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Review of European registries for psoriasis
Mina Amin1, Erica B Lee2, Tina Bhutani3
1a Department of Medicine , Kaiser Permanente Los Angeles Medical Center , Los Angeles , CA , USA.
Background:
Patient registries are databases that contain clinical data for patients with a specific disease or medical condition.
Objective:
The purpose was to identify psoriasis registries in Europe and examine their characteristics and implications.
Methods:
We searched Google, the Registry of Patient Registries, and ClinicalTrials.gov to generate a list of European psoriasis registries. We also conducted a literature review for publications related to the psoriasis registries in Europe using PubMed.
Results:
We identified 13 psoriasis patient registries in Europe.
Conclusions:
Patient registries are routinely used in dermatology and psoriasis registries offer pertinent long-term safety information regarding conventional systemic therapies and biologic agents for psoriasis.
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