RWJF Scholar examines neighborhood-based death rates from opiate-based painkiller overdoses, compared with heroin overdose deaths.
The Task Force for Child Survival and Development in Decatur, Ga., worked for four years (20002004) with federal, state and local public health agencies across the nation to foster the development of computerized child health information systems that integrate data from multiple sources.
In response to low immunization rates among preschool children, the Robert Wood Johnson Foundation (RWJF) in 1991 initiated a national program called All Kids Count: Establishing Immunization Monitoring and Follow-up Systems to create immunization registries (for more information see Grant Results).
An immunization registry is a computerized information system that collects child vaccination records from multiple health care providers in a geographic area.
In July 2000, the RWJF Board of Trustees funded an All Kids Count technical resource center.
The project staff formed a collaborative of health organizations working to integrate child health information systems. The goal of the collaborative, called Connections, was to provide a forum for members to learn from one another and to document best practices.
Members were eligible for mini-grants to support their local integration initiatives. In addition to Connections, which continued with federal funding after the project ended, the staff convened an invitational conference and produced various publications to encourage the development of integrated child health information systems.
RWJF supported the All Kids Count project with a $4,999,270 grant between August 2000 and July 2004.
Integrated child health information systems consolidate data on multiple health care services that children receive from various sources in a community. These computerized systems help public health agencies evaluate the health status of children and identify gaps where additional services are needed. (For a more comprehensive explanation of integrated systems and their potential benefits to health care providers and families as well as public health agencies, see Appendix 1.)
There are barriers to implementing integrated child health information systems, however. One major challenge is that, historically, state and local health agencies have developed separate information systems for different diseases and health programs. The result has been a proliferation of what are known as information "silos" unconnected, incompatible single-focus data systems that are unable to exchange information with each other.
While technology to link separate systems exists, the coordination necessary to set standards for systems architecture and data collection policies has been lacking. Setting privacy guidelines to protect the confidentiality of the information and identifying funding mechanisms to sustain integrated systems also have proved difficult.
The public health community's interest in integrated information is part of an effort by the entire health sector to move more decisively into the computer age. Health care systems, hospitals and individual providers increasingly are investing in electronic medical record systems as a means of improving the safety, quality and efficiency of care delivery. In the late 1990s, the National Committee on Vital and Health Statistics, a federal advisory committee to the U.S. Department of Health and Human Services (DHHS), initiated work on the National Health Information Infrastructure a concept for pulling health information networks serving both clinical medicine and public health into one coordinated framework.
In response to low immunization rates among preschool children, RWJF in 1991 initiated a national program called All Kids Count: Establishing Immunization Monitoring and Follow-up Systems, to create immunization registries. An immunization registry is a computerized information system that collects child vaccination records from multiple health care providers in a geographic area.
For public health authorities, an immunization registry is a useful tool to assess vaccination coverage rates and identify pockets of underimmunization where children could be at risk for vaccine-preventable diseases. A registry also allows health care providers to identify the immunization needs of specific patients and send out notices when shots are due an especially valuable tool to track children whose families are medically mobile. An estimated 25 percent of American children under age three receive their immunizations from more than one provider, in part because their families move about.
RWJF established a National Program Office to manage the work of All Kids Count at the Task Force for Child Survival and Development, a nonprofit public health organization based in Decatur, Ga., an Atlanta suburb. Phase I of the program (19911997) supported initial development work on 24 state and local registries. Phase II (19972001) provided implementation grants to 16 registry projects. Altogether, RWJF invested more than $20 million in the effort. For a comprehensive description of both phases, see the All Kids Count Grant Results.
As Phase II neared its end, a number of the All Kids Count grantees were interested in connecting immunization registries to other child health information systems. Health care organizations not directly involved in the program also sought leadership from the national program staff.
As a result, in June 2000, the task force proposed a Phase III of All Kids Count to stimulate development of integrated child health information systems to facilitate the assessment for and prompt provision of requisite services to ensure an optimal healthy start for all children and improve the health of children.
To achieve this outcome, integrated child health information systems must share information and knowledge appropriately and efficiently so that it is readily available to patients, families, health care and public health professionals and public agencies. This challenge is especially important for children who are born with heritable and congenital conditions identified through newborn dried blood spot screening and universal newborn hearing screening.
