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Precision Implementation of Minimal Erythema Dose MED Testing to Assess Individual Variation in Human Inflammatory Response
Published on: October 3, 2019
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Equipment developed for simplifying routine phototesting in dermatology
Hans Christian Wulf1, Jakob Heydenreich2, Peter Alshede Philipsen2
1Department of Dermatology, Copenhagen University Hospital-Bispebjerg and Frederiksberg, Nielsine Nielsens Vej 9, Entrance 4, 2400, Copenhagen, Denmark. h.wulf@regionh.dk.
Summary
A new MED Test Patch and solar simulator improve photosensitivity testing. This standardized method enhances accuracy for diagnosing abnormal skin reactions to ultraviolet radiation (UVR).
Area of Science:
- Dermatology
- Photobiology
- Medical Device Development
Background:
- Photosensitivity causes abnormal skin reactions like burns or rashes upon UVR exposure.
- Current minimal erythema dose (MED) testing faces challenges with skin area selection, patient movement, and clear erythema border definition.
Purpose of the Study:
- To develop and evaluate a novel MED Test Patch and associated solar simulator for improved photosensitivity assessment.
- To address limitations in current MED testing procedures for enhanced accuracy and standardization.
Main Methods:
- Development of a MED Test Patch with six irradiation fields and 20% decremental UVR doses.
- Construction of a solar simulator with LED lamps (309 nm, 370 nm, 415 nm) for MED and photoprovocation testing.
- Utilizing the back for testing due to assumed uniform UVR sensitivity and ample space.
Main Results:
- The MED Test Patch ensures sharp erythema borders and accommodates patient movement.
- The system allows for simultaneous MED and photoprovocation testing.
- UVA and UVB MED tests can be completed within 1 hour, improving efficiency.
Conclusions:
- The developed MED Test Patch and solar simulator offer an easy-to-use, standardized method for photosensitivity testing.
- This innovative approach significantly improves the accuracy of MED determination and photoprovocation tests.
- The advancements facilitate more reliable diagnosis of abnormal skin reactions to UVR.

