[HTML][HTML] Impairment of hypoxic pulmonary vasoconstriction in acute respiratory distress syndrome

M Gierhardt, O Pak, D Walmrath… - European …, 2021 - Eur Respiratory Soc
Acute respiratory distress syndrome (ARDS) is a serious complication of severe systemic or
local pulmonary inflammation, such as caused by severe acute respiratory syndrome …

Pulmonary hypertension

D Poch, J Mandel - Annals of internal medicine, 2021 - acpjournals.org
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 …

Efficacy and safety of sildenafil added to pirfenidone in patients with advanced idiopathic pulmonary fibrosis and risk of pulmonary hypertension: a double-blind …

J Behr, SD Nathan, WA Wuyts, NM Bishop… - The Lancet …, 2021 - thelancet.com
Background The benefit of sildenafil in patients with advanced idiopathic pulmonary fibrosis
(IPF) at risk of poor outcomes from pulmonary hypertension, whether already present or …

Comparison of three different aqueous microenvironments for enhancing oral bioavailability of sildenafil: solid self-nanoemulsifying drug delivery system, amorphous …

JS Kim, F Din, SM Lee, DS Kim, MR Woo… - International journal …, 2021 - Taylor & Francis
Background The purpose of this study was to screen various drug delivery systems for
improving the aqueous solubility and oral bioavailability of sildenafil. Three representative …

Trends in systemic sclerosis mortality over Forty‐Eight years, 1968–2015: a US Population–Based study

EY Yen, DR Singh, RR Singh - Arthritis care & research, 2021 - Wiley Online Library
Objective To identify secular trends associated with systemic sclerosis (SSc) mortality over a
48‐year period. Methods Using national mortality data compiled by the Centers for Disease …

Idiopathic pulmonary fibrosis and pulmonary hypertension: Heracles meets the Hydra

K Rajagopal, AJ Bryant, S Sahay… - British journal of …, 2021 - Wiley Online Library
Idiopathic pulmonary fibrosis (IPF) is a fatal lung disease where the additional presence of
pulmonary hypertension (PH) reduces survival. In particular, the presence of coexistent …

Multi-institutional prospective cohort study of patients with pulmonary hypertension associated with respiratory diseases

N Tanabe, H Kumamaru, Y Tamura, H Taniguchi… - Circulation …, 2021 - jstage.jst.go.jp
Background: There is limited evidence for pulmonary arterial hypertension (PAH)-targeted
therapy in patients with pulmonary hypertension associated with respiratory disease (R-PH) …

Assessing pulmonary hypertension severity in lung disease is a key step to improving outcomes: embrace resistance and don't be pressurised to go with the flow

DG Kiely, R Condliffe - European Respiratory Journal, 2021 - Eur Respiratory Soc
Managing patients with pulmonary hypertension (PH) in association with chronic lung
disease and/or hypoxia (PH-CLD) remains one of the most challenging areas in pulmonary …

[HTML][HTML] Vardenafil activity in lung fibrosis and in vitro synergy with nintedanib

MH Bourne Jr, TJ Kottom, DM Hebrink, M Choudhury… - Cells, 2021 - mdpi.com
Idiopathic pulmonary fibrosis (IPF) remains an intractably fatal disorder, despite the recent
advent of anti-fibrotic medication. Successful treatment of IPF, like many chronic diseases …

Pulmonary arterial hypertension secondary to drugs and toxins

RL Ramirez, SM Pienkos… - Clinics in Chest …, 2021 - chestmed.theclinics.com
Since its description by Romberg in 1891, 1 pulmonary arterial hypertension (PAH) was a
disease with low incidence and prevalence. However, in the 1960s a surge in PAH cases …