Electronic Dose Monitoring Identifies a High-Risk Subpopulation in the Treatment of Drug-resistant Tuberculosis and Human Immunodeficiency Virus.


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:
05 10 2021
Historique:
received: 23 06 2020
pubmed: 15 10 2020
medline: 21 10 2021
entrez: 14 10 2020
Statut: ppublish

Résumé

In generalized drug-resistant tuberculosis (DR-TB) human immunodeficiency virus (HIV) epidemics, identifying subpopulations at high risk for treatment failure and loss to care is critically important to improve treatment outcomes and prevent amplification of drug resistance. We hypothesized that an electronic dose-monitoring (EDM) device could empirically identify adherence-challenged patients and that a mixed-methods approach would characterize treatment challenges. A prospective study of patients with DR-TB HIV on antiretroviral therapy (ART) initiating bedaquiline-containing regimens in KwaZulu-Natal, South Africa. Separate EDM devices measured adherence for bedaquiline and ART. Patients with low adherence (<85%) to both bedaquiline and ART were identified as high risk for poor outcomes. Baseline survey, study visit notes, and focus group discussions characterized treatment challenges. From December 2016-February 2018, 32 of 198 (16%) enrolled patients with DR-TB HIV were identified as dual-adherence challenged. In a multivariate model including baseline characteristics, only receiving a disability grant was significantly associated with dual nonadherence at 6 months. Mixed-methods identified treatment barriers including alcohol abuse, family conflicts, and mental health issues. Compared with adherent patients, dual-adherence-challenged patients struggled to prioritize treatment and lacked support, and dual-adherence-challenged patients experienced higher rates of detectable HIV viral load and mortality than more adherent patients. EDM empirically identified a subpopulation of patients with DR-TB HIV with dual-adherence challenges early in treatment. Mixed-methods revealed intense psychosocial, behavioral, and structural barriers to care in this subpopulation. Our data support developing differential, patient-centered, adherence support interventions focused on psychosocial and structural challenges for subpopulations of at-risk DR-TB HIV patients.

Sections du résumé

BACKGROUND
In generalized drug-resistant tuberculosis (DR-TB) human immunodeficiency virus (HIV) epidemics, identifying subpopulations at high risk for treatment failure and loss to care is critically important to improve treatment outcomes and prevent amplification of drug resistance. We hypothesized that an electronic dose-monitoring (EDM) device could empirically identify adherence-challenged patients and that a mixed-methods approach would characterize treatment challenges.
METHODS
A prospective study of patients with DR-TB HIV on antiretroviral therapy (ART) initiating bedaquiline-containing regimens in KwaZulu-Natal, South Africa. Separate EDM devices measured adherence for bedaquiline and ART. Patients with low adherence (<85%) to both bedaquiline and ART were identified as high risk for poor outcomes. Baseline survey, study visit notes, and focus group discussions characterized treatment challenges.
RESULTS
From December 2016-February 2018, 32 of 198 (16%) enrolled patients with DR-TB HIV were identified as dual-adherence challenged. In a multivariate model including baseline characteristics, only receiving a disability grant was significantly associated with dual nonadherence at 6 months. Mixed-methods identified treatment barriers including alcohol abuse, family conflicts, and mental health issues. Compared with adherent patients, dual-adherence-challenged patients struggled to prioritize treatment and lacked support, and dual-adherence-challenged patients experienced higher rates of detectable HIV viral load and mortality than more adherent patients.
CONCLUSIONS
EDM empirically identified a subpopulation of patients with DR-TB HIV with dual-adherence challenges early in treatment. Mixed-methods revealed intense psychosocial, behavioral, and structural barriers to care in this subpopulation. Our data support developing differential, patient-centered, adherence support interventions focused on psychosocial and structural challenges for subpopulations of at-risk DR-TB HIV patients.

Identifiants

pubmed: 33053186
pii: 5923372
doi: 10.1093/cid/ciaa1557
pmc: PMC8492155
doi:

Substances chimiques

Antitubercular Agents 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1901-e1910

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI114900
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI124413
Pays : United States
Organisme : FIC NIH HHS
ID : R21 TW011077
Pays : United States

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

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Auteurs

Jennifer R Zelnick (JR)

Graduate School of Social Work, Touro College and University System, New York, New York, USA.

Amrita Daftary (A)

Dahdaleh Institute of Global Health Research, School of Global Health, York University, Toronto, Canada.
Center for the AIDS Programme of Research in South Africa, Medical Research Council HIV-TB Pathogenesis and Treatment Research Unit (CAPRISA MRC-HIV-TB), Durban, South Africa.

Christina Hwang (C)

Department of Epidemiology, Mailman School of Public Health, Columbia University Medical Center, New York, New York, USA.

Amy S Labar (AS)

Vagelos College of Physician and Surgeons, Columbia University, New York, New York, USA.

Resha Boodhram (R)

Center for the AIDS Programme of Research in South Africa, Medical Research Council HIV-TB Pathogenesis and Treatment Research Unit (CAPRISA MRC-HIV-TB), Durban, South Africa.

Bhavna Maharaj (B)

Center for the AIDS Programme of Research in South Africa, Medical Research Council HIV-TB Pathogenesis and Treatment Research Unit (CAPRISA MRC-HIV-TB), Durban, South Africa.

Allison K Wolf (AK)

Division of Pulmonary, Allergy, and Critical Care Medicine, Columbia University Medical Center, New York, New York, USA.

Shinjini Mondal (S)

Department of Family Medicine, McGill University, Montreal, Canada.

K Rivet Amico (KR)

University of Michigan School of Public Health, Ann Arbor, Michigan, USA.

Catherine Orrell (C)

Desmond Tutu HIV Centre, Institute of Infectious Disease and Molecular Medicine and Department of Medicine, University of Cape Town, Cape Town, South Africa.

Boitumelo Seepamore (B)

University of Kwazulu-Natal, Durban, South Africa.

Gerald Friedland (G)

Yale School of Medicine, New Haven, Connecticut, USA.

Nesri Padayatchi (N)

Center for the AIDS Programme of Research in South Africa, Medical Research Council HIV-TB Pathogenesis and Treatment Research Unit (CAPRISA MRC-HIV-TB), Durban, South Africa.

Max R O'Donnell (MR)

Center for the AIDS Programme of Research in South Africa, Medical Research Council HIV-TB Pathogenesis and Treatment Research Unit (CAPRISA MRC-HIV-TB), Durban, South Africa.
Department of Epidemiology, Mailman School of Public Health, Columbia University Medical Center, New York, New York, USA.
Division of Pulmonary, Allergy, and Critical Care Medicine, Columbia University Medical Center, New York, New York, USA.

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