J. Vorobioff et al., PROPRANOLOL COMPARED WITH PROPRANOLOL PLUS ISOSORBIDE DINITRATE IN PORTAL-HYPERTENSIVE PATIENTS - LONG-TERM HEMODYNAMIC AND RENAL EFFECTS, Hepatology, 18(3), 1993, pp. 477-484
The long-term hemodynamic and renal effects of propranolol were compar
ed with those of propranolol plus isosorbide dinitrate in 44 portal-hy
pertensive alcoholic cirrhotic patients. Eight control patients, 8 pat
ients receiving propranolol and 14 patients receiving propranolol plus
isosorbide dinitrate were hemodynamically evaluated. Renal function w
as studied in a fourth group of 14 patients receiving propranolol plus
isosorbide dinitrate. Portal pressure decreased more (p < 0.05) with
combined therapy (-21.6%, from 19.5 +/- 4.8 to 15.4 +/- 4.3 mm Hg) tha
n with propranolol alone (-12.5%, from 19.9 +/- 1.2 to 17.4 +/- 1.8 mm
Hg). Serum urea and creatinine levels, plasma sodium concentration, u
rine volume and urinary sodium excretion showed nonsignificant changes
in all groups studied. Combined therapy induced a significant (p < 0.
05) decrease in plasma renin activity (from 4.42 +/- 4.7 to 1.59 +/- 1
.9 ng/ml/hr) and nonsignificant reductions in plasma aldosterone conce
ntration and creatinine clearance. None of the eight patients with asc
ites or history of ascites not receiving isosorbide dinitrate showed e
vidence of impairment in renal sodium metabolism during the study peri
od. In contrast, 8 of the 14 patients (57%) with ascites or history of
ascites receiving isosorbide dinitrate showed impairment in renal sod
ium metabolism (p < 0.01), as reflected by the development or worsenin
g of ascites and the need of higher diuretic requirements. Long-term c
ombined administration of propranolol plus isosorbide dinitrate is sup
erior to propranolol alone in the pharmacological treatment of portal
hypertension. However, the deleterious effects observed in patients wi
th ascites or even with a prior history of ascites preclude recommenda
tion of this therapy for all patients, making it more suitable for pat
ients without advanced liver disease.