3D-Printed Coronary Implants Are Effective for Percutaneous Creation of Swine Models with Focal Coronary Stenosis.
Animals
Coronary Circulation
Coronary Stenosis
/ diagnostic imaging
Disease Models, Animal
Feasibility Studies
Magnetic Resonance Imaging, Cine
Male
Myocardial Infarction
/ diagnostic imaging
Myocardial Perfusion Imaging
Printing, Three-Dimensional
Proof of Concept Study
Prosthesis Design
Prosthesis Implantation
/ instrumentation
Sus scrofa
3D printing
Acute swine model
Ischemic heart disease
MRI
Minimally invasive
Stress testing
Journal
Journal of cardiovascular translational research
ISSN: 1937-5395
Titre abrégé: J Cardiovasc Transl Res
Pays: United States
ID NLM: 101468585
Informations de publication
Date de publication:
12 2020
12 2020
Historique:
received:
22
11
2019
accepted:
28
04
2020
pubmed:
13
5
2020
medline:
26
1
2021
entrez:
13
5
2020
Statut:
ppublish
Résumé
Reliable, closed-chest methods for creating large animal models of acute myocardial hypoperfusion are limited. We demonstrated the feasibility and efficacy of using magnetic resonance (MR)-compatible 3D-printed coronary implants for establishing swine models of myocardial hypoperfusion. We designed, manufactured, and percutaneously deployed implants in 13 swine to selectively create focal coronary stenosis. To test the efficacy of the implants to cause hypoperfusion or ischemia in the perfused territory, we evaluated regional wall motion, myocardial perfusion, and infarction using MR imaging. The overall swine survival rate was 85% (11 of 13). The implant retrieval rate was 92% (12 of 13). Fluoroscopic angiography confirmed focal stenosis. Cine and perfusion MRI showed regional wall motion abnormalities and inducible ischemia, respectively. Late gadolinium enhancement and histopathology showed no myocardial infarction. Our minimally invasive technique has promising applications for validation of new diagnostic methods in cardiac MR. Graphical abstract Our new minimally invasive, percutaneous method for creating swine models of acute focal coronary stenosis can be used for magnetic resonance imaging studies of myocardial ischemia. Comparable to existing methods in its efficacy and reliability, this rapid prototyping technique will allow researchers to more easily conduct translational cardiac imaging studies of coronary artery disease in large animal models.
Identifiants
pubmed: 32394352
doi: 10.1007/s12265-020-10018-3
pii: 10.1007/s12265-020-10018-3
pmc: PMC9667863
mid: NIHMS1841458
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
1033-1043Subventions
Organisme : NHLBI NIH HHS
ID : R01 HL127153
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL137562
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL133407
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL147133
Pays : United States
Organisme : CSRD VA
ID : I01 CX001901
Pays : United States
Organisme : NHLBI NIH HHS
ID : DP2 HL142045
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL136578
Pays : United States
Organisme : American Heart Association-American Stroke Association
ID : 18TPA34170049
Pays : United States
Références
J Appl Physiol. 1969 Sep;27(3):419-21
pubmed: 5804143
Am Heart J. 1957 Apr;53(4):505-18
pubmed: 13402712
Invest Radiol. 2005 Jan;40(1):14-8
pubmed: 15597015
Eur Heart J Cardiovasc Imaging. 2015 Oct;16(10):1082-92
pubmed: 25812572
J Vis Exp. 2017 Oct 9;(128):
pubmed: 29053673
Transl Res. 2019 Sep;211:35-45
pubmed: 31034816
BMC Med Imaging. 2019 Jul 26;19(1):58
pubmed: 31349798
Adv Drug Deliv Rev. 2017 Mar;112:12-23
pubmed: 28042080
Invest Radiol. 2000 Jul;35(7):445-51
pubmed: 10901107
Am J Physiol Heart Circ Physiol. 2013 Nov 1;305(9):H1297-308
pubmed: 23997096
Cell Physiol Biochem. 2018;49(4):1277-1288
pubmed: 30205393
J Am Coll Surg. 2012 Nov;215(5):681-9
pubmed: 22867714
Circulation. 2010 Sep 14;122(11 Suppl):S142-9
pubmed: 20837905
J Cardiovasc Transl Res. 2013 Aug;6(4):640-8
pubmed: 23733543
J Biomed Res. 2015 Aug 20;30:
pubmed: 26585560
Eur Heart J. 2005 Aug;26(15):1461-74
pubmed: 15831557
J Magn Reson Imaging. 2005 Jul;22(1):125-35
pubmed: 15971171
J Pharmacol Sci. 2011;115(2):115-21
pubmed: 21258170
JACC Cardiovasc Imaging. 2019 Aug;12(8 Pt 1):1582-1584
pubmed: 30878418
Int J Cardiovasc Imaging. 2010 Mar;26(3):299-308
pubmed: 20012206
Nat Rev Cardiol. 2016 Dec;13(12):701-718
pubmed: 27786234
Am Heart J. 1981 May;101(5):593-600
pubmed: 6164281
Transl Res. 2019 Sep;211:64-83
pubmed: 31078513
J Surg Res. 2013 Aug;183(2):531-6
pubmed: 23622724
Expert Rev Cardiovasc Ther. 2018 Jul;16(7):465-477
pubmed: 29923434
Am J Physiol Heart Circ Physiol. 2018 Apr 01;314(4):H812-H838
pubmed: 29351451
Basic Res Cardiol. 1980 Jul-Aug;75(4):537-43
pubmed: 7436997
Heart Lung Circ. 2019 Oct;28(10):1525-1534
pubmed: 31176626
J Vis Exp. 2020 Feb 18;(156):
pubmed: 32150171
J Am Coll Cardiol. 2018 Mar 6;71(9):957-968
pubmed: 29495995
Circulation. 2008 Mar 11;117(10):1283-91
pubmed: 18268144
J Appl Physiol (1985). 2003 May;94(5):1689-701
pubmed: 12679343
Vet Pathol. 2012 Mar;49(2):344-56
pubmed: 21441112
Radiology. 2002 Oct;225(1):104-12
pubmed: 12354992
J Am Coll Cardiol. 2000 Nov 15;36(6):1985-91
pubmed: 11092675
Cardiol Young. 2019 Jun;29(6):733-743
pubmed: 31198120