dc.contributor.author | Dadi, Tegene Legese | |
dc.contributor.author | Wiemers, Anja M. C. | |
dc.contributor.author | Tegene, Yadessa | |
dc.contributor.author | Medhin, Girmay | |
dc.contributor.author | Spigt, Marcus | |
dc.date.accessioned | 2024-09-06T11:22:43Z | |
dc.date.available | 2024-09-06T11:22:43Z | |
dc.date.issued | 2024-01-31 | |
dc.description.abstract | Introduction Availability of anti-retroviral treatment has changed HIV in to a manageable chronic disease, making efective self-management essential. However, only a few studies in low- and middle-income countries (LMICs)
reported experiences of people living with HIV (PLWH) on self-management.<p>
<p>Methods This meta-synthesis of qualitative studies investigated perspectives of PLWH in LMICs on self-management.
Various databases, including PubMed, EMBASE, EBSCO, and CINHAL, were searched through June 2022. Relevant
additional articles were also included using cross-referencing of the identified papers. We used a thematic synthesis
guided by the "Model of the Individual and Family Self-Management Theory" (IFSMT).
<p>Result PLWH in LIMICs experience a variety of challenges that restrict their options for effective self-management
and compromises their quality of life. The main ones include: misconceptions about the disease, poor self-efficacy
and self-management skills, negative social perceptions, and a non-patient-centered model of care that reduces
the role of patients. The experiences that influenced the ability to practice self-management are summarized in context (the condition itself, physical and environmental factors, individual and family factors) and process factors (knowledge and beliefs, relationship with the health care worker, self-regulation skills and abilities, and social facilitation).
Context and process greatly impacted quality of life through the self-management practices of the patients.
<p>Conclusion and recommendation PLWH encounter multiple challenges, are not empowered enough to manage their own chronic condition, and their needs beyond medical care are not addressed by service providers.
Self-management practice of these patients is poor, and service providers do not follow service delivery approaches
that empower patients to be at the center of their own care and to achieve an effective and sustainable outcome
from treatment. These findings call for a comprehensive well thought self-management interventions. | en_US |
dc.identifier.citation | Dadi, Wiemers, Tegene, Medhin, Spigt. Experiences of people living with HIV in low- and middle-income countries and their perspectives in self-management: a meta-synthesis. AIDS research and therapy. 2024;21(1) | en_US |
dc.identifier.cristinID | FRIDAID 2245329 | |
dc.identifier.doi | 10.1186/s12981-024-00595-7 | |
dc.identifier.issn | 1742-6405 | |
dc.identifier.uri | https://hdl.handle.net/10037/34544 | |
dc.language.iso | eng | en_US |
dc.publisher | BMC | en_US |
dc.relation.journal | AIDS research and therapy | |
dc.rights.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2024 The Author(s) | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0 | en_US |
dc.rights | Attribution 4.0 International (CC BY 4.0) | en_US |
dc.title | Experiences of people living with HIV in low- and middle-income countries and their perspectives in self-management: a meta-synthesis | en_US |
dc.type.version | publishedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |