Under Review: No
Issued by Council: January 1, 2010
Reissued by Council: June 2016
- A regulated member must obtain a patient’s informed consenti prior to an examination, assessment, treatment or procedure; such consent may be implied, expressed orally or in writing as appropriate.
- If a patient is under the age of 18 years, a regulated member must:
- determine whether the patient is a mature minor with the capacity to give informed consenti; and
- if the patient is not a mature minor, seek informed consent from the patient’s legal guardian, in accordance with legislation.i
- If an adult patient lacks capacity to give informed consent, a regulated member must seek informed consent from the patient’s legal guardian or substitute decision maker, in accordance with legislation.i
- A regulated member who has reasonable grounds to believe an informed consent decision by a legal guardian or substitute decision maker is not in the best interests of the patient must seek legal advice, such as from the Canadian Medical Protective Association, or advice from the College.
- A regulated member obtaining informed consent from a patient, or the patient’s legal guardian or substitute decision maker must ensure the decision maker:
- is aware of his/her right to withdraw consent at any time;
- is free of undue influence, duress or coercion in making the consent decision;
- receives a proper explanation that includes but is not limited to:
- diagnosis reached;
- advised interventions and treatments;
- exact nature and anticipated benefits of the proposed examination, assessment, treatment or procedure;
- common risks and significant risks;
- reasonable alternative treatments available, and the associated common risks and significant risks; and
- natural history of the condition and the consequences of forgoing treatment;
- demonstrates a reasonable understanding of the information provided and the reasonably foreseeable consequences of both a decision and a failure to make a decision.
- A regulated member who assesses the capacity of a patient to give informed consent must:
- use accepted capacity assessment processes;
- to the extent possible, conduct the capacity assessment at a time and under circumstances in which the patient is likely to be able to demonstrate full capacity; and
- inform the patient of the nature and consequences of the capacity assessment.
- A regulated member obtaining informed consent for a patient to participate in health research must comply with the College’s Human Health Research standard of practice.
- A regulated member may delegate responsibility for obtaining informed consent to another healthcare professional only when confident the delegate has the appropriate knowledge, skill and judgment to meet the expectations of this standard.
Related Standards of PracticeAll Resources
Other resources related to this standardAll Resources
Consent: A guide for Canadian physiciansCanadian Medical Protective Association (CMPA) Click to view files
Resources for Capacity Assessors, Alberta Adult Guardianship and Trusteeship ActGovernment of Alberta Click to view files
Guide to Capacity Assessment Under the Personal Directives ActGovernment of Alberta Click to view files
Good Practices Guide: Informed Consent (CMPA)Canadian Medical Protective Association (CMPA) Click to view files
Goals of Care (AHS)Alberta Health Services (AHS) Click to view files
Informed ConsentCanadian Medical Protective Association (CMPA) Click to view files
About the Standards of Practice
The CPSA Standards of Practice are the minimum standards of professional behaviour and ethical conduct expected of all physicians registered in Alberta. Standards of practice are enforceable under the Health Professions Act and will be referenced in the management of complaints and in discipline hearings.
For questions or archived standards, policies and guidelines contact our Standards of Practice Advisor.