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A BILL TO BE ENTITLED
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AN ACT
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relating to consent requirements for the prescription of certain |
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psychoactive medications to residents of nursing facilities and |
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related institutions. |
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BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS: |
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SECTION 1. Section 242.505, Health and Safety Code, is |
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amended by amending Subsection (c) and adding Subsections (g), (h), |
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and (i) to read as follows: |
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(c) Subject to Subsection (g), consent [Consent] to the |
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prescription of psychoactive medication given by a resident or by a |
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person authorized by law to consent on behalf of the resident is |
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valid only if: |
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(1) the consent is given voluntarily and without |
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coercive or undue influence; |
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(2) the person prescribing the medication or that |
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person's designee provided the following information, in a standard |
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format approved by the department, to the resident and, if |
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applicable, to the person authorized by law to consent on behalf of |
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the resident: |
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(A) the specific condition to be treated; |
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(B) the beneficial effects on that condition |
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expected from the medication; |
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(C) the probable clinically significant side |
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effects and risks associated with the medication; and |
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(D) the proposed course of the medication; |
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(3) the resident and, if appropriate, the person |
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authorized by law to consent on behalf of the resident are informed |
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in writing that consent may be revoked; and |
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(4) the consent is evidenced in the resident's |
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clinical record by: |
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(A) a signed form prescribed by the facility or |
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by a statement of the person prescribing the medication or that |
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person's designee that documents that consent was given by the |
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appropriate person and the circumstances under which the consent |
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was obtained; and |
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(B) the original or a copy of the written consent |
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required by Subsection (g), if applicable. |
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(g) In addition to the requirements of Subsection (c), |
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consent to the prescription of an antipsychotic or neuroleptic |
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medication is valid only if: |
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(1) the consent to the prescription of that medication |
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is given in writing by a resident or by a person authorized by law to |
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consent on behalf of the resident; and |
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(2) the person prescribing the medication or that |
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person's designee provides the information listed in Subsection |
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(h), in a standard format approved by the department, to the |
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resident and, if applicable, to the person authorized by law to |
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consent on behalf of the resident. |
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(h) The information required under Subsection (g)(2) must |
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include: |
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(1) the nature of the medication; |
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(2) the means of administering the medication, |
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including: |
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(A) the dosage; |
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(B) the administration schedule; |
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(C) the method of delivery; and |
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(D) the expected duration of administration; |
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(3) the right of the resident or a person authorized by |
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law to consent on behalf of the resident to refuse medication; |
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(4) the potential medical and clinical consequences of |
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refusing the medication; and |
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(5) an explanation of treatment alternatives and the |
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right of the resident or a person authorized by law to consent on |
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behalf of the resident to choose such treatments. |
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(i) In addition to other requirements of this section, |
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before administering an antipsychotic or neuroleptic medication, |
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the facility shall inform the resident or a person authorized to |
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consent on behalf of the resident about facility policies and |
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procedures relating to consent and, on request of the resident or |
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authorized person, shall make available a written copy of those |
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policies and procedures. |
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SECTION 2. This Act takes effect September 1, 2019. |