Amended in Senate June 15, 2014

Amended in Senate June 12, 2014

California Legislature—2013–14 Regular Session

Assembly BillNo. 1474


Introduced by Committee on Budget (Skinner (Chair), Bloom, Campos, Chesbro, Dababneh, Daly, Dickinson, Gordon, Jones-Sawyer, Mullin, Muratsuchi, Nazarian, Rodriguez, Stone, Ting, and Weber)

January 9, 2014


An act to amend Section 1374.34 of, to add Chapter 13.6 (commencing with Section 121287) to Part 4 of Division 105 of, and to add and repeal Section 128225.5 of, the Health and Safety Code, to amend Sections 14105.33, 14105.436, and 14105.86 of, to amend, repeal, and add Section 14593 of, and to add Sections 14087.9730 and 14132.56 to, the Welfare and Institutions Code, relating to health, and making an appropriation therefor, to take effect immediately, bill related to the budget.

LEGISLATIVE COUNSEL’S DIGEST

AB 1474, as amended, Committee on Budget. Health.

(1) Existing law makes provisions for programs relating to treatment of persons with human immunodeficiency virus (HIV) and the acquired immunodeficiency syndrome (AIDS). Under existing law, the Office of AIDS, in the State Department of Public Health, is the lead agency within the state responsible for coordinating state programs, services, and activities relating to HIV and AIDS, and AIDS-related conditions.

This bill would authorize the department to implement up to 4 demonstration projects that may operate for a period of up to 2 years to allow for innovative, evidence-based approaches to provide outreach, HIV and Hepatitis C screenings, and linkage to, and retention in, quality health care for the most vulnerable and underserved individuals with a high risk for HIV infection. The bill would require, upon appropriation in the annual Budget Act, the department to award funding, on a competitive basis, to a community-based organization or local health jurisdiction to operate a demonstration project, as specified. The bill would require the department, at the conclusion of the demonstration projects, to review the effectiveness of each demonstration project and determine whether the demonstration project model can be implemented on a statewide basis.

(2) Existing law, the Song-Brown Health Care Workforce Training Act, establishes a state medical contract program with accredited medical schools, programs that train primary care physician’s assistants, programs that train primary care nurse practitioners and registered nurses, hospitals, and other health care delivery systems.

Existing law establishes the California Healthcare Workforce Policy Commission to, among other things, identify specific areas of the state where unmet priority needs for primary care family physicians and registered nurses exist and to make recommendations to the Director of Statewide Health Planning and Development with regard to the funding of specific programs. Existing law requires the director to select and contract on behalf of the state with accredited medical schools and the other above-described entities for the purpose of, among other things, training medical students and residents in the specialty of family practice, subject to criteria established by the commission.

This bill would require, only until January 1, 2018, the director to select and contract on behalf of the state with accredited primary care or family medicine residency programs for the purpose of providing grants to support newly created residency positions, and would require the commission to review and make recommendations to the director concerning the provision of those grants. These provisions would be operative only if funds are appropriated for these purposes in the Budget Act of 2014.

(3) Existing law provides for the Medi-Cal program, which is administered by the State Department of Health Care Services, under which qualified low-income individuals receive health care services. The Medi-Cal program is, in part, governed and funded by federal Medicaid Program provisions. Under existing law, one of the methods by which Medi-Cal services are provided is pursuant to contracts with various types of managed care plans.

This bill would require the department to establish a 3-year pilot program in the County of Los Angeles that enables school districts to allow students enrolled in Medi-Cal managed care plans the ability to receive vision care services at the school site through the use of a mobile vision service provider. The bill would generally require the Medi-Cal managed care plans in the County of Los Angeles to, in consultation with the department, jointly identify and develop standards and participation criteria that the participating mobile vision service provider would be required to meet in order to be deemed qualified to participate in the pilot program. The bill would authorize the Director of Health Care Services to extend the pilot program to Medi-Cal managed care plans in other counties and applicable local jurisdictions, as specified.

Existing law provides for a schedule of benefits under the Medi-Cal program, which includes Early and Periodic Screening, Diagnosis, and Treatment for any individual under 21 years of age, consistent with the requirements of federal law.

This bill would provide, only to the extent required by the federal government and effective no sooner than required by the federal government, that behavioral health treatment (BHT), as defined, is a covered service for individuals under 21 years of age, as specified. The bill would require that the department only implement these provisions, or continue to implement these provisions, if the department receives all necessary federal approvals to obtain federal funds for the service, the department seeksbegin delete and obtainsend delete an appropriation that would provide the necessary state funding estimated to be required for the applicable fiscal year, and the department consults with stakeholders. The bill would state that it is the intent of the Legislature, to the extent the federal government requires BHT to be a covered Medi-Cal service, that the department seek statutory authority to implement this new benefit.

Existing law also includes in the schedule of benefits for Medi-Cal prescribed drugs subject to the Medi-Cal list of contract drugs. Existing law authorizes the department to enter into contracts with manufacturers of single-source and multiple-source drugs, on a bid or nonbid basis, for drugs from each major therapeutic category. Existing law requires these contracts to provide for a state rebate to be remitted to the department quarterly. Existing law also requires pharmaceutical manufacturers to provide to the department a state rebate for any drug products that have been added to the Medi-Cal list of contract drugs related to drugs used to treat AIDS and cancer. Existing law requires that the utilization data to determine these rebates exclude data from specified entities and capitated plans. Existing law also requires the department to collect a state rebate for blood factors reimbursed by specified programs.

This bill would make those data exclusions inoperative when the department takes specified actions, and would, commencing July 1, 2014, specify that utilization data used to determine the rebates include data from all health plans with specified exceptions. The bill would require the department to develop coverage policies, in consultation with clinical experts, Medi-Cal managed care plans, and other stakeholders, for prescription drugs that the department reimburses managed care plans through separate capitated rate payments or other supplemental payments.

Existing federal law establishes the Program of All-Inclusive Care for the Elderly (PACE), which provides specified services for older individuals so that they may continue living in the community. Federal law authorizes states to implement the PACE program as a Medicaid state option. Existing law authorizes the department to enter into contracts with up to 15 PACE organizations, as defined, to implement the PACE program, as specified. Existing law requires the department to establish capitation rates paid to each PACE organization at no less than 90% of the fee-for-service equivalent cost, including the department’s cost of administration, that the department estimates would be payable for all services covered under the PACE organization contract if all those services were to be furnished to Medi-Cal beneficiaries under the fee-for-service program.

This bill would instead require, on and after April 1, 2015, that the department establish capitation rates paid to each PACE organization at no less than 95% of that amount.

(4) Existing law, the Knox-Keene Health Care Service Plan Act of 1975 (Knox-Keene Act), provides for the licensure and regulation of health care service plans by the Department of Managed Health Care and makes a willful violation of the Knox-Keene Act a crime. Existing law establishes the Independent Medical Review System to make determinations when a health care service that is eligible for coverage has been denied, modified, or delayed by a decision of the plan, or by one of its contracting providers, in whole or in part due to a finding that the service is not medically necessary. Existing law requires the Director of the Department of Managed Health Care to review individual cases submitted for independent medical review to determine whether any enforcement actions, including penalties, may be appropriate.

This bill would prohibit the director from taking an enforcement action against a plan if the plan provides prescription drugs to a Medi-Cal beneficiary pursuant to State Department of Health Care Services guidelines.

(5) This bill would state the intent of the Legislature that the State Department of Health Care Services continue to monitor access to and utilization of Medi-Cal services in the fee-for-service and managed care settings during the 2014-15 fiscal year, as specified and would require the department to use this information to evaluate current reimbursement levels for Medi-Cal providers and to make recommendations for targeted changes to the extent the department finds those changes appropriate.

