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Hydralazine-associated adverse events: a report of two cases of hydralazine-induced ANCA vasculitis

Hydralazine is a direct-acting vasodilator, which has been used in treatment for hypertension (HTN) since the 1950s. While it is well known to cause drug-induced lupus (DIL), recent reports are indicating the emergence of the drug-induced anti-neutrophil cytoplasmic antibody (ANCA) associated vascul...

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Autores principales: Zuckerman, Roman, Patel, Mayurkumar, Costanzo, Eric J, Dounis, Harry, Haj, Rany Al, Seyedali, Seyedehsara, Asif, Arif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Nefrologia 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533989/
https://www.ncbi.nlm.nih.gov/pubmed/29738027
http://dx.doi.org/10.1590/2175-8239-JBN-3858
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author Zuckerman, Roman
Patel, Mayurkumar
Costanzo, Eric J
Dounis, Harry
Haj, Rany Al
Seyedali, Seyedehsara
Asif, Arif
author_facet Zuckerman, Roman
Patel, Mayurkumar
Costanzo, Eric J
Dounis, Harry
Haj, Rany Al
Seyedali, Seyedehsara
Asif, Arif
author_sort Zuckerman, Roman
collection PubMed
description Hydralazine is a direct-acting vasodilator, which has been used in treatment for hypertension (HTN) since the 1950s. While it is well known to cause drug-induced lupus (DIL), recent reports are indicating the emergence of the drug-induced anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis (DIV). Herein, we describe two patients (aged 57 and 87 years) who presented with severe acute kidney injury (AKI), proteinuria, and hematuria. Both were receiving hydralazine for the treatment of hypertension. ANCA serology was positive in both patients along with anti-histone antibodies (commonly seen in drug-induced vasculitis). Renal biopsy revealed classic crescentic (pauci-immune) glomerulonephritis in these patients and hydralazine was discontinued. During the hospital course, the 57-year-old patient required dialysis therapy and was treated with steroids and rituximab for the ANCA disease. Renal function improved and the patient was discharged (off dialysis) with a serum creatinine of 3.6 mg/dL (baseline = 0.9 mg/dL). At a follow-up of 2 years, the patient remained off dialysis with advanced chronic kidney disease (CKD) (stage IIIb). The 87-year-old patient had severe AKI with serum creatinine at 10.41 mg/dL (baseline = 2.27 mg/dL). The patient required hemodialysis and was treated with steroids, rituximab, and plasmapheresis. Unfortunately, the patient developed catheter-induced bacteremia and subsequently died of sepsis. Hydralazine can cause severe AKI resulting in CKD or death. Given this extremely unfavorable adverse-event profile and the widespread availability of alternative anti-hypertensive agents, the use of hydralazine should be carefully considered.
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spelling pubmed-65339892019-06-17 Hydralazine-associated adverse events: a report of two cases of hydralazine-induced ANCA vasculitis Zuckerman, Roman Patel, Mayurkumar Costanzo, Eric J Dounis, Harry Haj, Rany Al Seyedali, Seyedehsara Asif, Arif J Bras Nefrol Case Reports Hydralazine is a direct-acting vasodilator, which has been used in treatment for hypertension (HTN) since the 1950s. While it is well known to cause drug-induced lupus (DIL), recent reports are indicating the emergence of the drug-induced anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis (DIV). Herein, we describe two patients (aged 57 and 87 years) who presented with severe acute kidney injury (AKI), proteinuria, and hematuria. Both were receiving hydralazine for the treatment of hypertension. ANCA serology was positive in both patients along with anti-histone antibodies (commonly seen in drug-induced vasculitis). Renal biopsy revealed classic crescentic (pauci-immune) glomerulonephritis in these patients and hydralazine was discontinued. During the hospital course, the 57-year-old patient required dialysis therapy and was treated with steroids and rituximab for the ANCA disease. Renal function improved and the patient was discharged (off dialysis) with a serum creatinine of 3.6 mg/dL (baseline = 0.9 mg/dL). At a follow-up of 2 years, the patient remained off dialysis with advanced chronic kidney disease (CKD) (stage IIIb). The 87-year-old patient had severe AKI with serum creatinine at 10.41 mg/dL (baseline = 2.27 mg/dL). The patient required hemodialysis and was treated with steroids, rituximab, and plasmapheresis. Unfortunately, the patient developed catheter-induced bacteremia and subsequently died of sepsis. Hydralazine can cause severe AKI resulting in CKD or death. Given this extremely unfavorable adverse-event profile and the widespread availability of alternative anti-hypertensive agents, the use of hydralazine should be carefully considered. Sociedade Brasileira de Nefrologia 2018-05-07 2018 /pmc/articles/PMC6533989/ /pubmed/29738027 http://dx.doi.org/10.1590/2175-8239-JBN-3858 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Zuckerman, Roman
Patel, Mayurkumar
Costanzo, Eric J
Dounis, Harry
Haj, Rany Al
Seyedali, Seyedehsara
Asif, Arif
Hydralazine-associated adverse events: a report of two cases of hydralazine-induced ANCA vasculitis
title Hydralazine-associated adverse events: a report of two cases of hydralazine-induced ANCA vasculitis
title_full Hydralazine-associated adverse events: a report of two cases of hydralazine-induced ANCA vasculitis
title_fullStr Hydralazine-associated adverse events: a report of two cases of hydralazine-induced ANCA vasculitis
title_full_unstemmed Hydralazine-associated adverse events: a report of two cases of hydralazine-induced ANCA vasculitis
title_short Hydralazine-associated adverse events: a report of two cases of hydralazine-induced ANCA vasculitis
title_sort hydralazine-associated adverse events: a report of two cases of hydralazine-induced anca vasculitis
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533989/
https://www.ncbi.nlm.nih.gov/pubmed/29738027
http://dx.doi.org/10.1590/2175-8239-JBN-3858
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