Collected Dataset / SSCS_pSS_Followup 9

The population is composed of adult patients with primary Sjoegren's syndrome from 8 different Swiss hospitals.

Information on patient’s age, sex, ethnicity, educational status, tobacco use, body mass index (BMI), disease duration since diagnosis, disease activity using the Physician's Global Assessment score (PGA) and damage, and treatment modalities were collected during the medical visit. Data on health-related quality of life (HRQoL) and fatigue were or will be assessed with the Short Form 36 (SF36) and the Fatigue Assessment Scale (FAS). Blood and urine samples were or will be collected.