(6) Item 4300-101-0001 of the Budget Act of 2009, as added by Chapter 1 of the 3rd Extraordinary Session, appropriated $24,553,000 to the State Department of Developmental Services for the support of the department, payable from the General Fund. Item 4300-101-0001 of the Budget Act of 2010, as added by Chapter 712 of the Statutes of 2010, appropriated $24,391,000 to the department for its support, payable from the General Fund.

This bill would reappropriate the balances of those amounts to the department, subject to specified purposes, and would provide that those funds would be available for liquidation until June 30, 2015.

The bill also would, for the 2014-15 fiscal year, appropriate $3,200,000 from the Major Risk Medical Insurance Fund to the State Department of Health Care Services for allocation to health benefit plans that meet specified requirements.

This bill would, for the 2014-15 fiscal year, appropriate $3,750,000 from the Major Risk Medical Insurance Fund to the State Department of Health Care Services for purposes of electronic health records technical assistance in accordance with the State Medicaid Health Information Technology Plan, as specified.

(7) This bill would declare that it is to take effect immediately as a bill providing for appropriations related to the Budget Bill.

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

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

P6    1

SECTION 1.  

Section 1374.34 of the Health and Safety Code
2 is amended to read:

3

1374.34.  

(a) Upon receiving the decision adopted by the
4director pursuant to Section 1374.33 that a disputed health care
5service is medically necessary, the plan shall promptly implement
6the decision. In the case of reimbursement for services already
7rendered, the plan shall reimburse the provider or enrollee,
8whichever applies, within five working days. In the case of services
9not yet rendered, the plan shall authorize the services within five
10working days of receipt of the written decision from the director,
11or sooner if appropriate for the nature of the enrollee’s medical
12condition, and shall inform the enrollee and provider of the
13authorization in accordance with the requirements of paragraph
14(3) of subdivision (h) of Section 1367.01.

15(b) A plan shall not engage in any conduct that has the effect
16of prolonging the independent review process. The engaging in
17that conduct or the failure of the plan to promptly implement the
18decision is a violation of this chapter and, in addition to any other
19fines, penalties, and other remedies available to the director under
20this chapter, the plan shall be subject to an administrative penalty
21of not less than five thousand dollars ($5,000) for each day that
22the decision is not implemented. The administrative penalties shall
23be paid to the Managed Care Administrative Fines and Penalties
24Fund and shall be used for the purposes specified in Section
251341.45.

26(c) The director shall require the plan to promptly reimburse
27the enrollee for any reasonable costs associated with those services
28when the director finds that the disputed health care services were
29a covered benefit under the terms and conditions of the health care
30service plan contract, and the services are found by the independent
31medical review organization to have been medically necessary
32pursuant to Section 1374.33, and either the enrollee’s decision to
33secure the services outside of the plan provider network was
34reasonable under the emergency or urgent medical circumstances,
35or the health care service plan contract does not require or provide
36prior authorization before the health care services are provided to
37the enrollee.

P7    1(d) In addition to requiring plan compliance regarding
2subdivisions (a), (b), and (c) the director shall review individual
3cases submitted for independent medical review to determine
4whether any enforcement actions, including penalties, may be
5appropriate. In particular, where substantial harm, as defined in
6Section 3428 of the Civil Code, to an enrollee has already occurred
7because of the decision of a plan, or one of its contracting
8providers, to delay, deny, or modify covered health care services
9that an independent medical review determines to be medically
10necessary pursuant to Section 1374.33, the director shall impose
11penalties.

12(e) Pursuant to Section 1368.04, the director shall perform an
13annual audit of independent medical review cases for the dual
14purposes of education and the opportunity to determine if any
15investigative or enforcement actions should be undertaken by the
16department, particularly if a plan repeatedly fails to act promptly
17and reasonably to resolve grievances associated with a delay,
18denial, or modification of medically necessary health care services
19when the obligation of the plan to provide those health care services
20to enrollees or subscribers is reasonably clear.

21(f) A plan’s provision of prescription drugs to a Medi-Cal
22beneficiary pursuant to paragraph (5) of subdivision (b) of Section
2314105.33 of the Welfare and Institutions Code and in accordance
24with the State Department of Health Care Services coverage
25policies shall not be a ground for an enforcement action. Nothing
26in this article is intended to limit a plan’s responsibility to provide
27medically necessary health care services pursuant to this chapter.

28

SEC. 2.  

Chapter 13.6 (commencing with Section 121287) is
29added to Part 4 of Division 105 of the Health and Safety Code, to
30read:

31 

32Chapter  13.6. Public Health Demonstration Projects
33

 

34

121287.  

(a) There are hereby established public health
35demonstration projects to allow for innovative, evidence-based
36approaches to provide outreach, HIV and Hepatitis C screenings,
37and linkage to, and retention in, quality health care for the most
38vulnerable and underserved individuals with a high risk for HIV
39infection.

P8    1(b) The demonstration projects may operate for a period of up
2to two years. The department shall implement up to four
3demonstration projects. The demonstration projects shall be
4designed to be capable of replication and expansion on a statewide
5basis.

6(c) After conclusion of the demonstration projects, the
7department shall review the effectiveness of each demonstration
8project and make a determination of whether the demonstration
9project model can be implemented on a statewide basis.

10

121288.  

Upon an appropriation for this purpose in the annual
11Budget Act, the department shall award funding, on a competitive
12basis, to a community-based organization or local health
13jurisdiction to operate a demonstration project pursuant to this
14chapter. The department shall determine the funding levels of each
15demonstration project based on scope and geographic area. An
16applicant shall demonstrate each of the following qualifications:

17(a) Leadership on access to HIV care and testing issues and
18experience addressing the needs of highly marginalized populations
19in accessing medical and HIV care and support.

20(b) Experience with the target population or relationships with
21community-based organizations or nongovernmental organizations,
22or both, that demonstrate expertise, history, and credibility working
23successfully in engaging the target population.

24(c) Experience working with nontraditional collaborators who
25work within and beyond the field of HIV/AIDS education and
26outreach, including areas of reproductive health, housing,
27immigration, and mental health.

28(d) Strong relationships with community-based HIV health care
29providers that have the trust of the targeted populations.

30(e) Strong relationships with the state and local health
31departments.

32(f) Capacity to coordinate a communitywide planning phase
33involving multiple community collaborators.

34(g) Experience implementing evidence-based programs or
35generating innovative strategies, or both, with at least preliminary
36evidence of program effectiveness.

37(h) Administrative systems and accountability mechanisms for
38grant management.

39(i) Capacity to participate in evaluation activities.

P9    1(j) Strong communication systems that are in place to participate
2in public relations activities.

3

121289.  

Each demonstration project shall prepare and
4disseminate information regarding best practices for, and the
5lessons learned regarding, providing outreach and education to the
6most vulnerable and underserved individuals with a high risk for
7HIV infection for use by providers, the Office of AIDS, State
8Department of Public Health, federal departments and agencies,
9including the Department of Health and Human Services, and other
10national HIV/AIDS groups.

11

SEC. 3.  

Section 128225.5 is added to the Health and Safety
12Code
, to read:

13

128225.5.  

(a) The commission shall review and make
14recommendations to the Director of the Office of Statewide Health
15Planning and Development concerning the provision of grants
16pursuant to this section. In making recommendations, the
17commission shall give priority to residency programs that
18demonstrate all of the following:

19(1)  That the grant will be used to support new primary care
20physician slots.

