Standards and Guidelines for Cancer Registration in Europe PDF Download
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Author: European Network of Cancer Registries
Publisher: World Health Organization
ISBN: 9789283224228
Category : Medical
Languages : en
Pages : 97
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Book Description
This is a handbook for cancer registries bringing together all recommendations and guidelines that have been prepared so far by the ENCR Working Groups, as well as recommendations prepared by the International Association of Cancer Registries (IACR) and adapted by the Network. Several appendices provide information on the EUROCIM software and databases, the ACCIS project on childhood cancers, automated registration, and structured registry reviews. The complete address list of the ENCR member registries and a list of selected ENCR publications are also included.
Author: European Network of Cancer Registries
Publisher: World Health Organization
ISBN: 9789283224228
Category : Medical
Languages : en
Pages : 97
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Book Description
This is a handbook for cancer registries bringing together all recommendations and guidelines that have been prepared so far by the ENCR Working Groups, as well as recommendations prepared by the International Association of Cancer Registries (IACR) and adapted by the Network. Several appendices provide information on the EUROCIM software and databases, the ACCIS project on childhood cancers, automated registration, and structured registry reviews. The complete address list of the ENCR member registries and a list of selected ENCR publications are also included.
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: Marc Arbyn
Publisher:
ISBN:
Category : Cancer
Languages : en
Pages : 328
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Book Description
Recoge: 1. Epidemiological guidelines for quality assurance in cervical cancer screening - 2. Methods for screening and diagnosis - 3. Laboratory guidelines and quality assurance practices for cytology - 4. Techniques and quality assurance guidelines for histopathology - 5. Management of abnormal cervical cytology - 6. Key performance indicators - 7. Annexes.
Author: Guy Launoy
Publisher: Springer Nature
ISBN: 3030693295
Category : Medical
Languages : en
Pages : 323
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Book Description
This contributed volume addresses the link between the social environment and cancer in Europe. The authors document the wide range and diverse trends in cancer incidence and patient survival in Europe, and they identify the main mechanisms and key influences that underlie these inequalities. They suggest a series of actions and programmes to tackle these inequalities in Europe, within the conceptual framework of intervention research. The influence of the social environment on the risk of suffering and dying from cancer is obviously a global phenomenon, as evidenced by a growing number of studies and books. In part, the underlying mechanisms are universal. Given the availability of a new standardised measure for social deprivation in Europe (the European Deprivation Index), the networking of population-based cancer registries across Europe as efficient surveillance tools, the increasing comparability of the organisation of care in European countries, and the recent launch of Europe’s Beating Cancer Plan, this extensive review of social inequalities in cancer on a European scale is both relevant and timely. The book consists of 21 chapters organised in four sections: Part I – General Considerations and Methodologic Aspects Part II – Social Disparities in Cancer Incidence and Survival – Reports Part III – Social Disparities in Cancer Incidence and Survival – Mechanisms Part IV – Towards an Evidence-Based Policy for Tackling Social Inequalities in Cancer Social Environment and Cancer in Europe: Towards an Evidence-Based Public Health Policy is a unique resource that presents up-to-date methods for analysing quantitative data. It focusses on inequalities in cancer incidence and survival within the wider framework of inequalities in health. This book will be an essential reference for policy-makers, researchers, public health professionals, social scientists and oncologists.
Author: Ichiro Kawachi
Publisher: Oxford University Press
ISBN: 0192520601
Category : Medical
Languages : en
Pages : 816
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Book Description
Fully revised and updated for the fourth edition, the award-winning Oxford Handbook of Public Health Practice remains the first resort for practitioners in the field. Structured into practical sections addressed towards professional competencies and translating evidence into policy, this Handbook provides concise summaries and covers real issues from across the globe, providing a world of experience at your fingertips. Easy-to-use, concise, and practical, this Handbook is divided into seven parts that focus on the vital areas of this broad discipline. Reflecting recent advances, the most promising developments in the practice of public health are presented, along with essential summaries of the core disciplines. Specific sections are devoted to the development of professional competencies including negotiation, communicating risk to the public, community action, and translating evidence into policy. Written by an international team of experts, and considering both social and scientific advances since the previous edition, this Handbook will assist students, trainees and practitioners around the world with its enriched information on the management of disasters, epidemics, health behaviour, acute and chronic disease prevention, community and government action, environmental heath, vulnerable populations, and more.
