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Transition to dolutegravir-based ART in 35 low- and middle-income countries: a global survey of HIV care clinics

杜鲁特格拉维尔 医学 家庭医学 抗逆转录病毒疗法 病毒载量 拉丁美洲 人类免疫缺陷病毒(HIV) 人口学 儿科 政治学 社会学 法学
作者
Elizabeth Zaniewski,Veronika Skrivankova,Ellen Brazier,Anchalee Avihingsanon,Sandra Wagner Cardoso,Carina César,Henri Chenal,Brenda Crabtree‐Ramírez,Rossana Ditangco,Peter Vanes Ebasone,Brian Eley,Jonathan Euvrard,Geoffrey Fatti,Jacqueline Huwa,Andrew Edmonds,Daisy Maria Machado,Xavier Anglaret,Albert Minga,Joseph Muleebwa,Sanjay Mundhe,Gad Murenzi,Winnie Muyindike,Dominique Nsonde,Sarah Obatsa,Joseph Odhiambo,Hans Prozesky,Supattra Rungmaitree,Aggrey Semeere,Moussa Seydi,Nosisa Sipambo,Tavitiya Sudjaritruk,Karl‐Günter Technau,Thierry Tiendrebeogo,Christella Twizere,Marie Ballif
出处
期刊:AIDS [Lippincott Williams & Wilkins]
标识
DOI:10.1097/qad.0000000000004007
摘要

Objective: We studied the transition to dolutegravir-containing antiretroviral therapy (ART) at HIV treatment clinics within the International epidemiology Databases to Evaluate AIDS (IeDEA). Design: Site-level survey conducted in 2020–2021 among HIV clinics in low- and middle-income countries (LMICs). Methods: We assessed the status of dolutegravir rollout and viral load and drug resistance testing practices for patients on ART switching to dolutegravir-based regimens. We used generalized estimating equations to assess associations between clinic rollout of both first- and second-line dolutegravir-based ART regimens (dual rollout) and site-level factors. Results: Of 179 surveyed clinics, 175 (98%) participated; 137 (78%) from Africa, 30 (17%) from the Asia-Pacific, and 8 (5%) from Latin America. Most clinics (80%) were in low- or lower-middle-income countries, and there were a mix of primary-, secondary- and tertiary-level clinics. Ninety percent reported rollout of first-line dolutegravir, 59% of second-line, 94% of first- or second-line and 55% of dual rollout. The adjusted odds of dual rollout were higher among tertiary-level (aOR 4.00; 95% CI 1.39 to 11.47) and secondary-level clinics (aOR 3.66; 95% CI 2.19 to 6.11) than in primary-level clinics. Over half (59%) of clinics that introduced first- or second-line dolutegravir-based ART required recent viral load testing before switching to dolutegravir, and 15% performed genotypic resistance testing at switch. Conclusions: Dolutegravir-based ART was rolled out at nearly all IeDEA clinics in LMICs, yet many switched patients to dolutegravir without recent viral load testing and drug resistance testing was rarely performed. Without such testing, drug resistance among patient switching to dolutegravir may go undetected.

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