M. Yücel, Hayrullah Alp, Alaaddin Yorulmaz, Sevim Karaarslan, T. Baysal
2019.9.1Turk Kardiyoloji Dernegi Arsivi-Archives of the Turkish Society of Cardiology
tlooto Summary
The right ventricular Tei Index values in children with CHD and a left-to-right shunt can be used as a parameter to follow up on the potential development of PAH, to make a diagnosis in the early period, and tomake a timely decision about surgery.
Abstract
OBJECTIVE The aim of this study was to determine the usefulness of the Tei Index, an echocardiographic parameter, in the early determination of pulmonary artery pressure (PAP) in congenital heart disease (CHD) with a left-to-right shunt.
METHODS Right and left ventricular functions were evaluated using Tei Index values determined with tissue Doppler echocardiography. Cardiac catheterization was performed in all cases. The presence of pulmonary arterial hypertension (PAH) was defined as a mean PAP of ≥25 mm Hg and a pulmonary vascular resistance index of >3 WU/m2. Patients with a pulmonary/systemic blood flow ratio of ≥2 were considered candidates for surgery.
RESULTS The Tei Index values measured from the left ventricular posterior wall and the right ventricular anterior wall were found to be significantly higher in the patients with PAH (0.68±0.18, 0.67±0.16, respectively) compared with the patients without PAH (0.56±0.16, p=0.027; 0.51±0.12 p=0.001). A significant correlation was detected between the Tei Index value measured from the left ventricular posterior wall and the mean PAP (correlation coefficient: 0.491).
CONCLUSION The right ventricular Tei Index values in children with CHD and a left-to-right shunt can be used as a parameter to follow up on the potential development of PAH, to make a diagnosis in the early period, and to make a timely decision about surgery.
Citation format
YÜCEL, M., et al. Prediction of the development of pulmonary arterial hypertension with tei index in congenital heart diseases with left-to-right shunt. Turk Kardiyoloji Dernegi Arsivi-Archives of the Turkish Society of Cardiology, 2019, 47 6: 466–475.