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The group was derived from the Observational Medical Outcomes Partnership (OMOP), a public-private consortium based in the United States of America, created with the goal of improving the state of observational health data for better drug development, which started in response to the U.S. Food and Drug Administration (FDA) Amendments Act of 2007.
OMOP: It is an acronym for Observational Medical Outcomes Partnership. The OMOP research program was initially established under Foundation for NIH) and created first version of OMOP common data model. The common data model was able to accommodate observational data of different types (both claims and electronic health records). It has a single ...
Within genomic and medical data, the Observational Medical Outcomes Partnership (OMOP) research program established under the U.S. National Institutes of Health has created a common data model for claims and electronic health records which can accommodate data from different sources around the world.
The STROBE Statement has also been adapted as a public, open-source repository for epidemiological research methods and reporting skills for observational studies. Epidemiologists, statisticians, and public health researchers are able to comment and edit the tool to inform future updates of the reporting guideline. [27]
The Patient-Reported Outcomes Measurement Information System [1] (PROMIS) provides clinicians and researchers access to reliable, valid, and flexible measures of health status that assess physical, mental, and social well–being from the patient perspective. PROMIS measures are standardized, allowing for assessment of many patient-reported ...
Observational data forms the foundation of a significant body of knowledge. Observer bias can be seen as a significant issue in medical research and treatment. There is greater potential for variance in observations made where subjective judgement is required, when compared with observation of objective data where there is a much lower risk of ...
Wiklund I., Assessment of patient-reported outcomes in clinical trials: the example of health-related quality of life, Fundam Clin Pharmacol. 2004 Jun;18(3):351-63. Willke RJ, Burke LB, Erickson P., Measuring treatment impact: a review of patient-reported outcomes and other efficacy endpoints in approved product labels, Control Clin Trials ...
Behavioral health outcome management (BHOM) involves the use of behavioral health outcome measurement data to help guide and inform the treatment of each individual patient. Like blood pressure, cholesterol and other routine lab work that helps to guide and inform general medical practice, the use of routine measurement in behavioral health is ...