Results 11 to 20 of about 674,291 (325)

Sarcopenia in Patients with Chronic Thromboembolic Pulmonary Hypertension [PDF]

open access: yesJournal of Cardiovascular Development and Disease
Background: Sarcopenia, or loss of skeletal muscle mass, has been associated with poor outcomes (e.g., functional decline, increased mortality, and low quality of life), but its role in CTEPH remains unclear.
Steven Hopkins   +8 more
doaj   +2 more sources

Pulmonary hypertension [PDF]

open access: yesEuropean Respiratory Review, 2016
In 2015, more than 800 papers were published in the field of pulmonary hypertension. A Clinical Year in Review article cannot possibly incorporate all this work and needs to be selective. The recently published European guidelines for the diagnosis and treatment of pulmonary hypertension contain an inclusive summary of all published clinical studies ...
Noordegraaf, Anton Vonk   +2 more
  +14 more sources

Pulmonary Hypertension [PDF]

open access: yesPulmonary Medicine, 2012
Pulmonary hypertension (PH), defined as elevated pulmonary artery pressure, is common in the general population and associated with increased mortality. Accordingly, physicians commonly encounter patients with dyspnea, exercise intolerance, and/or right heart failure who have elevated pulmonary artery systolic pressure (PASP) on echocardiography ...
Ilknur Basyigit   +4 more
  +7 more sources

Prognosis and Treatment With Phosphodiesterase 5 Inhibitors in Combined Post‐ and Precapillary Pulmonary Hypertension: A Propensity Score‐Matched Analysis From the Hellenic Pulmonary Hypertension Registry [PDF]

open access: yesPulmonary Circulation
Combined post‐ and precapillary pulmonary hypertension (CpcPH) comprises the most severe form of postcapillary PH. A severe precapillary component (pulmonary vascular resistance [PVR] > 5 WU) is critical for therapeutic decisions.
Georgios E. Papadopoulos   +15 more
doaj   +2 more sources

Transient but not genetic loss of miR-451 attenuates the development of pulmonary arterial hypertension [PDF]

open access: yes, 2013
<b>Rationale:</b> MicroRNAs are small non-coding RNAs involved in the regulation of gene expression and have recently been implicated in the development of pulmonary arterial hypertension (PAH).
Baker, Andrew H.   +5 more
core   +17 more sources

Incidence and outcomes of pulmonary hypertension in the Ireland

open access: yesBMJ Open Respiratory Research, 2022
Introduction Pulmonary hypertension (PH) is a progressive disease of the pulmonary vasculature, which is characterised by premature morbidity and mortality.
Sarah Cullivan   +5 more
doaj   +1 more source

Pulmonary Hypertension [PDF]

open access: yesAnnals of Internal Medicine, 2013
Pulmonary hypertension is the term used to describe a group of disorders characterized by abnormally high pressures in the pulmonary arteries. Initial evaluation is focused on identifying the cause, which helps guide appropriate treatment. Pulmonary hypertension is often a feature of advanced common diseases, such as chronic obstructive pulmonary ...
Jess Mandel, David Poch
openaire   +7 more sources

Characteristics of chronic thromboembolic pulmonary hypertension in Ireland

open access: yesPulmonary Circulation, 2021
Chronic thromboembolic pulmonary hypertension (CTEPH) is a rare and under‐recognised complication of acute pulmonary embolism. Information regarding the characteristics of CTEPH in Ireland is limited, and the aim of this retrospective cohort study was to
Sarah Cullivan   +6 more
doaj   +1 more source

Tolerability, safety and survival in patients with severe pulmonary arterial hypertension treated with intravenous epoprostenol (Veletri®): a prospective, 6-months, open label, observational, non-interventional study

open access: yesRespiratory Research, 2023
Background Epoprostenol AS (Veletri®), a thermostable epoprostenol formulation, provides better drug stability and improved clinical use compared to previous epoprostenol formulations. This study aims to expand clinical experience in the use of Veletri®,
Julia Degering   +9 more
doaj   +1 more source

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