Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12530/19948
Title: Sjögren SER: National registry of the Spanish Society of Rheumatology of patients with primary Sjögren syndrome: Objectives and methodology.
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Issue Date: Jul-2016
Citation: Reumatol Clin.;(12)4:184-9
Abstract: To describe the objectives and methods of the Spanish Society of Rheumatology primary Sjögren syndrome (pSS) registry (SJOGREN-SER) METHODS: This is a multicenter descriptive transversal study of a cohort of pSS patients fulfilling European/American consensus criteria collected from Rheumatology clinics all over Spain. Patients were included by randomisation from an anonymised list provided by every department. Data were collected by reviewing clinical records and an interviewing the patients. Two hundred and ninety eight variables were investigated: epidemiological, clinical, serological characteristics, treatments and complications. Informed consent was obtained and local ethics committees approved the study. Variables were analysed by descriptive statistical methods, using means, medians, and rates, with their deviations and interquartile ranges (p25-p75).
PMID: 26617051
URI: https://hdl.handle.net/20.500.12530/19948
Appears in Collections:Hospitales > H. U. Infanta Sofía > Artículos

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