Results 11 to 20 of about 827,342 (360)

Isolated major aortopulmonary collateral as the sole pulmonary blood supply to an entire lung segment [PDF]

open access: yes, 2017
Congenital systemic-to-pulmonary collateral arteries or major aortopulmonary collaterals are associated with cyanotic congenital heart disease with decreased pulmonary blood flow.
Grady, R. Mark   +2 more
core   +3 more sources

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

open access: yesESC Heart Failure, 2021
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.
Andrew Constantine   +5 more
doaj   +1 more source

Pulmonary Hypertension in Congenital Heart Disease [PDF]

open access: yesFuture Cardiology, 2018
Pulmonary hypertension is defined as a mean pulmonary arterial pressure ≥25 mmHg. We focus on its relevance in congenital heart disease, reviewing pathophysiology, diagnosis and management. Pulmonary hypertension is a relatively common complication of congenital heart disease, with adult prevalence between 5 and 10%.
Pascall, Emma, Tulloh, Robert M.R.
openaire   +5 more sources

Interdisciplinary three-step strategy to treat aortic stenosis and coronary artery disease in a patient with end-stage chronic obstructive pulmonary disease [PDF]

open access: yes, 2012
Background: Valvular aortic stenosis is a common disease in the elderly, often in multimorbid patients. It is often associated with coronary artery disease and peripheral artery disease.
Beiras Fernández, Andrés   +6 more
core   +2 more sources

Under pressure: pulmonary hypertension associated with left heart disease. [PDF]

open access: yes, 2015
© ERS 2015.Pulmonary hypertension (PH) associated with left heart disease (PH-LHD) is the most common type of PH, but its natural history is not well understood.
Farber, HW, Gibbs, S
core   +2 more sources

ACVIM consensus statement guidelines for the diagnosis, classification, treatment, and monitoring of pulmonary hypertension in dogs. [PDF]

open access: yes, 2020
Pulmonary hypertension (PH), defined by increased pressure within the pulmonary vasculature, is a hemodynamic and pathophysiologic state present in a wide variety of cardiovascular, respiratory, and systemic diseases.
Abbott, Jonathan   +9 more
core   +3 more sources

A Case of Pulmonary Hypertension Recurred by Graves’ Disease [PDF]

open access: yesKosin Medical Journal, 2013
A few cases of severe pulmonary hypertension with right heart failure associated with Graves’ disease were reported in the literature. However, cases of pulmonary hypertension with right heart failure recurred by Graves’ disease is very rare. We describe
Jun Seop Lee   +5 more
doaj   +1 more source

Do patients with suspected heart failure and preserved left ventricular systolic function suffer from "diastolic heart failure" or from misdiagnosis? A prospective descriptive study [PDF]

open access: yes, 2000
OBJECTIVES: To characterise the clinical features of patients with suspected heart failure but preserved left ventricular systolic function to determine if they have other potential causes for their symptoms rather than being diagnosed with 'diastolic ...
Caruana, L.   +3 more
core   +2 more sources

Adult congenital heart care in the COVID-19 era, and beyond: A call for actionKey Points

open access: yesInternational Journal of Cardiology Congenital Heart Disease, 2020
While virus epidemics are nothing new to man, the scale, speed of global spread and immediacy of the COVID-19 pandemic have been truly unprecedented [1].
Michael A. Gatzoulis   +8 more
doaj   +1 more source

The use of Macitentan in Fontan circulation: a case report

open access: yesBMC Cardiovascular Disorders, 2017
Background The Fontan circulation, a result of a palliative procedure in patients with single systemic ventricles, is defined by chronically elevated pulmonary vascular resistance.
Polyvios Demetriades   +4 more
doaj   +1 more source

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