Alarm Summit Agenda
Tuesday, October 4, 2011 |
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8:45-9:15 am |
Keynote Presentation |
| George Blike, MD, Dartmouth-Hitchcock Medical Center | |
9:15-10:30 am
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Defining the Problem: It's More Than A "Nuisance" |
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James Blum, MD, University of Michigan Health System Barbara Drew, RN, PhD, FAAN, FAHA, Univeristy of California, San Francisco |
| Hundreds of preventable patient deaths in a five-year period are attributed to “alarm fatigue.” It’s easy to say the problem is “too many nuisance alarms.” It’s far more crucial to expand our understanding, to include the multiple facets in a complex system of systems. Panelists will help define the problem from various stakeholder perspectives, followed by a moderated discussion with the audience. |
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10:45-Noon |
How We Got Here: Regulatory, Liability, and Risk Management Limitations Impacting Medical Device Alarms (Unintended Consequences of a “No Risk Tolerated” World) |
| Felipe Aguel, PhD, U.S. Food and Drug Administration James Keller, MS, ECRI Institute Katie McDermott, Morgan, Lewis & Bockius LLP |
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| Panelists will provide an overview of the medical-legal issues and regulations related to health provider behavior with alarm management; alarm parameters, including how they relate to appropriate specificity and sensitivity settings; and obstacles that must be overcome to spur innovation and reduce “nuisance” alarms. The moderator will engage the audience and panelists in a discussion about experiences with these issues and areas for improvement. | |
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Noon-1:00 pm |
Simulation Testing For Medical Device Alarms |
| Richard McNeer, MD, PhD, University of Miami | |
1:00-2:45 pm |
“We Didn’t Hear It:” Optimizing the Environment of Care |
| Ilene Busch-Vishniac, PhD, McMaster University Maria Cvach, MS, RN, CCRN, Johns Hopkins Hospital, and Kathryn Pelczarski, ECRI Institute Rebecca Shultz and Elena Simoncini, VA Boston Healthcare System |
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| Panelists will identify the numerous environmental factors that impact the way clinicians pay attention and respond or “don’t respond to” medical device alarms. Workflow, system management challenges and opportunities, and overall environmental noise also will be addressed. The moderator will then ask the audience to further identify and discuss the issues and set priorities for potential changes that need to be addressed for an optimal culture, human, physical, workflow, and technology integration and interaction in order to improve monitoring systems and the environment of care, and ultimately improve patient safety. | |
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3:00-4:15 pm |
Industry Can Help: Alarm Design |
| David Barash, MD, GE Healthcare Julian Goldman, MD, Massachusetts General Hospital Michael O’Reilly, MD, Masimo Corporation Michael Wiklund, PE, CHFP, Wiklund Research & Design |
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| Panelists will address how some alarm problems can be solved by re-design. Problem areas they will discuss include escalated alarms, delayed signals, alarm settings and ease of use, number of severity categories are “how many are enough?,” design trade-offs, and more. The moderator will ask audience members to participate in a discussion of these and other design issues, and what it will take to achieve consensus on potential solutions that could benefit the entire healthcare system. | |
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4:15-5:00 pm |
Yes, They Matter: Medical Device Alarms Related Standards |
| Frank Block, MD Oliver Christ, Prosystem AG David Osborn, Philips Healthcare |
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| Panelists will provide a brief overview of medical device alarm related standards and discuss reasons these standards have not been fully adopted throughout the healthcare system. The moderator will ask audience members to provide input on the weaknesses of current alarm standards and to identify ways to strengthen them. | |
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5:00-5:30 pm |
First Day Wrap-up |
| The Summit Moderator will review discussions from Day 1, and review the schedule for Day 2. Audience members will have the opportunity to bring up their observations from the day or ask additional questions about the discussions. | |

