听力与言语-语言病理学

行为科学

医学伦理学

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  • The turn for ultimate harm: a reply to Fenton.

    abstract::Elizabeth Fenton has criticised an earlier article by the authors in which the claim was made that, by providing humankind with means of causing its destruction, the advance of science and technology has put it in a perilous condition that might take the development of genetic or biomedical techniques of moral enhance...

    journal_title:Journal of medical ethics

    pub_type: 评论,杂志文章

    doi:10.1136/jme.2010.036962

    authors: Persson I,Savulescu J

    更新日期:2011-07-01 00:00:00

  • A taxonomy of multinational ethical and methodological standards for clinical trials of therapeutic interventions.

    abstract:BACKGROUND:If trials of therapeutic interventions are to serve society's interests, they must be of high methodological quality and must satisfy moral commitments to human subjects. The authors set out to develop a clinical-trials compendium in which standards for the ethical treatment of human subjects are integrated ...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2010.039255

    authors: Ashton CM,Wray NP,Jarman AF,Kolman JM,Wenner DM,Brody BA

    更新日期:2011-06-01 00:00:00

  • Veterinary surgeons' attitudes towards physician-assisted suicide: an empirical study of Swedish experts on euthanasia.

    abstract:AIM:To examine the hypothesis that knowledge about physician-assisted suicide (PAS) and euthanasia is associated with a more restrictive attitude towards PAS. DESIGN:A questionnaire about attitudes towards PAS, including prioritization of arguments pro and contra, was sent to Swedish veterinary surgeons. The results w...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2010.038901

    authors: Lerner H,Lindblad A,Algers B,Lynöe N

    更新日期:2011-05-01 00:00:00

  • Disclosure of individual research results in clinico-genomic trials: challenges, classification and criteria for decision-making.

    abstract::While an ethical obligation to report findings of clinical research to trial participants is increasingly recognised, the academic debate is often vague about what kinds of data should be fed back and how such a process should be organised. In this article, we present a classification of different actors, processes an...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.034041

    authors: Kollek R,Petersen I

    更新日期:2011-05-01 00:00:00

  • Parental procreative obligation and the categorisation of disease: the case of cystic fibrosis.

    abstract::The advent of prenatal genetic diagnosis has sparked debates among ethicists and philosophers regarding parental responsibility towards potential offspring. Some have attempted to place moral obligations on parents to not bring about children with certain diseases in order to prevent harm to such children. There has b...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2010.039230

    authors: Bosslet GT

    更新日期:2011-05-01 00:00:00

  • Ethically complex decisions in the neonatal intensive care unit: impact of the new French legislation on attitudes and practices of physicians and nurses.

    abstract:OBJECTIVES:A statute enacted in 2005 modified the legislative framework of the rights of terminally ill persons in France. Ten years after the EURONIC study, which described the self-reported practices of neonatal caregivers towards ethical decision-making, a new study was conducted to assess the impact of the new law ...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2010.038356

    authors: Garel M,Caeymaex L,Goffinet F,Cuttini M,Kaminski M

    更新日期:2011-04-01 00:00:00

  • What sort of bioethical values are the evidence-based medicine and the GRADE approaches willing to deal with?

    abstract::The concept of evidence-based medicine (EBM) has been invented by physicians mostly from English Canada, mostly from McMaster University, Ontario, Canada. The term EBM first appeared in the biomedical literature in 1991 in an article written by a prominent member of this group-Gordon Guyatt from McMaster University. T...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2010.039735

    authors: Watine J

    更新日期:2011-03-01 00:00:00

  • Facebook activity of residents and fellows and its impact on the doctor-patient relationship.

    abstract:AIM:Facebook is an increasingly popular online social networking site. The purpose of this study was to describe the Facebook activity of residents and fellows and their opinions regarding the impact of Facebook on the doctor-patient relationship. METHODS:An anonymous questionnaire was emailed to 405 residents and fel...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2010.036293

    authors: Moubarak G,Guiot A,Benhamou Y,Benhamou A,Hariri S

    更新日期:2011-02-01 00:00:00

  • Scientific evidence and best patient care practices should guide the ethics of Lyme disease activism.

    abstract::Johnson and Stricker published an opinion piece in the Journal of Medical Ethics presenting their perspective on the 2008 agreement between the Infectious Diseases Society of America (IDSA) and the Connecticut Attorney General with regard to the 2006 IDSA treatment guideline for Lyme disease. Their writings indicate t...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.032896

    authors: Auwaerter PG,Bakken JS,Dattwyler RJ,Dumler JS,Halperin JJ,McSweegan E,Nadelman RB,O'Connell S,Sood SK,Weinstein A,Wormser GP

    更新日期:2011-02-01 00:00:00

  • Public attitudes to the use in research of personal health information from general practitioners' records: a survey of the Irish general public.

