Temporary scaffolding of coronary arteries with bioabsorbable magnesium stents:: a prospective, non-randomised multicentre trial

被引:1067
作者
Erbel, Raimund
Di Mario, Carlo
Bartunek, Jozef
Bonnier, Johann
de Bruyne, Bernard
Eberli, Franz R.
Erne, Paul
Haude, Michael
Heublein, Bernd
Horrigan, Mark
Ilsley, Charles
Boese, Dirk
Koolen, Jacques
Luescher, Thomas F.
Weissman, Neil
Waksman, Ron
机构
[1] Univ Duisburg Essen, W German Heart Ctr, Dept Cardiol, D-45122 Essen, Germany
[2] Royal Brompton Hosp, London SW3 6LY, England
[3] Harefield Hosp, London, England
[4] Univ London Imperial Coll Sci Technol & Med, London, England
[5] Catharina Hosp, Dept Cardiol, Eindhoven, Netherlands
[6] Onze Lieve Vrouw Hosp, Ctr Cardiovasc, Aalst, Belgium
[7] Univ Zurich Hosp, Dept Cardiol, CH-8091 Zurich, Switzerland
[8] Kantonal Hosp, Dept Cardiol, Luzern, Switzerland
[9] Hannover Med Sch, Leibniz Lab Biotechnol & Artificial Organs, D-3000 Hannover, Germany
[10] Austin & Repatriat Med Ctr, Dept Cardiol, Melbourne, Vic, Australia
[11] Washington Hosp Ctr, Washington, DC 20010 USA
关键词
D O I
10.1016/S0140-6736(07)60853-8
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background Coronary stents improve immediate and late results of balloon angioplasty by tacking up dissections and preventing wall recoil. These goals are achieved within weeks after angioplasty, but with current technology stents permanently remain in the artery, with many limitations including the need for long-term antiplatelet treatment to avoid thrombosis. We report a prospective multicentre clinical trial of coronary implantations of absorbable magnesium stents. Methods We enrolled 63 patients (44 men; mean age 61.3 [SD 9.5 years]) in eight centres with single de novo lesions in a native coronary artery in a multicentre, non-randomised prospective study. Follow-up included coronary angiography and intravascular ultrasound at 4 months and clinical assessment at 6 months and 12 months. The primary endpoint was cardiac death, non-fatal myocardial infarction, or clinically driven target lesion revascularisation at 4 months Findings 71 stents, 10-15 mm in length and 3.0-3.5 mm in diameter, were successfully implanted after pre-dilatation in 63 patients. Diameter stenosis was reduced from 61.5 (SD 13.1%) to 12.6 (5.6%) with an acute gain of 1.41 mm (0.46 mm) and in-stent late loss of 1.08 mm (0.49 mm). The ischaemia-driven target lesion revascularisation rate was 23.8% after 4 months, and the overall target lesion revascularisation rate was 45% after 1 year. No myocardial infarction, subacute or late thrombosis, or death occurred. Angiography at 4 months showed an increased diameter stenosis of 48.4 (17. 0%). After serial intravascular ultrasound examinations, only small remnants of the original struts were visible, well embedded into the intima. Neointimal growth and negative remodelling were the main operating mechanisms of restenosis. Interpretation This study shows that biodegradable magnesium stents can achieve an immediate angiographic result similar to the result of other metal stents and can be safely degraded after 4 months. Modifications of stent characteristics with prolonged degradation and drug elution are currently in development.
引用
收藏
页码:1869 / 1875
页数:7
相关论文
共 32 条
[1]
Intravascular ultrasound stent area of sirolimus-eluting stents and its impact on late outcome [J].
Cheneau, E ;
Pichard, AD ;
Satler, LF ;
Suddath, WO ;
Weissman, NJ ;
Waksman, R .
AMERICAN JOURNAL OF CARDIOLOGY, 2005, 95 (10) :1240-1242
[2]
Results of coronary stenting for restenosis [J].
Colombo, A ;
Ferraro, M ;
Itoh, A ;
Martini, G ;
Blengino, S ;
Finci, L .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1996, 28 (04) :830-836
[3]
Di Mario Carlo, 2004, J Interv Cardiol, V17, P391, DOI 10.1111/j.1540-8183.2004.04081.x
[4]
Novel magnetic resonance-compatible coronary stent -: The absorbable magnesium-alloy stent [J].
Eggebrecht, H ;
Rodermann, J ;
Hunold, P ;
Schmermund, A ;
Böse, D ;
Haude, M ;
Erbel, R .
CIRCULATION, 2005, 112 (18) :E303-E304
[5]
Coronary-artery stenting compared with balloon angioplasty for restenosis after initial balloon angioplasty [J].
Erbel, R ;
Haude, M ;
Höpp, HW ;
Franzen, D ;
Rupprecht, HJ ;
Heublein, B ;
Fischer, K ;
De Jaegere, P ;
Serruys, P ;
Rutsch, W ;
Probst, P .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (23) :1672-1678
[6]
Maintenance of long-term clinical benefit with sirolimus-eluting coronary stents -: Three-year results of the RAVEL trial [J].
Fajadet, J ;
Morice, MC ;
Bode, C ;
Barragan, P ;
Serruys, PW ;
Wijns, W ;
Constantini, CR ;
Guermonprez, JL ;
Eltchaninoff, H ;
Blanchard, D ;
Bartorelli, A ;
Laarman, GJ ;
Perin, MA ;
Sousa, JE ;
Schuler, G ;
Molnar, F ;
Guagliumi, G ;
Colombo, A ;
Hayashi, EB ;
Wülfert, E .
CIRCULATION, 2005, 111 (08) :1040-1044
[7]
Inhibition of restenosis with a paclitaxel-eluting, polymer-free coronary stent - The European evaLUation of pacliTaxel Eluting Stent (ELUTES) trial [J].
Gershlick, A ;
De Scheerder, I ;
Chevalier, B ;
Stephens-Lloyd, A ;
Camenzind, E ;
Vrints, C ;
Reifart, N ;
Missault, L ;
Goy, JJ ;
Brinker, JA ;
Raizner, AE ;
Urban, P ;
Heldman, AW .
CIRCULATION, 2004, 109 (04) :487-493
[8]
Six- and twelve-month results from a randomized, double-blind trial on a slow-release paclitaxel-eluting stent for de novo coronary lesions [J].
Grube, E ;
Silber, S ;
Hauptmann, KE ;
Mueller, R ;
Buellesfeld, L ;
Gerckens, U ;
Russell, ME .
CIRCULATION, 2003, 107 (01) :38-42
[9]
Haude M, 2000, Am Heart J, V140, pe26
[10]
Biocorrosion of magnesium alloys: a new principle in cardiovascular implant technology? [J].
Heublein, B ;
Rohde, R ;
Kaese, V ;
Niemeyer, M ;
Hartung, W ;
Haverich, A .
HEART, 2003, 89 (06) :651-656