‘National Progress Report on eHealth’ Shows Significant Progress in Last 3 Years

eHealth Initiative Survey Identifies Challenges with Consumer Outreach and Understanding of Value
eHealth Initiative (eHI) issued the following press release on July 1, 2010.

WASHINGTON, DC – July 1, 2010 -
Today, the eHealth Initiative (eHI) released the “National Progress Report on eHealth,” which tracks the progress of eHealth in the wake of the American Recovery and Reinvestment Act of 2009.

National Progress Report on eHealth 2010

National Progress Report on eHealth 2010

The National Progress Report on eHealth includes a review of progress made over the last three years relative to strategies and actions proposed in a 2007 eHI report. Over one hundred individuals participated on committees charged with assessing progress in five focus areas: Aligning Incentives; Engaging Consumers; Improving Population Health; Managing Privacy, Security & Confidentiality; and, Transforming Care Delivery. The report highlights key trends, actions, and strategies that still need to be addressed.

The report reveals a number of high-level findings including:

  • Significant progress has been made over the last three years as a result of public and private sector initiatives. The American Recovery and Reinvestment Act (ARRA) was the key driver of progress.
  • Many providers are concerned about the lack of coordination across the government health and health information technology (HIT) initiatives.
  • More education and outreach to consumers about HIT and health information exchange (HIE) is required.
  • Knowledge and transparency of privacy and security policies will be the key to building consumer trust of HIT and HIE.

As part of the assessment process, eHI conducted an informal online survey to gauge perceptions of progress. The survey responses offer a snapshot about the eHealth landscape. Some findings include:

  • The majority of respondents believe significant progress has been made: 61 percent of respondents agree or strongly agree with the statement that significant progress has been made in the successful adoption and use of HIT since 2007.
  • The value of HIE is not clearly understood by the majority of respondents: 54.9 percent disagree or strongly disagree with the statement that the value of HIE is clearly understood.
  • The majority of respondents believe outreach to consumers about the value of EHRs and HIE is not effective: 66.6 percent disagree or strongly disagree with the statement that current outreach to consumers about the value of EHRs and HIE is effective.
  • The majority believe Regional Extension Centers and the National Health Information Technology Research Center (HITRC) will be vital to educating providers: 66.1 percent of respondents agree or strongly agree with the view that Regional Extension Centers and the HITRC will be vital to educating providers about adoption and meaningful use of HIT.

“Contributors to the report found that, while considerable progress has been made over the past three years, challenges remain,” noted Jennifer Covich Bordenick, eHealth Initiative’s Chief Executive Officer. “Coordinating public and private sector efforts, and communicating the true value of HIT and HIE to consumers will be critical as we move forward.”

As part of its work, the eHealth Initiative collected information on dozens of existing and new HIT initiatives occurring across the country. An online version of the current activities is available in the report and online.

The National Progress Report on eHealth was supported by the Commonwealth Fund, a private foundation supporting independent research on health policy reform and a high performance health system.

The report is available on the eHI website at: http://www.ehealthinitiative.org/

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About eHealth Initiative
The eHealth Initiative (eHI) is an independent, non-profit, multi-stakeholder organization whose mission is to drive improvements in the quality, safety, and efficiency of healthcare through information and information technology (IT). eHI is the only organization that represents all of the stakeholders in the healthcare industry. eHI advocates for the use of HIT that is practical, sustainable and addresses stakeholder needs, particularly those of patients. For more information, visit http://www.ehealthinitiative.org/
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Jennifer Lubell, HITS staff writer, reported July 2, 2010 in ModernHealthcare.com on National Progress Report,
“Electronic healthcare initiatives have made headway over the last several years, but health information technology remains an undervalued tool, a new report concludes.”

ONC Health IT Stories from the EHR Road: Update

New “Journey Stories” on Implementing EHRs
Excerpts from stories collected by Office of National Coordinator (ONC) for Health IT based on physician practices around the country.  Earlier stories repeated from a previous post on e-Healthcare Marketing.com . All carry a map and a quote from the practice.

The Heart of Texas Community Health Center considers their implementation of health IT a success. Their leadership states that the effort towards EHR implementation had the right people on the leadership team, the right product/vendor, and the good fortune to obtain a significant amount of funding at a critical time in the project. A map shows the geographical location of McLennan County, TX.

Dr. Lisa Moreno
Queens pediatric allergist and immunology specialist starts her practice from the cutting edge of HIT.
Queens, New York
Posted June 28, 2010

Cooley Dickinson Hospital
EHR adoption marks a time of rebirth for Massachusetts hospital. Northampton, Massachussetts
Posted June 28, 2010

Heart of Texas Community Health Center
McLennan County, Texas
Posted June 28, 2010

White River Rural Health Center
High standards for care and safety are met with the implementation of EHRs.
Augusta, Arkansas
Posted June 10, 2010

Thayer County Health Services
Five rural health centers and a 19 bed critical access hospital implement EHRs and HIE to benefit county residents.
Hebron, Nebraska
Posted June 10, 2010

Dr. Russell Kohl, Green Country Family Medicine
A two-doctor practice in rural Oklahoma creatively funds the practice’s journey to health IT implementation.
Vinita, Oklahoma
May 27, 2010

Urban Health Plan
The implementation of EHRs improves access to care and reduces health disparities for the urban underserved in the South Bronx.
South Bronx, NY
May 27, 2010

Toward Enhanced Information Capacities for Health: Achieving the Promise: NCVHS

NCVHS Concept Paper Looks How to Achieve the
Promise of Health Reform and Electronic Health Records
The National Committee on Vital and Health Statistics (NCVHS) met June 16-17, 2010 in Washington, DC, and used the NCVHS concept paper “Toward Enhanced Information Capacities for Health” as the basis of discussions for their 6oth Anniversary Symposium of the committee. The paper, issued May 26, 2010, focuses on policies HHS could establish to maximize the benefits that could be acheived through the appropriate use of the tremendous amount of health data that will be generated with Electronic Health Records.

The committee advises the Secretary of  HHS on policies toward health data, statistics, privacy, national health information policy, and Administrative Simplication of HIPAA.

NCVHS Concept Paper
“Toward Enhanced Information Capabilities for Health”
PDF FORMAT
The text of the 11-page paper is reproduced in whole below.

EXECUTIVE SUMMARYHealth care reform and federal stimulus legislation have created an unprecedented opportunity to improve health and health care in the United States. The nation’s ability to seize this opportunity will depend greatly on the existence of robust health information capacities. The National Committee on Vital and Health Statistics (NCVHS) is the statutory advisory body on health information policy to the Department of Health and Human Services. On the occasion of the Committee’s 60th anniversary, this concept paper outlines its current thinking about the necessary information capacities and how NCVHS can help the Department guide their development.

We are entering a new chapter in the health and health care of Americans. The expansion of health care coverage, the infusion of new funds and adoption of standards for electronic health records (EHRs), and increased administrative simplification offer us the potential to use the enriched data generated to better address our country’s health and health care challenges. Having better information with which to measure and understand the processes, episodes, and outcomes of care as well as the determinants of health can bring considerable health benefits, not only to individuals but also to the population as a whole.

To be able to achieve the promise of these new developments, we need to be attentive to the underpinnings of the data, ensuring that they are easy to generate and use at the front lines as well as easy to reuse, manipulate, link, and learn from within a mantle of privacy and security. It is important to remember that the new data sources are not necessarily a replacement for traditional sources such as administrative and survey data, which play a key role in our infrastructure. Rather, the new sources present an opportunity to augment and enrich traditional sources. While efficiency may be gained by replacing some survey and administrative data with newer EHR data, we must continue to nourish and sustain the traditional data sources that offer unique and irreplaceable information for both clinical and population health purposes.

National health information capacities must enable not just better clinical care but also population health and the many synergies between the two. More specifically, health information policy should foster improved access to affordable, efficient, quality health care; enhanced clinical care delivery; greater patient safety; empowered and engaged patients and consumers; patient trust in the protection of their health information; continuous improvement in population health and the elimination of health disparities; and support of clinical and health services research. A major priority of health information policy should be to enable the multiple uses of data, drawn from the full range of sources, while minimizing burden. Most sources have primary uses for which they were designed; however, with adequate standardization, privacy protections, and technology, the data from many sources can be used for multiple purposes. Realizing the collective potential of all information sources is what will allow the U.S. to maximize the return on its investments in system reform and health IT for the benefit of all Americans.

As information capacities expand, it is critical that the information be comprehensive, timely, efficiently retrievable, and usable, with full individual privacy protections in place. “Comprehensive” refers to the inclusion not just of traditional health-related data, but also of data on the full array of determinants of health, including community attributes and cultural context. Usability of the data—whether for initial use or reuse―requires a well-coordinated effort to assure the accessibility and availability of information as well as its standardization.

NCVHS will continue to use its consultative and deliberative processes, working collaboratively with other HHS advisory committees, to help the Department meet these opportunities and challenges. Given the rapidity of the changes now under way, we cannot over-emphasize the urgency of this endeavor and the need to move ahead with deliberate speed.

INTRODUCTION

Health care reform and federal stimulus legislation have created an unprecedented opportunity to improve health and health care in the United States. The nation’s ability to seize this opportunity will depend greatly on the existence of robust health information capacities. 1 To maximize the return on these enormous investments and make it possible to evaluate their impact, health information capacities must be carefully developed with an eye to their uses for improving health care and health for all Americans. New investments in EHRs and health information exchanges are important contributors, especially for clinical care, but the benefits from these investments will be limited unless the synergies with other types of health information are recognized and used. Population-level data from vital statistics systems, surveys, and public health surveillance and health care administrative data are equally important information sources. Assuring that all these sources are adequately developed and supported and can be integrated appropriately is essential to developing the information capacities the nation needs.