As a starting point, the principal focus was on four programmatic areas: newborn dried blood spot screening (a blood test for certain metabolic and other inherited disorders); early hearing detection and intervention; immunizations and vital registration; as well as information from Medicaid and the Special Supplemental Nutrition Program for Women, Infants and Children (WIC).
The proposal called for the All Kids Count staff to work with public agencies and private organizations to develop a "shared vision" of integrated preventive child health information systems. The vision was to include:
RWJF program staff considered All Kids Count Phases I and II to have been successful in demonstrating the feasibility and effectiveness of immunization registries and believed the proposed new phase, to establish a resource and technical assistance center, would build on that earlier work and on the credibility that the program office had established in the health information field. In July 2000, the Board of Trustees approved a $5-million grant (ID# 039374) to fund the All Kids Count technical resource center for three years, later extended to four years.
Laying the Groundwork
In addition to its broadened focus, the technical resource center differed in two key respects from the earlier All Kids Count program. First, unlike the first two phases, it did not entail separate RWJF funding for pilot projects. Instead, the $5-million grant included $1.3 million to be disbursed by the task force staff as technical assistance mini-grants to organizations working on integrated systems. (Of the remaining $3.7 million, $2.4 million was to support the project staff and $1.3 million was to cover expenses for communications, travel, meetings and consultants.)
Second, without pilot projects to select and oversee, the approximately 12-member All Kids Count staff concentrated its efforts more heavily on providing technical assistance to and building partnerships with government agencies and nongovernment health organizations. Reflecting that shift, the staff traded its designation as a National Program Office for the new classification of Technical Resource Center.
While much of the Phase II staff remained unchanged, David A. Ross, Sc.D., an expert in health information systems, took over as All Kids Count director. (The program had been directed by William H. Foege, M.D., M.P.H., from December 1991 through July 1997 and by William C. Watson, Jr., M.P.A., from August 1997 through July 2001.) Ross, a retired U.S. Public Health Service officer, had been assistant director for information and communications services at the federal Centers for Disease Control and Prevention (CDC) and more recently, an executive with the Cerner Corp., a supplier of health care information technology.
The staff spent the first six months researching child health information systems and meeting with government agencies and private organizations involved in child health programs to discuss integration efforts. These included the following:
The staff hired a consultant to research medical software systems used in preventive child health programs and convened a working group. This group of information system experts and former All Kids Count grantees was to consider information system models and the costs and benefits of integration.
The technical resource center staff defined technical assistance broadly to cover a wide range of activities, including educating health policy leaders on integration issues, documenting and disseminating best practices in the integration of child health information systems and helping organizations during their planning and implementation phases.
For example, the project staff contracted with the American Immunization Registry Association, a membership organization that grew out of All Kids Count Phase II, to conduct workshops on information integration. It also sponsored a meeting on linkages between immunization registries and the Vaccine Adverse Event Reporting System, a cooperative safety program of the CDC and the U.S. Food and Drug Administration.
To gain greater knowledge of the field, the staff surveyed 18 public health departments involved in integration efforts around the nation about their information systems. Staff also conducted telephone interviews with parents of children with special health care problems to learn their needs for and perspective on child health information.
Connections: The Major Activity
To stimulate integrated child health information systems, provide technical assistance and build partnerships, the project staff organized a forum or collaborative named Connections open to public health agencies and others interested in working cooperatively to advance the field of information integration. The collaborative was not part of the grant proposal, but it quickly evolved into the principal technical resource center activity and focus.
The staff saw Connections as a means of bringing states and communities together to share their experiences and knowledge on a peer-to-peer basis and to identify best practices in data integration. As Ross explains, Connections provided a trusted, learning environment that encouraged stakeholders to share their failures as well as their successes. He characterized Connections as a community of practice, a term for an informal group whose participants share a common pursuit.
Connections attracted 11 members. Some had been All Kids Count Phase II grantees, and some had federal funding from HRSA/MCHB to work on information integration projects. (See HRSA: A Key Partnership.) All were involved in linking at least two child health information systems.
