Acta Dermato-Venereologica Suppl 219 AbstractPsoriasis2018 | Page 15

Poster abstracts 13 Results: Among respondents with PsO alone 38.9% had seen a dermatologist in the past year, and 10.7% had never seen a derma- tologist; 60.9% of those with PsA ± PsO had seen a rheumatologist in the past year; 14.3% had never seen a rheumatologist. Systemic treatments had been used by 14.6% of respondents with PsO alone and 58.5% with PsA ± PsO. Respondents with self-perceived severe symptoms and patient organization members (POMs) were more likely than those with non-severe symptoms or non-members, to have discussed systemic treatments with their physician and to have used the treatments; however, 35.2% of respondents with self-perceived severe symptoms had never discussed systemic treatment with their physician. Asked about long-term health risks of systemic treatments, 18–44 year-olds and POMs were less likely to answer “don’t know” than 45–74 year-olds (47.7%–49.1% vs 66.7%–72.9%) or non-members (26.1%–30.7% vs 66.8%–70.4%). Biologics had been used by 40.7% of POMs vs 6.9% of non- members, and 21.5% of 18–44 year-olds vs 8.1% of 45–74 year- olds. Among respondents using oral/injectable methotrexate 30.5% were dissatisfied, 60.2% citing side-effects as the reason; 22.9% of biologics users were dissatisfied, 28.9% citing lack of effect and 28.1% citing side-effects. Conclusion: In Scandinavia POMs and young patients are more likely to receive systemic treatment. A high proportion of patients are dissatisfied with their treatment because of side effects. a normal everyday life (83%), and needing less time for daily treatment (80%). Based on a clinically meaningful PBI score ≥1, 78% of pts achieved a benefit with APR after 6 mo. Mean (SD) PBI score was 2.2 (1.3) and increased to 2.5 (1.2) for pts on continued APR at 6 mo vs 1.6 (1.3) for pts who discontinued APR. Pts achieved benefit related to skin involvement (60%), confidence in healing (70%), itch (69%), side effects (60%), be- ing able to lead a normal everyday life (72%), and needing less time for daily treatment (65%). Consistent with phase 3 studies, most frequently reported AEs were diarrhea (19.2%), nausea (16.4%), and headache (11.5%); 25% of pts reported weight loss (no change, 71%; gain, 4%). Conclusions: This interim analysis indicates main pt needs from a therapy extend beyond skin improvement. Findings indicate APR may address diverse pt needs. P024 Dermatologikum Hamburg and SCIderm Research Institute, Hamburg, Praxis Dr. med. S. Rotterdam, Gelsenkirchen-Feldmark, 3 Priv. Doz. Dr. med. Korge, Düren, 4 Derma Nord Hautarztpraxen Dr. med. Schwichten- berg, Bremen, 5 Celgene GmbH, Munich, Germany FIRST PATIENT-REPORTED INSIGHTS FROM A MULTINATIONAL, RETROSPECTIVE, CROSS- SECTIONAL STUDY OF REAL-WORLD EXPERIENCE OF PSORIASIS PATIENTS TREATED WITH APREMILAST IN CLINICAL DERMATOLOGY PRACTICE (APPRECIATE) Matthias Augustin 1 , Marc Alexander Radtke 1 , Kilian Eyerich 2 , Mona Ståhle 3 , Christine Bundy 4 , Myriam Cordey 5 , Volker Kosci- elny 5 , C. Elise Kleyn 6 , Christopher EM Griffiths 6 Institute for Health Services Research in Dermatology and Nursing, University Medical Center Hamburg-Eppendorf, Hamburg, 2 Department of Dermatology and Allergy, Technical University of Munich, Munich, Germany, 3 Department of Medicine, Karolinska Institute, Solna, Sweden, 4 School of Healthcare Sciences, College of Biomedical and Life Sciences, Cardiff University, Cardiff, UK, 5 Celgene International, Boudry, Switzer- land, 6 Dermatology Centre, Salford Royal NHS Foundation Trust, Univer- sity of Manchester, Manchester Academic Health Science Centre, Man- chester, UK 1 Introduction: Patient (pt)-centered care is gaining traction in long-term disease management. We report on a multinational, retrospective, cross-sectional study in psoriasis pts treated with apremilast (APR), an oral phosphodiesterase 4 inhibitor, in a real- world clinical setting. Objectives: The study aims to identify important pt needs and therapeutic benefits of APR. Methods: Consecutive pts with chronic plaque psoriasis treated according to routine clinical practice who could be contacted 6 ± 1 mo after APR initiation were enrolled. Medical chart review, standardized pt-reported outcome tools (PBI, TSQM-9), and pt/ physician questionnaires were used. An interim analysis of the first 104 pts from 40 sites in Germany (42), UK (31), and Sweden (31) was performed using predefined descriptive statistics. Results: 102 pt questionnaires were analyzed (98%). At 6 ± 1 mo, 74 pts (71%) continued APR; 30 (29%) had discontinued APR (lack of efficacy [14%], safety/tolerability [11%], other [4%]). Assessment of pts’ main needs from a therapy (quite/very im- portant on the PBI) revealed the importance pts attributed to skin involvement (93% of responders), confidence in healing (92%), being itch free (85%), fewer side effects (84%), being able to lead Prior Presentation: EADV 2017 P025 PHYSICIAN- AND PATIENT-REPORTED OUTCOMES WITH APREMILAST FOR PATIENTS WITH PLAQUE PSORIASIS DURING ROUTINE DERMATOLOGY CARE IN GERMANY: A SECOND INTERIM ANALYSIS Kristian Reich 1 , Stefanie Bomas 2 , Bernhard Korge 3 , Uwe Schwich- tenberg 4 , Hannah Mentz 5 , Kathrin Groegel 5 , Natalie Núnez Gómez 5 1 2 Introduction: LAPIS-PSO is an ongoing, 52-week, prospective, multicenter, observational cohort study in real-world dermatology clinical settings in Germany. Objectives: To present a 4-month interim analysis of patient (pt)- reported outcomes and efficacy assessments of apremilast (APR) among pts (n = 294; full analysis set [FAS], n = 1