SYSTSCLE_STRICT
scleroderma: Scleroderma is a rare autoimmune connective tissue disorder characterized by abnormal hardening of the skin and, sometimes, other organs. It is classified into two main forms: localized scleroderma and systemic sclerosis (SSc), the latter comprising three subsets; diffuse cutaneous SSc (dcSSc), limited cutaneous SSc (lcSSc) and limited SSc (lSSc) (see these terms).
321302 individuals
Apply sex-specific rule None
321302
Check conditions
485
Check pre-conditions, main-only, mode, ICD version None
171
Check minimum number of events None
171
Include endpoints None
171
Extra metadata
List of similar endpoints to
Systemic sclerosis,strict definition
based on the number of shared cases.
Broader endpoints:
Narrower endpoints:
None
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 164 | 144 | 20 |
| Unadjusted prevalence (%) | 0.05 | 0.08 | 0.01 |
| Mean age at first event (years) | 54.49 | 54.36 | 55.44 |
| Follow-up | Absolute risk | HR [95% CI] | p | N |
|---|---|---|---|---|
| 1998–2019 | - | - | - | - |
| 15 years | - | - | - | - |
| 5 years | - | - | - | - |
| 1 year | - | - | - | - |
Index endpoint: SYSTSCLE_STRICT – Systemic sclerosis,strict definition
GWS hits:
before Systemic sclerosis,strict definition
after Systemic sclerosis,strict definition
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