One member was CalOptima, a health system that administers state Medicaid benefits in Orange County, Calif. The other 10 were public health agencies:
It was to members of Connections and only members were eligible that the project staff offered technical assistance mini-grants. In May 2001, the project staff issued a Call for Proposals soliciting projects aimed at developing some aspect of an integrated child health information system. In addition to testing technology to link disparate systems, projects could focus on less technical tasks, such as:
The staff conducted two competitive funding rounds and awarded a total of 16 grants (the term grants was used; but legally they were contracts). Fourteen grants of about $50,000 each went to single members of Connections, and two grants totaling $104,000 supported projects involving multiple Connections members. Five members of Connections received grants in both funding rounds, while two members received no grant funding.
The funded Connections projects differed widely. For example, one project examined different software products that clean data to facilitate merger of electronic records. Another analyzed the business case for an integrated information system. A third created a marketing plan to promote the use of an integrated information by health care providers and families. (See Appendix 2 for a description of all 16 projects.)
Connections held its initial meeting in June 2001 in Atlanta and thereafter met at five different members' sites. Each site meeting lasted two-and-a-half days, split evenly between learning about the project of the host organization and considering more general integration issues.
Representatives of federal public health agencies participated in Connections as ad hoc members, and consultants to the member organizations and other invitees also attended meetings. For example, one session featured a panel of health care providers. Between meetings, the staff and Connections members communicated through conference calls, a listserv and an interactive Web site. The staff used various communications mechanisms to share the knowledge developed by Connections with stakeholders and other interested parties. (See Communications for an account of these dissemination efforts.)
Conference Planning: Another Key Activity
To develop a shared vision of information integration, the grant proposal called for the project to produce a white paper endorsed by key stakeholder groups in the public and private sector. However, in November 2001, the National Committee on Vital and Health Statistics published the report Information for Health: A Strategy for Building the National Health Information Infrastructure, which outlined a vision for information exchange to improve the health of communities and individuals. This report was widely endorsed and, consequently, All Kids Count staff felt their efforts should be focused on delineating specific recommendations for the future of child health information systems versus duplicating the national efforts.
As the momentum for the national information infrastructure initiative (NHII) grew over the next two years, the staff felt the time was ripe to proceed with plans to host an invitational conference aimed at fostering development of a shared vision for integrated systems. The staff formed a planning committee with representatives from other organizations and held what was informally called the "vision conference" on December 34, 2003, at the Emory Conference Center in Atlanta. Seventeen agencies and organizations agreed to support the conference as nonfunding cosponsors. (See Appendix 3 for the list.)
HRSA: A Key Partnership
The project staff worked closely with the Genetic Services Branch of HRSA's Maternal and Child Health Bureau. A mission of the Genetic Services Branch is to facilitate the early identification of individuals with genetic conditions and integrate them into systems of care that are comprehensive, accessible, available, affordable, acceptable, population and community-based, culturally appropriate and family-centered. In 1999, HRSA/MCHB began a grant initiative to facilitate program integration and further infrastructure development at the state level around newborn screening and genetics. The purpose of these state-based programs is the early identification of conditions for which early and timely interventions can lead to the elimination or reduction of associated mortality, morbidity and disability. The system must ensure that the results of newborn screens are shared with the child's medical home for long-term follow-up and care.
During the term of the grant for the technical resource center, the task force received two HRSA contracts worth a total of $875,000 to support HRSA/MCHB efforts in information integration. For example, task force staff identified key elements of a successful integrated information systems project and reported on best practices of seven HRSA/MCHB-funded integration projects on the key elements. Also, HRSA/MCHB and the All Kids Count technical resource center jointly convened a workgroup to identify the principles, core functions and performance measures that an integrated system should be able to perform.
To house the All Kids Count technical resource center activities supported by RWJF and the complementary activities undertaken for HRSA/MCHB, the task force formed an internal umbrella component called the Center for Innovation in Health Information Systems. The same staff members did the work for both All Kids Count and HRSA/MCHB. (Also, with funding from CDC, the same staff helped the Association for State and Territorial Health Officers develop a community of practice to share best practices among states related to emergency response and bioterrorism planning.
In 2002, the task force received additional RJWF funding to support expanded efforts to upgrade the public health information infrastructure (ID#s 043745, 046025 and 046085). At that time, the task force started the Public Health Informatics Institute, and the All Kids Count technical resource center became a program within the institute. (See After the Grant for additional information about the institute.)
