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Adverse ventricular–ventricular interactions in right ventricular pressure load: Insights from pediatric pulmonary hypertension versus pulmonary stenosis

Right ventricular (RV) pressure overload has a vastly different clinical course in children with idiopathic pulmonary arterial hypertension (iPAH) than in children with pulmonary stenosis (PS). While RV function is well recognized as a key prognostic factor in iPAH, adverse ventricular–ventricular i...

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Bibliographic Details
Published in:Physiological reports 2016-06, Vol.4 (11), p.e12833-n/a
Main Authors: Driessen, Mieke M. P., Hui, Wei, Bijnens, Bart H., Dragulescu, Andreea, Mertens, Luc, Meijboom, Folkert J., Friedberg, Mark K.
Format: Article
Language:English
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Summary:Right ventricular (RV) pressure overload has a vastly different clinical course in children with idiopathic pulmonary arterial hypertension (iPAH) than in children with pulmonary stenosis (PS). While RV function is well recognized as a key prognostic factor in iPAH, adverse ventricular–ventricular interactions and LV dysfunction are less well characterized and the pathophysiology is incompletely understood. We compared ventricular–ventricular interactions as hypothesized drivers of biventricular dysfunction in pediatric iPAH versus PS. Eighteen iPAH, 16 PS patients and 18 age‐ and size‐matched controls were retrospectively studied. Cardiac cycle events were measured by M‐mode and Doppler echocardiography. Measurements were compared between groups using ANOVA with post hoc Dunnet's or ANCOVA including RV systolic pressure (RVSP; iPAH 96.8 ± 25.4 mmHg vs. PS 75.4 ± 18.9 mmHg; P = 0.011) as a covariate. RV‐free wall thickening was prolonged in iPAH versus PS, extending beyond pulmonary valve closure (638 ± 76 msec vs. 562 ± 76 msec vs. 473 ± 59 msec controls). LV and RV isovolumetric relaxation were prolonged in iPAH (P 
ISSN:2051-817X
2051-817X
DOI:10.14814/phy2.12833