Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10514977 | Journal of Clinical Epidemiology | 2005 | 6 Pages |
Abstract
With guidelines for data collection, the quality of research data is enhanced. A well-designed case record form and a handbook for standardized data collection are essential for training the data collectors and for ensuring fastidious searching of the record; however, certain kinds of information are not always well documented in patient records. Consequently, it is essential to perform a pilot study to assess the study design and to use additional questionnaires. Correct interpretation of clinical outcomes documented in the medical records often necessitates an independent adjudication committee to prevent bias in outcome definition.
Related Topics
Health Sciences
Medicine and Dentistry
Public Health and Health Policy
Authors
Angelique C.M. Jansen, Emily S. van Aalst-Cohen, Barbara A. Hutten, Harry R. Büller, John J.P. Kastelein, Martin H. Prins,