Author:
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 76

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Author:
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages :

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Author: Ole Møller Jensen
Publisher: IARC
ISBN: 9283211952
Category : Medical
Languages : en
Pages : 295

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Book Description
Data obtained by population based cancer registries have a pivotal role in cancer control. Now also available in Spanish and French, this volume, which contains 15 authored chapters and four useful appendices, remains a standard reference for those planning to establish new cancer registries and those keen to adopt recognized methodologies. Information is given on the techniques required to collect, store, analyse and interpret data.

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.

Author: Herman R. Menck
Publisher:
ISBN: 9780757569005
Category : Cancer
Languages : en
Pages : 0

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Author: VIRUTI SHIVAN
Publisher: Viruti Satyan Shivan
ISBN:
Category : Medical
Languages : en
Pages : 225

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Book Description
In the rapidly evolving field of oncology, the role of a Cancer Registry Manager has never been more critical. "Cancer Registry Manager - The Comprehensive Guide" serves as an indispensable resource, offering a deep dive into the complexities of cancer data management and patient tracking. This book stands out by equipping readers with the knowledge and tools necessary to navigate the intricacies of the profession, from regulatory compliance to advanced data analysis techniques. Without relying on images or illustrations to circumvent copyright issues, the guide focuses on rich, textual content that brings clarity to complex concepts and procedures, making it a vital asset for both aspiring managers and seasoned professionals looking to refine their skills. At its core, this guide is designed to transform theoretical knowledge into practical expertise. Readers will find themselves immersed in a world where data becomes the foundation for groundbreaking research and personalized patient care. Through engaging narratives, personal anecdotes, and hypothetical scenarios, the book paints a vivid picture of the challenges and triumphs encountered by cancer registry managers. Whether you're looking to make a significant impact in the field of oncology, streamline cancer registry operations, or enhance patient outcomes through meticulous data management, this book is your quintessential companion on a journey towards excellence in cancer care.

Author: National Cancer Registrars Assn
Publisher: Kendall Hunt
ISBN: 9780757501920
Category :
Languages : en
Pages : 580

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Book Description
If you are a member of NCRA and would like to receive member discount pricing on this item, please contact customer service at 800-228-0810. Discounted orders cannot be processed via the website.

Author: Herman Menck
Publisher: CRC Press
ISBN: 9783718605873
Category : Cancer
Languages : en
Pages : 334

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Book Description
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.

Author:
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 252

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Author: National Research Council
Publisher: National Academies Press
ISBN: 0309255716
Category : Medical
Languages : en
Pages : 424

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Book Description
In the late 1980s, the National Cancer Institute initiated an investigation of cancer risks in populations near 52 commercial nuclear power plants and 10 Department of Energy nuclear facilities (including research and nuclear weapons production facilities and one reprocessing plant) in the United States. The results of the NCI investigation were used a primary resource for communicating with the public about the cancer risks near the nuclear facilities. However, this study is now over 20 years old. The U.S. Nuclear Regulatory Commission requested that the National Academy of Sciences provide an updated assessment of cancer risks in populations near USNRC-licensed nuclear facilities that utilize or process uranium for the production of electricity. Analysis of Cancer Risks in Populations near Nuclear Facilities: Phase 1 focuses on identifying scientifically sound approaches for carrying out an assessment of cancer risks associated with living near a nuclear facility, judgments about the strengths and weaknesses of various statistical power, ability to assess potential confounding factors, possible biases, and required effort. The results from this Phase 1 study will be used to inform the design of cancer risk assessment, which will be carried out in Phase 2. This report is beneficial for the general public, communities near nuclear facilities, stakeholders, healthcare providers, policy makers, state and local officials, community leaders, and the media.