2009
DOI: 10.1007/s00246-009-9574-3
|View full text |Cite
|
Sign up to set email alerts
|

Late Pulmonary Valve Replacement in Congenital Heart Disease Patients Without Original Congenital Pulmonary Valve Pathology

Abstract: Many congenital heart defects with pulmonary valve pathology are repaired or palliated in childhood. It is anticipated that these patients will need subsequent pulmonary valve replacement due to the pulmonary regurgitation or right ventricular dilation/failure that results from their original operation. Interestingly, some patients with prior congenital heart surgery and no congenital pulmonary valve pathology require pulmonary valve replacement in adulthood. The current study analyzed this subset of patients.… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
4
0

Year Published

2010
2010
2016
2016

Publication Types

Select...
4
1

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(4 citation statements)
references
References 7 publications
0
4
0
Order By: Relevance
“…We further assumed the mechanical contributions of elastin (e), collagen (c), and smooth muscle (m), are weighted by their respective volume fractions é (1) where C = F-F^ is the left Cauchy-Green stretch tensor. We further assumed the mechanical contributions of elastin (e), collagen (c), and smooth muscle (m), are weighted by their respective volume fractions é (1) where C = F-F^ is the left Cauchy-Green stretch tensor.…”
Section: Tissue Level Strain Energy Functionmentioning
confidence: 99%
“…We further assumed the mechanical contributions of elastin (e), collagen (c), and smooth muscle (m), are weighted by their respective volume fractions é (1) where C = F-F^ is the left Cauchy-Green stretch tensor. We further assumed the mechanical contributions of elastin (e), collagen (c), and smooth muscle (m), are weighted by their respective volume fractions é (1) where C = F-F^ is the left Cauchy-Green stretch tensor.…”
Section: Tissue Level Strain Energy Functionmentioning
confidence: 99%
“…The normal development of the pulmonary artery (PA) can be greatly affected in many congenital heart defects, often leading to pulmonary hypertension if left untreated [1,2]. Congenital abnormalities of these arteries often necessitate surgical repair or the use of a valved conduit replacement [3][4][5], requiring multiple reinterventions due to regurgitation or failure of the prosthetic conduit [6]. In recent years, there has been a growing interest in the development of a living autologous tissue graft that could address the critical need for growing substitutes in the repair of congenital cardiovascular defects [7][8][9].…”
Section: Introductionmentioning
confidence: 99%
“…Regardless of the particulars of the therapeutic approach, the detailed growth characteristics of the native artery are required to establish the baseline dimensional changes post-implantation. Moreover, delineating the normal arterial growth patterns has implications for the timing and nature of surgical repair [3,10]. The geometries of the PA and ascending aorta (AA) are also important indicators of pulmonary and systolic hypertension [11], such as the ratio of diameters of the PA to the AA is an important measure of pulmonary hypertension in younger adults [12].…”
Section: Introductionmentioning
confidence: 99%
“…Congenital abnormalities of these arteries often necessitate surgical repair or the use of autologous tissue and synthetic biomaterials as vascular grafts [8][9][10]. The patency of the synthetic conduit replacements is limited, often requiring further surgical reinterventions due to lack of adaptation to the normal growth of the child and/or functional failure of the graft [11].…”
Section: Introductionmentioning
confidence: 99%