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NC Trauma Registry Single Variable Data Validation Form January 2005 Updated December 2008 Run frequencies of data items and check for a valid response in each of the data fields Change all default values to appropriate response. See explanation key at end. NCDVS1 Demographics Sex Valid Responses Default Value blank F M Do not leave at default value Race A B H I M O W Age Age range 0 to 100 autocalculated DOB If age unknown try to estimate age based on information available in patient record...
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What is trauma registry data validation?
Trauma registry data validation is the process of ensuring the accuracy and completeness of data collected in a trauma registry. It involves verifying the information entered, identifying errors or inconsistencies, and making necessary corrections or updates.
Who is required to file trauma registry data validation?
Trauma registries are typically maintained by hospitals or healthcare institutions. The responsibility for filing trauma registry data validation lies with the healthcare professionals or designated staff members who are responsible for managing the registry.
How to fill out trauma registry data validation?
The process of filling out trauma registry data validation involves reviewing the collected data for accuracy and completeness. Any errors or inconsistencies found should be corrected or updated. Depending on the specific system or software used for the registry, there may be specific steps or guidelines provided for data validation.
What is the purpose of trauma registry data validation?
The purpose of trauma registry data validation is to ensure the reliability and quality of the data collected. Validating the data helps in improving the accuracy of research studies, monitoring the performance of trauma care systems, identifying trends and patterns, and ultimately improving patient outcomes.
What information must be reported on trauma registry data validation?
The information reported on trauma registry data validation includes various data elements related to trauma patients, such as demographic information, injury severity scores, clinical interventions, outcomes, and follow-up information. The specific data elements may vary depending on the requirements of the trauma registry and the specific reporting standards used.
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