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Change Expectations > Change Technology > Change Healthcare The Medical Device "Plug-and-Play" (MD PnP) Interoperability Program is promoting innovation in patient safety and clinical care by leading the adoption of patient-centric medical device integration. |
Medical Device "Plug-and-Play" Interoperability Program
| QUICK LINKS > MD PnP White Paper > ICE Standard (ASTM F2761) > MD FIRE > QMDI Project > Program Leadership > Upcoming Events ............................................ BECOME A MEMBER > Benefits of Membership > Membership Application ............................................ CONTACT INFORMATION MD PnP Program 65 Landsdowne St., Suite 200 Cambridge, MA 02139 info@mdpnp.org Julian M. Goldman, MD Program Director jgoldman@mdpnp.org Sue Whitehead Program Manager 617-768-8760 swhitehead@partners.org ............................................ NEWS 3/4/13 - MD PnP at HIMSS: MD PnP research demonstrations in the ONC Area of the Interoperability Showcase at HIMSS, New Orleans Read about the demonstrations here 2/1/13 - Two new articles about the current state of interoperability feature interviews with Julian Goldman Find them on our Publications page > MORE NEWS |
The Challenge: How can we better use medical devices to improve the safety of medical care?
Medical devices are essential to the practice of modern medicine. Clinical measurements such as blood pressure and temperature, x-ray and ultrasound imaging, administration of intravenous medications, and support of critical life functions all require medical devices. However, despite our reliance on sophisticated medical equipment, most devices are not designed to interconnect with other devices. Therefore, it is difficult to connect individual devices into integrated medical systems to improve patient care and avoid unnecessary accidents.
The Answer: Facilitate the adoption of open standards and interoperable technologies to integrate the clinical environment.
The Medical Device “Plug-and-Play” (MD PnP) Interoperability Program is accelerating the adoption of medical device interoperability to enable the creation of complete and accurate electronic health records and the cost-effective development of innovative third-party medical “apps” for diagnosis, treatment, research, safety and quality improvements, equipment management, and adverse event detection and reporting when using networked medical devices for clinical care. Our team is working to develop sharable databases, tools, and applications that will enable a broader community of researchers and manufacturers to implement medical device interoperability. We have taken a multi-faceted approach to reduce key barriers to achieving interoperability, including:
- Development and support of suitable open standards (e.g. ASTM F2761, Integrated Clinical Environment, or “ICE”)
- Elicitation, analysis, and modeling of clinical use cases and system engineering requirements for an open architecture instantiation of ICE as a platform and “ecosystem”
- Alignment of clinical, manufacturer, and FDA regulatory expectations
- Implementation of prototype use cases in an open “sandbox” environment