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Author: Joanna Manning
Publisher: Bridget Williams Books
ISBN: 1877242454
Category : Health & Fitness
Languages : en
Pages : 225
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Book Description
The Cervical Cancer Inquiry and its report (known as the Cartwright Report) were momentous events in the recent history of New Zealand. Critical issues were at stake: matters of life and death; the life's work of leaders within the medical profession; professional reputations; public trust in the profession, and its own sense of self-worth. After seven months of considering evidence, Judge Silvia Cartwright, assisted by expert medical and legal teams and drawing on specialist opinion from all over the world, concluded that Associate Professor Herbert Green had been conducting unethical research at National Women's Hospital, and that many women had been affected. This book of essays recounts some of this history. Several of the contributors were participants: Clare Matheson writes as one of the patients; Professor Charlotte Paul was a medical adviser to the Inquiry; Sandra Coney (with Phillida Bunkle) wrote the article leading to the Inquiry; Dr Ron Jones was one of the three authors of the 1984 article, using data from Green's own patients, that demonstrated that carcinoma of the cervix had a significant invasive potential. Other authors are specialists in other fields: Professor Alastair Campbell and Associate Professor Joanna Manning comment from the perspective of medical ethics and medical law respectively; Ron Paterson is the Health and Disability Commissioner; Jan Crosthwaite is a philosopher with expertise in medical ethics. These essays not only review the history but also document how the Cartwright Report changed the whole landscape of medical practice and biomedical research in this country, leading to far better protections for both patients and research participants. Yet despite all the regulatory changes, the most significant change to which the Cartwright Report contributed was attitudinal - a rejection of medical paternalism and a new expectation that patients would be treated as partners in their care. The findings of the Report remain controversial and continue to be debated to this day. This book provides a perspective on the current debates and helps place them in context. As Clare Matheson (one of Green's patients) said: 'We must never forget lest it happen again'. Contributors include: Alastair Campbell, Silvia Cartwright, Sandra Coney, Jan Crosthwaite, Ron Jones, Joanna Manning, Clare Matheson, Ron Paterson, Charlotte Paul.
Author: Joanna Manning
Publisher: Bridget Williams Books
ISBN: 1877242454
Category : Health & Fitness
Languages : en
Pages : 225
Get Book Here
Book Description
The Cervical Cancer Inquiry and its report (known as the Cartwright Report) were momentous events in the recent history of New Zealand. Critical issues were at stake: matters of life and death; the life's work of leaders within the medical profession; professional reputations; public trust in the profession, and its own sense of self-worth. After seven months of considering evidence, Judge Silvia Cartwright, assisted by expert medical and legal teams and drawing on specialist opinion from all over the world, concluded that Associate Professor Herbert Green had been conducting unethical research at National Women's Hospital, and that many women had been affected. This book of essays recounts some of this history. Several of the contributors were participants: Clare Matheson writes as one of the patients; Professor Charlotte Paul was a medical adviser to the Inquiry; Sandra Coney (with Phillida Bunkle) wrote the article leading to the Inquiry; Dr Ron Jones was one of the three authors of the 1984 article, using data from Green's own patients, that demonstrated that carcinoma of the cervix had a significant invasive potential. Other authors are specialists in other fields: Professor Alastair Campbell and Associate Professor Joanna Manning comment from the perspective of medical ethics and medical law respectively; Ron Paterson is the Health and Disability Commissioner; Jan Crosthwaite is a philosopher with expertise in medical ethics. These essays not only review the history but also document how the Cartwright Report changed the whole landscape of medical practice and biomedical research in this country, leading to far better protections for both patients and research participants. Yet despite all the regulatory changes, the most significant change to which the Cartwright Report contributed was attitudinal - a rejection of medical paternalism and a new expectation that patients would be treated as partners in their care. The findings of the Report remain controversial and continue to be debated to this day. This book provides a perspective on the current debates and helps place them in context. As Clare Matheson (one of Green's patients) said: 'We must never forget lest it happen again'. Contributors include: Alastair Campbell, Silvia Cartwright, Sandra Coney, Jan Crosthwaite, Ron Jones, Joanna Manning, Clare Matheson, Ron Paterson, Charlotte Paul.
Author: Sheila A. M. McLean
Publisher: Routledge
ISBN: 1317134982
Category : Law
Languages : en
Pages : 622
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Book Description
This collection brings together essays from leading figures in the field of medical law and ethics which address the key issues currently challenging scholars in the field. It has also been compiled as a lasting testimony to the work of one of the most eminent scholars in the area, Professor Ken Mason. The collection marks the academic crowning of a career which has laid one of the foundation stones of an entire discipline. The wide-ranging contents and the standing of the contributors mean that the volume will be an invaluable resource for anyone studying or working in medical law or medical ethics.
Author: Edward S. Dove
Publisher: Edward Elgar Publishing
ISBN: 1788975359
Category : Law
Languages : en
Pages : 288
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Book Description
This timely book examines the interaction of health research and regulation with law through empirical analysis and the application of key anthropological concepts to reveal the inner workings of human health research. Through ground-breaking empirical inquiry, Regulatory Stewardship of Health Research explores how research ethics committees (RECs) work in practice to both protect research participants and promote ethical research. This thought-provoking book provides a new perspective on the regulation of health research by demonstrating how RECs and other regulatory actors seek to fulfil these two functions by performing a role of ‘regulatory stewardship’.
