Pulmonary hypertension in chronic lung disease and hypoxia

SD Nathan, JA Barbera, SP Gaine… - European …, 2019 - Eur Respiratory Soc
Pulmonary hypertension (PH) frequently complicates the course of patients with various
forms of chronic lung disease (CLD). CLD-associated PH (CLD-PH) is invariably associated …

Group 3 pulmonary hypertension: from bench to bedside

N Singh, P Dorfmüller, OA Shlobin… - Circulation …, 2022 - Am Heart Assoc
Pulmonary hypertension (PH) because of chronic lung disease is categorized as Group 3
PH in the most recent classification system. Prevalence of these diseases is increasing over …

Pulmonary hypertension secondary to pulmonary fibrosis: clinical data, histopathology and molecular insights

G Ruffenach, J Hong, M Vaillancourt, L Medzikovic… - Respiratory …, 2020 - Springer
Pulmonary hypertension (PH) developing secondarily in pulmonary fibrosis (PF) patients
(PF-PH) is a frequent co-morbidity. The high prevalence of PH in PF patients is very …

[HTML][HTML] Screening strategies for pulmonary hypertension in patients with interstitial lung disease: a multidisciplinary Delphi study

FF Rahaghi, NA Kolaitis, A Adegunsoye… - Chest, 2022 - Elsevier
Background Pulmonary hypertension (PH) is a common complication of interstitial lung
disease (ILD) and is associated with worse outcomes and increased mortality. Evaluation of …

Updated perspectives on pulmonary hypertension in COPD

I Blanco, O Tura-Ceide, VI Peinado… - International Journal of …, 2020 - Taylor & Francis
Pulmonary hypertension (PH) is a frequent and important complication of chronic obstructive
pulmonary disease (COPD). It is associated with worse clinical courses with more frequent …

Pulmonary hypertension in patients with interstitial lung disease: a tool for early detection

R Parikh, I Konstantinidis, DM O'Sullivan… - Pulmonary …, 2022 - Wiley Online Library
Pulmonary hypertension (PH) complicates the treatment of interstitial lung disease (ILD)
patients resulting in poor functional status and worse outcomes. Early recognition of PH in …

Pulmonary hypertension in interstitial lung disease: screening, diagnosis and treatment

J Behr, SD Nathan - Current Opinion in Pulmonary Medicine, 2021 - journals.lww.com
Pulmonary hypertension in interstitial lung disease: screeni... : Current Opinion in
Pulmonary Medicine Pulmonary hypertension in interstitial lung disease: screening …

CT‐determined pulmonary artery to aorta ratio as a predictor of elevated pulmonary artery pressure and survival in idiopathic pulmonary fibrosis

M Yagi, H Taniguchi, Y Kondoh, M Ando… - …, 2017 - Wiley Online Library
Background and objective Elevated mean pulmonary artery pressure (mPAP) is a significant
prognostic indicator in idiopathic pulmonary fibrosis (IPF). It has been reported that the …

Pulmonary hypertension in interstitial lung disease: limitations of echocardiography compared to cardiac catheterization

GJ Keir, SJ Wort, M Kokosi, PM George… - …, 2018 - Wiley Online Library
Background and objective In interstitial lung disease (ILD), pulmonary hypertension (PH) is
a major adverse prognostic determinant. Transthoracic echocardiography (TTE) is the most …

Pulmonary hypertension associated with lung diseases

OA Shlobin, Y Adir, JA Barbera, V Cottin… - European …, 2024 - erj.ersjournals.com
Pulmonary hypertension (PH) associated with chronic lung disease (CLD) is both common
and underrecognised. The presence of PH in the setting of lung disease has been …