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    Plast Reconstr Surg. 2008 Mar;121(3):781-93.

    A novel biomimetic material for engineering postsurgical adhesion using the injured digital flexor tendon-synovial complex as an in vivo model.

    Branford OA, Mudera V, Brown RA, McGrouther DA, Grobbelaar AO.

    RAFT, Mount Vernon Hospital, Northwood, Middlesex HA6 2RN, United Kingdom. olivier.branford@totalise.co.uk

    BACKGROUND: Many surgical procedures are complicated by adhesions. These restrictive fibrotic bands form between normally separate gliding tissue layers, potentially impairing function. The authors tested the adhesion-modifying effect of a novel fibronectin-derived biomimetic biomaterial in a tendon-synovial complex injury model. METHODS: The deep flexor tendons of digits 2 and 4 in the right forepaw of 15 New Zealand White rabbits were subjected to 5-mm-long partial tenotomies. Animals were randomized to receive biomaterial tubes enveloping the tendon injuries or left untreated. Digits, amputated at 2 weeks, were randomized to mechanical pullout assessments of adhesion strength or to quantitative histologic cellularity and immunohistochemical proliferation (Ki67) assessments. RESULTS: The mean peak pullout force required to break the adhesions was reduced from 7.70 N (n = 6) in untreated digits to 0.31 N (n = 7) in biomaterial-treated digits (p = 0.001). The mean structural stiffness of the adhesions was also significantly reduced (p = 0.001). Histologically, treated and untreated digits demonstrated an equal incidence of adhesions. The treated adhesions were 55 percent less cellular at their surface than the untreated injured controls (p = 0.003). Treated tendons were 8 percent more cellular (with equal numbers of proliferating cells) at their surface and significantly more cellular within their bulk than positive controls (p <or= 0.05). CONCLUSION: This study suggests a significant reduction in the restrictive nature of postsurgical adhesions following treatment with the antiadhesive biomaterial without compromising tendon cellularity.

    PMID: 18317128 [PubMed - indexed for MEDLINE]

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