Article Text
Abstract
A recent article from Archives of Disease in Childhood outlined problems with the act of gaining child assent for research participation. However the arguments used in the article are incomplete or misguided. Rather than being harmful, assent should be seen as an ethically-appropriate way in which we can engage with the child about his participation in research. While additional clarification of the concept of assent is needed, the child's family context can provide us with a valuable guide to the way we involve him in the decision-making process.
- Autonomy
- informed consent
- minors/parental consent
- public health ethics
- family
- cloning
- virtue theory and bioethics
- resource allocation/ priority setting
- artificial reproduction
- biotechnology
- paediatrics
- medical ethics
- newborns and minors
- allowing minors to die
- donation/procurement of organs/tissues
- prolongation of life and euthanasia
- quality/value of life/personhood
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- Autonomy
- informed consent
- minors/parental consent
- public health ethics
- family
- cloning
- virtue theory and bioethics
- resource allocation/ priority setting
- artificial reproduction
- biotechnology
- paediatrics
- medical ethics
- newborns and minors
- allowing minors to die
- donation/procurement of organs/tissues
- prolongation of life and euthanasia
- quality/value of life/personhood
Footnotes
Linked article 100242.
Funding AS and MS receive funding from the Department of Health's NIHR Oxford Biomedical Research Centre. AJP is a Jenner Investigator and James Martin Senior Fellow.
Competing interests None.
Provenance and peer review Commissioned; internally peer reviewed.
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