Challenges and Changes
To pursue the issue of information privacy, the staff attended conferences on privacy law and funded a Connections member (Rhode Island Department of Health) to produce a white paper assessing that state's data system's compliance with privacy standards. However, the evolving nature of federal confidentiality requirements prevented development of a comprehensive set of privacy guidelines as the project proposal had contemplated.
The Health Insurance Portability and Accountability Act of 1996 (HIPAA) mandated adoption of federal privacy protections for certain health information. In 2000 and again in 2002, DHHS issued HIPAA regulations detailing specific privacy requirements. This unsettled legal and policy landscape, with uncertainty over the interpretation of HIPAA regulations and their effect on individual state privacy requirements, made setting confidentiality guidelines impractical.
Also, after initial study, the technical resource center staff concluded that the field of information integration was too new and full of unknowns to document reliable cost and benefit estimates for child health data. Consequently, the staff postponed the effort to produce a comprehensive cost-benefit analysis, although one of the Connections grantees (Maine Department of Health and Human Services) conducted a cost study of its integration project. The institute is currently developing the business case for integrating child health information systems.
Early in the technical resource center grant, the staff hired a contractor to develop a computer tool named Catalyst to help public health organizations formulate information systems strategy. However, the work required cost and outcome data that were not readily available. Given that difficulty, the expense of the undertaking and a determination that the tool was a low priority for health care organizations, the staff discontinued the development effort in the project's second year.
The September 11, 2001, terrorist attacks on New York and Washington and the subsequent anthrax scare also had an impact on the work of the technical resource center. In response to the threat of bioterrorism, public health agencies stepped up their preparedness efforts, causing some to divert resources and personnel from other activities, including information integration.
In summary, national initiatives and events overtook some aspects of the project plans, says Alan R. Hinman, M.D., M.P.H., principal investigator on the All Kids Count technical resource center staff.
In interviews conducted for this report, a report from the technical resource center staff to RWJF and articles published in a supplement to the November 2004 issue of the Journal of Public Health Management and Practice, the staff identified the following among the project's accomplishments and conclusions:
In an article in the November 2004 journal supplement, the project's top staff members identified four "common threads" in recommendations made by participants at the December 2003 "vision" conference. The authors (Ross, Saarlas and Hinman) emphasized that the recommendations were by individuals and had not been officially endorsed by any of the 17 agencies and organizations that cosponsored the conference.
The four common-thread recommendations identified by the staff were:
(For a full discussion of the conference recommendations, see "A Vision for Child Health Information Systems: Developing Child Health Information Systems to Meet Medical Care and Public Health Needs" in the November 2004 supplement online.)
The technical resource center staff used a variety of means to disseminate the results of their work. Foremost was support for a journal supplement devoted to child health data integration. The 104-page supplement to the November 2004 issue of the Journal of Public Health Management and Practice contained 16 articles on activities, results and lessons from All Kids Count, related work supported by HRSA/MCHB and state and local information efforts. Some 2,500 copies of the supplement went to journal subscribers and others, and the full text was also available on the Public Health Informatics Institute Web site.
The staff also published two volumes describing the 16 state and local integration projects undertaken by members of Connections. Both volumes entitled Creating a Road Map: Sharing Knowledge about Integrating Child Health Information Systems were accessible on the project Web site and the institute site.
In cooperation with HRSA/MCHB, the project published a "sourcebook" for organizations interested in integrating newborn screening data with other child health information that documented best practices and lessons from seven HRSA/MCHB-funded integration projects. A companion tool for assessment and planning enabled agencies to assess their readiness for integrating information systems.
The December 2003 "vision conference" was another key communications effort. The two-day invitational meeting drew about 100 people representing 55 government agencies and private organizations. Richard Shiffman, M.D., M.C.I.S., associate professor of pediatrics at the Yale School of Medicine and associate director of the Yale Center for Medical Informatics, delivered the keynote address. Fourteen additional speakers including staff members from the technical resource center, HRSA and state and local public health institutions discussed information integration from various perspectives. Participants divided into breakout sessions to consider and make recommendations in specific areas.
