Profiles of HIV Care Disruptions Among Adult Patients Lost to Follow-up in Zambia: A Latent Class Analysis.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
01 01 2021
Historique:
pubmed: 27 10 2020
medline: 16 7 2021
entrez: 26 10 2020
Statut: ppublish

Résumé

Patients report varied barriers to HIV care across multiple domains, but specific barrier patterns may be driven by underlying, but unobserved, behavioral profiles. We traced a probability sample of patients lost to follow-up (>90 days late) as of July 31, 2015 from 64 clinics in Zambia. Among those found alive, we ascertained patient-reported reasons for care disruptions. We performed latent class analysis to identify patient subgroups with similar patterns of reasons reported and assessed the association between class membership and care status (ie, disengaged versus silently transferred to a new site). Among 547 patients, we identified 5 profiles of care disruptions: (1) "Livelihood and Mobility" (30.6% of the population) reported work/school obligations and mobility/travel as reasons for care disruptions; (2) "Clinic Accessibility" (28.9%) reported challenges with attending clinic; (3) "Mobility and Family" (21.9%) reported family obligations, mobility/travel, and transport-related reasons; (4) "Doubting Need for HIV care" (10.2%) reported uncertainty around HIV status or need for clinical care, and (5) "Multidimensional Barriers to Care" (8.3%) reported numerous (mean 5.6) reasons across multiple domains. Patient profiles were significantly associated with care status. The "Doubting Need for HIV Care" class were mostly disengaged (97.9%), followed by the "Multidimensional Barriers to Care" (62.8%), "Clinic Accessibility" (62.4%), "Livelihood and Mobility" (43.6%), and "Mobility and Family" (23.5%) classes. There are distinct HIV care disruption profiles that are strongly associated with patients' current engagement status. Interventions targeting these unique profiles may enable more effective and tailored strategies for improving HIV treatment outcomes.

Sections du résumé

BACKGROUND
Patients report varied barriers to HIV care across multiple domains, but specific barrier patterns may be driven by underlying, but unobserved, behavioral profiles.
METHODS
We traced a probability sample of patients lost to follow-up (>90 days late) as of July 31, 2015 from 64 clinics in Zambia. Among those found alive, we ascertained patient-reported reasons for care disruptions. We performed latent class analysis to identify patient subgroups with similar patterns of reasons reported and assessed the association between class membership and care status (ie, disengaged versus silently transferred to a new site).
RESULTS
Among 547 patients, we identified 5 profiles of care disruptions: (1) "Livelihood and Mobility" (30.6% of the population) reported work/school obligations and mobility/travel as reasons for care disruptions; (2) "Clinic Accessibility" (28.9%) reported challenges with attending clinic; (3) "Mobility and Family" (21.9%) reported family obligations, mobility/travel, and transport-related reasons; (4) "Doubting Need for HIV care" (10.2%) reported uncertainty around HIV status or need for clinical care, and (5) "Multidimensional Barriers to Care" (8.3%) reported numerous (mean 5.6) reasons across multiple domains. Patient profiles were significantly associated with care status. The "Doubting Need for HIV Care" class were mostly disengaged (97.9%), followed by the "Multidimensional Barriers to Care" (62.8%), "Clinic Accessibility" (62.4%), "Livelihood and Mobility" (43.6%), and "Mobility and Family" (23.5%) classes.
CONCLUSION
There are distinct HIV care disruption profiles that are strongly associated with patients' current engagement status. Interventions targeting these unique profiles may enable more effective and tailored strategies for improving HIV treatment outcomes.

Identifiants

pubmed: 33105396
doi: 10.1097/QAI.0000000000002530
pmc: PMC7722465
pii: 00126334-202101010-00010
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

62-72

Subventions

Organisme : NCATS NIH HHS
ID : KL2 TR002346
Pays : United States
Organisme : NIAID NIH HHS
ID : T32 AI060530
Pays : United States
Organisme : NIAID NIH HHS
ID : K24 AI134413
Pays : United States

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Auteurs

Aaloke Mody (A)

Division of Infectious Diseases, Washington University School of Medicine, St. Louis, MO.

Kombatende Sikombe (K)

Centre for Infectious Diseases Research in Zambia, Lusaka, Zambia.
Department of Public Health Environments and Society, Faculty of Public Health and Policy, London School of Hygiene and Tropical Medicine, London, United Kingdom.

Laura K Beres (LK)

Department of International Health, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD.

Sandra Simbeza (S)

Centre for Infectious Diseases Research in Zambia, Lusaka, Zambia.

Njekwa Mukamba (N)

Centre for Infectious Diseases Research in Zambia, Lusaka, Zambia.

Ingrid Eshun-Wilson (I)

Division of Infectious Diseases, Washington University School of Medicine, St. Louis, MO.

Sheree Schwartz (S)

Department of International Health, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD.

Jake Pry (J)

Division of Infectious Diseases, Washington University School of Medicine, St. Louis, MO.
Centre for Infectious Diseases Research in Zambia, Lusaka, Zambia.

Nancy Padian (N)

Division of Epidemiology, University of California, Berkeley, Berkeley, CA.

Charles B Holmes (CB)

Department of Medicine, Georgetown University, Washington, DC; and.

Carolyn Bolton-Moore (C)

Centre for Infectious Diseases Research in Zambia, Lusaka, Zambia.
Division of Infectious Diseases, University of Alabama, Birmingham, AL.

Izukanji Sikazwe (I)

Centre for Infectious Diseases Research in Zambia, Lusaka, Zambia.

Elvin H Geng (EH)

Division of Infectious Diseases, Washington University School of Medicine, St. Louis, MO.

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