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Pulmonary arterial hypertension in congenital heart disease

Pulmonary arterial hypertension in congenital heart disease

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2890361911

Pulmonary arterial hypertension in congenital heart disease

About this item

Full title

Pulmonary arterial hypertension in congenital heart disease

Publisher

England: BMJ Publishing Group Ltd and British Cardiovascular Society

Journal title

Heart (British Cardiac Society), 2024-08, Vol.110 (18), p.1145-1152

Language

English

Formats

Publication information

Publisher

England: BMJ Publishing Group Ltd and British Cardiovascular Society

More information

Scope and Contents

Contents

PH is classified into five distinct groups based on underlying pathophysiology and haemodynamics (figure 1).1 2 Patients with pulmonary arterial hypertension (PAH) have precapillary PH haemodynamics, defined as a mean PAP above 20 mm Hg, a pulmonary vascular resistance (PVR) >2 Wood units (WU) and a pulmonary capillary wedge pressure (PCWP) ≤15 mm...

Alternative Titles

Full title

Pulmonary arterial hypertension in congenital heart disease

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2890361911

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2890361911

Other Identifiers

ISSN

1355-6037,1468-201X

E-ISSN

1468-201X

DOI

10.1136/heartjnl-2023-322890

How to access this item