Tandon Anushka, Saseen Joseph J, Fink Rhianna M, Billups Sarah J
Department of Clinical Pharmacy, University of Colorado Skaggs School of Pharmacy and Pharmaceutical Sciences, Aurora, CO, USA.
Department of Family Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
AIDS Behav. 2024 Apr;28(4):1270-1275. doi: 10.1007/s10461-023-04154-5. Epub 2023 Aug 5.
This study aimed to compare primary care (PC) and infectious diseases (ID) provider adherence to HIV pre-exposure prophylaxis (PrEP) prescribing and monitoring parameters outlined in Centers for Disease Control/Department of Health and Human Services (CDC/DHHS) guidelines. This retrospective cohort analysis from 2017 to 2022 used prescription and laboratory order data to identify patients prescribed PrEP by PC or ID providers. Primary endpoints assessed were adherence to baseline and follow-up HIV monitoring recommendations in the 12 months following the initial PrEP prescription. Secondary endpoints included appropriate PrEP prescription order quantities (≤ 90-day supply), appropriate renal function monitoring, and identification of factors independently associated with follow-up HIV monitoring adherence. Of the 324 eligible patients identified, 112 received PrEP from an ID specialist and 212 from a PC provider. Patients prescribed PrEP from an ID specialist were more likely to have appropriately completed baseline HIV monitoring (OR = 2.56, 95% CI 1.20, 5.47), follow-up HIV monitoring (OR = 1.81, 95% CI 1.08, 3.05), and renal function monitoring (OR = 2.81, 95% CI 1.69, 4.68); The ID group was also more likely to have PrEP prescriptions appropriately authorized for a days' supply of ≤ 90 days (OR = 4.41, 95% CI 2.60, 7.48). Patients receiving PrEP care from ID specialists had better adherence to all assessed PrEP prescribing and monitoring recommendations compared to those receiving care from PC providers.
本研究旨在比较初级保健(PC)提供者和传染病(ID)提供者对美国疾病控制与预防中心/卫生与公众服务部(CDC/DHHS)指南中概述的HIV暴露前预防(PrEP)处方和监测参数的遵循情况。这项2017年至2022年的回顾性队列分析使用处方和实验室检查医嘱数据,以确定由PC或ID提供者开具PrEP处方的患者。评估的主要终点是在首次开具PrEP处方后的12个月内对基线和随访HIV监测建议的遵循情况。次要终点包括适当的PrEP处方剂量(≤90天供应量)、适当的肾功能监测,以及识别与随访HIV监测遵循情况独立相关的因素。在确定的324名符合条件的患者中,112名从ID专科医生处接受PrEP治疗,212名从PC提供者处接受治疗。从ID专科医生处开具PrEP处方的患者更有可能适当完成基线HIV监测(OR = 2.56,95%CI 1.20,5.47)、随访HIV监测(OR = 1.81,95%CI 1.08,3.05)和肾功能监测(OR = 2.81,95%CI 1.69,4.68);ID组也更有可能获得≤90天供应量的适当授权的PrEP处方(OR = 4.41,95%CI 2.60,7.48)。与从PC提供者处接受治疗的患者相比,从ID专科医生处接受PrEP治疗的患者对所有评估的PrEP处方和监测建议的遵循情况更好。