Source: Annual Congress 2008 - Clinical aspects of interstitial lung disease
Disease area: Pulmonary vascular diseases, Respiratory critical care



Rating:

Share or cite this content

Citations should be made in the following way:
M. A. Dimadi, F. P. Kokkinis, I. Tsangaridou, P. Tsagouli, S. Tatsi, E. Seferos, L. Thanos (Athens, Lamia, Greece). Mean pulmonary artery diameter (MPAD) on CT scan versus pulmonary artery systolic pressure (PASP) on echocardiogram in interstitial lung disease (ILD) patients. Eur Respir J 2008; 32: Suppl. 52, 3467

Member's Comments

No comment yet.

Related content which might interest you: The relation between pulmonary artery pressure on echocardiography and pulmonary artery diameter on CT scan in patients with interstitial lung diseases Source: Eur Respir J 2007; 30: Suppl. 51, 119s Year: 2007 Diastolic pulmonary artery pressure (dPAP) at three months post pulmonary endarterectomy (PEA) as a new prognostic factor Source: Annual Congress 2010 - Pulmonary venous thromboembolic disease Year: 2010 Estimating pulmonary artery pressures by echocardiography in patients with emphysema Source: Eur Respir J 2007; 30: 914-921 Year: 2007 Acute exacerbation of idiopathic pulmonary fibrosis is associated to increase of pulmonary artery systolic pressure (PAPs) Source: Annual Congress 2010 - Clinical aspects in pulmonary fibrosis Year: 2010 Is there a fixed relationship between the mean and systolic pulmonary artery pressures in idiopathic pulmonary arterial hypertension (IPAH) and proximal chronic thromboembolic pulmonary hypertension (CTEPH) Source: Annual Congress 2009 - Pulmonary embolism Year: 2009 Mean pulmonary artery pressure-heart rate (mPAP-HR) relationship during submaximal supine exercise in idiopathic pulmonary arterial hypertension (iPAH) Source: Annual Congress 2005 - Exercise in pulmonary hypertension Year: 2005 Elevated pulmonary artery to aortic ratio measured with MRI identifies patients with pulmonary hypertension Source: Eur Respir J 2005; 26: Suppl. 49, 312s Year: 2005 The association between resting and mild-to-moderate exercise pulmonary artery pressure Source: Eur Respir J 2012; 39: 313-318 Year: 2012 Patterns of mean pulmonary artery pressure (mPAP)-flow relation changes following chronic therapy in idiopathic pulmonary arterial hypertension (IPAH) Source: Eur Respir J 2006; 28: Suppl. 50, 427s Year: 2006 Right ventricular (RV) diastolic function in patients with pulmonary hypertension (PH) due to chronic obstructive pulmonary disease (COPD) Source: Eur Respir J 2002; 20: Suppl. 38, 26s Year: 2002 The ratio of pulmonary artery to aortic size from CT scans: a predictor of COPD exacerbations Source: Annual Congress 2012 - ERS/NEJM Lunchtime session "Advances in asthma and COPD" Year: 2012 Analysis of the ratio of the main pulmonary artery to that of the aorta on chest CT in patients with combined pulmonary fibrosis and emphysema. Source: Virtual Congress 2020 – Prognosis and biomarkers of idiopathic pulmonary fibrosis Year: 2020 Change in right atrial minimal volume is a prognostic marker in pulmonary arterial hypertension (PAH) Source: International Congress 2016 – From microimaging to functional evaluation of the lung Year: 2016 The right ventricle (RV) in systemic sclerosis-associated pulmonary arterial hypertension (SSCPH) vs idiopathic pulmonary arterial hypertension (IPH): higher inflammatory status, no increase in interstitial fibrosis Source: Annual Congress 2009 - Pulmonary vascular diseases Year: 2009 Pulmonary arterial wedge pressure =21 mmHg during exercise unmasks occult left heart disease in exercise pulmonary hypertension Source: International Congress 2019 – Haemodynamics and chronic thromboembolic pulmonary hypertension Year: 2019 Inventive protocols of CT pulmonary angiography (CTPA) avoid artifacts in right pulmonary artery (rPA), improving detectability of pulmonary embolism (PE) Source: Annual Congress 2012 - Pulmonary circulation: clinical aspects of PAH, PTE and CTEPH Year: 2012 Pulmonary arterial hypertension (PAH) in patients with lung sarcoidosis (LS) Source: Annual Congress 2008 - Clinical aspects in the management of sarcoidosis Year: 2008 6MWD in patients with pulmonary arterial hypertension (PAH) Source: Eur Respir J 2003; 22: Suppl. 45, 464s Year: 2003 Pulmonary artery pressure (PAP) reduction by systemic and inhaled nitroglycerin (NTG) in an isolated rabbit lung model of pulmonary hypertension (PH) Source: Eur Respir J 2003; 22: Suppl. 45, 270s Year: 2003