It was a pleasure to work with you, as you and your team made this process a more pleasant experience for our team and the participants.
Several groups have submitted comments on CMS' proposed meaningful use modifications for 2015 through 2017, Clinical Innovation & Technology reports (Walsh, Clinical Innovation & Technology, 6/15).
Under the 2009 economic stimulus package, providers who demonstrate meaningful use of certified electronic health records can qualify for Medicaid and Medicare incentive payments.
In April, CMS released a proposed rule that would shorten Medicare and Medicaid meaningful use attestation for eligible professionals and hospitals to a 90-day period in 2015.
Overall, the proposed rule would:
In addition, the proposed rule would change Stage 2 meaningful use requirements related to patient engagement. Specifically, CMS proposed reducing the requirement for patients to use technology to electronically download, view and transmit their medical records from 5% of eligible providers' patients to just one patient (iHealthBeat, 4/13).
Comments on the proposed modifications were due June 15 (iHealthBeat, 5/28).
The American Medical Group Association in its comments praised CMS for easing the program's reporting requirements, as well as for proposing a shorter 90-day reporting period.
AMGA CEO Donald Fisher said, "This proposed rule reflects that CMS has been sensitive to the struggles that the health care industry has had with meaningful use by simplifying some of the reporting requirements through 2017."
The group also urged CMS to help strengthen the health IT infrastructure to support future data sharing requirements (AMGA release, 6/15).
Russell Branzell, president of the College of Healthcare Information Management Executives, in his comments called for a middle ground on patient engagement. He wrote that rather than requiring every specialist to demonstrate that patients can "view, download and transmit" their health information, those data should be aggregated into a single location for patients.
He added, "I definitely want patient data made accessible to patients or those taking care of them. But I don't want to get every note out of some subspecialty office" (Pittman et al., "Morning eHealth," Politico, 6/16).
Meanwhile, a group of 50 advocacy groups organized by the Consumer Partnership for eHealth and the Consumer-Purchase Alliance in its comments expressed disappointment, saying CMS' proposal to reduce patient engagement requirements would undermine patient engagement efforts (Clinical Innovation & Technology, 6/15). Specifically, CPeH said, "CMS' proposed amendments constitute a dramatic retreat from essential efforts to make patients and family caregivers true and equal partners in improving health through shared information, understanding and decision making" ("Morning eHealth," Politico, 6/16).
Debra Ness -- president of the National Partnership for Women & Families, which was part of the coalition -- said the groups "urge CMS to keep the existing patient engagement thresholds."
Meanwhile, Bill Kramer, co-chair of the Consumer-Purchase Alliance, noted that maintaining efforts to give patients and caregivers "electronic access to and use of their health information" is key to achieving interoperability in the U.S. health care system (Clinical Innovation & Technology, 6/15).
The Healthcare Information and Management Systems Society in a letter to CMS supported the agency's proposal to ease reporting requirements but urged CMS to be cautious moving forward with other proposals, Health Data Management reports.
Among other things, HIMSS recommended that CMS:
It was a pleasure to work with you, as you and your team made this process a more pleasant experience for our team and the participants.
I just want to tell you that I value people relations more than money. I remember how you were friendly and helpful not going against policies and contractual obligations at the same time, not using your power to make us feel stupid and small. It was a very rare and big experience for me. Really. I will always remember this.
The Usability People are all individuals that you can become friends with very easily. They have a lot of different interests and are a pleasure to work with. I was writing a PRD/MRD for a billing solution and worked with The Usability People in defining the user interface. They are receptive to ideas and are able to mold the user interface from an end-user's perspective. I really liked the idea of putting end-user photograph & short biography around the office to help understand the users