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艾滋病毒感染者的个人健康记录:综述

Personal health records for people living with HIV: a review.

作者信息

Turner Kea, Klaman Stacey L, Shea Christopher M

机构信息

a Department of Health Policy and Management , University of North Carolina at Chapel Hill , Chapel Hill , USA.

b Department of Maternal and Child Health , University of North Carolina at Chapel Hill , Chapel Hill , USA.

出版信息

AIDS Care. 2016 Sep;28(9):1181-7. doi: 10.1080/09540121.2016.1153594. Epub 2016 Feb 26.


DOI:10.1080/09540121.2016.1153594
PMID:26917113
Abstract

Personal health records have the potential to improve patient outcomes, but the state of the literature on personal health record usage by people living with the human immunodeficiency virus (HIV) is unclear. The purpose of this review is to examine the impact of personal health records on HIV-related health beliefs and behaviors. We used the Health Belief Model to guide a review of studies examining the impact of electronic personal health records on the health beliefs and behaviors among people living with HIV. The search yielded 434 results. Following abstract review, 19 papers were selected for full-text review, and 12 were included in the review. A limited number of studies in this review found a positive impact of personal health records on HIV-related beliefs and behaviors. Additional research is needed to identify which personal health record features are most influential in changing health behaviors and why adoption rates remain low, particularly for groups at greatest risk for poor HIV outcomes. Theory-informed interventions are needed to identify which patients are likely to benefit from using personal health records and how to reduce barriers to personal health record adoption for people living with HIV.

摘要

个人健康记录有改善患者治疗效果的潜力,但关于人类免疫缺陷病毒(HIV)感染者使用个人健康记录的文献状况尚不明晰。本综述的目的是研究个人健康记录对与HIV相关的健康信念和行为的影响。我们使用健康信念模型来指导对研究电子个人健康记录对HIV感染者健康信念和行为影响的研究进行综述。检索结果有434条。经过摘要审查,选择了19篇论文进行全文审查,其中12篇被纳入综述。本综述中数量有限的研究发现个人健康记录对与HIV相关的信念和行为有积极影响。需要进一步研究以确定哪些个人健康记录特征在改变健康行为方面最具影响力,以及为何采用率仍然较低,尤其是对于HIV治疗效果最差风险最高的群体。需要基于理论的干预措施来确定哪些患者可能从使用个人健康记录中受益,以及如何减少HIV感染者采用个人健康记录的障碍。

相似文献

[1]
Personal health records for people living with HIV: a review.

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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Electronic Patient Portal Access, Retention in Care, and Viral Suppression Among People Living With HIV in Southeastern United States: Observational Study.

JMIR Med Inform. 2022-7-25

[2]
PositiveLinks and the COVID-19 Response: Importance of Low-Barrier Messaging for PLWH in Non-urban Virginia in a Crisis.

AIDS Behav. 2021-11

[3]
Patient Portal Barriers and Group Differences: Cross-Sectional National Survey Study.

J Med Internet Res. 2020-9-17

[4]
Towards an Adoption Framework for Patient Access to Electronic Health Records: Systematic Literature Mapping Study.

JMIR Med Inform. 2020-3-30

[5]
Patient portal utilization: before and after stage 2 electronic health record meaningful use.

J Am Med Inform Assoc. 2019-10-1

[6]
Patient and clinician perspectives on optimizing graphical displays of longitudinal medication adherence data.

Patient Educ Couns. 2019-1-2

[7]
Methods to Evaluate the Effects of Internet-Based Digital Health Interventions for Citizens: Systematic Review of Reviews.

J Med Internet Res. 2018-6-7

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