Intracoronary streptokinase after primary percutaneous coronary intervention

被引:149
作者
Sezer, Murat [1 ]
Oflaz, Hueseyin [1 ]
Goeren, Taner [1 ]
Okcular, Irem [1 ]
Umman, Berrin [1 ]
Nisanci, Yilmaz [1 ]
Bilge, Ahmet Kaya [1 ]
Sanli, Yasemin [1 ]
Meric, Mehmet [1 ]
Umman, Sabahattin [1 ]
机构
[1] Istanbul Univ, Istanbul Fac Med, Dept Cardiol, Istanbul, Turkey
关键词
ACUTE MYOCARDIAL-INFARCTION; ST-SEGMENT ELEVATION; RANDOMIZED CONTROLLED-TRIAL; PRIMARY ANGIOPLASTY; MICROVASCULAR DYSFUNCTION; FLOW RESERVE; ISCHEMIC EVENTS; SIZE; MICROCIRCULATION; ECHOCARDIOGRAPHY;
D O I
10.1056/NEJMoa054374
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Microvascular perfusion is often impaired after primary percutaneous coronary intervention (PCI). We proposed that in situ thrombosis might contribute to poor myocardial perfusion in this setting. To test this hypothesis, we evaluated the effect of low-dose intracoronary streptokinase administered immediately after primary PCI. METHODS: Forty-one patients undergoing primary PCI were randomly assigned to receive intracoronary streptokinase (250 kU) or no additional therapy. Two days later, cardiac catheterization was repeated, and coronary hemodynamic end points were measured with the use of a guidewire tipped with pressure and temperature sensors. In patients with anterior myocardial infarction, the deceleration time of coronary diastolic flow was measured with transthoracic echocardiography. At 6 months, angiography, echocardiography, and technetium-99m single-photon-emission computed tomography were performed. RESULTS: Two days after PCI, all measures of microvascular function (means +/- SD) were significantly better in the streptokinase group than in the control group, including coronary flow reserve (2.01 +/- 0.57 vs. 1.39 +/- 0.31), the index of microvascular resistance (16.29 +/- 5.06 U vs. 32.49 +/- 11.04 U), the collateral-flow index (0.08 +/- 0.05 vs. 0.17 +/- 0.07), mean coronary wedge pressure (10.81 +/- 5.46 mm Hg vs. 17.20 +/- 7.93 mm Hg), systolic coronary wedge pressure (18.24 +/- 6.07 mm Hg vs. 33.80 +/- 11.00 mm Hg), and diastolic deceleration time (828 +/- 258 msec vs. 360 +/- 292 msec). The administration of intracoronary streptokinase was also associated with a significantly lower corrected Thrombolysis in Myocardial Infarction frame count (the number of cine frames required for dye to travel from the ostium of a coronary artery to a standardized distal coronary landmark) at 2 days. At 6 months, however, there was no evidence of a difference between the two study groups in left ventricular size or function. CONCLUSIONS: In our pilot trial, the administration of low-dose intracoronary streptokinase immediately after primary PCI improved myocardial reperfusion but not long-term left ventricular size or function. These findings require clarification in a larger trial.
引用
收藏
页码:1823 / 1834
页数:12
相关论文
共 34 条
[1]  
Antman Elliott M, 2004, J Am Coll Cardiol, V44, P671, DOI 10.1016/j.jacc.2004.07.002
[2]  
ANTMAN EM, 2005, J AM COLL CARDIOL, V45, P1376
[3]   Validation of coronary flow reserve measurements by thermodilution in clinical practice [J].
Barbato, E ;
Aarnoudse, W ;
Aengevaeren, WR ;
Werner, G ;
Klauss, V ;
Bojara, W ;
Herzfeld, I ;
Oldroyd, KG ;
Pijls, NHJ ;
De Bruyne, B .
EUROPEAN HEART JOURNAL, 2004, 25 (03) :219-223
[4]  
BEARON WF, 2003, CIRCULATION, V108, P3165
[5]   Thrombolytic therapy reduces red blood cell aggregation in plasma without affecting intrinsic aggregability [J].
Ben-Ami, R ;
Sheinman, G ;
Yedgar, S ;
Eldor, A ;
Roth, A ;
Berliner, AS ;
Barshtein, G .
THROMBOSIS RESEARCH, 2002, 105 (06) :487-492
[6]   Physiologically assessed coronary collateral flow and adverse cardiac ischemic events: A follow-up study in 403 patients with coronary artery disease [J].
Billinger, M ;
Kloos, P ;
Eberli, FR ;
Windecker, S ;
Meier, B ;
Seiler, C .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2002, 40 (09) :1545-1550
[7]   Impact of microvascular dysfunction on left ventricular remodeling and long-term clinical outcome after primary coronary angioplasty for acute myocardial infarction [J].
Bolognese, L ;
Carrabba, N ;
Parodi, G ;
Santoro, GM ;
Buonamici, P ;
Cerisano, G ;
Antoniucci, D .
CIRCULATION, 2004, 109 (09) :1121-1126
[8]   THROMBOLYSIS IN MYOCARDIAL-INFARCTION (TIMI) TRIAL, PHASE-I - A COMPARISON BETWEEN INTRAVENOUS TISSUE PLASMINOGEN-ACTIVATOR AND INTRAVENOUS STREPTOKINASE - CLINICAL FINDINGS THROUGH HOSPITAL DISCHARGE [J].
CHESEBRO, JH ;
KNATTERUD, G ;
ROBERTS, R ;
BORER, J ;
COHEN, LS ;
DALEN, J ;
DODGE, HT ;
FRANCIS, CK ;
HILLIS, D ;
LUDBROOK, P ;
MARKIS, JE ;
MUELLER, H ;
PASSAMANI, ER ;
POWERS, ER ;
RAO, AK ;
ROBERTSON, T ;
ROSS, A ;
RYAN, TJ ;
SOBEL, BE ;
WILLERSON, J ;
WILLIAMS, DO ;
ZARET, BL ;
BRAUNWALD, E .
CIRCULATION, 1987, 76 (01) :142-154
[9]   Coronary thermodilution to assess flow reserve - Experimental validation [J].
De Bruyne, B ;
Pijls, NHJ ;
Smith, L ;
Wievegg, M ;
Heyndrickx, GR .
CIRCULATION, 2001, 104 (17) :2003-2006
[10]   New tools for assessing microvascular obstruction in patients with ST elevation myocardial infarction [J].
de Lemos, JA ;
Warner, JJ .
HEART, 2004, 90 (02) :119-120