Also known as:informed consent doctrine · informed consent
Written by attorneys · grounded in primary & secondary sources — see below
2 senses
1
in torts and health law
An obligation requiring a physician to disclose material risks of and reasonable alternatives to a proposed treatment. The disclosure enables a competent patient to make a voluntary and informed decision whether to accept or refuse the intervention. Failure to provide the required information can support a claim for battery or negligence if the undisclosed risk materializes and causes harm.
2
in professional responsibility
Agreement by a client or former client to a proposed course of lawyer conduct after the lawyer communicates adequate information about material risks and reasonably available alternatives. The consent must be confirmed in writing when the applicable rule so requires. It permits representation that would otherwise be prohibited by conflict-of-interest rules.
Each sense below has its own examples, sources, and questions.
Sense 1
1
in torts and health law
An obligation requiring a physician to disclose material risks of and reasonable alternatives to a proposed treatment. The disclosure enables a competent patient to make a voluntary and informed decision whether to accept or refuse the intervention. Failure to provide the required information can support a claim for battery or negligence if the undisclosed risk materializes and causes harm.
Frequently Asked1
How does the doctrine of informed consent in torts differ from its use in professional responsibility?+
In torts the doctrine protects patient autonomy by requiring physicians to disclose material medical risks and alternatives before treatment. In professional responsibility it permits otherwise prohibited representations once clients receive adequate disclosure of risks and give written consent.
Sense 2
2
in professional responsibility
Agreement by a client or former client to a proposed course of lawyer conduct after the lawyer communicates adequate information about material risks and reasonably available alternatives. The consent must be confirmed in writing when the applicable rule so requires. It permits representation that would otherwise be prohibited by conflict-of-interest rules.
Examples6
Government Agency Consent to Former Private Matter
Destiny Davis left private practice to join a state agency. While there she was assigned to a regulatory enforcement action against a company she had previously represented on the identical issues. The agency reviewed the prior representation and gave written informed consent for her continued participation.
Delilah Duran’s firm represented Dixon Foods in a contract dispute while another office of the same firm sued Dixon Foods on an unrelated product-liability claim. Dixon Foods refused to give informed consent after full disclosure of the direct adversity, so the firm could not continue both matters.
Former Judge Representing Party in Prior Case
Damian Decker had served as a law clerk on an arbitration panel that decided a commercial dispute. After leaving the clerkship he sought to represent one of the same parties in related litigation. All parties gave written informed consent, allowing the representation to proceed.
Lawyer Must Promptly Seek Required Consent
Dustin Donovan discovered that his client’s matter now required informed consent under Rule 1.7 because of a newly arising conflict. He immediately disclosed the circumstances and risks in writing and obtained the client’s informed consent before continuing the representation.
Aggregate Settlement Needs Signed Consents
Denise Donovan represented three plaintiffs injured in the same accident. When the defendant offered a lump-sum settlement, she explained the total amount, each client’s share, and the risks of the aggregate deal. Each client signed a written consent after receiving that disclosure.
Former Firm’s Client Consent to New Representation
Diego Duarte joined a new firm that had previously represented a company now adverse to his current client in a substantially related matter. Duarte had acquired no material confidential information. After the former client gave written informed consent, the new firm could represent the current client.
Frequently Asked5
What information must a lawyer disclose before obtaining informed consent under the Model Rules?+
The lawyer must communicate adequate information and explanation about the material risks of and reasonably available alternatives to the proposed course of conduct. Rule 1.0(e) defines informed consent in these terms.
When is informed consent required for a lawyer to participate in a matter the lawyer previously handled in private practice?+
Rule 1.11(d)(2)(i) requires informed consent, confirmed in writing, from the appropriate government agency before the lawyer may participate in such a matter.
Does a former judge or arbitrator need informed consent to represent a party in a matter the judge previously decided?+
Rule 1.12(a) prohibits the representation unless all parties to the proceeding give informed consent confirmed in writing.
What must be disclosed to obtain valid informed consent for an aggregate settlement under Rule 1.8(g)?+
The lawyer must disclose the existence and nature of all claims or pleas involved and the participation of each person in the settlement, and each client must give consent in a writing signed by the client.
Can a lawyer continue joint representation after discovery reveals differing degrees of fault among clients?+
Continued representation is impermissible if the lawyer can no longer reasonably believe competent and diligent representation can be provided to each client, even if the clients previously gave informed consent.
is that the patient generally possesses the right not to
consent
, that is, to refuse treatment. See, e. g., In re Storar , 52 N. Y. 2d 363, 373, 420 N. E. 2d 64, 69 (1981); Superintendent…
has its roots in the law of battery. A physician who performs an operation without his patient’s
consent
is guilty of a battery. The
consent
must be an
informed
one. The patient must be…
: Debunking Myths and Misconceptions, 53 Food & Drug L. J. 71, 76-77 (1998) (noting that courts, several States, and the FDA itself recogniz[e] the value and propriety of off-label use).…
”. The issue involved is whether Oklahoma adheres to the
doctrine of informed consent
as the basis of an action for medical malpractice, and if so did the present instructions adequately advise the jury of defendant’s duty. Anglo-American law starts with the premise of…
Professional ResponsibilityRegulation of the legal profession · Multijurisdictional practiceMPREFoundational