Pujari Sanjay, Srasuebkul Preeyaporn, Sungkanuparph Somnuek, Lim Poh Lian, Kumarasamy Nagalingeswaran, Chuah John, Kumar Ritesh N, Chen Yi-Ming A, Oka Shinichi, Choi Jun Yong, Lee Man-Po, Phanuphak Praphan, Kamarulzaman Adeeba, Lee Christopher, Fujie Zhang, Ditangco Rosanna, Saphonn Vonthanak, Sirisanthana Thira, Merati Tuti Parwati, Smith Jeff, Law Matthew G
Institute of Infectious diseases, Pune India.
J Antivir Antiretrovir. 2009 Nov 1;1(1):28-35. doi: 10.4172/jaa.1000004.
Regimens containing protease inhibitors (PI) are less commonly used in developing countries due to high cost and less availability. We evaluated characteristics of patients initiating PI-based therapy according to previous antiretroviral (ARV) exposure; factors associated with initiating a PI-containing regimen using newer versus older PIs, and proportion of patients with detectable viral loads (VL) after initiating a PI-based regimen. METHODS: This analysis includes all patients who have initiated a PI-based regimen. ARV exposure was categorised: naïve (no previous ARV), 1st, 2nd, >/= 3rd switches; a switch was defined as starting or stopping any drug in a regimen. Newer PIs were defined as those approved by the US FDA after 1 January 2000. Detectable VL at 12 months was defined as VL >/= 400 copies/mL. Characteristics at PI initiation were evaluated. Logistic regression was used to determine factors associated with initiating a newer PI and detectable VL at 12 months after PI initiation. RESULTS: 1106 patients initiated PI-based therapy; of these, 618 (56%) were naïve patients. Overall, 22% (176) of patients had detectable VL at 12 months following the PI initiation. Being from a high income country (vs. mid/low income, OR = 1.80, p = 0.034) were more likely to be associated with detectable VL. CONCLUSION: The use of PIs in this cohort is dictated by accessibility and affordability issues particularly for the newer PIs. Short-term virological outcomes following PI-therapy in our cohort were good, and were associated with CD4 count at time of initiation.
由于成本高且可用性低,含蛋白酶抑制剂(PI)的治疗方案在发展中国家较少使用。我们根据先前的抗逆转录病毒(ARV)暴露情况评估了开始基于PI治疗的患者特征;使用新型与旧型PI启动含PI方案相关的因素,以及开始基于PI方案后病毒载量(VL)可检测的患者比例。方法:该分析纳入了所有开始基于PI方案的患者。ARV暴露情况分为:初治(无先前ARV治疗)、第1次、第2次、≥第3次换药;换药定义为开始或停止方案中的任何药物。新型PI定义为2000年1月1日后获美国食品药品监督管理局(FDA)批准的药物。12个月时可检测的VL定义为VL≥400拷贝/毫升。评估了开始使用PI时的特征。采用逻辑回归确定与开始使用新型PI以及开始使用PI后12个月时可检测VL相关的因素。结果:1106例患者开始基于PI的治疗;其中,618例(56%)为初治患者。总体而言,22%(176例)患者在开始使用PI后12个月时VL可检测。来自高收入国家(与中/低收入国家相比,比值比=1.80,p=0.034)更可能与VL可检测相关。结论:该队列中PI的使用受可及性和可负担性问题的支配,尤其是新型PI。我们队列中PI治疗后的短期病毒学结局良好,且与开始治疗时的CD4细胞计数相关。