SEER Program, Self Instructional Manual For Cancer Registrars, Book 1, Objectives And Functions Of Cancer Registries, Etc., Revised May 1999

SEER Program, Self Instructional Manual For Cancer Registrars, Book 1, Objectives And Functions Of Cancer Registries, Etc., Revised May 1999 PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 260

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Self Instructional Manual for Cancer Registrars

Self Instructional Manual for Cancer Registrars PDF Author:
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 252

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Self-instructional Manual for Tumor Registrars: Objectives and functions of tumor registry

Self-instructional Manual for Tumor Registrars: Objectives and functions of tumor registry PDF Author:
Publisher:
ISBN:
Category : Tumors
Languages : en
Pages : 260

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Self-instructional Manual for Tumor Registrars

Self-instructional Manual for Tumor Registrars PDF Author:
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 256

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The SEER Program

The SEER Program PDF Author: SEER Program (National Cancer Institute (U.S.))
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 104

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Registries for Evaluating Patient Outcomes

Registries for Evaluating Patient Outcomes PDF Author: Agency for Healthcare Research and Quality/AHRQ
Publisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 385

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Book Description
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.

The SEER Program Coding and Staging Manual 2004

The SEER Program Coding and Staging Manual 2004 PDF Author: SEER Program (National Cancer Institute (U.S.))
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 1036

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Cancer Registries Amendment Act

Cancer Registries Amendment Act PDF Author: United States
Publisher:
ISBN:
Category : Breast
Languages : en
Pages : 8

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Developing a Protocol for Observational Comparative Effectiveness Research: A User's Guide

Developing a Protocol for Observational Comparative Effectiveness Research: A User's Guide PDF Author: Agency for Health Care Research and Quality (U.S.)
Publisher: Government Printing Office
ISBN: 1587634236
Category : Medical
Languages : en
Pages : 236

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Book Description
This User’s Guide is a resource for investigators and stakeholders who develop and review observational comparative effectiveness research protocols. It explains how to (1) identify key considerations and best practices for research design; (2) build a protocol based on these standards and best practices; and (3) judge the adequacy and completeness of a protocol. Eleven chapters cover all aspects of research design, including: developing study objectives, defining and refining study questions, addressing the heterogeneity of treatment effect, characterizing exposure, selecting a comparator, defining and measuring outcomes, and identifying optimal data sources. Checklists of guidance and key considerations for protocols are provided at the end of each chapter. 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. More more information, please consult the Agency website: www.effectivehealthcare.ahrq.gov)

AJCC Cancer Staging Manual

AJCC Cancer Staging Manual PDF Author: Frederick L, Greene
Publisher: Springer Science & Business Media
ISBN: 1475736568
Category : Medical
Languages : en
Pages : 386

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Book Description
The American Joint Committee on Cancer's Cancer Staging Manual is used by physicians throughout the world to diagnose cancer and determine the extent to which cancer has progressed. All of the TNM staging information included in this Sixth Edition is uniform between the AJCC (American Joint Committee on Cancer) and the UICC (International Union Against Cancer). In addition to the information found in the Handbook, the Manual provides standardized data forms for each anatomic site, which can be utilized as permanent patient records, enabling clinicians and cancer research scientists to maintain consistency in evaluating the efficacy of diagnosis and treatment. The CD-ROM packaged with each Manual contains printable copies of each of the book’s 45 Staging Forms.