Helen Stanton Chapple, PhD, RN, CCRN, CT, is the Nurse Ethicist at Creighton University's Center for Health Policy and Ethics. Her twenty years of bedside nursing include oncology, research, hospice home care, cardiac and neuroscience critical care. A persistent interest in thanatology and the fate of hospitalized dying patients prompted her to pursue graduate degrees in bioethics and anthropology at the University of Virginia. She is the author of several articles in top anthropology and nursing journals.
"[S]he combined her study results with extensive supporting material from relevant research to present a convincing case for her conclusions. This is an aspect of the book that I particularly enjoyed--Chapple thoroughly reviews the literature (references run to 20TH pages), provides a theoretical view and makes it ''real'' with case studies. She achieves a good mix of presenting hospital procedures with the human results of those procedures. I highly recommend it and hope it reaches a wide audience." -Jeanne Boland, Death Studies"Helen Stanton Chapple does a masterful job of portraying the ways that rescue minimizes death and contributes to death denial in our culture. In hospitals where almost every aspect of care has a code or label, dying patients are uncategorized. Moreover, dying does not have an International Classification of Diseases Clinical Modification, Ninth Revision (ICD-9-CM) code. Clinicians in the acute care setting often feel helpless when a person is dying and see themselves as being held hostage to the dying instead of feeling a sense of honor. Acute and high tech care can support vital signs and delay death, but it also promotes the illusion that death can be infinitely postponed. Chapple argues that society's complacent confidence in its agents' ability to perform life-saving miracles distracts us from death's inevitability. When hospitalized dying patients are minimized, each member of society is shortchanged." -Gerontologist
"While rooted in an ethnographic study of staff in two quite different hospitals, her analysis embraces insights into the roles of economics, bioethics, the hospice and palliative care movement, and iconic American cultural beliefs. This volume would be rewarding reading for any student of American health care, including hospital administrators and board members as well as clinicians and change agents frustrated by the epidemic of over-treatment of hospitalized patients at the end of life. This volume would be rewarding reading for any student of American health care, including hospital administrators and board members as well as clinicians and change agents frustrated by the epidemic of over-treatment of hospitalized patients at the end of life. Th[e] book is loaded with serious, intellectually strenuous material, making some popular books on dying in America seem downright breezy by contrast. Because Dr. Chapple is a good writer and her volume is well organized, the book is dense only in the best sense. Most importantly, clearly told patients' stories and direct quotations from interviews with those who cared for them keeps the analysis grounded in hospital realities." -Patricia A. Murphy and David M. Price, Journal of Palliative Medicine
"Readers familiar with the inner workings of hospital care will instantly empathise with the 'ritual' described in all its guises in the text. Chapple's skill is in deploying such a description that raises awareness of the tacit cultural agendas that influence clinicians' practice. The stark point being made by Chapple is that dying patients often undergo rescue needlessly and that even if the ritual permits their re-labelling as 'dying' (considered, by the author, as a 'successful' outcome of the ritual), there follows a disappointing lack of co-ordinated clinical care to meet their and their loved one's particular needs at that crucial time. [Q]ualitative evidence of this sort must be welcomed. Given the equal-ninth ranking of the US and Canada on quality of death, according to the Economist Intelligence Unit , Chapple's analysis provides compelling evidence as to why this might be the case. Whilst the academic reader will welcome the amount of wider referencing and research that Chapple has used to develop her thesis, it is to her credit that a non-clinical, lay reader will also pick up this book and understand her points easily, thanks to the skilful and coherent organisation and presentation of the complex material she has chosen to study."- Milind Arolker, Sociology of Health and Illness
"The right to life is a hard right to refuse. No Place for Dying: Hospitals and the Ideology of Rescue is a text that discusses the legal place of the rights of the dying, the thought process behind these laws, and the position of modern medical facilities. The first chapters discuss situations where death is gauged between unavoidable and where rescue is successful. It then discusses the place of profit, and the drive to save lives in American culture. Finally, it analyzes culture and its own attitudes towards death. A complete and comprehensive text on the role hospitals play in death and dying, No Place for Dying is a scholarly and thoughtful work that would do well in community and college anthropology collections." - Five Stars from Midwest Book Review