Longitudinal Care Cascade Outcomes Among People Eligible for Antiretroviral Therapy Who Are Newly Linking to Care in Zambia: A Multistate Analysis.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
17 12 2020
Historique:
received: 10 12 2019
accepted: 13 03 2020
pubmed: 17 3 2020
medline: 29 4 2021
entrez: 17 3 2020
Statut: ppublish

Résumé

Retention in human immunodeficiency virus (HIV) care is dynamic, with patients frequently transitioning in and out of care. Analytical approaches (eg, survival analyses) commonly used to assess HIV care cascade outcomes fail to capture such transitions and therefore incompletely represent care outcomes over time. We analyzed antiretroviral therapy (ART)-eligible adults newly linking to care at 64 clinics in Zambia between 1 April 2014 and 31 July 2015. We used electronic medical record data and supplemented these with updated care outcomes ascertained by tracing a multistage random sample of patients lost to follow-up (LTFU, >90 days late for last appointment). We performed multistate analyses, incorporating weights from sampling, to estimate the prevalence of 9 care states over time since linkage with respect to ART initiation, retention in care, transfers, and mortality. In sum, 23 227 patients (58% female; median age 34 years [interquartile range 28-41]) were ART-eligible at enrollment. At 1 year, 75.2% had initiated ART and were in care: 61.8% were continuously retained, 6.1% had reengaged after LTFU, and 7.3% had transferred. Also, 10.1% were LTFU within 7 days of enrollment, and 15.2% were LTFU at 1 year (6.7% prior to ART). One year after LTFU, 51.6% of those LTFU prior to ART remained out of care compared to 30.2% of those LTFU after initiating ART. Overall, 6.9% of patients had died by 1 year with 3.0% dying prior to ART. Multistate analyses provide more complete assessments of longitudinal HIV cascade outcomes and reveal treatment gaps at distinct timepoints in care that will still need to be addressed even with universal treatment.

Sections du résumé

BACKGROUND
Retention in human immunodeficiency virus (HIV) care is dynamic, with patients frequently transitioning in and out of care. Analytical approaches (eg, survival analyses) commonly used to assess HIV care cascade outcomes fail to capture such transitions and therefore incompletely represent care outcomes over time.
METHODS
We analyzed antiretroviral therapy (ART)-eligible adults newly linking to care at 64 clinics in Zambia between 1 April 2014 and 31 July 2015. We used electronic medical record data and supplemented these with updated care outcomes ascertained by tracing a multistage random sample of patients lost to follow-up (LTFU, >90 days late for last appointment). We performed multistate analyses, incorporating weights from sampling, to estimate the prevalence of 9 care states over time since linkage with respect to ART initiation, retention in care, transfers, and mortality.
RESULTS
In sum, 23 227 patients (58% female; median age 34 years [interquartile range 28-41]) were ART-eligible at enrollment. At 1 year, 75.2% had initiated ART and were in care: 61.8% were continuously retained, 6.1% had reengaged after LTFU, and 7.3% had transferred. Also, 10.1% were LTFU within 7 days of enrollment, and 15.2% were LTFU at 1 year (6.7% prior to ART). One year after LTFU, 51.6% of those LTFU prior to ART remained out of care compared to 30.2% of those LTFU after initiating ART. Overall, 6.9% of patients had died by 1 year with 3.0% dying prior to ART.
CONCLUSION
Multistate analyses provide more complete assessments of longitudinal HIV cascade outcomes and reveal treatment gaps at distinct timepoints in care that will still need to be addressed even with universal treatment.

Identifiants

pubmed: 32173743
pii: 5805511
doi: 10.1093/cid/ciaa268
pmc: PMC7744998
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

e561-e570

Subventions

Organisme : NIAID NIH HHS
ID : T32 AI060530
Pays : United States
Organisme : NIAID NIH HHS
ID : K24 AI134413
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI027763
Pays : United States

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America.

Auteurs

Aaloke Mody (A)

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

David V Glidden (DV)

Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, California, USA.

Ingrid Eshun-Wilson (I)

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

Kombatende Sikombe (K)

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

Sandra Simbeza (S)

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

Njekwa Mukamba (N)

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

Paul Somwe (P)

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

Laura K Beres (LK)

Department of International Health, Johns Hopkins University School of Public Health, Baltimore, Maryland, USA.

Jake Pry (J)

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

Carolyn Bolton-Moore (C)

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

Nancy Padian (N)

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

Charles B Holmes (CB)

Department of Medicine, Georgetown University, Washington, D.C., USA.

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, Missouri, USA.

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