Department of Veterans Affairs, Center for Quality Management in Public Health, Palo Alto, CA, USA.
HIV Med. 2010 Mar;11(3):209-15. doi: 10.1111/j.1468-1293.2009.00764.x. Epub 2009 Oct 23.
The aim of the study was to describe Veterans Healthcare Administration (VHA) system-wide uptake of three HIV protease inhibitors: atazanavir, darunavir and tipranavir.
This retrospective cohort study evaluated VHA uptake of three target antiretrovirals and lopinavir/ritonavir in each complete 90-day quarter since approval to December 2007 using VHA HIV Clinical Case Registry data. We assessed uptake using number of new prescriptions, number of providers and facilities prescribing target agents, provider type, clinic type, facility size and location within four US regions.
Overall, 6551 HIV-infected veterans received target antiretrovirals. Uptake was generally greatest within the first year after Food and Drug Administration (FDA) approval, and then slightly declined and plateaued. Geographically, early adoption of new antiretroviral drugs tended to occur in the Western USA, as evidenced by comparison of uptake patterns of new antiretrovirals to use of all antiretroviral agents. A small percentage of prescribers of all antiretrovirals were responsible for new prescriptions for target medications, particularly for darunavir and tipranavir. Providers at almost 50% of VHA facilities were prescribing these agents within the first year.
Uptake of new antiretrovirals in the VHA generally reflected overall prescribing of all antiretrovirals, suggesting a lack of VHA impediments to new antiretrovirals in the healthcare system. Some regional variation in uptake among the targeted antiretrovirals occurred over time but tended to resolve after the first several months. Providers responsible for early prescribing of the target medications were limited to a fraction of providers who tended to be physicians who practised in infectious disease (ID) clinics at medium-sized facilities.
本研究旨在描述退伍军人医疗保健管理局(VHA)在全美范围内对三种 HIV 蛋白酶抑制剂(阿扎那韦、达芦那韦和替拉那韦)的采用情况。
本回顾性队列研究使用 VHA HIV 临床病例登记数据,评估了自 2007 年 12 月批准以来每个完整的 90 天季度中三种目标抗逆转录病毒药物和洛匹那韦/利托那韦的 VHA 采用情况。我们通过新处方数量、开具目标药物的提供者和医疗机构数量、提供者类型、诊所类型、机构规模以及美国四个地区的地理位置来评估采用情况。
总体而言,6551 名 HIV 感染退伍军人接受了目标抗逆转录病毒药物治疗。在 FDA 批准后的第一年,采用率通常最高,然后略有下降并趋于平稳。从地理上看,新抗逆转录病毒药物的早期采用往往发生在美国西部,这可以通过比较新抗逆转录病毒药物的采用模式与所有抗逆转录病毒药物的使用情况来证明。所有抗逆转录病毒药物的一小部分开处方者负责开具目标药物的新处方,尤其是达芦那韦和替拉那韦。在第一年,近 50%的 VHA 机构的提供者都在开具这些药物。
VHA 中新型抗逆转录病毒药物的采用情况总体上反映了所有抗逆转录病毒药物的总体使用情况,表明 VHA 系统中不存在新型抗逆转录病毒药物的障碍。在一段时间内,三种目标抗逆转录病毒药物的采用情况存在一些地区差异,但在最初几个月后往往会得到解决。负责早期开具目标药物的提供者仅限于少数提供者,这些提供者往往是在中型机构的传染病(ID)诊所工作的医生。