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Health IT | News, Analysis, Insights - HIT Consultant

46% of Patients Want Their Docs to Share Health Records Directly

by Fred Pennic 09/29/2015 Leave a Comment

46% of Patients Want Their Docs to Share Health Records Directly

By the year 2024, the U.S. Department of Health and Human Services wants interoperability between disparate electronic health records systems (EHRs) to be a common capability. This would allow patient data to be shared among authorized practitioners more seamlessly. But how do patients feel about this? According to a recent survey conducted by Software Advice, 46 percent of patients want their doctors to directly exchange the health records, and fewer (21 percent) favor in-person delivery.
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Can You Maintain HIPAA Consent While Using Email?

by Our Thought Leaders 09/29/2015 Leave a Comment

Editor's Note: Erik Kangas is the Presdient and CEO of LuxSci, a SaaS company specializing in security, privacy, HIPAA compliance, and all things email. He also consults on email best practices, secure web site architectures, and HIPAA compliance to organizations around the globe. The way personal health information has been gathered, stored, and protected over the years has seen a great number of changes. Up until 1996, when Congress first passed the Health Insurance Portability and
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Nuance Unveils Next-Gen Computer-Assisted Physician Documentation for ICD-10

by HITC Staff 09/28/2015 Leave a Comment

Today, Nuance Communications, Inc. has launched Dragon Medical Advisor, a next generation Computer-Assisted Physician Documentation (CAPD) solution that automatically provides real-time quality feedback to physicians while they are documenting patient encounters. This improves the completeness of clinical notes and helps provider organizations meet the impending ICD-10 requirements, justify medical necessity of care decisions, and support better patient care. Building on the work done in 2011
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lifeIMAGE Pulls In $5M for its Medical image Exchange Platform

by HITC Staff 09/28/2015 Leave a Comment

lifeIMAGE, a medical image exchange platform that enables imaging data interoperability across healthcare networks, providers, patients and technology systems, has received a $5 million strategic investment from Zaffre Investments, LLC, the investment arm of Blue Cross Blue Shield of Massachusetts (BCBSMA). As part of the investment, Zaffre Vice President, Steven J. Fox, will serve as board observer at lifeIMAGE, and will help identify opportunities to connect providers and patients in the
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WEDI, Nate Partner on Virtual Clipboard to Support Interoperability

by Fred Pennic 09/28/2015 Leave a Comment

WEDI Survey Reveals ICD-10 Delay Negatively Impacted Provider Readiness

The Workgroup for Electronic Data Interchange (WEDI), a nonprofit authority on the use of health IT to create efficiencies in healthcare information exchange, and the National Association for Trusted Exchange (NATE), a nonprofit authority in consumer-mediated electronic health information exchange, announced a partnership to cooperate on Phase II of the Virtual Clipboard Initiative and to advance research concerning healthcare interoperability. Virtual Clipboard Initiative Overview Built
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Virtual Town Hall Meeting Examines Reframing Meaningful Use Regulations

by Jasmine Pennic 09/24/2015 Leave a Comment

After sending letters to  Secretary of Health and Human Services Sylvia Burwell and Office of Management and Budget Director Shaun Donovan last week, the American Medical Association (AMA) and the Massachusetts Medical Society (MMS) will hold a virtual town hall meeting to give physicians and others a chance to discuss concerns with poorly designed EHRs and the impact these systems have on patient care. The U.S. government has spent $25 billion under the Meaningful Use program to promote a
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5 Best Practices for Healthcare Organizations’ Working on UDI Compliance

by HITC Staff 09/24/2015 Leave a Comment

Healthcare Organizations’ Working on UDI Compliance

Today, the healthcare industry crosses another Unique Device Identifier (UDI) milestone: the deadline requiring all implantable, life-supporting and life-sustaining devices to be labeled with a UDI. Two years ago, the U.S. Food and Drug Administration (FDA) issued its UDI Rule. Since then, Global Healthcare Exchange, LLC (GHX) has worked closely with healthcare suppliers to help them navigate the complexities of becoming UDI compliant and to leverage the rule to improve how they manage product
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Leidos Donates $40k to Fund Pilot Healthcare Data Analytics Platform

by HITC Staff 09/24/2015 Leave a Comment

Leidos, a national security, health, and engineering solutions company, has donated $40,000 to the Georgia Institute of Technology to fund a pilot program in healthcare data analytics. The funding will help support the development of a pilot data analytics platform in the I3L designed to improve the quality and efficiency of healthcare through data transparency. The donation marks Leidos’ third to Tech’s Interoperability & Integration Innovation Lab (I3L) since 2013. Healthcare Data
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Accenture Acquires Sagacious Consultants to Expand Epic Consulting Capabilities

by HITC Staff 09/23/2015 Leave a Comment

Accenture and TPP Complete First Phase of Digitizing Patient Records

Global management consultant firm Accenture,  today announced that it has finalized its agreement to acquire Sagacious Consultants, an Epic-focused EHR consulting firm to expand its capabilities for helping clients to better manage healthcare quality, efficiency and costs. Financial terms of the transaction were not disclosed. Founded in 2009 by former Epic consultant Shane Adams, approximately 250 employees from Sagacious Consultants will bring to Accenture their specialized skills in
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FDA Launches First-Ever Patient Engagement Advisory Committee

by HITC Staff 09/22/2015 Leave a Comment

Medical Device_FDA Recalls McKesson's Anesthesia Care for False Patient-Matching

On Friday, the FDA announced its first-ever Patient Engagement Advisory Committee (PEAC) that will provide advisory support to the FDA Commissioner on a range of complex issues relating to medical devices, the regulation of devices, and their use by patients. These ultimate goal of the PEAC is to helping to drive more patient-centered medical product development and assessment process. Other topics the committee may consider include: - Agency guidance and policies - clinical trial or
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