Literature DB >> 28183857

Coexistent Sickle Cell Disease Has No Impact on the Safety or Outcome of Lytic Therapy in Acute Ischemic Stroke: Findings From Get With The Guidelines-Stroke.

Robert J Adams1, Margueritte Cox2, Shelly D Ozark2, Julie Kanter2, Phillip J Schulte2, Ying Xian2, Gregg C Fonarow2, Eric E Smith2, Lee H Schwamm2.   

Abstract

BACKGROUND AND
PURPOSE: The recommended treatment for ischemic stroke is tPA (tissue-type plasminogen activator). Although sickle cell disease (SCD) represents no known contraindication to tPA, National Heart Lung and Blood Institute of the National Institutes of Health recommended acute exchange transfusion for stroke in SCD, not tPA. Data on safety and outcomes of tPA in patients are needed to guide tPA use in SCD.
METHODS: We matched patients from the American Heart Association and American Stroke Association Get With The Guidelines-Stroke registry with SCD to patients without SCD and compared usage, complications, and discharge outcomes after tPA. Multivariable logistic regression models using generalized estimating equations were used to assess outcomes.
RESULTS: From 2 016 652 stroke patients admitted to Get With The Guidelines-Stroke sites in the United States, 832 SCD and 3328 non-SCD controls with no differences in admission National Institutes of Health Stroke Scale or blood pressure were identified. Neither the fraction receiving thrombolytic therapy (8.2% for SCD versus 9.4% non-SCD) nor symptomatic intracranial hemorrhage (4.9% of SCD versus 3.2% non-SCD; P=0.4502) was different. There was no difference in a prespecified set of outcome measures for those with SCD compared with controls.
CONCLUSIONS: Coexistent SCD had no significant impact on the safety or outcome of thrombolytic therapy in acute ischemic stroke. Although the sample size is relatively small, these data suggest that adults with SCD and acute ischemic stroke should be treated with thrombolysis, if they otherwise qualify. Addition studies, however, should track the intracranial hemorrhage rate and provide information on other SCD-related care such as transfusion.
© 2017 American Heart Association, Inc.

Entities:  

Keywords:  brain infarction; quality improvement; sickle cell disease; stroke; thrombolytic therapy

Mesh:

Substances:

Year:  2017        PMID: 28183857     DOI: 10.1161/STROKEAHA.116.015412

Source DB:  PubMed          Journal:  Stroke        ISSN: 0039-2499            Impact factor:   7.914


  8 in total

1.  Thrombolytic therapy for the treatment of acute ischaemic stroke in adults with homozygous sickle cell disease.

Authors:  Loubna Majhadi; David Calvet; Charlotte Rosso; Pablo Bartolucci
Journal:  BMJ Case Rep       Date:  2017-07-28

2.  Sickle Mice Are Sensitive to Hypoxia/Ischemia-Induced Stroke but Respond to Tissue-Type Plasminogen Activator Treatment.

Authors:  Yu-Yo Sun; Jolly Lee; Henry Huang; Mary B Wagner; Clinton H Joiner; David R Archer; Chia-Yi Kuan
Journal:  Stroke       Date:  2017-11-10       Impact factor: 7.914

3.  Optimal disease management and health monitoring in adults with sickle cell disease.

Authors:  Jo Howard; Swee Lay Thein
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2019-12-06

Review 4.  Neurologic Complications of Sickle Cell Disease.

Authors:  Shama Farooq; Fernando D Testai
Journal:  Curr Neurol Neurosci Rep       Date:  2019-02-28       Impact factor: 5.081

5.  More Than Meets the Eye: Cerebrovascular Disease in Sickle Cell Disease Is About More Than Sickling.

Authors:  Sneha Jacob; Amelia Adcock; Ann Murray; Joanna Kolodney
Journal:  Stroke       Date:  2018-04-25       Impact factor: 7.914

Review 6.  The American Heart Association's Get With the Guidelines (GWTG)-Stroke development and impact on stroke care.

Authors:  Cora H Ormseth; Kevin N Sheth; Jeffrey L Saver; Gregg C Fonarow; Lee H Schwamm
Journal:  Stroke Vasc Neurol       Date:  2017-05-29

7.  Cerebrovascular manifestations in hematological diseases: an update.

Authors:  José M Ferro; Joana Infante
Journal:  J Neurol       Date:  2021-02-13       Impact factor: 4.849

8.  American Society of Hematology 2020 guidelines for sickle cell disease: prevention, diagnosis, and treatment of cerebrovascular disease in children and adults.

Authors:  M R DeBaun; L C Jordan; A A King; J Schatz; E Vichinsky; C K Fox; R C McKinstry; P Telfer; M A Kraut; L Daraz; F J Kirkham; M H Murad
Journal:  Blood Adv       Date:  2020-04-28
  8 in total

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