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contributor authorBellofiore, A.
contributor authorHenningsen, J.
contributor authorLepak, C. G.
contributor authorTian, L.
contributor authorRoldan
contributor authorKellihan, H. B.
contributor authorConsigny, D. W.
contributor authorFrancois, C. J.
contributor authorChesler, N. C.
date accessioned2017-05-09T01:15:07Z
date available2017-05-09T01:15:07Z
date issued2015
identifier issn0148-0731
identifier otherbio_137_04_044501.pdf
identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/157104
description abstractPulmonary arteries (PAs) distend to accommodate increases in cardiac output. PA distensibility protects the right ventricle (RV) from excessive increases in pressure. Loss of PA distensibility plays a critical role in the fatal progression of pulmonary arterial hypertension (PAH) toward RV failure. However, it is unclear how PA distensibility is distributed across the generations of PA branches, mainly because of the lack of appropriate in vivo methods to measure distensibility of vessels other than the large, conduit PAs. In this study, we propose a novel approach to assess the distensibility of individual PA branches. The metric of PA distensibility we used is the slope of the stretch ratio–pressure relationship. To measure distensibility, we combined invasive measurements of mean PA pressure with angiographic imaging of the PA network of six healthy female dogs. Stacks of 2D images of the PAs, obtained from either contrast enhanced magnetic resonance angiography (CEMRA) or computed tomography digital subtraction angiography (CTDSA), were used to reconstruct 3D surface models of the PA network, from the first bifurcation down to the sixth generation of branches. For each branch of the PA, we calculated radial and longitudinal stretch between baseline and a pressurized state obtained via acute embolization of the pulmonary vasculature. Our results indicated that large and intermediate PA branches have a radial distensibility consistently close to 2%/mmHg. Our axial distensibility data, albeit affected by larger variability, suggested that the PAs distal to the first generation may not significantly elongate in vivo, presumably due to spatial constraints. Results from both angiographic techniques were comparable to data from established phasecontrast (PC) magnetic resonance imaging (MRI) and ex vivo mechanical tests, which can only be used in the first branch generation. Our novel method can be used to characterize PA distensibility in PAH patients undergoing clinical right heart catheterization (RHC) in combination with MRI.
publisherThe American Society of Mechanical Engineers (ASME)
titleA Novel In Vivo Approach to Assess Radial and Axial Distensibility of Large and Intermediate Pulmonary Artery Branches
typeJournal Paper
journal volume137
journal issue4
journal titleJournal of Biomechanical Engineering
identifier doi10.1115/1.4029578
journal fristpage44501
journal lastpage44501
identifier eissn1528-8951
treeJournal of Biomechanical Engineering:;2015:;volume( 137 ):;issue: 004
contenttypeFulltext


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