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      Risk‐based versus universal PrEP delivery during pregnancy: a cluster randomized trial in Western Kenya from 2018 to 2019

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          Abstract

          Introduction

          Integrating pre‐exposure prophylaxis (PrEP) delivery for pregnant and postpartum women within maternal and child health (MCH) clinics is feasible and acceptable. It is unknown whether a risk‐guided model would facilitate appropriate PrEP use among MCH attendees better than universally offering PrEP.

          Methods

          The PrEP Implementation for Mothers in Antenatal Care (PrIMA) study was a cluster randomized trial to assess two models for PrEP delivery among pregnant women seeking routine MCH care at 20 public clinics in Kenya between January 2018 and July 2019 (NCT03070600). In the Universal arm, all participants received PrEP counselling and self‐selected whether to initiate PrEP. In the Targeted arm, participants underwent an HIV risk assessment, including an objective risk‐scoring tool and an offer of HIV self‐tests for at‐home partner testing; those determined to be at high risk received a PrEP offer. Participants were followed through 9 months postpartum. Primary outcomes included incident HIV and appropriate PrEP use (defined as PrEP uptake among those at high risk and no PrEP uptake for those not at risk). Outcomes were compared using intention‐to‐treat analyses, adjusting for baseline HIV risk and marital status.

          Results

          Among 4447 women enrolled, the median age was 24.0 years (interquartile range [IQR]: 20.9, 28.3), and most were married (84.8%). The median gestational age at enrolment was 24 weeks (IQR: 20, 30). Women in the Targeted arm were more likely to be at high risk for HIV acquisition at baseline (51.6% vs. 33.3%). During 4638 person‐years (p‐yr) of follow‐up, there were 16 maternal HIV infections with no difference in maternal HIV incidence between arms: 0.31/100 p‐yr (95% CI: 0.15, 0.65) Targeted and 0.38/100p‐yr (95% CI: 0.20, 0.73) Universal (adjusted relative risk [aRR]: 0.85 [CI: 0.28, 2.55]). There was no significant difference in the frequency of appropriate PrEP use between the arms (68.2% vs. 59.1% in Targeted vs. Universal, respectively) (aRR: 1.03 [CI: 0.96, 1.10]).

          Conclusions

          Given comparable maternal HIV incidence and PrEP uptake in Universal and Targeted approaches, and the simplicity that universal PrEP offers, our findings suggest that universal PrEP counselling is optimal for integrating PrEP in MCH systems.

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          Most cited references37

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          Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.

          Research electronic data capture (REDCap) is a novel workflow methodology and software solution designed for rapid development and deployment of electronic data capture tools to support clinical and translational research. We present: (1) a brief description of the REDCap metadata-driven software toolset; (2) detail concerning the capture and use of study-related metadata from scientific research teams; (3) measures of impact for REDCap; (4) details concerning a consortium network of domestic and international institutions collaborating on the project; and (5) strengths and limitations of the REDCap system. REDCap is currently supporting 286 translational research projects in a growing collaborative network including 27 active partner institutions.
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            The Patient Health Questionnaire-2: validity of a two-item depression screener.

            A number of self-administered questionnaires are available for assessing depression severity, including the 9-item Patient Health Questionnaire depression module (PHQ-9). Because even briefer measures might be desirable for use in busy clinical settings or as part of comprehensive health questionnaires, we evaluated a 2-item version of the PHQ depression module, the PHQ-2. The PHQ-2 inquires about the frequency of depressed mood and anhedonia over the past 2 weeks, scoring each as 0 ("not at all") to 3 ("nearly every day"). The PHQ-2 was completed by 6000 patients in 8 primary care clinics and 7 obstetrics-gynecology clinics. Construct validity was assessed using the 20-item Short-Form General Health Survey, self-reported sick days and clinic visits, and symptom-related difficulty. Criterion validity was assessed against an independent structured mental health professional (MHP) interview in a sample of 580 patients. As PHQ-2 depression severity increased from 0 to 6, there was a substantial decrease in functional status on all 6 SF-20 subscales. Also, symptom-related difficulty, sick days, and healthcare utilization increased. Using the MHP reinterview as the criterion standard, a PHQ-2 score > or =3 had a sensitivity of 83% and a specificity of 92% for major depression. Likelihood ratio and receiver operator characteristic analysis identified a PHQ-2 score of 3 as the optimal cutpoint for screening purposes. Results were similar in the primary care and obstetrics-gynecology samples. The construct and criterion validity of the PHQ-2 make it an attractive measure for depression screening.
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              Effectiveness and safety of oral HIV preexposure prophylaxis for all populations

