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   <subfield code="a">Accuracy of Doppler-Derived Estimation of Pulmonary Vascular Resistance in Congenital Heart Disease: An Index of Operability</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Gholam Ajami, Sirous Cheriki, Hamid Amoozgar, Mohammad Borzouee, Manoucher Soltani]</subfield>
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   <subfield code="a">Pulmonary vascular resistance (PVR) is a critical and essential parameter during the assessment and selection of modality of treatment in patients with congenital heart disease (CHD) accompanied by pulmonary arterial hypertension (PAH). Cardiac catheterization is the &quot;gold standard” but is an invasive method for PVR measurement. A noninvasive and reliable method for estimation of PVR in children has been a major challenge and most desirable during past decades, especially for those who need repeated measurements. In a prospective study and among consecutive patients who were referred for cardiac catheterizations, PVR was calculated as the ratio of the transpulmonary pressure gradient (∆P) to the amount of the pulmonary flow (QP) accordingly for 20 patients with CHD and high PAH. Subsequently and noninvasively, PVR was assessed for these patients by a Doppler echocardiography-derived index defined as the ratio of the tricuspid regurgitation velocity (TRVm/s) to the velocity time integral (VTIcm) of the right-ventricular outflow tract (RVOT). There was a good correlation between PVR measured at catheterization (PVRcath) and TRV/VTIm ratio; the mean of three measurements of VTI (VTIm) with R 2=0.53 (p=0.008). In addition, a TRV/VTIm value of 0.2 provided a sensitivity of 71.4% and a specificity of 100% for PVR &gt;6 Woods units (WU) as well as sensitivity of 90% and specificity of 90% for a PVR equal to 8 WU. PVR value between 6 and 8 WU by catheterization has been considered as a cut-off point for intervention in children with left-to-right shunts and PAH. In conclusion, Doppler-derived TRV/VTIm ratio is a reliable index that may be helpful as a supplementary diagnostic tool for the selection of modality of treatment and follow-up of patients with PAH and increased PVR.</subfield>
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   <subfield code="a">Congenital heart disease</subfield>
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   <subfield code="a">Pulmonary vascular resistance</subfield>
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   <subfield code="a">Doppler estimation</subfield>
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   <subfield code="a">Ajami</subfield>
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   <subfield code="u">Department of Pediatrics, Division of Pediatric Cardiology, Namazi Hospital, Shiraz University of Medical Sciences, 71937-11351, Shiraz, Iran</subfield>
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   <subfield code="a">Amoozgar</subfield>
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