21(2)  That priority in filling the position shall be given to
22physicians who have graduated from a California-based medical
23school.

24(3)  That the new primary care physician residency positions
25have been, or will be, approved by the Accreditation Council for
26Graduate Medical Education prior to the first distribution of grant
27funds.

28(b) The director shall do both of the following:

29(1) Determine whether the residency programs recommended
30by the commission meet the standards established by this section.

31(2) Select and contract on behalf of the state with accredited
32primary care or family medicine residency programs for the
33purpose of providing grants for the support of newly created
34residency positions.

35(c) This section does not apply to funding appropriated in the
36annual Budget Act for the Song-Brown Health Care Workforce
37Training Act (Article 1 (commencing with Section 128200)).

38(d) This section shall be operative only if funds are appropriated
39in the Budget Act of 2014 for the purposes described in this section.

P10   1(e) This section shall remain in effect only until January 1, 2018,
2and as of that date is repealed, unless a later enacted statute, that
3is enacted before January 1, 2018, deletes or extends that date.

4

SEC. 4.  

Section 14087.9730 is added to the Welfare and
5Institutions Code
, immediately following Section 14087.9725, to
6read:

7

14087.9730.  

(a) In an effort to determine whether children’s
8access to, and utilization of, vision care services can be increased
9by providing vision care services at schools, the department shall
10establish a pilot program in the County of Los Angeles that enables
11school districts to allow students enrolled in Medi-Cal managed
12care plans to receive vision care services at the school site through
13the use of a mobile vision service provider. The vision care services
14available under this pilot program are limited to vision
15examinations and providing eyeglasses.

16(b) The Medi-Cal managed care plans in the County of Los
17Angeles shall jointly identify and develop standards and
18participation criteria that the participating mobile vision service
19provider shall meet in order to be deemed qualified to participate
20in the pilot program, in consultation with the department and
21consistent with any applicable federal requirements governing
22Medicaid managed care contracts. In the event the Medi-Cal
23managed care plans have not developed standards and participation
24criteria by January 1, 2015, or by the scheduled start date of the
25pilot program if later, the department shall determine the standards
26and participating criteria for purposes of this pilot program.

27(c) This section shall not be construed to preclude Los Angeles
28County school district students not enrolled in Medi-Cal managed
29care from accessing vision care services from a mobile vision
30service provider participating in this pilot program.

31(d) Under the pilot program, if a school district in the County
32of Los Angeles enters into a written memorandum of understanding
33with a mobile vision care service provider allowing the provider
34to offer the vision care services described in this section to students,
35all of the following shall apply:

36(1) The two Medi-Cal managed care plans in the County of Los
37Angeles shall contract with one or more mobile vision care service
38providers that meets the standards and participation criteria
39developed pursuant to subdivision (b) for the delivery of those
40vision care services to any student enrolled in the Medi-Cal
P11   1managed care plan who chooses to receive his or her vision care
2services from the provider at that school site. This contracting
3requirement is contingent upon agreement between each of the
4two Medi-Cal managed care plans in the County of Los Angeles
5and a mobile vision care service provider with respect to
6reimbursement rates applicable to the services under this pilot.

7(2) Neither this pilot program nor the Medi-Cal managed care
8plan shall require that a Medi-Cal beneficiary receive the vision
9care services described in this section through a mobile vision care
10provider on site at the school.

11(3) Prior to a Medi-Cal beneficiary receiving mobile vision care
12services at the school site, the parents, guardians, or legal
13representative of the student shall consent in writing to the
14Medi-Cal beneficiary receiving the services through a mobile
15vision care provider on site at the school.

16(e) An optometrist or ophthalmologist prescribing glasses to a
17Medi-Cal managed care beneficiary as part of services provided
18at a school site by a mobile vision care service provider pursuant
19to this pilot program shall be enrolled in the Medi-Cal program as
20an Ordering/Referring/Prescribing provider. For any other purposes
21under the pilot program, the licensed health professional shall
22satisfy all requirements for enrollment as a provider in the
23Medi-Cal program.

24(f) (1) The Medi-Cal managed care plan shall compensate the
25mobile vision services provider for the cost of the vision
26examination, dispensing of the lenses, and eyeglass frames.

27(2) Ophthalmic eyeglasses lenses prescribed by optometrists or
28ophthalmologists for a Medi-Cal managed care plan enrollee as
29part of the services provided at a school site by a mobile vision
30services provider shall be fabricated through optical laboratories
31the department contracts with pursuant to subdivision (b) of Section
3214105.3.

33(g) (1) The department shall annually adjust capitation rates
34for the Medi-Cal managed care plans operating in the County of
35Los Angeles as necessary to account for projected changes in the
36costs and utilization of the services provided pursuant to this
37section by mobile vision service providers.

38(2) Capitation rate adjustments pursuant to this section shall be
39actuarially based and developed using projections of contingent
40events including targeted populations who will receive these
P12   1services, and shall otherwise be in accordance with requirements
2necessary to secure federal financial participation.

3(3) Capitation rate adjustments pursuant to this section shall be
4limited to those related to vision examinations, dispensing of
5lenses, and eyeglass frames. The fabrication of optical lenses
6pursuant to this section shall be paid on a fee-for-service basis in
7accordance with the department’s applicable contract under
8subdivision (b) of Section 14105.3.

9(h) The pilot program shall last three years, starting no sooner
10 than January 1, 2015, and concluding December 31, 2017, or three
11years from the start date of the pilot if later. The department shall
12evaluate the impact of the pilot program on access to, and
13utilization of, vision care services by children by monitoring the
14managed care plan utilization data for vision services, as well as
15the lens fabrication data.

16(i) The department may terminate the pilot program at any time
17with 90 days advance notice to the Medi-Cal managed care plans
18for reasons that include, but are not limited to, any of the following:

19(1) The department determines that the pilot program is resulting
20in a lower level of access to, or use of, vision care services for
21children under the participating health plans.

22(2) The department determines that the pilot program is resulting
23in fraud, waste, or abuse of Medi-Cal funds.

24(3) The department determines there is a lack of funding for the
25vision care services provided in the pilot program.

26(j) Notwithstanding Chapter 3.5 (commencing with Section
2711340) of Part 1 of Division 3 of Title 2 of the Government Code,
28the department may implement, interpret, or make specific this
29section and any applicable federal waivers and state plan
30amendments by means of all-county letters, plan letters, plan or
31provider bulletins, or similar instructions, without taking regulatory
32action.

33(k) The department shall obtain any federal approvals necessary
34to implement this section and to obtain federal matching funds to
35the maximum extent permitted by federal law.

36(l) This section shall be implemented only if and to the extent
37all federal approvals are obtained and federal financial participation
38is available.

P13   1(m) This section shall be implemented only to the extent an
2annual appropriation is made available to the department each
3fiscal year for the specific purpose of implementing this section.

4(n) If the department determines, pursuant to subdivision (h),
5that the pilot program is having a positive impact on access and
6utilization and that additional funds are available, the director may
7extend the pilot program described in this section to Medi-Cal
8managed care plans in other counties and applicable local
9jurisdictions. Any extension shall be implemented only to the
10extent that any additional and necessary federal approvals are
11obtained, and if sufficient funds are made available to participating
12plans for this purpose. The department may accept funding from
13private foundations in order to implement an extension under this
14subdivision to the extent that federal financial participation is
15available.

16(o) The department shall post on its Internet Web site a notice
17that has terminated or expanded the pilot program, including
18identification of the geographic locations, and shall notify
19appropriate fiscal and policy committees of both houses of the
20Legislature.

21

SEC. 5.  

