Abstract
We present a report on children with severe pulmonary hypertension secondary to congenital heart disease who received 6 months of beraprost therapy. The children had an increase in intracardiac left-to-right shunt and a reduction of the pulmonary-to-systemic vascular resistance ratio, whereas the pulmonary artery pressure was not significantly changed.
| Original language | English |
|---|---|
| Pages (from-to) | 787-791 |
| Number of pages | 5 |
| Journal | Pediatric Cardiology |
| Volume | 26 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - Dec 2005 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- Congenital heart disease
- Eisenmenger syndrome
- Pulmonary hypertension
Fingerprint
Dive into the research topics of 'Beraprost therapy in children with pulmonary hypertension secondary to congenital heart disease'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver