DeMasi R A, Graham N M, Tolson J M, Pham S V, Capuano G A, Fisher R L, Shaefer M S, Pakes G E, Sawyerr G A, Eron J J
Glaxo Wellcome Inc., Research Triangle Park, North Carolina, USA.
Adv Ther. 2001 Jul-Aug;18(4):163-73. doi: 10.1007/BF02850110.
The Patient Medication Adherence Questionnaire Version 1.0 (PMAQ-V1.0) is a patient-reported adherence instrument to assess medication-taking behaviors and identify barriers to adherence with antiretroviral therapy. To assess the correlation between adherence and virologic outcome, the PMAQ-V1.0 was administered to 194 antiretroviral-experienced adults with HIV infection enrolled in a 16-week evaluation of protease inhibitor-containing regimens featuring a lamivudine/zidovudine combination tablet. At baseline, plasma HIV-1 RNA levels were less than 10,000 copies/mL and CD4(+)-cell counts were equal to or greater than 300 x 10(6)/L; patients had been receiving a conventional regimen of lamivudine + zidovudine (separately) plus a protease inhibitor for at least 10 weeks immediately prior to the study. Forty-eight percent of patients who reported missing at least one dose of a nucleoside reverse-transcriptase inhibitor (NRTI) during the study had detectable plasma HIV-1 RNA, compared with 26% of patients who reported no missed doses (P = .002). Patients who missed at least one dose of an NRTI or protease inhibitor were 2.5 times more likely to have quantifiable HIV-1 RNA than those who reported no missed doses. Patients who reported fewer barriers and more motivators to adherence had better virologic outcomes (P = .001). Several dimensions of the PMAQ-V1.0 did not function as well as hypothesized. In this study, self-reported adherence derived from the PMAQ-V1.0 predicted virologic outcomes, but further refinement of the dimensions appears warranted.
患者药物依从性问卷第1.0版(PMAQ-V1.0)是一种由患者报告的依从性工具,用于评估服药行为并识别抗逆转录病毒治疗依从性的障碍。为了评估依从性与病毒学结果之间的相关性,对194名有抗逆转录病毒治疗经验的HIV感染成人进行了PMAQ-V1.0评估,这些患者参加了一项为期16周的含蛋白酶抑制剂方案评估,该方案以拉米夫定/齐多夫定组合片剂为特色。基线时,血浆HIV-1 RNA水平低于10,000拷贝/mL,CD4(+)细胞计数等于或大于300×10(6)/L;患者在研究前至少10周一直接受拉米夫定+齐多夫定(分别服用)加蛋白酶抑制剂的传统方案。在研究期间报告至少漏服一剂核苷类逆转录酶抑制剂(NRTI)的患者中,48%的患者血浆HIV-1 RNA可检测到,而报告无漏服剂量的患者中这一比例为26%(P = .002)。漏服至少一剂NRTI或蛋白酶抑制剂的患者出现可量化HIV-1 RNA的可能性是报告无漏服剂量患者的2.5倍。报告依从性障碍较少且动机较多的患者病毒学结果较好(P = .001)。PMAQ-V1.0的几个维度并未如预期那样发挥良好作用。在本研究中,源自PMAQ-V1.0的自我报告依从性可预测病毒学结果,但各维度似乎仍需进一步完善。