Most childhood immune thrombocytopenic purpure is benign, self-limiting and requires no therapy. However, questions remain: (i) to treat or not; (ii) bone marrow examination or not; and (iii) admit to hospital or not. These questions have dominated the literature and we still need a prospective large multi-centre study of these issues to determine a useful bleeding score, quality of life measure and a measure of parental anxiety. © 2011 Paediatrics and Child Health Division (Royal Australasian College of Physicians).
CITATION STYLE
Cole, C. H. (2012, May). Rapid update on childhood immune thrombocytopenic purpure. Journal of Paediatrics and Child Health. https://doi.org/10.1111/j.1440-1754.2011.02207.x
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