    abstract:INTRODUCTION:Understanding the views of the public is essential if generally acceptable policies are to be devised that balance research access to general practice patient records with protection of patients' privacy. However, few large studies have been conducted about public attitudes to research access to personal h...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2010.037903

    authors: Buckley BS,Murphy AW,MacFarlane AE

    更新日期:2011-01-01 00:00:00

  • Developing ethics guidance for HIV prevention research: the HIV Prevention Trials Network approach.

    abstract::More than 25 years into the HIV epidemic, in excess of 2 million new infections continue to occur each year. HIV prevention research is crucial for groups at heightened risk for HIV, but the design and conduct of HIV prevention research with vulnerable populations worldwide raises considerable ethical challenge...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2010.035444

    authors: Rennie S,Sugarman J

    更新日期:2010-12-01 00:00:00

  • Ancillary care duties: the demands of justice.

    abstract::Ancillary care is care that research participants need that is not essential to make the research safe or scientifically valid and is not needed to remedy injuries that eventuate as a result of the research project itself. Ancillary care duties have recently been defended on the grounds of beneficence, entrustment, ut...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2010.035758

    authors: Hooper CR

    更新日期:2010-11-01 00:00:00

  • The potential impact of an opt-out system for organ donation in the UK.

    abstract::The recent report of the UK government's Organ Donation Taskforce is in favour of continuing with the current organ donation system rather than changing to an opt-out system where people are assumed to be willing to donate. How did it reach this decision and is it correct? ...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.031757

    authors: Rieu R

    更新日期:2010-09-01 00:00:00

  • Disclosures of funding sources and conflicts of interest in published HIV/AIDS research conducted in developing countries.

    abstract:OBJECTIVES:Disclosures of funding sources and conflicts of interests (COI) in published peer-reviewed journal articles have recently begun to receive some attention, but many critical questions remain, for example, how often such reporting occurs concerning research conducted in the developing world and what factors ma...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2010.035394

    authors: Klitzman R,Chin LJ,Rifai-Bishjawish H,Kleinert K,Leu CS

    更新日期:2010-08-01 00:00:00

  • Coercive offers and research participation: a comment on Wertheimer and Miller.

    abstract::Concepts such as 'coercion' and 'inducement' are often used within bioethics without much reflection upon what they mean. This is particularly so in research ethics where they are assumed to imply that payment for research participation is unethical. Wertheimer and Miller advance our thinking about these concepts and ...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2010.035931

    authors: McMillan J

    更新日期:2010-07-01 00:00:00

  • Non-equivalent stringency of ethical review in the Baltic States: a sign of a systematic problem in Europe?

    abstract::We analyse the system of ethical review of human research in the Baltic States by introducing the principle of equivalent stringency of ethical review, that is, research projects imposing equal risks and inconveniences on research participants should be subjected to equally stringent review procedures. We examine seve...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.035030

    authors: Gefenas E,Dranseika V,Cekanauskaite A,Hug K,Mezinska S,Peicius E,Silis V,Soosaar A,Strosberg M

    更新日期:2010-07-01 00:00:00

  • Therapeutic privilege: between the ethics of lying and the practice of truth.

    abstract::The 'right to the truth' involves disclosing all the pertinent facts to a patient so that an informed decision can be made. However, this concept of a 'right to the truth' entails certain ambiguities, especially since it is difficult to apply the concept in medical practice based mainly on current evidence-based data ...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.033340

    authors: Richard C,Lajeunesse Y,Lussier MT

    更新日期:2010-06-01 00:00:00

  • When enough is enough; terminating life-sustaining treatment at the patient's request: a survey of attitudes among Swedish physicians and the general public.

    abstract:OBJECTIVES:To explore attitudes and reasoning among Swedish physicians and the general public regarding the withdrawal of life-sustaining treatment at a competent patient's request. DESIGN:A vignette-based postal questionnaire including 1202 randomly selected individuals in the county of Stockholm and 1200 randomly se...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.034967

    authors: Lindblad A,Juth N,Fürst CJ,Lynöe N

    更新日期:2010-05-01 00:00:00

  • Translational ethics? The theory-practice gap in medical ethics.

    abstract::Translational research is now a critically important current in academic medicine. Researchers in all health-related fields are being encouraged not only to demonstrate the potential benefits of their research but also to help identify the steps through which their research might be 'made practical'. This paper consid...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.029785

    authors: Cribb A

    更新日期:2010-04-01 00:00:00

  • Do strong value-based attitudes influence estimations of future events?

    abstract::The purpose of the present study was to examine whether or not strong values might influence physicians' estimations of future events. In an empirical study about physicians' attitudes towards physician assisted suicide (PAS) we asked about the physicians' main reasons for being pro, doubtful or contra PAS and also as...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.033506

    authors: Juth N,Lynöe N

    更新日期:2010-04-01 00:00:00

  • Evolution of hospital clinical ethics committees in Canada.

