Ji. Elizalde et al., EFFECTS OF INCREASING BLOOD HEMOGLOBIN LEVELS ON SYSTEMIC HEMODYNAMICS OF ACUTELY ANEMIC CIRRHOTIC-PATIENTS, Journal of hepatology, 29(5), 1998, pp. 789-795
Background/Aims: In experimental portal hypertension, blood hemoglobin
levels have been shown to influence the hyperdynamic circulatory stat
e. The aim of this study was to assess the hemodynamic effects of incr
easing hemoglobin concentration in human portal hypertension. Methods:
Sixteen cirrhotic patients recovering from a variceal bleeding episod
e were randomly assigned to receive two units of packed red cells or 5
00 ml of a protein solution, Systemic and portal hemodynamics, and rhe
ological and hormonal parameters were measured at baseline and after e
xpansion. Results: Both groups were similar with respect to the degree
of liver failure, severity of the bleeding episode, activation of the
endogenous vasopressor systems, and hemodynamic parameters. The admin
istration of either erythrocytes or a protein solution prompted a simi
lar increase in total blood volume and suppression of vasopressor syst
ems, Both groups of patients experienced similar increases in wedged h
epatic venous pressure. Hepatic venous pressure gradient was not signi
ficantly modified but tended to increase in erythrocyte-transfused pat
ients. Cardiopulmonary pressures increased, but this increment was sig
nificant in the non-blood-trans-fused patients only Cardiac output dec
reased in erythrocyte-transfused patients, while it increased in the g
roup receiving a protein solution. Red blood cell transfusion resulted
in an increase in systemic vascular hindrance (resistance/blood visco
sity), whereas the administration of a protein solution prompted a dec
rease in this parameter, thus reflecting true vasoconstriction and vas
odilation, respectively. Conclusions: An increase in blood hemoglobin
in acutely anemic cirrhotic patients attenuates their hyperdynamic cir
culation beyond viscosity-dependent changes, an effect which might be
counteracted by the effects on portal venous pressure gradient.