Use of a hydrocapillary dressing in the management of highly exuding ulcers: a comparative study
Autor: | M A de Mena, A Svensson, Vytautas Dargis, N Serra, I Moll, J K Thomsen, N Ivins, K Carter, A Hauschild, A Norkus, Finn Gottrup, O G Torres de Castro, J L Blanco, Jytte Roed-Petersen, Keith G Harding, A Galindo, Klaus Ejner Andersen |
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Rok vydání: | 2005 |
Předmět: |
Adult
Male medicine.medical_specialty Nursing (miscellaneous) Healing time Patient satisfaction Hypersensitivity Humans Medicine Aged Aged 80 and over integumentary system business.industry Leg Ulcer Significant difference Exudates and Transudates Middle Aged equipment and supplies Surgery Clinical trial Treatment Outcome Leg ulcer Wound area Erythema Patient Satisfaction Quality of Life Absorption capacity Female Fundamentals and skills business human activities Ankle–brachial pressure index Bandages Hydrocolloid |
Zdroj: | Norkus, A, Dargis, V, Thomsen, J K, Harding, K G, Ivins, N, Serra, N, Torres de Castro, O G, Galindo, A, Andersen, K E, Roed-Petersen, J, Gottrup, F, Blanco, J L, de Mena, M A, Hauschild, A, Moll, I, Svenson, A & Carter, K 2005, ' Use of hydrocapillary dressing in the management of highly exuding ulcers : a comparative study. ', Journal of Wound Care, vol. 14, no. 9, pp. 429-432 . https://doi.org/10.12968/jowc.2005.14.9.26837 |
ISSN: | 2052-2916 0969-0700 |
Popis: | Objective: To evaluate the safety and performance of Alione Hydrocapillary dressing (Coloplast A/S) in the management of highly exuding chronic venous leg ulcers and compare it with two hydropolymer dressings, Tielle and Tielle Plus (Johnson & Johnson). Method: A comparative clinical trial was conducted on 97 patients with an ankle brachial pressure index ≥0.8 and a highly exuding leg ulcer. Ulcer duration was at least four weeks. Treatment continued until healing or for a maximum of 12 months. Results: There was no statistically significant difference in healing time or wound area reduction between the two treatment protocols. The test dressing (Alione Hydrocapillary) had better absorption capacity and was more comfortable for the patients than the comparator dressings (Tielle/Tielle Plus) and adhered less to the wound bed. Also, more patients preferred the test dressing to their previous treatment. Although severe leakage and maceration were observed more frequently in the comparator group compared with the test group, this was not statistically significant. Conclusion: Both treatment protocols were safe and effective in treating highly exuding chronic venous leg ulcers. The test dressing performed as well as or better than the comparator dressings for all study parameters and more patients preferred the test dressing to their previous dressing compared with the comparator dressings. Declaration of interest: The study was funded by Coloplast A/S, Humlebaek, Denmark. |
Databáze: | OpenAIRE |
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