Why the study?
Does a single oral dose of beraprost sodium reduce pulmonary vascular resistance in children with pulmonary hypertension secondary to congenital heart disease?
Does a single oral dose of beraprost sodium reduce pulmonary vascular resistance in children with pulmonary hypertension secondary to congenital heart disease?
A single oral dose of beraprost sodium effectively reduces pulmonary vascular resistance in children with pulmonary hypertension secondary to congenital heart disease, offering a potential novel oral option for vasoreactivity screening and treatment.
Answers are grounded in this paper and cite their sources.
May support oral vasoreactivity testing in children with congenital heart disease-associated PH; hypothesis-generating and requires randomized confirmation before practice change.
To determine whether a newly synthesized oral analog of prostacyclin, called beraprost sodium, could cause pulmonary vasodilation, we studied its hemodynamic effect on pulmonary hypertension of children, comparing it to other vasodilatory agents, such as nitric oxide and tolazoline. We studied 20 children (mean age 24 months) having pulmonary hypertension secondary to congenital heart disease. A single oral dose of beraprost sodium resulted in an appreciable reduction of pulmonary vascular resistance (mean 34%), which was comparable to that induced by inhalation of nitric oxide and intravenous delivery of tolazoline (mean 41% and 31%, respectively). The results suggest that beraprost sodium may serve as a novel and safe vasodilator for the screening of pulmonary vasoreactivity, as well as the treatment of pulmonary hypertension in children.
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Ichida et al. (1998) studied pulmonary hypertension secondary to congenital heart disease (n=20). Beraprost sodium vs. Nitric oxide and tolazoline was evaluated on Reduction of pulmonary vascular resistance (mean 34% reduction).
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