Thromboembolism in paediatric lupus patients
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D M Levy1, M P Massicotte, E Harvey
1Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto, Canada.
Insights
Pediatric patients with lupus anticoagulant (LAC)-positive systemic lupus erythematosus (SLE) face a high risk of thromboembolic events (TE). Lifelong anticoagulation is recommended after an initial TE to reduce recurrent events and associated morbidity.
Area of Science:
- Rheumatology
- Pediatric Hematology
- Thrombosis Research
Background:
- Systemic lupus erythematosus (SLE) in children is a chronic autoimmune disease.
- Antiphospholipid antibodies (aPL), particularly lupus anticoagulants (LAC), are associated with increased thrombotic risk.
- Thromboembolic events (TE) are a significant cause of morbidity and mortality in pediatric SLE patients.
Purpose of the Study:
- To determine the prevalence of TE in pediatric SLE patients with LAC.
- To evaluate the effectiveness of anticoagulation in preventing recurrent TE and reducing morbidity.
- To inform clinical management strategies for this high-risk population.
Main Methods:
- Retrospective review of 149 pediatric SLE patients treated over a 10-year period.
- Identification of LAC-positive patients and analysis of TE incidence, type, and timing.
- Assessment of anticoagulation strategies and outcomes, including recurrent TE and long-term management.
Main Results:
- 16% of pediatric SLE patients were LAC-positive (24/149).
- 54% of LAC-positive patients experienced TE (13/24), with events including cerebral venous thrombosis, arterial stroke, and deep venous thrombosis.
- Recurrent TE occurred in 31% of affected patients, with some events happening despite anticoagulation.
Conclusions:
- Thromboembolic events are highly prevalent in pediatric SLE patients with LAC.
- Lifelong anticoagulation should be strongly considered following an initial TE in this population.
- Effective management strategies are crucial to mitigate the risk of recurrent TE and improve outcomes.
Abstract:
Paediatric patients with systemic lupus erythematosus (SLE) and antiphospholipid antibodies (aPL), specifically lupus anticoagulants (LAC) are at high risk of developing thromboembolic events (TE). Our objectives were to determine the prevalence of TE in paediatric SLE patients with LAC and to determine if anticoagulation was effective to decrease morbidity, and prevent recurrent TE. We reviewed data on 149 paediatric SLE patients treated over 10 years. In all, 24 patients (16%) were LAC positive, and 21 TE occurred in 13 of these LAC positive patients (54% incidence of TE in LAC positive patients). The events were cerebral venous thrombosis (9), arterial stroke (3), deep venous thrombosis (4), pulmonary embolism (2), other venous event (1) and other arterial events (2). The median duration between SLE diagnosis and first TE was 15.2 months (range 0-62), and the median age at first TE was 15.1 years (range 11.4-18.4). Long-term anticoagulation was prescribed, and eight patients (62%) were transferred to adult care on lifelong oral warfarin; four (31%) remain under our care on lifelong warfarin, and one patient died of causes unrelated to her TE. No patient has been identified with deficiencies of protein C, protein S or antithrombin III. One patient is heterozygous for Factor V Leiden, and one is heterozygous for both the Prothrombin 20210A mutation and the MTHFR (methylene tetrahydrofolate reductase) mutation. Four patients had recurrent TE (31%), and three were not anticoagulated at the time of their second event. One patient had two recurrences on therapeutic anticoagulation. Thromboembolic events are prevalent in the LAC positive paediatric SLE population, and consideration for lifelong anticoagulation must occur after an initial TE.
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