The SEER Program Coding and Staging Manual 2004

The SEER Program Coding and Staging Manual 2004
Title The SEER Program Coding and Staging Manual 2004 PDF eBook
Author SEER Program (National Cancer Institute (U.S.))
Publisher
Pages 1036
Release 2004
Genre Cancer
ISBN

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SEER Summary Staging Manual 2000

SEER Summary Staging Manual 2000
Title SEER Summary Staging Manual 2000 PDF eBook
Author National Cancer Institute (U.S.). Cancer Statistics Branch
Publisher
Pages 293
Release 2001-10
Genre Cancer
ISBN 9780756714406

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From the Surveill., Epidem., & End Results (SEER) Prog. based at the Nat. Cancer Inst. Intended as a coding manual beginning with cases diagnosed from Jan. 1, 2001 rather than a staging guide. Each anatomic site in the Topography Sect. of the Internat. Class. of Disease for Oncology -- 3rd Ed. (ICD-0-3) has a corresponding summary staging scheme. Certain specific histologic types also have specific staging schemes. In some cases, sites which previously had separate guides (such as the segments of the colon) have a single staging scheme (colon), whereas some sites which previously had a single guide (e.g., larynx) have separate schemes for each sub-site of the larynx.

Cancer Registries Amendment Act

Cancer Registries Amendment Act
Title Cancer Registries Amendment Act PDF eBook
Author United States
Publisher
Pages 8
Release 1992
Genre Breast
ISBN

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Registries for Evaluating Patient Outcomes

Registries for Evaluating Patient Outcomes
Title Registries for Evaluating Patient Outcomes PDF eBook
Author Agency for Healthcare Research and Quality/AHRQ
Publisher Government Printing Office
Pages 385
Release 2014-04-01
Genre Medical
ISBN 1587634333

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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.

Race, Ethnicity, and Language Data

Race, Ethnicity, and Language Data
Title Race, Ethnicity, and Language Data PDF eBook
Author Institute of Medicine
Publisher National Academies Press
Pages 286
Release 2009-12-30
Genre Medical
ISBN 0309140129

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The goal of eliminating disparities in health care in the United States remains elusive. Even as quality improves on specific measures, disparities often persist. Addressing these disparities must begin with the fundamental step of bringing the nature of the disparities and the groups at risk for those disparities to light by collecting health care quality information stratified by race, ethnicity and language data. Then attention can be focused on where interventions might be best applied, and on planning and evaluating those efforts to inform the development of policy and the application of resources. A lack of standardization of categories for race, ethnicity, and language data has been suggested as one obstacle to achieving more widespread collection and utilization of these data. Race, Ethnicity, and Language Data identifies current models for collecting and coding race, ethnicity, and language data; reviews challenges involved in obtaining these data, and makes recommendations for a nationally standardized approach for use in health care quality improvement.

Sentinel Lymph Node Biopsy

Sentinel Lymph Node Biopsy
Title Sentinel Lymph Node Biopsy PDF eBook
Author Hiram S. Cody
Publisher CRC Press
Pages 300
Release 2001-11-08
Genre Medical
ISBN 9781841840345

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An intuitive, ingenious and powerful technique, sentinel lymph node biopsy has entered clinical practice with astonishing rapidity and now represents a new standard of care for melanoma and breast cancer patients, while showing great promise for the treatment of urologic, colorectal, gynecologic, and head and neck cancers. This text, written by international experts in the technique, provides a clear and comprehensive guide, presenting a detailed overview and discussing the various mapping techniques available and how these are applied in a number of leading institutions. This essential resource for surgical onocologists, pathologists, and specialists in nuclear medicine will also provide key information for those planning to start a sentinel lymph node program.

The SEER Program Coding and Staging Manual 2004

The SEER Program Coding and Staging Manual 2004
Title The SEER Program Coding and Staging Manual 2004 PDF eBook
Author SEER Program (National Cancer Institute (U.S.))
Publisher
Pages
Release 2004
Genre Cancer
ISBN

Download The SEER Program Coding and Staging Manual 2004 Book in PDF, Epub and Kindle