Author:
Publisher: World Health Organization
ISBN: 9240025278
Category : Medical
Languages : en
Pages : 126
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Book Description
This framework document is a “how-to” guide for policy-makers and programme managers to effectively implement the CureAll pillars and enablers. It provides justification for action, posits priority interventions and proposes a monitoring framework. Key components needed to establish, scale up and sustain a well-functioning national childhood cancer programme are explained.The scope of this framework document is centrally defined by the programmes, services and policies that support children with cancer in the context of the health system. For the Initiative, children are defined as those aged 19 years or younger. Childhood cancer care requires cross-cutting strategies, such as workforce training, that often have overlap with broader child health and/or cancer control programmes. These synergies are highlighted and considered in scope for the Initiative and for an integrated response in childhood cancer control. The primary audience for this framework document are policy-makers, cancer control programme managers and hospital managers at the country level. Additional key stakeholders may also find the information in this guide beneficial, including clinicians, parent groups, civil society, academia and interested parties in the private sector. The primary audience for this framework document are policy-makers, cancer control programme managers and hospital managers at the country level. Additional key stakeholders may also find the information in this guide beneficial, including clinicians, parent groups, civil society, academia and interested parties in the private sector.
Author: Guy Launoy
Publisher:
ISBN: 9783030693305
Category : Cancer
Languages : en
Pages : 324
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Book Description
This contributed volume addresses the link between the social environment and cancer in Europe. The authors document the wide range and diverse trends in cancer incidence and patient survival in Europe, and they identify the main mechanisms and key influences that underlie these inequalities. They suggest a series of actions and programmes to tackle these inequalities in Europe, within the conceptual framework of intervention research. The influence of the social environment on the risk of suffering and dying from cancer is obviously a global phenomenon, as evidenced by a growing number of studies and books. In part, the underlying mechanisms are universal. Given the availability of a new standardised measure for social deprivation in Europe (the European Deprivation Index), the networking of population-based cancer registries across Europe as efficient surveillance tools, the increasing comparability of the organisation of care in European countries, and the recent launch of Europes Beating Cancer Plan, this extensive review of social inequalities in cancer on a European scale is both relevant and timely. The book consists of 21 chapters organised in four sections: Part I General Considerations and Methodologic Aspects Part II Social Disparities in Cancer Incidence and Survival Reports Part III Social Disparities in Cancer Incidence and Survival Mechanisms Part IV Towards an Evidence-Based Policy for Tackling Social Inequalities in Cancer Social Environment and Cancer in Europe: Towards an Evidence-Based Public Health Policy is a unique resource that presents up-to-date methods for analysing quantitative data. It focusses on inequalities in cancer incidence and survival within the wider framework of inequalities in health. This book will be an essential reference for policy-makers, researchers, public health professionals, social scientists and oncologists.
Author: Helena Legido-Quigley
Publisher: World Health Organization
ISBN: 9289071931
Category : Medical
Languages : en
Pages : 242
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Book Description
People have always travelled within Europe for work and leisure, although never before with the current intensity. Now, however, they are travelling for many other reasons, including the quest for key services such as health care. Whatever the reason for travelling, one question they ask is "If I fall ill, will the health care I receive be of a high standard?" This book examines, for the first time, the systems that have been put in place in all of the European Union's 27 Member States. The picture it paints is mixed. Some have well developed systems, setting standards based on the best available evidence, monitoring the care provided, and taking action where it falls short. Others need to overcome significant obstacles.
Author: F. Berrino
Publisher:
ISBN:
Category : Medical
Languages : en
Pages : 490
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Book Description
This book is a compilation and discussion of data on the survival of cancer patients in 12 European countries. Measures of incidence, survival and mortality are critical to the interpretation of data on progress in the fight against cancer, and in the evaluation of the overall effectiveness of cancer control programmes. Randomized controlled clinical trials have shown many modern protocols for cancer treatment to be more effective than earlier treatments, but until now, comparable population-based survival figures have raraly been available. EUROCARE is a concerted action among European cancer registries, aimed at estimating and comparing the survival of cancer patients in different European populations. The rationale behind this project is to optimize the comparability of survival data by using an agreed and standard definition of the diseases for which survival is to be compared, and by taking due account of basic demographic variables. The EUROCARE Working Group succeeded in collecting, checking and editing data on cancer survival from 30 cancer registries in 12 countries, and established a database covering some 800,000 cancer patients in the period 1978-85 and followed up to the end of 1990. This database forms the raw material for this monograph.
Author: Agency for Healthcare Research and Quality/AHRQ
Publisher: Government Printing Office
ISBN: 1587634333
Category : Medical
Languages : en
Pages : 396
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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.
