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ACE-I/ARB Therapy prior to Contrast Exposure: What Should the Clinician Do?
Author(s) -
Robert Kalyesubula,
Peace Bagasha,
Mark A. Perazella
Publication year - 2014
Publication title -
biomed research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 126
eISSN - 2314-6141
pISSN - 2314-6133
DOI - 10.1155/2014/423848
Subject(s) - medicine , contrast induced nephropathy , acute kidney injury , nephropathy , intensive care medicine , disease , contrast (vision) , ace inhibitor , angiotensin receptor blockers , kidney disease , renin–angiotensin system , angiotensin converting enzyme , endocrinology , diabetes mellitus , blood pressure , artificial intelligence , computer science
Contrast-induced nephropathy (CIN) is now one of the three leading causes of acute kidney injury in the world. A lot is known about the risk factors of CIN, yet it remains a major cause of morbidity, end stage renal disease, prolonged hospital stay, and increased costs as well as a high mortality. Many patients undergoing contrast-based radiological investigations are treated with angiotensin converting inhibitors (ACE-Is) or angiotensin receptor blockers (ARBs) for their cardiac and renal benefits and their known mortality benefits. However, controversy exists among clinicians as to whether ACE-Is and ARBs should be continued or discontinued prior to contrast media exposure. In this paper we review the current evidence on ACE-I/ARB therapy for patients undergoing procedures involving use of contrast media and provide recommendations as to whether these drugs should be continued or held prior to contrast exposure.

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