Microvessels in Chronic Total Occlusions: Pathways for Successful Guidewire Crossing?

Journal of Interventional Cardiology - Tập 18 Số 6 - Trang 425-436 - 2005
Bradley H. Strauss1, Amit Segev2, Graham A. Wright3,4, Beiping Qiang1, Nigel R. Munce3, Kevan Anderson3, General Leung3, Alexander Dick4, Renu Virmani5, Jagdish Butany6
1The Roy and Ann Foss Cardiovascular Research Program, Terrence Donnelly Heart Center, St. Michael's Hospital, Toronto, Ontario, Canada.
2Sheba Medical Center, Tel Aviv, Israel
3Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada
4Sunnybrook and Women's College Health Sciences Center, Toronto, Ontario, Canada
5CV Path, Gaithersburg, Maryland
6University Health Network, Toronto, Ontario, Canada

Tóm tắt

Arterial chronic total occlusions (CTO) are a common and clinically relevant problem in patients with coronary artery disease. Percutaneous coronary intervention (PCI) success rates in a wide range of CTO are low, primarily due to inability of guidewire crossing. The pathophysiology of CTO is poorly understood and limits our ability to introduce innovative therapies. Recent studies from our laboratory have suggested that microvessel formation within arterial CTO is a complex process with temporal and regional differences. Moreover, there is evidence from pilot studies that the presence of either microvessels or the particular extracellular matrix environment in the adjacent perivascular tissue can facilitate guidewire crossing and successful PCI. Currently, studies are underway in our experimental CTO model to delineate the pathophysiology of microvessel formation in CTO and its potential role in PCI.

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Tài liệu tham khảo

Baim DS, 1988, Use of coronary angioplasty: Results of a current survey, Am J Cardiol, 61, 3G, 10.1016/S0002-9149(88)80025-0

10.1002/(SICI)1522-726X(200003)49:3<258::AID-CCD7>3.0.CO;2-L

10.1161/01.CIR.85.1.106

10.1016/0002-9149(94)90809-5

10.1016/S0735-1097(96)00276-8

10.1053/euhj.1997.0617

10.1016/S0002-9149(96)00411-0

10.1161/01.CIR.92.5.1101

10.1016/S0735-1097(01)01349-3

Ramanathan K, 2001, Successful percutaneous recanalization of a non‐acute occluded coronary artery predicts clinical outcomes and survival, Circulation, 104, 415A

Srinivas VS, 2002, Contemporary percutaneous coronary intervention versus balloon angioplasty for multivessel coronary artery disease, A comparison of the National Heart, Lung, and Blood Institute Dynamic Registry and the Bypass Angioplasty Revascularization Investigation (BARI) study. Circulation, 106, 1627

10.1056/NEJM199410203311602

10.1053/euhj.2000.2295

10.1016/S0735-1097(97)00490-7

10.1016/0735-1097(90)90285-W

10.1056/NEJMoa012843

10.1016/j.jacc.2004.01.045

10.1002/ccd.10402

10.1016/S0002-9149(03)00841-5

10.1161/01.CIR.0000086320.24172.A1

10.1016/S0735-1097(97)00035-1

Stone GW, 2005, Percutaneous recanalization of chronically occluded coronary arteries: A consensus document. Part 1, Circulation

10.1016/S0002-9149(01)01614-9

10.1016/0735-1097(93)90091-E

10.1172/JCI1568

10.1016/S0735-1097(98)00482-3

CheemaAN HongT NiliN et al.Adventitial microvessel formation after coronary stenting and the effects of SU11218 a tyrosine kinase inhibitor. Submitted.

De Martin R, 2000, The transcription factor NF‐kappa B and the regulation of vascular cell function, Arterioscler Thromb Vasc Biol, 20, E83

10.1038/86490

10.1016/S0735-1097(01)01301-8

10.1161/01.CIR.99.13.1726

10.1038/89961

10.1016/S0008-6363(98)00255-7

10.1002/(SICI)1096-9896(199906)188:2<189::AID-PATH336>3.0.CO;2-N

10.1002/path.1700750102

10.1016/S0741-5214(99)70013-3

10.1016/S0967-2109(97)00162-2

10.1055/s-0037-1615957

Sevitt S, 1970, Organic canalisation and vascularisation of deep vein thrombi studied with dyed‐micropaque injected at necropsy, J Pathol, 100, I

10.1161/01.CIR.0000050149.22928.39

10.1067/mva.2000.110882

10.1136/heart.87.2.158

Majno G, 1996, In Principles of General Pathology

10.1016/0033-0620(91)90019-I

10.1016/j.cardiores.2004.10.012

10.1002/path.1711170203

10.1007/BF00734508

Leu HJ, 1988, Differentiation of mononuclear blood cells into macrophages, fibroblasts and endothelial cells in thrombus organization, Exp Cell Biol, 56, 201

10.1111/j.1432-0436.1993.tb00653.x

10.1016/0092-8674(91)90308-L

10.1016/S0065-230X(08)60772-1

10.1152/ajpheart.00478.2002

10.1177/002215540305101101

10.1172/JCI200113738

10.1016/j.cardiores.2004.03.028

10.1096/fj.03-0545fje

10.1023/A:1024540701634

10.1006/mvre.2001.2311

10.1038/sj.onc.1205595

10.1161/hh1601.095596

10.1097/00002142-200106000-00006

10.1002/jmri.1880070113

10.1002/(SICI)1522-2586(200005)11:5<488::AID-JMRI4>3.0.CO;2-V

10.1002/mrm.10066

10.1016/S1051-0443(96)70735-2

10.1126/science.237.4821.1439

10.1161/01.HYP.31.1.440

10.1016/0002-9149(87)91164-7

QiX BurnsP HongJ et al.Characterizing Blood Volume Fraction (BVF) in a VX2 Tumour by MRI and Ultrasound 10th Scientific Meeting of International Society for Magnetic Resonance in Medicine number 2106 May 1824 2002.