Section 14105.33 of the Welfare and Institutions Code
22 is amended to read:

23

14105.33.  

(a) The department may enter into contracts with
24manufacturers of single-source and multiple-source drugs, on a
25bid or nonbid basis, for drugs from each major therapeutic category,
26and shall maintain a list of those drugs for which contracts have
27been executed.

28(b) (1) Contracts executed pursuant to this section shall be for
29the manufacturer’s best price, as defined in Section 14105.31,
30which shall be specified in the contract, and subject to agreed-upon
31price escalators, as defined in that section. The contracts shall
32provide for a state rebate, as defined in Section 14105.31, to be
33remitted to the department quarterly. The department shall submit
34an invoice to each manufacturer for the state rebate, including
35supporting utilization data from the department’s prescription drug
36paid claims tapes within 30 days of receipt of the federal Centers
37for Medicare and Medicaid Services’ file of manufacturer rebate
38information. In lieu of paying the entire invoiced amount, a
39manufacturer may contest the invoiced amount pursuant to
40procedures established by the federal Centers for Medicare and
P14   1Medicaid Services’ Medicaid Drug Rebate Program Releases or
2regulations by mailing a notice, that shall set forth its grounds for
3contesting the invoiced amount, to the department within 38 days
4of the department’s mailing of the state invoice and supporting
5utilization data. For purposes of state accounting practices only,
6the contested balance shall not be considered an accounts receivable
7amount until final resolution of the dispute pursuant to procedures
8established by the federal Centers for Medicare and Medicaid
9Services’ Medicaid Drug Rebate Program Releases or regulations
10that results in a finding of an underpayment by the manufacturer.
11Manufacturers may request, and the department shall timely
12provide, at cost, Medi-Cal provider level drug utilization data, and
13other Medi-Cal utilization data necessary to resolve a contested
14department-invoiced rebate amount.

15(2) The department shall provide for an annual audit of
16utilization data used to calculate the state rebate to verify the
17accuracy of that data. The findings of the audit shall be documented
18in a written audit report to be made available to manufacturers
19within 90 days of receipt of the report from the auditor. Any
20manufacturer may receive a copy of the audit report upon written
21request. Contracts between the department and manufacturers shall
22provide for any equalization payment adjustments determined
23necessary pursuant to an audit.

24(3) (A) Utilization data used to determine the state rebate shall
25exclude data from both of the following:

26(i) Health maintenance organizations, as defined in Section
27300e(a) of Title 42 of the United States Code, including those
28organizations that contract under Section 1396b(m) of Title 42 of
29the United States Code.

30(ii) Capitated plans that include a prescription drug benefit in
31the capitated rate, and that have negotiated contracts for rebates
32or discounts with manufacturers.

33(B) This paragraph shall become inoperative on July 1, 2014.

34(4) Commencing July 1, 2014, utilization data used to determine
35the state rebate shall include data from all programs, including,
36but not limited to, fee-for-service Medi-Cal, and utilization data,
37as limited in paragraph (5), from health plans contracting with the
38department to provide services to beneficiaries pursuant to this
39chapter, Chapter 8 (commencing with Section 14200), or Chapter
408.75 (commencing with Section 14591), that qualify for federal
P15   1drug rebates pursuant to Section 1927 of the federal Social Security
2Act (42 U.S.C. Sec. 1396r-8) or that otherwise qualify for federal
3funds under Title XIX of the federal Social Security Act (42 U.S.C.
4Sec. 1396 et seq.) pursuant to the Medicaid state plan or waivers.

5(5) Health plan utilization data shall be limited to those drugs
6 for which a health plan is authorizing a prescription drug described
7in subparagraph (A), and pursuant to the coverage policies
8established in subparagraph (B):

9(A) A prescription drug for which the department reimburses
10the health plan through a separate capitated payment or other
11supplemental payment. Payment shall not be withheld for decisions
12determined pursuant to Section 1374.34 of the Health and Safety
13Code.

14(B) The department shall develop coverage policies, consistent
15with the criteria set forth in paragraph (1) of subdivision (c) of
16Section 14105.39 and in consultation with clinical experts,
17Medi-Cal managed care plans, and other stakeholders, for
18prescription drugs described in subparagraph (A). These coverage
19policies shall apply to the entire Medi-Cal program, including
20fee-for-service and Medi-Cal managed care, through the Medi-Cal
21List of Contract Drugs or through provider bulletins, all plan letters,
22or similar instructions. Coverage policies developed pursuant to
23this section shall be revised on a semiannual basis or upon approval
24by the Food and Drug Administration of a new drug subject to
25subparagraph (A). For the purposes of this section, “coverage
26policies” include, but are not limited to, clinical guidelines and
27treatment and utilization policies.

28(6) For prescription drugs not subject to the requirements of
29paragraph (5), utilization data used to determine the state rebate
30shall include all data from health plans, except for health
31maintenance organizations, as defined in Section 300e(a) of Title
3242 of the United States Code, including those organizations that
33contract pursuant to Section 1396b(m) of Title 42 of the United
34States Code.

35(7) Notwithstanding Chapter 3.5 (commencing with Section
3611340) of Part 1 of Division 3 of Title 2 of the Government Code,
37the department, without taking any further regulatory action, shall
38implement, interpret, or make specific paragraph (5) by means of
39all-county letters, plan letters, plan or provider bulletins, or similar
40instructions, until the time regulations are adopted. The department
P16   1shall adopt regulations by October 1, 2017, in accordance with the
2requirements of Chapter 3.5 (commencing with Section 11340) of
3Part 1 of Division 3 of Title 2 of the Government Code.
4Notwithstanding Section 10231.5 of the Government Code,
5beginning six months after the effective date of this section, the
6department shall provide a status report to the Legislature on a
7semiannual basis, in compliance with Section 9795 of the
8Government Code, until regulations have been adopted.

9(c) In order that Medi-Cal beneficiaries may have access to a
10comprehensive range of therapeutic agents, the department shall
11ensure that there is representation on the list of contract drugs in
12all major therapeutic categories. Except as provided in subdivision
13(a) of Section 14105.35, the department shall not be required to
14contract with all manufacturers who negotiate for a contract in a
15particular category. The department shall ensure that there is
16sufficient representation of single-source and multiple-source
17drugs, as appropriate, in each major therapeutic category.

18(d) The department shall select the therapeutic categories to be
19included on the list of contract drugs, and the order in which it
20seeks contracts for those categories. The department may establish
21different contracting schedules for single-source and
22multiple-source drugs within a given therapeutic category.

23(e) (1) In order to fully implement subdivision (d), the
24department shall, to the extent necessary, negotiate or renegotiate
25contracts to ensure there are as many single-source drugs within
26each therapeutic category or subcategory as the department
27determines necessary to meet the health needs of the Medi-Cal
28population. The department may determine in selected therapeutic
29categories or subcategories that no single-source drugs are
30necessary because there are currently sufficient multiple-source
31drugs in the therapeutic category or subcategory on the list of
32contract drugs to meet the health needs of the Medi-Cal population.
33However, in no event shall a beneficiary be denied continued use
34of a drug which is part of a prescribed therapy in effect as of
35September 2, 1992, until the prescribed therapy is no longer
36prescribed.

37(2) In the development of decisions by the department on the
38required number of single-source drugs in a therapeutic category
39or subcategory, and the relative therapeutic merits of each drug in
40a therapeutic category or subcategory, the department shall consult
P17   1with the Medi-Cal Contract Drug Advisory Committee. The
2committee members shall communicate their comments and
3recommendations to the department within 30 business days of a
4request for consultation, and shall disclose any associations with
5pharmaceutical manufacturers or any remuneration from
6pharmaceutical manufacturers.

