(a) It is the responsibility of the attending licensed healthcare
practitioner acting within the scope of his or her professional licensure
to determine what information a reasonable person in the patient's
condition and circumstances would consider material to a decision to
accept or refuse a proposed treatment or procedure. Information that
is commonly appreciated need not be disclosed. The disclosure of the
material information and obtaining informed consent shall be the
responsibility of the licensed healthcare practitioner who, acting within
the scope of his or her professional licensure, performs or orders the
procedure or treatment for which informed consent is required.
(b) The information material to a decision concerning the
administration of a psychotherapeutic drug or physical restraint, or the
prolonged use of a device that may lead to the inability of the patient
to regain use of a normal bodily function shall include at least the
following:
(1) The reason for the treatment and the nature and seriousness of
the patient's illness.
(2) The nature of the procedures to be used in the proposed treatment
including their probable frequency and duration
(3) The probable degree and duration (temporary or permanent) of
improvement or remission, expected with or without such treatment.
(4) The nature, degree, duration and probability of the side effects and
significant risks, commonly known by the health professions.
(5) The reasonable alternative treatments and risks, and why the
health professional is recommending this particular treatment.
(6) That the patient has the right to accept or refuse the proposed
treatment, and if he or she consents, has the right to revoke his or her
consent for any reason at any time.
(c) Before initiating the administration of psychotherapeutic drugs, or
physical restraints, or the prolonged use of a device that may lead to