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      Oral preexposure prophylaxis uptake, adherence, and persistence during periconception periods among women in South Africa

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          Abstract

          Objective:

          We developed the Healthy Families-PrEP intervention to support HIV-prevention during periconception and pregnancy. We evaluated preexposure prophylaxis (PrEP) use with three objective measures.

          Design:

          This single-arm intervention study enrolled women in KwaZulu-Natal, South Africa, who were HIV-uninfected, not pregnant, in a relationship with a partner with HIV or unknown-serostatus, and with pregnancy plans. PrEP was offered as part of a comprehensive HIV prevention intervention. Participants were followed for 12 months.

          Methods:

          We evaluated periconception PrEP uptake and adherence using quarterly plasma tenofovir concentrations. We modeled factors associated with PrEP uptake and high plasma tenofovir (past day dosing). Patterns of use were analyzed using electronic pillcap data. Dried blood spots to measure intracellular tenofovir product (past 2 months dosing) were analyzed for a subset of women.

          Results:

          Three hundred thirty women with median age 24 (IQR: 22–27) years enrolled. Partner HIV-serostatus was unknown by 96% ( N = 316); 60% (195) initiated PrEP. High plasma tenofovir concentrations were seen in 35, 25, 22, and 20% of samples at 3, 6, 9, and 12 months, respectively. Similar adherence was measured by pillcap and dried blood spots. In adjusted models, lower income, alcohol use, and higher HIV stigma were associated with high plasma tenofovir. Eleven HIV-seroconversions were observed (incidence rate: 4.04/100 person-years [95% confidence interval: 2.24–7.30]). None had detectable plasma tenofovir.

          Conclusion:

          The Healthy Families-PrEP intervention supported women in PrEP use. We observed high interest in periconception PrEP and over one-third adhered to PrEP in the first quarter; one-fifth were adherent over a year. High HIV incidence highlights the importance of strategies to reduce HIV incidence among periconception women.

          Clinical Trial Number:

          NCT03194308

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          Most cited references48

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          The Hopkins Symptom Checklist (HSCL): A self-report symptom inventory

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            The Duke-UNC Functional Social Support Questionnaire. Measurement of social support in family medicine patients.

            A 14-item, self-administered, multidimensional, functional social support questionnaire was designed and evaluated on 401 patients attending a family medicine clinic. Patients were selected from randomized time-frame sampling blocks during regular office hours. The population was predominantly white, female, married, and under age 45. Eleven items remained after test-retest reliability was assessed over a 1- to 4-week follow-up period. Factor analysis and item remainder analysis reduced the remaining 11 items to a brief and easy-to-complete two-scale, eight-item functional social support instrument. Construct validity, concurrent validity, and discriminant validity are demonstrated for the two scales (confidant support--five items and affective support--three items). Factor analysis and correlations with other measures of social support suggest that the three remaining items (visits, instrumental support, and praise) are distinct entities that may need further study.
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              The Dyadic Trust Scale: Toward Understanding Interpersonal Trust in Close Relationships

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                Author and article information

                Journal
                AIDS
                AIDS
                AIDS
                AIDS (London, England)
                Lippincott Williams & Wilkins (Hagerstown, MD )
                0269-9370
                1473-5571
                15 July 2024
                27 May 2024
                : 38
                : 9
                : 1342-1354
                Affiliations
                [a ]Division of Infectious Diseases, University of Alabama at Birmingham, Birmingham, Alabama, USA
                [b ]Maternal Adolescent and Child Health Research Unit (MRU), Department of Obstetrics and Gynaecology, University of the Witwatersrand, Faculty of Health Sciences, Durban, South Africa
                [c ]Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts
                [d ]Department of Global Health
                [e ]Division of Allergy and Infectious Diseases, University of Washington, Seattle, Washington
                [f ]Department of Medicine (Clinical Pharmacology), Johns Hopkins University, School of Medicine, Baltimore, Maryland
                [g ]Department of Global Health & Social Medicine, Harvard Medical School
                [h ]Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts
                [i ]University of KwaZulu-Natal, School of Laboratory Medicine and Medical Sciences, National Health Laboratory Service
                [j ]Department of Virology, National Health Laboratory Service, Durban, South Africa
                [k ]Target RWE, Durham, North Carolina
                [l ]Department of Biostatistics, School of Public Health, University of Alabama at Birmingham, Birmingham, Alabama
                [m ]Department of Psychiatry, Behavioural Medicine Program, Massachusetts General Hospital, Boston, Massachusetts, USA
                [n ]Vinh University College of Health Sciences, Hanoi, Vietnam.
                Author notes
                Correspondence to Lynn T. Matthews, 1900 University Blvd, THT215E, Birmingham, AL 35294, USA. Tel: +1 (205) 934 8148; e-mail: lynnmatthews@ 123456uabmc.edu
                Article
                AIDS-D-24-00036 00008
                10.1097/QAD.0000000000003925
                11211057
                38752557
                01e95e2e-e3a6-4e90-9611-74d84f681b9b
                Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc.

                This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0

                History
                : 18 January 2024
                : 01 April 2024
                : 08 April 2024
                Categories
                Clinical Science
                Custom metadata
                TRUE

                adherence,hiv-prevention,periconception,perinatal,pre-exposure prophylaxis,south africa

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