autoimmune thrombocytopenic purpura: An autoimmune disorder in which the number of circulating platelets is reduced due to their antibody-mediated destruction. ITP is a diagnosis of exclusion and is heterogeneous in origin.
| Name | D3_ITP |
|---|---|
| Long name | Idiopathic thrombocytopenic purpura |
| Hospital Discharge registry | ICD-10: D693, ICD-9: 2873A, ICD-8: 28710 |
| Cause of Death registry | ICD-10: D693, ICD-9: 2873A, ICD-8: 28710 |
| Level in the ICD-hierarchy | 4 |
| First defined in version | DF2 |
| Latin name | Purpura idiopathica thrombocytopenica |
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 394 | 208 | 186 |
| Unadjusted prevalence (%) | 0.18 | 0.17 | 0.20 |
| Mean age at first event (years) | 48.41 | 44.08 | 53.26 |
| Case fatality at 5-years (%) | 5.58 | 2.88 | 8.60 |
| All | Female | Male | |
|---|---|---|---|
| Median nb. of events per indiv. | 2.0 | 2.0 | 2.0 |
| Recurrence at 6 months (%) | 53.05 | 52.88 | 53.23 |
before Idiopathic thrombocytopenic purpura
after Idiopathic thrombocytopenic purpura
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