The National Committee on Vital and Health Statistics, the Department’s statutory advisory body on health information policy, has long assisted the Department in the development of national health information policy, providing thought leadership and expert advice in the areas of population health, privacy, standards, the NHII/NHIN, health care quality, and more. Nearly ten years ago, NCVHS put forward a vision for a national health information infrastructure in its 2001 report, Information for Health,2 followed in 2002 by a vision for 21st century health statistics.3 Today, as data and communication capacities explode and health care coverage expands, new thinking and visioning are needed to clarify the information capacities that will make it possible to meet our national goals for better health and health care for all Americans. On the occasion of the Committee’s 60th anniversary, this concept paper outlines its current thinking about the required capacities and their development.

In 2009, as course-altering legislation was unfolding, NCVHS began to consider how it could assist the Department’s development of the necessary information capacities.4 All four NCVHS subcommittees have contributed to the early thinking on this subject, and all plan further work

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1 We use the term capacities in the sense of the ability to perform or produce. That is, information capacities are understood in relation to specific needs, purposes, and functions of information.
2 NCVHS, Information for Health: A Strategy for Building the National Health Information Infrastructure, November 2001.
3 NCVHS, Shaping a Health Statistics Vision for the 21st Century, November 2002.
4 As part of this process, NCVHS in 2009 commissioned two authors of the 2002 health statistics vision report to help the Committee consolidate and update its recommendations. Their report to the Committee is posted on the NCVHS website. < http://www.ncvhs.hhs.gov/090922p3.pdf >
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in their respective domains, as described below. 5 The Committee has crafted a highly effective process for bringing multiple points of view and areas of expertise to bear as it develops recommendations to the Secretary, and this process is well suited to the work that lies ahead. NCVHS will continue to use its consultative process to create venues for dialog, eliciting input and perspectives from stakeholders and experts regarding critical challenges, potential opportunities, and next steps. It will use this external input and its own broad expertise to help the Department develop health information policies that are commensurate with new opportunities and needs. Given the rapidity of the changes now under way, we cannot over- emphasize the urgency of this endeavor and the need to move ahead with deliberate speed.

INFORMATION CAPACITIES FOR HEALTH AND HEALTH CAREPublic sector involvement in health information has a long history. State, local, and federal agencies have gathered information through vital records, hospital and ambulatory data sets, public health surveillance, population surveys, and other sources to monitor health trends, identify threats, and guide interventions to protect and promote health. Congress initiated a new type of government involvement in 1996 when the Health Information Portability and Accountability Act (HIPAA) recognized the importance of protecting individuals’ health care information while improving the efficiency of health care delivery through standardized electronic administrative transactions. Most recently, the American Recovery and Reinvestment Act of 2009 (ARRA) began another type of intervention, providing financial incentives for health IT adoption in the nation’s hospitals and physician offices as well as funding for infrastructure support.

While much current attention is focused on the ARRA funding of health IT and critical associated tasks such as defining and implementing “meaningful use” of EHRs, a broader perspective is required to take full advantage of evolving opportunities. Widespread use of optimally configured, standardized EHRs will greatly expand the information available on health care services, users, and providers. However, promoting the health and wellness of the population also requires information about those who have not received health care services, among other things, as well as information on other determinants of health beyond traditional health care, including environmental, social, and economic factors.6

In short, national health information capacities must support a broad array of uses and purposes that include improving access to affordable and efficient quality health care, supporting clinicians in delivering care, empowering and engaging patients and consumers in their care,
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5 At present, NCVHS has subcommittees on population health, standards, quality, and privacy/confidentiality/security.
6 See the NCVHS-developed graphic of the determinants of health on page 9 of its report on a vision for 21st century health statistics (see note 3).
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ensuring patient safety, promoting patient trust, eliminating health disparities, monitoring and improving population health, and supporting health services and clinical research. As these capacities are developed, it is critical that the information being collected be comprehensive, timely, efficiently retrievable, and usable, and that individual privacy be protected.

In the Committee’s view, this requires a well-coordinated effort that assures the following:

1.  Accessibility and availability of information. The availability of sufficient, timely information from relevant sources must be assured to meet the priority needs of diverse users (including clinicians, consumers, purchasers, payors, researchers, public health officials, regulators, and policymakers) for taking action and evaluating outcomes. To minimize burden, wherever possible data should be collected once, for multiple appropriate uses by authorized users. Where appropriate, the capacity to connect data from multiple sources should be provided.

2.  Standardization. Standardization is necessary to enable interoperability for the efficient collection and timely sharing of information among all types of users. Robust standards should be assured through the definition, application, and adoption of terminologies, codes, and messaging in the areas of reimbursement, public health, regulation, statistical use, clinical use, e-prescribing, and clinical documents.

3.  Privacy, confidentiality, and security protections. With the increasing adoption of interoperable electronic health records technology, along with the move toward global access to health data and emerging new uses of data, methods of access and information availability raise significant new and unique privacy and security concerns. Appropriate privacy, confidentiality, and security protections; data stewardship; governance; and an understanding of shared responsibility for the proper collection, management, sharing, and use of health data are critical to addressing these concerns.

Each is briefly discussed below.

1. ACCESSIBILITY AND AVAILABILITY OF INFORMATION

In today’s world, the boundaries between health care, population health, and even individual personal health management are permeable, and information exchange is increasingly multi- directional. The domains traditionally called “public health” and “health care” are increasingly intertwined, often sharing broad, common information sources and capacities. For example, promoting the health and wellness of individuals and the population requires attention to health determinants including not only the treatment and prevention of disease and the nature of community health resources but also environmental, housing, educational, nutritional, economic, and other influences. Continuously improving the quality, value, and safety of health care involves, among other things, research and knowledge management, meaningful performance measurement, education and workforce development, and support for personal and family health management. Finally, improving health and health care on a national scale requires monitoring and eliminating health disparities and assessing the health status of all Americans, including vulnerable sub-populations.

A major priority of health information policy should be to facilitate these interconnections and enable the multiple uses of information for current and emerging data needs. With health IT, complemented by the necessary privacy protections and data stewardship and facilitated by well designed standards, data can be combined to create richer information and used to address a broad array of current and emerging health and health care issues. Realizing the collective potential of all information sources is what will allow the U.S. to maximize the return on its investments in system reform and health IT for the benefit of all Americans.

At present, the major sources of data on health are:

       Surveys (interview and examination) and Censuses    Public health surveillance data (e.g., notifiable disease reporting, medical device reporting)        Health care data (EHRs, HIEs, registries, and other such as prescription history, labs, imaging)
      Administrative data (claims, hospital discharge data, vital records)
      Research data (community-based studies, clinical trials, research data repositories)

Another essential set of sources for understanding health is the information on influences on health (including transportation, housing, air and water quality, land use, education, and economic factors) managed by various public and private sector agencies. In addition to all these well-established sources, new ones such as personal health records and computerized personal health monitoring devices are emerging with the potential to contribute to understanding health at individual and population levels. Social networking content has the potential to provide yet another new and novel resource.

Most data sources have primary uses for which they were designed. However, given adequate standardization, privacy protections, and informatics technology, these sources have great potential to be used for multiple purposes. For example, EHR data elements are collected to document and manage clinical care, but also can be used for public health reporting (such as communicable diseases and medication safety) and to evaluate population health and conduct health services research. Surveys are principally for population-level analysis, but survey information also contributes to clinical care. Vital records not only provide information about births and deaths, but also serve as the “bookends” of population health data. Administrative data (ICD-9-CM disease codes and CPT-4/HCPS procedure codes) were initially used for management and reimbursement, but today play a critical role in quality assessment and public health monitoring (e.g., quality and safety indicators and disease prevalence evaluation). As we look to the future, the goal is to leverage all these sources, when appropriate, and expand their utility for understanding personal and population health and their determinants while carefully protecting the confidentiality of the data they contain.

To bring about the needed improvements and efficiencies and draw all possible benefit from the large and growing investment in health IT, the emerging information capacities must enable both more effective and cost-effective clinical services and population health promotion, and their many synergies. This can be facilitated through multi-directional data sharing and linkages to generate information that is comprehensive and broadly representative. It will be critical to break down the silos that now make it difficult to share and connect data. This requires addressing the policy, institutional, technical, and other barriers that contribute to the existing silos. A workforce trained to take advantage of the broader data and informatics capacities is also essential. Detailed local data are needed to enable understanding of health and health care at local neighborhood, community, sub-population, and other levels of aggregation. Key decisions about health and health care are made at the local level, and we envision the potential to meet these needs in ways not previously possible. Finally, a critical use of population health data, especially with the advent of health care reform, is to assess the effectiveness, comparative effectiveness, and equity of health care.

Because resources are limited and burden must be minimized, information policy must set priorities regarding which data are most important in order to target investments in data collection. As noted, burden can be minimized by collecting data once for multiple uses. At least in the near term, provided that data can be put in the hands of trusted stewards, enhanced administrative data may be a powerful component that reduces the burden of multiple collections. As new capacities come on line, it may be possible to curtail or redirect some current collection activities.

An important criterion is that information, whatever its source, must be meaningful to users. Experience has demonstrated that having relevant data and information available does not ensure that it is accessible in a timely manner and useful form to the full range of potential users. Delays may be created by approval processes or regulatory requirements, as well as by the lack of data handling and analysis capacities that could enable a user to pose a question, indentify relevant data sources, and request a report that is understandable and protects the privacy of data sources. Ensuring access to useful information is a critical part of the challenge. An overarching goal of all these endeavors is to assure that data can be converted into information and ultimately into knowledge that can answer the priority questions about personal and population health in the U.S. and enable effective decisions and actions to improve them.

