Objective: It was the objective of this product evaluation to assess peristomal skin health in the presence of a ceramide infused skin barrier.
Results: Of interest was the condition of peristomal skin prior to the use of ceramide infused skin barriers, and after. Peristomal skin condition was assessed using the Skin Assessment Tool1 (DET; scale = 0-15), and categorized according to Meisner2 as mild skin (<4), moderate (≥ 4 and < 7), and severe (≥ 7). The data indicates that of 66 ostomy patients assessed as having a severe peristomal skin condition prior to the use of ceramide infused skin barriers, 52% were assessed as having mild peristomal skin and 24% were assessed as having moderate peristomal skin condition after the use of ceramide infused skin barriers (24% remained unchanged). The data also indicates that of 78 patients assessed with a moderate peristomal skin condition prior to the use of ceramide infused, 74% were assessed as having mild peristomal skin condition after the use of ceramide infused skin barriers (22% remained the same).
For those patients in which skin conditions improved an approximate 1 day longer product wear time was observed, while the use of topical medications and accessories were indicated as having been reduced in 37% of patients and 48% of patients respectively.
Conclusions: In this product evaluation improvements in peristomal skin condition were associated with the use of a ceramide infused skin barrier.