Ethics Final Notes New
Ethics Final Notes New
Ethics Final Notes New
Age.
Ethnicity.
Citizenship.
Disability.
Sexual orientation.
Organ donation is the process of removing an organ from one person and surgically placing it in another
person. Many organs can be donated. Donations include the liver, kidney, pancreas, and heart.
Ethics of organ transplantation refers to the ethical concerns on organ transplantation procedures . Both
the source and method of obtaining the organ to transplant are major ethical issues to consider, as well as
the notion of distributive justice.
Organ harvesting from live people is one of the most frequently discussed debate topic in organ
transplantation. The World Health Organization argues that transplantation promote health, but the notion
of “transplantation tourism” has the potential to violate human rights or exploit the poor, to have
unintended health consequences, and to provide unequal access to services, all of which ultimately may
cause harm. Thus WHO called to ban compensated organ transplanting and asked member states to
protect the most vulnerable from transplant tourism and organ trade. However, as disincentives becomes a
must, adding incentives back, such as improving life condition for organ donors after donation, becomes
difficult.
There is also a powerful opposing view, that trade in organs, if properly and effectively regulated to ensure
that the seller is fully informed of all the consequences of donation, is a mutually beneficial transaction
between two consenting adults, and that prohibiting it would itself be a violation of Articles 3 and 29 of
the Universal Declaration of Human Rights.
Controversies also raise on how to assume consent of organ donation for dead people. In practice most
countries, have legislation allowing for implied consent, asking people to opt out of organ donation instead
of opt in, but allow family refusal
Q4. Malpractice
Medical malpractice occurs when a hospital, doctor or other health care professional, through a negligent
act or omission, causes an injury to a patient. The negligence might be the result of errors in diagnosis,
treatment, aftercare or health management.
Characteristics:
A violation of the standard of care - The law acknowledges that there are certain medical standards
that are recognized by the profession as being acceptable medical treatment by reasonably prudent
health care professionals under like or similar circumstances. This is known as the standard of care. A
patient has the right to expect that health care professionals will deliver care that is consistent with
these standards. If it is determined that the standard of care has not been met, then negligence may
be established.
An injury was caused by the negligence - For a medical malpractice claim to be valid, it is not
sufficient that a health care professional simply violated the standard of care. The patient must also
prove he or she sustained an injury that would not have occurred in the absence of negligence. An
unfavorable outcome by itself is not malpractice. The patient must prove that the negligence caused
the injury. If there is an injury without negligence or negligence that did not cause an injury, there is
no case.
The injury resulted in significant damages - Medical malpractice lawsuits are extremely expensive
to litigate, frequently requiring testimony of numerous medical experts and countless hours of
deposition testimony. For a case to be viable, the patient must show that significant damages resulted
from an injury received due to the medical negligence. If the damages are small, the cost of pursuing
the case might be greater than the eventual recovery. To pursue a medical malpractice claim, the
patient must show that the injury resulted in disability, loss of income, unusual pain, suffering and
hardship, or significant past and future medical bills.
Fair treatment
Employees are expected to act fairly at all times. This includes not allowing undue external factors to
interfere with the implementation of our fair-treatment policy and avoiding actions that might create a
perception that suppliers or contractors have “a friend at Bechtel” who could exert improper influence on
their behalf.
No misrepresentation
Honesty is an integral part of ethical behavior, and trustworthiness is essential for strong, lasting
relationships. employees may not misrepresent themselves, including their level of authority, or the
company to anyone. We expect the same of our suppliers.
The general principles of what is considered confidential have been outlined in common law. A duty of
confidence arises when one person discloses information to another (e.g. a patient to a doctor) in
circumstances where it is reasonable to expect that the information be held in confidence. To represent a
breach, confidential information must: Enforcement of a legal duty in the UK has to date been relatively
weak. There has to date been no criminal conviction of a doctor for breach of confidence, although civil
claims in negligence have occurred and damages awarded when confidence has been breached by
revealing medical information without explicit consent.
have the necessary quality of confidence,
be imparted in circumstances importing an obligation of confidence,
be disclosed without the permission and to the detriment of the person originally communicating it,
not already be in the public domain,
be in the public interest to protect it.
Q7. Research Ethics:
Research that involves human subjects or participants raises unique and complex ethical, legal, social and
political issues. Research ethics is specifically interested in the analysis of ethical issues that are raised
when people are involved as participants in research. There are three objectives in research ethics. The first
and broadest objective is to protect human participants. The second objective is to ensure that research is
conducted in a way that serves interests of individuals, groups and/or society as a whole. Finally, the third
objective is to examine specific research activities and projects for their ethical soundness, looking at issues
such as the management of risk, protection of confidentiality and the process of informed consent.
For the most part, research ethics has traditionally focused on issues in biomedical research. The
application of research ethics to examine and evaluate biomedical research has been well developed over
the last century and has influenced much of the existing statutes and guidelines for the ethical conduct of
research. However in humanities and social science research, different kinds of ethical issues arise. New
and emerging methods of conducting research, such as auto-ethnography and participatory action research
raise important but markedly different ethical issues and obligations for researchers.
Research involving vulnerable persons, which may include children, persons with developmental or
cognitive disabilities, persons who are institutionalized, the homeless or those without legal status, also
raises unique issues in any research context.
Research ethicists everywhere today are challenged by issues that reflect global concerns in other domains,
such as the conduct of research in developing countries, the limits of research involving genetic material
and the protection of privacy in light of advances in technology and Internet capabilities.
In Canada, current debates and challenges in research ethics include the changing notions of what
constitutes research and therefore requires formal ethics review, the oversight and monitoring of the work
of Research Ethics Boards (known as Institutional Review Boards, in the U.S.) at federal and provincial
levels, the jurisdiction of Research Ethics Boards in academic, clinical and corporate settings, the increasing
multidisciplinary of research collaborations and pursuits and challenges created by rigorous federal and
provincial privacy legislation. This is by no means an exhaustive list of the kinds of live issues there are in
research ethics today. Aside from the epistemological and philosophical issues in this dynamic field,
research ethicists also face anecdotal issues at the level of individual research ethics reviews, systemic
issues related to the institutions in which research ethics reviews are carried out and social, legal and
political issues related to governance and oversight of research ethics activities.