Related Experiment Video
Updated: Dec 23, 2025

07:56
Scanning Skeletal Remains for Bone Mineral Density in Forensic Contexts
Published on: January 29, 2018
18.1K
Reasonable Persons, Autonomous Persons, and Lady Hale: Determining a Standard for Risk Disclosure
The Hastings Center Report
|April 21, 2020
Summary
The "reasonable person" standard is inadequate for determining essential medical risk disclosures. Courts adjudicate informed consent cases by examining specific patient needs, not a hypothetical individual.
Area of Science:
- Medical Ethics
- Legal Medicine
- Patient Rights
Background:
- Risk disclosure is crucial in clinical and research settings.
- Determining what information a 'reasonable person' needs is a persistent challenge.
- Informed consent requires healthcare providers to disclose relevant risks.
Purpose of the Study:
- To critically evaluate the 'reasonable person' standard in medical risk disclosure.
- To analyze how Western courts handle 'negligent nondisclosure' claims.
- To examine the implications of the Montgomery v. Lanarkshire Health Board decision.
Main Methods:
- Analysis of the 'reasonable person' construct's limitations.
- Review of legal precedents in negligent nondisclosure cases.
- Scrutiny of the UK Supreme Court's ruling in Montgomery v. Lanarkshire Health Board.
Main Results:
- The 'reasonable person' standard is deemed insufficient for defining necessary risk disclosures.
- Courts often consider individual patient circumstances rather than a generalized standard.
- The Montgomery decision highlights a shift towards a more patient-centric approach to informed consent.
Conclusions:
- The 'reasonable person' standard is ill-equipped to guide medical risk disclosure.
- Legal adjudication of informed consent disputes relies on specific patient contexts.
- A patient-centered approach is essential for upholding informed consent rights.

