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Case Studies
An Evaluation of Mepiform for the Management of Hypertrophic Scars

Louisiana State University Medical Center
Department of Rehabilitation and Regional Burn Center - Shreveport, LA

Scar Management and Reduction
with Tendra
Safetac Technology
by Mölnlycke







  • CASE STUDY #1

    •
        LW is a 32 year old female who had a partial liver resection for a large benign tumor. Initial scar assessment indicated height less than 2mm, vascularity was red with flexible pliability. Half the scar was treated with Mepiform and the remainder of the scar was not treated.

    After fourteen days of treatment the patient observed that the scar was becoming softer under Mepiform. On day 57, compression therapy was added to the scar regime. By day 84, scar vascularity changed from red to pink. LW noted the scar area treated with Mepiform felt smoother than the non-treated area. By day 112, the scar height decreased to Imm as compared to 2mm on the control site. Mepiform was rated positively for ease of application, repositioning and removal, overall appearance, quality, ability to cut the dressing and low dressing profile.

    The progress continued and by day 273 the patient reported that the scar's appearance continued to improve and the scar under Mepiform was smooth and moist. At day 360, it was noted the scar's vascularity was pink and normalizing.

    At the conclusion of the study, LW rated Mepiform's overall performance as good. The dressing exceeded expectations in the following areas: ease of application and removal, dressing appearance, quality, ability to reapply and reposition the dressing, dressing profile and color. The dressing met her expectations in the following areas: ability to use with a compression device, average dressing wear time (minimum of 3 days) and ability of the dressing to remain in place during activities of daily living.



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