Guest post by Sandra Martins Pereira, Roeline Pasman and Bregje Onwuteaka-Philipsen Decisions to forgo treatment are embedded in clinical, socio-cultural, philosophical, religious, legal and ethical contexts and beliefs, and they cannot be considered as representing good or poor quality care. Particularly for older people, it is sometimes argued that treatment is aggressive, and that there may […]
Category: clinical ethics
The Talking Cure Taboo
Guest post by C Blease Talking cures have never been so accessible. Since 2007 the UK government has invested £300 million launching its Improved Access to Psychological Treatments scheme. The goal is to train up to 4000 therapists in a particular branch of psychotherapy – cognitive behavioural therapy (CBT). CBT is the most widely researched […]
The Death of Sidaway: Values, Judgments and Informed Consent
Guest post by Kirsty Keywood (University of Manchester) On 11th March Nadine Montgomery won her case before the UK Supreme Court to gain compensation for the failure of her obstetrician to warn her of risks associated with the vaginal delivery of a large infant – a risk which she would have averted by requesting a […]
Does Religion Deserve a Place in Secular Medicine?
By Brian D. Earp The latest issue of the Journal of Medical Ethics is out, and in it, Professor Nigel Biggar—an Oxford theologian—argues that “religion” should have a place in secular medicine (click here for a link to the article). Some people will feel a shiver go down their spines—and not only the non-religious. After […]
Physicians and Euthanasia: What about Psychiatric Illness, Dementia and Weltschmerz?
Guest Post by Eva Bolt In the Netherlands, requests for euthanasia are not uncommon. A physician who grants a request for euthanasia in the Netherlands is not prosecuted if the criteria for due care (described in the Euthanasia Act) are met. An example of one of these criteria is the presence of unbearable suffering without […]
Growing a Kidney Inside a Pig Using your own DNA: The Ethics of ‘Chimera Organs’
Guest post by David Shaw Imagine that you’re in dire need of a new kidney. You’re near the top of the waiting list, but time is running out and you might not be lucky enough to receive a new organ from a deceased or living donor. But another option is now available: scientists could take […]
Once More unto the Breach of Covenant?
The “Military Covenant” is in the news again: The government is failing to abide by its military covenant, medical experts who treat injured soldiers have said. Leading professors in psychology and orthopaedics say the healthcare system is not providing veterans with the service they have been promised. […] The moral obligation to treat veterans should […]
Paper Preview: Implementation of a Consent for Chart Review and Contact
Guest post by Irena Druce Our article “Implementation of a Consent for Chart Review and Contact and its Impact in one Clinical Centre” focuses on issues regarding patient health information privacy and recruitment for medical research studies. Research studies are an integral part of the advancement of medical therapies; however, recruitment into research studies can […]
Adrenaline, Information Provision and the Benefits of a Non-Randomised Methodology
Guest Post by Ruth Stirton and Lindsay Stirton, University of Sheffield One of us – Ruth – was on Newsnight on Wednesday the 13th August talking about the PARAMEDIC2 trial. The trial is a double blind, individually randomised, placebo controlled trial of adrenaline v. normal saline injections in cardiac arrest patients treated outside hospital. In simpler terms, if […]
Advance Directives, Critical Interests, and Dementia Research
Guest post by Tom Buller, Illinois State University In my paper, “Advance Directives, Critical Interests, and Dementia Research”, I investigate whether advance directives can be applied in the context of dementia research. Consider, for the sake of argument, the following fictional case. William, a 77-year-old man who has moderate to severe dementia. When he was first […]