Class 6 - Childhood Ethics Flashcards
two “small cases” often seen in childhood ethics
Situation where a child shares a secret with you and do not want you to tell parents
Situations where you have concerns about treatment, or they way people are approaching the child… where the child seems to be resisting and you do not know if the child’s views are being respected adequately
4 ways children are disadvantaged
Physically
Smaller and less powerful = making them prone to physical vulnerability
They could be physically exploited and controlled and taken advantage of by bigger, more powerful, older people (‘grown ups’)
Psychologically
They might not have certain types of relational experiences
May not know how to navigate things like trust. How are they supposed to know when they can believe what someone is telling them? When they can cooperate of what someone is asking of them? How do they know when it is safe or unsafe to do so?
With relational experiences we tend to understand how to navigate and read these situations
Socially
They are economically dependent on others for the necessities of living
They can’t sustain themselves, they are dependent on the benevolence of others (commonly their family) to ensure that their basic needs are being met
Legally
Being a minor entails some legal vulnerabilities because they are not independent to act entirely on their own
They cannot independently pursue that their rights are going to be respected adequately
They always require a legal representative, a surrogate, who can act on their behalf and advocate
examples that multiply the vulnerability of children
Disabled
Mental health concerns
LGBTQ2A
Newborns
Indigenous
Migrant newcomers
Low income/Poverty
Cultural/religious/racial diversity
Child welfare (youth protection)
Pediatric palliative care
Global child health
5 recurring themes (ethical challenges) in nursing children and families
Which criteria determine whether therapies should be provided?
What criteria would be ethically correct
How do we judge that?
Who should make such decisions?
Who should have the authority to decide what healthcare approach is ethically optimal for the particular child ?
What about the voice of the child?
Where does their voice fit in?
Does the voice of the child always matter? Does age and so called maturity? Capacity?
Do some children’s voices merit more ethical grounds for being respected than other children? How do we figure that out?
What about confidentiality?
Are children owed a respect for privacy and confidentiality?
Are we bound to respect their wishes when they say “do not tell my parents”?
Considerations in pediatric palliative care
How do we relate end of life or other types of palliative care challenges that children confront … .how does good ethical nursing navigate these situations?
Help define what type of norms we ought to be drawing on in order to help clarify what would be the ethical superior way forward
statement from the Canadian Pediatric Society
3 important statements from the Canadian Paediatric Society Position Statement “Tx decisions regarding infants, children and adolescents”
All infants, children and adolescents – regardless of physical or mental disability - have dignity, intrinsic value, and a claim to respect, protection, and medical treatment that serves their best interests.
In most cases, parents are appropriate surrogate decision makers for their children and should give primacy to the best interests of their child.
Children and adolescents should be appropriately involved in decisions affecting them. Once they have sufficient decision- making capacity, they should become the principal decision maker for themselves
why is Qb different from other provinces
All other provinces are not the same, but they are rooted in Common Law which we do not have in Quebec.
In Quebec it varies quite a lot because it is a Civil Code system, so the way the law operates is quite different
Medical decision-making in paediatrics: Infancy to adolescence
(name a few key points from the Canadian Paediatric Society)
Children’s/ adolescents’ participation in medical decision-making should besought in proportion to developmental capacity to understand nature & consequences of their medical problem and to reasonably foreseeable risks & benefits of treatment proposed
HCPs & SDMs should be informed about, and act in accordance with, laws and regulations governing consent to treatment within their jurisdiction
HCPs must provide patients and their SDMs with all the information they need to participate effectively in the decision-making process
Assent/dissent should be respected whenever possible; it is recognized that in absence of capacity, minimizing harms & maximizing patient’s best interests is the priority
HCPs, patients & families should work together to reach medical decisions based on the patient’s best interests or outcomes
In cases of serious disagreement/competing interests, HCP’s primary responsibility is to the patient
In complex social situations, a collaborative process should be agreed upon to clearly identify the SDM(s) in a timely fashion
HCPs should be aware of conflict resolution process in place in their practice environment In situations of conflict, HCPs have an obligation to seek and access resources to help resolve that conflict & to facilitate patient and family access to such assistance as well
Which criteria should determine whether therapies ought to be provided?
(2)
Child’s best interests
Proportional weighing of benefits and burdens
What does best interest mean?
There is not one clear universal definition. In general, it is widely agreed that the best interest implies the course of option where the benefits are proportionally greater to the burdens.
Which benefits and burdens are most important - when we are discussion best interest?
We do not have a universal consensus on that
We know that many families have relative differences on quantity of life in relation to quality of life
Some families, whether it is cultural, religious or just personal convictions; might believe that prolonging life (even for another day) is always worth it - no matter how intrusive some of the treatments might be
For some families, quality of life is important. They do not view doing very intrusive things as worth it if the QOL during treatment is going to be severely difficult, and the long term outcome is going to be compromised in relation to what the parent’s aspirations are and the parent’s conception of what is best for the child would be.
Gets into very sensitive topics relating to how do different forms of disability, and other types of outcomes, matter in terms of a child’s best interest (**in recent years interesting work on this area)
Who should decide which treatment is best?
Legally, the person with the ultimate authority on what course of Tx would optimize the child’s best interest, in the context of Canadian Jurisdiction, would be the parents.
When it comes to consenting to treatment, the authority commonly would be the parent. In certain circumstances it could be the child.
All the others who are involved in the duty of care to the child (physicians, nurses, RT, psychologist, social workers, etc) also have to make decisions on what is in the child’s best interest, in how they make decisions about their own actions.
Ultimately, in deciding what will be the goals and the master care plan here = the parents or person’s with parental authority are the legal decisions makers
Consent (adapted)
There are certain standards in which the child is recognized as being capable, or in fact required to consent to treatment. Either independently or sometimes with parenteral collaboration.
This is specified by law in every jurisdiction
Assent
Even when the child is not of that age or threshold of capacity to decide for themselves, within childhood ethics, many have been promoting recognizing the child’s capacity to ASSENT to care.
Assent is NOT consent
Ultimately, you may still do certain things to a child without their consent. We will try the best we can to elicit their voluntary cooperation
So if a younger child is not legally allowed to provide consent = a legal standard. We then provide in Childhood Ethics is a way of recognizing the younger child as a person, they still have a voice and a say in how they will be treated to the extent of what is possible and realistic to their voluntary collaboration
An ethical analysis has been able to make a compelling case that we can still move forward with this intervention regardless of the child’s dissent (clear expression of rejection). Regardless, we would have done the best we can to be mindful of the child’s preferences
what is our responsibility to the parents of a child who is 14 or over and hospitalized for > 12 hours?
The civil code allows us and requires us that we breach the privacy and confidentiality of the child in a narrow way = in the chance that they would be hospitalized for 12 hours or more
We have an obligation, and the parent’s have a right to know this
Only to know that the child is there
Does not allow us to explain any of the circumstances related to the child’s condition, health and so on; UNLESS the child is unconscious, illness or medication has rendered them incapable of deciding for themselves → in that case the parent would be the decision maker for the child and should received required information, ONLY the information required for them to make Tx decisions for that minor