Tenofovir-Associated Acute and Chronic Kidney Disease: A Case of Multiple Drug Interactions
Author(s) -
Anthony E. Zimmermann,
T. Pizzoferrato,
Jennifer J. Bedford,
Alan H. Morris,
Robert P. Hoffman,
Gregory L. Braden
Publication year - 2005
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1086/499048
Subject(s) - medicine , atazanavir , lopinavir , ritonavir , discontinuation , tenofovir , fanconi syndrome , didanosine , acute tubular necrosis , renal function , creatinine , kidney disease , gastroenterology , drug , nephrotoxicity , kidney , disease , viral load , sida , pharmacology , viral disease , immunology , human immunodeficiency virus (hiv) , antiretroviral therapy , infectious disease (medical specialty) , covid-19
Tenofovir therapy in patients with human immunodeficiency virus (HIV) infection has been associated with acute renal failure (ARF) and Fanconi syndrome. In the past 2 years, we diagnosed tenofovir-associated ARF in 5 HIV-infected patients who were receiving tenofovir therapy and who had classic findings of acute tubular necrosis, and we compared findings for our patients with data on 22 patients described in the literature. The mean serum creatinine level increased from 0.9 to 3.9 mg/dL, and it decreased to 1.2 mg/dL during recovery. ARF resolved in 22 of 27 patients after discontinuation of tenofovir therapy. The most common drugs given with tenofovir were ritonavir or lopinavir-ritonavir (21 of 27 patients), atazanavir (5 of 27 patients), and didanosine (9 of 27 patients). Tenofovir-associated ARF manifests as acute tubular necrosis that may not resolve with tenofovir withdrawal. Tenofovir is associated with multiple drug interactions, leading to an increased risk of ARF. Frequent monitoring of renal function is warranted for any patient receiving these combinations.
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