Author: Sally Robinson
Publisher: Edward Elgar Publishing
ISBN: 1800373651
Category : Social Science
Languages : en
Pages : 889
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Book Description
Examining how policy affects the human rights of people with disabilities, this topical Handbook presents diverse empirical experiences of disability policy and identifies the changes that are necessary to achieve social justice.
Author: New Zealand. Ministry of Health
Publisher:
ISBN: 9781990029523
Category : Diet
Languages : en
Pages :
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Book Description
"These Guidelines provide the current evidence-based recommendations on healthy eating and physical activity for New Zealand adults, including pregnant and breastfeeding women. ... focus on the detail practitioners need at a glance: that is, what people need to eat or do, a summary of the rationale - 'why' - and a little on how to put the recommendations into practice"--Page iv.
Author: Geraint Lewis
Publisher: CRC Press
ISBN: 1444152696
Category : Medical
Languages : en
Pages : 736
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Book Description
Mastering Public Health: A Postgraduate Guide to Examinations and Revalidation, Second Edition is an essential study aid for all those preparing for postgraduate, masters, and higher examinations in public health. Now updated and revised for the second edition, the book continues to provide all postgraduate students taking higher public health examinations with a proven, successful core revision text. The book covers the five key areas of public health knowledge: research methods; disease prevention and health promotion; health information; sociology, policy, and health economics; and organisation and management of health care. It is structured to follow the entire MFPH Part A exam syllabus, with appendices on revision strategies, exam technique and essay frameworks. Written in conjunction with an international team of editors, the book is aimed at public health practitioners who are training or re-validating in the UK and worldwide. Its concise format also serves as a quick reference text for the specialty.
Author: Sandra Coney
Publisher: Viking Penguin
ISBN:
Category : Cancer
Languages : en
Pages : 300
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Book Description
In 1984 the medical journal Obstetrics and Gynecology published a paper that would initiate an investigation into one of the greatest medical scandals of the late twentieth century. Titled "The Invasive Potential of Carcinoma in Situ of the Cervix", it discussed the results of an experiment that had been run at the National Women’s Hospital in Auckland, New Zealand, since 1955. The experiment looked at the natural history of cervical carcinoma in situ (CIS) – in other words, what happens if no treatment is initiated in a condition suspected (when the experiment began) to lead to cervical cancer. The paper divided participants into two groups, one that had negative results after biopsy or treatment, and one smaller group that continued to test positive. This second group had a significant rate of cervical cancer; some of these women were followed for twenty-five years without treatment, and in only 5% did the disease spontaneously resolve. For the other 95%, outcomes ranged from positive but localised results to metastatic disease and death. The authors said these results were in contrast with other, earlier papers about the experiment. After much research, Sandra Coney, one-time editor of a NZ feminist magazine, and Phyllida Bunkle, a women’s studies lecturer, wrote an article about the experiment, exposing the unauthorised research performed by one prominent gynaecologist in support of his belief that CIS was not associated with cervical cancer. Professor Herbert Green, a physician of considerable influence and power throughout New Zealand, persisted in his belief despite increasingly convincing proof of a progressive connection between the two conditions, never sought permission from his patients, or even told them what he was doing.
Author: Anne Good
Publisher: Emerald Group Publishing
ISBN: 1787693112
Category : Social Science
Languages : en
Pages : 190
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Book Description
Considering important aspects of general ethical research principles, this volume establishes an inspiring vision for both present and future improvements across all levels of disability research.
Author: Catriona Ida Macleod
Publisher: Springer
ISBN: 3319747215
Category : Psychology
Languages : en
Pages : 469
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Book Description
This handbook highlights the growing tensions surrounding the current dominant ethical clearance model which is increasingly being questioned, particularly in critical research. It draws on stories from the field in critical research conducted in a range of contexts and countries and on an array of topics. The authors involved in this collection encountered dilemmas, contradictions and surprises that brought about a change in their understanding of ethics. Throughout the book they discuss how ethics is an ongoing and situated struggle that requires researchers, at times, to traverse traditional ethical imperatives. Four sections lead readers through the complexities of grounded ethical practice: encountering systems, including Ethics Committees and institutions; blurring boundaries within research; the politics of voice, anonymity and confidentiality; and power relations in researching ‘down’, ‘up’, and ‘alongside’. This handbook is a resource for social science researchers using critical methodologies across a range of disciplines, as well as for students and teachers of ethics, in navigating the quandaries of ‘doing good’ while doing good research.
Author: Mark Henaghan
Publisher: Routledge
ISBN: 1136621067
Category : Business & Economics
Languages : en
Pages : 157
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Book Description
Over the past twenty years there has been a shift in medical law and practise to increasingly distrust the judgement of health professionals. This book will look comparatively at a number of countries, showing through analysis of case law, legislation and protocols produced by hospitals, how the shift from trust to lack of trust has happened.
