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.
Filter registries Inpat., Oupat., Death
Check pre-conditions None
Include endpoints None
Check conditions None
Apply sex-specific rule None
D3_ITP
Extra metadata
List of similar endpoints to
Idiopathic thrombocytopenic purpura
based on the number of shared cases.
Broader endpoints:
Narrower endpoints:
None
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 494 | 263 | 231 |
| Unadjusted prevalence (%) | 0.19 | 0.18 | 0.20 |
| Mean age at first event (years) | 48.32 | 42.99 | 54.39 |
| Follow-up | Absolute risk | HR [95% CI] | p | N |
|---|---|---|---|---|
| 1998–2019 | 0.04 | 3.04 [1.43, 6.47] | 3.8e-3 | 68 |
| 15 years | 0.02 | 3.65 [1.85, 7.19] | 1.9e-4 | 58 |
| 5 years | 0.01 | 7.69 [4.36, 13.56] | 1.8e-12 | 33 |
| 1 year | - | - | - | - |
Index endpoint: D3_ITP – Idiopathic thrombocytopenic purpura
GWS hits: 0
before Idiopathic thrombocytopenic purpura
after Idiopathic thrombocytopenic purpura
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