Wilson's disease is an inherited autosomal recessive disorder of copper balance leading to accumulation of copper mainly in liver and

BackgroundThere are few recent large cohort epidemiological studies that analyse the clinical profile of patients with psoriatic arthritis (PsA) who require biological treatment, as well as pharmacological survival and reasons for the suspension of these treatments.Abstract AB0900 – Table 1N383Basal radiological involvement Age at PsA (years), mean (SD)45.9 (14.5)Erosive arthritis (%)33.1 Male sex, n (%)203 (53)Mutilating arthritis (%)1.9History of psoriasis (%)84.8Sacroiliitis (%)21.2Nail involvement (%)46.3Syndesmophytes (%)5Dactylitis (%)32.9ImmunityEnthesitis (%)36.9RF positive (%)6.3DAS-28 (ESR), mean (SD)3.5 (1.46)ANA positive (%)14.5CRP mg/L, mean (SD)8.11 (15.9)HLA B27 positive (%)14.1ESR mm/h, mean (SD)20.3 (19.2)TreatmentComorbiditiesNSAID (%)96.7Dyslipidemia (%)34.2csDMARDs (%)84.8AH (%)20.9bDMARDs (%)32.3Obesity (%)28.2CRP: C-reactive protein; ESR: erythrocyte sedimentation rate; AH: arterial hypertension; RF rheumatoid factor; ANA: anti-nucleotide antibodies; NSAID: non-steroidal anti-inflammatory drugs; csDMARDs: conventional synthetic disease-modifying antirheumatic drugs; bDMARDs: biological disease-modifying antirheumatic drugs.ObjectivesTo describe the clinical, demographic, epidemiological and radiographic characteristics of patients with PsA in our centre, as well as pharmacological survival and reasons for the suspension of different biological treatments.MethodsRetrospective analysis of patients with PsA treated between 1985 and 2015 at a University Hospital with a referral area of 8 50 000 inhabitants. Demographic, clinical, laboratory and imaging data, as well as patients’ clinical and medical treatment records.ResultsThe main characteristics of the cohort are summarised in table 1:Approximately one third of patients with PsA (32.3%) required treatment with a biological drug during the course of their disease. The most frequently prescribed first-line drugs (89.5%) were tumour necrosis factor-α inhibitors (TNFi).During the course of their disease, 27 (21.9%) patients who started biological treatment received a biological drug other than TNFi. Of the 124 patients who started treatment with a biological DMARD, more than half (65, 52.8%) required a change to a second drug, and of these, 27 (41.5%) changed to a third, with up to 7 different biological drugs required in one case. The mean survival time for the first bDMARD was 42.8±42.3 months, with secondary failure the most frequent cause of treatment change (37.8%), followed by adverse effects (27.1%) and primary failure (18.9%). The adverse effects registered were: 20% infections, 20% appearance of neoplasms, 5% allergic reactions and 55% other causes.ConclusionsPsA presents a similar distribution by sex and is usually diagnosed at around the age of 50, having been preceded by cutaneous involvement. PsA is an entity of considerable severity and up to a third of patients will require biological treatments during its evolution. More than half of them will receive a second biological treatment. The retention rate of each drug varies but tends t...