Informed patients have lower readmission rates, better therapy adherence and reduced miscommunication errors among providers, outlining the critical need for providers to share patient data and engage with patients. Historically, such initiatives have often failed or have been underutilized. Nevertheless, the need and desire for patient engagement programs have increased in recent years, partially due to quality programs introduced with value-based care requirements, but also because of improvements and innovation in digital and mobile technology.
In determining the right way to engage patients, it is important to first examine previous initiatives and why they were unsuccessful. Under Meaningful Use, for example, five percent of patients were required to view and download their records. Many providers had a hard time meeting this requirement, and in order to comply, many resorted to patient rounds, traveling bed-to-bed, to request patients to download their records.
Many other initiatives have leveraged patient portals in efforts to increase engagement. When using such portals, patients are often faced with confusion surrounding the correct one to use – a hospital-specific portal, the primary physician’s portal, the surgeon’s portal or the payer’s portal? According to one client, portal usage statistics reveal patients are really only using them for financial information and not on a regular basis to manage care.
Other initiatives have attempted to gauge why patients are not leveraging information provided to them. The Centers for Medicare and Medicaid Services (CMS) conducted a survey regarding their “Blue Button” initiative, which gave patients the ability to view, print and download their personal health information and customize the view of their record. Survey results showed a critical need for patients to have access to their online records. However, three years after the initiative started, only three in ten patients knew they had access to their information online, and one in three patients had to address miscommunication among providers and a delay in information being shared because of the program.
There were some successes with Blue Button, however. Nearly three-fourths of patients used their online information to monitor their health and share information with their providers and care managers, which is a significant rate of acceptance. While the number of providers sharing information digitally has increased and will inevitably continue to grow, the use of such an opportunity is still in a nascent stage.
Geisinger Health System, a leading Pennsylvania-based health maintenance organization (HMO), also conducted an initiative to monitor Congestive Heart Failure (CHF) patients’ weight using Bluetooth scales. This initiative had positive results, with a reported 40 percent reduction in emergency departments and direct admits, and a higher patient satisfaction rate.1 This initiative involved heavy involvement from care management staff, making it viable only for the highest risk patients. How can this improve?
By reviewing previous initiatives, it’s clear that when there is actionable information, patients are much more willing to engage. Below are some best practices for communicating with patients:
On the business side of it, bundled payments, value-based initiatives and shared savings are some of the key initiatives that require coordinated care. Most providers have started to understand the value and are taking steps to introduce these programs in their business strategy and roadmap. Patient engagement presents an opportunity to drive the coordination between providers by actively involving the patient as the glue that drives meaningful change.
1 http://www.amchealth.com/_files/published-outcomes/PopulationHealthManagement-GeisingerHFStudy-May2014.pdf
2 https://health.gov/communication/literacy/issuebrief/
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