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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 ...
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.
The STROBE Statement was developed by the STROBE Initiative, an international collaboration of epidemiologists, methodologists, statisticians, researchers and journal editors with the aim to assist authors when writing up analytical observational studies, to support editors and reviewers when considering such articles for publication, and to help readers when critically appraising published ...
Anthropological survey paper from 1961 by Juhan Aul from University of Tartu who measured about 50 000 people. In fields such as epidemiology, social sciences, psychology and statistics, an observational study draws inferences from a sample to a population where the independent variable is not under the control of the researcher because of ethical concerns or logistical constraints.
One can find reports of routine health outcomes measurement in many medical specialties and in many countries. However, the vast majority of these reports are by or about enthusiasts who have set up essentially local systems, with little connection with other similar systems elsewhere, even down the street.
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 ...
[9] [10] [2] Patient-centered outcomes research involves questions and outcomes that are "meaningful and important to patients and caregivers" [11] in order to help those individuals make informed decisions for their own care. As of 2019, there have been 65 research standards developed to support patient-centered outcomes research. [12]
"Effects of Cost Sharing on Use of Medical Services and Health" (PDF). Medical Practice Management. 8: 317– 321. – summarizes major findings of the RAND Health Insurance Experiment; Normand, C (June 25, 1994). "Views and reviews – Free for All: Lessons from the RAND Health Insurance Experiment". The BMJ. 308. BMJ Publishing Group Ltd: 1724.