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Antiretroviral adherence program in HIV patients: a feasibility study in the Swiss HIV Cohort Study.

机译:HIV患者的抗逆转录病毒依从性计划:瑞士HIV队列研究中的可行性研究。

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OBJECTIVE: To evaluate the feasibility of a comprehensive, interdisciplinary adherence program aimed at HIV patients. SETTING: Two centers of the Swiss HIV Cohort Study: Lausanne and Basel. METHOD: 6-month, pilot, quasi-experimental, 2-arm design (control and intervention). Patients starting a first or second combined antiretroviral therapy line were invited to participate in the study. Patients entering the intervention arm were proposed a multifactorial intervention along with an electronic drug monitor. It consisted of a maximum of six 30-min sessions with the interventionist coinciding with routine HIV check-up. The sessions relied on individualized semi-structured motivational interviews. Patients in the control arm used directly blinded EDM and did not participate in motivational interviews. MAIN OUTCOME MEASURES: Rate of patients' acceptance to take part in the HIV-adherence program and rate of patients' retention in this program assessed in both intervention and control groups. Persistence, execution and adherence. RESULTS: The study was feasible in one center but not in the other one. Hence, the control group previously planned in Basel was recruited in Lausanne. Inclusion rate was 84% (n = 21) in the intervention versus 52% (n = 11) in the control group (P = 0.027). Retention rate was 91% in the intervention versus 82% in the control group (P = ns). Regarding adherence, execution was high in both groups (97 vs. 95%). Interestingly, the statistical model showed that adherence decreased more quickly in the control versus the intervention group (interaction group x time P < 0.0001). CONCLUSION: The encountered difficulties rely on the implementation, i.e., on the program and the health care system levels rather than on the patient level. Implementation needs to be evaluated further; to be feasible a new adherence program needs to fit into the daily routine of the centre and has to be supported by all trained healthcare providers. However, this study shows that patients' adherence behavior evolved differently in both groups; it decreased more quickly over time in the control than in the intervention group. RCTs are eventually needed to assess the clinical impact of such an adherence program and to verify whether skilled pharmacists can ensure continuity of care for HIV outpatients.
机译:目的:评估针对艾滋病毒患者的综合,跨学科依从性计划的可行性。地点:瑞士艾滋病毒队列研究的两个中心:洛桑和巴塞尔。方法:6个月,飞行员,准实验,2臂设计(控制和干预)。开始第一个或第二个联合抗逆转录病毒疗法的患者被邀请参加研究。建议进入介入治疗的患者进行多因素干预,并配备电子药物监控器。它包括最多六个30分钟的疗程,干预医师与例行HIV检查相吻合。这些会议依赖于个性化的半结构化动机访谈。对照组的患者直接使用盲目EDM,不参加动机性访谈。主要观察指标:在干预组和对照组中评估患者参加艾滋病毒依从性计划的接受率以及该方案中患者的保留率。坚持,执行和坚持。结果:该研究在一个中心是可行的,但在另一中心则不可行。因此,先前在巴塞尔计划的对照组在洛桑被招募。干预组的纳入率为84%(n = 21),而对照组为52%(n = 11)(P = 0.027)。干预组的保留率为91%,而对照组为82%(P = ns)。关于依从性,两组的执行率均很高(97比95%)。有趣的是,统计模型显示,与干预组相比,对照组的依从性下降得更快(互动组x时间P <0.0001)。结论:所遇到的困难取决于实施,即取决于计划和卫生保健系统级别,而不是患者级别。需要进一步评估执行情况;为了切实可行,新的遵守计划必须适合该中心的日常工作,并且必须得到所有训练有素的医疗服务提供者的支持。然而,这项研究表明,两组患者的依从性行为有所不同。与对照组相比,对照组的随时间推移其下降速度更快。最终需要RCT来评估这种依从性计划的临床影响,并验证熟练的药剂师是否可以确保对HIV门诊病人的护理连续性。

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