Department of Infectious Diseases, Hospital Ramón y Cajal, Madrid, Spain.
AIDS. 2011 Apr 24;25(7):1006-9. doi: 10.1097/QAD.0b013e3283466f85.
Although atazanavir is widely used in hepatitis C virus (HCV)-HIV-1 patients, little is known about its safety in advanced liver disease. We studied 34 HCV-HIV-1 patients with cirrhosis receiving atazanavir. After 551.2 patient-months of follow-up, there were no cases of serious liver toxicity or cirrhosis decompensation, and only 18.5% discontinued the drug. Despite median bilirubin level at inclusion was 1.5 mg/ml, increases in bilirubin level were mild. Model for end-stage liver disease score (MELD) increased to 1.35 points (95% confidence interval 0.13-2.6), but no patient changed their pretreatment situation after atazanavir introduction. Atazanavir is a well tolerated option in cirrhosis, and significant alterations in bilirubin or MELD were not observed.
虽然阿扎那韦在丙型肝炎病毒 (HCV)-HIV-1 患者中被广泛应用,但对于其在晚期肝病中的安全性知之甚少。我们研究了 34 例接受阿扎那韦治疗的 HCV-HIV-1 合并肝硬化患者。经过 551.2 个患者月的随访,没有出现严重肝毒性或肝硬化失代偿的病例,仅有 18.5%的患者停药。尽管纳入时中位胆红素水平为 1.5mg/ml,但胆红素水平升高较轻。终末期肝病模型评分(MELD)增加至 1.35 分(95%置信区间 0.13-2.6),但在阿扎那韦应用后,没有患者的预处理情况发生改变。阿扎那韦在肝硬化中耐受良好,胆红素或 MELD 没有明显变化。