2021
DOI: 10.1002/ehf2.13263
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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 practice, little is known on how to interpret their results and manage PAH-CHD patients with evidence of impaired health-related quality of life, especially those with advanced disease and palliative care needs. Methods and re… Show more

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Cited by 9 publications
(1 citation statement)
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References 72 publications
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“…Palliative care referral and assessment should be undertaken in parallel with active treatment and initiation/escalation of PAH therapies, to optimize patient physical and emotional well-being. 151 152 Patients with advanced PH typically develop refractory heart failure with multiorgan involvement; hence, a holistic multidisciplinary approach is needed that combines active treatment with supportive and palliative care.…”
Section: Cardiopulmonary Resuscitation and End-of-life Managementmentioning
confidence: 99%
“…Palliative care referral and assessment should be undertaken in parallel with active treatment and initiation/escalation of PAH therapies, to optimize patient physical and emotional well-being. 151 152 Patients with advanced PH typically develop refractory heart failure with multiorgan involvement; hence, a holistic multidisciplinary approach is needed that combines active treatment with supportive and palliative care.…”
Section: Cardiopulmonary Resuscitation and End-of-life Managementmentioning
confidence: 99%