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A BILL TO BE ENTITLED
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AN ACT
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relating to reimbursement under the state Medicaid program for |
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health care services associated with certain adverse events. |
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BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS: |
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SECTION 1. Subchapter B, Chapter 32, Human Resources Code, |
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is amended by adding Section 32.0312 to read as follows: |
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Sec. 32.0312. REIMBURSEMENT PROHIBITED FOR SERVICES |
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ASSOCIATED WITH PREVENTABLE ADVERSE EVENTS. (a) In this section: |
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(1) "Health care facility" means a hospital or |
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ambulatory surgical center. |
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(2) "Health care provider" means a physician or health |
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care facility. |
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(3) "Infant" means a child younger than one year of |
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age. |
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(4) "Serious disability" means: |
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(A) a physical or mental impairment that |
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substantially limits one or more major life activities of an |
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individual such as seeing, hearing, speaking, walking, or |
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breathing, or a loss of a bodily function, if the impairment or loss |
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lasts more than seven days or is still present at the time of |
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discharge from an inpatient health care facility; or |
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(B) loss of a body part. |
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(5) "Serious injury" means a bodily injury that |
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results in: |
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(A) death; |
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(B) permanent and serious impairment of an |
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important bodily function; or |
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(C) permanent and significant disfigurement. |
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(b) The department may not provide reimbursement under the |
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medical assistance program to a health care provider for a health |
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care service provided in association with a preventable adverse |
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event involving a recipient of medical assistance while in the |
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provider's care, including a health care service provided as a |
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result of or to correct the consequences of a preventable adverse |
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event. |
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(c) For purposes of this section, a preventable adverse |
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event is any of the following events involving a recipient of |
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medical assistance: |
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(1) surgery performed on the wrong body part that is |
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not consistent with the documented informed consent for that |
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recipient, excluding a situation requiring prompt action that |
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occurs in the course of surgery or an urgent situation that |
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precludes obtaining informed consent; |
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(2) surgery performed on the wrong person; |
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(3) the wrong surgical procedure performed on the |
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recipient that is not consistent with the documented informed |
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consent for that recipient, excluding a situation requiring prompt |
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action that occurs in the course of surgery or an urgent situation |
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that precludes obtaining informed consent; |
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(4) the unintended retention of a foreign object in |
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the recipient after surgery or another procedure; |
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(5) death during or immediately after surgery if the |
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recipient would be classified as a normal, healthy patient under |
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guidelines published by a national association of |
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anesthesiologists; |
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(6) death or serious disability caused by the use of a |
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contaminated drug, device, or biologic provided by a health care |
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provider if the contamination is the result of a generally |
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detectable contaminant in drugs, devices, or biologics regardless |
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of the source of the contamination or product; |
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(7) death or serious disability caused by the use or |
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function of a device during the recipient's care in which the device |
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is used for a function other than as intended; |
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(8) death or serious disability caused by an |
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intravascular air embolism that occurs while the recipient is |
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receiving care in a health care facility, excluding a death |
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associated with a neurological procedure known to present a high |
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risk of intravascular air emoblism; |
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(9) an infant being discharged to the wrong person; |
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(10) death or serious disability associated with the |
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recipient's disappearance for more than four hours, excluding the |
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death or serious disability of an adult recipient who has |
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decision-making capacity; |
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(11) suicide or attempted suicide resulting in serious |
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disability while the recipient is receiving care in a health care |
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facility if the suicide or attempted suicide is due to the |
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recipient's actions after admission to the facility, excluding a |
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death resulting from a self-inflicted injury that was the reason |
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for the recipient's admission to the facility; |
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(12) death or serious disability caused by a |
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medication error, including an error involving the wrong drug, |
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wrong dose, wrong patient, wrong time, wrong rate, wrong |
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preparation, or wrong route of administration; |
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(13) death or serious disability caused by a hemolytic |
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reaction resulting from the administration of ABO- or |
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HLA-incompatible blood or blood products; |
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(14) subject to Subsection (d), death or serious |
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disability caused by labor or delivery in a low-risk pregnancy |
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while the recipient is receiving care in a health care facility, |
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including death or serious disability occurring not later than 42 |
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days after the delivery date; |
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(15) death or serious disability directly related to |
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hypoglycemia, the onset of which occurs while the recipient is |
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receiving care in a health care facility; |
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(16) death or serious disability, including |
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kernicterus, caused by failure to identify and treat |
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hyperbilirubinemia in a neonate before discharge from a health care |
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facility; |
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(17) stage three or four pressure ulcers acquired |
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after admission to a health care facility, excluding progression |
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from stage two to stage three if stage two was recognized on |
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admission; |
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(18) death or serious disability resulting from spinal |
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manipulative therapy; |
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(19) death or serious disability caused by an electric |
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shock while the recipient is receiving care in a health care |
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facility, excluding an event involving a planned treatment such as |
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electric countershock; |
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(20) an incident in which a line designated for oxygen |
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or other gas to be delivered to the recipient contains the wrong gas |
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or is contaminated by a toxic substance; |
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(21) death or serious disability caused by a burn |
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incurred from any source while the recipient is receiving care in a |
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health care facility; |
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(22) death or serious disability caused by a fall |
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while the recipient is receiving care in a health care facility; |
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(23) death or serious disability caused by the use of a |
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restraint or bed rail while the recipient is receiving care in a |
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health care facility; |
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(24) an instance of care for the recipient ordered or |
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provided by an individual impersonating a physician, nurse, |
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pharmacist, or other licensed health care professional; |
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(25) abduction of the recipient from a health care |
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facility; |
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(26) sexual assault of the recipient within or on the |
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grounds of a health care facility; |
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(27) death or significant injury resulting from a |
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physical assault of the recipient that occurs within or on the |
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grounds of a health care facility; and |
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(28) artificial insemination with the wrong donor |
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sperm or donor egg. |
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(d) For purposes of Subsection (c)(14), the death of a |
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recipient of medical assistance resulting from pulmonary or |
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amniotic fluid embolism, acute fatty liver of pregnancy, or |
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cardiomyopathy during the course of labor or delivery is not |
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considered a preventable adverse event. |
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(e) The department's refusal to reimburse a health care |
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provider under this section does not in itself create civil |
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liability and is not subject to discovery or admissible in any civil |
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action against the provider. |
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SECTION 2. Not later than November 1, 2009, the executive |
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commissioner of the Health and Human Services Commission shall |
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adopt rules necessary to implement Section 32.0312, Human Resources |
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Code, as added by this Act. |
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SECTION 3. Section 32.0312, Human Resources Code, as added |
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by this Act, applies only to a preventable adverse event occurring |
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on or after the effective date of the rules adopted by the executive |
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commissioner of the Health and Human Services Commission under |
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Section 2 of this Act. |
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SECTION 4. If before implementing any provision of this Act |
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a state agency determines that a waiver or authorization from a |
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federal agency is necessary for implementation of that provision, |
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the agency affected by the provision shall request the waiver or |
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authorization and may delay implementing that provision until the |
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waiver or authorization is granted. |
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SECTION 5. This Act takes effect September 1, 2009. |