Cardiovascular medicine
Long term treatment of pulmonary arterial hypertension with
beraprost, an oral prostacyclin analogue
C D Vizzaa, S Sciomera, S Morellib, C Lavallea, P Di Marziob, D Padovania, R Badagliaccaa, A R Vestria, R Naeijec, F Fedelea
a Department of
Cardiovascular and Respiratory Sciences, University La Sapienza, Rome,
Italy, b Institute of Internal Medicine, University La
Sapienza, c Department of Pathophysiology, Erasme University
Hospital, Erasme Campus CP 604, 808 Lennik Road, B-1070 Brussels,
Belgium
Correspondence to: Dr Naeije rnaeije{at}ulb.ac.be
Accepted 12 July 2001
OBJECTIVE
To evaluate the effects of
one year's treatment with beraprost, an orally active prostacyclin
analogue, in patients with severe pulmonary hypertension.
PATIENTS
13 patients with severe
pulmonary hypertension. This was primary in nine, thromboembolic in
three, and caused by Eisenmenger syndrome in one.
METHODS
All patients underwent right
heart catheterisation. Mean (SD) right atrial pressure was 5 (3) mm Hg, mean pulmonary artery pressure was 48 (12) mm Hg,
cardiac index was 2.6 (0.8) l/min/m2, and mixed venous
oxygen saturation was 68 (7)%. Beraprost was started at the dose of
20 µg three to four times a day (1 µg/kg/day), increasing after
one month to 40 µg three to four times a day (2 µg/kg/day), with
further increases of 20 µg three to four times a day in case of
clinical deterioration.
MAIN OUTCOME MEASURES
New York Heart
Association (NYHA) functional class, exercise capacity measured by
distance walked in six minutes, and systolic pulmonary pressure (by
echocardiography) were evaluated at baseline, after one month's
treatment, and then every three months for a year.
RESULTS
After the first month of
treatment, NYHA class decreased from 3.4 (0.7) to 2.9 (0.7)
(p < 0.05), the six minute walking distance increased from 213 (64)
to 276 (101) m (p < 0.05), and systolic pulmonary artery pressure
decreased from 93 (15) to 85 (18) mm Hg (NS). One patient died after
40 days from refractory right heart failure, and another was lost for
follow up at six months. The 11 remaining patients had persistent
improvements in functional class and exercise capacity and a
significant decrease in systolic pulmonary artery pressure in the
period from 1-12 months. Side effects were minor.
CONCLUSIONS
Oral administration of
beraprost may result in long lasting clinical and haemodynamic
improvements in patients with severe pulmonary hypertension.
Keywords: pulmonary arterial hypertension; prostacyclin; beraprost
© 2001 by Heart
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