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Electronic Health Records and Electronic Medical Records. Administrative Data. Claims Data. Patient / Disease Registries. Health Surveys. Clinical Trial Data. Genomic Data.
Data collection in healthcare is the process of collecting, analyzing, and using the data for patient documentation and resources. This technology allows patient data to be immediately available system-wide and the collaborative efforts within any medical system can improve the accuracy of medical data collection.
Depending on the measure, data can be collected from different sources, including medical records, patient surveys, and administrative databases used to pay bills or to manage care.
These databases contain a wealth of information, including patient medical records, treatment outcomes, and healthcare provider performance data. By analyzing this data, healthcare organizations can gain valuable insights into the quality of care being provided.
A patient registry can be a powerful tool to observe the course of disease; to understand variations in treatment and outcomes; to examine factors that influence prognosis and quality of life; to describe care patterns, including appropriateness of care and disparities in the delivery of care; to assess effectiveness;
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Healthcare data refers to information collected from patients, including diagnoses, medications, treatment plans, and test results, stored digitally for personalized healthcare and improved patient-doctor communication.
Clinical data registries record information about patients health status and the care they receive over time.

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