Amended in Assembly April 23, 2013

Amended in Assembly March 21, 2013

California Legislature—2013–14 Regular Session

Assembly BillNo. 889


Introduced by Assembly Member Frazier

February 22, 2013


An act to add Section 1367.243 to the Health and Safety Code, and to add Section 10123.192 to the Insurance Code, relating to health care coverage.

LEGISLATIVE COUNSEL’S DIGEST

AB 889, as amended, Frazier. Health care coverage: prescription drugs.

Existing law, the Knox-Keene Health Care Service Plan Act of 1975, provides for the licensure and regulation of health care service plans by the Department of Managed Health Care and makes a willful violation of that act a crime. Existing law also provides for the regulation of health insurers by the Department of Insurance. Commonly referred to as utilization review, existing law governs the procedures that apply to every health care service plan and health insurer that prospectively, retrospectively, or concurrently reviews and approves, modifies, delays, or denies, based on medical necessity, requests by providers prior to, retrospectively, or concurrent with, providing health care services to enrollees or insureds, as specified.

Existing law also imposes various requirements and restrictions on health care service plans and health insurers, including, among other things, requiring a health care service plan that provides prescription drug benefits to maintain an expeditious process by which prescribing providers, as described, may obtain authorization for a medically necessary nonformulary prescription drug, according to certain procedures. Existing law also requires every health care service plan that provides prescription drug benefits that maintains one or more drug formularies to provide to members of the public, upon request, a copy of the most current list of prescription drugs on the formulary.

This bill would impose specified requirements on health care service plans or health insurers thatbegin delete restrictend deletebegin insert provide coverage forend insert medications pursuant to step therapy or fail first protocol. The bill would require a plan or insurer to have an expeditious process in place to authorize exceptions to step therapy when medically necessary and to conform effectively and efficiently to continuity of care. The bill would require the duration of any step therapy or fail first protocol to be consistent with up-to-datebegin delete evidence-based outcomes and current publishedend delete peer-reviewedbegin insert, scientific,end insert medical and pharmaceuticalbegin delete literatureend deletebegin insert evidenceend insert, and would, except under certain conditions, prohibit a health care service plan or health insurer from requiring that a patient try and fail on more than 2 medications before allowing the patient access to other medication prescribed by the prescribing provider, as specified.begin insert The bill, with regard to an enrollee or insured changing plans or policies, would prohibit a new plan or insurer from requiring the enrollee or insured to repeat step therapy when that person is already being treated for a medical condition by a prescription drug, as specified. The bill would specify that these provisions would not apply to accident-only, specified disease, hospital indemnity, Medicare supplement, dental-only, or vision-only contracts or policies.end insert

Because a willful violation of these requirements with respect to health care service plans would be a crime, the bill would impose a state-mandated local program.

The California Constitution requires the state to reimburse local agencies and school districts for certain costs mandated by the state. Statutory provisions establish procedures for making that reimbursement.

This bill would provide that no reimbursement is required by this act for a specified reason.

Vote: majority. Appropriation: no. Fiscal committee: yes. State-mandated local program: yes.

The people of the State of California do enact as follows:

P3    1

SECTION 1.  

Section 1367.243 is added to the Health and
2Safety Code
, to read:

3

1367.243.  

(a) Notwithstanding any other law, a health care
4service plan thatbegin delete restrictsend deletebegin insert provides coverage forend insert medications
5pursuant to step therapy or fail first protocol shall be subject to the
6following requirements:

7(1) The health care service plan shall have an expeditious
8process in place to authorize exceptions to step therapy when
9medically necessary and to conform effectively and efficiently to
10continuity of care.

11(2) The duration of any step therapy or fail first protocol shall
12be consistent with up-to-datebegin delete evidence-based outcomes and current
13publishedend delete
peer-reviewedbegin insert, scientific,end insert medical and pharmaceutical
14begin delete literatureend deletebegin insert evidenceend insert.

15(3) The health care service plan shall not require a patient to try
16and fail on more than two medications before allowing the patient
17access to the medication, or generically equivalent drug, prescribed
18by the prescribing provider, unless the FDA-approved label
19indication,begin insert peer-reviewed, scientific, medical and pharmaceutical
20evidence,end insert
or clinical research trials focusing on clinical outcomes,
21supports that more than two prior therapies should be used before
22using the requested medications.

begin insert

23(4) In circumstances where an enrollee is changing plans, the
24new plan shall not require the enrollee to repeat step therapy when
25that enrollee is already being treated for a medical condition by
26a prescription drug provided that the drug is appropriately
27prescribed and is considered safe and effective for the enrollee’s
28condition.

end insert

29(b) For purposes of this section, the following shall apply:

30(1) “Prescribing provider” shall include a provider who is
31authorized to write a prescription, as described in subdivision (a)
32of Section 4040 of the Business and Professions Code, to treat a
33medical condition of an enrollee.

