
Platelet count remains the most objective measure of ITP severity and the efficacy of ITP treatment. However, with the exception of severe cases (counts below 10,000/µL), platelet counts may not tell the whole story. Most patients will do well if their platelet count remains over 30,000/µL. At that level, there is a minimal risk of bleeding and no demonstrated higher risk of mortality than in the general population.1
These questions merit further investigation:
As treatment options evolve and improve, therapeutic guidelines should be updated so that both physician and patient have a reasonable set of expectations about lifestyle, treatment, and the long-term approach to ITP.
References
1. Chong BH, Ho S-J. Autoimmune thrombocytopenia. J Thromb Haemost. 2005;3(8):1763-1772.
2. Cines DB, Blanchette VS. Immune thrombocytopenic purpura. N Engl J Med. 2002;346(13):995-1008.
3. Cines DB, Bussel JB. How I treat idiopathic thrombocytopenic purpura (ITP). Blood. 2005;106(7):2244-2251.