Tenofovir-induced Fanconi syndrome in chronic hepatitis B monoinfected patients that reverted after tenofovir withdrawal

被引:56
作者
Vigano, Mauro [2 ]
Brocchieri, Alessandra [3 ]
Spinetti, Angiola [4 ,5 ]
Zaltron, Serena [4 ,5 ]
Mangia, Giampaolo [1 ]
Facchetti, Floriana [1 ]
Fugazza, Alessandro [3 ]
Castelli, Francesco [4 ,5 ]
Colombo, Massimo [1 ]
Lampertico, Pietro [1 ]
机构
[1] Univ Milan, Gastroenterol Unit 1, Fdn IRCCS Ca Granda Osped Maggiore Policlin, I-20122 Milan, Italy
[2] Univ Milan, Osped San Giuseppe, Liver Unit, I-20122 Milan, Italy
[3] Osped Maggiore Lodi, Liver Unit, Lodi, Italy
[4] Univ Brescia, Univ Div Infect & Trop Dis, Brescia, Italy
[5] Brescia Spedali Civili Gen Hosp, Brescia, Italy
关键词
Adverse drug reaction; Fanconi syndrome; Tenofovir; Hepatitis B virus; Entecavir; KIDNEY TUBULAR DYSFUNCTION; HIV-INFECTED PATIENTS; CLINICAL-PRACTICE; VIRUS INFECTION;
D O I
10.1016/j.jcv.2014.09.016
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Tenofovir disoproxil fumarate (TDF) is a nucleotide reverse transcriptase inhibitor widely used to treat patients with human immunodeficiency virus (HIV) and hepatitis B virus (HBV) infection. Despite the excellent safety records of this regimen, a few cases of acute renal failure and Fanconi syndrome have been reported among HIV patients exposed to TDF. In the HBV monoinfection scenario, only two cases of TDF-associated Fanconi syndrome have been reported thus far. Here, we describe two additional patients with chronic hepatitis B (CHB) who developed a TDF-induced Fanconi syndrome that reverted after TDF withdrawal and had viral replication fully suppressed upon switching to entecavir (ETV). Though the overall risk of TDF associated severe renal toxicity in HBV patients appears to be negligible, both glomerular and tubular function should be monitored in patients exposed to TDF, especially when other renal risk factors or a history of previous exposure to adefovir dipivoxil (ADV) are present. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:600 / 603
页数:4
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