Distal microcirculatory protection during percutaneous coronary intervention in acute ST-segment elevation myocardial infarction - A randomized controlled trial

被引:420
作者
Stone, GW
Webb, J
Cox, DA
Brodie, BR
Qureshi, M
Kalynych, A
Turco, M
Schultheiss, HP
Dulas, D
Rutherford, BD
Antoniucci, D
Krucoff, MW
Gibbons, RJ
Jones, D
Lansky, AJ
Mehran, R
机构
[1] Columbia Univ, Med Ctr, New York, NY 10022 USA
[2] Cardiovasc Res Fdn, New York, NY 10022 USA
[3] St Pauls Hosp, Vancouver, BC V6Z 1Y6, Canada
[4] Mid Carolina Cardiol, Charlotte, NC USA
[5] Moses Cone Hosp, Greensboro, NC USA
[6] St Joseph Mercy Hosp, Ypsilanti, MI USA
[7] Emory Univ, Crawford Long Hosp, Atlanta, GA 30365 USA
[8] Washington Adventist Hosp, Takoma Pk, MD USA
[9] Univ Hosp Benjamin Franklin, Berlin, Germany
[10] Mercy Hosp, Coon Rapids, MN USA
[11] St Lukes Hosp, Kansas City, MO USA
[12] Policlin Careggi, Florence, Italy
[13] Duke Univ, Med Ctr, Durham, NC USA
[14] Mayo Clin Fdn, Rochester, MN USA
[15] Medtron Corp, Santa Rosa, CA USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2005年 / 293卷 / 09期
关键词
D O I
10.1001/jama.293.9.1063
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Atheromatous and thrombotic embolization during percutaneous coronary intervention (PCI in acute myocardial infarction is common and may result in microcirculatory dysfunction, the prevention of which may improve reperfusion success, reduce infarct size, and enhance event-free survival. Objective To determine whether protection of the distal microcirculation from thromboembolic debris liberated during primary PCI results in improved reperfusion and decreased infarct size. Design, Setting, and Patients Prospective randomized controlled trial at 38 academic and community-based institutions in 7 countries enrolling 501 patients aged 18 years or older with ST-segment elevation myocardial infarction (STEMI) presenting within 6 hours of symptom onset and undergoing primary PCI or rescue intervention after failed thrombolysis. Interventions Patients were randomized between May 20, 2002, and November 21, 2003, to receive PCI with a balloon occlusion and aspiration distal microcirculatory protection system vs angioplasty without distal protection. Main Outcome Measures Coprimary end points were ST-segment resolution (STR) measured 30 minutes after PCI by continuous Holter monitoring and infarct size measured by technetium Tc 99m sestamibi imaging between days 5 and 14. Secondary end points included major adverse cardiac events. Results Among 252 patients assigned to distal protection, aspiration was performed in 97% (242/251), all angioplasty balloon inflations were fully protected in 79% (193/245), and visible debris was retrieved from 73 % (182/250). Complete STR was achieved in a similar proportion reperfused with vs without distal protection (63.3% [152/240] vs 61.9% [148/2391, respectively; absolute difference, 1.4% [95% confidence interval, -7.7% to 10.5%; P=.781), and left ventricular infarct size was similar in both groups (median, 12.0% [n=2291 vs9.5% [n=2081, respectively; P=.15). Major adverse cardiac events at 6 months occurred with similar frequency in the distal protection and control groups (10.0% vs 11.0%, respectively; P=.66). Conclusions A distal balloon occlusion and aspiration system effectively retrieves embolic debris in most patients with acute STEMI undergoing emergent PCI. Nonetheless, distal embolic protection did not result in improved microvascular flow, greater reperfusion success, reduced infarct size, or enhanced event-free survival.
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收藏
页码:1063 / 1072
页数:10
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