Arkansas § 17-95-108 Informed consent required for gastric bypass surgery

Arkansas Statutes

§ 17-95-108 — Informed consent required for gastric bypass surgery

Arkansas § 17-95-108

Title17

This text of Arkansas § 17-95-108 (Informed consent required for gastric bypass surgery) is published on Counsel Stack Legal Research, covering Arkansas primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook

Ark. Code Ann. § 17-95-108 (2026).

Text

(a)No gastric bypass surgery may be performed in this state unless the physician who will perform the surgery has informed the patient in writing, as evidenced by the patient's signature, of the known risks and complications of the procedure, including, but not limited to:

(1)The surgery itself;

(2)All known and documented future complications that may occur as a result of the procedure;

(3)Side effects that may result from vitamin deficiency and malnutrition; and (4) The requirements for appropriate follow up.

(b)(1) The Arkansas State Medical Board shall promulgate rules to enforce this section within six (6) months of July 16, 2003.

(2)The rules shall utilize scientifically accepted information from national medical specialty boards, organizations, or governmental agencies in dete

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(a) No gastric bypass surgery may be performed in this state unless the physician who will perform the surgery has informed the patient in writing, as evidenced by the patient's signature, of the known risks and complications of the procedure, including, but not limited to: (1) The surgery itself; (2) All known and documented future complications that may occur as a result of the procedure; (3) Side effects that may result from vitamin deficiency and malnutrition; and (4) The requirements for appropriate follow up. (b) (1) The Arkansas State Medical Board shall promulgate rules to enforce this section within six (6) months of July 16, 2003. (2) The rules shall utilize scientifically accepted information from national medical specialty boards, organizations, or governmental agencies in determining the specific content and lists of complications or side effects, or both, that must be included in the informed consent.