Early in the life of the technical resource center, the staff targeted its communications activities to inform stakeholders of the expansion of All Kids Count from immunization registries to information networking. The technical resource center commissioned a new All Kids Count logo and graphic identity and developed and disseminated a brochure explaining the need for integrated child health information systems. Another brochure explained the purpose of Connections, and the staff also published a quarterly Connections newsletter about activities of the collaborative and its members.
Over the course of the project, the staff issued several news releases, including one identifying the first-round recipients of technical assistance grants. Staff members made numerous presentations to health organizations about the project and information integration issues.
The All Kids Count Web site, which is still accessible, includes information about the purpose of the technical resource center as well as many of the project documents. Information, much of it duplicative, is also available at the Institute site.
(See Bibliography for details of the technical resource center's major dissemination efforts.)
Although RWJF itself did not evaluate the technical resource center, the staff used a portion of the RWJF grant to hire a consultant, Silver Creek Associates, in Alexandria, Va., to assess the effectiveness of Connections. The two-member evaluation team interviewed 26 Connections participants, conducted a Web-based survey of the members and examined written records. The firm's January 30, 2004, report included the following findings and recommendations:
(For a full discussion of the evaluation findings, see "All Kids Count Connections: A Community of Practice on Integrating Child Health Information Systems" in the November 2004 supplement online.)
In "All Kids Count 19912004: Developing Information Systems to Improve Child Health and the Delivery of Immunizations and Preventive Services" in the November 2004 supplement, program staff members said the combined phases of All Kids Count provided several general lessons for health information projects, including:
The September 11, 2001, terrorist attacks on New York and Washington and subsequent anthrax incidents focused increased attention on bioterrorism and the ability of public health agencies to detect and react to disease outbreaks.
In response, RWJF in 2002 awarded the task force a $2.87-million, 23-month grant (ID# 046026) to undertake additional activities aimed at upgrading the public health surveillance and information infrastructure, including improving the information management systems used by public health laboratories.
As noted previously, the task force created the Public Health Informatics Institute to perform this work simultaneously with the All Kids Count technical resource center. In May 2004, as the grant for the technical resource center was nearing its end, RWJF awarded the task force a $3.2-million, two-year grant (ID# 046085) to continue the efforts of the Public Health Informatics Institute.
The new grant called for the institute to use its collaborative model to:
The institute's other funders include HRSA/MCHB, the Association of Public Health Laboratories and the Minnesota Department of Health. Connections continues with HRSA/MCHB support, its membership enlarged to include additional federal grantees.
All Kids Count: Technical Resource Center to Foster Development of Integrated Preventive Health Information Systems
Task Force for Child Survival and Development (Decatur, GA)
The Definition and Potential Benefits of Integrated Child Health Information Systems
Integrated child health information systems consolidate data on multiple health care services delivered to children and make the information useful to families, medical providers and public health authorities. Integrated systems are accessible through a convenient point of access, ensure optimal health care service delivery and follow-up and support population health assessment.
Integration projects now underway focus on the integration of information systems of four programmatic areas: immunizations; newborn dried blood spot screening; early hearing detection and intervention; and vital registration, as well as others.
For public health officials, integrated systems:
For parents and providers, these systems:
Results of Projects Supported by the All Kids Count Technical Resource Center
The All Kids Count technical resource center provided 16 technical assistance "mini-grants" to support development of integrated preventive health information systems. Following are brief descriptions of each project as reported in Volumes One and Two of Creating a Road Map: Sharing Knowledge about Integrating Child Health Information Systems.
The first nine projects received funding during 20012002 in the initial round of grants and are the subject of Volume One. The other seven projects received funding in 2003 in a second round and are covered in Volume Two.
Round One Projects
Project title: Recruitment and Retention Plan for CalOptima's Login Information Network for Kids
This Medicaid managed care organization in California's Orange County evaluated pilot sites using a Web-based children information network (LINK) and developed recruitment plans to expand the network's use by the larger pediatric provider community. Pilot site staff and physicians who were interviewed all viewed LINK as a positive resource but some expressed concerns about the availability of data and ease of use of the system. Project staff concluded, for both pilot and newly recruited sites, physicians and staff members need adequate training, support and awareness of the information available on the system.
