Publications by authors named "Alexander Ruck Keene"

Article Synopsis
  • Dementia is a big health problem for many countries, including the UK, and finding solutions is very important for everyone.
  • To help people with dementia, researchers need to conduct studies, but it's tricky to work with participants who may not fully understand what they’re agreeing to.
  • The article talks about legal rules and ethical challenges researchers face and suggests ways to improve how they conduct studies involving people with dementia.
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The overwhelming weight of legal authority in the USA and Canada holds that consent is not required for brain death testing. The situation in England and Wales is similar but different. While clinicians in England and Wales may have a prima facie duty to obtain consent, lack of consent has not barred testing.

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All contemporary frameworks of mental capacity stipulate that we must begin from the presumption that an adult has capacity. This presumption is crucial, as it manifests respect for autonomy and guards against prejudice and paternalism on the part of the evaluator.Given its ubiquity, we might presume that we all understand the presumption's meaning and application in the same way.

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  • This paper looks into a feeling called 'clinical unease' that doctors and healthcare workers have when they face tough decisions where there are different right ways to act.
  • It asks if courts can help make things clearer by deciding on these tricky legal and ethical questions, even when no one is arguing about it.
  • The paper also shares made-up scenarios where doctors might want a court's opinion and discusses if going to court is really the best option for solving these problems.
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In February 2022, the Court of Protection was faced with the question of whether a kidney transplant was in the best interests of William Verden. The case highlighted the legal, ethical and clinical complexities of treating potential kidney transplant patients with impaired decision-making. Above all, it exposed the potential risk of discrimination on the basis of disability when treatment decisions in relation to potential kidney recipients with impaired capacity are being made.

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Taken together, Sections 145 and 63 of the Mental Health Act 1983 (MHA) provide for treatment without consent of physical illness ancillary to the mental disorder with which a patient presents. On a daily basis, clinicians make both the decision that the Act's authority can be applied to their patient's case, and that it should be applied. But in the unusual circumstances where there is uncertainty as to the applicability of the MHA to the ancillary treatment of physical illness, the assistance of a court may be sought.

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Most jurisdictions require that a mental capacity assessment be conducted using a functional model whose definition includes several abilities. In England and Wales and in increasing number of countries, the law requires a person be able to understand, to retain, to use or weigh relevant information and to communicate one's decision. But interpreting and applying broad and vague criteria, such as the ability 'to use or weigh' to a diverse range of presentations is challenging.

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Article Synopsis
  • The COVID-19 pandemic stressed healthcare systems, making it difficult to decide who gets treated first, especially for older people.
  • A study in the UK asked people how they feel about using age and other factors in these tough choices about care during the pandemic.
  • Participants agreed that while some form of triage is needed, they preferred fairness, helping as many people as possible, and caring for those who are vulnerable over just focusing on maximizing life years.
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This article investigates the lawfulness of isolating residents of care and group homes during the COVID-19 pandemic. Many residents are mobile, and their freedom to move is a central ethical tenet and human right. It is not however an absolute right and trade-offs between autonomy, liberty and health need to be made since COVID-19 is highly infectious and poses serious risks of critical illness and death.

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Article Synopsis
  • The movement against traditional ways of making medical decisions for patients who can't decide for themselves is growing, focusing on what patients would have wanted instead of just what's best for them.
  • In England and Wales, a law called the Mental Capacity Act 2005 emphasizes the importance of patients’ past wishes and beliefs when making decisions about their care.
  • A recent court case showed that while this approach tries to respect patients’ views, it might lead to problems like not considering the patients' actual medical needs and relying too much on what their caregivers think instead of what the patients might choose if they could.
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Article Synopsis
  • Two authors share their thoughts on what happens when ambulance workers find someone who has died and the family doesn’t want them to try to save that person.
  • They talk about the rules and support for ambulance workers, but notice there isn’t enough help for families in these tough situations.
  • The authors suggest changes to the rules to keep everyone safe, including the ambulance workers, the patients, and their families.
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What contribution can rhetoric make to socio-legal studies? Though now a byword for deception and spin, rhetoric was long identified with the very substance of law and politics. Latterly radical scholars have foregrounded an understanding of law as rhetoric in their polemics against legal formalism, but it needs to be complemented by a critical perspective which goes beyond simple revivalism, taking account of rhetoric's own blind spots, inquiring into the means by which some speakers and listeners are privileged and others excluded or silenced. The critical potential of legal rhetoric is tested here through a review of the developing law on mental capacity and the best interests of people with disabilities in England and Wales.

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Article Synopsis
  • The article discusses legal and ethical issues about stopping life support for people in long-term comas, inspired by Charles Foster's essay and Vincent Lambert's case.
  • It reviews laws from different sources, including European rights laws, to see how they apply to these situations.
  • The article suggests that decisions should focus more on each person as an individual and not just general ideas about their quality of life or treatment burden.
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This article argues that, properly analysed, the common law and the European Convention on Human Rights (ECHR) march hand in hand with the provisions of the Mental Capacity Act 2005 (MCA 2005) so as to impose a set of requirements on litigation friends acting for the subject of applications of proceedings before the Court of Protection ('P') which are very different to those currently understood by practitioners and the judiciary. The authors examine critically current practice and procedures and provide a set of proposals for reforms.

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This comment responds to the comment by Jonathan Youngs in St George's Healthcare NHS Trust v P(1) entitled 'Can the courts force the doctor's hand?' Vol. 24, No. 1, pp.

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