2.  STANDARDS FOR INTEROPERABILITY, USABILITY, QUALITY, SAFETY, AND EFFICIENCY

The purposes of health information standards are to ensure the efficient, secure, safe, and effective delivery of high quality health care and population health services; to support the information exchange needs of health care, public health, and research; and to empower consumers to improve their health.

The impending implementation of the next generation of HIPAA standards, the enactment of The Health Information Technology for Economic and Clinical Health (HITECH) Act in 2009, and the recent signing of health reform into law are creating an unprecedented convergence of driving forces, foundational components, technology advances and capabilities, and regulatory requirements. Together, these assets can help create a common national pathway toward achieving the vision and policy priorities of a 21st century health system that relies on a strong health information and health information technology foundation. The past five years have seen a remarkable transformation in the adoption and use of standards for electronic exchange of health information. The transformation encompasses privacy and security standards, standards for administrative and financial transactions, the establishment of unique identifiers, and more recently the adoption of standards for codifying, packaging, and transmitting clinical information between and across health care organizations. This rapidly evolving transformation is moving us closer to the ideal of a fully interoperable electronic health information collection and exchange environment that supports all functions and needs of the country’s health and health care ecosystem, as discussed in the previous pages.

Data standards provide a key architectural building block that supports the collection, use, and exchange of health information. Health information standards have been developed and are being adopted and implemented in many different areas. Capturing information in codified format through standard representations such as clinical vocabularies and terminologies, code sets, classification systems, and definitions is a key strategy for achieving semantic interoperability. The inclusion of standardized metadata, which describe characteristics of the data such as provenance, increases the potential for assessing the reliability and validity of the data for aggregation, research, and other uses. Organizing and packaging data through defined electronic message and document standards to be accessed and exchanged via standardized electronic transport mechanisms and protocols achieves access and exchange of health information. The availability and integrity of health information is protected and ensured through the deployment of security standards, thus guaranteeing confidentiality and privacy of protected health information. Finally, the certification of health information technology for Meaningful Use depends on the wise deployment and use of health information standards.

3. PRIVACY, CONFIDENTIALITY, SECURITY

With the move toward the management of health data in electronic form, there is a significant opportunity to enhance health data access, utility in patient care, and important secondary uses. The opportunity is further enhanced through the emergence of new methods to exchange health data, both on a regional and national basis. However, the ability to realize the potential of electronic health data depends greatly on ensuring that uses are appropriate and individuals’ reasonable privacy, confidentiality, and security expectations are met.

Individuals should have the right to understand how their health data may be used, and to provide consent where appropriate. Often, consent is difficult, as not all uses are known at the time the health data are collected. Further, standards do not yet exist to track an individual’s consent as data are exchanged. Although many of the population health uses described in this concept paper involve aggregated or de-identified health data, legitimate concerns exist about group harms and possible re-identification. In addition, the possibility of using health data from emerging information sources, such as personal health record systems, raises unique privacy concerns.

NCVHS has discussed many of these privacy challenges in numerous reports and letters to the Secretary. Most notably, NCVHS published two reports, a Primer on health data stewardship 7 and Recommendations on Privacy and Confidentiality, 2006-2008. Both are available on the NVCHS website.8

Further work is necessary to develop the privacy, confidentiality, and security standards that should apply as these data uses continue to evolve. In addition, work is needed to establish governance structures to provide the proper oversight of entities that exchange and use health data. In essence, governance is the accountability for ensuring that proper data stewardship (as described in the NCVHS Primer cited above) is practiced. To differentiate between governance and data stewardship, data stewardship is focused on the internal practices of the entity that uses health data, whereas governance is focused on the oversight of such entities to ensure that their data stewardship practices are adequate. Such oversight includes initially approving entities that have access to data, ensuring that such entities appropriately use and protect data, and ensuring that entities that misuse data are appropriately sanctioned.

THE WAY FORWARDTaken together, today’s emerging policy opportunities and the nation’s longstanding health challenges create a situation of considerable urgency for the United States. The openness to bold new approaches offered by recent legislation will disappear quickly. Given that the U.S. lags behind most other industrialized countries in the health status of its citizens, we must seize the opportunities to maximize the health benefits and begin to assess whether the huge investments are indeed having the desired impact.

This paper has noted the critical federal role in devising health information policy to support national health goals. Federal leadership is more needed than ever to create the comprehensive approaches that will guide the development of information capacities and coordinate efforts by actors in the public and private sectors. Whatever progress is made in the critical transition to electronic health records, clinical data alone will not suffice; broad information capacities that

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7
An NCVHS Primer: Health Data Stewardship―What, Why, Who, How, December 2009.
8 http://www.ncvhs.hhs.gov
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draw on all the sources and serve all the purposes discussed in this paper will be necessary. This will require shoring up the data resources for public functions such as surveys, safety surveillance, and vital records, along with strategic thinking to determine what capacities will be needed in the future and how to guide their development. Many issues require research and demonstration as part of a prioritized, adequately funded research agenda. In addition, further investments in a trained workforce are needed, to ensure the availability of professionals and leaders who can properly use information resources for analysis and decision-making.

As it develops policies and strategies, the Department has always invited input from experts and stakeholders; and NCVHS has long helped to facilitate this dialogue and distill the key messages and lessons. NCVHS will continue to use its consultative and deliberative processes, working collaboratively with other HHS advisory committees, to help the Department meet the current opportunities and challenges. As noted, all NCVHS subcommittees plan to be involved in this effort; this report is an early installment on subcommittee and full Committee work plans for the coming 18 months or more. NCVHS expects to develop recommendations on a research agenda, which may be the focus of one or more hearings. Each of the subcommittees is identifying the key issues in its domain, to be pursued through workshops, hearings, and internal deliberations as NCVHS develops recommendations for the Secretary. The subcommittees’ preliminary thinking is outlined below.

SUBCOMMITTEE ON QUALITY

Over the next two years, the NCVHS Subcommittee on Quality will focus on supporting the development of meaningful measures, leveraging both existing and emerging data sources (e.g., patient-generated data, remote monitoring, personal health records), and in particular identifying significant opportunities and gaps. Critical to meaningful measurement is the availability of relevant data elements that could be easily captured using certified EHR technology and functionality, among other tools. The Subcommittee on Quality will identify emerging health data needs for a health system where the individual engages in his or her health and health care. As a near-term priority, the Subcommittee will address the data needs of person-centered health and health care, emphasizing coordination and continuity of care across a continuum of services. A longer term goal is to develop a national strategy to leverage clinically rich health data to address important national questions about determinants of health and disease.

SUBCOMMITTEE ON PRIVACY, CONFIDENTIALITY AND SECURITY

The NCVHS Subcommittee on Privacy, Confidentiality and Security will focus its efforts on providing recommendations that support national priorities, in coordination with such groups as the ONC HIT Policy Committee’s Privacy and Security Workgroup. In the next year, the Subcommittee plans to develop recommendations regarding governance as well as a framework for the identification and appropriate management of sensitive data. The Subcommittee will also consider transparency and the role of patient consent. In addition, it will continue to review and make recommendations regarding new privacy, confidentiality, and security regulations; compliance with these regulations; and strategies for effective enforcement.

SUBCOMMITTEE ON STANDARDS

Health care reform legislation now provides a new opportunity to continue the administrative simplification that began under HIPAA―a process in which NCVHS will remain heavily involved. The NCVHS Subcommittee on Standards will continue to meet its responsibilities related to HIPAA; will implement the many administrative simplification responsibilities assigned by the Health Reform Act of 2010; and will meet new requests for recommendations on the use of standards to enhance interoperability of the transmission and semantics of health data as they arise. As we look to the future, several goals stand out with respect to standards. The Subcommittee will seek to ensure a comprehensive framework and roadmap for health information standards that support the national health IT strategic framework, vision and policy priorities; the public health policy agenda; the NCVHS proposed data stewardship framework; a national research agenda that includes comparative effectiveness; and the needs of all data users.

SUBCOMMITTEE ON POPULATION HEALTH

Understanding the population’s health and its determinants relies on multiple data sources, including population surveys, clinical data, administrative data (notably, birth and death records and billing data on use of health services), and public health and environmental reporting systems. At the national level, Federal agencies such as the National Center for Health Statistics are charged with developing methods, assessing validity, and reporting national population health information. As we envision building a comparable capacity for communities and states across America, the quality of information and its timeliness will be central to success. The Subcommittee on Population Health will focus on facilitators and barriers to data linkage at state and local levels as a critical part of health information infrastructure, specifically linking EHR data with existing administrative and local survey data. Fundamental to understanding population health is describing the underlying population, which also comprises those who have not seen a doctor recently or have refused to respond to a survey. The work of the Subcommittee will focus on methods to ensure that linked data sources provide valid health information, including methods to adjust for missing data and methods to protect privacy.

AHRQ Webinar: Quality Measures to Improve Patient Care: June 23

Impact of Health IT on Quality Assessment:
Innovations in Measurement and Reporting

Excerpted from AHRQ on June 20, 2010
This free 90-minute teleconference will explore the use of quality measures to improve patient care.
 
Date: June 23
Time: 2:00 – 3:30 p.m., ET
Sponsored by the Agency for Healthcare Research and Quality’s (AHRQ) National Resource Center for Health IT

To register, click here.

