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Appendix E <br />NCRPCD Data Dissemination Policy & <br />Guidelines for Requesting De -identified Dataset <br />DATA DISSEMINATION POLICY <br />Mission <br />The purpose of the Child Death Review (CDR) Case Reporting System of the National Center <br />for the Review and Prevention of Child Deaths (NCRPCD) is to systematically collect, analyze, <br />and report on information surrounding deaths of individual children around the country. The <br />information can then be used at the local, state, and national levels to inform improvement in <br />child health and safety and to prevent deaths. The data collected with the System includes the <br />following: <br />• information about the child, family, supervisor and perpetrator; <br />• the types of action taken during the investigation; <br />• the scene, incident, and background information on the cause of death, including <br />the risk and protective factors; <br />• the services provided or needed as a result of the death; <br />• a description of the teams' recommendations, as well as the policies, practices, <br />and other actions taken to prevent other child deaths; and <br />• factors affecting the quality of the case review. <br />The web -based CDR Case Reporting System (CDR -CRS) was first implemented in May 2004 in <br />14 pilot states. Version 1 was made available for widespread use in January 2007; Version 2 was <br />released in January 2008; and Version 3 was issued in October 2013. Updated information on <br />the number of participating states, number of entered cases and number of cases migrated into <br />the system from older state reporting systems is available from NCRPCD. The CDR -CRS is <br />supported primarily by the HRSA Maternal and Child Health Bureaus and secondarily by the US <br />Centers for Disease Control and Prevention. Data submitted by states resides on servers at the <br />Michigan Public Health Institute (MPHI). <br />Data Sources <br />Data collected by the CDR -CRS are the result of multi -disciplinary processes that bring together <br />state and/or community agencies to share information on child death events and to identify the <br />risk factors in these deaths. Data entered into the System may include, but are not limited to, <br />information gathered from the following data sources: birth certificates, death certificates, law <br />enforcement records, medical records, autopsy reports, child protective services reports, and <br />Emergency Medical Services run reports. <br />I Grant No. 1 U49 MC 00225-11-00 from the Maternal and Child Health Bureau (Title V, Social Security Act), Health <br />Resources and Services Administration, Department of Health and Human Services. <br />2 Number 200-2012-M-51198 from the US Centers for Disease Control and Prevention. <br />13 <br />