Round versus tape sutures with interference fit anchors perform similarly in cadaveric glenoid and greater tuberosity biomechanical testing - Scorecard - MDSpire
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Round and tape sutures show comparable biomechanical performance with interference-fit anchors in cadaveric glenoid and greater tuberosity testing

  • By

  • James D Dimitroff

  • Conor Smith

  • Stefan Hanish

  • Lasun O. Oladeji

  • Will Bezold

  • Clayton W Nuelle

  • Matthew J Smith

  • October 7, 2026

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Clinical Scorecard: Round and Tape Sutures Show Comparable Biomechanical Performance with Interference-Fit Anchors in Cadaveric Glenoid and Greater Tuberosity Testing

At a Glance

CategoryDetail
ConditionBiomechanical performance of suture configurations in interference-fit anchors used in shoulder repair models
Key MechanismsInterference-fit anchors secure sutures by compressing them against bone within the anchor; suture slippage is a possible failure mechanism.
Target PopulationThe study tested fresh-frozen cadaveric shoulders; it did not study living patients.
Care SettingPreclinical biomechanical testing relevant to arthroscopic rotator cuff and labral repair.

Key Highlights

  • The study compared three suture-anchor combinations in posterior glenoid specimens using 2.9-mm interference-fit anchors: 1.3-mm SutureTape, 1.5-mm LabralTape, and #2 FiberWire.
  • Four of five glenoid pairs were included; one pair was excluded because improper storage made the specimens unsuitable.
  • Within each shoulder, suture-type placement alternated, and locations were staggered between shoulders to reduce glenoid position as a confounding variable.
  • The supplied excerpt ends during the humeral methods and does not report biomechanical results; comparative performance cannot be summarized from this excerpt.

Guideline-Based Recommendations

Diagnosis

    Management

      Monitoring & Follow-up

        Risks

          Patient & Prescribing Data

          The study used commercially obtained fresh-frozen cadaveric shoulders from donors aged 32–50 years; the excerpt does not describe enrollment of living patients.

          The excerpt describes biomechanical testing of suture-anchor constructs and does not report treatment or prescribing outcomes.

          Clinical Best Practices

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