    abstract::To investigate the current status of hospital clinical ethics committees (CEC) and how they have evolved in Canada over the past 20 years, this paper presents an overview of the findings from a 2008 survey and compares these findings with two previous Canadian surveys conducted in 1989 and 1984. All Canadian hospitals...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.032607

    authors: Gaudine A,Thorne L,LeFort SM,Lamb M

    更新日期:2010-03-01 00:00:00

  • Advance commitment: an alternative approach to the family veto problem in organ procurement.

    abstract::This article tackles the current deficit in the supply of cadaveric organs by addressing the family veto in organ donation. The authors believe that the family veto matters-ethically as well as practically-and that policies that completely disregard the views of the family in this decision are likely to be counterprod...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.032912

    authors: De Wispelaere J,Stirton L

    更新日期:2010-03-01 00:00:00

  • Tailor-made finance versus tailor-made care. Can the state strengthen consumer choice in healthcare by reforming the financial structure of long-term care?

    abstract:BACKGROUND:Policy instruments based on the working of markets have been introduced to empower consumers of healthcare. However, it is still not easy to become a critical consumer of healthcare. OBJECTIVES:The aim of this study is to analyse the possibilities of the state to strengthen the position of patients with the...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.030536

    authors: Grit K,de Bont A

    更新日期:2010-02-01 00:00:00

  • Post-recruitment confirmation of informed consent by SMS.

    abstract:BACKGROUND:To allow patients to reflect about a decision to participate in a clinical trial, guidelines suggest a 24-h delay from when they are informed about the trial to when they give consent. In certain clinical settings, this is likely to hamper recruitment. METHOD:After oral and written information about the tri...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.033456

    authors: Gulbrandsen P,Jensen BF

    更新日期:2010-02-01 00:00:00

  • The right not to know and preimplantation genetic diagnosis for Huntington's disease.

    abstract::The right not to know is underappreciated in policy-making. Despite its articulation in medical law and ethics, policy-makers too easily let other concerns override the right not to know. This observation is triggered by a recent decision of the Dutch government on embryo selection for Huntington's disease. This is a ...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.031047

    authors: Asscher E,Koops BJ

    更新日期:2010-01-01 00:00:00

  • Can the Catholic Church agree to condom use by HIV-discordant couples?

    abstract::Does the position of the Roman Catholic Church on contraception also imply that the usage of condoms by HIV-discordant couples is illicit? A standard argument is to appeal to the doctrine of double effect to condone such usage, but this meets with the objection that there exists an alternative action that brings about...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.030767

    authors: Bovens L

    更新日期:2009-12-01 00:00:00

  • Agency, duties and the "Ashley treatment".

    abstract::In 2006, a paper in the journal Archives of Pediatric and Adolescent Medicine described a novel case of growth attenuation therapy and other treatments carried out on Ashley, a severely cognitively, neurologically and physically disabled 6-year-old girl. Some of the moral arguments that have sprung up in respect of th...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.029934

    authors: Tan N,Brassington I

    更新日期:2009-11-01 00:00:00

  • Who should consent for research in adult intensive care? Preferences of patients and their relatives: a pilot study.

    abstract:INTRODUCTION:Research in intensive care is necessary for the continuing advancement of patient care. In research, informed consent is considered essential for patient protection. In intensive care, the modalities of informed consent are currently being debated by both lawyers and the medical community. The preferences ...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2008.028068

    authors: Chenaud C,Merlani P,Verdon M,Ricou B

    更新日期:2009-11-01 00:00:00

  • All hail the new flesh: some thoughts on scarification, children and adults.

    abstract::Body art as expressed through non-therapeutic bodily modification is extremely popular, with techniques ranging from the commonplace such as ear piercing to the more esoteric forms such as tongue splitting. Scarification is one such body art practice that is becoming popular as an alternative to tattooing and ear pier...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2008.027615

    authors: Oultram S

    更新日期:2009-10-01 00:00:00

  • Euthanasia and eudaimonia.

    abstract::This paper re-evaluates euthanasia and assisted suicide from the perspective of eudaimonia, the ancient Greek conception of happiness across one's whole life. It is argued that one cannot be said to have fully flourished or had a truly happy life if one's death is preceded by a period of unbearable pain or suffering t...

    journal_title:Journal of medical ethics

    pub_type: 历史文章,杂志文章

    doi:10.1136/jme.2008.028852

    authors: Shaw DM

    更新日期:2009-09-01 00:00:00

  • Medical professionalism in the age of online social networking.

