Bill Text: TX HB1464 | 2017-2018 | 85th Legislature | Comm Sub
Bill Title: Relating to step therapy protocols required by a health benefit plan in connection with prescription drug coverage.
Spectrum: Bipartisan Bill
Status: (Introduced - Dead) 2017-05-08 - Laid on the table subject to call [HB1464 Detail]
Download: Texas-2017-HB1464-Comm_Sub.html
85R23121 PMO-F | |||
By: Bonnen of Galveston, Parker, | H.B. No. 1464 | ||
Thompson of Harris, Bernal, Villalba, | |||
et al. | |||
Substitute the following for H.B. |
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relating to step therapy protocols required by a health benefit | ||
plan in connection with prescription drug coverage. | ||
BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS: | ||
SECTION 1. Section 1369.051, Insurance Code, is amended by | ||
amending Subdivision (1) and adding Subdivisions (1-a), (1-b), and | ||
(5) to read as follows: | ||
(1) "Clinical practice guideline" means a statement | ||
systematically developed by a multidisciplinary panel of experts | ||
composed of physicians and, as necessary, other health care | ||
providers to assist a patient or health care provider in making a | ||
decision about appropriate health care for a specific clinical | ||
circumstance or condition. | ||
(1-a) "Clinical review criteria" means the written | ||
screening procedures, decision abstracts, clinical protocols, and | ||
clinical practice guidelines used by a health benefit plan issuer, | ||
utilization review organization, or independent review | ||
organization to determine the medical necessity and | ||
appropriateness or the experimental or investigational nature of a | ||
health care service or prescription drug. | ||
(1-b) "Drug formulary" means a list of drugs: | ||
(A) for which a health benefit plan provides | ||
coverage; | ||
(B) for which a health benefit plan issuer | ||
approves payment; or | ||
(C) that a health benefit plan issuer encourages | ||
or offers incentives for physicians to prescribe. | ||
(5) "Step therapy protocol" means a protocol that | ||
requires an enrollee to use a prescription drug or sequence of | ||
prescription drugs other than the drug that the enrollee's | ||
physician recommends for the enrollee's treatment before the health | ||
benefit plan provides coverage for the recommended drug. | ||
SECTION 2. Subchapter B, Chapter 1369, Insurance Code, is | ||
amended by adding Sections 1369.0545 and 1369.0546 to read as | ||
follows: | ||
Sec. 1369.0545. STEP THERAPY PROTOCOLS. (a) A health | ||
benefit plan issuer that requires a step therapy protocol before | ||
providing coverage for a prescription drug must establish, | ||
implement, and administer the step therapy protocol in accordance | ||
with clinical review criteria readily available to the health care | ||
industry. The health benefit plan issuer shall take into account | ||
the needs of atypical patient populations and diagnoses in | ||
establishing the clinical review criteria. The clinical review | ||
criteria: | ||
(1) must consider generally accepted clinical | ||
practice guidelines that are: | ||
(A) developed and endorsed by a | ||
multidisciplinary panel of experts described by Subsection (b); | ||
(B) based on high quality studies, research, and | ||
medical practice; | ||
(C) created by an explicit and transparent | ||
process that: | ||
(i) minimizes bias and conflicts of | ||
interest; | ||
(ii) explains the relationship between | ||
treatment options and outcomes; | ||
(iii) rates the quality of the evidence | ||
supporting the recommendations; and | ||
(iv) considers relevant patient subgroups | ||
and preferences; and | ||
(D) updated at appropriate intervals after a | ||
review of new evidence, research, and treatments; or | ||
(2) if clinical practice guidelines described by | ||
Subdivision (1) are not reasonably available, may be based on | ||
peer-reviewed publications developed by independent experts, which | ||
may include physicians, with expertise applicable to the relevant | ||
health condition. | ||
(b) A multidisciplinary panel of experts composed of | ||
physicians and, as necessary, other health care providers that | ||
develops and endorses clinical practice guidelines under | ||
Subsection (a)(1) must manage conflicts of interest by: | ||
(1) requiring each member of the panel's writing or | ||
review group to: | ||
(A) disclose any potential conflict of interest, | ||
including a conflict of interest involving an insurer, health | ||
benefit plan issuer, or pharmaceutical manufacturer; and | ||
(B) recuse himself or herself in any situation in | ||
which the member has a conflict of interest; | ||
(2) using a methodologist to work with writing groups | ||
to provide objectivity in data analysis and the ranking of evidence | ||
by preparing evidence tables and facilitating consensus; and | ||
(3) offering an opportunity for public review and | ||
comment. | ||
(c) Subsection (b) does not apply to a panel or committee of | ||
experts, including a pharmacy and therapeutics committee, | ||
established by a health benefit plan issuer or a pharmacy benefit | ||
manager that advises the health benefit plan issuer or pharmacy | ||
benefit manager regarding drugs or formularies. | ||
Sec. 1369.0546. STEP THERAPY PROTOCOL EXCEPTION REQUESTS. | ||
(a) A health benefit plan issuer shall establish a process in a | ||
user-friendly format that is readily accessible to a patient and | ||
prescribing provider, in the health benefit plan's formulary | ||
document and otherwise, through which an exception request under | ||
this section may be submitted by the provider. | ||
(b) A prescribing provider on behalf of a patient may submit | ||
to the patient's health benefit plan issuer a written request for an | ||
