Membrane-covered stents: A new treatment strategy for saphenous vein graft lesions

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Membrane-covered stents: A new treatment strategy for saphenous vein graft lesions. / Baldus, Stephan; Kster, Ralf; Reimers, Jacobus; Khler, Jan; Meinertz, Thomas; Hamm, Christian W.

In: CATHETER CARDIO INTE, Vol. 53, No. 1, 2001, p. 1-4.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Baldus, S, Kster, R, Reimers, J, Khler, J, Meinertz, T & Hamm, CW 2001, 'Membrane-covered stents: A new treatment strategy for saphenous vein graft lesions', CATHETER CARDIO INTE, vol. 53, no. 1, pp. 1-4. https://doi.org/10.1002/ccd.1119

APA

Baldus, S., Kster, R., Reimers, J., Khler, J., Meinertz, T., & Hamm, C. W. (2001). Membrane-covered stents: A new treatment strategy for saphenous vein graft lesions. CATHETER CARDIO INTE, 53(1), 1-4. https://doi.org/10.1002/ccd.1119

Vancouver

Bibtex

@article{b9b4e065b7b54d59aecf79b6f629dd5c,
title = "Membrane-covered stents: A new treatment strategy for saphenous vein graft lesions",
abstract = "The restenosis rate after stenting of lesions in aortocoronary venous bypass grafts still has to be considered unsatisfactorily high. We investigated a new stent design characterized by an expandable polytetrafluorethylene (PTFE) membrane in between two layers of struts. Five consecutive male patients (age 70 ± 6 years) were followed prospectively who presented with at least two de novo lesions in different grafts 13 ± 3 years after bypass surgery. A total of 11 lesions were treated located in grafts anastomosed to the circumflex (n = 3), to the LAD (n = 7), and to the right coronary artery (n = 1). Within the same procedure, every patient received membrane-covered stents (n = 6) and conventional stents (n = 5) in either of their lesions. All patients underwent successful interventions. The minimal luminal diameter increased from 1.0 ± 0.5 to 2.9 ± 0.6 mm in lesions treated by the membrane-covered stents and from 0.8 ± 0.4 to 2.4 ± 0.7 mm in the lesions treated by conventional stents. During follow-up, four out of five patients required angioplasty for in-stent restenosis of lesions covered by a conventional stent, whereas no patient underwent revascularization for a lesion treated by a membrane-covered device. The mean minimal luminal diameter of lesions covered by a conventional stent decreased by 42% to 1.4 ± 0.6 mm; the mean minimal luminal diameter of the lesions treated by a stent graft declined by 9% to 2.8 ± 0.6 mm (P < 0.05). This series of intraindividual comparisons suggests that membrane-covered stents may have the power to reduce in-stent restenosis in obstructed aortocoronary venous bypass grafts.",
keywords = "Coronary in-stent restenosis, Polytetrafluorethylene, Venous bypass graft",
author = "Stephan Baldus and Ralf Kster and Jacobus Reimers and Jan Khler and Thomas Meinertz and Hamm, {Christian W.}",
year = "2001",
doi = "10.1002/ccd.1119",
language = "English",
volume = "53",
pages = "1--4",
journal = "CATHETER CARDIO INTE",
issn = "1522-1946",
publisher = "Wiley-Liss Inc.",
number = "1",

}

RIS

TY - JOUR

T1 - Membrane-covered stents: A new treatment strategy for saphenous vein graft lesions

AU - Baldus, Stephan

AU - Kster, Ralf

AU - Reimers, Jacobus

AU - Khler, Jan

AU - Meinertz, Thomas

AU - Hamm, Christian W.

PY - 2001

Y1 - 2001

N2 - The restenosis rate after stenting of lesions in aortocoronary venous bypass grafts still has to be considered unsatisfactorily high. We investigated a new stent design characterized by an expandable polytetrafluorethylene (PTFE) membrane in between two layers of struts. Five consecutive male patients (age 70 ± 6 years) were followed prospectively who presented with at least two de novo lesions in different grafts 13 ± 3 years after bypass surgery. A total of 11 lesions were treated located in grafts anastomosed to the circumflex (n = 3), to the LAD (n = 7), and to the right coronary artery (n = 1). Within the same procedure, every patient received membrane-covered stents (n = 6) and conventional stents (n = 5) in either of their lesions. All patients underwent successful interventions. The minimal luminal diameter increased from 1.0 ± 0.5 to 2.9 ± 0.6 mm in lesions treated by the membrane-covered stents and from 0.8 ± 0.4 to 2.4 ± 0.7 mm in the lesions treated by conventional stents. During follow-up, four out of five patients required angioplasty for in-stent restenosis of lesions covered by a conventional stent, whereas no patient underwent revascularization for a lesion treated by a membrane-covered device. The mean minimal luminal diameter of lesions covered by a conventional stent decreased by 42% to 1.4 ± 0.6 mm; the mean minimal luminal diameter of the lesions treated by a stent graft declined by 9% to 2.8 ± 0.6 mm (P < 0.05). This series of intraindividual comparisons suggests that membrane-covered stents may have the power to reduce in-stent restenosis in obstructed aortocoronary venous bypass grafts.

AB - The restenosis rate after stenting of lesions in aortocoronary venous bypass grafts still has to be considered unsatisfactorily high. We investigated a new stent design characterized by an expandable polytetrafluorethylene (PTFE) membrane in between two layers of struts. Five consecutive male patients (age 70 ± 6 years) were followed prospectively who presented with at least two de novo lesions in different grafts 13 ± 3 years after bypass surgery. A total of 11 lesions were treated located in grafts anastomosed to the circumflex (n = 3), to the LAD (n = 7), and to the right coronary artery (n = 1). Within the same procedure, every patient received membrane-covered stents (n = 6) and conventional stents (n = 5) in either of their lesions. All patients underwent successful interventions. The minimal luminal diameter increased from 1.0 ± 0.5 to 2.9 ± 0.6 mm in lesions treated by the membrane-covered stents and from 0.8 ± 0.4 to 2.4 ± 0.7 mm in the lesions treated by conventional stents. During follow-up, four out of five patients required angioplasty for in-stent restenosis of lesions covered by a conventional stent, whereas no patient underwent revascularization for a lesion treated by a membrane-covered device. The mean minimal luminal diameter of lesions covered by a conventional stent decreased by 42% to 1.4 ± 0.6 mm; the mean minimal luminal diameter of the lesions treated by a stent graft declined by 9% to 2.8 ± 0.6 mm (P < 0.05). This series of intraindividual comparisons suggests that membrane-covered stents may have the power to reduce in-stent restenosis in obstructed aortocoronary venous bypass grafts.

KW - Coronary in-stent restenosis

KW - Polytetrafluorethylene

KW - Venous bypass graft

UR - http://www.scopus.com/inward/record.url?scp=0035041121&partnerID=8YFLogxK

U2 - 10.1002/ccd.1119

DO - 10.1002/ccd.1119

M3 - SCORING: Journal article

C2 - 11329208

AN - SCOPUS:0035041121

VL - 53

SP - 1

EP - 4

JO - CATHETER CARDIO INTE

JF - CATHETER CARDIO INTE

SN - 1522-1946

IS - 1

ER -