Stroke in the TOTAL trial: a randomized trial of routine thrombectomy vs. percutaneous coronary intervention alone in ST elevation myocardial infarction
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články, multicentrická studie, randomizované kontrolované studie, práce podpořená grantem
Grantová podpora
Canadian Institutes of Health Research - Canada
PubMed
26129947
PubMed Central
PMC4568405
DOI
10.1093/eurheartj/ehv296
PII: ehv296
Knihovny.cz E-zdroje
- Klíčová slova
- Meta-analysis, Randomized trial, STEMI, Stroke, Thrombectomy,
- MeSH
- cévní mozková příhoda etiologie mortalita MeSH
- infarkt myokardu mortalita chirurgie MeSH
- Kaplanův-Meierův odhad MeSH
- koronární angioplastika metody mortalita MeSH
- lidé MeSH
- pooperační komplikace etiologie MeSH
- senioři MeSH
- trombektomie metody mortalita MeSH
- výsledek terapie MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- srovnávací studie MeSH
AIMS: TOTAL (N = 10 732), a randomized trial of routine manual thrombectomy vs. percutaneous coronary intervention alone in ST elevation myocardial infarction, showed no difference in the primary efficacy outcome but a significant increase in stroke. We sought to understand these findings. METHODS AND RESULTS: A detailed analysis of stroke timing, stroke severity, and stroke subtype was performed. Strokes were adjudicated by neurologists blinded to treatment assignment. Stroke within 30 days, the primary safety outcome, was increased [33 (0.7%) vs. 16 (0.3%), hazard ratio (HR) 2.06; 95% confidence interval (CI) 1.13-3.75]. The difference in stroke was apparent within 48 h [15 (0.3%) vs. 5 (0.1%), HR 3.00; 95% CI 1.09-8.25]. There was an increase in strokes within 180 days with minor or no disability (Rankin 0-2) [18 (0.4%) vs. 13 (0.3%) HR 1.38; 95% CI 0.68-2.82] and in strokes with major disability or fatal (Rankin 3-6) [35 (0.7%) vs. 13 (0.3%), HR 2.69; 95% CI 1.42-5.08]. Most of the absolute difference was due to an increase in ischaemic strokes within 180 days [37 (0.7%) vs. 21 (0.4%), HR 1.71; 95% CI 1.03-3.00], but there was also an increase in haemorrhagic strokes [10 (0.2%) vs. 2 (0.04%), HR 4.98; 95% CI 1.09-22.7]. Patients that had a stroke had a mortality of 30.8% within 180 days vs. 3.4% without a stroke (P < 0.001). A meta-analysis of randomized trials (N = 21 173) showed an increase in risk of stroke (odds ratio 1.59; 95% CI 1.11-2.27) but a trend towards reduction in mortality odds ratio (odds ratio 0.87; 95% CI 0.76-1.00). CONCLUSION: Thrombectomy was associated with a significant increase in stroke. Based on these findings, future trials must carefully collect stroke to determine safety in addition to efficacy.
Central Manchester Foundation Trust Manchester Academic Health Science Centre Manchester UK
CK Hui Heart Centre Edmonton AB Canada
Department of Medicine University of British Columbia Vancouver BC Canada
Division of Cardiology Vancouver General Hospital University of British Columbia Vancouver BC Canada
Heart Centre Kuopio University Hospital Kuopio Finland
Krajská Nemocnice Liberec Liberec Czech Republic
Patras University Hospital Patras Greece
Peter Munk Cardiac Centre University Health Network Toronto ON Canada
Rouge Valley Health System Toronto ON Canada
University Clinic of Cardiology Sts Cyril and Methodius University Skopje Macedonia
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ClinicalTrials.gov
NCT01149044