exception to a step therapy protocol required by the patient's | ||
health benefit plan. The provider shall submit the request on the | ||
standard form prescribed by the commissioner under Section | ||
1369.304. | ||
(c) A health benefit plan issuer shall grant a written | ||
request under Subsection (b) if the request includes the | ||
prescribing provider's written statement, with supporting | ||
documentation, stating that: | ||
(1) the drug required under the step therapy protocol: | ||
(A) is contraindicated; | ||
(B) will likely cause an adverse reaction in or | ||
physical or mental harm to the patient; or | ||
(C) is expected to be ineffective based on the | ||
known clinical characteristics of the patient and the known | ||
characteristics of the prescription drug regimen; | ||
(2) the patient previously discontinued taking the | ||
drug required under the step therapy protocol, or another | ||
prescription drug in the same pharmacologic class or with the same | ||
mechanism of action as the required drug, while under the health | ||
benefit plan currently in force or while covered under another | ||
health benefit plan because the drug was not effective or had a | ||
diminished effect or because of an adverse event; | ||
(3) the drug required under the step therapy protocol | ||
is not in the best interest of the patient, based on clinical | ||
appropriateness, because the patient's use of the drug is expected | ||
to: | ||
(A) cause a significant barrier to the patient's | ||
adherence to or compliance with the patient's plan of care; | ||
(B) worsen a comorbid condition of the patient; | ||
or | ||
(C) decrease the patient's ability to achieve or | ||
maintain reasonable functional ability in performing daily | ||
activities; or | ||
(4)(A) the drug that is subject to the step therapy | ||
protocol was prescribed for the patient's condition; | ||
(B) the patient: | ||
(i) received benefits for the drug under | ||
the health benefit plan currently in force or a previous health | ||
benefit plan; and | ||
(ii) is stable on the drug; and | ||
(C) the change in the patient's prescription drug | ||
regimen required by the step therapy protocol is expected to be | ||
ineffective or cause harm to the patient based on the known clinical | ||
characteristics of the patient and the known characteristics of the | ||
required prescription drug regimen. | ||
(d) Except as provided by Subsection (e), if a health | ||
benefit plan issuer does not deny an exception request described by | ||
Subsection (c) before 72 hours after the health benefit plan issuer | ||
receives the request, the request is considered granted. | ||
(e) If an exception request described by Subsection (c) also | ||
states that the prescribing provider reasonably believes that | ||
denial of the request makes the death of or serious harm to the | ||
patient probable, the request is considered granted if the health | ||
benefit plan issuer does not deny the request before 24 hours after | ||
the health benefit plan issuer receives the request. | ||
(f) The denial of an exception request under this section is | ||
an adverse determination for purposes of Section 4201.002 and is | ||
subject to appeal under Subchapters H and I, Chapter 4201. | ||
SECTION 3. Section 4201.357, Insurance Code, is amended by | ||
adding Subsection (a-2) to read as follows: | ||
(a-2) An adverse determination under Section 1369.0546 is | ||
entitled to an expedited appeal. The physician or, if appropriate, | ||
other health care provider deciding the appeal must consider | ||
atypical diagnoses and the needs of atypical patient populations. | ||
SECTION 4. Section 4202.003, Insurance Code, is amended to | ||
read as follows: | ||
Sec. 4202.003. REQUIREMENTS REGARDING TIMELINESS OF | ||
DETERMINATION. The standards adopted under Section 4202.002 must | ||
require each independent review organization to make the | ||
organization's determination: | ||
(1) for a life-threatening condition as defined by | ||
Section 4201.002, [ |
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intravenous infusions for which the patient is receiving benefits | ||
under the health insurance policy, or a review of a step therapy | ||
protocol exception request under Section 1369.0546, not later than | ||
the earlier of the third day after the date the organization | ||
receives the information necessary to make the determination or, | ||
with respect to: | ||
(A) a review of a health care service provided to | ||
a person with a life-threatening condition eligible for workers' | ||
compensation medical benefits, the eighth day after the date the | ||
organization receives the request that the determination be made; | ||
or | ||
(B) a review of a health care service other than a | ||
service described by Paragraph (A), the third day after the date the | ||
organization receives the request that the determination be made; | ||
or | ||
(2) for a situation other than a situation described | ||
by Subdivision (1), not later than the earlier of: | ||
(A) the 15th day after the date the organization | ||
receives the information necessary to make the determination; or | ||
(B) the 20th day after the date the organization | ||
receives the request that the determination be made. | ||
SECTION 5. The changes in law made by this Act apply only to | ||
a health benefit plan that is delivered, issued for delivery, or | ||
renewed on or after January 1, 2018. A health benefit plan | ||
delivered, issued for delivery, or renewed before January 1, 2018, | ||
is governed by the law as it existed immediately before the | ||
effective date of this Act, and that law is continued in effect for | ||
that purpose. | ||
SECTION 6. This Act takes effect September 1, 2017. |