In today’s complex healthcare environment, Biomed and IT staff face growing challenges in supporting clinicians’ patient care information needs, with vast amounts of patient data generated from countless medical devices, including ventilators, dialysis machines, patient monitors and other devices for monitoring and treating patients.
In fact, more than two million different types of medical devices exist on the global market, according to the World Health Organization.[1] The volume, complexity and variety of patient data from these devices can feel overwhelming.
Add to this the steady influx of medical technologies available to providers, an evolving regulatory landscape of requirements, and the adoption of measurement devices used outside traditional healthcare settings, and you have a “perfect storm” in which healthcare organizations are struggling to deal with:
Because of all these factors, 99% of data generated by healthcare devices goes unused, according to a report from the World Economic Forum.[2]
Medical device data continues to be siloed across various departments and care settings or even within the confines of a device manufacturer’s proprietary system, unable to flow freely across healthcare information systems where it could contribute to discovery of meaningful insights by clinicians.
In fact, 94% of healthcare leaders say their organization experiences at least one data integration challenge that impacts its ability to provide timely, high-quality care, according to the Philips Future Health Index (FHI) 2024 Global Report.[3]
All that unused data is a lost opportunity for improving care with insights that potentially could have led to better optimized treatment plans, faster diagnosis, and greater ability to predict and prevent adverse health events.
Having so much data generated, but unused, makes it impossible to harness the full potential of data-driven insights.
Over the last 20+ years, industry organizations such as Health Level Seven (HL7) International, and various governments’ agencies such as the Office of the National Coordinator for Health Information Technology (ONC) in the U.S., have promoted standards and specifications to support interoperability and the secure integration, transfer and sharing of medical data between disparate devices and systems.
While there has been significant improvement in recent years, the percentage of hospitals routinely engaging in all four domains of interoperable exchange as defined by ONC (send, receive, find, and integrate) still remains at 43% — less than half. And, while most hospitals send health information electronically, only about three-quarters integrate the information they receive into their electronic health records (EHRs).[4]
Part of the problem is that most medical device manufacturers have proprietary protocols that make it difficult to convert to an industry-wide standards approach. In addition, hospitals are still using hundreds of older, legacy medical device models that might not be able to comply with new standards for interoperability.
Further, concerns about cyberattacks and data breaches have increased significantly within the healthcare industry over the past decade with the prevalence of electronic medical records (EMRs) and electronic health records (EHRs). To withstand today’s security challenges, each medical device and system may have specific IT requirements that ensure secure deployment, but those same requirements often prevent the data from being easily shared or transferred to other clinical systems.
To overcome these data integration challenges, many health systems turn to a vendor-agnostic medical device connectivity solution. Medical device connectivity can help organizations bring together disparate data from myriad devices that have different protocols and integrate that data into a cohesive patient story that can help support timely, accurate care.
But what should health systems consider when investing in a solution to integrate their medical data?
Here are a few suggestions:
Health systems that implement a scalable, secure, vendor-agnostic medical device connectivity solution can solve the problem of siloed, unused, unstructured medical device data and provide clinicians with richer, more powerful insights, including comprehensive, high-fidelity and live-streaming data that can contribute to predictive analytics. In addition, medical device connectivity will help Biomed and IT staff achieve their clinical users’ medical device information demands.
Please let us know what you think about your current medical device connectivity – we want to hear about your experiences with medical device connectivity! Please reach out at MDIProdMgmt@philips.com to share your thoughts.
Libby Bucsi is a Product Management Leader for medical device integration at Philips Capsule.
Learn more about device connectivity and Philips Medical Device Integration.
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