2. Kansas Integrated Public Health System
Project title: Childhood Lead Poisoning Prevention Information System Support for a Collaborative Childhood Lead Poisoning Prevention Program
The Kansas project planned to define requirements for an information system to address lead poisoning prevention. The Sedgwick County Health Department was the project sponsor; other partners included the Kansas Department of Health and Environment, the Women, Infant and Children's Program, the state preschool association and the Kansas City Housing Authority. Project staff was not able to complete the project as envisioned because of staff turnover and other competing priorities for the collaboration. Project staff instead began to define the business requirements for an information system that would support all community level public health activities. Project staff reported that an important lesson learned was that the role and expectations of the sponsor in a collaborative effort must be understood.
3. Maine Bureau of Health
Project title: Development of the Business Case Analysis for the Maine Integrated Public Health Information System
The Maine agency contracted with the Maine Health Research Institute to conduct a business case analysis of the agency's integrated information system. The project resulted in a business model, a funding plan and a draft of uniform core data elements and business rules for the system. In the next project phase, staff planned to use these products to recruit the leadership of the Bureau of Health and other community stakeholders to the vision of an integrated public health information system and the possible benefits of this re-engineering.
4. Michigan Department of Community Health
Project title: Envisioning Real-Time Access to Child Health Data by Providers
The agency initiated a systematic process to identify specific child health programs that can be linked with the Michigan Childhood Immunization Registry. The project evaluated the importance, interest and impediments to the potential linkages and developed a plan for eventually integrating these disparate data resources. The evaluation concluded that health data must serve three distinct functions within the system: client services (real-time access and reporting on services provided), health surveillance (epidemiological research on outbreaks of communicable disease, patterns of chronic illness, vital statistics and registries) and administration (managing Medicaid funds and enrollment and preventing fraud and abuse). Project staff noted the need for improvements to the data collected, including standardization and quality, and the creation of a patient identifier.
5. Missouri Department of Health and Senior Services
Project title: Increasing the Quantity and Timeliness of Immunization and Other Reportable Conditions Data in Missouri
The agency worked with a billing data clearinghouse to determine the feasibility of abstracting immunization and other public health reportable conditions data from billing data submitted by health care providers. Preliminary results indicated data abstraction from billing claims provides timely information and is a viable option for obtaining information on vaccine doses provided to clients. Project staff recommended expanding electronic file submissions to include communicable diseases and other reportable conditions.
6. New York City Department of Health and Mental Hygiene
Project title: A Pilot Data Exchange between the Master Child Index and the New York State Medicaid Database
The city agency piloted a data exchange between the city's Master Child Index database and the state Medicaid Management Information System. The pilot project demonstrated the feasibility of ongoing data exchanges with the state system. Staff reported lessons learned included: (1) allow sufficient amounts of time to negotiate between public health agencies and gain program approval and legal consent for data involving Medicaid; (2) pursue and obtain support from people able to influence the Medicaid data exchange process along; and (3) before integrating databases, conduct a pilot.
7. Oregon Department of Human Services
Project title: Communication Plan for FamilyNet, Oregon's Consolidated Health Data System
The Oregon agency created a marketing plan to communicate the benefits of the state's child health data system to health care providers and families. The project identified key stakeholders in the system: health care providers, parents and parent advocacy groups and medical associations. Results of focus groups with parents and providers revealed that for parents the main concerns of a health data system were confidentiality and misuse of data; providers' concerns were the responsibility for gathering and maintaining data and the need to explain the data gathering to parents. Staff produced the creative components of a marketing effort to address perceived barriers and highlight benefits. Elements included endorsements, public relations education and advertising to reach the two audiences of parents and providers.
8. Rhode Island Department of Health
Project title: Confidentiality: The Challenge of Time, Growth and Change
Agency staff assessed its data confidentiality, security and access policies for compliance with federal and state laws and standards. The agency revised some of its processes and materials related to data confidentiality and created a model document for data sharing among programs affiliated with KIDSNET, the statewide integrated child health information system.
9. Utah Department of Health
Project title: Developing Child Health Advanced Records Management (CHARM)
The agency created a data stewardship policy for intra-agency, program-to-program data sharing in connection with CHARM, a state initiative to manage online, real-time communication and data sharing among information systems.
