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Meaningful Use Stage 3 Should Address Care Disparities

Posted on September 13, 2013 I Written By

Anne Zieger is veteran healthcare consultant and analyst with 20 years of industry experience. Zieger formerly served as editor-in-chief of FierceHealthcare.com and her commentaries have appeared in dozens of international business publications, including Forbes, Business Week and Information Week. She has also contributed content to hundreds of healthcare and health IT organizations, including several Fortune 500 companies. Contact her at @ziegerhealth on Twitter or visit her site at Zieger Healthcare.

A consumer coalition of more than 50 consumer, patient and labor organizations has published a plan designed to thrust care disparities into center stage as part of Stage 3 of Meaningful Use, according to Healthcare IT News.

According to data from the Joint Center for Political and Economic Studies, the combined costs of premature death and health disparities in the U.S. were $1.24 trillion between 2003 and 2006. The group, the Consumer Partnership for eHealth, argues that these disparities will only increase as the country grows more diverse.

CPeH developed the plan after a year-long review of scientific literature, along with collaboration with experts on disparities in care and health IT. The plan focuses on data collection and use to identify disparities; language; literacy and communication and care coordination and planning, HIN reports.

The plan is designed to integrate disparities reduction with the other Stage 3 criteria to improve the identification and understanding of health disparities. The CPeH has submitted the plan to the Health IT Policy Committee, and has asked the committee to act on its recommendations.

Right now, the Meaningful Use program only requires basic identification of race, ethnicity and gender data collection. But the action plan would like to see Stage 3 include more stringent data collection standards designed by HHS, which would include disability status, sexual orientation and gender identity.

The group’s action plan includes recommendations that:

* EMRs have the ability to stratify patients’ specific conditions by demographic variables such as race, ethnicity, language, gender identity, sexual orientation and socio-economic status

* Providers make greater use of patient data collected and shared through mobile health applications

* Clinicians effectively communicate EMR information to patients, so patients can better make use of its benefits

While the goals outlined here are laudable, my sense is that even for doctors ready for Stage 3 Meaningful Use, requiring this level of data collection and analysis would be a difficult burden. I guess this one is a “wait and see” proposition.

Consumer Engagement in Healthcare by CPeH

Posted on May 10, 2011 I Written By

John Lynn is the Founder of the HealthcareScene.com blog network which currently consists of 10 blogs containing over 8000 articles with John having written over 4000 of the articles himself. These EMR and Healthcare IT related articles have been viewed over 16 million times. John also manages Healthcare IT Central and Healthcare IT Today, the leading career Health IT job board and blog. John is co-founder of InfluentialNetworks.com and Physia.com. John is highly involved in social media, and in addition to his blogs can also be found on Twitter: @techguy and @ehrandhit and LinkedIn.

Today, I came across this PDF file which was called “The Consumer Platform for Health IT.” Here’s the first paragraph:

Members of the Consumer Partnership for eHealth (CPeH) have been working for more than five years to advance patient-centered, consumer-focused health IT (information technology). We believe our nation is at a pivotal moment for transforming our health care system with the support of better information. This platform outlines a vision for how health IT can help patients, and how consumer groups can work alongside other stakeholders to improve health outcomes.

To be honest, I know nothing about the CPeH organization. I think that’s the actual problem. I’ve been working in healthcare IT and very active in the community of engagement consumers in healthcare for 5+ years myself and I’ve never heard of them. Unfortunately, it seems that CPeH has spent far too much time focused on creating a lengthy PDF of their vision and not enough time actually engaging consumers and producing results.

Although, I guess many might argue that I’ve spent too much time engaging with doctors, patients and other healthcare IT stakeholders and could spend more time on my vision. I’ll take that imbalance any day.