Low-dose fluconazole as primary prophylaxis for cryptococcal infection in AIDS patients with CD4 cell counts of <=100/mm(3): Demonstration of efficacy in a prospective, multicenter trial

被引:32
作者
Singh, N
Barnish, MJ
Berman, S
Bender, BS
Wagener, MM
Rinaldi, MG
Yu, VL
机构
[1] VET AFFAIRS MED CTR,INFECT DIS SECT,PITTSBURGH,PA 15240
[2] UNIV PITTSBURGH,PITTSBURGH,PA 15260
[3] KENNEDY MEM HOSP,STRATFORD,NJ
[4] VET AFFAIRS MED CTR,LONG BEACH,CA
[5] VET AFFAIRS MED CTR,GAINESVILLE,FL 32608
[6] UNIV FLORIDA,GAINESVILLE,FL 32611
[7] UNIV TEXAS,HLTH SCI CTR,SAN ANTONIO,TX
关键词
D O I
10.1093/clinids/23.6.1282
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The efficacy of low-dose fluconazole (200 mg orally administered thrice weekly) as primary prophylaxis for cryptococcal infection was prospectively assessed in a multicenter trial involving 218 patients who were infected with human immunodeficiency virus (HIV) and who had CD4 cell counts of less than or equal to 100/mm(3). The median CD4 cell count at baseline was 39/mm(3); 58% of the patients had an AIDS-defining illness or infection prior to enrollment. Cryptococcal meningitis occurred in 0.4% (1) of the 218 patients. The breakthrough isolate was susceptible to fluconazole, and the fluconazole kinetic study demonstrated adequate drug absorption and serum fluconazole levels; noncompliance could not be excluded in this case. Mucocutaneous and/or esophageal candidiasis developed in 18% (40) of the patients, Noncompliance with fluconazole therapy was the only variable independently associated with breakthrough candidiasis in the study patients (P = .00002). Thus, fluconazole (200 mg thrice weekly) given to HIV-infected patients with CD4 cell counts of less than or equal to 100/mm(3) was efficacious as primary prophylaxis for cryptococcosis, with notably lower costs acid increased convenience for patients in comparison with daily administration of the drug.
引用
收藏
页码:1282 / 1286
页数:5
相关论文
共 17 条
[1]   PHARMACOKINETICS AND BIOAVAILABILITY OF FLUCONAZOLE IN PATIENTS WITH AIDS [J].
DEMURIA, D ;
FORREST, A ;
RICH, J ;
SCAVONE, JM ;
COHEN, LG ;
KAZANJIAN, PH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (10) :2187-2192
[2]   UNDERSTANDING AND IMPROVING PATIENT COMPLIANCE [J].
ERAKER, SA ;
KIRSCHT, JP ;
BECKER, MH .
ANNALS OF INTERNAL MEDICINE, 1984, 100 (02) :258-268
[3]   ASSAY OF FLUCONAZOLE BY MEGABORE CAPILLARY GAS-LIQUID-CHROMATOGRAPHY WITH NITROGEN-SELECTIVE DETECTION [J].
HARRIS, SC ;
WALLACE, JE ;
FOULDS, G ;
RINALDI, MG .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (05) :714-716
[4]  
HEALD A, 1994, 34 INT C ANT AG CHEM
[5]   FLUCONAZOLE-RESISTANT CANDIDA IN AIDS PATIENTS [J].
HEINIC, GS ;
STEVENS, DA ;
GREENSPAN, D ;
MACPHAIL, LA ;
DODD, CL ;
STRINGARI, S ;
STRULL, WM ;
HOLLANDER, H .
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS, 1993, 76 (06) :711-715
[6]  
LAGUNA F, 1994, 34 INT C ANT AG CHEM
[7]   PHARMACOKINETICS OF FLUCONAZOLE IN CEREBROSPINAL-FLUID AND SERUM OF RABBITS - VALIDATION OF AN ANIMAL-MODEL USED TO MEASURE DRUG CONCENTRATIONS IN CEREBROSPINAL-FLUID [J].
MADU, A ;
CIOFFE, C ;
MIAN, U ;
BURROUGHS, M ;
TUOMANEN, E ;
MAYERS, M ;
SCHWARTZ, E ;
MILLER, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (09) :2111-2115
[8]  
MONANE M, 1993, HOSP PHYSICIAN APR, P35
[9]  
*NAT COMM CLIN LAB, 1995, M27T NCCLS
[10]   IN-VITRO EVALUATION OF COMBINATION OF FLUCONAZOLE AND FLUCYTOSINE AGAINST CRYPTOCOCCUS-NEOFORMANS VAR NEOFORMANS [J].
NGUYEN, MH ;
BARCHIESI, F ;
MCGOUGH, DA ;
YU, VL ;
RINALDI, MG .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (08) :1691-1695