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Independent Clinical Research Confirms Clinical Efficacy and Cost-Effectiveness of the SurgiCount Safety-Sponge® System
Date:1/18/2011

IRVINE, Calif. and DUBLIN, Ohio, Jan. 18, 2011 /PRNewswire/ -- Results of a multi-year, independent clinical research study on retained surgical sponges published in the February edition of The Joint Commission Journal on Quality and Patient Safety show that the institution implementing the SurgiCount Safety-Sponge® System eliminated the occurrence of retained surgical sponges and the costs associated with these preventable surgical errors.  

The peer-reviewed publication details two, randomized, controlled trials conducted at a high-volume surgical practice, the subsequent implementation of the Safety-Sponge® System across all of the 128 operating rooms at the affiliated institution and a comprehensive evaluation of the solution after 18 months of use. The evaluation considered variables including system effectiveness on reducing retained surgical sponges, efficiency, impact on operative time, ergonomics and staff satisfaction.      

Key results and conclusions of the study include:

  • Prior to implementation, a retained surgical sponge occurred at the institution on average every 64 days. During the study, 87,404 procedures were performed over 18 months using 1,862,373 Safety-Sponges®, and none were retained.  
  • Use of the Safety-Sponge® System caused no workflow disruption or increase in case duration.
  • Staff satisfaction with the Safety-Sponge® System was acceptable with a high degree of trust in the system.
  • The Safety-Sponge® System was found to be highly reliable and cost-effective.

"To my knowledge this is by far the most extensive study ever performed on this important patient safety issue, and we are proud to have this comprehensive, independent research validate the SurgiCount Safety-Sponge® System," said Brian E. Stewart, president and chief executive officer of Patient Safety Technologies, the
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SOURCE Cardinal Health, Inc.
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