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A case study exploring the ethical and policy dimensions of allocating acute care resources to a dying patient
Author(s) -
Cooke Mary,
Hurley Ciarán
Publication year - 2008
Publication title -
journal of clinical nursing
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.94
H-Index - 102
eISSN - 1365-2702
pISSN - 0962-1067
DOI - 10.1111/j.1365-2702.2006.01929.x
Subject(s) - general partnership , nursing , health care , acute care , medicine , flexibility (engineering) , business , psychology , political science , finance , law , statistics , mathematics
Aims. We aimed to identify policy, process and ethical issues related to allocation of National Health Service resources when patients with end‐of‐life illness are referred to acute care services. Background. Sharing healthcare decisions denotes a different partnership between professionals and patients when patients are empowered to define their needs. Implementation of a transition from professional to patient decision‐making appears to be dependent upon its interpretation by personnel delivering care using the local trust policy. The outcome of this is a reformation of responsibility for budget allocation, choice of acute care provider and selecting services, currently in the realm of primary care; be it the general practitioner, community practitioners, or the patient. Design. We used a ‘lens’ approach to case study analysis in which the lens is constructed of a model of policy analysis and four principles of biomedical ethics. A patient's decision to decline care proposed by an Accident and Emergency department nurse and the nurse's response to that decision expose a policy that restricts the use of ambulance transport and with that, flexibility in responses to patients’ decisions. Findings. End‐of‐life care partnership decisions require sensitivity and flexibility from all healthcare practitioners. We found that policy‐based systems currently used to deliver care across the primary care – hospital care border are far from seamless and can lead to foreseeable problems. Conclusions. Health professionals responsible for the care of a patient at the end of life should consider the holistic outcomes of resource allocation decisions for patients. Relevance to clinical practice. Government and health professional agenda suggest that patients should be given a greater element of control over their healthcare than has historically been the case. When patients take responsibility for their decisions, healthcare personnel should recognize that this signals a shift in the nature of the professional–patient relationship to one of partnership.