In 2018, throughout the United States, the health care sector saw 15 million patient records compromised in 503 breaches. This was three times the number seen in 2017, according to the Protenus Barometer report, a quarterly snapshot of disclosed breaches impacting the health care industry.
Cyberattacks in health care are similar to attacks on enterprise organizations: publicly available vulnerability exploit kits (or preconfigured hacking tools) combined with misconfiguration and coding errors provide an open door for an aspiring hacker.
In fact, hacking has turned into a lucrative day job with better hours, higher pay and less risk/consequence compared to other illegal activities. It only takes one vulnerability in a single device to shut down an entire network and/or hospital until a ransom is paid. And on the black market, a single patient health record can sell for $1,000.
Hackers probe and scan the state of Minnesota's computers 3 million times per day. As a major health care hub, Minnesota has a host of high-profile health care insurance companies, medical device manufacturers, and provider networks, all of which face threats against cybersecurity every day.
Recently, we spoke with several health care IT experts in Minnesota, who all said cybersecurity has become a pivotal focus in their day-to-day planning activities. Whether securing protected personal health information (PHI) or safeguarding against targeted device attacks, cybersecurity is no longer an afterthought but, instead, something that is addressed in the early stages of IT development.
The threats include:
Device-specific attacks. There are many types of health care cybersecurity attacks. Perhaps the most sensationalized, yet the least likely, are attacks to implantable cardiac devices, whereby a hacker can hijack the device and administer shocks on command, disable the features, and intentionally wear out the battery. Similar vulnerabilities have been identified in drug infusion systems and insulin pumps.
Given the importance of cybersecurity, the FDA has updated its draft guidance for implementing security measures during device development. Security measures are no longer considered after a device is developed.