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Immune thrombocytopenia (ITP) is an acquired immune- Nugent, 2006; Psaila & Bussel, 2007; Glanz et al, 2008). Under-
mediated disorder characterized by low blood platelet counts diagnosis may be particularly common among children as
(<150 · 109/l), or thrombocytopenia (Rodeghiero, 2003). The episodes of ITP tend to be of shorter duration.
course of ITP can be acute, (i.e. spontaneously resolving within It has been suggested that childhood ITP may be a distinct
a few months), persistent, (i.e. of 3–12 months duration), or entity from adult ITP, as a low proportion of paediatric cases
chronic (i.e. lasting ‡12 months) Rodeghiero, 2009. ITP in has chronic disease and incidence distribution between genders
children is usually short-lived, with the onset typically being is similar among children. This is in contrast to adult ITP,
acute and frequently occurring a few days or weeks after viral where the majority of cases has a chronic form of ITP with
infection or vaccination (Cines & Blanchette, 2002; Nugent, more women affected than men (Cines & Blanchette, 2002).
2006; Psaila & Bussel, 2007; Le Meignen et al, 2008). We have previously described the sex- and age-specific
The diagnosis of ITP is made by excluding other causes of incidence estimates of ITP using the large United Kingdom
thrombocytopenia. The basic diagnostic approach to ITP (UK) population-based General Practice Research Database
includes a patient history, physical examination, complete (GPRD) (Schoonen et al, 2009). Here we provide a more
blood count, and examination of a peripheral blood smear detailed description of the incidence estimates of paediatric
(Provan & Newland, 2002). In children, two-thirds of patients ITP and directly compare these to incidence estimates of adult
have been reported to recover within 6 months and to improve ITP from the same database. We also examined prior
spontaneously with no specific treatment (Kuhne et al, 2001; infections and immunizations, the platelet count distribution