Arthroscopy: The Journal of Arthroscopic and Related Surgery
Volume 22, Issue 7 , Pages 700-709, July 2006

Rotator Cuff Repair Using an Acellular Dermal Matrix Graft: An In Vivo Study in a Canine Model

  • Julie E. Adams, M.D.

      Affiliations

    • Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, U.S.A.
  • ,
  • Mark E. Zobitz, M.S.

      Affiliations

    • Biomechanics Laboratory, Mayo Clinic, Rochester, Minnesota, U.S.A.
  • ,
  • John S. Reach Jr, M.D.

      Affiliations

    • Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, U.S.A.
  • ,
  • Kai-Nan An, Ph.D.

      Affiliations

    • Biomechanics Laboratory, Mayo Clinic, Rochester, Minnesota, U.S.A.
  • ,
  • Scott P. Steinmann, M.D.

      Affiliations

    • Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, U.S.A.
    • Corresponding Author InformationAddress correspondence and reprint requests to Scott P. Steinmann, M.D., Department of Orthopedic Surgery, Mayo Clinic, E14 Mayo Building, 200 First St SW, Rochester, Minnesota 55905, U.S.A.

Purpose: Large rotator cuff tears present a challenge to orthopaedic surgeons. Because tissue may be insufficient or of inadequate quality to undergo repair, a variety of materials have been used as adjuncts. Human dermal tissue may be processed to render it acellular, and thus less immunogenic, but with the extracellular matrix left intact, creating a collagen scaffold with favorable characteristics. Because of these traits, use in rotator cuff repair was proposed. Methods: A canine model for a full-thickness infraspinatus tendon tear was used. Tendon was excised from the bony interface to the myotendinous junction, and a human acellular dermal matrix graft (experimental) or the autologous excised tendon (control) was used to bridge the defect. Animals were sacrificed, and shoulders were evaluated histologically and biomechanically. Results: At time 0, strength of control and experimental repairs was similar. At 6 weeks, the strength of the experimental repair was half that of the control side. Strength of control specimens remained the same at 6 and 12 weeks, but by 12 weeks, the strength of the experimental repair was equal to that of the control. Histologically, cells infiltrated the control and experimental specimens by 6 weeks; chronic inflammation was consistent with surgery and repair. At 6 months, control and experimental specimens mimicked normal tendon structure grossly and histologically. Conclusions: Use of human acellular dermal matrix as a patch is a viable option in this model of large rotator cuff defects. Within 6 weeks, histologic evidence of native cell infiltration and neotendon development was observed. Within 12 weeks, the strength of the dermal matrix graft repair was equivalent to that of autologous tendon. At 6 months, control and graft specimens mimicked normal tendon structure grossly and histologically. Clinical Relevance: This study provides in vivo animal data to support the use of this acellular dermal matrix graft for repair of full-thickness rotator cuff defects. Additional studies are indicated to determine the role of this material in the treatment of humans with rotator cuff tears.

Key Words:  Rotator cuff , Patch graft , Rotator cuff repair , Full-thickness rotator cuff defect , Irreparable rotator cuff tear

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 Supported in part by a research grant from Wright Medical Technology, Arlington, Tennessee. Additional institutional support was provided by the Mayo Foundation, Rochester, Minnesota.

PII: S0749-8063(06)00554-8

doi:10.1016/j.arthro.2006.03.016

Arthroscopy: The Journal of Arthroscopic and Related Surgery
Volume 22, Issue 7 , Pages 700-709, July 2006