Self-instructional Manual for Tumor Registrars: Tumor registrar vocabulary PDF Download
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Author:
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Category : Tumors
Languages : en
Pages : 236
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Author:
Publisher:
ISBN:
Category : Tumors
Languages : en
Pages : 236
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Author:
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ISBN:
Category : Cancer
Languages : en
Pages : 256
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Author:
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ISBN:
Category : Tumors
Languages : en
Pages : 260
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Author:
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ISBN:
Category : Cancer
Languages : en
Pages : 252
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Author:
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ISBN:
Category :
Languages : en
Pages : 260
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Author: Herman Menck
Publisher: CRC Press
ISBN: 9783718605873
Category : Medical
Languages : en
Pages : 334
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Practical issues, including the use of computers, selection and training of professional, administrative and technical staff are included, along with quality control procedures, essential to assure the integrity of information kept by the registry. Follow-up procedures, sources of population data, calculation and interpretation of incidence rates and survival rates, and the differences between case-control studies and cohort studies (based on registry data) are also described. Prevention and control applications, and legal issues relative to the confidentiality of information in the data files are also examined. This book covers the goals and objectives of U.S. central cancer registries; the kinds of information they can produce and how this information can be used. The practical considerations involved in case-finding are discussed, covering sources of case reports, and how the central registry works with doctors and hospitals.
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Category : Government publications
Languages : en
Pages : 1102
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Author:
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ISBN:
Category : Cancer
Languages : en
Pages : 560
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Author: Agency for Healthcare Research and Quality/AHRQ
Publisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 385
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This User’s Guide is intended to support the design, implementation, analysis, interpretation, and quality evaluation of registries created to increase understanding of patient outcomes. For the purposes of this guide, a patient registry is an organized system that uses observational study methods to collect uniform data (clinical and other) to evaluate specified outcomes for a population defined by a particular disease, condition, or exposure, and that serves one or more predetermined scientific, clinical, or policy purposes. A registry database is a file (or files) derived from the registry. Although registries can serve many purposes, this guide focuses on registries created for one or more of the following purposes: to describe the natural history of disease, to determine clinical effectiveness or cost-effectiveness of health care products and services, to measure or monitor safety and harm, and/or to measure quality of care. Registries are classified according to how their populations are defined. For example, product registries include patients who have been exposed to biopharmaceutical products or medical devices. Health services registries consist of patients who have had a common procedure, clinical encounter, or hospitalization. Disease or condition registries are defined by patients having the same diagnosis, such as cystic fibrosis or heart failure. The User’s Guide was created by researchers affiliated with AHRQ’s Effective Health Care Program, particularly those who participated in AHRQ’s DEcIDE (Developing Evidence to Inform Decisions About Effectiveness) program. Chapters were subject to multiple internal and external independent reviews.
Author:
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ISBN:
Category : Education
Languages : en
Pages : 1148
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