    abstract::The rapid emergence and exploding usage of online social networking forums, which are frequented by millions, present clinicians with new ethical and professional challenges. Particularly among a younger generation of physicians and patients, the use of online social networking forums has become widespread. In this ar...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2009.029231

    authors: Guseh JS 2nd,Brendel RW,Brendel DH

    更新日期:2009-09-01 00:00:00

  • Functional neuroimaging and withdrawal of life-sustaining treatment from vegetative patients.

    abstract::Recent studies using functional magnetic resonance imaging of patients in a vegetative state have raised the possibility that such patients retain some degree of consciousness. In this paper, the ethical implications of such findings are outlined, in particular in relation to decisions about withdrawing life-sustainin...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2008.029165

    authors: Wilkinson DJ,Kahane G,Horne M,Savulescu J

    更新日期:2009-08-01 00:00:00

  • Understanding respect: learning from patients.

    abstract:BACKGROUND:The importance of respecting patients and participants in clinical research is widely recognised. However, what it means to respect persons beyond recognising them as autonomous is unclear, and little is known about what patients find to be respectful. OBJECTIVE:To understand patients' conceptions of respec...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2008.027235

    authors: Dickert NW,Kass NE

    更新日期:2009-07-01 00:00:00

  • Tobacco regulation: autonomy up in smoke?

    abstract::Over the past few decades, "Big Tobacco" has spread its tentacles across the developing world with devastating results. The global incidence of smoking has increased exponentially in Africa, Asia and South America and it is leading to an equally rapid increase in the incidence of smoking-induced morbidity and mortalit...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2008.027847

    authors: Hooper CR,Agule C

    更新日期:2009-06-01 00:00:00

  • Under what conditions do patients want to be informed about their risk of a complication? A vignette study.

    abstract:BACKGROUND:Discussing treatment risks has become increasingly important in medical communication. Still, despite regulations, physicians must decide how much and what kind of information to present. OBJECTIVE:To investigate patients' preference for information about a small risk of a complication of colonoscopy, and w...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2008.025031

    authors: Janssen NB,Oort FJ,Fockens P,Willems DL,de Haes HC,Smets EM

    更新日期:2009-05-01 00:00:00

  • Erring on the side of life: the case of Terri Schiavo.

    abstract::In debates over life and death it is often said that one should err on the side of caution--that is, on the side of life. In the light of the recent case of Terri Schiavo, it is explained how the "err-on-the-side-of-life" argument proceeds, and an objection to it is offered. ...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2007.023002

    authors: Merrell DA

    更新日期:2009-05-01 00:00:00

  • The justificatory power of moral experience.

    abstract::A recurrent issue in the vast amount of literature on reasoning models in ethics is the role and nature of moral intuitions. In this paper, we start from the view that people who work and live in a certain moral practice usually possess specific moral wisdom. If we manage to incorporate their moral intuitions in ethic...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2008.026559

    authors: van Thiel GJ,van Delden JJ

    更新日期:2009-04-01 00:00:00

  • Opinions of private medical practitioners in Bloemfontein, South Africa, regarding euthanasia of terminally ill patients.

    abstract::The aim of this study was to determine the opinions of private medical practitioners in Bloemfontein, South Africa, regarding euthanasia of terminally ill patients. This descriptive study was performed amongst a simple random sample of 100 of 230 private medical practitioners in Bloemfontein. Information was obtained ...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2008.027417

    authors: Brits L,Human L,Pieterse L,Sonnekus P,Joubert G

    更新日期:2009-03-01 00:00:00

  • Holding personal information in a disease-specific register: the perspectives of people with multiple sclerosis and professionals on consent and access.

    abstract:OBJECTIVE:To determine the views of people with multiple sclerosis (MS) and professionals in relation to confidentiality, consent and access to data within a proposed MS register in the UK. DESIGN:Qualitative study using focus groups (10) and interviews (13). SETTING:England and Northern Ireland. PARTICIPANTS:68 peo...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2008.025304

    authors: Baird W,Jackson R,Ford H,Evangelou N,Busby M,Bull P,Zajicek J

    更新日期:2009-02-01 00:00:00

  • Ethical aspects of research into Alzheimer disease. A European Delphi Study focused on genetic and non-genetic research.

    abstract:BACKGROUND:Although genetic research into Alzheimer disease (AD) is increasing, the ethical aspects of this kind of research and the differences between ethical issues related to genetic and non-genetic research into AD have not yet received much attention. OBJECTIVES:(1) To identify and compare the five ethical issue...

    journal_title:Journal of medical ethics

    pub_type: 杂志文章

    doi:10.1136/jme.2008.025049

    authors: van der Vorm A,Vernooij-Dassen MJ,Kehoe PG,Olde Rikkert MG,van Leeuwen E,Dekkers WJ

    更新日期:2009-02-01 00:00:00

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