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KECORT Study: An International e-Delphi Study on the Treatment of KEloids Using Intralesional CORTicosteroids in
Qi Yin1, Albert Wolkerstorfer2, Oren Lapid3,4,5
1Department of Dermatology, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, 1100 DD, Amsterdam, The Netherlands. q.yin@amsterdamumc.nl.
Intralesional corticosteroid administration (ICA) for keloids shows practice variability. This study established consensus on key ICA aspects, aiming to standardize treatment and improve outcomes for keloid patients.
Area of Science:
- Dermatology
- Plastic Surgery
- Wound Healing
Background:
- Intralesional corticosteroid administration (ICA) is a primary treatment for keloids.
- Significant variability exists in current ICA clinical practices, hindering treatment result comparisons.
Purpose of the Study:
- To achieve international expert consensus on intralesional corticosteroid administration (ICA) for keloid treatment.
- To develop evidence-based clinical recommendations for physicians managing keloids.
Main Methods:
- An international panel of 23 dermatologists and plastic surgeons specialized in keloid treatment participated.
- A two-round online e-Delphi survey was conducted, followed by consensus meetings.
- Consensus was defined as agreement by at least 75% of participants.
Main Results:
- Consensus was achieved on treatment goals, indications, preferred corticosteroid (triamcinolone acetonide 40 mg/mL), maximum dosage (80 mg/month), injection intervals (4 weeks), pain minimization, syringe/needle size (1 mL, 25/27G), endpoint (blanching), and technique (avoiding subcutaneous injection, multiple passes for firm keloids).
- Areas without consensus included specific dosing, local anesthesia methods, and injection sites.
Conclusions:
- This e-Delphi study provides crucial clinical recommendations for ICA in keloid management.
- Implementing these consensus-based guidelines can enhance treatment uniformity and potentially improve keloid treatment outcomes.
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