Echocardiography may help detect pulmonary vasculopathy in the early stages of pulmonary artery hypertension associated with systemic sclerosis


Background Pulmonary arterial hypertension (PAH) in patients with systemic sclerosis is associated with a poor prognosis, but this can be improved by early disease detection. Abnormal pulmonary and cardiac function can be detected early by means of echocardiography, whereas right heart catheterization is usually performed later.Objectives The purpose of this prospective study was to detect early the presence of pulmonary artery vasculopathy in patients with verified systemic sclerosis without significant pulmonary fibrosis, normal lung volumes and a mildly reduced lung diffusion capacity of carbon monoxide (DLCO).Methods Nineteen consecutive female NYHA class I-II patients with scleroderma and aPAPs of >35 mm/Hg measured by echocardiography, were enrolled between September 2007 andSeptember 2009.

They had a mean age of 51+/-13 years, body mass index of 25+/-5 kg/m2). They allunderwent complete Doppler echocardiography, CPET, a pulmonary ventilation test (carbon monoxidelung diffusion, DLCO), HRCT.

To investigate PAH by means of complete resting Dopplerechocardiography estimates of systolic pulmonary artery pressure (PAPs) derived from tricuspidregurgitation, mean PAP derived from pulmonary regurgitation, pulmonary vessel resistance (PVR)derived from the acceleration time of the pulmonary outflow tract (ACTpo), and right ventricularfunction derived from tricuspid annular plane systolic excursion (TAPSE). Right heart catheterisationwas conducted only, if pulmonary hypertension was suggested by echocardiography and an abnormalventilator test.The data are given as mean values +/- SD, unless otherwise stated.

The correlations between thevariables were analysed using Pearson's r coefficient, and the predictive value of the variables wascalculated using linearregression analysis. A p value of <0.05 was considered significant.Results Right heart catheterization detected PAH in 15/19 patients; mean PAP was 30.5 mm/Hg and RVP 3.6 UW.

Coronary angiography of the patients aged more than 55 years showed some evidence of significant coronary artery disease. Echocardiography showed high systolic PAP values (46+/-8 mmHg), whereas right ventricular function was normal (TAPSE 23+/-3 mm), and in line with the NYHA class.

ACTpo was reduced in the patients with a systolic PAP of >46 mm/Hg (p<0.001) and positively correlated with DLCO (p<0.001) and the hemodynamic data.There was a good correlation between ACTpo and PVR (hemodynamic data) (r=-0615; p<0.01).Conclusions Although they need to be confirmed by studies of larger series of patients, our findings suggest that, in comparison with hemodynamic data, non-invasive echocardiographic measurements are an excellent means of identifying early-stage PAH.

Author: Walter SerraAlfredo ChettaDaniele SantilliFlavio MozzaniPier Paolo Dall'AglioDario OlivieriMaria Alberta CattabianiDiego ArdissinoTiziano Gherli
Credits/Source: Cardiovascular Ultrasound 2010, 8:25



Published on: 2010-07-05



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