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Wound Complications Following the Use of FiberWire in Lower-Extremity Traumatic AmputationsA Case Series
Andrew W. Mack, MD1; Brett A. Freedman, MD1; Scott B. Shawen, MD1; Donald A. Gajewski, MD1; Victor F. Kalasinsky, PhD2; Michael R. Lewin-Smith, MB, BS2
1 Orthopaedic Surgery Service, Walter Reed Army Medical Center, 6900 Georgia Avenue, N.W., Washington, DC 20307. E-mail address for A.W. Mack: andrew.mack@amedd.army.mil
2 Department of Environmental and Toxicologic Pathology, Armed Forces Institute of Pathology, 14th Street and Alaska Avenue, N.W., Washington, DC 20306-6000
The Journal of Bone & Joint Surgery.  2009; 91:680-685  doi:10.2106/JBJS.H.00110
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Extract

With the development of new arthroscopic approaches over the last decade, one innovation that has facilitated this trend has been the introduction of high-tensile-strength sutures. These nonabsorbable sutures allow for the reliable and secure fixation of soft tissues, such as the glenoid labrum and rotator cuff, to bone by means of anchors1,2. Similarly, these sutures have gained great acceptance in open procedures, such as tendon repairs and suture fixation of fracture fragments3. FiberWire (Arthrex, Naples, Florida) is one of the first members of this family of sutures. Currently, it is one of the most commonly used high-tensile-strength sutures in orthopaedic surgery.
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    These activities have been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of the American Academy of Orthopaedic Surgeons and The Journal of Bone and Joint Surgery, Inc. The American Academy of Orthopaedic Surgeons is accredited by the ACCME to provide continuing medical education for physicians.
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