The natural history of atherosclerotic and fibrous renal artery disease |
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Authors: | Martin J Schreiber Jr Andrew C Novick Marc A Pohl |
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Institution: | (1) Department of Hypertension and Nephrology, Desk A-101, The Cleveland Clinic Foundation, 9500 Euclid Avenue, 44195-5042 Cleveland, Ohio, USA;(2) Department of Urology, The Cleveland Clinic Foundation, 9500 Euclid Avenue, 44195-5042 Cleveland, Ohio, USA |
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Abstract: | Summary Individuals with atherosclerotic or fibrous renal artery disease may develop renovascular hypertension and/or renal dysfunction. Traditionally, the motivation for identifying patients with renal artery stenosis was the treatment of renovascular hypertension. However, recent interest has centered on the investigation of patients suspected of having renal artery stenosis that might account for progressive azotemia. While specific forms of fibrous and/or atherosclerotic renal artery disease can lead to a compromise in renal function, differences may exist in the age of presentation, predominat sex, angiographic appearance and overal natural history. Recognition of these differences is helpful in deciding on the most likely lesion type, appropriate workup and treatment. Since renal artery stenosis can lead to radiologic and functional alterations, clinical markers of progression, such as renal size and serum creatinine measurements, are helpful in identifying patients with advancing disease. The regulators of fibrous disease progression are less clear than those responsible for atherosclerotic progression in the renal artery. Uncontrolled systemic hypertension, intrarenal hypertension, hyperlipidemia, cigarette smoking, and obesity all may potentially contribute to progressive atherosclerosis. Individuals identified with progressive azotemia due to renal artery stenosis may benefit from improved perfusion flow by renal revascularization or balloon angioplasty provided no significant parenchymal disease is present. |
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