Trajectories of Oral PrEP Adherence Among Young Kenyan Women: Implications for Promoting Effective PrEP Use.


Journal

AIDS and behavior
ISSN: 1573-3254
Titre abrégé: AIDS Behav
Pays: United States
ID NLM: 9712133

Informations de publication

Date de publication:
Jan 2023
Historique:
accepted: 08 06 2022
pubmed: 17 7 2022
medline: 24 1 2023
entrez: 16 7 2022
Statut: ppublish

Résumé

Using data from a 2-year study of young women at high HIV risk in Thika and Kisumu, Kenya, we identified group-based trajectories of PrEP adherence based on electronic pillcap-monitoring and assessed potentially associated demographic and socio-behavioral factors. Among 348 women, we selected a three-trajectory adherence model: low and declining (N = 211, 61%), moderate but declining (N = 119, 34%) and steady high adherers (N = 18, 5%). We also identified a two-trajectory HIV risk model based on self-perceived risk in the past week: high and increasing (N = 28, 8%) and steady low (N = 320, 92%) risk. The Kisumu site was associated with the moderate but declining and steady high adherence trajectories, while increasing VOICE risk score was associated with the low and declining adherence trajectory. We found no association between the adherence and risk trajectories. Our findings suggest adherence support may need tailoring by setting. Early, sustained support may also help those at highest risk of non-adherence. Utilizando datos de un estudio de dos años de duración en mujeres jóvenes con alto riesgo de VIH en Thika y Kisumu, Kenia, identificamos trayectorias grupales de adherencia a la PrEP basadas en el monitoreo electrónico de pillcap y evaluamos los factores demográficos, sociales y de comportamiento potencialmente asociados con la adherencia. En un grupo de 348 mujeres, seleccionamos un modelo de adherencia de tres trayectorias: baja y decreciente (N = 211, 61%), moderada pero decreciente (N = 119, 34%) y altas constantes (N = 18, 5%). También identificamos un modelo de riesgo de VIH de dos trayectorias basado en el riesgo autopercibido en la última semana: riesgo alto y creciente (N = 28, 8%) y riesgo bajo constante (N = 320, 92%). El sitio de Kisumu estuvo asociado con las trayectorias de adherencia alta moderadas pero decrecientes y constantes, mientras que el aumento de la puntuación de riesgo de VOICE se asoció con la trayectoria de adherencia baja y decreciente. No se encontró asociación entre la adherencia y las trayectorias de riesgo. Nuestros hallazgos sugieren que el apoyo a la adherencia podría individualizarse de acuerdo con el entorno. El apoyo temprano y sostenido a la adherencia también puede ayudar a las personas con mayor riesgo de no adherencia.

Autres résumés

Type: Publisher (spa)
Utilizando datos de un estudio de dos años de duración en mujeres jóvenes con alto riesgo de VIH en Thika y Kisumu, Kenia, identificamos trayectorias grupales de adherencia a la PrEP basadas en el monitoreo electrónico de pillcap y evaluamos los factores demográficos, sociales y de comportamiento potencialmente asociados con la adherencia. En un grupo de 348 mujeres, seleccionamos un modelo de adherencia de tres trayectorias: baja y decreciente (N = 211, 61%), moderada pero decreciente (N = 119, 34%) y altas constantes (N = 18, 5%). También identificamos un modelo de riesgo de VIH de dos trayectorias basado en el riesgo autopercibido en la última semana: riesgo alto y creciente (N = 28, 8%) y riesgo bajo constante (N = 320, 92%). El sitio de Kisumu estuvo asociado con las trayectorias de adherencia alta moderadas pero decrecientes y constantes, mientras que el aumento de la puntuación de riesgo de VOICE se asoció con la trayectoria de adherencia baja y decreciente. No se encontró asociación entre la adherencia y las trayectorias de riesgo. Nuestros hallazgos sugieren que el apoyo a la adherencia podría individualizarse de acuerdo con el entorno. El apoyo temprano y sostenido a la adherencia también puede ayudar a las personas con mayor riesgo de no adherencia.

Identifiants

pubmed: 35841463
doi: 10.1007/s10461-022-03753-y
pii: 10.1007/s10461-022-03753-y
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

171-181

Subventions

Organisme : NIMH NIH HHS
ID : K24 MH114732
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH109309
Pays : United States
Organisme : NIH HHS
ID : R01MH109309
Pays : United States

Investigateurs

Jessica E Haberer (JE)
Jared M Baeten (JM)
Elizabeth Bukusi (E)
Nelly Mugo (N)
Kenneth Ngure (K)
Ruanne Barnabas (R)
Harsha Thirumurthy (H)
Ingrid Katz (I)
Kevin Kamolloh (K)
Josephine Odoyo (J)
Linda Aswani (L)
Lawrence Juma (L)
Elizabeth Koyo (E)
Bernard Rono (B)
Stanley Cheruiot (S)
Vallery Ogello (V)
Loice Okumu (L)
Violet Kwach (V)
Alfred Obiero (A)
Stella Njuguna (S)
Millicent Faith Akinyi (MF)
Lilian Adipo (L)
Sylvia Akinyi (S)
Catherine Kiptiness (C)
Nicholas Thuo (N)
Stephen Gakuo Maina (SG)
Irene Njeru (I)
Peter Mogere (P)
Sarah Mbaire (S)
Murugi Micheni (M)
Lynda Oluoch (L)
John Njoroge (J)
Snaidah Ongachi (S)
Jacinta Nyokabi (J)
Lindsey Garrison (L)
Maria Pyra (M)
Kathleen K Thomas (KK)
Nicholas Musinguzi (N)
Susie Valenzuela (S)
Susan Morrison (S)

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Nicholas Musinguzi (N)

Global Health Collaborative, Mbarara University of Science and Technology, Plot 10/24, Lower Circular Road, Mbarara, Uganda. nmusinguzi@gmail.com.

Maria Pyra (M)

Department of Medicine, University of Chicago, Chicago, USA.

Elizabeth A Bukusi (EA)

Department of Obstetrics and Gynecology, University of Washington, Seattle, USA.

Nelly R Mugo (NR)

Department of Obstetrics and Gynecology, University of Washington, Seattle, USA.
Center for Clinical Research (CCR), Kenya Medical Research Institute (KEMRI), Nairobi, Kenya.

Jared M Baeten (JM)

Department of Global Health, University of Washington, Seattle, USA.
Department of Epidemiology, University of Washington, Seattle, USA.
Department of Medicine, University of Washington, Seattle, USA.

Jessica E Haberer (JE)

Massachusetts General Hospital and Harvard Medical School, Boston, USA.
Department of Medicine, Harvard Medical School, Boston, MA, USA.

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