34(2) “Generically equivalent drug” means a drug product with
35the same active chemical ingredients of the same strength, quantity,
36and dosage form, and of the same generic drug name, as determined
37by the United States Adopted Names Council and accepted by the
P4    1federal Food and Drug Administration, as those drug products
2having the same chemical ingredient.

3(c) This section does not prohibit a health care service plan from
4charging a subscriber or enrollee a copaymentbegin insert, coinsurance,end insert or a
5deductible for prescription drug benefits or from setting forth, by
6contract, limitations on maximum coverage of prescription drug
7benefits, provided that the copayments,begin insert coinsurance,end insert deductibles,
8or limitations are reported to, and held unobjectionable by, the
9director and communicated to the subscriber or enrollee pursuant
10to the disclosure provisions of Section 1363.

11(d) Nothing in this section shall be construed to require coverage
12of prescription drugs not in a plan’s drug formulary or to prohibit
13generically equivalent drugs or generic drug substitutions as
14authorized by Section 4073 of the Business and Professions Code.

begin insert

15(e) This section shall not apply to accident-only, specified
16disease, hospital indemnity, Medicare supplement, dental-only, or
17vision-only health care service plan contracts.

end insert
18

SEC. 2.  

Section 10123.192 is added to the Insurance Code, to
19read:

20

10123.192.  

(a) Notwithstanding any other law, a health insurer
21thatbegin delete restrictsend deletebegin insert provides coverage forend insert medications pursuant to step
22therapy or fail first protocol shall be subject to the following
23requirements:

24(1) The health insurer shall have an expeditious process in place
25to authorize exceptions to step therapy when medically necessary
26and to conform effectively and efficiently to continuity of care.

27(2) The duration of any step therapy or fail first protocol shall
28be consistent with up-to-datebegin delete evidence-based outcomes and current
29publishedend delete
peer-reviewedbegin insert, scientific,end insert medical and pharmaceutical
30begin delete literatureend deletebegin insert evidenceend insert.

31(3) The health insurer shall not require a patient to try and fail
32on more than two medications before allowing the patient access
33to the medication, or generically equivalent drug, prescribed by
34the prescribing provider, unless the FDA-approved label indication,
35begin insert peer-reviewed, scientific, medical and pharmaceutical evidence,end insert
36 or clinical research trials focusing on clinical outcomes, supports
37that more than two prior therapies should be used before using the
38requested medications.

begin insert

39(4) In circumstances where an insured is changing plans or
40policies, the new plan or policy shall not require the insured to
P5    1repeat step therapy when that insured is already being treated for
2a medical condition by a prescription drug provided that the drug
3is appropriately prescribed and is considered safe and effective
4for the insured’s condition.

end insert

5(b) For purposes of this section, the following shall apply:

6(1) “Prescribing provider” shall include a provider who is
7authorized to write a prescription, as described in subdivision (a)
8of Section 4040 of the Business and Professions Code, to treat a
9medical condition of an insured.

10(2) “Generically equivalent drug” means a drug product with
11the same active chemical ingredients of the same strength, quantity,
12 and dosage form, and of the same generic drug name, as determined
13by the United States Adopted Names Council and accepted by the
14federal Food and Drug Administration, as those drug products
15having the same chemical ingredient.

16(c) This section does not prohibit a health insurer from charging
17an insured or policyholder a copaymentbegin insert, coend insertbegin insertinsurance,end insert or a
18deductible for prescription drug benefits or from setting forth, by
19contract, limitations on maximum coverage of prescription drug
20benefits, provided that the copayments,begin insert coinsurances,end insert deductibles,
21or limitations are reported to, and held unobjectionable by, the
22commissioner and communicated to the insured or policyholder
23pursuant to the disclosure provisions of Section 10603.

24(d) Nothing in this section shall be construed to require coverage
25of prescription drugs not in an insurer’s drug formulary or to
26prohibit generically equivalent drugs or generic drug substitutions
27as authorized by Section 4073 of the Business and Professions
28Code.

begin insert

29(e) This section shall not apply to accident-only, specified
30disease, hospital indemnity, Medicare supplement, dental-only, or
31vision-only health insurance policies.

end insert
32

SEC. 3.  

No reimbursement is required by this act pursuant to
33Section 6 of Article XIII B of the California Constitution because
34the only costs that may be incurred by a local agency or school
35district will be incurred because this act creates a new crime or
36infraction, eliminates a crime or infraction, or changes the penalty
37for a crime or infraction, within the meaning of Section 17556 of
38the Government Code, or changes the definition of a crime within
P6    1the meaning of Section 6 of Article XIII B of the California
2 Constitution.



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