Risk and prognosis of adult primary immune thrombocytopenia.

Abstract:

:Adult immune thrombocytopenia was previously considered a benign disease affecting young people and with a low risk of severe bleeding. This view was challenged by studies published during the past decade, as the median age of adult immune thrombocytopenia patients has been found to be 55-60 years and the incidence increases with age. Recent studies reported that mortality and morbidity are increased compared with the general population. In this review, we describe patient-specific factors associated with the outcome of disease, the clinical course of immune thrombocytopenia including the potential adverse impact of some treatments and finally the overall prognosis.

journal_name

Expert Rev Hematol

authors

Frederiksen H,Christiansen CF,Nørgaard M

doi

10.1586/ehm.12.7

subject

Has Abstract

pub_date

2012-04-01 00:00:00

pages

219-28

issue

2

eissn

1747-4086

issn

1747-4094

journal_volume

5

pub_type

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