Palliative care in pulmonary hypertension associated with congenital heart disease: systematic review and expert opinion

AIMS: Pulmonary arterial hypertension (PAH) is common amongst patients with congenital heart disease (CHD). It is a severe and complex condition that adversely affects quality of life and prognosis. While quality of life questionnaires are routinely used in clinical pulmonary hypertension practice,...

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Detalles Bibliográficos
Autores principales: Constantine, Andrew, Condliffe, Robin, Clift, Paul, Tulloh, Robert, Dimopoulos, Konstantinos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120400/
https://www.ncbi.nlm.nih.gov/pubmed/33660435
http://dx.doi.org/10.1002/ehf2.13263

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120400/
https://www.ncbi.nlm.nih.gov/pubmed/33660435
http://dx.doi.org/10.1002/ehf2.13263

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