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基于治疗药物监测,由替拉那韦/利托那韦 500/200 bid 简化为 500/100 bid 的获益。

The benefit of simplification from tipranavir/ritonavir 500/200 bid to 500/100 bid guided by therapeutic drug monitoring.

机构信息

Pharmacokinetic Unit, Hospital Carlos III, Madrid, Spain.

出版信息

Ther Drug Monit. 2010 Apr;32(2):242-4. doi: 10.1097/FTD.0b013e3181d3f97f.

Abstract

Despite being among the most potent protease inhibitors, the use of tipranavir (TPV) is hampered by a high pill burden and frequent side effects compared with other boosted protease inhibitors. A total of 10 patients receiving TPV/ritonavir (TPV/RTV) 500/200 for longer than 6 months were randomized to stay on the same dosing schedule or switch to TPV/RTV 500/100. Although all patients on TVP/RTV 500/200 remained stable for the next 12 weeks, 3 out of 5 patients who switched doses experienced benefits in terms of reducing aminotransferases and total cholesterol. Fasting triglycerides were also reduced in 2 of them. Plasma HIV-RNA remained undetectable in all patients, despite the observed decline in TPV trough concentrations.

摘要

尽管替拉那韦(TPV)是最有效的蛋白酶抑制剂之一,但与其他增效蛋白酶抑制剂相比,其较高的药物负担和频繁的副作用限制了其应用。共有 10 名接受替拉那韦/利托那韦(TPV/RTV)500/200 治疗超过 6 个月的患者被随机分为继续维持原剂量或换用替拉那韦/利托那韦 500/100。尽管所有接受 TPV/RTV 500/200 治疗的患者在接下来的 12 周内保持稳定,但换用剂量的 5 名患者中有 3 名在降低转氨酶和总胆固醇方面受益。其中 2 名患者的空腹甘油三酯也有所降低。尽管 TPV 谷浓度下降,但所有患者的血浆 HIV-RNA 仍保持不可检测。

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