Impact of portal hemodynamics on Doppler ultrasonography for predicting decompensation and long-term outcomes in patients with cirrhosis

Scand J Gastroenterol. 2016;51(2):236-44. doi: 10.3109/00365521.2015.1081275. Epub 2015 Sep 10.

Abstract

Objective: Significance of portal hemodynamics for non-invasive marker of cirrhosis remains unclear. The aim was to determine the value of portal hemodynamics on Doppler ultrasound for predicting decompensation and prognosis in cirrhosis.

Methods: This retrospective study comprised 236 cirrhotic patients (132 males, 104 females; age 63.7 ± 11.3 years; 110 compensated, 126 decompensated). Clinical data, including Doppler findings, were analyzed with respect to decompensation and prognosis. The median follow-up period was 33.2 months (0.1-95.4).

Results: Fifty-three patients developed clinical decompensation, 13 patients received liver transplantation, and 71 died. Higher model for end-stage liver disease score (p < 0.001) at baseline was the significant factor for the presence of decompensation. Higher alanine transaminase (p = 0.020), lower albumin (p = 0.002) and lower mean velocity in the portal trunk (p = 0.038) were significant factors for developing decompensation (best cut-off value: Alanine transaminase > 31 IU/L, albumin < 3.6 g/dL, and portal trunk < 12.8 cm/s). The cumulative incidence of decompensation was higher in patients with portal trunk < 12.8 cm/s (22.5% at 1 year, 71.2% at 5 years) than those without (6.9% at 1 year, 35.4% at 5 years; p < 0.001). The significant prognostic factors were hepatocellular carcinoma (p = 0.036) and lower albumin (p = 0.008) for compensated patients, and reversed portal flow (p = 0.028), overt ascites (p < 0.001), and higher bilirubin (p < 0.001) for decompensated patients.

Conclusion: Portal hemodynamics offer a non-invasive marker for decompensation and prognosis of cirrhosis, suggesting a future direction for practical management.

Keywords: Compensated cirrhosis; Doppler ultrasound; decompensated cirrhosis; portal hemodynamics.

MeSH terms

  • Aged
  • Alanine Transaminase / blood
  • Ascites / etiology
  • Bilirubin / blood
  • Blood Flow Velocity
  • Carcinoma, Hepatocellular / complications*
  • Disease Progression
  • End Stage Liver Disease / etiology
  • End Stage Liver Disease / physiopathology*
  • End Stage Liver Disease / surgery
  • Female
  • Follow-Up Studies
  • Hemodynamics
  • Humans
  • Liver Cirrhosis / complications
  • Liver Cirrhosis / physiopathology*
  • Liver Cirrhosis / surgery
  • Liver Neoplasms / complications*
  • Liver Transplantation
  • Male
  • Middle Aged
  • Portal Vein / diagnostic imaging*
  • Portal Vein / physiopathology
  • Predictive Value of Tests
  • Retrospective Studies
  • Risk Factors
  • Serum Albumin / metabolism
  • Severity of Illness Index
  • Ultrasonography, Doppler

Substances

  • Serum Albumin
  • Alanine Transaminase
  • Bilirubin