Round Two Projects
10. Kansas Integrated Public Health System
Project title: The Data Used in Your Secondary Use Application May Not Represent What You Think They Do
This project studied data elements in the Kansas integrated system and the secondary use of the data for public health decision-making. The objective was to create a classification scheme for data sources and identify appropriate and inappropriate data usage. In Volume Two of Creating a Road Map: Sharing Knowledge about Integrating Child Health Information Systems, project staff concluded, " the dream of a comprehensive, internally consistent set of data from disparate sources gathered into a secondary use environment in order to accurately measure the pulse of public health activity, effectiveness and efficiency is going to be a far more difficult undertaking than we initially believed."
11. Missouri Department of Health and Senior Services
Project title: Expansion of Missouri's Integrated Public Health Information System to Include Electronic Blood Lead Level Results: A Pilot Project for Electronic Reporting of Laboratory Blood Lead Level Results
The agency worked with public and private laboratories to increase the electronic laboratory reporting of blood lead level testing results for children 1272 months of age. The agency reported at the end of the project that much of the preparatory work necessary to implement the electronic reporting improvement had been completed.
12. New York City Department of Health and Mental Hygiene
Project title: Developing and Implementing a Batch Query Application
The agency developed and implemented an application that queried the city child health database and disseminated immunization and lead test information. The application increased the number of records returned to requesting providers and decreased the time spent by the agency on record reviews.
13. Oregon Department of Human Services
Project title: Using Nationally Accepted Standards to Exchange Data between an Immunization Registry and a Managed Care Organization
The agency's immunization registry implemented a synchronized data exchange that populated a Kaiser Permanente Northwest computerized system with information on patients up to age five. This prototype for exchanging data across different systems provided a model applicable to a planned data exchange between the immunization registry and FamilyNet, Oregon's health data system.
14. Utah Department of Health
Project title: Improving Data Quality through Electronic Data Capture
The agency hired a consulting firm to identify the procedures utilized at birthing hospitals to enter the birth record number (BRN) a unique identifier of newborns initiated by the agency in 2002 and to make recommendations to ensure data accuracy and completeness. (The BRN had proved beneficial in identifying unregistered births, missed hearing screenings and missed follow-up opportunities, but data entry errors and omissions had reduced the BRN's effectiveness.) Project staff concluded that the effectiveness of unique BRNs could be enhanced by (1) employing electronic data capture technology to enter the BRN, (2) enhancing the systems used for newborn screening and creating the birth registration and (3) improving operational processes to eliminate manual or redundant activities.
15. A group project involving seven organizations: Kansas Integrated Public Health System, Maine Bureau of Health, Missouri Department of Health and Senior Services, New York City Department of Health and Mental Hygiene, Oregon Department of Human Services, Rhode Island Department of Health and Utah Department Health
Project title: De-Duplication Technology and Practices for Integrated Child Health Information Systems.
De-duplication is the term for data cleaning activities performed to match and merge records appropriately. This study examined de-duplication software and approaches, performed limited testing and technical analysis of a number of products and compared their effectiveness, cost and other factors. The study did not identify one single best product but provided a framework to examine alternatives and trade-offs when choosing de-duplication products and strategies to meet integration requirements.
16. A group project involving six organizations: Maine Bureau of Health, Michigan Department of Community Health, New York City Department of Health and Mental Hygiene, Oregon Department of Human Services, Rhode Island Department of Health and Utah Department of Health.
Project title: All Kids Count Mobile Registry Application: A PDA-based Interface to Immunization Registries
A consulting firm worked with the above six organizations to design a personal digital assistant (PDA) product to accommodate the needs of a diverse set of registries. A PDA is a handheld device that combines computing, the Internet and other capabilities. The design team developed architecture and end-user, security and server integration requirements for this product.
Cosponsors of "A Vision for Child Health Information Systems: Developing Child Health Information Systems to Meet Medical Care and Public Health Needs," held December 34, 2003
(Current as of date of this report; as provided by grantee organization; not verified by RWJF; items not available from RWJF.)
Ross DA, Hinman AR, Saarlas K and Foege W. "Foreword." In Public Health Informatics and Information Systems, O'Carroll PW, Yasnoff WA, Ward ME, Ripp LH and Martin EL (eds.). New York: Springer, 2003.
