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A Review on the Innovative Surgical Suture and Needle Evaluation and Selection Program.

Robin R Szarmach1, Jean Livingston1, George T Rodeheaver2

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Summary

Surgical sutures and needles from United States Surgical/Davis & Geck Sutures (USS/D&G) demonstrated high clinical acceptability, with 98.1% of evaluations deemed successful. Surgeons found these essential surgical biomaterials reliable in diverse procedures.

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Area of Science:

  • Surgical biomaterials evaluation
  • Clinical performance assessment
  • Healthcare resource management

Background:

  • Collaboration between Consorta, Inc. (healthcare resource management) and United States Surgical/Davis & Geck Sutures (USS/D&G) (surgical biomaterials manufacturer).
  • Development of an innovative clinical evaluation program for surgical sutures and needles.

Purpose of the Study:

  • To assess the clinical performance of surgical needles and sutures manufactured by USS/D&G.
  • To gather surgeon feedback on various performance characteristics of surgical biomaterials.

Main Methods:

  • Nonexperimental observational study involving 699 surgeons across 19 hospitals.
  • Evaluation of 3407 surgical procedures over 30-day periods.
  • Assessment of packaging, needle sharpness/strength, tissue drag, knot security, and tensile strength.

Main Results:

  • Overall clinical acceptability rating of 98.1% for USS/D&G sutures and needles.
  • POLISORB* braided synthetic sutures showed 98.4% acceptability; SOFSILK* had 98.7%; monofilament nylon had 96.3%.
  • Surgical needles achieved a 97.9% clinical acceptability rating.

Conclusions:

  • The evaluated USS/D&G surgical sutures and needles are highly clinically acceptable.
  • The collaborative evaluation program successfully assessed the performance of surgical biomaterials.
  • High surgeon satisfaction indicates reliability of these surgical essentials in practice.