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Converge where Healthcare meets Innovation
2015-09-02 - 2015-09-03    
All Day
MedCity CONVERGE provides the most accurate picture of the future of medical innovation by gathering decision-makers from every sector to debate the challenges and opportunities [...]
11th Global Summit and Expo on Food & Beverages
2015-09-22 - 2015-09-24    
All Day
Event Date: September 22-24, 2016 Event Venue: Embassy Suites, Las Vegas, Nevada, USA Theme: Accentuate Innovations and Emerging Novel Research in Food and Beverage Sector [...]
2015 AHIMA Convention and Exhibit
2015-09-26 - 2015-09-30    
All Day
The Affordable Care Act, Meaningful Use, HIPAA, and of course, ICD-10 are changing healthcare. Central to healthcare today is health information. It is used throughout [...]
Transforming Medicine: Evidence-Driven mHealth
2015-09-30 - 2015-10-02    
8:00 am - 5:00 pm
September 30-October 2, 2015Digital Medicine 2015 Save the Date (PDF, 1.23 MB) Download the Scripps CME app to your smart phone and/or tablet for the conference [...]
Health 2.0 9th Annual Fall Conference
2015-10-04 - 2015-10-07    
All Day
October 4th - 7th, 2015 Join us for our 9th Annual Fall Conference, October 4-7th. Set over 3 1/2 days, the 9th Annual Fall Conference will [...]
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Articles

Nov 26: DNA links to skin diseases found in EMR data

tasmania lays foundations

Data contained in electronic medical records can help link genetic variants to previously unknown relationships with disease, according to research published at Nature Biotechnology.

Vanderbilt University researchers found links between DNA variants and skin diseases by surveying 13,000 EMRs. First they grouped around 15,000 billing codes from medical records into 1,600 disease categories, then they looked for looked for links to disease in records in which DNA data was available.

Links to skin diseases–non melanoma skin cancer and two forms of skin growths called keratosis, one of which is pre-cancerous–were found. The researchers were able to validate the connection between these conditions and their associated gene variants in other patient data, reports Technology Review.

Looking for various diseases at once might be less biased than research looking at a specific disease, the article says, and it might help researchers understand how single genes might affect multiple characteristics or conditions.

Even larger sets of EMRs could uncover even more rare and complex relationships, the authors said, such a drug side effect that occurs only in one of 10,000 patients.

A discussion paper released by the Institute of Medicine earlier this year proposed argued that the data collected in routine doctor visits could be used to improve care for all by creating a learning healthcare system.

“Currently, the information collected like blood pressure, weight, medications used, disease diagnoses and medical history are used only to inform decisions for that individual patient. We are missing a tremendous opportunity to turn our health care system into one that learns from each care experience and leads to better and more affordable care for all,” Michael D. Murray, the Regenstrief Institute investigator and Purdue University professor who was lead author on the paper, said.

In October, the National Science Foundation awarded grants totaling nearly $900,000 to The University of Texas at Arlington, Southern Methodist University and the University of Texas Southwest Medical Center at Dallas to develop data mining tools for electronic health records.

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