Circulation, Vol 65, 523-528, Copyright © 1982 by American Heart Association
RH Beekman, AP Rocchini and A Rosenthal
To evaluate the effects of acute afterload reduction, hydralazine, 0.2
mg/kg, was administered at cardiac catheterization to seven infants who had
a large ventricular septal defect (VSD). The infants were 2.5 - 11 months
old (mean 5.1 months). Before and 5, 15, 25 and 35 minutes after
hydralazine, aortic, pulmonary capillary wedge, pulmonary artery, right
atrial and superior vena caval pressures and saturations, heart rate and
oxygen consumption were measured. Hemodynamic effects were noted after 5
minutes but were most pronounced 35 minutes after hydralazine.
Prehydralazine baseline data were therefore compared with values 35 minutes
after hydralazine. Pulmonary flow did not changes, but systemic flow
increased significantly (4.5 +/- 0.2 to 6.7 +/- 0.5 liters/min/m2 [mean +/-
SEM], p less than 0.001). The pulmonary-to-systemic flow ratio decreased by
32% (3.4 +/- 0.4 to 2.3 +/- 0.2, p less than 0.001) and the absolute
left-to-right shunt decreased by 24% (10.8 +/- 1.3 to 8.2 +/- 1.2
liters/min/m2, p less than 0.01). Hydralazine caused a significant decrease
in systemic resistance (13.9 +/- 0.7 to 9.5 +/- 0.7 U, p less than 0.001).
Pulmonary resistance, aortic, pulmonary artery and pulmonary capillary
wedge pressures, heart rate and oxygen consumption did not change after
hydralazine. Right atrial pressure decreased slightly (4.0 +/- 0.6 to 2.4
+/- 0.6 mm Hg, p less than 0.05). In conclusion, hydralazine caused a
significant increase in systemic blood flow and a significant decrease in
both pulmonary-to- systemic flow ratio and absolute left-to-right shunt in
seven infants with a large VSD. These effects appear to be related to the
decrease in systemic resistance that occurred with hydralazine. Although
limited to the acute setting, these findings suggest that hydralazine may
be beneficial in the management of infants with a large VSD.
ARTICLES
Hemodynamic effects of hydralazine in infants with a large ventricular septal defect
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