              Objective: Preexposure prophylaxis (PrEP) offers a promising new approach to HIV prevention. This systematic review and meta-analysis evaluated the evidence for use of oral PrEP containing tenofovir disoproxil fumarate as an additional HIV prevention strategy in populations at substantial risk for HIV based on HIV acquisition, adverse events, drug resistance, sexual behavior, and reproductive health outcomes. Design: Rigorous systematic review and meta-analysis. Methods: A comprehensive search strategy reviewed three electronic databases and conference abstracts through April 2015. Pooled effect estimates were calculated using random-effects meta-analysis. Results: Eighteen studies were included, comprising data from 39 articles and six conference abstracts. Across populations and PrEP regimens, PrEP significantly reduced the risk of HIV acquisition compared with placebo. Trials with PrEP use more than 70% demonstrated the highest PrEP effectiveness (risk ratio = 0.30, 95% confidence interval: 0.21–0.45, P < 0.001) compared with placebo. Trials with low PrEP use did not show a significantly protective effect. Adverse events were similar between PrEP and placebo groups. More cases of drug-resistant HIV infection were found among PrEP users who initiated PrEP while acutely HIV-infected, but incidence of acquiring drug-resistant HIV during PrEP use was low. Studies consistently found no association between PrEP use and changes in sexual risk behavior. PrEP was not associated with increased pregnancy-related adverse events or hormonal contraception effectiveness. Conclusion: PrEP is protective against HIV infection across populations, presents few significant safety risks, and there is no evidence of behavioral risk compensation. The effective and cost-effective use of PrEP will require development of best practices for fostering uptake and adherence among people at substantial HIV risk.
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                Author and article information

                Contributors
                jcdettin@uw.edu
                Journal
                J Int AIDS Soc
                J Int AIDS Soc
                10.1002/(ISSN)1758-2652
                JIA2
                Journal of the International AIDS Society
                John Wiley and Sons Inc. (Hoboken )
                1758-2652
                20 February 2023
                February 2023
                : 26
                : 2 ( doiID: 10.1002/jia2.v26.2 )
                : e26061
                Affiliations
                [ 1 ] Department of Research and Programs Kenyatta National Hospital Nairobi Kenya
                [ 2 ] Department of Global Health University of Washington Seattle Washington USA
                [ 3 ] Department of Biostatistics University of Washington Seattle Washington USA
                [ 4 ] Division of Allergy and Infectious Diseases University of Washington Seattle Washington USA
                [ 5 ] Vaccine and Infectious Disease Division Fred Hutchinson Cancer Research Center Seattle Washington USA
                [ 6 ] Department of Behavioral Nursing & Health Informatics University of Washington Seattle Washington USA
                [ 7 ] Department of Epidemiology University of Washington Seattle Washington USA
                [ 8 ] Department of Medicine University of Washington Seattle Washington USA
                [ 9 ] Gilead Sciences Foster City California USA
                [ 10 ] Department of Pediatrics University of Washington Seattle Washington USA
                Author notes
                [*] [* ] Corresponding author: Julia C. Dettinger, Hans Rosling Center for Population Health, 3980 15th Ave NE, Box 351620, Seattle, WA 98195, USA. Tel: +206 221 1041. ( jcdettin@ 123456uw.edu )

                [#]

                Joint first authors have contributed equally to the work.

                [##]

                Joint last authors have contributed equally to the work.

                Author information
                https://orcid.org/0000-0002-9130-2666
                https://orcid.org/0000-0002-8767-1282
                https://orcid.org/0000-0003-1255-7191
                https://orcid.org/0000-0001-8242-8438
                Article
                JIA226061
                10.1002/jia2.26061
                9939942
                36807505
                59cf105e-643e-4175-a792-01fb8af6f59b
                © 2023 The Authors. Journal of the International AIDS Society published by John Wiley & Sons Ltd on behalf of the International AIDS Society.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 29 August 2022
                : 19 January 2023
                Page count
                Figures: 1, Tables: 4, Pages: 11, Words: 7487
                Funding
                Funded by: National Institutes of Health, National Institute of Allergy and Infectious Disease
                Award ID: GJS,JMB‐R01AI125498
                Funded by: Eunice Kennedy Shriver National Institute of Child Health & Human Development
                Award ID: GJS‐R01HD094630
                Award ID: JP‐R01HD100201
                Funded by: University of Washington's Center for AIDS Research Behavioral Sciences Core and Biometrics Core
                Award ID: P30AI027757
                Funded by: Global WACh
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                February 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.5 mode:remove_FC converted:20.02.2023

                Infectious disease & Microbiology
                pre‐exposure prophylaxis,pregnancy,postpartum,hiv prevention,breastfeeding,kenya

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