7(f) In order to achieve maximum cost savings, the Legislature
8declares that an expedited process for contracts under this section
9is necessary. Therefore, contracts entered into on a nonbid basis
10shall be exempt from Chapter 2 (commencing with Section 10290)
11of Part 2 of Division 2 of the Public Contract Code.

12(g) In no event shall a beneficiary be denied continued use of
13a drug that is part of a prescribed therapy in effect as of September
142, 1992, until the prescribed therapy is no longer prescribed.

15(h) Contracts executed pursuant to this section shall be
16confidential and shall be exempt from disclosure under the
17California Public Records Act (Chapter 3.5 (commencing with
18Section 6250) of Division 7 of Title 1 of the Government Code).

19(i) The department shall provide individual notice to Medi-Cal
20beneficiaries at least 60 calendar days prior to the effective date
21of the deletion or suspension of any drug from the list of contract
22drugs. The notice shall include a description of the beneficiary’s
23right to a fair hearing and shall encourage the beneficiary to consult
24a physician to determine if an appropriate substitute medication
25is available from Medi-Cal.

26(j) In carrying out the provisions of this section, the department
27may contract either directly, or through the fiscal intermediary,
28for pharmacy consultant staff necessary to initially accomplish the
29treatment authorization request reviews.

30(k) (1) Manufacturers shall calculate and pay interest on late
31or unpaid rebates. The interest shall not apply to any prior period
32adjustments of unit rebate amounts or department utilization
33adjustments.

34(2) For state rebate payments, manufacturers shall calculate and
35pay interest on late or unpaid rebates for quarters that begin on or
36after the effective date of the act that added this subdivision.

37(3) Following final resolution of any dispute pursuant to
38procedures established by the federal Centers for Medicare and
39Medicaid Services’ Medicaid Drug Rebate Program Releases or
40regulations regarding the amount of a rebate, any underpayment
P18   1by a manufacturer shall be paid with interest calculated pursuant
2to subdivisions (m) and (n), and any overpayment, together with
3interest at the rate calculated pursuant to subdivisions (m) and (n),
4shall be credited by the department against future rebates due.

5(l) Interest pursuant to subdivision (k) shall begin accruing 38
6calendar days from the date of mailing of the invoice, including
7supporting utilization data sent to the manufacturer. Interest shall
8continue to accrue until the date of mailing of the manufacturer’s
9payment.

10(m) Except as specified in subdivision (n), interest rates and
11calculations pursuant to subdivision (k) for Medicaid rebates and
12state rebates shall be identical and shall be determined by the
13federal Centers for Medicare and Medicaid Services’ Medicaid
14Drug Rebate Program Releases or regulations.

15(n) If the date of mailing of a state rebate payment is 69 days
16or more from the date of mailing of the invoice, including
17supporting utilization data sent to the manufacturer, the interest
18rate and calculations pursuant to subdivision (k) shall be as
19specified in subdivision (m), however the interest rate shall be
20increased by 10 percentage points. This subdivision shall apply to
21payments for amounts invoiced for any quarters that begin on or
22after the effective date of the act that added this subdivision.

23(o) If the rebate payment is not received, the department shall
24send overdue notices to the manufacturer at 38, 68, and 98 days
25after the date of mailing of the invoice, and supporting utilization
26data. If the department has not received a rebate payment, including
27interest, within 180 days of the date of mailing of the invoice,
28including supporting utilization data, the manufacturer’s contract
29with the department shall be deemed to be in default and the
30contract may be terminated in accordance with the terms of the
31contract. For all other manufacturers, if the department has not
32received a rebate payment, including interest, within 180 days of
33the date of mailing of the invoice, including supporting utilization
34data, all of the drug products of those manufacturers shall be made
35available only through prior authorization effective 270 days after
36the date of mailing of the invoice, including utilization data sent
37to manufacturers.

38(p) If the manufacturer provides payment or evidence of
39payment to the department at least 40 days prior to the proposed
40date the drug is to be made available only through prior
P19   1authorization pursuant to subdivision (o), the department shall
2terminate its actions to place the manufacturers’ drug products on
3prior authorization.

4(q) The department shall direct the state’s fiscal intermediary
5to remove prior authorization requirements imposed pursuant to
6subdivision (o) and notify providers within 60 days after payment
7by the manufacturer of the rebate, including interest. If a contract
8 was in place at the time the manufacturers’ drugs were placed on
9prior authorization, removal of prior authorization requirements
10shall be contingent upon good faith negotiations and a signed
11contract with the department.

12(r) A beneficiary may obtain drugs placed on prior authorization
13pursuant to subdivision (o) if the beneficiary qualifies for
14continuing care status. To be eligible for continuing care status, a
15beneficiary must be taking the drug when its manufacturer is placed
16on prior authorization status. Additionally, the department shall
17have received a claim for the drug with a date of service that is
18within 100 days prior to the date the manufacturer was placed on
19prior authorization.

20(s) A beneficiary may remain eligible for continuing care status,
21provided that a claim is submitted for the drug in question at least
22every 100 days and the date of service of the claim is within 100
23days of the date of service of the last claim submitted for the same
24drug.

25(t) Drugs covered pursuant to Sections 14105.43 and 14133.2
26shall not be subject to prior authorization pursuant to subdivision
27(o), and any other drug may be exempted from prior authorization
28by the department if the director determines that an essential need
29exists for that drug, and there are no other drugs currently available
30without prior authorization that meet that need.

31(u) It is the intent of the Legislature in enacting subdivisions
32(k) to (t), inclusive, that the department and manufacturers shall
33cooperate and make every effort to resolve rebate payment disputes
34within 90 days of notification by the manufacturer to the
35department of a dispute in the calculation of rebate payments.

36

SEC. 6.  

Section 14105.436 of the Welfare and Institutions
37Code
is amended to read:

38

14105.436.  

(a) Effective July 1, 2002, all pharmaceutical
39manufacturers shall provide to the department a state rebate, in
40addition to rebates pursuant to other provisions of state or federal
P20   1law, for any drug products that have been added to the Medi-Cal
2list of contract drugs pursuant to Section 14105.43 or 14133.2 and
3reimbursed through the Medi-Cal outpatient fee-for-service drug
4program. The state rebate shall be negotiated as necessary between
5the department and the pharmaceutical manufacturer. The
6negotiations shall take into account offers such as rebates,
7discounts, disease management programs, and other cost savings
8offerings and shall be retroactive to July 1, 2002.

9(b) The department may use existing administrative mechanisms
10for any drug for which the department does not obtain a rebate
11pursuant to subdivision (a). The department may only use those
12mechanisms in the event that, by February 1, 2003, the
13manufacturer refuses to provide the additional rebate. This
14subdivision shall become inoperative on January 1, 2010.

15(c) For purposes of this section, “Medi-Cal utilization data”
16means the data used by the department to reimburse providers
17under all programs that qualify for federal drug rebates pursuant
18to Section 1927 of the federal Social Security Act (42 U.S.C. Sec.
191396r-8) or that otherwise qualify for federal funds under Title
20XIX of the federal Social Security Act (42 U.S.C. Sec. 1396 et
21seq.) pursuant to the Medicaid state plan or waivers. Medi-Cal
22utilization data excludes data from covered entities identified in
23Section 256b(a)(4) of Title 42 of the United States Code in
24accordance with Sections 256b(a)(5)(A) and 1396r-8(a)(5)(C) of
25Title 42 of the United States Code, and those capitated plans that
26include a prescription drug benefit in the capitated rate and that
27have negotiated contracts for rebates or discounts with
28manufacturers.

