Thrombolysis in Patients With Mild Stroke: Results From the Austrian Stroke Unit Registry

Background and Purpose— Apart from missing the approved time window of 4.5 hours, one frequent cause for withholding recombinant tissue plasminogen activator (rt-PA) treatment in patients with ischemic stroke is presentation with mild deficit on admission. We analyzed in a large cohort of patients whether rt-PA treatment is beneficial for this group of patients. Methods— From a total of 54 917 patients with ischemic stroke prospectively enrolled in the Austrian Stroke Unit Registry, 890 patients with mild deficit defined as ⩽5 points in the National Institutes of Health Stroke Scale treated with and without rt-PA were matched for age, sex, prestroke disability, stroke severity, hypertension, diabetes mellitus, hypercholesterolemia, stroke cause, and clinical stroke syndrome. Functional outcome was assessed using the modified Rankin Scale at 3 months. For data visualization, weighted averages of outcome differences were computed for all age severity combinations and mapped to a color. For quantification of effect sizes, numbers need to treat were calculated. Results— rt-PA–treated patients with mild deficit had a better outcome after 3 months compared with matched cases without rt-PA treatment (odds ratio [OR], 1.49; 95% confidence interval [CI], 1.17–1.89; P<0.001). In rt-PA–treated patients with mild deficit, the numbers need to treat ranged from 8 to 14. Improvement achieved by rt-PA treatment was observed along the entire age range. Conclusions— In our study, intravenous rt-PA treatment was beneficial for patients with mild deficit. Given the observational nature of these results, our data might serve as an incentive for future randomized controlled trials to provide a basis for optimal patient selection.

[1]  D. Inzitari,et al.  Aphasia predicts unfavorable outcome in mild ischemic stroke patients and prompts thrombolytic treatment. , 2014, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

[2]  D. Leys,et al.  Ultra-Early Intravenous Stroke Thrombolysis: Do All Patients Benefit Similarly? , 2013, Stroke.

[3]  A. Rabinstein,et al.  Contraindications to intravenous rtPA for acute stroke: A critical reappraisal. , 2013, Neurology. Clinical practice.

[4]  M. Brainin,et al.  Time Trends in Patient Characteristics Treated on Acute Stroke-Units: Results From the Austrian Stroke Unit Registry 2003–2011 , 2013, Stroke.

[5]  Gerhard Schroth,et al.  National Institutes of Health Stroke Scale Score and Vessel Occlusion in 2152 Patients With Acute Ischemic Stroke , 2013, Stroke.

[6]  Laura Llull,et al.  The Outcome of Patients with Mild Stroke Improves after Treatment with Systemic Thrombolysis , 2013, PloS one.

[7]  A. Alexandrov,et al.  Thrombolysis in Stroke Despite Contraindications or Warnings? , 2013, Stroke.

[8]  P. Rothwell,et al.  Population-based study of capsular warning syndrome and prognosis after early recurrent TIA , 2012, Neurology.

[9]  Geoff Cohen,et al.  The benefits and harms of intravenous thrombolysis with recombinant tissue plasminogen activator within 6 h of acute ischaemic stroke (the third international stroke trial [IST-3]): a randomised controlled trial , 2012, The Lancet.

[10]  Eric E. Smith,et al.  Use of Tissue-Type Plasminogen Activator Before and After Publication of the European Cooperative Acute Stroke Study III in Get With The Guidelines-Stroke , 2012, Circulation. Cardiovascular quality and outcomes.

[11]  B. Norrving,et al.  Thrombolytic Therapy Rates and Stroke Severity: An Analysis of Data From the Swedish Stroke Register (Riks-Stroke) 2007–2010 , 2012, Stroke.

[12]  M. Conaway,et al.  Ninety-Day Outcome Rates of a Prospective Cohort of Consecutive Patients With Mild Ischemic Stroke , 2012, Stroke.

[13]  Eric E. Smith,et al.  Outcomes in Mild or Rapidly Improving Stroke Not Treated With Intravenous Recombinant Tissue-Type Plasminogen Activator: Findings From Get With The Guidelines–Stroke , 2011, Stroke.

[14]  J. Grotta,et al.  Thrombolysis Is Associated With Consistent Functional Improvement Across Baseline Stroke Severity: A Comparison of Outcomes in Patients From the Virtual International Stroke Trials Archive (VISTA) , 2010, Stroke.

[15]  Gerhard Schroth,et al.  What Is a Minor Stroke? , 2010, Stroke.

[16]  S. Kiechl,et al.  Early clinical worsening in patients with TIA or minor stroke , 2010, Neurology.

[17]  C. Gerloff,et al.  Thrombolysis targeting MRI defined tissue at risk in minor stroke , 2009, Journal of Neurology, Neurosurgery & Psychiatry.

[18]  R. Sacco,et al.  Long-Term Functional Recovery After First Ischemic Stroke: The Northern Manhattan Study , 2009, Stroke.

[19]  G. Schroth,et al.  Outcome of Stroke With Mild or Rapidly Improving Symptoms , 2007, Stroke.

[20]  Jeffery R. Alger,et al.  Early MRI and outcomes of untreated patients with mild or improving ischemic stroke , 2006, Neurology.

[21]  N. Newman,et al.  Natural history of homonymous hemianopia , 2006, Neurology.

[22]  Gerhard Schroth,et al.  NIHSS Score and Arteriographic Findings in Acute Ischemic Stroke , 2005, Stroke.

[23]  Joseph P. Broderick,et al.  Recombinant tissue plasminogen activator for minor strokes: the National Institute of Neurological Disorders and Stroke rt-PA Stroke Study experience. , 2005, Annals of emergency medicine.

[24]  J. Martí-Fàbregas,et al.  Reasons for exclusion from thrombolytic therapy following acute ischemic stroke , 2005, Neurology.

[25]  William P. Burdick,et al.  Recombinant tissue plasminogen activator for minor strokes: the National Institute of Neurological Disorders and Stroke rt-PA Stroke Study experience. , 2005, Annals of emergency medicine.

[26]  T. Louis,et al.  Findings From the Reanalysis of the NINDS Tissue Plasminogen Activator for Acute Ischemic Stroke Treatment Trial , 2004, Stroke.

[27]  R. Sacco,et al.  The Northern Manhattan Study , 2004 .

[28]  A. Demchuk,et al.  Why are stroke patients excluded from TPA therapy? , 2001, Neurology.

[29]  Koroshetz Wj,et al.  Tissue plasminogen activator for acute ischemic stroke. , 1996, The New England journal of medicine.

[30]  Joseph P. Broderick,et al.  Tissue plasminogen activator for acute ischemic stroke. The National Institute of Neurological Disorders and Stroke rt-PA Stroke Study Group. , 1995 .

[31]  David Lee Gordon,et al.  Classification of Subtype of Acute Ischemic Stroke: Definitions for Use in a Multicenter Clinical Trial , 1993, Stroke.

[32]  J. Bamford,et al.  Classification and natural history of clinically identifiable subtypes of cerebral infarction , 1991, The Lancet.

[33]  J. French,et al.  Recovery of visual fields in acute stroke: homonymous hemianopia associated with adverse prognosis. , 1989, Age and ageing.