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Epistaxis duration predicts bleeding in immune thrombocytopenia: a cohort study
Lianna Reynolds1, Benjamin David Williams2, John Grainger3
1Manchester University NHS Foundation Trust, Manchester, UK lianna.reynolds@nhs.net.
Prolonged nosebleeds (epistaxis) in children with immune thrombocytopenia (ITP) indicate a higher risk of significant bleeding events within a year. This finding aids in assessing ITP severity and guiding treatment decisions.
Area of Science:
- Pediatric Hematology
- Clinical Research
- Bleeding Disorders
Background:
- Immune thrombocytopenia (ITP) is an autoimmune disorder characterized by low platelet counts, increasing bleeding risk.
- Epistaxis is a common symptom in children with ITP, but its association with future bleeding severity is not well-defined.
Purpose of the Study:
- To investigate the relationship between the duration of epistaxis at presentation and the occurrence of clinically relevant bleeding events in children with ITP over a 12-month period.
Main Methods:
- A prospective cohort study was conducted using data from the national UK Paediatric ITP registry (2006-2020).
- Included were 1793 children (2 months to 16 years) with ITP, categorizing epistaxis duration at presentation (<10 min, 10-30 min, >30 min).
- Outcomes assessed included severe bleeds, moderate/severe bleeds, and hemoglobin drop (≥2 g/dL) within 12 months.
Main Results:
- Children with epistaxis lasting over 30 minutes had significantly increased odds of severe bleeds (OR 1.43-15.67), moderate/severe bleeds (OR 1.33-4.2), and hemoglobin drop (OR 1.23-6.91).
- No increased bleeding risk was associated with shorter epistaxis durations.
- A significant trend showed higher bleeding risk with longer epistaxis duration for all assessed outcomes.
Conclusions:
- The duration of epistaxis at presentation in children with ITP is a significant predictor of subsequent clinically relevant bleeding.
- Findings support using epistaxis duration to inform clinical severity assessments and treatment strategies for pediatric ITP.
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