Clinical vs haemodynamic response to drugs in portal hypertension

J Hepatol. 1998 Jun;28(6):1015-9. doi: 10.1016/s0168-8278(98)80351-6.

Abstract

Background/aims: The combination of non-selective beta-blockers and nitrates is an effective therapy for the prevention of rebleeding from oesophageal varices. However, a significant number of patients fail to respond and have further haemorrhage. It has been suggested that measurement of the hepatic venous pressure gradient response to long-term drug therapy may allow early selection of non-responders. We aimed to test this hypothesis in 63 patients with cirrhosis and variceal bleeding treated with propranolol+/-isosorbide mononitrate.

Methods: Hepatic venous pressure gradient was measured before and during treatment. Response was defined as a reduction of 20% or more in hepatic venous pressure gradient, or a fall in hepatic venous pressure gradient to 12 mmHg or less.

Results: Forty-four patients were evaluable: 28 responders and 16 non-responders. Hepatic venous pressure gradient fell significantly in the responder group (17.5+/-0.5 mmHg vs 12.2+/-0.5 mmHg; p<0.01) but not in the non-responders (18.0+/-1.0 vs 17.9+/-1.2 mmHg; p=n.s.). Overall, there was no difference in rebleeding rates between the two groups: responders 43%, non-responders 25%. However, rebleeding was uncommon in compliant patients with alcoholic cirrhosis, in whom the hepatic venous pressure gradient fell to less than 12 mmHg (9%).

Conclusions: In this study a fall in hepatic venous pressure gradient of 20% was not a reliable predictor of clinical response. A threshold value of 12 mmHg was useful, but applied to relatively few patients.

MeSH terms

  • Adrenergic beta-Antagonists / therapeutic use*
  • Blood Pressure / drug effects*
  • Esophageal and Gastric Varices / drug therapy*
  • Esophageal and Gastric Varices / physiopathology*
  • Esophageal and Gastric Varices / therapy
  • Female
  • Follow-Up Studies
  • Hemodynamics / drug effects
  • Humans
  • Hypertension, Portal / drug therapy
  • Hypertension, Portal / physiopathology
  • Isosorbide Dinitrate / analogs & derivatives*
  • Isosorbide Dinitrate / therapeutic use
  • Liver Cirrhosis / complications
  • Liver Cirrhosis, Alcoholic / complications
  • Liver Cirrhosis, Alcoholic / physiopathology
  • Male
  • Middle Aged
  • Octreotide / therapeutic use
  • Propranolol / therapeutic use*
  • Recurrence
  • Sclerotherapy
  • Time Factors
  • Treatment Outcome
  • Vasodilator Agents / therapeutic use*

Substances

  • Adrenergic beta-Antagonists
  • Vasodilator Agents
  • Propranolol
  • Isosorbide Dinitrate
  • isosorbide-5-mononitrate
  • Octreotide