首页> 外文期刊>Journal of Renal and Hepatic Disorders >Monitoring the Effects of Tenofovir Disoproxil Fumarate to Tenofovir Alafenamide Switch for Tubulotoxicity in Highly Treatment-Experienced or in Very Sick Individuals Infected with HIV
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Monitoring the Effects of Tenofovir Disoproxil Fumarate to Tenofovir Alafenamide Switch for Tubulotoxicity in Highly Treatment-Experienced or in Very Sick Individuals Infected with HIV

机译:监测Tenofovir Disoproxil Mumarate对替诺福韦的替诺夫血酰胺开关在高度治疗中或在感染HIV感染的病态的个体中的毒素毒性

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Tenofovir disoproxil fumarate (TDF) is a common antiretroviral utilised in the treatment of human immunodeficiency virus (HIV) and hepatitis B infections. It is associated with the development of tubulotoxicity and tubulopathies, and is not recommended in the treatment of patients with baseline chronic kidney disease. Until now, guidelines have suggested frequent monitoring of serum biochemistry to detect the development of such complications. In recent trials, a new prodrug formulation of tenofovir alafenamide (TAF) has been shown to exhibit less tubular toxicity than its counterpart due to a lower serum concentration of its metabolites. In this article, we share our experience with two patients who developed tubulotoxicity following the commencement of TDF-based regimens in HIV, and its improvement following its change to TAF, and review the available literature regarding tenofovir-based nephrotoxicity.
机译:Tenofovir Disoproxil umarate(TDF)是用于治疗人免疫缺陷病毒(HIV)和乙型肝炎感染的常见抗逆转录病毒。它与小管状毒性和微管疗法的发育有关,并不建议治疗基线慢性肾病的患者。到目前为止,指导方针表明频繁监测血清生物化学,以检测这种并发症的发展。最近的试验中,由于其代谢物的血清浓度较低的血清浓度较低,已经显示出替诺福韦醛酰胺(TAF)的新前药制剂表现出比其代谢物的血清浓度较低的对应物具有较少的管状毒性。在本文中,我们分享我们的经验,这些患者在艾滋病毒的基于TDF的基础方案开始后开发了滴管毒性,以及其改变对TAF后的改进,并审查了关于胞多夫罗基的肾毒性的可用文献。

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