Presenters:

•    Denni McColm, M.B.A., is Chief Information Officer for Citizens Memorial Healthcare. She has been at Citizens Memorial since 1988, serving as Director of Human Resources and Director of Finance before moving into the CIO role in June, 2003. Ms. McColm served on the Certification Commission for Health Information Technology as a Commissioner from 2006-2008. She also served on the Davies Awards of Excellence Organizational Selection Committee from 2006 -2008 and again in 2010.  She is a member of the Editorial Board for Healthcare IT News, published in partnership with HIMSS. Ms. McColm holds a Master of Business Administration degree from the University of Missouri-Columbia.
•    Karen Kmetik, Ph.D., is Vice President of Performance Improvement at the American Medical Association (AMA), where she provides strategic leadership for AMA initiatives in health care quality measurement and improvement.  She also leads the activities of the AMA-convened Physician Consortium for Performance Improvement® (PCPI) through continued development and effectiveness testing of performance measures, advancement of the   integration of the measures into health IT, and implementation in a variety of programs.  Dr. Kmetik is a founding member of the Collaborative for Performance Measure Integration with EHR Systems, co-sponsored by the AMA, the National Committee for Quality Assurance (NCQA), and the HIMSS Electronic Health Record Association (EHRA).
•     Henry Fischer, M.D., is an Assistant Professor at the University of Colorado Health Sciences Center and a practicing internist at Denver Health Medical Center (DH).  He is director of the diabetes collaborative at Denver Health, which serves over 7000 primarily indigent adult patients with diabetes.  He was the PI on an AHRQ funded study of,  i) the automated distribution of individualized diabetic performance report cards to patients by mail and at the point of care, and, ii) the electronic distribution of provider performance report cards on diabetes measures with patient-level data. He is currently studying the use of text messaging to help manage diabetes outside of clinic visits in a primarily low-income population.

Ms. McColm will begin the teleconference by providing an overview of the three year quality measurement project at Citizens Memorial Healthcare.  She will discuss the challenges involved with applying quality measurement in ambulatory care and describe how they were able to achieve their goals.  Dr. Kmetik will describe the Cardio-HIT project, whereby different practice sites with different EHRs exported data to a warehouse for the calculation of national performance measures.  She also will describe current efforts to design measure specifications to enable integration of measures into EHRs.  Dr. Fischer will conclude the event by presenting on the use of an integrated diabetes registry to improve the quality of care for adult diabetic patients in a safety net system.  He will describe the effects of providing both patients and providers information via report cards and the benefits and challenges of this process. 

Live Webcast Information
Start Time:
June 23, 2010 2:00 PM Eastern
1:00 PM Central, 12:00 PM Mountain, 11:00 AM Pacific
Estimated Length:
1 hour, 30 minutes
Registration Fee:

Blumenthal blogs on “Adoption of Health IT”

Health IT Buzz Blog:  Adoption of Health IT
Monday, June 14th, 2010 | Originally posted by Dr. David Blumenthal on ONC’s Health IT Buzz Blog and republished here.

Introducing change in health care is never easy. Historically, adopting our most fundamental medical technologies, from the stethoscope to the x-ray, were met with significant doubt and opposition. So it comes as no surprise that in the face of change as transformational as the adoption of health IT – even though it carries the promise of vastly improving the nation’s health care – some hospitals and providers push back. I resisted using EHRs while an internist in Boston, as I wrote in my blog, “Why Be a Meaningful User.” Over time, however, I found that working with health IT made me a better and safer physician. Most importantly, my patients received better, safer care and improved outcomes.

There are thousands of stories like mine across the nation. The question health care providers are facing today is whether we are pushing too hard, too fast to make this important change. I respectfully submit, no. In turn, I ask, “Can we make these changes expeditiously enough?”

Americans deserve better health care than they are currently receiving, and they need it delivered more efficiently. Every provider, every patient throughout our nation will benefit from the goals envisioned by the HITECH Act. Yes, this will be a challenge. While large hospital networks and smaller providers may be stretched to meet national health IT goals, it is not beyond their capacity for growth.

Doctors and hospitals will not have to go it alone. Programs, such as our 60 Regional Extension Centers located throughout the United States, are working hard to ensure that providers have all the necessary resources to meet the challenge. The incentive program will then provide reimbursement to providers who have achieved meaningful use.

This is the time to realize the promise of health IT. Information technology has improved every aspect of our lives, we need to channel information technology to improve our health and care. Providing patients with improved quality and safety, more efficient care and better outcomes is paramount. Physicians who adhere to the oath of Hippocrates believe we must act with all deliberate haste. More than two thousand years later, we can’t forestall health care quality improvements, not when so many patients entrust their providers for the best care they can possibly deliver. As the saying goes, “If not now, when?”

I welcome your comments, and ask you to share your stories on how health IT has changed your practice.
To comment directly on the Health IT Buzz Blog, click here.

Updates on ONC’s SHARP — Strategic Healthcare IT Advanced Research Projects

SHARP Awards for Health IT Establish Web Sites
Web sites have been launched for each of the four advanced research projects announced April 2, 2010 by the Office of the National Coordinator (ONC) for Health IT. The program called Strategic Healthcare IT Advanced Research Projects (SHARP), totalling $60 million over four years, taps into four consortia of leading reseach and academic institutions each led by a major research institution. “The research projects supported by the SHARP program will focus on solving current and expected future challenges that represent barriers to adoption and meaningful use of health IT. These projects will focus on areas where ‘breakthrough’ advances are needed to realize the full potential of health IT.” This chart was taken from the Mayo Clinic College of Medicine Wiki site for its project.

SHARP Organization
SHARP Organization

1. Security of Health IT
http://sharps.org
University of Illinois at Urbana-Champaign
Strategic Healthcare IT Advanced Research Projects on Security (SHARPS)
SHARPS is accociated with the Center for Health Information Privacy and Security in the Information Trust Institute at the University of Illinois at Urbana-Champaign
In their research overview, SHARPS describes the structure of their project, “SHARPS is organized around three major environments: Electronic Health Records (EHRs), Health Information Exchanges (HIEs), and Telemedicine  (TEL), with Personal Health Records (PHRs) included as a major subtopic. SHARPS research projects in these strategic areas are interconnected through three cross-cutting themes: conceptual and policy foundations, service models, and open validation.”
People
Research
Jobs
Publications
Links

2. Patient-Centered Congnitive Support
http://sharpc.org
The University of Texas Health Science Center at Houston
National Center for Cognitive Informatics and Decision Making in Healthcare (NCCD)
Alternative URL: http://www.uthouston.edu/nccd
Mission: “The mission of the NCCD is to bring together a collaborative, interdisciplinary team of researchers from across the nation; with the highest level of expertise in patient-centered cognitive support research from biomedical and health informatics, cognitive science, clinical sciences, industrial and systems engineering, and health services research. Additionally, the NCCD will conduct short-term research that addresses the urgent usability , workflow, and cognitive support issues of Health Information Technology ( HIT) as well as long-term, breakthrough research that can fundamentally remove the key cognitive barriers to HIT adoption and meaningful use. The center will translate research findings to the real world through a cooperative program involving researchers, patients, providers, HIT vendors, and other stakeholders.”

Projects

Project Title

 

Project 1 Work-Centered Design of Care Process Improvements in HIT  
Project 2A Cognitive Foundations for Decision Making: Implications for Decision Support  
Project 2B Modeling of Setting-Specific Factors to Enhance Clinical Decision Support Adaptation  
Project 3 Automated Model-based Clinical Summarization of Key Patient Data  
Project 4 Cognitive Information Design and Visualization: Enhancing Accessibility and Understanding  of Patient Data  
Project 5 Improving Communication in Distributed Team Environment  

3. Health Application and Network Platform Architectures
http://www.smartplatforms.org
Harvard University
Substitutable Medical Apps, reusable technologiesSMArt App

“A platform with substitutable apps constructed around core services is a promising approach to driving down healthcare costs, supporting standards evolution, accommodating differences in care workflow, fostering competition in the market, and accelerating innovation.”

The March 26, 2009 essay by Kenneth D. Mandl, MD, MPH, and Isaac S. Kohane, MD, PhD,   in New England Journal of Medicine  “No Small Change for the Health Information Economy”. They wrote “A health care system adapting to the effects of an aging population, growing expenditures, and a diminishing primary care workforce needs the support of a flexible information infrastructure that facilitates innovation in wellness, health care, and public health.” They reference the flexbility of applications and the stable platform provided by the iPhone.

Ten principles were developed at a subsuquent workshop setup on May 13, 2009 by the”Informatics Program at Children’s Hospital Boston (CHIP) “of leading experts in health, innovation and technology to define ten core principles of a platform that would support healthcare information technology.”  See “Ten Principles for Fostering Development of an ‘iPhone-like’ Platform for Healthcare Information Technology”

4. Secondary Use of EHR Data
http://sharpn.org
Mayo Clinic College of Medicine
Per Mayo Clinic College of Medicine Wiki: “We propose research that will generate a framework of open-source services that can be dynamically configured to transform EHR data into standards-conforming, comparable information suitable for large-scale analyses, inferencing, and integration of disparate health data. We will apply these services to phenotype recognition (disease, risk factor, eligibility, or adverse event) in medical centers and population-based settings. Finally, we will examine data quality and repair strategies with real-world evaluations of their behavior in Clinical and Translational Science Awards (CTSAs), health information exchanges (HIEs), and National Health Information Network (NHIN) connections.

“We have assembled a federated informatics research community committed to open-source resources that can industrially scale to address barriers to the broad-based, facile, and ethical use of EHR data for secondary purposes. We will collaborate to create, evaluate, and refine informatics artifacts that advance the capacity to efficiently leverage EHR data to improve care, generate new knowledge, and address population needs. Our goal is to make these artifacts available to the community of secondary EHR data users, manifest as open-source tools, services, and scalable software. In addition, we have partnered with industry developers who can make these resources available with commercial deployment. We propose to assemble modular services and agents from existing open-source software to improve the utilization of EHR data for a spectrum of use-cases and focus on three themes: Normalization, Phenotypes, and Data Quality/Evaluation. Our six projects span one or more of these themes, though together constitute a coherent ensemble of related research and development. Finally, these services will have open-source deployments as well as commercially supported implementations.

