Microcrystalline cellulose membrane for re‐epithelisation of chronic leg wounds: a prospective open study
Identifieur interne : 005C64 ( Main/Exploration ); précédent : 005C63; suivant : 005C65Microcrystalline cellulose membrane for re‐epithelisation of chronic leg wounds: a prospective open study
Auteurs : Elia B. Ricci [Italie] ; Roberto Cassino [Italie] ; Cristiana Di Campli [Italie]Source :
- International Wound Journal [ 1742-4801 ] ; 2010-12.
Abstract
Treatment of chronic leg ulcers remains a major health care issue. Although many reports have examined different topical dressings, none have specifically looked at microcrystalline cellulose (MCC). We aimed to evaluate in a prospective, open study the safety and performance of a MCC membrane (Veloderm) in a series of chronic leg wounds of different aetiology. Fifty‐five patients participated in this study. The membrane was applied every 5–10 days for 1 month, immediately after surgical debridement. The wound bed was assessed on days 7, 15 and 30 for erythema, pain, exudate level and infection. The wound size change at 30 days was the primary efficacy parameter and any adverse events were collected and analysed. A wound size change of 55% was achieved at the end of follow‐up, with an improvement in all the collected parameters, but the erythema, which showed a mild increase. To date, this is the largest experience with a MCC product in chronic wounds. Our study suggests that this treatment may be safe and useful and deserves further investigation.
Url:
DOI: 10.1111/j.1742-481X.2010.00707.x
Affiliations:
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Although many reports have examined different topical dressings, none have specifically looked at microcrystalline cellulose (MCC). We aimed to evaluate in a prospective, open study the safety and performance of a MCC membrane (Veloderm) in a series of chronic leg wounds of different aetiology. Fifty‐five patients participated in this study. The membrane was applied every 5–10 days for 1 month, immediately after surgical debridement. The wound bed was assessed on days 7, 15 and 30 for erythema, pain, exudate level and infection. The wound size change at 30 days was the primary efficacy parameter and any adverse events were collected and analysed. A wound size change of 55% was achieved at the end of follow‐up, with an improvement in all the collected parameters, but the erythema, which showed a mild increase. To date, this is the largest experience with a MCC product in chronic wounds. Our study suggests that this treatment may be safe and useful and deserves further investigation.</div></front></TEI><affiliations><list><country><li>Italie</li></country><region><li>Latium</li><li>Piémont</li></region><settlement><li>Rome</li><li>Turin</li></settlement></list><tree><country name="Italie"><region name="Piémont"><name sortKey="Ricci, Elia B" sort="Ricci, Elia B" uniqKey="Ricci E" first="Elia B" last="Ricci">Elia B. Ricci</name></region><name sortKey="Cassino, Roberto" sort="Cassino, Roberto" uniqKey="Cassino R" first="Roberto" last="Cassino">Roberto Cassino</name><name sortKey="Di Campli, Cristiana" sort="Di Campli, Cristiana" uniqKey="Di Campli C" first="Cristiana" last="Di Campli">Cristiana Di Campli</name><name sortKey="Di Campli, Cristiana" sort="Di Campli, Cristiana" uniqKey="Di Campli C" first="Cristiana" last="Di Campli">Cristiana Di Campli</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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