Health Information Exchange, Interoperability, and Network Effects

Health Information Exchange, Interoperability, and Network Effects

Author: Sunita Desai

Publisher:

Published: 2015

Total Pages: 178

ISBN-13:

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Health information exchange (HIE) is the electronic exchange of patient medical records among hospitals. I investigate how two defining characteristics of HIE can cause under-adoption. First, HIE represents an information-sharing network, and participation for any hospital is valuable if others participate. This is a network effect. Second, HIE involves exchange of medical records, which may be competitive assets for hospitals. Therefore, hospitals may have disincentive to exchange with competitors despite social benefits. This is a competitive effect. I present a theoretical framework of hospitals' decisions to adopt HIE and show how presence of network and competitive effects can result in under-adoption relative to the social optimal. I then test for evidence of network and competitive effects in hospital HIE adoption. In the empirical analysis, I use two measure of HIE adoption. The first is a measure of general adoption in which all hospitals that have adopted any HIE capability are assumed to be able to exchange information with each other. The second takes into account that much information-sharing occurs through interoperable IT systems and currently, most IT systems of different vendors are not interoperable. I find evidence of network effects in general HIE adoption and vendor choice. I find that a 10% increase in market adoption rate results in a hospital being 9.2% more likely to adopt HIE. I also find that a 10% increase in adoption rate of a vendor results in a hospital being 1.5% more likely to adopt the vendor. I also find evidence of competitive effects. Specifically, hospitals that are more vulnerable to losing market share are less likely to adopt a prominent vendor in a market. I estimate a model of patients' hospital preferences and hospitals' HIE adoption decision. Through counterfactual simulation, I show effects of widespread HIE adoption on market share redistribution. Finally, I evaluate current policies such as the federal government's $30 billion adoption incentive program (HITECH Act). The program may be inadequate to promote widespread interoperability in the presence of competitive effects. I also discuss the implications of network effects for competition and innovation in the health IT industry.


Health Information Exchange

Health Information Exchange

Author: Brian Dixon

Publisher: Academic Press

Published: 2022-11-13

Total Pages: 733

ISBN-13: 0323908039

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Health Information Exchange: Navigating and Managing a Network of Health Information Systems, Second Edition, now fully updated, is a practical guide on how to understand, manage and make use of a health information exchange infrastructure, which moves patient-centered information within the health care system. The book informs and guides the development of new infrastructures as well as the management of existing and expanding infrastructures across the globe. Sections explore the reasons for the health information exchange (HIE) infrastructures, how to manage them, examines the key drivers of HIE, and barriers to their widespread use. In addition, the book explains the underlying technologies and methods for conducting HIE across communities as well as nations. Finally, the book explains the principles of governing an organization that chiefly moves protected health information around. The text unravels the complexities of HIE and provides guidance for those who need to access HIE data and support operations. Encompasses comprehensive knowledge on the technology and governance of health information exchanges (HIEs) Presents business school style case studies that explore why a given HIE has or hasn't been successful Discusses the kinds of data and practical examples of the infrastructure required to exchange clinical data to support modern medicine in a world of disparate EHR systems


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.


Electronic Health Information Exchange, Switching Costs, and Network Effects

Electronic Health Information Exchange, Switching Costs, and Network Effects

Author: Sunita Desai

Publisher:

Published: 2014

Total Pages: 0

ISBN-13:

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As in most industries, in health care, information is a competitive asset, and we expect that health care providers may have incentive to protect their information from competitors. This study aims to understand how this incentive to protect information may be a barrier to the development of a health information network. Health information networks are designed to facilitate electronic information sharing across health care providers. The electronic exchange of health information is widely considered a promising tool to improve quality, costs, and efficiency of health care. Federal and state governments have invested over $30 billion dollars to support the development of health information networks and electronic health information sharing. However, uptake has been slow suggesting that barriers to adoption exist. We first develop a model of firms' decisions to enter a health information network given this potential loss of competitive advantage. Guided by implications of the model, we conduct a two part empirical analysis to test for evidence that providers may be reluctant to join a health information network out of competitive concern. First, we conduct a national hospital-level analysis. Second, we construct a novel data set to conduct a physician-level analysis focused on New York state. In both analyses, we find supporting evidence that competitive pressure may be a barrier to entry by health care firms. We discuss implications for policy and network design given our findings.


Public Health Informatics and Information Systems

Public Health Informatics and Information Systems

Author: J.A. Magnuson

Publisher: Springer Science & Business Media

Published: 2013-11-29

Total Pages: 665

ISBN-13: 1447142373

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This revised edition covers all aspects of public health informatics and discusses the creation and management of an information technology infrastructure that is essential in linking state and local organizations in their efforts to gather data for the surveillance and prevention. Public health officials will have to understand basic principles of information resource management in order to make the appropriate technology choices that will guide the future of their organizations. Public health continues to be at the forefront of modern medicine, given the importance of implementing a population-based health approach and to addressing chronic health conditions. This book provides informatics principles and examples of practice in a public health context. In doing so, it clarifies the ways in which newer information technologies will improve individual and community health status. This book's primary purpose is to consolidate key information and promote a strategic approach to information systems and development, making it a resource for use by faculty and students of public health, as well as the practicing public health professional. Chapter highlights include: The Governmental and Legislative Context of Informatics; Assessing the Value of Information Systems; Ethics, Information Technology, and Public Health; and Privacy, Confidentiality, and Security. Review questions are featured at the end of every chapter. Aside from its use for public health professionals, the book will be used by schools of public health, clinical and public health nurses and students, schools of social work, allied health, and environmental sciences.