29(d) Subdivision (c) shall become inoperative when the
30department implements paragraphs (4) and (5) of subdivision (b)
31of Section 14105.33. The department shall post on its Internet Web
32site a notice that it has implemented paragraphs (4) and (5) of
33subdivision (b) of Section 14105.33.

34(e) Effective July 1, 2009, all pharmaceutical manufacturers
35shall provide to the department a state rebate, in addition to rebates
36pursuant to other provisions of state or federal law, equal to an
37amount not less than 10 percent of the average manufacturer price
38based on Medi-Cal utilization data for any drug products that have
39been added to the Medi-Cal list of contract drugs pursuant to
40Section 14105.43 or 14133.2.

P21   1(f) Pharmaceutical manufacturers shall, by January 1, 2010,
2enter into a supplemental rebate agreement for the rebate required
3in subdivision (d) for drug products added to the Medi-Cal list of
4contract drugs on or before December 31, 2009.

5(g) Effective January 1, 2010, all pharmaceutical manufacturers
6who have not entered into a supplemental rebate agreement
7pursuant to subdivisions (d) and (e), shall provide to the department
8a state rebate, in addition to rebates pursuant to other provisions
9of state or federal law, equal to an amount not less than 20 percent
10of the average manufacturer price based on Medi-Cal utilization
11data for any drug products that have been added to the Medi-Cal
12list of contract drugs pursuant to Section 14105.43 or 14133.2
13prior to January 1, 2010. If the pharmaceutical manufacturer does
14not enter into a supplemental rebate agreement by March 1, 2010,
15the manufacturer’s drug product shall be made available only
16through an approved treatment authorization request pursuant to
17subdivision (h).

18(h) For a drug product added to the Medi-Cal list of contract
19drugs pursuant to Section 14105.43 or 14133.2 on or after January
201, 2010, a pharmaceutical manufacturer shall provide to the
21department a state rebate pursuant to subdivision (d). If the
22pharmaceutical manufacturer does not enter into a supplemental
23rebate agreement within 60 days after the addition of the drug to
24the Medi-Cal list of contract drugs, the manufacturer shall provide
25to the department a state rebate equal to not less than 20 percent
26of the average manufacturers price based on Medi-Cal utilization
27data for any drug products that have been added to the Medi-Cal
28list of contract drugs pursuant to Section 14105.43 or 14133.2. If
29the pharmaceutical manufacturer does not enter into a supplemental
30rebate agreement within 120 days after the addition of the drug to
31the Medi-Cal list of contract drugs, the pharmaceutical
32manufacturer’s drug product shall be made available only through
33an approved treatment authorization request pursuant to subdivision
34(h). For supplemental rebate agreements executed more than 120
35days after the addition of the drug product to the Medi-Cal list of
36contract drugs, the state rebate shall equal an amount not less than
3720 percent of the average manufacturers price based on Medi-Cal
38utilization data for any drug products that have been added to the
39Medi-Cal list of contract drugs pursuant to Section 14105.43 or
4014133.2.

P22   1(i) Notwithstanding any other provision of law, drug products
2added to the Medi-Cal list of contract drugs pursuant to Section
314105.43 or 14133.2 of manufacturers who do not execute an
4agreement to pay additional rebates pursuant to this section, shall
5be available only through an approved treatment authorization
6request.

7(j) For drug products added on or before December 31, 2009,
8a beneficiary may obtain a drug product that requires a treatment
9authorization request pursuant to subdivision (h) if the beneficiary
10qualifies for continuing care status. To be eligible for continuing
11care status, a beneficiary must be taking the drug product and the
12department must have record of a reimbursed claim for the drug
13product with a date of service that is within 100 days prior to the
14date the drug product was placed on treatment authorization request
15status. A beneficiary may remain eligible for continuing care status,
16provided that a claim is submitted for the drug product in question
17at least every 100 days and the date of service of the claim is within
18100 days of the date of service of the last claim submitted for the
19same drug product.

20(k) Changes made to the Medi-Cal list of contract drugs under
21this section shall be exempt from the requirements of the
22Administrative Procedure Act (Chapter 3.5 (commencing with
23Section 11340), Chapter 4 (commencing with Section 11370), and
24Chapter 5 (commencing with Section 11500) of Part 1 of Division
253 of Title 2 of the Government Code), and shall not be subject to
26the review and approval of the Office of Administrative Law.

27

SEC. 7.  

Section 14105.86 of the Welfare and Institutions Code
28 is amended to read:

29

14105.86.  

(a) For the purposes of this section, the following
30definitions apply:

31(1) (A) “Average sales price” means the price reported to the
32federal Centers for Medicare and Medicaid Services by the
33manufacturer pursuant to Section 1847A of the federal Social
34Security Act (42 U.S.C. Sec. 1395w-3a).

35(B) “Average manufacturer price” means the price reported to
36the federal Centers for Medicare and Medicaid Services pursuant
37to Section 1927 of the federal Social Security Act (42 U.S.C. Sec.
381396r-8).

P23   1(2) “Blood factors” means plasma protein therapies and their
2recombinant analogs. Blood factors include, but are not limited
3to, all of the following:

4(A) Coagulation factors, including:

5(i) Factor VIII, nonrecombinant.

6(ii) Factor VIII, porcine.

7(iii) Factor VIII, recombinant.

8(iv) Factor IX, nonrecombinant.

9(v) Factor IX, complex.

10(vi) Factor IX, recombinant.

11(vii) Antithrombin III.

12(viii) Anti-inhibitor factor.

13(ix) Von Willebrand factor.

14(x) Factor VIIa, recombinant.

15(B) Immune Globulin Intravenous.

16(C) Alpha-1 Proteinase Inhibitor.

17(b) The reimbursement for blood factors shall be by national
18drug code number and shall not exceed 120 percent of the average
19sales price of the last quarter reported.

20(c) The average sales price for blood factors of manufacturers
21or distributors that do not report an average sales price pursuant
22to subdivision (a) shall be identical to the average manufacturer
23price. The average sales price for new products that do not have
24a calculable average sales price or average manufacturer price
25shall be equal to a projected sales price, as reported by the
26manufacturer to the department. Manufacturers reporting a
27projected sales price for a new product shall report the first monthly
28average manufacturer price reported to the federal Centers for
29Medicare and Medicaid Services. The reporting of an average sales
30price that does not meet the requirement of this subdivision shall
31result in that blood factor no longer being considered a covered
32benefit.

33(d) The average sales price shall be reported at the national drug
34code level to the department on a quarterly basis.

35(e) (1) Effective July 1, 2008, the department shall collect a
36state rebate, in addition to rebates pursuant to other provisions of
37state or federal law, for blood factors reimbursed pursuant to this
38section by programs that qualify for federal drug rebates pursuant
39to Section 1927 of the federal Social Security Act (42 U.S.C. Sec.
401396r-8) or otherwise qualify for federal funds under Title XIX
P24   1of the federal Social Security Act (42 U.S.C. Sec. 1396 et seq.)
2pursuant to the medicaid state plan or waivers and the programs
3authorized by Article 5 (commencing with Section 123800) of
4Chapter 3 of Part 2 of, and Article 1 (commencing with Section
5125125) of Chapter 2 of Part 5 of, Division 106 of the Health and
6Safety Code.

7(2) Paragraph (1) shall become inoperative when the department
8implements paragraphs (4) and (5) of subdivision (b) of Section
914105.33. The department shall post on its Internet Web site a
10notice that it has implemented paragraphs (4) and (5) of subdivision
11(b) of Section 14105.33.

