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从包含相同抗逆转录病毒药物的多片剂方案转换为单片剂方案是否能提高依从性?基于群组的轨迹建模分析。

Does switching from multiple to single-tablet regimen containing the same antiretroviral drugs improve adherence? A group-based trajectory modeling analysis.

机构信息

Department of Social Pharmacy, School of Pharmacy, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Canada.

出版信息

AIDS Care. 2020 Oct;32(10):1268-1276. doi: 10.1080/09540121.2020.1736258. Epub 2020 Mar 8.

Abstract

Combination Antiretroviral Therapy (cART) in single-tablet regimens (STR) is a simplification strategy that can potentially improve medication adherence and clinical outcomes. We conducted a retrospective cohort study of 1206 patients using efavirenz, tenofovir and lamivudine in multiple-tablet regimen who switched to the STR containing the same active ingredients in a southeast metropolis in Brazil. We measured adherence using the proportion of days covered (PDC≥95%) and evaluated this outcome before and after the switch using paired non-parametric statistics. Additionally, we used group-based trajectory modeling to identify adherence patterns to cART for each period and evaluate the migration behavior of patients between the trajectory groups. We observed a 14% increase in the proportion of adherent patients after switching to STR and a 6.2% increase in the proportion of patients with CD4 count>500 cells/μl ( < 0.001), without changes in viral load outcomes. We identified four adherence trajectories in each period. Most patients (60%,  = 722) migrated towards a group with better adherence trajectory or remained in the trajectory group with the highest probability of adherence after the switch. Our findings suggest that the implementation of the STR had a positive impact on adherence and CD4 count. This may potentially improve virologic outcomes later on treatment.

摘要

联合抗逆转录病毒疗法(cART)在单一片剂方案(STR)中是一种简化策略,可能会提高药物依从性和临床结果。我们在巴西东南部的一个大都市对使用依非韦伦、替诺福韦和拉米夫定的多片方案治疗的 1206 名患者进行了回顾性队列研究,这些患者转换为含有相同活性成分的 STR。我们使用覆盖率(PDC≥95%)来衡量依从性,并使用配对非参数统计来评估转换前后的结果。此外,我们使用基于组的轨迹建模来识别每个时期对 cART 的依从性模式,并评估患者在轨迹组之间的迁移行为。我们发现,转换为 STR 后,依从性患者的比例增加了 14%,CD4 计数>500 个细胞/μl 的患者比例增加了 6.2%(<0.001),病毒载量结果没有变化。我们在每个时期都发现了四个依从性轨迹。大多数患者(60%,n=722)在转换后朝着依从性更好的轨迹组迁移,或者在转换后仍留在具有最高依从性概率的轨迹组中。我们的研究结果表明,STR 的实施对依从性和 CD4 计数有积极影响。这可能会在以后的治疗中改善病毒学结果。

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