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首页> 外文期刊>The Southeast Asian journal of tropical medicine and public health >EFFECTIVENESS OF FIXED-DOSE COMBINATION STAVUDINE, LAMIVUDINE AND NEVIRAPINE (GPO-VIR) FOR TREATMENT OF NAIVE HIV PATIENTS IN THAILAND: A 3-YEAR FOLLOW-UP
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EFFECTIVENESS OF FIXED-DOSE COMBINATION STAVUDINE, LAMIVUDINE AND NEVIRAPINE (GPO-VIR) FOR TREATMENT OF NAIVE HIV PATIENTS IN THAILAND: A 3-YEAR FOLLOW-UP

机译:固定剂量司他定,拉米夫定和尼维拉平联合用药治疗泰国纯净艾滋病毒患者的三年随访

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摘要

Generic fixed dose combination stavudine (d4T), lamivudine (3TC) and nevirapine (NVP), named GPO-VIR is recommended in the HIV treatment guidelines for Thailand. The long term effectiveness and adverse effects of this drug combination for the treatment of HIV were evaluated in an ambispective study at Bamrasnaradura Infectious Diseases Institute, Nonthaburi Province, Thailand from March 2002 to January 2006. A total of 152 adult treatment naive HIV patients who had received at least 12 months of GPO-VIR were enrolled. The median (IQR) CD4 cell count increased from 23 (8-94) cells/mul at baseline to 126 (38-180), 136 (98-189), 199 (141-255) and 334 (243-414) cells/ul at 3, 6,12 and 24 months (p<0.001), respectively. The median (IQR) percentage of body weights increased from baseline by 3.0% (0.3-6.3), 6.2% (2.2-9.3), 7.3% (3.9-10.9) and 8.1% (3.4-11.9) at 3, 6, 12 and 24 months, respectively and then remained at a plateau until the end of the 3-year study. The occurrence of new opportunistic infections decreased significantly (p<0.001) with GPO-VIR treatment. Drug resistance occurred in 5 cases (3.3%) with a median (IQR) time of 18.0 (16.5-32.5) months to occurrence. Adverse effects included hypercholesterolemia (43.2%), lipodystrophy (35.5%), hypertriglyceridemia (25%), hypertension (13.1%), peripheral neuropathy (11.9%), hyperlactatemia (2.6%) and lactic acidosis (1.3%). Thirty-six patients (27%) switched from GPO-VIR to other anti-retro viral drugs regimens due to lipodystrophy. This study showed GPO-VIR had clinical and immunological benefits, but one-third of patients had adverse effects.
机译:在泰国的HIV治疗指南中建议使用通用固定剂量组合司他夫定(d4T),拉米夫定(3TC)和奈韦拉平(NVP),称为GPO-VIR。 2002年3月至2006年1月,在泰国暖武里府Bamrasnaradura传染病研究所进行的一项前瞻性研究中,评估了该药物组合治疗HIV的长期有效性和不良反应。总共152例成人HIV初治患者至少接受了12个月的GPO-VIR登记。中位数(IQR)CD4细胞计数从基线的23(8-94)个细胞/ mul增加到126(38-180),136(98-189),199(141-255)和334(243-414)个细胞分别在3、6、12和24个月时/ ul(p <0.001)。在3、6、12时,体重的中位数(IQR)百分比较基线分别增加了3.0%(0.3-6.3),6.2%(2.2-9.3),7.3%(3.9-10.9)和8.1%(3.4-11.9)分别为24个月和24个月,然后保持稳定,直到3年研究结束。使用GPO-VIR治疗后,新的机会感染的发生率显着降低(p <0.001)。 5例(3.3%)发生了耐药,发生中位时间(IQR)为18.0(16.5-32.5)个月。不良反应包括高胆固醇血症(43.2%),脂肪营养不良(35.5%),高甘油三酯血症(25%),高血压(13.1%),周围神经病变(11.9%),高乳酸血症(2.6%)和乳酸性酸中毒(1.3%)。三十六名患者(占27%)由于脂肪营养不良而从GPO-VIR转向其他抗逆转录病毒药物治疗方案。这项研究显示GPO-VIR具有临床和免疫学益处,但三分之一的患者有不良反应。

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