National Control Program for HIV/AIDS/STI, República del Paraguay Ministry of Public Health and Social Welfare, Asunción, Paraguay.
Department of Medicine, Center for Public Health Research, University of California, San Francisco, California, USA.
J Med Virol. 2022 Oct;94(10):5061-5065. doi: 10.1002/jmv.27933. Epub 2022 Jun 30.
Human immunodeficiency virus (HIV) drug resistance increases mortality and morbidity and antiretroviral therapy (ART) costs. We describe Paraguay's first nationally representative survey on pretreatment drug resistance (PDR) conducted among persons who initiated or reinitiated ART in 2019. We conducted a cross-sectional survey of antiretroviral (ARV) drug resistance in Paraguay in 2019. Participants were sampled at four comprehensive care clinics where 90% of patients with HIV in Paraguay initiate ART. Patients included were adults ≥18 years old who initiated first-line ART or reinitiated the same first-line ART regimen after ≥3 months of discontinuation. Of 208 patients, 93.8% had no prior ART exposure, 3.8% reinitiated the same regimen, 2.4% had unknown prior ART exposure; and 31.3% had a CD4 count <200 cells/µl. Mutations associated with resistance were present in 15.4% of patients. Mutations associated with resistance to nonnucleoside reverse transcriptase inhibitors (NNRTI) were present in 13.0% of patients, nucleoside reverse transcriptase inhibitors in 4.3%, and integrase inhibitors in 3.4%. Mutations associated with resistance to tenofovir were present in 1.0% of patients and emtricitabine/lamivudine in 1.4%. Nearly one in six patients had PDR in Paraguay's first nationally representative sample. High NNRTI PDR prevalence underscores the need to accelerate the transition to dolutegravir-based first-line ART. The low PDR prevalence of tenofovir and emtricitabine is reassuring as these ARVs are part of the World Health Organization (WHO)-recommended oral pre-exposure prophylaxis regimen. The high proportion of individuals initiating ART at a late disease stage highlights the need to improve treatment linkage strategies and implement WHO rapid ART initiation recommendations.
人类免疫缺陷病毒(HIV)耐药性增加了死亡率和发病率,以及抗逆转录病毒治疗(ART)的费用。我们描述了巴拉圭在 2019 年对开始或重新开始 ART 的患者进行的首次全国代表性预处理耐药性(PDR)调查。我们在 2019 年对巴拉圭的抗逆转录病毒(ARV)耐药性进行了横断面调查。参与者是在四家综合护理诊所中抽取的,巴拉圭 90%的 HIV 患者在这些诊所开始接受 ART。纳入的患者为年龄≥18 岁的成年人,他们首次接受一线 ART 或在停药≥3 个月后重新开始同一线 ART 方案。在 208 名患者中,93.8%的患者无既往 ART 暴露史,3.8%的患者重新开始同一方案,2.4%的患者既往 ART 暴露史未知;31.3%的患者 CD4 计数<200 个/µl。15.4%的患者存在与耐药相关的突变。与非核苷类逆转录酶抑制剂(NNRTI)耐药相关的突变存在于 13.0%的患者中,核苷类逆转录酶抑制剂存在于 4.3%的患者中,整合酶抑制剂存在于 3.4%的患者中。与替诺福韦耐药相关的突变存在于 1.0%的患者中,与恩曲他滨/拉米夫定耐药相关的突变存在于 1.4%的患者中。在巴拉圭首次全国代表性样本中,近六分之一的患者存在 PDR。高 NNRTI PDR 流行率突出表明需要加快向基于度鲁特韦的一线 ART 过渡。替诺福韦和恩曲他滨/拉米夫定的低 PDR 流行率令人欣慰,因为这些 ARV 是世界卫生组织(WHO)推荐的口服暴露前预防方案的一部分。大量个体在疾病晚期开始接受 ART,这突出表明需要改善治疗衔接策略并实施 WHO 快速开始 ART 的建议。