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2013 | OriginalPaper | Hoofdstuk

10. Pulmonale hypertensie en het Eisenmenger-syndroom

Auteurs : B.J. Bouma, A.P.J. van Dijk, B.J.M. Mulder

Gepubliceerd in: Aangeboren hartafwijkingen bij volwassenen

Uitgeverij: Bohn Stafleu van Loghum

Inleiding

PH wordt gekenmerkt door verhoogde druk in de art. pulmonalis en secundair RV-falen. De progressie van de ziekte is zeer variabel. PH is door de World Health Organization op grond van het mechanisme ingedeeld in vijf groepen:

vorige hoofdstuk Persisterende ductus Botalli

volgende hoofdstuk LVOT-obstructies

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Titel: Pulmonale hypertensie en het Eisenmenger-syndroom
Auteurs: B.J. Bouma
A.P.J. van Dijk
B.J.M. Mulder
Uitgeverij: Bohn Stafleu van Loghum
Boek: Aangeboren hartafwijkingen bij volwassenen
Print ISBN: 978-90-368-0306-9

Elektronisch ISBN: 978-90-368-0307-6

Copyright: 2013
DOI: https://doi.org/10.1007/978-90-368-0307-6_10

Bohn Stafleu van Loghum

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Inleiding

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