Manual for Cancer Registry Personnel

Manual for Cancer Registry Personnel PDF

Author: Divina Esteban

Publisher:

Published: 1995

Total Pages:

ISBN-13:

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A complete training guide and day-to-day reference for personnel working in population-based cancer registries. Firmly rooted in practical experience, the manual aims to provide all the information needed to help personnel exercise good judgement as well as follow standard procedures of abstracting and coding. Explanations of specific tasks are complemented by numerous reference tables and charts, definitions, exercises, questions and answers, model forms, and examples of typical reports and records. Details range from a flow chart for finding cancer cases in hospitals, through exercises for practice in abstracting and coding, to advice on how to interpret ambiguous terms often used by physicians. The manual, which is presented in the form of a loose-leaf binder, is suitable for use by anyone starting to work in a cancer registry, and most especially for the many who arrive without special training in medicine. Chapters provide general information on the symptoms of cancer, methods of detection, and forms of treatment, and offer a step-by-step guide to the location, collection, extraction, and abstracting of data from all relevant hospital departments, emphasizing procedures of case-finding needed to achieve complete registration. Exercises are included to let readers practice abstracting relevant information from a range of typical hospital reports. Coding is covered in the main chapter, which explains how to convert the diagnosis of cancer into coded form, following the rules developed for ICD-10 and ICD-O. Other chapters cover document management, security and confidentiality, and quality control. The manual concludes with a 90-page course designed to facilitate a thorough understanding of the medical terminology commonly used in cancer centres.

Registries for Evaluating Patient Outcomes

Registries for Evaluating Patient Outcomes PDF

Author: Agency for Healthcare Research and Quality/AHRQ

Publisher: Government Printing Office

Published: 2014-04-01

Total Pages: 396

ISBN-13: 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.

Cancer Registry Management

Cancer Registry Management PDF

Author: National Cancer Registrars Assn

Publisher: Kendall Hunt

Published: 2004-06-11

Total Pages: 580

ISBN-13: 9780757501920

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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.

Cancer Registry Manager - The Comprehensive Guide

Cancer Registry Manager - The Comprehensive Guide PDF

Author: VIRUTI SHIVAN

Publisher: Viruti Satyan Shivan

Published:

Total Pages: 225

ISBN-13:

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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.

Cancer Registration

Cancer Registration PDF

Author: Ole Møller Jensen

Publisher: IARC

Published: 1991

Total Pages: 295

ISBN-13: 9283211952

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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.