4.7 Article

Understanding the Risks and Benefits of a Patient Portal Configured for HIV Care: Patient and Healthcare Professional Perspectives

期刊

JOURNAL OF PERSONALIZED MEDICINE
卷 12, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/jpm12020314

关键词

HIV; chronic disease; patient portal; patient engagement; qualitative research; self-management; health information technology (HIT); mobile health

资金

  1. Canadian Institutes for Health Research (CIHR), Strategy for Patient-Oriented Research (SPOR) Mentorship Chair in Innovative Clinical Trials in HIV
  2. Quebec SPOR Support Unit -McGill Methodological Developments Platform
  3. Assistance Publique-Hopitaux de Paris Foundation
  4. MSD Avenir Foundation [DS-2018-0072]
  5. Quebec's Ministry of Health for researchers in Family Medicine [LE 250]
  6. Fonds de Recherche du Quebec-Sante (FRQS) doctoral training program

向作者/读者索取更多资源

The study found that both people living with HIV and healthcare professionals have consensus on the risks and benefits of using a patient portal in HIV care. By engaging stakeholders, the configuration of a patient portal can be optimized and concerns during implementation can be mitigated.
Background: Like other chronic viral illnesses, HIV infection necessitates consistent self-management and adherence to care and treatment, which in turn relies on optimal collaboration between patients and healthcare professionals (HCPs), including physicians, nurses, pharmacists, and clinical care coordinators. By providing people living with HIV (PLHIV) with access to their personal health information, educational material, and a communication channel with HCPs, a tailored patient portal could support their engagement in care. Our team intends to implement a patient portal in HIV-specialized clinics in Canada and France. We sought to understand the perceived risks and benefits among PLHIV and HCPs of patient portal use in HIV clinical care. Methods: This qualitative study recruited PLHIV and HIV-specialized HCPs, through maximum variation sampling and purposeful sampling, respectively. Semi-structured focus group discussions (FGDs) were held separately with PLHIV and HCPs between August 2019 and January 2020. FGDs were recorded, transcribed, coded using NVivo 12 software, and analyzed using content analysis. Results: A total of twenty-eight PLHIV participated in four FGDs, and thirty-one HCPs participated in six FGDs. PLHIV included eighteen men, nine women, and one person identifying as other; while, HCPs included ten men, twenty women, and one person identifying as other. A multi-disciplinary team of HCPs were included, involving physicians, nurses, pharmacists, social workers, and clinical coordinators. Participants identified five potential risks: (1) breach of confidentiality, (2) stress or uncertainty, (3) contribution to the digital divide, (4) dehumanization of care, and (5) increase in HCPs' workload. They also highlighted four main benefits of using a patient portal: (1) improvement in HIV self-management, (2) facilitation of patient visits, (3) responsiveness to patient preferences, and (4) fulfillment of current or evolving patient needs. Conclusion: PLHIV and HCPs identified both risks and benefits of using a patient portal in HIV care. By engaging stakeholders and understanding their perspectives, the configuration of a patient portal can be optimized for end-users and concerns may be mitigated during its implementation.

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