About Julian Goldman, MD

Dr. Goldman is an anesthesiologist at the MGH and Medical Director of Biomedical Engineering for Partners HealthCare. He is the Director of the Medical Device Interoperability Program - a multi-institutional federally program founded in 2004 to advance medical device interoperability to improve patient safety and HIT innovation. http://www.mdpnp.org

Dr. Goldman completed his anesthesiology residency and medical device informatics fellowship at the Univ. of Colorado, and served as a Visiting Scholar in the FDA as well as an executive of a medical device company. He is an IEEE EMBS Distinguished Lecturer, chairs several national and international committees that develop standards for the safety, performance, and interoperability of medical equipment. His awards include the AAMI Foundation/Institute for Technology in Health Care Clinical Application Award, the International Council on Systems Engineering Pioneer Award, and the American College of Clinical Engineering award for Professional Achievement in Technology. More information is available at www.jgoldman.info

Departments, Centers, & Programs:

Clinical Interests:

Treats:

Locations

Anesthesia, Critical Care and Pain Medicine
55 Fruit Street
Boston, MA 02114-2696
617-768-8765
Fax: 617-726-7536

Medical Education

  • MD, SUNY at New York City (Downstate)
  • Residency, University of Colorado Health
  • Fellowship, University of Colorado Health Sciences Center

American Board Certifications

  • Anesthesiology, American Board of Anesthesiology
  • Clinical Informatics, American Board of Preventitive Medicine

Accepted Insurance Plans

Note: This provider may accept more insurance plans than shown; please call the practice to find out if your plan is accepted.


Research

Research Areas

  • Medical device interoperability to build smarter and safer clinical environments
  • Development of medical device safety and performance standards
  • Foundational requirements for the deployment of apps for advanced clinical capabilities such as smart alarms, safety interlocks, and closed-loop control

 

Description of Research

My research group, the Medical Device Plug-and-Play (MD PnP) Interoperability Program, is accelerating the adoption of safe, secure, interoperable medical devices to enable the creation of complete and accurate electronic health records and the cost-effective development of innovative medical apps for diagnosis, treatment, research, safety and quality improvements, equipment management, and adverse event detection and reporting. Our team is working to develop sharable software tools and applications that will enable a broader community of researchers and manufacturers to implement medical device interoperability with a focus on improving patient safety. Our work includes identifying clinical problems that could be solved through reliable, comprehensive medical system integration, and the implementation of those solutions through the development of open standards and technology in our Cambridge MD PnP lab " sandbox". We work closely with the FDA, DoD, VA, NIST, NSF, NIH, manufacturers, and other groups to help align clinical, research, manufacturing, policy, and regulatory needs. In addition our team is involved with the development of international safety and performance standards for anesthesia and respiratory care equipment and interoperability. These synergistic research and standardization activities provide diverse opportunities for residents and fellows to contribute to creating healthcare environments of the future. Our program website contains information about specific initiatives.

Publications

  • View my most recent publications at PubMed

    Select Publications:

    • Arney D, Fischmeister S, Goldman JM, Lee I, Trausmuth R. Plug-and-play for medical devices: experiences from a case study. Biomed Instrum Technol 2009; 43:313-317. PMID: 19670943
    • Hatcliff J, King A, Lee I, MacDonald A, Fernando A, Robkin M, Vasserman E, Weininger S, Goldman JM. Rationale and architecture principles for medical application platforms. In: Proceedings from the IEEE/ACM Third International Conference on Cyber-Physical Systems (ICCPS); 2012: 3-12.
    • Goldman JM, Schrenker R, Melendez L, Hampton R, Driscoll W. Implications of the New FDA Medical Device Data System (MDDS) Regulation for Automated Clinical Documentation. Proceedings of American Society of Anesthesiologists: Equipment, Monitoring and Technology. October 2011.
    • Arney D, Goldman JM, Bhargav-Spantzel A, Basu A, Taborn M, Pappas G, Robkin M. Simulation of Medical Device Network Performance and Requirements for an Integrated Clinical Environment. Biomed Instrum Technol 2012 Jul-Aug;46(4):308-15.