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Seattle University Collaborative Projects - International Academy of ...

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Restriction, Deprivation, and Detention: Limits to Freedom within EnglishMental Health and Mental Capacity LegislationIsabel Clare, <strong>University</strong> <strong>of</strong> Cambridge (ichc2@medschl.cam.ac.uk)In England and Wales, the freedom <strong>of</strong> men and women with a mental disorder or who lackcapacity to make decisions about their own care and treatment can, in certain circumstances, belimited lawfully through the use <strong>of</strong> appropriate legal frameworks. We use data from a mixedmethodsempirical research study to discuss how such frameworks are used in general and/orpsychiatric hospitals. We will illustrate the breadth <strong>of</strong> the relevant legislation, which includesboth unconscious patients who are receiving life-saving medical treatment and highly mobilepatients receiving predominantly nursing care. We will also illustrate the confusion relating tothe meaning <strong>of</strong> “care” and “treatment” and the emergence <strong>of</strong> new concepts, for example, that <strong>of</strong>“active” treatment, and rules <strong>of</strong> thumb differentiating those who are or are not expected tobenefit from treatment. We argue that clinicians struggle to apply these legal frameworks to therealities <strong>of</strong> patient care.Making Best Interest Decisions for Dementia Patients on Discharge fromGeneral Hospital: Do Family and Friends Fulfil an Effective SafeguardingFunction Under English Law?Charlotte Emmett, Northumbria Law School (charlotte.emmett@northumbria.ac.uk)In this paper we explore the role <strong>of</strong> family members and friends in the best interests decisionmakingprocess under the Mental Capacity Act 2005 in England and Wales. We ask whether, inthe absence <strong>of</strong> Independent Mental Capacity Advocates (IMCAs), close family and friends <strong>of</strong>older people with dementia are capable <strong>of</strong> fulfilling a safeguarding function when decisions arebeing made about where that person should live on discharge from general hospital. Our findingsare grounded in ethnographic ward-based observations and qualitative interviews conducted inthree hospital wards, in two hospitals (acute and rehabilitation), within two NHS healthcaretrusts in the North <strong>of</strong> England over a period <strong>of</strong> nine months from June 2008 to June 2009. Weask: Are family and friends there simply in an advisory/supportive capacity or are they <strong>of</strong>tenseen as the primary decision-makers by pr<strong>of</strong>essionals? Does this role accord with the incapableperson’s (P’s) view or the family and friend’s own views and expectations <strong>of</strong> their role? Is thisperception promoted by pr<strong>of</strong>essionals? Can relatives and friends really be expected to makeobjective assessments <strong>of</strong> P’s best interests in the context <strong>of</strong> decisions about where to live andfulfil an effective safeguarding function? Or are there simply too many competing tensions? Ourconclusions suggest that family and friends can only begin to act as an effective safeguard forthose they care about if communication with pr<strong>of</strong>essionals is improved and they are involvedmore fully in the hospital discharge planning process.243

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