I have started a series for the Human Factors MD blog on the design, presentation, and evaluation of safety information (warnings, precautions, and contraindications) in medical device labeling.
Last week I posted the first in the series that provided an overview of the challenges medical device companies face when developing safety information for their products. Yesterday, I posted the second in the series that discussed the four components (signal word, identification of the hazard, information on how to avoid the hazard, and consequences for failing to avoid the hazard) typically included when developing safety information.
Some of the additional topics that will be covered in the series include:
- Purpose of safety information
- When safety information is required
- Challenges developing safety information
- Why safety information isn’t always effective
- Questions to ask when developing safety information
- Design considerations when developing safety information
- Issues seen in device labeling safety information
Last month, I led a 90-minute webinar on Warnings and Safety Information in Device Labeling, Part 2: Design Best Practices for the AAMI University Distance Learning Program. Topics included:
- Reviewing seven initial questions to ask before designing warnings and safety information in medical device labeling.
- Discussing five overarching design considerations when developing warnings and safety information in medical device labeling.
- Describing which features contribute to effective warnings and safety information for medical device labeling.
- Identifying best practices of warnings and safety information in medical device labeling.
- Providing resources for instructional designers to use when developing warnings and safety information for medical device labeling.
If you missed the two-part webinar, you can purchase access to the archived webinar here.
The ECRI Institute has published their annual Top 10 Health Technology Hazards for 2017. As noted in the brief, the list is published each year to identify:
“…the potential sources of danger that we believe warrant the greatest attention for the coming year. The list does not enumerate the most frequently reported problems or the ones associated with the most severe consequences—although we do consider such information in our analysis. Rather, the list reflects our judgment about which risks should receive priority now.” (p. 3)
The list includes:
- Infusion Errors Can Be Deadly If Simple Safety Steps Are Overlooked
- Inadequate Cleaning of Complex Reusable Instruments Can Lead to Infections
- Missed Ventilator Alarms Can Lead to Patient Harm
- Undetected Opioid-Induced Respiratory Depression
- Infection Risks with Heater-Cooler Devices Used in Cardiothoracic Surgery
- Software Management Gaps Put Patients, and Patient Data, at Risk
- Occupational Radiation Hazards in Hybrid ORs
- Automated Dispensing Cabinet Setup and Use Errors May Cause Medication Mishaps
- Surgical Stapler Misuse and Malfunctions
- Device Failures Caused by Cleaning Products and Practices
If you’re interested in getting your own copy of the Executive Brief, visit this link.
Last Thursday, I led a 90-minute webinar on Warnings and Safety Information in Device Labeling, Part 1: A Primer on the Science for the AAMI University Distance Learning program. Topics included:
- Describing the purposes, parts, and pitfalls of warnings and safety information
- Reviewing the state of the science of warnings and safety information, specifically as it pertains to medical device labeling
- Examining how warnings and safety information development aligns with a typical usability engineering process
- Explaining why warnings and safety information are not always effective
- Discussing product liability challenges due to defective warnings and safety information
This week I will present Part 2 which will focus on medical device labeling design best practices. The webinar will be on November 10th from 11:00 am – 12:30 pm EST. If you’re interested in participating, you can register for the webinar here.
On November 9th, The Core will host the MedBuild 2016 Summit. The second annual summit is being held at Boise State University and seeks to connect innovators, companies, and investors with the intent of growing the nascent medical technology industry in Idaho.
The two-track summit will feature a keynote address by Debra Beresini and have educational sessions focusing on investing, reimbursements, and working with startups and universities. There will also be company spotlight presentations, where I’ll be speaking about the capabilities of Human Factors MD. The day will end with a networking reception.
For those interested in attending, you can purchase tickets here.
On November 3rd and 10th, I’ll be presenting a two-part webinar on Warnings and Safety Information in Device Labeling for the AAMI University Distance Learning program.
Part I will introduce attendees to the science of warnings and safety information. Part II will focus on highlighting the best practices of designing and presenting warnings and safety information in device labeling. Each session will last 90 minutes and start at 11:00 am EST.
To learn more about the webinar, including how to register, visit the following link.
On March 5th – 8th, the Human Factors and Ergonomics Society (@HFES) will hold the 2017 International Symposium on Human Factors and Ergonomics in Health Care at the Sheraton New Orleans Hotel in New Orleans, Louisiana.
The symposium will include lectures, panels, and posters in four program tracks:
- Consumer and Clinical Health Care IT
- Hospital Environments
- Medical and Drug-Delivery Devices
- Patient Safety Research and Initiatives
It should be another great opportunity to meet, reconnect, and learn from practitioners, industry representatives, researchers, students, and the human factors staff at the FDA. Hope to see you in New Orleans!