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Updated: Aug 2, 2025

The Goeckerman Regimen for the Treatment of Moderate to Severe Psoriasis
Published on: July 11, 2013
Clinical Unmet Needs and Treatment Patterns of Paediatric Psoriasis Patients: A Real-World Evidence Study in Spain
R de Lucas1, A Vicente2, C Richardson3
1Department of Dermatology, Universitary Hospital of La Paz, Madrid, España.
Insights
Real-world data on paediatric psoriasis (PsO) in Spain is scarce. This study reveals current treatment patterns and disease burden, highlighting needs for improved healthcare professional education and regional guidelines for managing paediatric psoriasis.
Area of Science:
- Dermatology
- Paediatric Medicine
- Real-World Evidence
Background:
- Limited real-world data exists for paediatric psoriasis (PsO) in Spain.
- Understanding the current disease burden and treatment landscape is crucial.
Purpose of the Study:
- To identify physician-reported disease burden in paediatric PsO patients in Spain.
- To analyze current treatment patterns for paediatric PsO in a real-world setting.
- To inform the development of regional guidelines for paediatric PsO management.
Main Methods:
- Retrospective analysis of a cross-sectional market research survey.
- Data collected from primary care and specialist physicians in Spain.
- Utilized the Adelphi Real World Paediatric PsO Disease-Specific Program (DSP™) data from Feb-Oct 2020.
Main Results:
- Data from 57 physicians and 378 paediatric PsO patients were analyzed.
- At sampling, 84.1% had mild, 15.3% moderate, and 0.5% severe PsO.
- Current treatments included topical therapies (89.3%), phototherapy (8.8%), conventional systemics (10.4%), and biologics (14.9%).
Conclusions:
- Real-world data confirms the current burden and treatment landscape of paediatric PsO in Spain.
- Improved management necessitates enhanced healthcare professional education.
- Development of regional guidelines is recommended for paediatric PsO care.
Background And Objective:
Real-world evidence of paediatric psoriasis (PsO) is lacking in Spain. The purpose of this study was to identify physician-reported disease burden and current treatment patterns in a real-world paediatric PsO patient cohort in Spain. This will enhance our understanding of the disease and contribute to the development of regional guidelines.
Material And Method:
This retrospective analysis of a cross-sectional market research survey assessed the clinical unmet needs and treatment patterns in patients with paediatric PsO in Spain, as reported by their primary care and specialist physicians, using data collected as part of the Adelphi Real World Paediatric PsO Disease-Specific Program (DSP™) between February and October 2020.
Results:
Survey data from 57 treating physicians were included (71.9% [N = 41] dermatologists, 17.6% [N = 10] general practitioners/primary care physicians, and 10.5% [N = 6] paediatricians); the final analysis included 378 patients. At sampling, 84.1% (318/378) of patients had mild disease, 15.3% (58/378) had moderate disease and 0.5% (2/378) had severe disease. Retrospectively reported physician-judged severity at the time of PsO diagnosis recorded 41.8% (158/378) of patients with mild disease, 51.3% (194/378) with moderate disease and 6.9% (26/378) with severe disease. Overall, 89.3% (335/375) of patients were currently receiving topical PsO therapy, while 8.8% (33/375), 10.4% (39/375) and 14.9% (56/375) of patients were currently receiving phototherapy, conventional systemics and biologics, respectively.
Conclusions:
These real-world data reflect the current burden and treatment landscape of paediatric PsO in Spain. The management of patients with paediatric PsO could be improved by further educating healthcare professionals and developing regional guidelines.
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