首页> 外文期刊>Therapeutic Drug Monitoring >Pharmacokinetics and Pharmacodynamics of Sildenafil in a Patient Treated With Human Immunodeficiency Virus Protease Inhibitors.
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Pharmacokinetics and Pharmacodynamics of Sildenafil in a Patient Treated With Human Immunodeficiency Virus Protease Inhibitors.

机译:西地那非在用人类免疫缺陷病毒蛋白酶抑制剂治疗的患者中的药代动力学和药效学。

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We describe a 44-year-old male patient with human immunodeficiency virus (HIV) infection and pulmonary arterial hypertension who was treated with several protease inhibitors and with sildenafil. In order to guide treatment with sildenafil, the pharmacokinetics and dynamics of sildenafil were monitored at various time points. In comparison with healthy subjects, the maximal concentration in plasma (Cmax), area under the curve (AUC), and elimination half-life of sildenafil were approximately doubled in the patient. After increasing the sildenafil dose to ensure therapeutic drug levels over 24 hours, the pulmonary arterial hypertension and physical performance of the patient improved significantly. We conclude that the elimination of sildenafil is impaired in patients treated with protease inhibitors, but to a lesser extent than predicted from single-dose studies reported in the literature. Patients treated concomitantly with protease inhibitors and sildenafil need close monitoring of plasma levels, pharmacodynamics, and toxicity of sildenafil in order to be treated optimally.
机译:我们描述了一名患有人类免疫缺陷病毒(HIV)感染和肺动脉高压的44岁男性患者,该患者接受了几种蛋白酶抑制剂和西地那非的治疗。为了指导西地那非的治疗,在各个时间点监测西地那非的药代动力学和动力学。与健康受试者相比,西地那非的最大血浆浓度(Cmax),曲线下面积(AUC)和消除半衰期大约增加了一倍。在增加西地那非的剂量以确保超过24小时的治疗药物水平后,患者的肺动脉高压和身体机能明显改善。我们得出的结论是,用蛋白酶抑制剂治疗的患者西地那非的消除受到损害,但程度比文献报道的单剂量研究预测的程度要小。同时接受蛋白酶抑制剂和西地那非治疗的患者需要密切监测血浆水平,西地那非的药效学和毒性,以便对其进行最佳治疗。

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