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Pediatric catastrophic antiphospholipid syndrome: descriptive analysis of 45 patients from the "CAPS Registry"
Horacio Berman1, Ignasi Rodríguez-Pintó, Ricard Cervera
1Department of Autoimmune Diseases, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Hospital Clinic, Barcelona, Catalonia, Spain.
Insights
Pediatric catastrophic antiphospholipid syndrome (APS) is rare, with infections triggering events more often than in adults. While outcomes are similar, children less frequently present with APS as their initial diagnosis.
Area of Science:
- Rheumatology
- Pediatric Medicine
- Immunology
Background:
- Catastrophic Antiphospholipid Syndrome (APS) is a rare, severe condition with limited data in pediatric populations.
- Understanding pediatric catastrophic APS is crucial for timely diagnosis and management.
Purpose of the Study:
- To describe clinical characteristics, laboratory findings, treatment, and outcomes of pediatric catastrophic APS.
- To compare these features with adult patients diagnosed with catastrophic APS.
Main Methods:
- Analysis of data from the international registry of patients with catastrophic APS (CAPS Registry).
- Inclusion of patients diagnosed before 18 years of age.
- Comparison of demographic, clinical, laboratory, treatment, and outcome data between pediatric and adult cohorts.
Main Results:
- Infections were a more frequent precipitating factor in pediatric catastrophic APS (60.9%) versus adults (26.8%).
- Peripheral vessel thrombosis was more prevalent in children (52.2%) compared to adults (34.3%).
- Catastrophic APS presented as the initial manifestation of APS more often in pediatric patients (86.6%) than in adults (45.2%).
Conclusions:
- Catastrophic APS in children is rare, sharing many similarities with adult cases.
- Key differences include a higher incidence of infections as triggers and peripheral thrombosis in pediatric patients.
- Pediatric patients showed a trend towards lower mortality, though not statistically significant.
Abstract:
Given the lack of information about catastrophic antiphospholipid syndrome (APS) in pediatric patients, the objective of the current study was to describe the clinical characteristics, laboratory features, treatment, and outcome of pediatric patients with catastrophic APS and compare them with the adult patients with catastrophic APS. We identified patients who were under 18years of age at time of catastrophic APS diagnosis included in the international registry of patients with catastrophic APS (CAPS Registry). Their main demographic and clinical characteristics, laboratory features, treatment, and outcome were described and compared with those of adult patients with catastrophic APS. From the 446 patients included in the CAPS Registry as of May 2013, 45 (10.3%) patients developed 46 catastrophic events before 18years of age (one patient presented two episodes). Overall, 32 (71.1%) patients were female and the mean age was 11.5±4.6years (range, 3months-18years). A total of 31 (68.9%) patients suffered from primary APS and 13 (28.9%) from systemic lupus erythematosus (SLE). The main differences between the two groups of patients were the higher prevalence of infections as precipitating factor for catastrophic event in the pediatric population (60.9% versus 26.8% in the adult population, p<0.001) and of peripheral vessel thrombosis (52.2% versus 34.3%, p=0.017). In addition, catastrophic APS was the first manifestation of APS more frequently in pediatric patients (86.6% versus 45.2%, p<0.001). Interestingly, pediatric patients showed a trend of lower mortality, although the difference was not statistically significant (26.1% versus 40.2%; odds ratio, 1.9; 95% confidence interval, 0.96-3.79; p=0.063). No differences were found neither in the laboratory features nor in the isolated or combination treatments between groups. Catastrophic APS in pediatric patients is a rare disease. There are minimal differences in the clinical and laboratory features, treatment, and outcome of pediatric and adult catastrophic APS patients.
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