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

Abstract 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 pr...

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Kaydedildi:
Asıl Yazarlar: Andrew Constantine, Robin Condliffe, Paul Clift, Robert Tulloh, Konstantinos Dimopoulos, the CHAMPION Steering Committee
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2021-06-01
Seri Bilgileri:ESC Heart Failure
Konular:
Congenital heart defects
Pulmonary hypertension
Palliative care
End‐of‐life care
Advance care planning
Systematic review
Online Erişim:https://doi.org/10.1002/ehf2.13263
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