Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
Add more filters










Database
Publication year range
1.
Swiss Med Wkly ; 142: w13667, 2012.
Article in English | MEDLINE | ID: mdl-22903228

ABSTRACT

In 1968, an Ad Hoc committee at the Harvard Medical School advanced new criteria for determining death. It proposed that patients in irreversible coma with no discernible central nervous system activity were actually dead. The committee paved the way for the "whole brain" definition of death, which has reached broad public acceptance and legal enactment in many countries. Despite this, the philosophical and ethical debate about the "whole brain" definition of death is far from being closed. This paper analyses the ongoing controversy and evaluates the recent revision of the Swiss Academy of Medical Sciences guidelines for determining death.


Subject(s)
Brain Death/diagnosis , Death , Ethics, Medical , Brain Death/legislation & jurisprudence , Humans , Practice Guidelines as Topic , Switzerland , Terminology as Topic , Tissue and Organ Procurement/ethics
2.
Dtsch Med Wochenschr ; 134(49): 2525-8, 2009 Dec.
Article in German | MEDLINE | ID: mdl-19941238

ABSTRACT

The World Medical Association's Declaration of Helsinki is one of the most influential documents in research ethics. A revised version of the Declaration was adopted in October 2008. This paper discusses selected changes regarding the Declaration's normative status, subject protection and issues in international research in light of current debates in research ethics.


Subject(s)
Ethics, Research , Helsinki Declaration , Europe , Humans , Informed Consent/ethics , Informed Consent/legislation & jurisprudence , Internationality , Mental Competency/legislation & jurisprudence , Moral Obligations , Patient Selection/ethics , Risk Assessment , Vulnerable Populations/legislation & jurisprudence
3.
J Med Ethics ; 35(9): 558-64, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19717695

ABSTRACT

BACKGROUND: It is often claimed that a regulated kidney market would significantly reduce the kidney shortage, thus saving or improving many lives. Data are lacking, however, on how many people would consider selling a kidney in such a market. METHODS: A survey instrument, developed to assess behavioural dispositions to and attitudes about a hypothetical regulated kidney market, was given to Swiss third-year medical students. RESULTS: Respondents' (n = 178) median age was 23 years. Their socioeconomic status was high or middle (94.6%). 48 (27%) considered selling a kidney in a regulated kidney market, of whom 31 (66%) would sell only to overcome a particularly difficult financial situation. High social status and male gender was the strongest predictor of a disposition to sell. 32 of all respondents (18%) supported legalising a regulated kidney market. This attitude was not associated with a disposition to sell a kidney. 5 respondents (2.8%) endorsed a market and considered providing a kidney to a stranger if and only if paid. 4 of those 5 would sell only under financial duress. CONCLUSIONS: Current understanding of a regulated kidney market is insufficient. It is unclear whether a regulated market would result in a net gain of kidneys. Most possible kidney vendors would only sell in a particularly difficult financial situation, raising concerns about the validity of consent and inequities in the provision of organs. Further empirical and normative analysis of these issues is required. Any calls to implement and evaluate a regulated kidney market in pilot studies are therefore premature.


Subject(s)
Commerce/ethics , Kidney , Tissue Donors/psychology , Tissue and Organ Procurement/ethics , Adult , Commerce/economics , Female , Health Knowledge, Attitudes, Practice , Humans , Male , Socioeconomic Factors , Switzerland , Tissue and Organ Procurement/economics , Tissue and Organ Procurement/legislation & jurisprudence , Waiting Lists , Young Adult
4.
J Med Ethics ; 35(1): 12-6, 2009 Jan.
Article in English | MEDLINE | ID: mdl-19103936

ABSTRACT

Norman Daniels' theory of justice and health faces a serious practical problem: his theory can ground the special moral importance of health and allows distinguishing just from unjust health inequalities, but it provides little practical guidance for allocating resources when they are especially scarce. Daniels' solution to this problem is a fair process that he specifies as "accountability for reasonableness". Daniels claims that accountability for reasonableness makes limit-setting decisions in healthcare not only legitimate, but also fair. This paper assesses the latter claim. Does accountability for reasonableness result in fair limit-setting decisions? It is argued that the answer to this question is not a clear yes. Daniels is remarkably unclear about the criterion of fairness that accountability for reasonableness satisfies. The paper discusses different options for resolving this lack of clarity and examines how they apply to Daniels' accountability for reasonableness framework. It is concluded, first, that accountability for reasonableness is not a paradigm case of any of the classic notions of procedural justice; second, that what might be called "constrained pure procedural justice" best reflects how accountability for reasonableness results in fair limit-setting decisions; and third, that the procedural conditions of accountability for reasonableness must be further specified and amended to better achieve a fair process, and hence fair limit-setting decisions.


Subject(s)
Decision Making/ethics , Health Care Rationing/ethics , Social Justice/ethics , Bioethics , Health Care Rationing/legislation & jurisprudence , Health Policy/legislation & jurisprudence , Humans , Socioeconomic Factors
SELECTION OF CITATIONS
SEARCH DETAIL
...