Thrombus Aspiration during ST-Segment Elevation Myocardial InfarctionDept Cardiol, Landspitali University Hospital Iceland, Reykjavik, Iceland; Cardiovasc Res Ctr, Landspitali Univ Hosp Iceland, Reykjavik, Iceland.
Dept Cardiol, Aarhus University Hospital, Aarhus, Denmark.
Dept Cardiol, Södersjukhuset, Karolinska Institute, Stockholm, Sweden.
Dept Cardiol, Sahlgrenska University Hospital, Gothenburg, Sweden.
Dept Cardiol, Karlstad Hospital, Karlstad, Sweden.
Dept Cardiol, Lund University Hospital, Lund, Sweden.
Dept Cardiol, Gävle Central Hospital, Gävle, Sweden.
Dept Med, Cardiol Unit, Karolinska University Hospital, Stockholm, Sweden.
PCI Unit, Sunderby Hospital, Sunderby, Sweden.
Dept Cardiol, Västerås Hospital, Västerås, Sweden.
Dept Cardiol, Ctr Heart, Umeå University, Umeå, Sweden.
Dept Cardiol, Borås Hospital, Borås, Sweden.
Dept Radiol, Helsingborg Hospital, Helsingborg, Sweden.
Dept Cardiol, Falun Central Hospital, Falun, Sweden.
Dept Med Sci, Uppsala University, Uppsala, Sweden; Clin Res Ctr, Uppsala University, Uppsala, Sweden.
Dept Cardiol, Lund University Hospital, Lund, Sweden.
Dept Med Sci, Uppsala University, Uppsala, Sweden; Clin Res Ctr, Uppsala University, Uppsala, Sweden.
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2013 (English)In: New England Journal of Medicine, ISSN 0028-4793, E-ISSN 1533-4406, Vol. 369, no 17, p. 1587-1597Article in journal (Refereed) Published
Abstract [en]
Background:The clinical effect of routine intracoronary thrombus aspiration before primary percutaneous coronary intervention (PCI) in patients with ST-segment elevation myocardial infarction (STEMI) is uncertain. We aimed to evaluate whether thrombus aspiration reduces mortality. Methods: We conducted a multicenter, prospective, randomized, controlled, open-label clinical trial, with enrollment of patients from the national comprehensive Swedish Coronary Angiography and Angioplasty Registry (SCAAR) and end points evaluated through national registries. A total of 7244 patients with STEMI undergoing PCI were randomly assigned to manual thrombus aspiration followed by PCI or to PCI only. The primary end point was all-cause mortality at 30 days. ResultsNo patients were lost to follow-up. Death from any cause occurred in 2.8% of the patients in the thrombus-aspiration group (103 of 3621), as compared with 3.0% in the PCI-only group (110 of 3623) (hazard ratio, 0.94; 95% confidence interval [CI], 0.72 to 1.22; P=0.63). The rates of hospitalization for recurrent myocardial infarction at 30 days were 0.5% and 0.9% in the two groups, respectively (hazard ratio, 0.61; 95% CI, 0.34 to 1.07; P=0.09), and the rates of stent thrombosis were 0.2% and 0.5%, respectively (hazard ratio, 0.47; 95% CI, 0.20 to 1.02; P=0.06). There were no significant differences between the groups with respect to the rate of stroke or neurologic complications at the time of discharge (P=0.87). The results were consistent across all major prespecified subgroups, including subgroups defined according to thrombus burden and coronary flow before PCI. ConclusionsRoutine thrombus aspiration before PCI as compared with PCI alone did not reduce 30-day mortality among patients with STEMI. (Funded by the Swedish Research Council and others; ClinicalTrials.gov number, NCT01093404.)
Place, publisher, year, edition, pages
2013. Vol. 369, no 17, p. 1587-1597
National Category
Cardiac and Cardiovascular Systems
Identifiers
URN: urn:nbn:se:oru:diva-56534DOI: 10.1056/NEJMoa1308789ISI: 000326031100008PubMedID: 23991656OAI: oai:DiVA.org:oru-56534DiVA, id: diva2:1082672
2017-03-172017-03-172024-01-16Bibliographically approved