Ethical Practice Flashcards
Bioethics - What are ethics?
Ethics are not a set of rules, they are a process of critical reflection.
Using an analytical approach (System 2 decision-making) helps
us to consider ethical issues from a number of different perspectives.
brief history of ethics
- Prior to the mid-20th Century paternalism was dominant in
medicine - Paternalism is the idea that “Father knows best”
- An unquestioning faith in the doctor’s knowledge and ability
- Since then we have seen the rise of:
- Patient centred care
- Greater knowledge and participation by the patient and carers
- Greater autonomy of the patient and carers
Post - mid 20th Century
Since then we have seen the rise of:
* Person centred care
* Greater knowledge and participation by the patient and carers
Reduction of authoritarian/paternalistic approach
Greater diversity of health practitioners and greater team based care
Focus on previous unethical behaviour
* Such as lack of Informed Consent in medical research
Ethics today
Delivery of Health Care
* Who gets treated? (Access and Equity)
* Who decides the treatment? (Paternalism versus Autonomy)
Ethics in research
* Is the experiment justified? (especially in regard to animals)
* Will anyone be potentially harmed?
Bioethics
“Bioethics is concerned with questions about basic human values such as the rights to life and health, and the rightness or wrongness of certain developments in healthcare institutions, life technology, medicine, the health professions and about society’s responsibility for the life and health of its members.”
Bioethics cont.
Childress and Beauchamp (2001)
It is a framework, and not a set of rules.
- Respect for autonomy
- Beneficence
- Non maleficence
- Justice
Can All Four Principles be Satisfied?
- The Bioethics framework is not a set of rules.
- Rarely can all four principles be satisfied.
- It is a process for critical reflection.
- We use each principle as a lens to examine the issue.
Autonomy
“Respecting the decision-making capacities of autonomous persons, enabling individuals to make reasoned informed choices.”
- The patient’s right to make the decision
- The patient’s ability to make an informed decision
Informed Consent
AUTONOMY»_space; INFORMED CONSENT»_space; INFORMATION + CAPACITY TO CONSENT»_space; TYPES OF CONSENT»_space; WHEN + WHO
Autonomy relies on informed Consent
Health Practitioners need to obtain informed consent before they treat patients
Health Practitioner needs to ensure that the patient:
* fully understands what is involved in the treatment
* has the capacity to consent
Understanding the Information
The patient or representative must demonstrate that they understand the information given.
- Has the information been delivered in a way which can be
understood? - Appropriate to their level of health literacy
- Accommodating language and cultural issues
- In consideration of the circumstances of the patient (such as place and time)
- Does the person have the capacity to consent based on this
information?
Capacity to Consent
Under the Victoria Medical Treatment Act 1988, a patient must be of sound mind and over 18 years of age in order to give or refuse valid informed consent. Competency is to be assumed unless there is clear evidence to the contrary. If there are any questions around a patient’s competence, an assessment should be undertaken by the treating
doctor or other appropriate personnel, e.g. psychiatrist.
Capacity to consent
All patients may be considered capable of consent if they are:
- Sufficiently mature and intellectually capable of understanding the procedure (age may not be a factor)
- Over 18
Where the patient is a minor (under 18) or incapacitated: - Under 18 – parent or guardian consent usually required
- Guardianship Legislation (such as Medical Power of Attorney)
When is Informed Consent Required?
Except in life saving, emergency situations, consent is always
required.
The patient (or nominated representative) must be told the:
* Diagnosis and prognosis
* Explanation of the treatment, including:
* What it will be
* Who will perform it and where
* Potential risks, complications and side effects
* Expected outcomes
* Alternatives
Types of consent
Written consent is where a document is signed (e.g. a consent form).
* Usually only where there is significant risk, such as a surgical
procedure.
Verbal consent is where the patient states their consent
* Used in low risk situations
Implied consent is where the patient indicates agreement through their actions or by cooperating with the health practitioner’s instructions.
* Used in routine situations (such as receiving a medication)