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抗逆转录病毒治疗的 HIV 患者服药依从性障碍问卷(ABQ-HIV)的适应和验证。

Adaption and validation of the adherence barriers questionnaire for HIV patients on antiretroviral therapy (ABQ-HIV).

机构信息

Ingress-Health HWM GmbH, Wismar, Germany.

Universitaetmedizin Mainz, Universitaetsmedizin, Germany.

出版信息

BMC Infect Dis. 2018 Nov 28;18(1):599. doi: 10.1186/s12879-018-3530-x.


DOI:10.1186/s12879-018-3530-x
PMID:30486795
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6264035/
Abstract

BACKGROUND: Despite substantial advances in antiretroviral therapy (ART) for human immunodeficiency virus (HIV) in the last decades, non-adherence (NA) continues to be a major challenge in the real-life treatment. To meet this challenge, adherence-promoting interventions with a tailored approach towards patient-specific adherence barriers that are identified using a reliable and practicable questionnaire are needed. The aim of this investigation was to develop and validate a respective questionnaire (Adherence Barriers Questionnaire for HIV: ABQ-HIV), based on an earlier version of the ABQ. METHODS: The existing ABQ was discussed by an expert panel and revised according to the specifications of ART therapy for HIV patients. Initially, the ABQ-HIV consisted of 17 items formulated as statements (4-point-Likert-scale ranging from "strongly agree" to "strongly disagree"). A higher score indicates a higher influence of a certain barrier on patient's perceptions. The ABQ-HIV was applied in a cross-sectional survey of German HIV patients. Evaluation of the questionnaire included an assessment of internal consistency as well as factor analysis. Convergent validity was assessed by comparing the ABQ-HIV score with the degree of self-reported adherence measured by the 8-item Morisky Medication Adherence Scale (MMAS-8©). RESULTS: Three hundred seventy patients were able to be included in all validation analyses. The included patients had a mean age of 51.2 years, and 15.7% were female. The mean HIV infection time was 11.7 years, and the mean duration of treatment since first starting ART was 8.7 years. Twenty-five patients - excluded from all further analyses - were not able/willing to answer all ABQ-HIV questions. The results of the reliability analysis showed a Cronbach's α of 0.708 for the initial 17-items in the ABQ-HIV draft. Two items were eliminated from the initial questionnaire, resulting in a Cronbach's α of 0.720 and a split-half reliability of 0.724 (Spearman-Brown coefficient). Based on the reduced 15-item scale, the factor analysis resulted in three different components of the questionnaire. Component 1, with seven items, represents the unintentional adherence barriers. The second component, which contains five items, can be labelled as a subscale describing barriers associated with disease/treatment knowledge. Finally, three items, which can be summarized as intentional adherence barriers, show maximum loading in the third component. The score of the reduced 15-item ABQ-HIV scale, as well as the scores of the three subscales, correlated significantly with the MMAS score. All correlation coefficients were negative, indicating that higher burdens of adherence barriers measured by ABQ-HIV or its subscales were associated with a lower MMAS score and thus, with a lower adherence level. The ROC analysis using the MMAS low adherence classification as its state variable provided a cut-off for the ABQ-HIV scale of > 28 (sensitivity: 61.5%, specificity: 83.3%). In our sample, 85 patients (23.0%) reached a score of > 28 and appeared to face a high non-adherence risk. CONCLUSIONS: The ABQ-HIV is a practical, reliable, and valid instrument for identifying patient-specific barriers to adherence in the HIV treatment. It is also useful in identifying HIV patient subgroups, according to adherence barriers specific to these patients.

摘要

背景:尽管在过去几十年中,人类免疫缺陷病毒(HIV)的抗逆转录病毒治疗(ART)取得了重大进展,但不依从(NA)仍然是现实生活中治疗的主要挑战。为了应对这一挑战,需要采用基于可靠且可行的问卷识别患者特定依从障碍的方法来提供促进依从性的干预措施。本研究的目的是基于早期版本的 ABQ,开发和验证相应的问卷(HIV 依从性障碍问卷:ABQ-HIV)。

方法:一个专家小组讨论了现有的 ABQ,并根据 HIV 患者的 ART 治疗规范进行了修订。最初,ABQ-HIV 由 17 个项目组成,这些项目被表述为陈述(4 点李克特量表,范围从“非常同意”到“非常不同意”)。分数越高表示该障碍对患者认知的影响越大。ABQ-HIV 应用于德国 HIV 患者的横断面调查。问卷评估包括内部一致性评估和因子分析。通过将 ABQ-HIV 评分与 8 项 Morisky 用药依从性量表(MMAS-8©)测量的自我报告依从性程度进行比较,评估了其聚合效度。

结果:共有 370 名患者能够参与所有验证分析。纳入的患者平均年龄为 51.2 岁,15.7%为女性。平均 HIV 感染时间为 11.7 年,自首次开始 ART 以来的治疗时间平均为 8.7 年。25 名患者 - 被排除在所有进一步的分析之外 - 无法/不愿回答 ABQ-HIV 的所有问题。可靠性分析的结果显示,ABQ-HIV 草案最初的 17 个项目的 Cronbach's α 为 0.708。从最初的问卷中删除了两个项目,Cronbach's α 为 0.720,半分可靠性为 0.724(Spearman-Brown 系数)。基于简化的 15 项量表,因子分析产生了问卷的三个不同组成部分。第一部分包含七个项目,代表非故意的依从障碍。第二部分包含五个项目,可以将其标记为与疾病/治疗知识相关的障碍的亚量表。最后,三个项目可以概括为有意的依从障碍,在第三个组成部分中表现出最大的负荷。简化的 15 项 ABQ-HIV 量表的评分以及三个子量表的评分与 MMAS 评分显著相关。所有相关系数均为负值,这表明 ABQ-HIV 或其子量表中测量的依从性障碍负担越高,与 MMAS 评分越低,从而与依从性水平越低相关。使用 MMAS 低依从性分类作为其状态变量的 ROC 分析为 ABQ-HIV 量表提供了 >28 的截止值(灵敏度:61.5%,特异性:83.3%)。在我们的样本中,85 名患者(23.0%)的得分>28,似乎面临着较高的不依从风险。

结论:ABQ-HIV 是一种实用、可靠且有效的工具,可用于识别 HIV 治疗中患者特定的依从障碍。它还可用于根据特定于这些患者的依从障碍来识别 HIV 患者亚组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d7/6264035/1022c8643fd8/12879_2018_3530_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d7/6264035/1022c8643fd8/12879_2018_3530_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9d7/6264035/1022c8643fd8/12879_2018_3530_Fig1_HTML.jpg

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