PMID: 18720579Aug 30, 2008Paper

Pulmonary hypertension in interstitial lung disease

International Journal of Clinical Practice. Supplement
S D Nathan

Abstract

Pulmonary hypertension (PH) may complicate the course of many forms of advanced interstitial lung disease (ILD) and has been shown to portend a worse outcome. The aetiology of PH is likely multifactorial with variable contribution of factors amongst the different diseases. The most common such conditions include idiopathic pulmonary fibrosis, sarcoidosis, connective tissue disease-related ILD and pulmonary langerhans cell histiocytosis. Whether the course and impact of PH in these conditions can be modified by therapy requires further study.

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Citations

Jul 14, 2019·The Clinical Respiratory Journal·Rajiv SontiSteven D Nathan
Aug 11, 2020·Seminars in Respiratory and Critical Care Medicine·Marloes P HuitemaMarco C Post
Mar 7, 2009·American Journal of Respiratory and Critical Care Medicine·Juergen Behr, Victor J Thannickal
May 17, 2014·Respirology : Official Journal of the Asian Pacific Society of Respirology·Afroditi K BoutouParaskevi Argyropoulou
May 1, 2020·The International Journal of Cardiovascular Imaging·M P HuitemaM C Post
Jan 14, 2021·The New England Journal of Medicine·Aaron WaxmanSteven D Nathan
May 5, 2012·Pulmonary Circulation·Robert W HallowellReda E Girgis

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