Midterm stability and hemodynamic performance of a transfemorally implantable nonmetallic, retrievable, and repositionable aortic valve in patients with severe aortic stenosis. Up to 2-year follow-up of the direct-flow medical valve: a pilot study

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Midterm stability and hemodynamic performance of a transfemorally implantable nonmetallic, retrievable, and repositionable aortic valve in patients with severe aortic stenosis. Up to 2-year follow-up of the direct-flow medical valve: a pilot study. / Bijuklic, Klaudija; Tuebler, Thilo; Reichenspurner, Hermann; Treede, Hendrik; Wandler, Andreas; Harreld, John H; Low, Reginald I; Schofer, Joachim.

in: CIRC-CARDIOVASC INTE, Jahrgang 4, Nr. 6, 01.12.2011, S. 595-601.

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@article{40d701cf96114027bdb1039d157e022f,
title = "Midterm stability and hemodynamic performance of a transfemorally implantable nonmetallic, retrievable, and repositionable aortic valve in patients with severe aortic stenosis. Up to 2-year follow-up of the direct-flow medical valve: a pilot study",
abstract = "BACKGROUND: Misplacement during percutaneous aortic valve implantation can be associated with severe complications. The direct flow medical (DFM) valve is repositionable and retrievable; however, the nonmetallic inflatable and conformable design of the valve results in less radial force, which may have an impact on stability and valve function over time. We, therefore, analyzed the midterm stability of the position, shape, and hemodynamic performance of the DFM percutaneous aortic valve.METHODS AND RESULTS: Sixteen symptomatic high-risk for surgery patients with aortic stenosis and a logistic EuroSCORE >20 underwent implantation and were the subject of this analysis. Clinical, echocardiographic, and dual-source multislice computed tomography data were obtained during 2-year follow-up. The 1- and 2-year survival rates were 81% and 69%, respectively. The dual-source multislice computed tomography follow-up indicated no changes in position, diameter, and orifice area of the DFM valve over time. Echocardiography revealed a significant decrease of the mean gradient from baseline (50.1±11.3 mm Hg) to 30 days (19.6±5.7 mm Hg, P<0.001), which remained stable over 2 years. The aortic valve area increased from 0.57±0.15 cm(2) at baseline to 1.47±0.35 cm(2) at 30 days (P<0.001) and did not significantly change during 2-year follow-up. Of the patients, 73% had no aortic regurgitation (AR) and 27% had minimal AR.CONCLUSIONS: In this preliminary series, the 2-year follow-up data of patients, in whom the nonmetallic, repositionable, and retrievable DFM valve was successfully implanted, show stability of the position, shape, and hemodynamic performance, with no AR in most patients.",
keywords = "Aged, Aged, 80 and over, Angioplasty/methods, Aortic Valve/diagnostic imaging, Aortic Valve Stenosis/mortality, Echocardiography, Female, Femoral Vein, Follow-Up Studies, Heart Valve Prosthesis, Heart Valve Prosthesis Implantation/methods, Hemodynamics/physiology, Humans, Kaplan-Meier Estimate, Male, Multidetector Computed Tomography, Pilot Projects, Regional Blood Flow/physiology, Severity of Illness Index, Treatment Outcome",
author = "Klaudija Bijuklic and Thilo Tuebler and Hermann Reichenspurner and Hendrik Treede and Andreas Wandler and Harreld, {John H} and Low, {Reginald I} and Joachim Schofer",
year = "2011",
month = dec,
day = "1",
doi = "10.1161/CIRCINTERVENTIONS.111.964072",
language = "English",
volume = "4",
pages = "595--601",
journal = "CIRC-CARDIOVASC INTE",
issn = "1941-7640",
publisher = "Lippincott Williams and Wilkins",
number = "6",

}

RIS

TY - JOUR

T1 - Midterm stability and hemodynamic performance of a transfemorally implantable nonmetallic, retrievable, and repositionable aortic valve in patients with severe aortic stenosis. Up to 2-year follow-up of the direct-flow medical valve: a pilot study

