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Published by American Society of Hematology (ASH)
Immune Thrombocytopenia (ITP) is a rare autoimmune disorder where the immune system destroys platelets, causing significant bleeding episodes. The guidelines offer updated treatment evidence to optimize care and avoid unnecessary interventions, particularly in children.
Key Takeaways
Avoid unnecessary treatment in children, specifically interventions and treatments that have little evidence of success and may have side effects that outweigh potential benefits.
Keep the course of corticosteroid treatment as short as possible, as long-term corticosteroid use can cause harm without additional benefit.
Delay splenectomy for at least a year due to the life-long side effects that can result from the procedure.
When considering TPO-RAs and rituximab, consider differences in the route of administration, duration of disease, short versus long-term treatment, and patient co-morbidities to make the best choice for the individual patient.
Clinical Topic
Immune Thrombocytopenia
Objectives
Produce and maintain evidence-based guidelines that will support health care providers and patients in making the best care decisions.
Target Patient Population
Adults and children with Immune Thrombocytopenia (ITP)
Target Providers
Therapeutic Area
HematologyGuideline Scope
Special Populations
Monitoring Guidance
Provides guidance on how corticosteroid usage should be monitored.
Difficulty
intermediate
Learning Paths