12(3) The state rebate shall be negotiated as necessary between
13the department and the manufacturer. Manufacturers who do not
14execute an agreement to pay additional rebates pursuant to this
15section shall have their blood factors available only through an
16approved treatment or service authorization request. All blood
17factors that meet the definition of a covered outpatient drug
18pursuant to Section 1927 of the federal Social Security Act (42
19U.S.C. Sec. 1396r-8) shall remain a benefit subject to the utilization
20controls provided for in this section.

21(4) In reviewing authorization requests, the department shall
22approve the lowest net cost product that meets the beneficiary’s
23medical need. The review of medical need shall take into account
24a beneficiary’s clinical history or the use of the blood factor
25pursuant to payment by another third party, or both.

26(f) A beneficiary may obtain blood factors that require a
27treatment or service authorization request pursuant to subdivision
28(e) if the beneficiary qualifies for continuing care status. To be
29eligible for continuing care status, a beneficiary must be taking
30the blood factor and the department has reimbursed a claim for
31the blood factor with a date of service that is within 100 days prior
32to the date the blood factor was placed on treatment authorization
33request status. A beneficiary may remain eligible for continuing
34care status, provided that a claim is submitted for the blood factor
35in question at least every 100 days and the date of service of the
36claim is within 100 days of the date of service of the last claim
37submitted for the same blood factor.

38(g) Changes made to the list of covered blood factors under this
39or any other section shall be exempt from the requirements of the
40Administrative Procedure Act (Chapter 3.5 (commencing with
P25   1Section 11340), Chapter 4 (commencing with Section 11370), and
2Chapter 5 (commencing with Section 11500) of Part 1 of Division
33 of Title 2 of the Government Code), and shall not be subject to
4the review and approval of the Office of Administrative Law.

5

SEC. 8.  

Section 14132.56 is added to the Welfare and
6Institutions Code
, to read:

7

14132.56.  

(a) (1) Only to the extent required by the federal
8government and effective no sooner than required by the federal
9government, behavioral health treatment (BHT), as defined by
10Section 1374.73 of the Health and Safety Code, shall be a covered
11Medi-Cal service for individuals under 21 years of age.

12(2) It is the intent of the Legislature that, to the extent the federal
13government requires BHT to be a covered Medi-Cal service, the
14department shall seek statutory authority to implement this new
15benefit in Medi-Cal.

16(b) The department shall implement, or continue to implement,
17this section only after all of the following occurs or has occurred:

18(1) The department receives all necessary federal approvals to
19obtain federal funds for the service.

20(2) The department seeksbegin delete and obtainsend delete an appropriation that
21would provide the necessary state funding estimated to be required
22for the applicable fiscal year.

23(3) The department consults with stakeholders.

24(c) The department shall develop and define eligibility criteria,
25provider participation criteria, utilization controls, and delivery
26system structure for services under this section, subject to
27limitations allowable under federal law, in consultation with
28stakeholders.

29(d) Notwithstanding Chapter 3.5 (commencing with Section
3011340) of Part 1 of Division 3 of Title 2 of the Government Code,
31 the department, without taking any further regulatory action, shall
32implement, interpret, or make specific this section by means of
33all-county letters, plan letters, plan or provider bulletins, or similar
34instructions until regulations are adopted. The department shall
35adopt regulations by July 1, 2017, in accordance with the
36requirements of Chapter 3.5 (commencing with Section 11340) of
37Part 1 of Division 3 of Title 2 of the Government Code.
38Notwithstanding Section 10231.5 of the Government Code,
39beginning six months after the effective date of this section, the
40department shall provide semiannual status reports to the
P26   1Legislature, in compliance with Section 9795 of the Government
2Code, until regulations have been adopted.

3(e) For the purposes of implementing this section, the department
4may enter into exclusive or nonexclusive contracts on a bid or
5negotiated basis, including contracts for the purpose of obtaining
6subject matter expertise or other technical assistance. Contracts
7may be statewide or on a more limited geographic basis. Contracts
8entered into or amended under this subdivision shall be exempt
9from Part 2 (commencing with Section 10100) of Division 2 of
10the Public Contract Code and Chapter 6 (commencing with Section
1114825) of Part 5.5 of Division 3 of the Government Code, and
12shall be exempt from the review or approval of any division of the
13Department of General Services.

14(f) The department may seek approval of any necessary state
15plan amendments or waivers to implement this section. The
16department shall make any state plan amendments or waiver
17requests public at least 30 days prior to submitting to the federal
18Centers for Medicare and Medicaid Services, and the department
19shall work with stakeholders to address the public comments in
20the state plan amendment or waiver request.

21(g) This section shall be implemented only to the extent that
22federal financial participation is available and any necessary federal
23approvals have been obtained.

24

SEC. 9.  

Section 14593 of the Welfare and Institutions Code is
25amended to read:

26

14593.  

(a) (1) The department may enter into contracts with
27public or private nonprofit organizations for implementation of
28the PACE program, and also may enter into separate contracts
29with PACE organizations, to fully implement the single state
30agency responsibilities assumed by the department in those
31contracts, Section 14132.94, and any other state requirement found
32necessary by the department to provide comprehensive
33community-based, risk-based, and capitated long-term care services
34to California’s frail elderly.

35(2) The department may enter into separate contracts as specified
36in subdivision (a) with up to 15 PACE organizations.

37(b) The requirements of the PACE model, as provided for
38pursuant to Section 1894 (42 U.S.C. Sec. 1395eee) and Section
391934 (42 U.S.C. Sec. 1396u-4) of the federal Social Security Act,
P27   1shall not be waived or modified. The requirements that shall not
2be waived or modified include all of the following:

3(1) The focus on frail elderly qualifying individuals who require
4the level of care provided in a nursing facility.

5(2) The delivery of comprehensive, integrated acute and
6long-term care services.

7(3) The interdisciplinary team approach to care management
8and service delivery.

9(4) Capitated, integrated financing that allows the provider to
10pool payments received from public and private programs and
11individuals.

12(5) The assumption by the provider of full financial risk.

13(6) The provision of a PACE benefit package for all participants,
14regardless of source of payment, that shall include all of the
15following:

16(A) All Medicare-covered items and services.

17(B) All Medicaid-covered items and services, as specified in
18the state’s Medicaid plan.

19(C) Other services determined necessary by the interdisciplinary
20team to improve and maintain the participant’s overall health status.

21(c) Sections 14002, 14005.12, 14005.17, and 14006 shall apply
22when determining the eligibility for Medi-Cal of a person receiving
23the services from an organization providing services under this
24chapter.

25(d) Provisions governing the treatment of income and resources
26of a married couple, for the purposes of determining the eligibility
27of a nursing-facility certifiable or institutionalized spouse, shall
28be established so as to qualify for federal financial participation.

29(e) (1) The department shall establish capitation rates paid to
30each PACE organization at no less than 90 percent of the
31fee-for-service equivalent cost, including the department’s cost of
32administration, that the department estimates would be payable
33for all services covered under the PACE organization contract if
34all those services were to be furnished to Medi-Cal beneficiaries
35under the fee-for-service Medi-Cal program provided for pursuant
36to Chapter 7 (commencing with Section 14000).

37(2)  This subdivision shall be implemented only to the extent
38that federal financial participation is available.

P28   1(f) Contracts under this chapter may be on a nonbid basis and
2shall be exempt from Chapter 2 (commencing with Section 10290)
3of Part 2 of Division 2 of the Public Contract Code.