AU - Bijuklic, Klaudija

AU - Tuebler, Thilo

AU - Reichenspurner, Hermann

AU - Treede, Hendrik

AU - Wandler, Andreas

AU - Harreld, John H

AU - Low, Reginald I

AU - Schofer, Joachim

PY - 2011/12/1

Y1 - 2011/12/1

N2 - BACKGROUND: Misplacement during percutaneous aortic valve implantation can be associated with severe complications. The direct flow medical (DFM) valve is repositionable and retrievable; however, the nonmetallic inflatable and conformable design of the valve results in less radial force, which may have an impact on stability and valve function over time. We, therefore, analyzed the midterm stability of the position, shape, and hemodynamic performance of the DFM percutaneous aortic valve.METHODS AND RESULTS: Sixteen symptomatic high-risk for surgery patients with aortic stenosis and a logistic EuroSCORE >20 underwent implantation and were the subject of this analysis. Clinical, echocardiographic, and dual-source multislice computed tomography data were obtained during 2-year follow-up. The 1- and 2-year survival rates were 81% and 69%, respectively. The dual-source multislice computed tomography follow-up indicated no changes in position, diameter, and orifice area of the DFM valve over time. Echocardiography revealed a significant decrease of the mean gradient from baseline (50.1±11.3 mm Hg) to 30 days (19.6±5.7 mm Hg, P<0.001), which remained stable over 2 years. The aortic valve area increased from 0.57±0.15 cm(2) at baseline to 1.47±0.35 cm(2) at 30 days (P<0.001) and did not significantly change during 2-year follow-up. Of the patients, 73% had no aortic regurgitation (AR) and 27% had minimal AR.CONCLUSIONS: In this preliminary series, the 2-year follow-up data of patients, in whom the nonmetallic, repositionable, and retrievable DFM valve was successfully implanted, show stability of the position, shape, and hemodynamic performance, with no AR in most patients.

AB - BACKGROUND: Misplacement during percutaneous aortic valve implantation can be associated with severe complications. The direct flow medical (DFM) valve is repositionable and retrievable; however, the nonmetallic inflatable and conformable design of the valve results in less radial force, which may have an impact on stability and valve function over time. We, therefore, analyzed the midterm stability of the position, shape, and hemodynamic performance of the DFM percutaneous aortic valve.METHODS AND RESULTS: Sixteen symptomatic high-risk for surgery patients with aortic stenosis and a logistic EuroSCORE >20 underwent implantation and were the subject of this analysis. Clinical, echocardiographic, and dual-source multislice computed tomography data were obtained during 2-year follow-up. The 1- and 2-year survival rates were 81% and 69%, respectively. The dual-source multislice computed tomography follow-up indicated no changes in position, diameter, and orifice area of the DFM valve over time. Echocardiography revealed a significant decrease of the mean gradient from baseline (50.1±11.3 mm Hg) to 30 days (19.6±5.7 mm Hg, P<0.001), which remained stable over 2 years. The aortic valve area increased from 0.57±0.15 cm(2) at baseline to 1.47±0.35 cm(2) at 30 days (P<0.001) and did not significantly change during 2-year follow-up. Of the patients, 73% had no aortic regurgitation (AR) and 27% had minimal AR.CONCLUSIONS: In this preliminary series, the 2-year follow-up data of patients, in whom the nonmetallic, repositionable, and retrievable DFM valve was successfully implanted, show stability of the position, shape, and hemodynamic performance, with no AR in most patients.

KW - Aged

KW - Aged, 80 and over

KW - Angioplasty/methods

KW - Aortic Valve/diagnostic imaging

KW - Aortic Valve Stenosis/mortality

KW - Echocardiography

KW - Female

KW - Femoral Vein

KW - Follow-Up Studies

KW - Heart Valve Prosthesis

KW - Heart Valve Prosthesis Implantation/methods

KW - Hemodynamics/physiology

KW - Humans

KW - Kaplan-Meier Estimate

KW - Male

KW - Multidetector Computed Tomography

KW - Pilot Projects

KW - Regional Blood Flow/physiology

KW - Severity of Illness Index

KW - Treatment Outcome

U2 - 10.1161/CIRCINTERVENTIONS.111.964072

DO - 10.1161/CIRCINTERVENTIONS.111.964072

M3 - SCORING: Journal article

C2 - 22128202

VL - 4

SP - 595

EP - 601

JO - CIRC-CARDIOVASC INTE

JF - CIRC-CARDIOVASC INTE

SN - 1941-7640

IS - 6

ER -