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替诺福韦引起的肾衰竭早期发病:病例报告及文献综述

Early onset of tenofovir-induced renal failure: case report and review of the literature.

作者信息

Patel Shilpa M, Zembower Teresa R, Palella Frank, Kanwar Yashpal S, Ahya Shubhada N

机构信息

Northwestern University, Feinberg School of Medicine, Department of InternalMedicine, Division of Infectious Diseases, Chicago, IL, USA.

出版信息

ScientificWorldJournal. 2007 Jul 27;7:1140-8. doi: 10.1100/tsw.2007.164.

Abstract

Tenofovir is an acyclic nucleotide analogue reverse transcriptase inhibitor that is commonly prescribed as part of a highly active antiretroviral therapy (HAART) regimen in HIV-infected patients. Although it is generally well tolerated, renal insufficiency has been associated with its use. We report a biopsy-proven case of acute renal failure that developed within weeks of initiating a HAART regimen containing tenofovir, and review the literature with specific attention to cases of renal failure occurring within 8 weeks of tenofovir initiation. Our patient developed renal insufficiency within 3 weeks of initiating tenofovir-containing HAART and overt renal failure was noted within 5 weeks. Renal biopsy demonstrated histopathologic changes suggestive of HIV nephropathy, despite normal baseline serum creatinine values. Thirty additional cases of tenofovir-associated renal failure have been reported. In the majority (n = 22, 73%), renal failure occurred months after initiating therapy (range: 5-26 months). However, in a significant subset (n = 8, 27%), renal failure occurred within 8 weeks of treatment initiation. Our data suggest that some patients are at risk for developing renal failure within weeks of tenofovir initiation. Thorough evaluation of renal function should be undertaken before prescription of tenofovir-containing HAART. For those in whom subclinical renal disease is discerned, added vigilance when monitoring renal function may be warranted.

摘要

替诺福韦是一种无环核苷酸类似物逆转录酶抑制剂,常用于为感染HIV的患者开具高效抗逆转录病毒治疗(HAART)方案。尽管它总体耐受性良好,但使用时曾出现过肾功能不全的情况。我们报告了1例经活检证实的急性肾衰竭病例,该病例在开始含替诺福韦的HAART方案数周内出现,并回顾了相关文献,特别关注在开始使用替诺福韦8周内发生肾衰竭的病例。我们的患者在开始含替诺福韦的HAART方案3周内出现肾功能不全,5周内出现明显肾衰竭。肾活检显示组织病理学变化提示为HIV相关性肾病,尽管基线血清肌酐值正常。另外还报告了30例与替诺福韦相关的肾衰竭病例。大多数(n = 22,73%)肾衰竭发生在开始治疗数月后(范围:5 - 26个月)。然而,有相当一部分(n = 8,27%)肾衰竭发生在开始治疗8周内。我们的数据表明,一些患者在开始使用替诺福韦数周内有发生肾衰竭的风险。在开具含替诺福韦的HAART处方前,应全面评估肾功能。对于那些发现有亚临床肾病的患者,监测肾功能时可能需要格外警惕。

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