Leaders Discuss Implications of New Connectors
The Joint Commission urges vigilance and planning in preparation for new connectors
Last month, The Joint Commission published Sentinel Event Alert Issue 53, which addresses the need to manage risk during the transition to new connectors. The publication reinforces the importance of the new standard and offers strategies to help health care organizations get ready for the change. “The new connectors greatly reduce the risk of tubing misconnections, but organizations still need to take a coordinated, mindful approach to identify and mitigate potential misconnection hazards during the transition to the new ISO connectors,” said Gerard Castro, Project Director for Patient Safety Initiatives in the Office of Patient Safety at The Joint Commission.
Download the Sentinel Event Alert
Coming in Q4 — The transition to safer connectors begins!
Introduction of transition sets in the US, Canada, Puerto Rico
Tell your colleagues
Did you know? Medication Safety Collaborative
Stay Connected is a global initiative, and individual markets have different yet coordinated schedules for the transition. Each downloadable brochure outlines that market’s schedule. Brochures available in Dutch, English, French, German, Italian, Portuguese, and Spanish.
Download a brochure for your market
Do you have? Raising Awareness
Transition Checklists
Your team may be familiar with the Stay Connected initiative and aware of the transition to new connectors—now they need to prepare for the change. Download a transition checklist to help get started.
Download a transition checklist for:
Facilities & Institutions
Nurses & Clinicians
Supply Chain
Home Care Providers
Patients & Caregivers
Have you met?
Ana McKee, M.D.
Executive Vice President and Chief Medical Officer
The Joint Commission
Ana focuses on and develops policies and strategies for promoting patient safety and quality improvement in health care. Her responsibilities include supporting The Joint Commission’s Patient Safety Advisory Group; overseeing work related to the development of the Sentinel Event Policy, National Patient Safety Goals and Sentinel Event Alerts; supervising the Sentinel Event Database; and overseeing the functions of the Standards Interpretation Group and the Office of Quality Monitoring.
“Tubing misconnections are the contributory factor of too many tragic patient safety events and The Joint Commission is committed to helping health care organizations prevent them. The redesign of these standards is a perfect example of how The Joint Commission is working collaboratively to determine the cause of the problem and re-design processes to improve patient safety.”   —Dr. Ana McKee, The Joint Commission
Have you told?
Make sure your Patient Safety officers are ready
Share this email and other Stay Connected tools and information with patient safety directors, managers, and coordinators, quality improvement directors, and risk management personnel to help smooth the transition to the new ENFit connectors.
Forward this email to your colleagues
Where to Find Us
October 7 The American Society for Healthcare Risk Management (ASHRM) and the Association for Healthcare Resource and Materials Management’s (AHRMM) Stay Connected Webinar
October 14-15 BAPEN 2014 Annual Conference, North Yorkshire, England
October 19-22 The LeadingAge Annual Meeting and EXPO, Nashville, TN
October 26-29 ASHRM Annual Conference & Exhibition, Anaheim, CA
December 7-11 ASHP Midyear Clinical Meeting and Exhibition, Orange County, CA
The Stay Connected initiative is organized by the Global Enteral Device Supplier Association (GEDSA) in partnership with leading regulators, associations and other supporting organizations.
If this email was forwarded to you and you would like to sign up to Stay Connected, click here.
©2014 GEDSA, all rights reserved
692 N. High St. Suite 207
Columbus, OH 43215 USA
GEDSA is a 501(c)(6) federal tax exempt Non-Profit Trade Association incorporated in the State of Ohio, USA. GEDSA’s mission is to promote initiatives surrounding safe and optimal delivery of enteral feeding and connectivity. It is GEDSA’s policy and the responsibility of every GEDSA member to comply in all respects with federal, state and international antitrust laws. Any discussion is strictly prohibited for the purpose of raising, lowering, or stabilizing prices; regulating production; allocating markets; encouraging boycotts; fostering unfair trade practices; or assisting monopolization at any GEDSA function. Any questions regarding the meaning or applicability of this policy, as well as any concerns regarding activities or discussions at GEDSA functions, should be promptly brought to the attention of GEDSA’s executive director, officers, and/or legal counsel.
All material provided in this email is intended for informational purposes only and should not be used to replace regulatory or company-specific documents, nor should it replace the advice of a qualified professional. This information is based on the draft ISO 80369 standard; does not imply or suggest any regulatory clearance of any specific product and may not be predictive of clinical outcomes. Images provided do not imply endorsement of any specific product. All products and product designs are the responsibility of each specific legal manufacturer, distributor or supplier. Products with these design features may be pending regulatory clearance or may not be available in a specific geography. Consult your supplier representative for product-specific availability, indications, contraindications, precautions, and warnings.

This email was sent to <<Email Address>>
why did I get this?    unsubscribe from this list    update subscription preferences
GEDSA · 692 N. High St. Suite 304 · Columbus, OH 43215 · USA

Email Marketing Powered by Mailchimp