Electronic Health Records Nonfederal Efforts to Help Achieve Health Information Interoperability

Electronic Health Records Nonfederal Efforts to Help Achieve Health Information Interoperability

Author: Government Accountability Office

Publisher: Createspace Independent Publishing Platform

Published: 2016-10-07

Total Pages: 30

ISBN-13: 9781539396260

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Representatives from the 18 nonfederal initiatives GAO reviewed described a variety of efforts they are undertaking to achieve or facilitate electronic health record (EHR) interoperability, but most of these initiatives remain works in progress. EHR interoperability is the ability of systems to exchange electronic health information with other systems and process the information without special effort by the user, such as a health care provider. These initiatives' efforts include creating guidance related to health data standards, encouraging the adoption of certain health data standards or policies that facilitate interoperability, and operating networks that connect EHR systems to enable interoperability. The initiatives varied in a number of other ways, including the types of electronic systems the initiatives are working to make interoperable, the cost of their products or services, the geographic area served, patient use of the products or services, and their organizational structures. For example, GAO found that while some initiatives are making their products or services available at no cost, others are charging a fee for their products or services based on the type of entity using the product or service (e.g., individual physician or hospital) or the amount of data exchanged. Similarly, over half of the initiatives were using varying approaches to facilitate patient access to and control over their health information. The majority of the initiatives GAO selected are still in the process of developing, or encouraging others to adopt, their products or services. Most of the initiatives' products or services were not widely available at the time of GAO's review, but initiative representatives anticipated greater availability of their products or services in the next 2 years. Stakeholders and initiative representatives GAO interviewed described five key challenges to achieving EHR interoperability, which are consistent with challenges described in past GAO work. Specifically, the challenges they described are (1) insufficiencies in health data standards, (2) variation in state privacy rules, (3) accurately matching patients' health records, (4) costs associated with interoperability, and (5) the need for governance and trust among entities, such as agreements to facilitate the sharing of information among all participants in an initiative. Representatives from the 18 initiatives GAO reviewed said they are working to address these key challenges using different approaches. Each key challenge is in the process of being addressed by some initiatives. To move interoperability forward, initiative representatives noted, among other issues, that providers need to see an EHR system as a valuable tool for improving clinical care. The Department of Health and Human Services provided technical comments on a draft of this report, which GAO incorporated as appropriate.


Electronic Health Records

Electronic Health Records

Author: United States Government Accountability Office

Publisher: Createspace Independent Publishing Platform

Published: 2017-12-24

Total Pages: 30

ISBN-13: 9781982006730

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ELECTRONIC HEALTH RECORDS: Nonfederal Efforts to Help Achieve Health Information Interoperability


Electronic Health Records

Electronic Health Records

Author: U S Government Accountability Offi Gao

Publisher: Independently Published

Published: 2019-06-07

Total Pages: 30

ISBN-13: 9781072517382

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ELECTRONIC HEALTH RECORDS: Nonfederal Efforts to Help Achieve Health Information Interoperability


Electronic Health Records, Nonfederal Efforts to Help Achieve Health Information Interoperability

Electronic Health Records, Nonfederal Efforts to Help Achieve Health Information Interoperability

Author: U.s. Government Accountability Office

Publisher: Createspace Independent Publishing Platform

Published: 2017-07-27

Total Pages: 30

ISBN-13: 9781973955894

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" EHR interoperability is viewed by many health care stakeholders as a necessary step toward improving health care. However, interoperability has remained limited. Although the federal government plays a key role in guiding movement toward interoperability, many of the actions are to be completed by nonfederal stakeholders. GAO was asked to review the status of efforts by entities other than the federal government to develop infrastructure that could lead to nationwide interoperability of health information. This report describes the (1) characteristics of selected nonfederal initiatives intended to facilitate EHR interoperability, and (2) key challenges related to EHR interoperability and the extent to which selected nonfederal initiatives are addressing these challenges. GAO interviewed representatives from 18 selected nonfederal initiatives that were frequently mentioned by stakeholders GAO interviewed, and reflected a range of approaches. GAO reviewed documents from these initiatives as well as other published research.


