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      <abstract xml:lang="en">Patients, diagnosed with spondyloarthritis, were identified through the healthcare system in Region Scania between 2003-2007. The cohort responded to two questionnaires, 2009 and 2011. The first questionnaire was answered by 2785 respondents (48 %) and the second was answered by 2037 respondents (58 %). The questionnaires consisted of validated instruments as well as separate issues (for example patient characteristics, demographics, lifestyle, physical activity, fatigue and pain, health-related quality of life, depression and anxiety, self-efficacy, work and issues related to health economics).  Purpose:  The aim is to create a longitudinal cohort of patients with spondyloarthritis and study the consequences of the disease on individuals and society.</abstract><abstract xml:lang="sv">Patientkohorten identifierades genom att söka efter individer med minst en spondylartritrelaterad diagnos (ICD-10-kod) registrerad i Region Skånes vårddatabas mellan 2003 och 2007. Kohorten besvarade två postenkäter, genomförda 2009 och 2011. Den första enkäten sändes till patienter som var ≥18 år, bosatta i Skåne och i livet per maj 2009 (n=5771). Den besvarades av 2785 respondenter (48%). Den andra enkäten sändes ut 2,5 år efter den första. Den skickades till de patienter som fortfarande var bosatta i Skåne och i livet per november 2011 och som inte tackat nej till fortsatt medverkan i studien (n=3513). Den senare enkäten besvarades av 2037 respondenter (58%). Enkäterna bestod av validerade instrument (8 resp 12) liksom separata frågor och berörde bla patientegenskaper, demografi, livsstil, fysisk aktivitet, trötthet och smärta, hälsorelaterad livskvalitet, sjukdomsaktivitet coh fysisk funktion, depression och ångest, self-efficacy, arbetsförmåga och frågor relaterade till hälsoekonomi.  Syfte:  Syftet med studien är att skapa en longitudinell kohort bestående av patienter med spondylartrit och studera sjukdomens konsekvenser för individen och samhället.</abstract>
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