Electronic Personal Health Information Exchange

Electronic Personal Health Information Exchange

Author: Valerie C. Melvin

Publisher: DIANE Publishing

Published: 2010-08

Total Pages: 51

ISBN-13: 1437929524

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To promote the use of info. tech. (IT) for the electronic exchange of personal health info. among providers and other health care entities (HCE), Congress passed the Health IT for Economic and Clinical Health Act. It provides incentives to promote the adoption of IT that supports the electronic sharing of data among hospitals, physicians, and other HCE. This report on practices implemented by health info. exchange org., providers, and other HCE that disclose electronic personal health info. describes: (1) the practices implemented for disclosing personal health info. for purposes of treatment, incl. the use of electronic means for obtaining consent; and (2) the effects of the electronic sharing of health info. on the quality of care for patients. Charts and tables.


Principles of Health Interoperability

Principles of Health Interoperability

Author: Tim Benson

Publisher: Springer

Published: 2016-06-22

Total Pages: 461

ISBN-13: 3319303708

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This book provides an introduction to health interoperability and the main standards used. Health interoperability delivers health information where and when it is needed. Everybody stands to gain from safer more soundly based decisions and less duplication, delays, waste and errors. The third edition of Principles of Health Interoperability includes a new part on FHIR (Fast Health Interoperability Resources), the most important new health interoperability standard for a generation. FHIR combines the best features of HL7’s v2, v3 and CDA while leveraging the latest web standards and a tight focus on implementability. FHIR can be implemented at a fraction of the price of existing alternatives and is well suited for use in mobile phone apps, cloud communications and EHRs. The book is organised into four parts. The first part covers the principles of health interoperability, why it matters, why it is hard and why models are an important part of the solution. The second part covers clinical terminology and SNOMED CT. The third part covers the main HL7 standards: v2, v3, CDA and IHE XDS. The new fourth part covers FHIR and has been contributed by Grahame Grieve, the original FHIR chief.


Interoperability in Healthcare Information Systems: Standards, Management, and Technology

Interoperability in Healthcare Information Systems: Standards, Management, and Technology

Author: Sicilia, Miguel Ángel

Publisher: IGI Global

Published: 2013-06-30

Total Pages: 336

ISBN-13: 1466630019

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Although the standards in electronic health records and general healthcare services continue to evolve, many organizations push to connect interoperability with public service and basic citizenship rights. This poses significant technical and organizational challenges that are the focus of many research and standardization efforts. Interoperability in Healthcare Information Systems: Standards, Management and Technology provides a comprehensive collection on the overview of electronic health records and health services interoperability and the different aspects representing its outlook in a framework that is useful for practitioners, researchers, and decision-makers.


Integrating Social Care into the Delivery of Health Care

Integrating Social Care into the Delivery of Health Care

Author: National Academies of Sciences, Engineering, and Medicine

Publisher: National Academies Press

Published: 2020-01-30

Total Pages: 195

ISBN-13: 0309493439

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Integrating Social Care into the Delivery of Health Care: Moving Upstream to Improve the Nation's Health was released in September 2019, before the World Health Organization declared COVID-19 a global pandemic in March 2020. Improving social conditions remains critical to improving health outcomes, and integrating social care into health care delivery is more relevant than ever in the context of the pandemic and increased strains placed on the U.S. health care system. The report and its related products ultimately aim to help improve health and health equity, during COVID-19 and beyond. The consistent and compelling evidence on how social determinants shape health has led to a growing recognition throughout the health care sector that improving health and health equity is likely to depend â€" at least in part â€" on mitigating adverse social determinants. This recognition has been bolstered by a shift in the health care sector towards value-based payment, which incentivizes improved health outcomes for persons and populations rather than service delivery alone. The combined result of these changes has been a growing emphasis on health care systems addressing patients' social risk factors and social needs with the aim of improving health outcomes. This may involve health care systems linking individual patients with government and community social services, but important questions need to be answered about when and how health care systems should integrate social care into their practices and what kinds of infrastructure are required to facilitate such activities. Integrating Social Care into the Delivery of Health Care: Moving Upstream to Improve the Nation's Health examines the potential for integrating services addressing social needs and the social determinants of health into the delivery of health care to achieve better health outcomes. This report assesses approaches to social care integration currently being taken by health care providers and systems, and new or emerging approaches and opportunities; current roles in such integration by different disciplines and organizations, and new or emerging roles and types of providers; and current and emerging efforts to design health care systems to improve the nation's health and reduce health inequities.