Functional hepatic flow in patients with liver cirrhosis

World J Gastroenterol. 2004 Mar 15;10(6):915-8. doi: 10.3748/wjg.v10.i6.915.

Abstract

Aim: To evaluate hepatic reserve function by investigating the change of functional hepatic flow and total hepatic flow in cirrhotic patients with portal hypertension.

Methods: HPLC method was employed for the determination of concentration of D-sorbitol in human plasma and urine. The functional hepatic flow (FHF) and total hepatic flow (THF) were determined by means of modified hepatic clearance of D-sorbitol combined with duplex doppler color sonography in 20 patients with cirrhosis and 10 healthy volunteers.

Results: FHF, evaluated by means of the D-sorbitol clearance, was significantly reduced in patients with cirrhosis in comparison to controls (764.74+/-167.91 vs 1195.04+/-242.97 mL/min, P<0.01). While THF was significantly increased in patients with cirrhosis in comparison to controls (1605.23+/-279.99 vs 1256.12+/-198.34 mL/min, P<0.01). Portal blood flow and hepatic artery flow all were increased in cirrhosis compared to controls (P<0.05 and P<0.01). D-sorbitol total clearance was significantly reduced in cirrhosis compared to control (P<0.01), while D-sorbitol renal clearance was significantly increased in cirrhosis (P<0.05). In controls FHF was similar to THF (1195.05+/-242.97 vs 1256.12+/-198.34 mL/min, P=0.636), while FHF was significantly reduced compared with THF in cirrhosis (764.74+/-167.91 vs 1605.23+/-279.99 mL/min, P<0.01).

Conclusion: Our method that combined modified hepatic clearance of D-sorbitol with duplex doppler color sonography is effective in the measurement of FHF and THF. FHF can be used to estimate hepatic reserve function.

MeSH terms

  • Adult
  • Aged
  • Case-Control Studies
  • Female
  • Hepatic Artery / physiopathology
  • Humans
  • Hypertension, Portal / complications*
  • Indicators and Reagents / pharmacokinetics
  • Kidney / metabolism
  • Liver Circulation*
  • Liver Cirrhosis / etiology*
  • Liver Cirrhosis / physiopathology*
  • Male
  • Middle Aged
  • Portal System / physiopathology
  • Sorbitol / pharmacokinetics

Substances

  • Indicators and Reagents
  • Sorbitol