Safety of anticoagulants in children with arterial ischemic stroke

Author:

Schechter Tal12,Kirton Adam3,Laughlin Suzanne45,Pontigon Ann-Marie6,Finkelstein Yaron278,MacGregor Daune26,Chan Anthony9,deVeber Gabrielle26,Brandão Leonardo R.12

Affiliation:

1. Division of Hematology/Oncology, Department of Pediatrics, The Hospital for Sick Children, Toronto, ON;

2. Department of Pediatrics, University of Toronto, Toronto, ON;

3. Stroke Program, Alberta Children's Hospital, Pediatric and Clinical Neuroscience, University of Calgary, Calgary, AB;

4. Department of Diagnostic Imaging, The Hospital for Sick Children, Toronto, ON;

5. Department of Medical Imaging, University of Toronto, Toronto, ON;

6. Children's Stroke Program, Division of Neurology, Department of Pediatrics;

7. Division of Pediatric Emergency Medicine; and

8. Division of Clinical Pharmacology and Toxicology, The Hospital for Sick Children, Toronto, ON; and

9. Division of Pediatric Hematology/Oncology, McMaster University, Hamilton, ON

Abstract

Abstract Pediatric arterial ischemic stroke (AIS) is increasingly diagnosed and carries significant risks of recurrence, morbidity, and mortality. Anticoagulant therapy (ACT) is commonly prescribed in childhood AIS. Hemorrhagic complication rates in pediatric stroke are unknown, and adult safety data are of limited applicability. We analyzed a prospectively enrolled cohort of children (aged 1 month-18 years) with acute AIS selected using standardized criteria for protocol-based ACT over14-year period. We assessed ACT-associated intracranial hemorrhage (ICH), including frequency, clinical and radiologic characteristics, predictors, and outcome. Among 215 children with AIS, 123 received ACT within 7 days after diagnosis. During anticoagulation, 14 (11%) children developed new or increased ICH, all within 26 days from diagnosis. ICH was symptomatic in 5 (4%), asymptomatic in 9 (7%), and mild (European Cooperative Acute Stroke Study grades HI1 or HI2) in all but 1 child (ECASS PH-2). Long-term neurologic outcomes after ACT-associated ICH in survivors were abnormal in 73% (8/11). Comparably, 12 of 75 (16%) children treated without anticoagulation developed new or increased ICH on follow-up imaging (P = .3507). We conclude that ACT is relatively safe in children with AIS, with a 4% risk of symptomatic ICH. Based on the safety of ACT in our study, clinical trials of ACT in childhood AIS are warranted.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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