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Informed consent: myths and risk management alternatives
QRB. Quality Review Bulletin
|December 1, 1986
Summary
Informed consent, often misunderstood, is key to reducing malpractice claims and advancing risk management goals. This article clarifies common myths and offers solutions for better informed consent practices.
Area of Science:
- Healthcare Law
- Risk Management
- Medical Ethics
Background:
- The doctrine of informed consent is frequently misunderstood by risk management personnel.
- Misperceptions surrounding informed consent contribute to numerous malpractice claims.
- Despite challenges, informed consent is a valuable concept for achieving risk management objectives.
Purpose of the Study:
- To analyze common myths and misperceptions regarding informed consent in the context of risk management.
- To provide practical strategies for addressing risk management challenges associated with informed consent.
Main Methods:
- Analysis of seven prevalent "myths" or misperceptions about informed consent.
- Development of five actionable recommendations for risk management improvement.
Main Results:
- Identified and deconstructed seven common misunderstandings of informed consent.
- Proposed five practical strategies to mitigate risks and enhance informed consent processes.
Conclusions:
- Addressing misconceptions about informed consent is crucial for effective risk management.
- Implementing suggested strategies can improve patient safety and reduce malpractice litigation.