Response to lamivudine-zidovudine plus abacavir twice daily in antiretroviral-naive, incarcerated patients with HIV infection taking directly observed treatment

被引:55
作者
Kirkland, LR
Fischl, MA
Tashima, KT
Paar, D
Gensler, T
Graham, NM
Gao, H
Rosenzweig, JRC
McClernon, DR
Pittman, G
Hessenthaler, SM
Hernandez, JE
机构
[1] Univ Miami, Sch Med, Dept Med, Miami, FL 33136 USA
[2] Burnside Clin, Columbia, SC USA
[3] Univ Miami, Sch Med, Coral Gables, FL 33124 USA
[4] Miriam Hosp, Providence, RI 02906 USA
[5] Univ Texas, Med Branch, Galveston, TX 77550 USA
[6] Correct Med Serv, Pine Bluff, AR USA
[7] Glaxo Wellcome Inc, Res Triangle Pk, NC 27709 USA
关键词
D O I
10.1086/338400
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Prison inmates with human immunodeficiency virus (HIV) infection can be difficult to treat because of the complexity and intrusiveness of many combination antiretroviral therapy regimens. NZTA4007, a 24-week open-label, single-arm clinical trial involving 108 antiretroviral therapy-naive, incarcerated, HIV-infected persons, was conducted to evaluate a compact regimen (4 tablets per day) consisting of 1 lamivudine-zidovudine (150 mg/300 mg) combination tablet (COM) and one 300-mg abacavir tablet administered twice daily under directly observed treatment conditions. In the intent-to-treat observed analysis, the plasma HIV type 1 (HIV-1) RNA level remained at less than or equal to400 copies/mL in 85% of the patients and at ! 50 copies/mL in 75% of the patients. Median change from baseline was -2.41 log(10) copies/mL for the HIV-1 RNA level and +111 cells/mm(3) for the CD4 cell count. The overall adherence to prescribed doses was 94% for patients who remained enrolled in the study. COM-abacavir given twice daily was generally well tolerated, and adverse events prompted only 4 patients to withdraw from the study.
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页码:511 / 518
页数:8
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