CLINICAL INFECTIOUS DISEASES, 2010, 50 (11) : 1539 - 1541
  • [8] Gynecomastia in HIV-infected patients receiving antiretroviral therapy
    García-Benayas, T
    Blanco, F
    Martín-Carbonero, L
    Valencia, E
    Barrios, A
    González-Lahoz, J
    Soriano, V
    AIDS RESEARCH AND HUMAN RETROVIRUSES, 2003, 19 (09) : 739 - 741
  • [9] Gastroduodenal opportunistic infections and dyspepsia in HIV-infected patients in the era of Highly Active Antiretroviral Therapy
    Werneck-Silva, Ana Luiza
    Prado, Ivete Bedin
    JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2009, 24 (01) : 135 - 139
  • [10] Operationalizing early antiretroviral therapy in HIV-infected in-patients with opportunistic infections including tuberculosis
    Sunpath, H.
    Edwin, C.
    Chelin, N.
    Nadesan, S.
    Maharaj, R.
    Moosa, Y.
    Smeaton, L.
    Court, R.
    Knight, S.
    Gwyther, E.
    Murphy, R. A.
    INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE, 2012, 16 (07) : 917 - 923