Publikationen

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2023

Disease burden and patient needs in women of childbearing age with psoriasis: a comparative study with same-age men and older women using data from the German PsoBest registries

N. da Silva

52. Jahrestagung der Deutschen Dermatologischen Gesellschaft (DDG-Tagung), Berlin, Germany (Oral presentation): ID FV01/04

Predictors of and Interventions Against Self Stigmatisation Results of Two Systematic Reviews

J. Traxler, CFZ. Stuhlmann, V. Paucke, L. Westphal, H. Graf, R. Sommer

Poster presented at the EADV Congress 2023, Berlin, Germany.

Patient-reported Well-being in Value-based Care Using Tildrakizumab in a Real-world Setting: Protocol of a Multinational, Phase IV, 1-cohort Prospective Observational Study (the POSITIVE Study)

M. Augustin, R. Sommer, E. Daudén, P. Laws, E. de Jong, G. Fabbrocini, L. Naldi, A. Navarini, J. Lambert, Z. Reguiai, S. Gerdes, E. Massana, T. Obis, I. Kasujee & U. Mrowietz

Psoriasis is a chronic inflammatory skin disease that negatively impacts the quality of life of patients and their families. However, the most commonly used decision-making tools in psoriasis, Psoriasis Area and Severity Index (PASI), Physician Global Assessment (PGA) and Dermatology Life Quality Index (DLQI), do not fully capture the impact of psoriasis on patients' lives. In contrast, the well-established 5-item WHO Well-being Index (WHO-5) assesses the subjective psychological well-being of patients. Moreover, while drug innovations became available for psoriasis, data on the impact of these therapies on patients' lives and their closest environment (family, physicians) are limited. This study will assess the effect of tildrakizumab, an interleukin-23p19 inhibitor, on the overall well-being of patients with moderate-to-severe psoriasis. Moreover, the long-term benefit of tildrakizumab on physicians' satisfaction and partners' lives of patients with psoriasis will be evaluated.

Development of Measurement Tools to Assess Cumulative Life Course Impairment in Patients with Chronic Skin Diseases

C.C. Braren-von Stülpnagel, M. Augustin, L. Westphal & R. Sommer

Patients with chronic skin diseases suffer from physical, psychological, emotional and social impairments. The overall burden has significant impact on patients' life, contributing to irreversible damage across many domains, known as cumulative life course impairment (CLCI). The aim of this project was to develop instruments which (a) measure persisting CLCI and (b) identify patients at risk for developing future CLCI.

Psychosocial health and quality of life in ICSI and naturally conceived adolescents: a cross-sectional comparison

N. Eisemann, M. Schnoor, E. Rakuska, C.C. Braren-von Stülpnagel, A. Katalinic, M. Ludwig, B. Sonntag, A.K. Ludwig & S.A. Elsner

Psychosocial health and quality of life in ICSI and naturally conceived adolescents: a cross-sectional comparison