Electronic Health Records

Electronic Health Records

Author: Joel C. Willemssen

Publisher: DIANE Publishing

Published: 2010-08

Total Pages: 31

ISBN-13: 1437928919

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The Nat. Defense Authorization Act for FY 2008 required the DoD and the VA to accelerate their exchange of health information and to develop capabilities that allow for interoperability (the ability of systems to exchange data) by Sept. 30, 2009. It also required compliance with federal standards and the establishment of a joint interagency program office to function as a single point of accountability for the effort. This report determined the extent to which: (1) DoD and VA developed and implemented electronic health record systems or capabilities that allowed for full interoperability by Sept. 30, 2009; and (2) the interagency program office established by the act is functioning as a single point of accountability. Charts and tables.


Registries for Evaluating Patient Outcomes

Registries for Evaluating Patient Outcomes

Author: Agency for Healthcare Research and Quality/AHRQ

Publisher: Government Printing Office

Published: 2014-04-01

Total Pages: 385

ISBN-13: 1587634333

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This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.


Portable Health Records in a Mobile Society

Portable Health Records in a Mobile Society

Author: Egondu R. Onyejekwe

Publisher: Springer Nature

Published: 2019-09-06

Total Pages: 325

ISBN-13: 3030199371

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This book details how electronic health records (EHRs) and medical records (EMRs) can be optimized to enable meaningful interactions between provider and patient to enhance quality of care in this new era of mHealth. As the technologies evolve to provide greater opportunities for mHealth applications, so do the challenges. This book addresses the issues of interoperability limitations, data processing errors and patient data privacy while providing instruction on how blockchain-like processes can potentially ensure the integrity of an externally maintained EHR. Portable Health Records in a Mobile Society identifies important issues and promising solutions to create a truly portable EHRs. It is a valuable resource for all informaticians and healthcare providers seeking an up-to-date resource on how to improve the availability, reliability, integrity and sustainability of these revolutionary developments in healthcare management.


Building a Roadmap for Health Information Systems Interoperability for Public Health

Building a Roadmap for Health Information Systems Interoperability for Public Health

Author:

Publisher:

Published: 2008

Total Pages: 66

ISBN-13:

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"The development of this White Paper has been facilitated by the Public Health Data Standards Consortium (PHDSC) and the Integrating the Healthcare Enterprise (IHE). The White Paper was developed by the participants of the PHDSC-IHE Task Force. The information in this document represents the views of the individual Task Force participants and may not represent the views of their organizations. The vision for this Roadmap is data interoperability throughout the complex web of the entire public health and healthcare enterprise for efficient exchange of health data for public health query. The overall goal of this effort is to facilitate the necessary linkages, standardization and integration of health data between clinical care and public health to create robust overarching health information exchanges. The objective is to engage the public health community in a dialogue with health information technology (HIT) vendors to assure that the work processes and data needs of public health stakeholders in health information exchanges are 1) well understood and agreed upon by stakeholders themselves, and then (2) communicated clearly to the developers of the interoperable clinical Electronic Health Record (EHR) systems and Public Health information systems (EHR-PH Systems). The White Paper consists of three sections. The first section describes public health and population health practices of governmental public health agencies that require access to health information exchanges incorporating clinical care data. The second and third sections describe examples of public health domains/programs (Immunization and Cancer) in the outline of the IHE Technical Tasks for Information Exchanges. Brief descriptions of practices and challenges of health information exchanges in other public health domains (research, chronic care, personal health record, surveys, obesity, trauma, pharmaco-vigilance, etc.) is provided in Appendix 1. Standardization of clinical-public health information exchanges in these domains may be included in the future public health activities at IHE."--Page 5.


Electronic Health Records

Electronic Health Records

Author: United States Government Account Office

Publisher: Createspace Independent Publishing Platform

Published: 2018-01-15

Total Pages: 36

ISBN-13: 9781983866203

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Electronic Health Records: DOD and VA Efforts to Achieve Full Interoperability Are Ongoing; Program Office Management Needs Improvement