“There are six strongly intertwined, mutually dependent projects, including: 1) Semantic and Syntactic Normalization; 2) Natural Language Processing (NLP); 3) Phenotype Applications; 4) Performance Optimization; 5) Data Quality Metrics; and 6) Evaluation Frameworks. The first two projects align with our Data Normalization theme, while Phenotype Applications and Performance Optimization span themes 1 and 2 (Normalization and Phenotyping); while the last two projects correspond to our third theme.”

SHARP Program Organization
SHARP Area 4: Themes & Projects
Project Initiation Meeting Slides PDF

For more recent post about SHARP Program on e-Healthcare Marketing, click here.

ONC’s Seidman Blogs on Health IT Disparities Meeting + June 4 Agenda

Using Health IT to Eliminate Disparities: A Focus on Solutions
Posted originally on Office of Nat’l Coordinator for Health IT’s
Federal Advisory Committee Blog: 
Wednesday, June 2nd, 2010 
by  Joshua Seidman PhD 
See June 4, 2010 Meaningul Use Workgroup Agenda Below

The meaningful use (MU) of electronic health records (EHRs) has great potential to improve the quality, efficiency and safety of health care. If we are not careful, however, benefits may disproportionately accrue to those best positioned to implement and use new technologies. That could have the unintended consequence of growing health, health care and health information disparities.

On the other hand, ignoring technological innovation is not a viable option for preventing exacerbation of disparities. Moreover, many innovators have demonstrated that—deployed thoughtfully—health IT solutions can improve access to, and understanding of, important personal health information.

That is the focus of the June 4 public hearing being convened in Washington, DC by the Health IT Policy Committee’s MU Workgroup. Given the great research that already exists on what causes disparities, we are focusing this discussion specifically on solutions—that is, how can meaningful use of health IT solutions help us reduce disparities?

In this context, disparities can refer to differences in health, health care and health information. They may be caused by inadequate health literacy or by cultural or language issues that affect communication. In many cases, disparities can also be caused by access to care, to technology, or to meaningful and useful health information.

Like the Workgroup’s previous hearing on patient and family engagement, we will build on the live public testimony and discussion through this FACA Blog. The April 20 hearing generated more than 50 thoughtful comments that have been incorporated into the public record as we begin the process of building the definition for future stages of meaningful use.

We hope that we have an equally robust online discussion that provides valuable input on this topic. As with the previous hearing, all comments are welcome but we particularly encourage you to consider the following questions that we posed to the panelists.  

1. What do you see as the greatest risks posed by the implementation of HIT in relationship to potentially increasing disparities in health processes and outcomes? 

2. What are you, or others with whom you work, doing (or planning to do) to reduce the risk of exacerbating disparities as HIT is implemented across the county?

3. What research is being done, or needs to be done, in this area to inform the HIT Policy Committee in trying to establish guidelines that will move providers to implement methods of using HIT to reduce disparities?

4. With patient and family engagement in care at the forefront of our thinking about improving our Nation’s health, what particular strategies would you recommend to us as potential meaningful use requirements in 2013 and 2015 for the vulnerable populations we have asked you to address?

5. How can the meaningful use of HIT specifically reduce a health disparity?

6. What specific HIT applications have been used to address health literacy (panel 1), culture (panel 2), or access (panel 3)?

7. Please share any relevant evidence on your topic.

Additional Questions for the Access Panel:

What tools can be used to improve access for those who face access barriers to healthcare or technology?

What are the most innovative solutions you have seen to overcome these challenges?
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To post comments directly on FACA blog article, click here.

AGENDA
(pdf version) excerpted from ONC site
HIT Policy Committee Meaningful Use Workgroup
Friday, June 4, 2010
9 a.m. to 3:30 p.m./
Eastern Time
Washington, DC

Hearing on “Using HIT to Eliminate Disparities: A Focus on Solutions
“As providers across the country begin to meaningfully use health information technology to improve care to vulnerable populations, we acknowledge the need to pay special attention to ensuring that we are improving disparities in healthcare processes and outcomes, not exacerbating them.”

9:00 a.m. Call to Order/Roll Call – Judy Sparrow, Office of the National Coordinator
9:05 a.m. Meeting Objectives and Outcomes:
Using HIT to Eliminate Disparities: A Focus on Solutions
– George Hripcsak, Co-Chair, and Neil Calman, The Institute for Family Health
9:15 a.m. Panel 1: Health Literacy & Data Collection
Moderator: Neil Calman
–Sara Czaja, University of Miami
–Cynthia Solomon, MiVia
–Geniene Wilson, The Institute for Family Health
–Silas Buchanan, The Cave Institute
10:45 a.m. Panel 2: Culture
Moderator: Joshua Seidman
–Russell Davis, National Health IT Collaborative for the Underserved
–M. Chris Gibbons, Johns Hopkins Urban Health Institute
–Dianne Hasselman, Center for Health Care Strategies
–Deeana Jang, Asian/Pacific Islander American Health Forum
12:15 p.m. LUNCH BREAK
1:15 p.m. Panel 3: Access
Moderator: George Hripcsak
–Carolyn Clancy, Agency for Healthcare Research & Quality, HHS
–Howard Hays, MD, Indian Health Service, HHS
–Ian Erlich, Maniilaq Association, Alaska
–R. Scott Hawkins, Boston Healthcare for the Homeless
–Cesar Palacios, Proyecto Salud Clinic
2:45 p.m. Meaningful Use Workgroup Discussion
3:15 p.m. Public Comment
3:30 p.m. Adjourn

To participate:
Webconference or iPhone
Audio
You may listen in via computer or telephone.
US toll free:   1-877-705-2976
International Direct:  1-201-689-8798

Beacon Community Program: Technical Call – June 1, 1pm EDT

Office of Nat’l Coordinator for Health IT Technical Assistance Call:
Tuesday 6/1/10, 1:00 – 2:00 PM EDT  (Link to slides below)

Excerpted from Office of National Coordinator for Health IT Web site and email on 6/1/10:
An additional $30.3 million is currently available to fund two additional Beacon Community cooperative agreement awards.  Please note that the Office of the National Coordinator for Health Information Technology is accepting Letters of Intent from potential applicants until 11:59 PM EDT June 9, 2010.”

“In addition, as was announced last week, ONC will be hosting a Technical Assistance call for potential applicants today, Tuesday, June 1 at 1:00 PM EDT.  This call will be a presentation on preparing proposals for this cooperative agreement. The purpose of this note is to pass on the specific dial-in information for today’s call.”

Technical Assistance Call (for round 2 Beacon applicants):  6/1/2010

Previous Technical Assistance Calls

Technical Assistance Call: 12/14/09

Technical Assistance Call:  1/20/2010

Learn more about the Beacon Community Cooperative Agreement Program:

Blumenthal Calls for Health IT Success stories on HIT Buzz Blog

Blumenthal’s Latest Post on ONC Blog:
Health IT Journey: Stories from the Road
Thursday, May 27, 2010;
Originally posted  on
Health IT Buzz blog by Dr. David Blumenthal 
                       

Across the country, in practices large and small, urban and rural, general and specialized, health care providers are beginning their journey towards the meaningful use of electronic health records (EHRs). Some practices are in the preliminary stages of learning about health IT, while others have already implemented systems and are using them to the benefit of patients.

We believe these real life experiences are valuable tools to share with other providers so they can learn from each other’s successes and the “speed bumps” along the way.  To facilitate this beneficial exchange, ONC has launched a new feature on its website—Health IT Journey: Stories from the Road. The site will be dedicated to collecting and sharing the personal experiences of real-world health IT users, and the lessons they have learned.

While the Regional Extension Centers will offer hands on assistance, and the Health Information Technology Research Center will disseminate best practices, Health IT Journeys will contribute a more personal component to the base of knowledge that will ultimately bring the meaningful use of health IT from vision to reality.

If you have struggled with a specific aspect of implementation, then no doubt other providers have, too. If you have discovered efficiencies and creative solutions, then others will likely benefit from your knowledge. You can make a difference in efforts to ensure the nationwide adoption of EHRs simply by sharing your story.

 For example: 

  • How did you decide on and then introduce health IT into your practice?
  • How are you working meaningful use of health IT into the day-to-day management of your practice?
  • What challenges have you faced along the way, and how did you overcome those challenges?
  • How is health IT affecting the quality of care you provide to your patients?

Let us know your experience.

With your help, we can make care better through the use of EHRs.
#        #       #

ONC requested that success stories be sent to: onc.request@hhs.gov

See previous post on e-Healthcare Marketing.

New AHRQ-Funded Report Provides Snapshot of Electronic Health Record (EHR) Vendor Usability Processes and Practices

New AHRQ-Funded Report Provides Snapshot of Electronic Health Record (EHR) Vendor Usability Processes and Practices

Received via email on May 27, 2010:  “The Agency for Healthcare Research and Quality (AHRQ) has issued a new report that focuses on assessing and improving the state of usability in Electronic Health Record (EHR) systems.  Key recommendations from the project’s expert panel include establishment of usability / information design of EHRs as an essential part of the certification requirements for EHRs, basing certification on a practical and fair process of usability evaluation, and designing certification programs for EHR usability in a way that focuses on objective and important aspects of system usability. Select to access the report and learn more about the panel’s recommendations.(PDF file).

