Background: Loss to follow-up (LTFU) has been reported as a recurrent challenge affecting the success of antiretroviral treatment among HIV-infected patients in low- and middle-income countries. Additionally, loss of follow-up is a significant problem associated with increased treatment failure, which can be presented through clinical, immunological, and virological failure. Lastly, LTFU exacerbates the rates of morbidity, mortality, and drug resistance among people living with HIV. Objective: The study explores underlying factors associated with loss to follow-up among patients living with HIV in selected public clinics under the DIMAMO surveillance area in the Capricorn district of Limpopo province. Methods: A qualitative research approach, particularly phenomenology, was adopted to explore and understand the experiences of registered nurses and community health workers caringfor patients receiving antiretroviral treatment at the selected public clinics. Twenty-eight (28) participants were purposively selected. Furthermore, data were collected using semi-structured interviews. Lastly, data was analysed using delve narrative analysis. Results: Following the process of data analysis, the study revealed that patients living with HIV often face diverse internal conflicts and significant barriers leading to loss of follow-up. The following themes emerged: (1) Patient-related factors identified in a form of denial related to perceptions of HIV, perceptions of being healed or healthy, and lastly, not accepting responsibility for HIV health status. (2) Significant barriers associated with disengagement from HIV care among patients were identified in the form of nondisclosure of HIV status to significant others, fear of stigmatisation, perceived breach of confidentiality, and lastly, resistance to or non-use of community healthcare interventions. Conclusion: In summary, the study identified the key challenges affecting HIV care, including internal conflicts, which manifested in the form of denial, and misconceptions about health status as reported by the participants. Thus, the significant barriers to care disengagement included non-disclosure of HIV status, fear of stigma, perceived breaches of confidentiality, and resistance to community healthcare interventions. Furthermore, these findings highlight the need for targeted interventions to improve patient retention rates. Notably, a comprehensive training program and information guide for healthcare providers can enhance their ability to support antiretroviral patients and improve treatment adherence and health outcomes.
Funding
This research received no external funding.
Institutional Review Board Statement
This study forms part of a PhD project and it was granted ethical clearance by the University of Limpopo, Turfloop Research Ethics Committee (TREC/100/2023:PG). the Limpopo provincial government (LP_202308-016), and the Capricorn Sub-district Manager (S.5/3/1/2).
Informed Consent Statement
Participants were reassured of the confidentiality of information collected from them. Furthermore, a written informed consent was obtained before participating in the study.
Data Availability Statement
The dataset in this study is available upon reasonable request from the author.
Conflicts of Interest
The Author declares no conflict of interest, financial or otherwise.
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