Prevention of Peritendinous Adhesions Using an Electrospun DegraPol Polymer Tube : A Histological, Ultrasonographic, and Biomechanical Study in Rabbits

Purpose. One of the great challenges in surgical tendon rupture repair is to minimize peritendinous adhesions. In order to reduce adhesion formation, a physical barrier was applied to a sutured rabbit Achilles tendon, with two different immobilization protocols used postoperatively. Methods. Thirty...

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Veröffentlicht in:BioMed research international 2014-01, Vol.2014 (2014), p.1-11
Hauptverfasser: Meier Bürgisser, Gabriella, Calcagni, Maurizio, Müller, Angela, Bonavoglia, Eliana, Fessel, Gion, Snedeker, Jess G., Giovanoli, Pietro, Buschmann, Johanna
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Sprache:eng
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Zusammenfassung:Purpose. One of the great challenges in surgical tendon rupture repair is to minimize peritendinous adhesions. In order to reduce adhesion formation, a physical barrier was applied to a sutured rabbit Achilles tendon, with two different immobilization protocols used postoperatively. Methods. Thirty New Zealand white rabbits received a laceration on the Achilles tendon, sutured with a 4-strand Becker suture, and half of the rabbits got a DegraPol tube at the repair site. While fifteen rabbits had their treated hind leg in a 180° stretched position during 6 weeks (adhesion provoking immobilization), the other fifteen rabbits were recasted with a 150° position after 3 weeks (adhesion inhibiting immobilization). Adhesion extent was analysed macroscopically, via ultrasound and histology. Inflammation was determined histologically. Biomechanical properties were analysed. Results. Application of a DegraPol tube reduced adhesion formation by approximately 20%—independently of the immobilization protocol. Biomechanical properties of extracted specimen were not affected by the tube application. There was no serious inflammatory reaction towards the implant material. Conclusions. Implantation of a DegraPol tube tightly set around a sutured tendon acts as a beneficial physical barrier and prevents adhesion formation significantly—without affecting the tendon healing process.
ISSN:2314-6133
2314-6141
DOI:10.1155/2014/656240