“AHRQ is working closely with the National Institute of Standards and Technology (NIST) and the Office of the National Coordinator to address the recommendations identified in its research.  In June, AHRQ plans to award a follow-on project for the development, testing and dissemination of an easy-to-use, objective and evidence-based toolkit that healthcare organizations can use to evaluate critical aspects of their EHR systems’ usability, accessibility and information design.  In addition, NIST is currently seeking applications for development of an EHR usability evaluation framework at a meeting, titled “Health Care IT Usability: Strategy, Research, Implementation,” to be held in Gaithersburg, MD, on July 13, (2010).”

The report was written by Cheryl McDonnell, Kristen Werner, and Lauren Wendel; and was prepared by James Bell Associates and The Altarum Institute. Suggested citation: McDonnell C, Werner K, Wendel L. Electronic Health Record Usability: Vendor Practices and Perspectives. AHRQ Publication No. 09(10)-0091-3-EF. Rockville, MD: Agency for Healthcare Research and Quality. May 2010.

Excerpted from the pdf report:
Electronic Health Record Usability:
Vendor Practices and Perspectives
May 2010

Executive Summary 

One of the key factors driving the adoption and appropriate utilization of electronic health record (EHR) systems is their usability. (1) However, a recent study funded by the Agency for Healthcare Research and Quality (AHRQ) identified information about current EHR vendor usability processes and practices during the different phases of product development and deployment as a key research gap. (2)To address this gap and identify actionable recommendations to move the field forward, AHRQ contracted with James Bell Associates and the Altarum Institute to conduct a series of structured discussions with selected certified EHR vendors and to solicit recommendations based on these findings from a panel of multidisciplinary experts in this area.

The objectives of the project were to understand processes and practices by these vendors with regard to:

     •   The existence and use of standards and “best practices” in designing, developing, and deploying products.

     •  Testing and evaluating usability throughout the product life cycle.

     •  Supporting postdeployment monitoring to ensure patient safety and effective use.

In addition, the project solicited the perspectives of certified EHR vendors with regard to the role of certification in evaluating and improving usability.

The key findings from the interviews are summarized below.

     •  All vendors expressed a deep commitment to the development and provision of usable EHR product(s) to the market.

     •  Although vendors described an array of usability engineering processes and the use of end users throughout the product life cycle, practices such as formal usability testing, the use of user-centered design processes, and specific resource personnel with expertise in usability engineering are not common.

     •  Specific best practices and standards of design, testing, and monitoring of the usability of EHR products are not readily available. Vendors reported use of general (software) and proprietary industry guidelines and best practices to support usability. Reported perspectives on critical issues such as allowable level of customization by customers varied dramatically.

     •  Many vendors did not initially address potential negative impacts of their products as a priority design issue. Vendors reported a variety of formal and informal processes for identifying, tracking, and addressing patient safety issues related to the usability of their products.

     •  Most vendors reported that they collect, but do not share, lists of incidents related to usability as a subset of user-reported “bugs” and product-enhancement requests. While all vendors described a process, procedures to classify and report usability issues of EHR  products are not standardized across the industry.

     •  No vendors reported placing specific contractual restrictions on disclosures by system users of patient safety incidents that were potentially related to their products.

     •  Disagreement exists among vendors as to the ideal method for ensuring usability standards, and best practices are evaluated and communicated across the industry as well as to customers. Many view the inclusion of usability as part of product certification as part of a larger “game” for staying competitive, but also as potentially too complex or something that will “stifle innovation” in this area.

     •  Because nearly all vendors view usability as their chief competitive differentiator, collaboration among vendors with regard to usability is almost nonexistent.

     •  To overcome competitive pressures, many vendors expressed interest in an independent body guiding the development of voluntary usability standards for EHRs. This body could build on existing models of vendor collaboration, which are currently focused predominantly on issues of interoperability.

Based on the feedback gained from the interviews and from their experience with usability best practices in health care and other industries, the project expert panel made the following recommendations:

     •  Encourage vendors to address key shortcomings that exist in current processes and practices related to the usability of their products. Most critical among these are lack of adherence to formal user-design processes and a lack of diversity in end users involved in the testing and evaluation process.

     • Include in the design and testing process, and collect feedback from, a variety of end-user contingents throughout the product life cycle. Potentially undersampled populations include end users from nonacademic backgrounds with limited past experience with health information technology and those with disabilities.

     •  Support an independent body for vendor collaboration and standards development to overcome market forces that discourage collaboration, development of best practices, and standards harmonization in this area.

     •  Develop standards and best practices in use of customization during EHR deployment.

     •  Encourage formal usability testing early in the design and development phase as a best practice, and discourage dependence on postdeployment review supporting usability assessments.

     •  Support research and development of tools that evaluate and report EHR ease of learning, effectiveness, and satisfaction both qualitatively and quantitatively.

     •  Increase research and development of best practices supporting designing for patient safety.

     •  Design certification programs for EHR usability in a way that focuses on objective and

important aspects of system usability.

Background

Encouraged by Federal leadership, significant investments in health information technology (IT) are being made across the country. While the influx of capital into the electronic health record (EHR)/health information exchange (HIE) market will undoubtedly stimulate innovation, there is the corresponding recognition that this may present an exceptional opportunity to guide that innovation in ways that benefit a significant majority of potential health IT users.

One of the key factors driving the adoption and appropriate utilization of EHR systems is their usability. (1) While recognized as critical, usability has not historically received the same level of attention as software features, functions, and technical standards. A recent analysis funded by the Agency for Healthcare Research and Quality (AHRQ) found that very little systematic evidence has been gathered on the usability of EHRs in practice. Further review established a foundation of EHR user-interface design considerations, and an action agenda was proposed for the application of information design principles to the use of health IT in primary care settings. (2), (3)

In response to these recommendations, AHRQ contracted with James Bell Associates and the Altarum Institute to evaluate current vendor-based practices for integrating usability during the entire life cycle of the product, including the design, testing, and postdeployment phases of EHR development. A selected group of EHR vendors, identified through the support of the Certification Commission for Health Information Technology (CCHIT) and AHRQ, participated in semistructured interviews. The discussions explored current standards and practices for ensuring the usability and safety of EHR products and assessed the vendors’ perspectives on how EHR usability and information design should be certified, measured, and addressed by the government, the EHR industry, and its customers. Summary interview findings were then distributed to experts in the field to gather implications and recommendations resulting from these discussions.

Vendor Profiles

The vendors interviewed were specifically chosen to represent a wide distribution of providers of ambulatory EHR products. There was a representation of small-sized businesses (less than 100 employees), medium-sized businesses (100-500 employees), and large-sized businesses (greater than 500 employees). The number of clinician users per company varied from 1,000 to over 7,000, and revenue ranged from $1 million to over $10 billion per year. The EHR products discussed came on the market in some form in the time period from the mid-1990s to 2007. All vendors except one had developed their EHR internally from the ground up, with the remaining one internally developing major enhancements for an acquired product. Many of these products were initially designed and developed based on a founding physician’s practice and/or established clinical processes. All companies reported that they are currently engaged in groundup development of new products and/or enhancements of their existing ambulatory products. Many enhancements of ambulatory products center on updates or improvements in usability. Examples of new developments include changes in products from client-based to Web-based EHRs; general changes to improve the overall usability and look and feel of the product; and the integration of new technologies such as patient portals, personal health records, and tablet devices.

The full list of vendors interviewed and a description of their key ambulatory EHR products are provided in Appendixes I and II. The following discussion provides a summary of the themes encountered in these interviews.

Standards in Design and Development

End-User InvolvementAll vendors reported actively involving their intended end users throughout the entirendesign and development process. Many vendors also have a staff member with clinical experience involved in the design and development process; for some companies the clinician was a founding member of the organization.nWorkgroups and advisory panels are the most common sources of feedback, with some vendors utilizing a more comprehensive participatory design approach, incorporating feedback from all stakeholders throughout the design process. Vendors seek this information to develop initial product requirements, as well as to define workflows, evaluate wireframes and prototypes, and participate in initial beta testing. When identifying users for workgroups, advisory panels, or beta sites, vendors look for clinicians who have a strong interest in technology, the ability to evaluate usability, and the patience to provide regular feedback. Clinicians meeting these requirements are most often found in academic medical centers. When the design concerns an enhancement to thencurrent product, vendors often look toward users familiar with the existing EHR to provide thismfeedback.

“We want to engage with leadership-level poartners as well as end users from all venues that may be impacted by out product.”

Design Standards and Best Practices

A reliance on end-user input and observation for ground-up development is seen as a requirement in the area of EHR design, where specific design standards and best practices are not yet well defined. Vendors indicated that appropriate and comprehensive standards were lacking for EHRspecific functionalities, and therefore they rely on general software design best practices to inform design, development, and usability. While these software design principles help to guide their processes, they must be adjusted to fit specific end-user needs within a health care setting. In addition to following existing general design guidelines such as Microsoft Common User Access, Windows User Interface, Nielsen Norman Group, human factors best practices, and releases from user interface (UI) and usability professional organizations, many vendors consult with Web sites, blogs, and professional organizations related to health IT to keep up to date with specific industry trends. Supplementing these outside resources, many vendors are actively developing internal documentation as their products grow and mature, with several reporting organized efforts to create internal documentation supporting product-specific standards and best practices that can be applied through future product updates and releases.

There are no standards most of the time, and when there are standards, there is no enforcement of them. The software industry has plenty of guidelines and good best practices, but in health IT, there are none.”