4(g) This section shall remain in effect only until April 1, 2015,
5and as of that date is repealed, unless a later enacted statute, that
6is enacted before April 1, 2015, deletes or extends that date.

7

SEC. 10.  

Section 14593 is added to the Welfare and Institutions
8Code
, to read:

9

14593.  

(a) (1) The department may enter into contracts with
10public or private nonprofit organizations for implementation of
11the PACE program, and also may enter into separate contracts
12with PACE organizations, to fully implement the single state
13agency responsibilities assumed by the department in those
14contracts, Section 14132.94, and any other state requirement found
15necessary by the department to provide comprehensive
16community-based, risk-based, and capitated long-term care services
17to California’s frail elderly.

18(2) The department may enter into separate contracts as specified
19in subdivision (a) with up to 15 PACE organizations.

20(b) The requirements of the PACE model, as provided for
21pursuant to Section 1894 (42 U.S.C. Sec. 1395eee) and Section
221934 (42 U.S.C. Sec. 1396u-4) of the federal Social Security Act,
23shall not be waived or modified. The requirements that shall not
24be waived or modified include all of the following:

25(1) The focus on frail elderly qualifying individuals who require
26the level of care provided in a nursing facility.

27(2) The delivery of comprehensive, integrated acute and
28long-term care services.

29(3) The interdisciplinary team approach to care management
30and service delivery.

31(4) Capitated, integrated financing that allows the provider to
32pool payments received from public and private programs and
33individuals.

34(5) The assumption by the provider of full financial risk.

35(6) The provision of a PACE benefit package for all participants,
36regardless of source of payment, that shall include all of the
37following:

38(A) All Medicare-covered items and services.

39(B) All Medicaid-covered items and services, as specified in
40the state’s Medicaid plan.

P29   1(C) Other services determined necessary by the interdisciplinary
2team to improve and maintain the participant’s overall health status.

3(c) Sections 14002, 14005.12, 14005.17, and 14006 shall apply
4when determining the eligibility for Medi-Cal of a person receiving
5the services from an organization providing services under this
6chapter.

7(d) Provisions governing the treatment of income and resources
8of a married couple, for the purposes of determining the eligibility
9of a nursing-facility certifiable or institutionalized spouse, shall
10be established so as to qualify for federal financial participation.

11(e) (1) The department shall establish capitation rates paid to
12each PACE organization at no less than 95 percent of the
13fee-for-service equivalent cost, including the department’s cost of
14administration, that the department estimates would be payable
15for all services covered under the PACE organization contract if
16all those services were to be furnished to Medi-Cal beneficiaries
17under the fee-for-service Medi-Cal program provided for pursuant
18to Chapter 7 (commencing with Section 14000).

19(2) This subdivision shall be implemented only to the extent
20that federal financial participation is available.

21(f) Contracts under this chapter may be on a nonbid basis and
22shall be exempt from Chapter 2 (commencing with Section 10290)
23of Part 2 of Division 2 of the Public Contract Code.

24(g) This section shall become operative on April 1, 2015.

25

SEC. 11.  

(a) With regard to Section 4 of this act, the
26Legislature finds and declares all of the following:

27(1) The County of Los Angeles has the largest number of school
28districts in the state and a correspondingly large Medi-Cal
29population with a lower than statewide average on utilization of
30Medi-Cal vision services.

31(2) The state contracts with two managed care health plans in
32the County of Los Angeles, which results in the delivery of
33Medi-Cal services to approximately 76 percent of the over 2.3
34million Medi-Cal beneficiaries in that county.

35(3) These 2.3 million beneficiaries are 24 percent of the state’s
36total number of Medi-Cal beneficiaries. Approximately one-half
37are under 21 years of age.

38(b) It is therefore the intent of the Legislature, in an effort to
39determine whether children’s access to, and utilization of, vision
40care services can be increased by providing vision care services
P30   1at schools, that the State Department of Health Care Services
2establish a pilot program in the County of Los Angeles that enables
3school districts to allow students enrolled in Medi-Cal managed
4care plans to receive vision care services at the school site through
5the use of a mobile vision service provider. It is the intent of the
6Legislature that the vision care services available under this pilot
7be limited to vision examinations and providing eyeglasses.

8

SEC. 12.  

It is the intent of the Legislature that the State
9Department of Health Care Services shall continue to monitor
10access to and utilization of Medi-Cal services in the fee-for-service
11and managed care settings during the 2014-15 fiscal year, in
12conjunction with the department’s federally approved plan to
13monitor health care access for Medi-Cal beneficiaries and any
14other methods deemed appropriate by the director. The department
15shall use this information to evaluate current reimbursement levels
16for Medi-Cal providers and to make recommendations for targeted
17changes to the reductions in reimbursement levels made pursuant
18to Chapter 3 of the Statutes of 2011 to the extent the department
19finds those changes appropriate.

20

SEC. 13.  

The balances of the reappropriations provided by
21Item 4300-490 of Section 2.00 of the Budget Act of 2013, as added
22by Chapters 20 and 354 of the Statutes of 2013, payable from the
23General Fund (Item 4300-101-0001, Budget Act of 2009 (Ch. 1,
242009-10 3rd Ex. Sess., as revised by Ch. 1, 2009-10 4th Ex. Sess.)
25and Item 4300-101-0001, Budget Act of 2010 (Ch. 712, Stats.
262010)), are hereby reappropriated for the purposes of, and subject
27to that Item 4300-490, and, notwithstanding any other law, shall
28be available for liquidation until June 30, 2015.

29

SEC. 14.  

(a) For the 2014-15 fiscal year, the sum of three
30million two hundred thousand dollars ($3,200,000) is hereby
31appropriated from the Major Risk Medical Insurance Fund to the
32State Department of Health Care Services for allocation to health
33benefit plans that meet all of the following requirements:

34(1) The health benefit plan has a valid exemption letter from
35the Internal Revenue Service pursuant to Section 501(c) (9) of the
36Internal Revenue Code.

37(2) The health benefit plan is a multiemployer plan, as defined
38in Section 3(37) of the federal Employee Retirement Income
39Security Act of 1974 (29 U.S.C. Sec. 1002(37)(A)).

P31   1(3) The health benefit plan is funded by contributions made by
2agricultural employers, as defined in subdivision (c) of the Section
31140.4 of the Labor Code, where 85 percent or more of the plan’s
4eligible participants are agricultural employees, as defined in
5subdivision (b) of Section 1140.4 of the Labor Code, for work
6performed and covered under a collective bargaining agreement.

7(b) On or before September 1, 2014, the State Department of
8Health Care Services shall pay the funds allocated pursuant to this
9section to the health plan that meets the criteria set forth in this
10section. The funds shall be used to provide health care coverage
11for agricultural employees and dependents.

12(c) The payment set forth in subdivision (b) shall not require
13the State Department of Health Care Services to contract with the
14recipient of the funds nor shall the payment of funds be subject to
15the requirements of Part 2 (commencing with Section 10100) of
16Division 2 of the Public Contract Code.

17

SEC. 15.  

For the 2014-15 fiscal year, the sum of three million
18seven hundred fifty thousand dollars ($3,750,000) is hereby
19appropriated from the Major Risk Medical Insurance Fund to the
20State Department of Health Care Services for purposes of electronic
21health records technical assistance in accordance with the State
22Medicaid Health Information Technology Plan as specified in
23Section 14046.1 of the Welfare and Institutions Code.

24

SEC. 16.  

This act is a bill providing for appropriations related
25to the Budget Bill within the meaning of subdivision (e) of Section
2612 of Article IV of the California Constitution, has been identified
27as related to the budget in the Budget Bill, and shall take effect
28immediately.



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