Archive | Meaningful Use

Meaningful Use is the new standard in healthcare, driven by the passage of HITECH.

The Secret Life of the SNOMED Code: Why Patient’s ‘Problem List’ is a Problem

In her debut on the blog, Mandi Bishop highlights how the one-to-many mapping of SNOMED codes could affect patient care and their medical history.

‘The purpose of the SNOMED problem list is to inform all providers in the patient’s care continuum of any active or chronic conditions needing assessment and monitoring. With the single-click application of any given SNOMED code to an entire population of patients, it is highly likely that some, if not many, patients will be incorrectly assigned. It is unlikely that the patient will be clinically educated enough to identify, let alone explain, the difference to the network of providers participating in his or her care.’

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GAO Report on Health Information Exchange Focuses on Standards

Meaningful use criteria are indeed shaping the industry and modernizing how health data is used, but the criteria isn’t a paint-by-numbers instruction manual. IT departments should not feel reliant on or handcuffed by the ONC. There is still plenty of room for IT leaders to set ambitious, innovative goals that help create a competitive advantage through data exchange.

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Big Things in Patient Engagement: Context and Transparency

It was apparent that health IT is really moving toward accountable, value-based care, which ultimately has its success rooted in better decisions by patients, physicians and caregivers. The interoperability must ultimately lead to delivering more transparent cost and quality data in context. To make effective decisions, and to effectively engage, we must understand all the factors influencing a person at a given time, we must understand contexts, and get key information placed into that context. That’s how we can put mHealth, interoperability and patient engagement into a framework that drives patient engagement.

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New ONC Leader Karen DeSalvo Discusses Priorities, Current Health IT Landscape at HIMSS14

This year’s HIMSS Annual Conference and Exhibition saw Karen DeSalvo, the new National Coordinator for Health Information Technology, take the stage and it was clear we are entering a new era under her leadership. She recognizes that we are at a pivot point in the history of health IT and sees the need for everyone to take a breath and possibly find some better ways to reach some of our goals. Brian Ahier discusses his first impressions and shares a comprehensive, one-on-one video interview he conducted at the conference.

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Should Physicians or Patients be Responsible for Health History Accuracy?

Jennifer Thew, RN, provides a personal story about medical errors that illustrates the need for better patient involvement in their care, which begins with ownership of patient data. The future possibility of patient-generated health data being incorporated into the patient’s actual medical record, per meaningful use proposals, poses many difficult questions such as, ‘Who needs to accept responsibility here?’ A great post that needs your comments.

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PGHD

Patient Generated Health Data: With Great Power Comes Great Responsibility

Will giving patients the privilege to capture and record their own health data, and have it incorporated into the EMR, be the first step to a future where patients are responsible (and held accountable through the documentation) for carrying out and documenting their physician’s orders? Will patients be penalized for failing their responsibility?

These questions, and more, will arise as we enter Meaningful Use Stage 3, which contains a provision allowing just that — the ability of the patient to input their data into their medical record. Let’s discuss this game-changing topic.

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