Hepatorenal syndrome overview: Difference between revisions
Line 8: | Line 8: | ||
==Historical Perspective== | ==Historical Perspective== | ||
Historically, the hepatorenal syndrome was first defined as acute renal failure that occurred in the setting of [[Bile duct|biliary surgery]]. The syndrome was soon associated with advanced liver disease. It was determined that kidneys transplanted from patients with hepatorenal syndrome were functional, leading to the hypothesis that hepatorenal syndrome was a systemic process as opposed to [[renal disease]], which affects the [[renal]] function. | Historically, the hepatorenal syndrome was first defined as acute renal failure that occurred in the setting of [[Bile duct|biliary surgery]]. The syndrome was soon associated with advanced [[Liver diseases|liver disease]]. It was determined that [[Kidney|kidneys]] transplanted from patients with hepatorenal syndrome were functional, leading to the hypothesis that hepatorenal syndrome was a systemic process as opposed to [[renal disease]], which affects the [[renal]] function. | ||
==Classification== | ==Classification== | ||
Line 14: | Line 14: | ||
==Pathophysiology== | ==Pathophysiology== | ||
The major pathophysiologic mechanism responsible for the clinical manifestation | The major pathophysiologic mechanism responsible for the clinical manifestation of hepatorenal syndrome is renal [[vasoconstriction]]. The hemodynamic disturbances include increased [[cardiac output]], systemic [[vasodilatation]] and low arterial [[blood pressure]]. Thus, [[renal]] vasoconstriction occurs even with a normal [[blood volume]] and increased [[cardiac output]]. | ||
==Causes== | ==Causes== |
Revision as of 20:08, 21 December 2017
Hepatorenal syndrome Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Hepatorenal syndrome overview On the Web |
American Roentgen Ray Society Images of Hepatorenal syndrome overview |
Risk calculators and risk factors for Hepatorenal syndrome overview |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Sunny Kumar MD [2], Mehrian Jafarizade, M.D [3]
Overview
Hepatorenal syndrome (HRS) refers to acute renal failure that occurs in the setting of cirrhosis or fulminant liver failure associated with portal hypertension, usually in the absence of other disease of the kidney. It is a direct result of changes in the splanchnic and systemic circulation from cirrhosis or fulminant hepatic failure. It is usually secondary to trigger events which cause multi-system organ failure.
Historical Perspective
Historically, the hepatorenal syndrome was first defined as acute renal failure that occurred in the setting of biliary surgery. The syndrome was soon associated with advanced liver disease. It was determined that kidneys transplanted from patients with hepatorenal syndrome were functional, leading to the hypothesis that hepatorenal syndrome was a systemic process as opposed to renal disease, which affects the renal function.
Classification
The classification of hepatorenal syndrome is based on the deteriorating function of kidney in to two types: type 1 rapidly progressive and type 2 HRS, slowly progressive.
Pathophysiology
The major pathophysiologic mechanism responsible for the clinical manifestation of hepatorenal syndrome is renal vasoconstriction. The hemodynamic disturbances include increased cardiac output, systemic vasodilatation and low arterial blood pressure. Thus, renal vasoconstriction occurs even with a normal blood volume and increased cardiac output.