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William Hyman: The Missing Link in Device Interoperability

October 6, 2017

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Last month, the FDA issued its guidance document Design Considerations and Premarket Submission Recommendations for Interoperable Medical Devices and a commentary by Bakul Patel. The essence of the form of interoperability addressed is the transfer of data from one medical device to another or perhaps from one or more medical devices to a separate processing […]

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Robert Sayle: Get Manufacturers on Board with Digital Certificates

September 19, 2017

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Hey, biomed! Thanks for waiting for me after the change control board meeting IT just had. I wanted to follow up on our discussion of supplicants for medical device cybersecurity because the best way to leverage 802.1X is to use digital certificates. Why would we do this? Because we can prepare your equipment for authentication […]

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Mike Ahmadi: When It Comes to Cybersecurity, the Regulatory Will Is Weak

August 3, 2017

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I want to tell a story. I grew up in Cleveland Ohio, a city that has always held its place in the top two or three cities that everyone likes to poke fun at for being a place where you do not want to live—or so it was for most of my life. Thankfully, it […]

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Robert Sayle: What Does Cybersecurity Need? Supplicants

July 18, 2017

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Mornin’, biomed! It’s Bob in IT. I was just on my way to a meeting next door, and I thought I’d drop by to say hello. I wanted to follow-up with you about my request to have you start collecting MAC addresses as part of your staging process. Here’s the thing: MAC addresses are what […]

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Emma Fauss: Remote Monitoring Is No Remote Concern for Hospitals

June 5, 2017

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Remote monitoring and virtual surveillance are quickly becoming a top priority at hospitals across the country. One of the main drivers is the growth of health systems where the main campus is looking for ways to remotely monitor its rural and sub-acute facility patients. Another driver is the desire to remotely monitor patients in higher […]

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Emma Fauss: Leverage Your Device Data for Advanced Event Detection

June 2, 2017

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Clinical staffers spend about 20% of their time on documentation alone. While it’s difficult to summarize the error rates, studies show that they range from 5% to 95%, depending upon the condition, patient, and measurement. Inaccurate documentation has many risks, from clinical risks such as cherry-picked vitals and handoff, to financial risks such as revenue […]

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Robert Sayle: A Conversation Worth Having for Network Security

May 26, 2017

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Hey, Information Security, how’s it going? You may remember me, Bob in IT. Thanks for meeting me over coffee. Did you order already? I did, too. While we’re waiting for them to bring it out, let me tell you about the conversation I had with our biomed colleagues. They heard about the recent WannaCry ransomware […]

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Samantha Jacques: Clinical Engineering Has Crucial Role in Facilities Projects

April 18, 2017

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For the past few years, AAMI, ACCE, HIMMS, and others have been working to bridge the gap between the clinical or biomedical engineering (or healthcare technology management) department and the information technology (IT) department within a hospital or hospital system. We continue to learn how valuable a relationship is between CE and IT and how […]

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Jennifer DeFrancesco: Are We Missing the Big Picture with Big Data?

April 13, 2017

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Healthcare technology management (HTM) prides itself on being driven by “big data.” We have more metrics and ways at making evidence-based decisions than most within the healthcare industry.  Now that we are well into the era of big data, the struggle has been making it relevant. Sure, as HTM, we have settled nicely into our […]

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Robert Sayle: Attention Biomeds! Your IT Colleague Would Like to Chat

April 4, 2017

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Hey, biomed! It’s me, Bob in IT. I’m from the networking team. I know we haven’t spoken much, but I think we should. You see, we’ve got some problems we need to solve. I have ideas on what to do, but I don’t totally understand your systems, so I need your input. Let’s take security […]

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