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      Preferences for long‐acting pre‐exposure prophylaxis among gay, bisexual and other men who have sex with men in Taiwan: findings from the 2021 HEART Survey

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          Abstract

          Introduction

          While various antiretrovirals have been studied as potential candidates for long‐acting pre‐exposure prophylaxis (PrEP), the bimonthly injectable cabotegravir the first long‐acting form of PrEP—was approved in 2021. Event‐driven (ED) PrEP has been the most prevalent dosing regimen among gay, bisexual and other men who have sex with men (GBMSM) in Taiwan, providing a unique setting to observe the preferences for long‐acting PrEP in a community where the daily regimen is not the mainstream method. This study aimed to determine the preferences for the different forms and dosing intervals of long‐acting PrEP that are currently in the development pipeline.

          Methods

          We conducted a survey in 2021 by convenience sampling the users of social networking applications for GBMSM in Taiwan. Our survey included questions on sexual behaviours, current PrEP regimens and the preferences for potential candidates of long‐acting PrEP, such as implants, intramuscular and subcutaneous injections. We compared the Likert‐scale preference ratings for potential long‐acting options, and conducted logistic regression analysis to examine the factors associated with a preference for bimonthly intramuscular injections (2M IM) over ED and daily PrEP regimens, respectively.

          Results

          A total of 1728 responses were eligible for analysis. Three percent of respondents ( n = 52) were daily PrEP users; 11.5% ( n = 198) were ED PrEP users. When not considering cost, current PrEP users—regardless of their original dosing regimen—were most likely to express preferences for monthly oral PrEP, followed by a 6‐month subcutaneous injectable (6M SC) and 2M IM. However, among non‐current PrEP users, monthly oral PrEP was the most preferred form, followed by ED, daily oral and 6M SC injectable. Multivariable logistic regression revealed that current daily users, those willing to take PrEP in the next 6 months and those with more sex partners in the last 12 months had a significant correlation with preferences for the 2M IM injectable over the ED PrEP.

          Conclusions

          The monthly oral form was the most preferable long‐acting PrEP among GBMSM in Taiwan. Current daily PrEP users preferred the 2M IM injectable over the ED PrEP, which made the 2M IM injectable a potential alternative. Further studies should focus on how the cost and delivery affect PrEP preferences and their actual uptake.

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          Most cited references26

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          Cabotegravir for HIV Prevention in Cisgender Men and Transgender Women

          Safe and effective long-acting injectable agents for preexposure prophylaxis (PrEP) for human immunodeficiency virus (HIV) infection are needed to increase the options for preventing HIV infection.
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            Cabotegravir for the prevention of HIV-1 in women: results from HPTN 084, a phase 3, randomised clinical trial

            Summary Background Oral pre-exposure prophylaxis has been introduced in more than 70 countries, including many in sub-Saharan Africa, but women experience considerable barriers to daily pill-taking, such as stigma, judgement, and the fear of violence. Safe and effective long-acting agents for HIV prevention are needed for women. We aimed to evaluate the safety and efficacy of injectable cabotegravir compared with daily oral tenofovir diphosphate plus emtricitabine (TDF-FTC) for HIV prevention in HIV-uninfected women. Methods HPTN 084 was a phase 3, randomised, double-blind, double-dummy, active-controlled, superiority trial in 20 clinical research sites in seven countries in sub-Saharan Africa. Participants were eligible for enrolment if they were assigned female sex at birth, were aged 18–45 years, reported at least two episodes of vaginal intercourse in the previous 30 days, were at risk of HIV infection based on an HIV risk score, and agreed to use a long-acting reversible contraceptive method. Participants were randomly assigned (1:1) to either active cabotegravir with TDF-FTC placebo (cabotegravir group) or active TDF-FTC with cabotegravir placebo (TDF-FTC group). Study staff and participants were masked to study group allocation, with the exception of the site pharmacist who was responsible for study product preparation. Participants were prescribed 5 weeks of daily oral product followed by intramuscular injections every 8 weeks after an initial 4-week interval load, alongside daily oral pills. Participants who discontinued injections were offered open-label daily TDF-FTC for 48 weeks. The primary endpoints of the study were incident HIV infection in the intention-to-treat population, and clinical and laboratory events that were grade 2 or higher in all women who had received at least one dose of study product. This study is registered with ClinicalTrials.gov, NCT03164564. Findings From Nov 27, 2017, to Nov 4, 2020, we enrolled 3224 participants (1614 in the cabotegravir group and 1610 in the TDF-FTC group). Median age was 25 years (IQR 22–30); 1755 (54·7%) of 3209 had two or more partners in the preceding month. 40 incident infections were observed over 3898 person-years (HIV incidence 1·0% [95% CI 0·73–1·40]); four in the cabotegravir group (HIV incidence 0·2 cases per 100 person-years [0·06–0·52]) and 36 in the TDF-FTC group (1·85 cases per 100 person-years [1·3–2·57]; hazard ratio 0·12 [0·05–0·31]; p<0·0001; risk difference –1·6% [–1·0% to –2·3%]. In a random subset of 405 TDF-FTC participants, 812 (42·1%) of 1929 plasma samples had tenofovir concentrations consistent with daily use. Injection coverage was 93% of the total number of person-years. Adverse event rates were similar across both groups, apart from injection site reactions, which were more frequent in the cabotegravir group than in the TDF-FTC group (577 [38·0%] of 1519 vs 162 [10·7%] of 1516]) but did not result in injection discontinuation. Confirmed pregnancy incidence was 1·3 per 100 person-years (0·9–1·7); no congenital birth anomalies were reported. Interpretation Although both products for HIV prevention were generally safe, well tolerated, and effective, cabotegravir was superior to TDF-FTC in preventing HIV infection in women. Funding National Institute of Allergy and Infectious Diseases, ViiV Healthcare, and the Bill & Melinda Gates Foundation. Additional support was provided through the National Institute of Mental Health, the National Institute on Drug Abuse, and the Eunice Kennedy Shriver National Institute of Child Health and Human Development. ViiV Healthcare and Gilead Sciences provided pharmaceutical support.
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              Medication adherence and discontinuation of long-acting injectable versus oral antipsychotics in patients with schizophrenia or bipolar disorder.

