The new committee's mandate will be to create and update policies that protect personal health information while expanding the state's ability to share electronic health records between healthcare providers, and with consumers and other health-related community organizations, according to a statement announcing the formation of the SHIN-NY Policy Committee.
Corinne Carey, one of the committee members and assistant legislative director at the New York Civil Liberties Union (NYCLU), joins 16 other members that include public officials, healthcare providers, attorneys, and public advocates.
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Carey told InformationWeek Healthcare that she would like the policy committee to "ask the state to conduct a thorough review of the policies and procedures governing health information exchange to determine if they are consistent with New York State law, in particular section 18 of the public health law which requires affirmative patient consent before any medical information is shared with a third party."
Recently, the NYCLU issued a report that bemoaned New York State's current privacy and security policies and procedures governing computer networks that share electronic medical records. The report concluded that under the state's current policies and procedures, providers are not required to have patient consent when they access a patient's medical record.
The report also noted that New York State is building a health information exchange that uploads the entire history of a patient's medical records, some of which is not required by specific providers to render adequate care. This allows, for example, a podiatrist to see the details of a sexually transmitted disease or a substance abuse disorder that occurred many years ago, information that's unrelated to the condition the podiatrist is treating.
Now that she's a member of the SHIN-NY Policy Committee, Carey is hoping these issues will be addressed. "We want the committee to put in place a policy that requires that health information exchange systems have the capacity to sort and segregate information so that both patients and providers have the ability to restrict access to certain portions of a medical record," Carey said.
She also wants the committee to revisit the policy that allows for the upload of patient information onto a health information exchange. In her view, patient consent should occur before the medical records are added to the network.
Officials at the NYeC said the organization is tasked with protecting the privacy and security of healthcare information. To advance this agenda, NYeC works with stakeholders from across the state and from a wide variety of interest groups to develop common policies, procedures, and technical approaches through an open and transparent process.
During 2010 and 2011, NYeC's privacy and security policy work focused mainly on reviewing the state's existing policy guidance on health IT, which directed the regional work of Regional Health Information Exchange Organizations (RHIOs).
With regional data now being tied together to provide for statewide exchange of healthcare data, the SHIN-NY Policy Committee will review and modify existing policy and explore the creation of a new policy as needed to improve interoperability while protecting patient information. New policy and policy amendments align with federal requirements, NYeC officials said in a statement.
"It's essential for the success of this electronic health information enterprise that it be transparent and that all stakeholders have a meaningful voice in its governance. This committee's diverse membership reflects that principle," Art Levin, director of the Center for Medical Consumers, member of the NYeC Board of Directors, and Co-Chair of the SHIN-NY Policy Committee, said in a statement.
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