Safety and outcomes of intravenous thrombolysis in dissection-related ischemic stroke: an international multicenter study and comprehensive meta-analysis of reported case series
Language English Country Germany Media print-electronic
Document type Journal Article, Meta-Analysis, Multicenter Study, Research Support, Non-U.S. Gov't
PubMed
26108410
DOI
10.1007/s00415-015-7829-x
PII: 10.1007/s00415-015-7829-x
Knihovny.cz E-resources
- Keywords
- Carotid artery dissection, Cervical artery dissection, Dissection-related ischemic stroke, Symptomatic intracranial hemorrhage, Thrombolysis, Tissue plasminogen activator, Vertebral artery dissection,
- MeSH
- Stroke drug therapy etiology MeSH
- Aortic Dissection complications MeSH
- Adult MeSH
- Fibrinolytic Agents adverse effects therapeutic use MeSH
- Brain Ischemia drug therapy etiology MeSH
- Middle Aged MeSH
- Humans MeSH
- Aged MeSH
- Tissue Plasminogen Activator adverse effects therapeutic use MeSH
- Thrombolytic Therapy adverse effects MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Meta-Analysis MeSH
- Multicenter Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Fibrinolytic Agents MeSH
- Tissue Plasminogen Activator MeSH
The safety and efficacy of intravenous thrombolysis (IVT) in dissection-related ischemic stroke (DRIS) has not been established. We sought to determine safety and recovery rates of IVT in DRIS using prospective, international, multicenter data and by conducting a comprehensive meta-analysis of reported case series. We analyzed consecutive DRIS patients treated with IVT according to national guidelines during a 5-year period at six tertiary-care stroke centers, and also conducted a comprehensive review and meta-analysis of all available case series reporting safety outcomes in DRIS treated with IVT according to PRISMA guidelines. A total of 39 DRIS patients (mean age 60 ± 18 years; 59% men; median NIHSS 13 points, IQR 9-17) received IVT in our multicenter study. Symptomatic intracranial hemorrhage (sICH), in-hospital mortality, complete recanalization, favorable functional outcome (FFO; mRS-score of 0-1) and functional independence (FI; mRS-score of 0-2) were 0% (adjusted Wald 95% CI 0-8%), 10% (3-24%), 55% (40-70%), 61% (45-74%) and 68% (52-81%). The pooled sICH and mortality rates in meta-analysis including 10 case series (234 IVT-DRIS patients) were 2% (0-5%) and 4% (0-8%). The pooled recanalization, FFO and FI rates were 45% (26-67%), 41% (29-54%) and 61% (48-72%), respectively. Substantial heterogeneity was only found for FFO (I(2) = 61%; p = 0.006). Subsequent meta-regression analysis identified baseline NIHSS and dissection in the posterior circulation as independent predictors of FFO (p < 0.05), accounting for FFO variance across different studies. Our prospective, international data coupled with comprehensive meta-analysis results underscore IVT safety in DRIS, while further independent validation is required in larger observational registries or RCTs.
Australian Catholic University Sydney Australia
Department of Neurology School of Medicine Democritus University of Thrace Alexandroupolis Greece
Department of Neurology St Josef Hospital Ruhr University Bochum Germany
Department of Neurology University of Tennessee Health Science Center Memphis TN USA
Division of Neurology Department of Medicine National University Hospital Singapore Singapore
International Clinical Research Center St Anne's University Hospital in Brno Brno Czech Republic
Stroke Unit Department of Neurology Brugmann University Hospital Brussels Belgium
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Stat Med. 2004 May 15;23(9):1351-75 PubMed
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Stroke. 2009 Jun;40(6):2085-91 PubMed
J Thromb Thrombolysis. 2014 May;37(4):557-64 PubMed
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Neurology. 2011 Sep 20;77(12):1174-81 PubMed
Stroke. 2011 Sep;42(9):2515-20 PubMed
Int J Stroke. 2012 Jan;7(1):7-13 PubMed
Neurology. 2005 May 10;64(9):1612-4 PubMed
JAMA. 2000 Apr 19;283(15):2008-12 PubMed
Eur J Neurol. 2009 May;16(5):646-9 PubMed
Stroke. 2007 Mar;38(3):961-6 PubMed
Int J Stroke. 2014 Jun;9(4):413-8 PubMed
Nat Clin Pract Neurol. 2008 Jan;4(1):34-42 PubMed
Eur J Neurol. 1999 Jan;6(1):51-5 PubMed
Neurotherapeutics. 2011 Jul;8(3):425-33 PubMed
Stroke. 2014 Sep;45(9):2662-9 PubMed
Neurologist. 2012 May;18(3):136-8 PubMed
Eur J Neurol. 2012 Sep;19(9):1199-206 PubMed
Arch Neurol. 2002 Apr;59(4):549-53 PubMed
Stroke. 2014 Nov;45(11):3352-9 PubMed
Eur J Neurol. 2012 Sep;19(9):1155-6 PubMed
Neurologist. 2012 Sep;18(5):273-6 PubMed
Stroke. 2013 Feb;44(2):394-400 PubMed
Stroke. 2011 Jun;42(6):1771-4 PubMed
J Clin Epidemiol. 2009 Oct;62(10):e1-34 PubMed
Clin Exp Hypertens. 2006 Apr-May;28(3-4):365-70 PubMed
BMJ. 1997 Sep 13;315(7109):629-34 PubMed
Stroke. 2007 Sep;38(9):2605-11 PubMed
Arch Neurol. 2011 Dec;68(12):1536-42 PubMed
Stroke. 2009 Dec;40(12):3772-6 PubMed
BMJ. 2011 Oct 18;343:d5928 PubMed
Eur J Neurol. 2009 Jun;16(6):656-61 PubMed
N Engl J Med. 1993 Sep 2;329(10 ):673-82 PubMed
Stroke. 2007 Sep;38(9):2612-8 PubMed