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Can "inoperable" congenital heart defects become operable in patients with pulmonary arterial hypertension? Dream or reality?Congenital heart disease, 7 1
- Publisher
- Springer International Publishing
- Copyright
- © Springer International Publishing AG, part of Springer Nature 2019. Translation from the German language edition: Pädiatrische Intensivmedizin – Kinderkardiologische Praxis, 2. erw. Auflage by D. Klauwer / C. Neuhäuser / J. Thul / R. Zimmermann, © Deutscher Ärzteverlag 2017
- ISBN
- 978-3-319-92440-3
- Pages
- 231 –250
- DOI
- 10.1007/978-3-319-92441-0_9
- Publisher site
- See Chapter on Publisher Site
Abstract
[Increases in pulmonary arterial resistance are playing an ever important role in pediatric cardiology. In addition to the clinical evaluation and terminological classification, the diagnostic approach to and treatment of the various forms of pulmonary hypertension are described in this chapter. General principles are discussed as well as specific drug entities, their modes of action, indications, and interactions. The benefits of temporarily increasing pulmonary resistance in balancing parallel circulations are described in addition to preoperative measurement of pulmonary resistance and its implications for the surgical procedure.]
Published: Nov 12, 2018
Keywords: Tricuspid Annular Plane Systolic Excursion (TAPSE); To Complications (TCPC); Pulmonary Arterial Wedge Pressure (PAWP); Pulmonary Arterial Hypertension (PAH); Transpulmonary Pressure Gradient (TPG)