Thrombus Aspiration during Primary Percutaneous Coronary Intervention
Tone Svilaas, M.D., Pieter J. Vlaar, M.Sc., Iwan C. van der Horst, M.D., Ph.D., Gilles F.H. Diercks, M.D., Ph.D., Bart J.G.L. de Smet, M.D., Ph.D., Ad F.M. van den Heuvel, M.D., Ph.D., Rutger L. Anthonio, M.D., Ph.D., Gillian A. Jessurun, M.D., Ph.D., Eng-Shiong Tan, M.D., Albert J.H. Suurmeijer, M.D., Ph.D., and Felix Zijlstra, M.D., Ph.D.
Background Primary percutaneous coronary intervention (PCI)is effective in opening the infarct-related artery in patientswith myocardial infarction with ST-segment elevation. However,the embolization of atherothrombotic debris induces microvascularobstruction and diminishes myocardial reperfusion.
Methods We performed a randomized trial assessing whether manualaspiration was superior to conventional treatment during primaryPCI. A total of 1071 patients were randomly assigned to thethrombus-aspiration group or the conventional-PCI group beforeundergoing coronary angiography. Aspiration was considered tobe successful if there was histopathological evidence of atherothromboticmaterial. We assessed angiographic and electrocardiographicsigns of myocardial reperfusion, as well as clinical outcome.The primary end point was a myocardial blush grade of 0 or 1(defined as absent or minimal myocardial reperfusion, respectively).
Results A myocardial blush grade of 0 or 1 occurred in 17.1%of the patients in the thrombus-aspiration group and in 26.3%of those in the conventional-PCI group (P<0.001). Completeresolution of ST-segment elevation occurred in 56.6% and 44.2%of patients, respectively (P<0.001). The benefit did notshow heterogeneity among the baseline levels of the prespecifiedcovariates. At 30 days, the rate of death in patients with amyocardial blush grade of 0 or 1, 2, and 3 was 5.2%, 2.9%, and1.0%, respectively (P=0.003), and the rate of adverse eventswas 14.1%, 8.8%, and 4.2%, respectively (P<0.001). Histopathologicalexamination confirmed successful aspiration in 72.9% of patients.
Conclusions Thrombus aspiration is applicable in a large majorityof patients with myocardial infarction with ST-segment elevation,and it results in better reperfusion and clinical outcomes thanconventional PCI, irrespective of clinical and angiographiccharacteristics at baseline. (Current Controlled Trials number,ISRCTN16716833
[controlled-trials.com]
.)
Source Information
From the University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Address reprint requests to Dr. Svilaas at the Thorax Center, Department of Cardiology, Triadegebouw, Gang LM1.004, University Medical Center Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, the Netherlands, or at fzijlstra{at}thorax.umcg.nl.
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