Discontinuation of primary prophylaxis against Pneumocystis carinii pneumonia in HIV-1-infected adults treated with combination antiretroviral therapy

被引:200
作者
Furrer, H [1 ]
Egger, M
Opravil, M
Bernasconi, E
Hirschel, B
Battegay, M
Telenti, A
Vernazza, PL
Rickenbach, M
Flepp, M
Malinverni, R
机构
[1] Inselspital, HIV Sprechstunde, CH-3010 Bern, Switzerland
[2] Univ Bristol, Dept Social Med, MRC, Hlth Serv Res Collaborat, Bristol, Avon, England
[3] Univ Spital Zurich, Abt Infektionskrankheiten & Spitalhyg, Zurich, Switzerland
[4] Osped Reg Lugano, Lugano, Switzerland
[5] Univ Geneva, Hop Cantonal, Div Malad Infect, CH-1211 Geneva, Switzerland
[6] Univ Basel, Kantonsspital, Med Poliklin, CH-4031 Basel, Switzerland
[7] CHU Vaudois, Div Malad Infect, CH-1011 Lausanne, Switzerland
[8] Kantonsspital, Klin Innere Med A, St Gallen, Switzerland
[9] Swiss HIV Cohort Study, Coordinat & Data Ctr, Lausanne, Switzerland
关键词
D O I
10.1056/NEJM199904293401701
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background It is unclear whether primary prophylaxis against Pneumocystis carinii pneumonia can be discontinued in patients infected with the human immunodeficiency virus (HIV) who are successfully treated with combination antiretroviral therapy. We prospectively studied the safety of stopping prophylaxis among patients in the Swiss HIV Cohort Study. Methods Patients were eligible for our study if their CD4 counts had increased to at least 200 cells per cubic millimeter and 14 percent of total lymphocytes while they were receiving combination antiretroviral therapy, with these levels sustained for at least 12 weeks. Prophylaxis was stopped at study entry, and patients were examined every three months thereafter. The development of P. carinii pneumonia was the primary end point, and the development of toxoplasmic encephalitis the secondary end point. Results Of the 262 patients included in our analysis, 121 (46.2 percent) were positive for IgG antibodies to Toxoplasma gondii at base line. The median CD4 count at study entry was 325 per cubic millimeter (range, 210 to 806); the median nadir CD4 count was 110 per cubic millimeter (range, 0 to 240). During a median follow-up of 11.3 months (range, 3.0 to 18.8), prophylaxis was resumed in nine patients, and two patients died. There were no cases of P. carinii pneumonia or toxoplasmic encephalitis. The one-sided upper 99 percent confidence limit for the incidence of P. carinii pneumonia was 1.9 cases per 100 patient-years (based on 238 patient-years of followup). The corresponding figure for toxoplasmic encephalitis was 4.2 per 100 patient-years (based on 110 patient-years of follow-up). Conclusions Stopping primary prophylaxis against Fl carinii pneumonia appears to be safe in HIV-infected patients who are receiving combination antiretroviral treatment and who have had a sustained increase in their CD4 counts to at least 200 cells per cubic millimeter and to at least 14 percent of total lymphocytes. (N Engl J Med 1999;340:1301-6.) (C)1999, Massachusetts Medical Society.
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页码:1301 / 1306
页数:6
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