Industry Collaboration

As these standards and best practices are being developed, they are not being disseminated throughout the industry. Vendors receive some information through professional  organizations and conferences, but they would like to see a stronger push toward an independent body, either governmental or research based, to establish some of these standards. The independent body would be required, as all vendors reported usability as a key competitive differentiator for their product;this creates a strong disincentive for industrywide collaboration. While all were eager to take advantage of any resources commonly applied across the industry, few were comfortable with sharing their internally developed designs or best practices for fear of losing a major component of their product’s competitiveness. Some vendors did report they collaborate informally within the health IT industry, particularly through professional societies, trade conferences, and serving on committees. For example, several vendors mentioned participation in the Electronic Health Record Association (EHRA), sponsored by the Healthcare Information and Management Systems Society (HIMSS), but noted that the focus of this group is on clinical vocabulary modeling rather than the usability of EHRs. Some interviewees expressed a desire to collaborate on standards issues that impact usability and patient safety through independent venues such as government or research agencies.

“The field is competitive so there is little sharing of best practices in the community. The industry should not look toward vendors to create these best practices. Other entities must step up and define [them] and let the industry adapt.”

Customization

In addition to the initial design and development process, vendors commonly work with end users to customize or configure specific parts of the EHR. Vendors differed in the extent to which they allowed and facilitated customization and noted the potential for introducing errors when customization is pursued. Most customizations involve setting security rules based on roles within a clinic and the creation of document templates that fit a clinic’s specific workflow. Many vendors view this process as a critical step toward a successful implementation and try to assist users to an extent in developing these items. While some vendors track these customizations as insight for future product design, they do not view the customizations as something that can be generalized to their entire user base, as so many are context specific. The level of customization varies according to vendor since vendors have different views about the extent to which their product can or should be customized. Vendors do not routinely make changes to the code or underlying interface based on a user request; however, the level to which end users can modify templates, workflows, and other interface-related characteristics varies greatly by vendor offering.

“You cannot possibly adapt technology to everyone’s workflow. You must provide the most optimum way of doing something which [users] can adapt.”

Usability Testing and Evaluation

Informal Usability Assessments

Formal usability assessments, such as task-centered user tests, heuristic evaluations, cognitive walkthroughs, and card sorts, are not a common activity during the design and development process for the majority of vendors. Lack of time, personnel, and budget resources were cited as reasons for this absence; however, the majority expressed a desire to increase these types of formal assessments. There was a common perception among the vendors that usability assessments are expensive and time consuming to implement during the design and development phase. The level of formal usability testing appeared to vary by vendor size, with larger companies having more staff and resources dedicated to usability testing while smaller vendors relied heavily on informal methods (e.g., observations, interviews), which were more integrated into the general development process. Although some reported that they conduct a full gamut of both formal and informal usability assessments for some parts of the design process, most reported restricting their use of formal methods to key points in the process (e.g., during the final design phase or for evaluation of specific critical features during development).

“Due to time and resource constraints, we do not do as much as we would like to do. It is an area in which we are looking to do more.”

Measurement

Functions are selected for usability testing according to several criteria: frequency of use, task criticality and complexity, customer feedback, difficult design areas, risk and liability, effects on revenue, compliance issues (e.g., Military Health System HIPAA [Health Insurance Portability and Accountability Act], and the American Recovery and Reinvestment Act) and potential impacts on patient safety. The most common or frequent tasks and tasks identified as inherently complex are specifically prioritized for usability testing. Neither benchmarks and standards for performance nor formalized measurements of these tasks are common in the industry. While some vendors do measure number of clicks and amount of time to complete a task, as well as error rates, most do not collect data on factors directly related to the usability of the product, such as ease of learning, effectiveness, and satisfaction. Many vendors reported that the amount of data collected does not allow for quantitative analysis, so instead they rely on more anecdotal and informal methods to ensure that their product works more effectively than paper-based methods and to inform their continuous improvements with up rades and releases.

“Testing is focused more on functionality rather than usability.”

Observation

Observation is the “gold standard” among all vendors for learning how users interact with their EHR. These observations usually take place within the user’s own medical practice, either in person or with software such as TechSmith’s Morae. (4) Vendors will occasionally solicit feedback on rototypes from user conferences in an informal lablike Sstting. These observations are typically used to gather information on clinical workflows or process flows, which are incorporated into the product design, particularly if the vendor is developing a new enhancement or entire product.

“[Methods with] low time and resource efforts are the best [to gather feedback]; wherever users are present, we will gather data.”

Changing Landscape

While informal methods of usability testing seem to be common across most vendors, the landscape appears to be changing toward increasing the importance of usability as a design necessity. Multiple vendors reported the current or recent development of formal in-house observation laboratories where usability testing could be more effectively conducted. Others reported the recent completion of policies and standards directly related to integrating usability more formally into the design process, and one reported a current contract with a third-party vendor to improve usability practices. While it is yet to be seen if these changes will materialize, it appeared that most respondents recognized the value of usability testing in the design process and were taking active steps to improve their practices.

Postdeployment Monitoring and Patient Safety

Feedback Solicitation

Vendors are beginning to incorporate more user feedback into earlier stages of product design and development; however, most of this feedback comes during the postdeployment phase. As all vendors interviewed are currently engaged in either the development of enhancements of current products or the creation of new products, the focus on incorporating feedback from intended end users at all stages of development has increased. Many of the EHRs have been on the market for over 10 years; as a result, many vendors rely heavily on this postdeployment feedback to evaluate product use and inform future product enhancements and designs. Maintaining contact with current users is of high priority to all EHR vendors interviewed and in many ways appeared to represent the most important source of product evaluation and improvement. Feedback is gathered through a variety of sources, including informal comments received by product staff, help desk support calls, training and implementation staff, sales personnel, online user communities, beta clients, advisory panels, and user conferences. With all of these avenues established, vendors appear to attempt to make it as easy as possible for current users to report potential issues as well as seek guidance from other users and the vendor alike.

“A lot of feedback and questions are often turned into enhancements, as they speak to the user experience of the product.”

Review and Response

Once the vendors receive both internal and external feedback, they organize it through a formal escalation process that ranks the severity of the issue based on factors such as number of users impacted, type of functionality involved, patient safety implications, effects on workflow, financial impact to client, regulation compliance, and the source of the problem, either implementation based or product based. In general, safety issues are given a high-priority tag. Based on this escalation process, priorities are set, resources within the organization are assigned, and timelines are created for directly addressing the reported issue. Multiple responses are possible depending on the problem. Responses can include additional user training, software updates included in the next product release, or the creation and release of immediate software patches to correct high-priority issues throughout the customer base.

“Every suggestion is not a good suggestion; some things do not help all users because not all workflows are the same.”

Patient Safety

Adoption of health IT has the potential for introducing beneficial outcomes along many dimensions. It is well recognized, however, that the actual results achieved vary from setting to setting, (5) and numerous studies have reported health IT implementations that introduced unintended adverse consequences detrimental to patient care practice. (6) Surprisingly, in many interviews patient safety was not initially verbalized as a priority issue. Initial comments focused on creating a useful, usable EHR product, not one that addresses potential negative impacts on patient safety. Vendors rely heavily on physcians to notice potential hazards and report these hazards to them through their initial design and development advisory panels and postdeployment feedback mechanisms. After further questioning specific to adverse events, however, most vendors did describe having processes in place for monitoring potential safety issues on a variety of fronts. Some vendors become aware of patient safety issues through user feedback collected from patient safety offices and field visits; others educate support staff as well as users on how to identify potential patient safety risks and properly notify those who can address the issue. Once patient safety issues are identified, vendors address them in various ways, including tracking and reporting potential issues online, using patient safety review boards to quantify risk, and engaging cognitive engineers to uncover root causes.

When asked about client contracts, no vendors reported placing specific contractual restrictions on disclosures by system users of patient safety incidents that were potentially related to the EHR products, sharing patient safety incidents with other customers or other clinicians, or publishing research on how the EHR system affects patient safety or their clinical operations.

“Physicians are very acutely aware of how technology is going to impact patient safety; that’s their focus and motivation.”Role of Certification in Evaluating Usability

Current Certification Strategies

The issue of certification is one that elicited strong opinions from most vendors. Certification of any type represents an investment of time and money to meet standards originating outside the organization. For many vendors, particularly the smaller ones, this investment was seen as burdensome. Vendors commonly described the current CCHIT certification process as part of a larger “game” they must play in order to remain viable in the marketplace, not as a way to improve theirnproduct(s). Accounts of functions added specifically for certification but not used by customers were common, as well as specific
instances where vendors felt meeting certification guidelines actually reduced aspects of their product’s quality. As one vendor noted, sometimes providing the functionality for “checking the box” to meet a certification requirement involves a backward step and a lowering of a potentially innovative internal standard. As meaningful use has entered the picture, however, vendors are striving to provide their customers with products that will comply with this definition and plan to participate in any associated certifications.

“We don’t want to get dinged for an innovative standard that we’ve developed and [that] tested well with users because it doesn’t fit the criteria.”

Subjectivity

Interviewees held mixed opinions on whether the certification process can effectively evaluate the usability aspect of EHR performance. Without exception, participating vendors had concerns about the inherent subjectivity of evaluation of usability, which can be strongly affected by the past EHR experience of the user, the context in which the product is used, and even the education and background of the evaluator. Methods for overcoming these types of bias issues included suggestions such as certifying workflows rather than attempting to measure usability, comparing objective product performance (time and error rates) for specific tasks, or measuring usability based on end-user surveys instead of juror analysis.

“Some products may be strong, but due to the familiarity of jurors of a product or technology, some products may be overrated or  underrated.”