              To examine medication adherence and discontinuation in two separate groups of patients with schizophrenia or bipolar disorder (BD), who began receiving a long-acting injectable antipsychotic (LAI) versus those who changed to a different oral antipsychotic monotherapy.
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                Author and article information

                Contributors
                carol.chiajung@gmail.com
                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
                07 September 2023
                September 2023
                : 26
                : 9 ( doiID: 10.1002/jia2.v26.9 )
                : e26163
                Affiliations
                [ 1 ] Department of Public Health College of Medicine National Cheng Kung University Tainan Taiwan
                [ 2 ] Division of Infectious Diseases Department of Medicine Taipei City Hospital Renai Branch Taipei Taiwan
                [ 3 ] HIV Education and Research Taiwan (HEART) Association Taipei Taiwan
                [ 4 ] Infection Control Center and Department of Internal Medicine National Cheng Kung University Hospital College of Medicine National Cheng Kung University Tainan Taiwan
                [ 5 ] Institute of Health Behaviors and Community Sciences National Taiwan University Taipei Taiwan
                [ 6 ] The Kirby Institute UNSW Sydney Sydney New South Wales Australia
                [ 7 ] Australian Research Centre in Sex Health and Society La Trobe University Melbourne Victoria Australia
                Author notes
                [*] [* ]Corresponding author: Carol Strong, Department of Public Health, College of Medicine, National Cheng Kung University, 8F‐8068, No. 138, ShengLi Rd., North Dist., Tainan 704, Taiwan.

                Tel: +886‐6‐2353535, ext 5963. ( carol.chiajung@ 123456gmail.com )

                [#]

                These authors have contributed equally to the work.

                Author information
                https://orcid.org/0000-0003-1007-9624
                https://orcid.org/0000-0001-7399-5852
                https://orcid.org/0000-0002-3319-5145
                https://orcid.org/0000-0002-5085-1976
                https://orcid.org/0000-0002-2934-5382
                Article
                JIA226163
                10.1002/jia2.26163
                10483501
                37675767
                13f5e9fd-518c-43e0-8a86-adbf624e00f6
                © 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
                : 19 March 2023
                : 22 August 2023
                Page count
                Figures: 1, Tables: 2, Pages: 8, Words: 4464
                Funding
                Funded by: National Cheng Kung University Hospital , doi 10.13039/501100004844;
                Award ID: NCKUH‐10902066
                Funded by: National Science and Technology Council , doi 10.13039/501100020950;
                Award ID: NSTC 108‐2636‐B‐006‐004
                Award ID: NSCT 109‐2636‐B‐006‐004
                Award ID: NSTC 110‐2636‐B‐006‐011
                Award ID: NSTC 111‐2636‐B‐006‐011
                Award ID: NSTC 112‐2636‐B‐006‐007
                Award ID: NSTC 112‐2314‐B‐006‐081‐MY3
                Categories
                Short Report
                Short Report
                Custom metadata
                2.0
                September 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.3.3 mode:remove_FC converted:07.09.2023

                Infectious disease & Microbiology
                asia,gay, bisexual and other men who have sex with men (gbmsm),hiv prevention,policy,pre‐exposure prophylaxis (prep),retention

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