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Lopinavir/ritonavir vs. indinavir/ritonavir in antiretroviral naive HIV-infected patients: immunovirological outcome and side effects.

机译:Lopinavir / ritonavir与indinavir / ritonavir在抗逆转录病毒初次感染HIV的患者中:免疫病毒学结果和副作用。

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摘要

We compared immunovirological outcomes and toxicities of HAART regimens including LPV/r and IDV/r in antiretroviral naive HIV-1 patients. We retrospectively selected 55 patients starting LPV/r and 52 starting IDV/r as first-line HAART. Immunovirological and metabolic parameters were recorded at baseline and every 3 months as were side effects, AIDS-defining events and deaths. Demographic characteristics and NRTIs included in the regimens were comparable. Both groups reached undetectable HIV-RNA plasma viremia from third month and maintained during follow-up. However, patients receiving IDV/r had a lower probability to obtain virological success (RH: 0.46). Patients receiving IDV/r patients showed a greater increase of total cholesterol (P = 0.01). Three patients on LPV/r and 21 on IDV/r discontinued the drug for toxicity, leading to a 8.40 higher risk of discontinuation in the latter group. In our clinical setting IDV/r showed to be less effective and more toxic than LPV/RTV as first-line HAART.
机译:我们比较了抗逆转录病毒初次感染HIV-1的HAART方案(包括LPV / r和IDV / r)的免疫病毒学结果和毒性。我们回顾性地选择55例开始LPV / r的患者和52例开始IDV / r的患者作为一线HAART。在基线和每三个月记录一次免疫病毒学和代谢参数,以及副作用,定义艾滋病的事件和死亡。方案中包括的人口统计学特征和NRTI相当。两组均从第三个月开始达到无法检测到的HIV-RNA血浆病毒血症,并在随访期间维持。但是,接受IDV / r的患者获得病毒学成功的可能性较低(RH:0.46)。接受IDV / r的患者的总胆固醇升高幅度更大(P = 0.01)。接受LPV / r治疗的三名患者和接受IDV / r治疗的21名患者因药物中毒而停药,导致后者中止风险高8.40。在我们的临床环境中,IDV / r作为一线HAART比LPV / RTV无效,毒性更高。

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