Innovation

Several interviewees also expressed concern about the effect of usability certification on innovation within the EHR marketplace. This seemed to stem from experience with CCHIT’s feature- and function-based criteria. It was noted that in the developing EHR marketplace, current systems are striving to make significant changes in the way physicians practice care, which has inherent negative implications for perceived usability early in the product’s release. Guidelines or ratings that are too prescriptive may have the effect of forcing vendors to create technologies that more directly mirror current practices, a strategy that could limit innovation and the overall effectiveness of EHRs.

“Products are picked on the amount of things they do, not how well they do them. CCHIT perpetuates this cycle; if a product contains certain functions, it is placed among the elite. That has nothing to do with usability.”

Recognized Need

Despite these concerns, vendors recognized the role certification could play both as an indicator to support customers in selecting EHRs and as a method through which established standards could be disseminated across the industry. While there is unease about the details of the conduct of certification, many vendors thought that some form of certification or evaluation had the potential to serve as a complement to what is now a predominantly market-driven issue. While each vendor viewed itself as a leader in the development of usable EHR systems and supported the role of consumer demand in continuing to improve product  usability, vendors recognized that there could be utility to more standardized testing that could be evenly applied throughout the industry.

“Being aware of standards and guidelines is
very important, but we also want to make sure we are not hamstrung by them.”

Conclusion

All vendors interviewed expressed a deep commitment to the continued development and provision of usable EHR product(s) to the market. Vendors believe that as features and functions become more standardized across the industry, industry leaders will begin to differentiate themselves from the rest of the market based on usability. Current best practices and standards of design, testing, and monitoring EHR product(s), particularly for usability, are varied and not well disseminated. While models for vendor collaboration for issues such as interoperability currently exist through EHRA and IHE (Integrating the Healthcare Enterprise), collaboration among vendors with regard to usability is almost nonexistent. Given the current move toward the adoption and meaningful use of health IT, and the role usability plays in realizing intended benefits, a transition from the current environment seems likely. This could be driven by many sources, including standards developed by academic research, certification required by government entities, collaboration through a nonprofit association such as EHRA or IHE, or simply market pressures demanding more usable offerings. Vendors recognize these pressures and the importance of usability to the continued success of their products. Disagreement exists as to the ideal method for ensuring that usability is evaluated and communicated across the industry as well as to customers. This disagreement exists even within companies, as well as across vendors. Regardless of this uncertainty, there is agreement that end users need to remain a central component within the development process, innovation needs to be encouraged, and usability needs to be a critical driver of efficient, effective, and safe EHRs.

Implications and Recommendations

The summary interview findings were distributed to selected experts in the field, who provided additional thoughts on the implications of these discussions and developed recommendations based on the discussions. A summary of these suggestions follows.

Standards in Design and Development

Increase diversity of users surveyed for pre-deployment feedback. While the use of subject-matter experts and inclusion of end-user feedback in the design and development process are beneficial and important approaches, the end-user selection process currently in use has a potential for bias. Vendors noted extensive use of volunteered feedback. Clinicians with a strong interest in technology, the ability to evaluate usability, and the patience to provide regular feedback are not indicative of the typical end user. Additionally, as these types of clinicians are commonly found in academic medical centers, they may rely on residents or other trainees to do most of the work involving the EHR. Similar issues exist when soliciting input from users familiar with the existing EHR; these users have potentially learned, sometimes unconsciously, to work around or ignore many of the usability problems of the current system. To some extent, vendors must utilize this “coalition of the willing” to gather feedback, given the extremely busy schedules of most practicing clinicians. However, steps must be taken both in the vendor community and by independent bodies to encourage inclusion of a more diverse range of users in all stages of the design process. This more inclusive approach will ultimately support a more usable end product.

Support an independent body for vendor collaboration and standards development. Lack of vendor collaboration resulting from attempts to protect intellectual property and uphold a competitive edge is understandable. However, with the accelerated adoption timeframe encouraged by recent legislation and increasing demand, letting the market act as a primary driver to dictate usability standards may not ensure that appropriate standards are adopted. The user base currently has relatively limited abilities to accurately determine product usability before purchase and, if dissatisfied after purchase, may incur significant expense to explore more usable products. Simply deeming an EHR usable or not usable does not create or disseminate standards and best practices for design. The market can provide direction, but more must be done to document trends and best practices, create new standards for design, and regulate implementation across the industry.

Develop standards and best practices in use of customization during EHR deployment. Customization is often a key to successful implementation within a site, as it can enable users to document the clinical visit in a way that accommodates their usual methods and existing workflow. However, customization may also serve to hide existing usability issues within an EHR, prevent users from interacting with advanced functions, or even create unintended consequences that negatively impact patient safety. There is an additional concern that customization may negatively impact future interoperability and consistency in design across the industry. Customer demand for customization exists and some level of customization can be beneficial to supporting individual workflows; however, more work must be done to evaluate the level of customization that maximizes the EHR’s benefits and limits its risks.

Usability Testing and Evaluation

Encourage formal usability testing early in the design and development phase as a best practice. Usability assessments can be resource intensive; however, it has been demonstrated that including them in the design and development phase is more effective and less expensive than responding to and correcting items after market release.7 Identifying and correcting issues before release also reduce help desk support and training costs. Vendors indicated an awareness of this tradeoff and a move toward investment in usability assessment up front. Further monitoring will be required to evaluate how the vendor community incorporates formal usability testing within future design and development practices.

Evaluate ease of learning, effectiveness, and satisfaction qualitatively and
quantitatively. Observations are an important component of usability testing but are insufficient for assessment of the root cause of usability issues. Alternatively, quantitative data such as number of clicks, time to complete tasks, and error rates can help the vendor identify tasks that may present usability issues but must be further explored to identify underlying issues. A mix of structured qualitative and quantitative approaches, incorporating at minimum an assessment of the three basic factors directly contributing to product usability—ease of learning, effectiveness, and satisfaction—will serve to broaden the impact of usability assessments beyond the informal methods commonly employed today.

Postdeployment Monitoring and Patient Safety

Decrease dependence on postdeployment review supporting usability assessments. Usability issues are usually not simple, one-function problems, but tend to be pervasive throughout the EHR. So while small-scale issues are often reported and corrected after deployment, the identified issue may not be the primary determinant of a product’s usability. It is chiefly within the main displays of information that are omnipresent, such as menu listings, use of pop-up boxes, and the interaction between screens, that the EHR’s usability is determined. Even with the best of intentions, it is unlikely that vendors will be able to resolve major usability issues after release. By not identifying critical usability issues through a wide range of user testing during design and development, vendors are opening the door to potential patient safety incidents and costly postrelease fixes.

Increase research and development of best practices supporting designing for patient safety. Monitoring and designing for patient safety, like usability testing, appear to be most prevalent late in the design of the product or during its release cycle. Vendors’ heavy reliance on end users or advisory panels to point out patient safety issues in many ways mirrors the informal  methods used to advance usability of their products. While patient safety similarly lacks specific standards for vendors to follow, vendors are currently collaborating on patient safety issues. These collaborations appear to be in their early stages, but they provide an opportunity toenhance vendor awareness and vendor response to potential patient safety issues within their products and improve their ability to incorporate patient safety much earlier in the design process. Further work must be done to directly connect design to patient safety and ensure that standards are created and disseminated throughout the industry.

Role of Certification in Evaluating Usability

Certification programs should be carefully designed and valid. Any certification or outside evaluation will be initially approached with questions as to its validity, and the concept of usability certification is no exception. Usability is a complex multifaceted system characteristic, and usability certification must reflect that complexity. Further complicating this issue is the fact that vendors have already participated in a certification process that most did not find particularly valuable in enhancing their product. Driving the EHR market toward creation of usable products requires development of a process that accurately identifies usable products, establishes and disseminates standards, and encourages innovation.

References

(1). Belden J, Grayson R, Barnes J. Defining and Testing EMR Usability: Principles and Proposed Methods of EMR Usability Evaluation and Rating. Healthcare Information Management and Systems Society Electronic Health Record Usability Task Force. Available at:
http://www.himss.org/content/files/HIMSS_DefiningandTestingEMRUsability.pdf
Accessed June 2009.

(2). Armijo D, McDonnell C, Werner K. Electronic Health Record Usability: Interface Design Considerations. AHRQ Publication No. 09(10)-0091-2-EF. Rockville, MD: Agency for Healthcare Research and Quality. October 2009.

(3). Armijo D, McDonnell C, Werner K. Electronic Health Record Usability: Evaluation and Use Case Framework. AHRQ Publication No. 09(10)-0091-1-EF. Rockville, MD: Agency for Healthcare Research and Quality. October 2009.

(4). TechSmith. Morae: usability testing and market research software. Available at: http://www.techsmith.com/morae.asp .

(5). Ammenwerth E, Talmon J, Ash JS, et al. Impact of CPOE on mortality rates—contradictory findings, important messages. Methods Inf Med 2006;45:586-93.

(6). Koppel R, Metlay JP, Cohen A, et al. Role of computerized physician order entry systems in facilitating medication errors. JAMA 2005;293:1197-203.

(7). Gilb T, Finzi S. Principles of software engineering management. Reading, MA: Addison-Wesley Pub. Co.; 1988

The report includes two appendices: Summary of Interviewed Vendors and Description of Electronic Health Records.

Vendors interviewed were
athenahealth, Inc. — athenaClinicals 9.15.1
Cerner Corporation –  Cerner Millenium Powerchart/PowerWorks EMR 2007.19
Criterions, LLC — Criterions 1.0.0
e-MDs — e-MDs Solution Series 6.3
EHS — CareRevolution 5.3
GE Healthcare — Centricity Electronic Medical Record 9.2
NextGen — NextGen EMR 5.5
Veterans Administration –VISTA

See PDF file for complete report.