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Safety of anticoagulants in children with arterial ischemic stroke
Tal Schechter1, Adam Kirton, Suzanne Laughlin
1Division of Hematology/Oncology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada. tal.schechter-finkelstein@sickkids.ca
Insights
Anticoagulant therapy (ACT) is relatively safe for pediatric arterial ischemic stroke (AIS), with a low risk of symptomatic intracranial hemorrhage (ICH). This finding supports further clinical trials of ACT in childhood AIS.
Area of Science:
- Neurology
- Pediatric Medicine
- Hematology
Background:
- Pediatric arterial ischemic stroke (AIS) is a growing concern with significant risks.
- Anticoagulant therapy (ACT) is frequently used in children with AIS.
- Data on hemorrhagic complications and adult safety data applicability in pediatric stroke are limited.
Purpose of the Study:
- To assess the frequency, characteristics, predictors, and outcomes of ACT-associated intracranial hemorrhage (ICH) in children with AIS.
- To evaluate the safety of ACT in this pediatric population.
Main Methods:
- Analysis of a prospectively enrolled cohort of children (1 month-18 years) with acute AIS.
- Protocol-based ACT was administered to selected patients over a 14-year period.
- Assessment of new or increased ICH during and after anticoagulation.
Main Results:
- 11% of children receiving ACT developed new or increased ICH within 26 days of diagnosis.
- Symptomatic ICH occurred in 4% of patients, with most cases being mild.
- Long-term outcomes after ICH were abnormal in 73% of survivors.
- 16% of children not treated with anticoagulation also developed ICH on follow-up.
Conclusions:
- ACT is relatively safe in pediatric AIS, with a 4% risk of symptomatic ICH.
- The safety profile supports the use of ACT in this population.
- Clinical trials investigating ACT for childhood AIS are warranted.
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 over 14-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.
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