A prospective study of discontinuing primary and secondary Pneumocystis carinii pneumonia prophylaxis after CD4 cell count increase to > 200 X 106/I

被引:25
作者
Koletar, SL
Heald, AE
Finkelstein, D
Hafner, R
Currier, JS
McCutchan, JA
Vallee, M
Torriani, FJ
Powderly, WG
Fass, RJ
Murphy, RL
机构
[1] Ohio State Univ Hosp, Columbus, OH 43210 USA
[2] Duke Univ, Med Ctr, Durham, NC USA
[3] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
[4] NIH, Bethesda, MD 20892 USA
[5] Univ Calif Los Angeles, Los Angeles, CA 90024 USA
[6] Univ Calif San Diego, San Diego, CA 92103 USA
[7] Washington Univ, Sch Med, St Louis, MO USA
[8] Northwestern Univ, Sch Med, Chicago, IL USA
关键词
discontinuing primary and secondary prophylaxis; Pneumocystis carinii pneumonia;
D O I
10.1097/00002030-200108170-00008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To assess the incidence of Pneumocystis carinii pneumonia (PCP) after discontinuation of either primary or secondary prophylaxis. Design: This was a prospective, non-randomized, non-blinded study. Setting: Twenty-five University-based AIDS Clinical Trials Group units. Participants: Participants either had a CD4 cell count less than or equal to 100 x 10(6)/l at any time in the past and no history of confirmed PCP (group I; n = 144), or had a confirmed episode of PCP greater than or equal to 6 months prior to study entry (group II; n = 129). All subjects had sustained CD4 cell counts > 200 x 10(6)/l in response to antiretroviral therapy. Interventions: Subjects discontinued PCP prophylaxis within 3 months or at the time of study entry. Evaluations for symptoms of PCP and CD4 cell counts were performed every 8 weeks. Prophylaxis was resumed if two consecutive CD4 cell counts were < 200 x 10(6)/l. Main outcome measure(s): The main outcome was development of PCP. Results: No cases of PCP occurred in 144 subjects (median follow-up, 82 weeks) in group I or in the 129 subjects (median follow-up, 63 weeks) in group II (95% upper confidence limits on the rates of 1.3 per 100 person-years and 1.96 per 100 person-years for groups I and II, respectively). Eight subjects (five in group I and three in group II) resumed PCP prophylaxis after two consecutive CD4 cell counts < 200 x 10(6)/l. Conclusions: The risk of developing initial or recurrent PCP after discontinuing prophylaxis is low in HIV-infected individuals who have sustained CD4 cell count increases in response to antiretroviral therapy. Neither lifelong primary nor secondary PCP prophylaxis is necessary. (C) 2001 Lippincott Williams & Wilkins.
引用
收藏
页码:1509 / 1515
页数:7
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