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Dive into the research topics where Juan F. Granada is active.

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Featured researches published by Juan F. Granada.


Jacc-cardiovascular Imaging | 2011

Intracoronary Transluminal Attenuation Gradient in Coronary CT Angiography for Determining Coronary Artery Stenosis

Jin Ho Choi; James K. Min; Troy LaBounty; Fay Y. Lin; Dorinna D. Mendoza; Dae Hee Shin; Nikki S. Ariaratnam; Sunaina Koduru; Juan F. Granada; Thomas C. Gerber; Jae K. Oh; Hyeon Cheol Gwon; Yeon Hyeon Choe

Coronary computed tomography angiography (CTA) assessment of calcified or complex coronary lesions is frequently challenging. Transluminal attenuation gradient (TAG), defined as the linear regression coefficient between luminal attenuation and axial distance, has a potential to evaluate the degree of coronary stenosis. We examined the value of TAG in determining the stenosis severity on 64-slice coronary CTA. The value of TAG of 370 major coronary arteries was measured from 7,263 intervals of 5-mm length. Compared with coronary CTA and invasive coronary angiography, TAG decreased consistently and significantly with maximum stenosis severity on a per-vessel basis, from -1.91 ± 4.25 Hounsfield units/10 mm for diameter stenosis of 0% to 49% to -13.37 ± 9.81 Hounsfield units/10 mm for diameter stenosis of 100% (p < 0.0001). Adding TAG to the interpretation of coronary CTA improved diagnostic accuracy (p = 0.001), especially in vessels with calcified lesions (N = 127; net reclassification improvement 0.095; p = 0.046). TAG appears to be able to contribute to improved classification of coronary artery stenosis severity in coronary CTA, especially in severely calcified lesions.


Circulation-cardiovascular Interventions | 2012

Impact of Parallel Micro-Engineered Stent Grooves on Endothelial Cell Migration, Proliferation, and Function An In Vivo Correlation Study of the Healing Response in the Coronary Swine Model

Eugene A. Sprague; Fermin O. Tio; S. Hinan Ahmed; Juan F. Granada; Steven R. Bailey

Background— Stent luminal surface characteristics influence surface endothelialization. We hypothesize that luminal stent microgrooves created in the direction of coronary flow accelerate endothelial cell migration, resulting in lower levels of neointimal formation. Methods and Results— Surface coverage efficiency was evaluated in vitro by allowing human aortic endothelial cells (HAEC) to migrate onto microgrooved (G) or smooth (NG) surfaces. HAEC functionality was assessed by proliferation rate, apoptosis rate, nitric oxide production, and inflammatory markers TNF-&agr; and VCAM-1 expression. Early endothelialization and restenosis studies were performed using the porcine coronary injury model. Stainless steel stents of identical design with (GS) and without (NGS) luminal microgrooves were used. The commercially available Multi-Link Vision (MLVS) stent of identical design was used as a control. The degree of GS and NGS surface endothelialization was compared at 3 days. Biocompatibility and tissue response outcomes were evaluated at 28 days. The in vitro study demonstrated that at 7 days the presence of surface microgrooves increased HAEC migration distance >2-fold. Cell proliferation rate and nitric oxide production were increased and apoptosis rate was decreased. There was no difference in inflammatory marker expression. At 3 days, coronary artery stent endothelialization was significantly increased in GS compared with NGS (81.3% versus 67.5%, P=0.0002). At 28 days, GS exhibited lower neointimal thickness compared with either NGS (21.1%, P=0.011) or MLVS (40.8%, P=0.014). Conclusion— Parallel microgrooves on coronary stent luminal surfaces promote endothelial cell migration and positively influence endothelial cell function, resulting in decreased neointimal formation in the porcine coronary injury model.


JACC: Basic to Translational Science | 2018

Catheter-Based Intervention of the “Forgotten” Valve: Time to Reconsider Tricuspid Valve Intervention?

Juan F. Granada; Torsten Vahl

Corresponding Author


Archive | 2003

Apparatus and Method for Delivery of Mitomycin Through an Eluting Biocompatible Implantable Medical Device

Juan F. Granada; Simon M. Furnish


Archive | 2007

Composite Vascular Prosthesis

Juan F. Granada; Simon M. Furnish


Eurointervention | 2008

Surface material, surface treatment and nanotechnology in cardiovascular stent development

Eugene A. Sprague; Mark Pomeranz; Ilana Odess; Simon M. Furnish; Juan F. Granada


Archive | 2007

Conformable vascular prosthesis delivery system

Juan F. Granada; Simon M. Furnish


Archive | 2007

Système de prothèse vasculaire adaptable

Juan F. Granada; Simon M. Furnish


Archive | 2007

Prothèse vasculaire composite

Juan F. Granada; Simon M. Furnish


Archive | 2003

Appareil et procede de distribution de mitomycine au moyen d'un dispositif medical d'elution biocompatible implantable

Juan F. Granada; Simon M. Furnish

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Simon M. Furnish

University of Texas Health Science Center at San Antonio

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Eugene A. Sprague

University of Texas Health Science Center at San Antonio

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Jin Ho Choi

Samsung Medical Center

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Fermin O. Tio

University of Texas Health Science Center at San Antonio

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Ilana Odess

University of Texas Health Science Center at San Antonio

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Mark Pomeranz

University of Texas Health Science Center at San Antonio

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