Ethical frameworks of informed consent in the age of pediatric ...

The challenge of informed consent arises in pediatric care, where the authority for consent to make decisions in care should be considered alongside objective ...

Here, we provide a high-level, clinical primer of (1) ethical informed consent frameworks widely used in clinical practice and (2) promising ...

(PDF) Ethical frameworks of informed consent in the age of pediatric ...

Ethics considerations for precision medicine research and genetic testing in low- and middle-income... ... Background: Genetic data transfer ...

Informed Consent in Decision-Making in Pediatric Practice

Informed consent should be seen as an essential part of health care practice; parental permission and childhood assent is an active process that engages ...

Informed Consent - Ethical Research Involving Children

Seeking informed consent from children and young people (as well as from their parent/carer) is central to an ethical, children's rights approach to ...

Ethics of Pediatric and Young Adult Medical Decision-Making

The third session taught the concepts of informed consent and assent, focusing on the variety of standards for adequate informed consent and the ...

Informed consent for pediatric research: Is it really possible?

At the most fundamental level is an existential question: “Can informed consent exist for pediatric research?” Pediatric ethics provides an important lens ...

Pediatric Decision Making - AMA Code of Medical Ethics

Informed consent to medical treatment is fundamental in both ethics and law. Patients have the right to receive information and ask questions about recommended ...

The informed consent in the mature minor: Understanding and ...

Paediatric clinical research has unique and complex ethical implications. Due to the vulnerability of minors and their lack of a legal right to consent, ...

Informed Consent in Decision-Making in Pediatric Practice

This policy statement provides a brief review of informed consent, including the ethical and legal roots, frameworks for surrogate decision- making, and ...

Do Pediatric Patients Have a Right to Know? - AMA Journal of Ethics

Commentary. Our general understanding of informed consent, based upon the conviction that moral agents have an (almost) unfettered right to control what happens ...

Informed consent instead of assent is appropriate in children from ...

... children's competence to give informed consent in medical settings concentrated on ethical and legal aspects ... children from the age of ...

clarifying consent and assent in medical and research settings

In adults, the 'primary justification' or underlying ethical value of informed consent is autonomy.2 For interventions involving children, the ...

Informed consent in paediatric clinical research ‐ a case study of ...

Determining who should act on behalf of the child is a matter of law, rather than ethical principle. But, if national laws are lacking or do not ...

Informed Consent in Pediatric Research

The process of informed consent and assent for these trials presents a major challenge. The aim of this review is to map historical, ethical and ...

Consent and Assent for Anesthesia in Infants and Children

principles. •List the elements of informed consent in adults. •Recognize differences of informed consent and assent in pediatrics. •Apply ethical principles to ...

The ethics of informed consent and shared decision-making in ...

Although the ethical principles underlying informed consent are shared by adult and pediatric medicine, there are many aspects which are unique to the ...

A Bioethics Framework for At-risk Child/Adolescent Access to Key ...

Informed consent is an ethical process and a legal issue. By law, children under 18 years are usually considered unauthorized to consent to medical procedures.

Moral structuring of children during the process of obtaining ...

Informed consent is an important factor in a child's moral structure from which different types of doctor–patient relationships arise.

Informed Consent FAQs - HHS.gov

The informed consent process involves three key features: (1) disclosing to potential research subjects information needed to make an informed decision; (2) ...