2025 Regular Session
Link to Bill History on Legacy Website (Click Here)Summary: To require all medical providers to orally explain any and all medical treatments and procedures and all possibilities for potential problems or complications or side effects to patients before proceeding with treatments.
PDF: hb2631 intr.pdf
DOCX: HB2631 INTR.docx
WEST VIRGINIA LEGISLATURE
2025 REGULAR SESSION
Introduced
House Bill 2631
By Delegates Vance, Worrell, McGeehan, Hornby, Jeffries, and Dean
[Introduced February 19, 2025; referred to the Committee on Health and Human Resources]
A BILL to amend the Code of West Virginia,1931, as amended, by adding thereto a new article, designated §16-3E-1, §16-3E-2, §16-3E-3, and §16-3E-4, all relating to requiring information to be provided orally to all patients in order for the patient to give informed consent knowing all potential outcomes for all medical tests, prescriptions, and treatments; providing a short title; defining terms; creating rights for patients; and establishing monetary penalties and revocation of licensure for violations.
Be it enacted by the Legislature of West Virginia:
article 3E. informed consent for all medical treatments.
§16-3E-1. Short title.
This article shall be known and may be cited as the Medical Informed Consent Act.
§16-3E-2. Definitions.
"Department" means the Department of Health;
"Emergency medical services provider" means that term as defined in §16-4C-3;
"Health care facility" means this term as defined in §16-2D-2;
"Health care provider" means that term as defined in §16-1A-3, as well as dentists, chiropractors, and podiatrists;
"Informed consent" means the right of all people to be fully informed about the risks and benefits of any medical intervention, to be provided with information about all possible treatment options and medications and the side effects, and free to make a voluntary decision on that intervention; and
"License" means a health care practitioner license issued by the Department of Health or a health care facility license issued by the Department of Health.
§16-3E-3. Informed consent requirements.
All medical treatment providers in this state are required to orally describe all possible treatment plans, including potential problems, complications, or side effects to each patient seeking medical advice, treatment, or testing. Upon being advised of all options and possible problems, complications, or side effects, the medical practitioner will obtain the patient's signature to attest that the patient has received this information.
§16-3E-4. Rights of patients; penalties.
(a) Summary of rights. -- The department shall publish on the department's publicly accessible Internet website a summary of the rights of a patient or parents or guardians of a patient under §16-3E-3, in any format the health care provider or health care facility chooses.
(b) Complaints. -- A health care provider and health care facility, if requested, shall inform patients of the address and telephone number of each state agency responsible for responding to patient complaints about a health care provider or health care facility’s alleged noncompliance with this article.
(c) Procedure for providing information on patient rights. -- A health care provider or facility shall adopt policies and procedures to ensure that a patient and the parent or guardian of a patient are provided the opportunity during the course of admission to receive information regarding the rights contained in §16-3E-3 and how to file complaints with the facility and appropriate state agency.
(d) The appropriate regulatory board or, if no board exists, the department may impose an administrative fine against a health care practitioner for failing to make available to patients a summary of their rights under §16-3E-3 and the following shall apply:
(1) A health care provider's first violation under this paragraph shall be subject to corrective action and shall not be subject to an administrative fine if the violation was unintentional;
(2) The appropriate licensing board or the department may levy a fine of not more than $100 for a second or subsequent unintentional violation under this subsection; and
(3) The appropriate licensing board or the department may levy a fine of not more than $500 for an intentional violation under this subsection, with each intentional violation constituting a separate violation subject to a separate fine.
(e) Determination of fine. -- In determining the amount of fine to be levied under subsection (d) of this section, the following factors shall be considered:
(1) The scope and severity of the violation, including the number of patients or parents or guardians of patients found not to have received notice of a patient’s rights under §16-3E-3, and whether the failure to provide the information to patients was willful;
(2) Actions taken by the health care provider or health care facility to correct violations or to remedy complaints; and
(3) Any previous violations under this article by a health care provider or health care facility.
NOTE: The purpose of this bill is to require information to be provided orally to all patients in order for the patient to give informed consent knowing all potential outcomes for all medical tests, prescriptions, and treatments; providing a short title; defining terms; creating rights for patients; and establishing monetary penalties.
Strike-throughs indicate language that would be stricken from a heading or the present law and underscoring indicates new language that would be added.