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Immunizations

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Data from Oklahoma's Immunization Registry Helps Shape CDC Policy on Polio Vaccine

June 1, 2002 | Program Result Report

In 1999, the Oklahoma immunization registry, OSIIS, helped shape the CDC's Advisory Committee on Immunization Practices (ACIP) recommendation on the use of inactivated polio vaccine (IPV) rather than oral polio vaccine (OPV).

Philadelphia Registry Increases Immunization Rates

June 1, 2002 | Program Result Report

Immunization registries working in collaboration with other public agencies and community organizations can have a substantial impact on increasing the immunization rate of a community's children.

Washington State: How an Immunization Registry Is Funded Can Determine Its Success

June 1, 2002 | Program Result Report

In Washington State where an unusual approach to funding the registry had been adopted in 1997.

Complex, High-Volume Immunization Registry Established In Michigan

June 17, 2002 | Program Result Report

Michigan represented All Kids Count's largest, and in many ways, most complex project. At the project's conclusion in June 2000, MCIR reported impressive statistics: it included 1.7 million child records and 14 million immunization records.

All Kids Count Project Builds Cooperation for Computerized Child Health Information Systems

July 1, 2005 | Program Result Report

The Task Force for Child Survival and Development worked for four years 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.

Planning a Web-Based Immunization Registry for Rhode Island

June 1, 2002 | Program Result Report

Rhode Island's KIDSNET wanted its registry to meet the needs of Rhode Island's private providers its success depended on it, since nearly 100 percent of immunizations in the state are given by private sector providers.

Bolstering Electronic Health Records at Four Community Health Centers in Chicago with Race, Ethnicity and Language Data

July 1, 2009 | Program Result Report

The Health Research and Educational Trust collected and integrated information on patients' race/ethnicity, primary language and socioeconomic status into an electronic health record system, and linked that information with clinical performance measures.

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