Journal of Public Health Management and Practice. November Supplement, 2004. The supplement consists of 16 articles describing activities, results and lessons learned from the All Kids Count III project, related work supported by the Health Resources and Services Administration, and state and local efforts to integrate child health information systems. The articles, which are also available online, are:
Hinman AR. "Public Health Information Systems: From Promise to Practice." Journal of Public Health Management and Practice, 8(3): 5458, 2002.
Hinman AR. "Tracking Immunization." Pediatric Annals, 33(9): 609615, 2004. Abstract available online.
Horne PR, Saarlas KN and Hinman AR. "Costs of Immunization Registries: Experiences from the All Kids Count II Project." American Journal of Preventive Medicine, 19(2): 9498, 2000. Abstract available online.
Horne PR, Saarlas KN and Hinman AR. "Update on Immunization Registries." American Journal of Preventive Medicine, 20(2): 174, 2001.
Ross DA. "Implications of Practicing Informatics in the Public Health Sector." Journal of Public Health Management and Practice, 8(3): vvi, 2002.
Saarlas KN, Edwards KC, Wild E and Richmond P. "Developing Performance Measures for Immunization Registries." Journal of Public Health Management and Practice, 9(1): 4757, 2003. Abstract available online.
All Kids Count. (Brochure) Atlanta: Public Health Informatics Institute, 2001.
All Kids Count and Public Health Informatics Institute. (Brochure) Atlanta: Public Health Informatics Institute, 2003.
All Kids Count Connections. (Brochure). Atlanta: Public Health Informatics Institute, 2001.
All Kids Count Connections Evaluation. Alexandria, Va.: Silver Creek Associates, 2004.
All Kids Count Vision Conference Proceedings. Decatur: Ga.: Public Health Informatics Institute, 2004. Available online.
Case Study: Developing Performance Measures for Immunization Registries. Atlanta: Public Health Informatics Institute, 2004. Available online.
Creating a Road Map: Sharing Knowledge about Integrating Child Health Information Systems, Volume One. Decatur, Ga.: Public Health Informatics Institute, 2003. Available online.
Creating a Road Map: Sharing Knowledge about Integrating Child Health Information Systems, Volume Two. Decatur, Ga.: Public Health Informatics Institute, 2004. Available online.
Current State of Integration Survey. Decatur, Ga.: Public Health Informatics Institute, 2003.
Hinman AR and Lloyd-Puryear MA. Integrating Child Health Information Systems. Proceedings of the 2004 Newborn Screening and Generic Testing Symposium. Atlanta: 2004.
Integration of Newborn Screening and Genetic Service Systems with Other Maternal and Child Health Systems: A Sourcebook for Planning and Development. Decatur, Ga.: Public Health Informatics Institute, 2003. Available online.
Integration of Newborn Screening and Genetic Service Systems with Other Maternal and Child Health Systems: A Tool for Assessment and Planning. Decatur, Ga.: Public Health Informatics Institute, 2003. Available online.
Topics in Public Health Informatics: Integrated Child Health Information Systems. Atlanta: Public Health Informatics Institute, 2004. Available online.
Connections, Integrated Child Health Information Systems Community of Practice, a CD-ROM containing visual aids on the information integration initiatives of the Oregon Department of Human Services. From a presentation at a meeting of the Connections collaborative in Portland, Ore., June 2527, 2002.
www.allkidscount.org. The public Web site of the All Kids Count program. Although the program itself has concluded, the site continues and contains information on activities, reports and findings related to the program's Phase III efforts to stimulate development of integrated preventive child health information systems. Atlanta: Public Health Informatics Institute, 2001.
www.ConnectionsZone.org. An interactive Web site for members of Connections and other public health practitioners. The site permits users to exchange ideas and address issues related to the integration of child public health information systems. Atlanta: Public Health Informatics Institute, 2001.
www.phii.org. The Web site of the Public Health Informatics Institute, a component of the Task Force for Child Survival and Development. The Institute seeks to advance the ability of the public health sector to apply information systems strategically to improve the health of communities and individuals. The site includes information about Institute activities and the field of health information systems, including access to reports, publications and other materials produced by the All Kids Count Phase III project. Atlanta: Public Health Informatics Institute, 2002.
Report prepared by: Michael H. Brown
Reviewed by: Janet Heroux
Reviewed by: Molly McKaughan
Program Officer: Susan B. Hassmiller
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