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通用抗逆转录病毒疗法(ART)和免费ART项目对印度金奈一家三级HIV护理中心开始ART治疗时间的影响。

Impact of generic antiretroviral therapy (ART) and free ART programs on time to initiation of ART at a tertiary HIV care center in Chennai, India.

作者信息

Solomon Sunil S, Lucas Gregory M, Kumarasamy Nagalingeswaran, Yepthomi Tokugha, Balakrishnan Pachamuthu, Ganesh Aylur K, Anand Santhanam, Moore Richard D, Solomon Suniti, Mehta Shruti H

机构信息

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

AIDS Care. 2013 Aug;25(8):931-6. doi: 10.1080/09540121.2012.748160. Epub 2012 Dec 7.

Abstract

Antiretroviral therapy (ART) access in the developing world has improved, but whether increased access has translated to more rapid treatment initiation among those who need it is unknown. We characterize time to ART initiation across three eras of ART availability in Chennai, India (1996-1999: pregeneric; 2000-2003: generic; 2004-2007: free rollout). Between 1996 and 2007, 11,171 patients registered for care at the YR Gaitonde Centre for AIDS Research and Education (YRGCARE), a tertiary HIV referral center in southern India. Of these, 5726 patients became eligible for ART during this period as per Indian guidelines for initiation of ART. Generalized gamma survival models were used to estimate relative times (RT) to ART initiation by calendar periods of eligibility. Time to initiation of ART among patients in Chennai, India was also compared to an HIV clinical cohort in Baltimore, USA. Median age of the YRGCARE patients was 34 years; 77% were male. The median CD4 at presentation was 140 cells/µl. After adjustment for demographics, CD4 and WHO stage, persons in the pregeneric era took 3.25 times longer (95% confidence interval [CI]: 2.53-4.17) to initiate ART versus the generic era and persons in the free rollout era initiated ART more rapidly than the generic era (RT: 0.73; 95% CI: 0.63-0.83). Adjusting for differences across centers, patients at YRGCARE took longer than patients in the Johns Hopkins Clinical Cohort (JHCC) to initiate ART in the pregeneric era (RT: 4.90; 95% CI: 3.37-7.13) but in the free rollout era, YRGCARE patients took only about a quarter of the time (RT: 0.31; 95% CI: 0.22-0.44). These data demonstrate the benefits of generic ART and government rollouts on time to initiation of ART in one developing country setting and suggests that access to ART may be comparable to developed country settings.

摘要

发展中国家抗逆转录病毒疗法(ART)的可及性有所改善,但可及性的提高是否转化为有需求者更快开始治疗尚不清楚。我们描述了印度钦奈三个抗逆转录病毒疗法可及时代(1996 - 1999年:非仿制药时代;2000 - 2003年:仿制药时代;2004 - 2007年:免费推广时代)开始接受抗逆转录病毒疗法的时间。1996年至2007年期间,11171名患者在印度南部一家三级艾滋病转诊中心YR盖通德艾滋病研究与教育中心(YRGCARE)登记接受治疗。其中,根据印度抗逆转录病毒疗法启动指南,有5726名患者在此期间符合接受抗逆转录病毒疗法的条件。使用广义伽马生存模型按符合条件的日历时间段估计开始接受抗逆转录病毒疗法的相对时间(RT)。还将印度钦奈患者开始接受抗逆转录病毒疗法的时间与美国巴尔的摩的一个艾滋病毒临床队列进行了比较。YRGCARE患者的中位年龄为34岁;77%为男性。就诊时的CD4中位数为140个细胞/微升。在对人口统计学、CD4和世界卫生组织(WHO)分期进行调整后,非仿制药时代的患者开始接受抗逆转录病毒疗法的时间比仿制药时代长3.25倍(95%置信区间[CI]:2.53 - 4.17),免费推广时代的患者开始接受抗逆转录病毒疗法的速度比仿制药时代更快(相对时间:0.73;95%置信区间:0.63 - 0.83)。考虑到不同中心之间的差异,YRGCARE的患者在非仿制药时代开始接受抗逆转录病毒疗法的时间比约翰·霍普金斯临床队列(JHCC)的患者长(相对时间:4.90;95%置信区间:3.37 - 7.13),但在免费推广时代,YRGCARE的患者所用时间仅约为其四分之一(相对时间:0.31;95%置信区间:0.22 - 0.44)。这些数据证明了仿制药和政府推广在一个发展中国家环境中对抗逆转录病毒疗法启动时间的益处,并表明抗逆转录病毒疗法的可及性可能与发达国家相当。

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