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Prognostic Factors for Immune Thrombocytopenia Outcome in Greek Children: A Retrospective Single-Centered Analysis
Alexandros Makis1, Athanasios Gkoutsias1, Theodoros Palianopoulos1
1Department of Pediatrics, University Hospital of Ioannina, Ioannina, Greece.
Insights
This study identified key differences in pediatric immune thrombocytopenia (ITP). Chronic ITP in Greek children is linked to older age, gradual onset, higher platelet counts, and immune markers, unlike newly diagnosed or persistent forms.
Area of Science:
- Pediatrics
- Hematology
- Immunology
Background:
- Immune thrombocytopenia (ITP) in children presents with varied clinical courses, categorized by duration: newly diagnosed (<3 months), persistent (3-12 months), and chronic (>12 months).
- Prognostic factors influencing ITP progression have been studied globally, but data specific to the Greek pediatric population was lacking.
Purpose of the Study:
- To identify prognostic markers differentiating the three forms of childhood ITP within a Greek cohort.
- To analyze clinical and immunological factors associated with disease course in pediatric ITP.
Main Methods:
- A retrospective analysis of 57 Greek children diagnosed with ITP over a 13-year period.
- Data collected included age, gender, preceding infections, bleeding patterns, symptom duration, platelet counts at diagnosis, treatment, disease course, and immunological markers.
Main Results:
- The study included 39 newly diagnosed, 4 persistent, and 14 chronic ITP cases.
- Children with chronic ITP were significantly older (>10 years), exhibited a gradual disease onset, had higher platelet counts (>10 × 10^9/L), and showed impaired immunological markers compared to newly diagnosed/persistent groups.
- A recent history of infection was more prevalent in the newly diagnosed/persistent ITP groups.
Conclusions:
- While childhood ITP generally follows a self-limited course with infrequent severe bleeding, the chronic form exhibits distinct predictive parameters.
- These identified prognostic markers for chronic ITP in children can potentially aid in clinical management and prediction.
Abstract:
Immune thrombocytopenia (ITP) in children has a varied course and according to duration is distinguished as newly diagnosed (<3 months), persistent (3-12), and chronic (>12) types. Several studies have evaluated the prognostic factors for the progression of the disease, but similar works have yet to be performed in Greece. We aimed to identify prognostic markers for the three forms of the disease in 57 Greek children during a 13-year period. Information regarding age, gender, preceding infection, bleeding type, duration of symptoms and platelets at diagnosis, treatment, disease course, and immunological markers was recorded. 39 children had newly diagnosed, 4 persistent, and 14 chronic disease. Chronic ITP children were more likely to be of age > 10 years (p = 0.015) and have gradual initiation of the disease (p = 0.001), platelets > 10 × 109/L (p = 0.01), and impaired immunological markers (p < 0.003) compared to newly diagnosed/persistent groups. Recent history of infection was found mainly in the newly diagnosed/persistent group (p = 0.013). None of the children exhibited severe spontaneous bleeding. Conclusion. Even though ITP in children usually has a self-limited course, with rare serious bleeding complications, the chronic form of the disease is characterized by different predictive parameters, which can be used in clinical practice.
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