Mild parenchymal lung disease and/or low diffusion capacity impacts survival and treatment response in patients diagnosed with idiopathic pulmonary arterial hypertension

R. Lewis (Sheffield (South Yorkshire), United Kingdom), A. Thompson (Sheffield (South Yorkshire), United Kingdom), C. Billings (Sheffield (South Yorkshire), United Kingdom), A. Charalampopoulos (Sheffield (South Yorkshire), United Kingdom), C. Elliot (Sheffield (South Yorkshire), United Kingdom), N. Hamilton (Sheffield (South Yorkshire), United Kingdom), C. Hill (Sheffield (South Yorkshire), United Kingdom), J. Hurdman (Sheffield (South Yorkshire), United Kingdom), S. Rajaram (Sheffield (South Yorkshire), United Kingdom), I. Sabroe (Sheffield (South Yorkshire), United Kingdom), A. Swift (Sheffield (South Yorkshire), United Kingdom), D. Kiely (Sheffield (South Yorkshire), United Kingdom), R. Condliffe (Sheffield (South Yorkshire), United Kingdom)

Source: Virtual Congress 2020 – Pulmonary hypertension in lung diseases
Session: Pulmonary hypertension in lung diseases
Session type: E-poster session
Number: 290
Disease area: Interstitial lung diseases, Pulmonary vascular diseases

Congress or journal article abstractE-poster

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R. Lewis (Sheffield (South Yorkshire), United Kingdom), A. Thompson (Sheffield (South Yorkshire), United Kingdom), C. Billings (Sheffield (South Yorkshire), United Kingdom), A. Charalampopoulos (Sheffield (South Yorkshire), United Kingdom), C. Elliot (Sheffield (South Yorkshire), United Kingdom), N. Hamilton (Sheffield (South Yorkshire), United Kingdom), C. Hill (Sheffield (South Yorkshire), United Kingdom), J. Hurdman (Sheffield (South Yorkshire), United Kingdom), S. Rajaram (Sheffield (South Yorkshire), United Kingdom), I. Sabroe (Sheffield (South Yorkshire), United Kingdom), A. Swift (Sheffield (South Yorkshire), United Kingdom), D. Kiely (Sheffield (South Yorkshire), United Kingdom), R. Condliffe (Sheffield (South Yorkshire), United Kingdom). Mild parenchymal lung disease and/or low diffusion capacity impacts survival and treatment response in patients diagnosed with idiopathic pulmonary arterial hypertension. 290

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