(E) Comply with the requirements governing provider and supplier requests for error correction established pursuant to Section 401.717 of Title 42 of the Code of Federal Regulations for all claims data received, including, but not limited to, data from sources other than Medicare.
(2) A prohibition on the nonprofit organization or organizations administering the California Health Care Cost and Quality Database from doing either of the following:
(A) Using the data received during the execution of the contract for any purpose not specified in this chapter or in the contract.
(B) Receiving funding from any other source to accomplish the same purposes sought to be accomplished under this chapter unless funding is received from another nonprofit or government source and is for the
purpose of research or education.
(3) A requirement that the nonprofit organization or organizations administering the California Health Care Cost and Quality Database identify, in accordance with this section, the type of data, purpose of use, and entities and individuals that are required to report to, or that may have access to, the California Health Care Cost and Quality Database. An entity or individual shall not be required to report to, and shall not have access to, the California Health Care Cost and Quality Database until the review committee established pursuant to Section 127672 has approved the nonprofit organization or organizations determination.
(c) (1) For the purpose of developing information for inclusion in the California Health Care Cost and Quality Database, a health care service plan, including a specialized
health care service plan, an insurer licensed to provide health insurance, as defined in Section 106 of the Insurance Code, a self-insured employer, a supplier, as defined in paragraph (3) of subdivision (b) of Section 1367.50, or a provider, as defined in paragraph (2) of subdivision (b) of Section 1367.50, shall, and a multiemployer self-insured plan that is responsible for paying for health care services provided to beneficiaries and the trust administrator for a multiemployer self-insured plan may, provide both all of the following to the nonprofit organization or organizations administering the California Health Care Cost and Quality Database:
(A) Utilization data from the health care service plans’ and insurers’ medical, dental, and pharmacy claims
or, in the case of entities that do not use claims data, including, but not limited to, integrated delivery systems, encounter data consistent with the core set of data elements for data submission proposed by the APCD Council, the University of New Hampshire, and the National Association of Health Data Organizations.
(B) Pricing information for health care items, services, and medical and surgical episodes of care gathered from allowed charges for covered health care items and services or, in the case of entities that do not use or produce individual claims, price information that is the best possible proxy to pricing information for health care items, services, and medical and surgical episodes of care available in lieu of actual cost data so to allow for meaningful comparisons of provider prices and treatment costs.
(C) Information sufficient to determine the impacts of social determinants of health, including age, gender, race, ethnicity, limited English proficiency, sexual orientation and gender identity, ZIP Code, and any other factors for which there is peer-reviewed evidence.
(2) (A) The nonprofit organization or organizations administering the California Health Care Cost and Quality Database may report an entity’s failure to comply with paragraph (1) to the entity’s regulating agency.
(B) The regulating agency of an entity described in paragraph (1) may enforce paragraph (1) using its existing enforcement procedures. Notwithstanding any other law, moneys collected pursuant to this authorization shall be subject to appropriation by the Legislature, and the failure to comply with
paragraph (1) shall not be a crime.
(d) (1) All uses and disclosures of data made pursuant to this section shall comply with all applicable state and federal laws for the protection of the privacy and security of data, including, but not limited to,
the Confidentiality of Medical Information Act (Part 2.6 (commencing with Section 56)) of Division 1 of the Civil Code), the Information Practices Act (Chapter 1 (commencing with Section 1798) of Title 1.8 of Part 4 of Division 3 of the Civil Code, Title 1.81 (commencing with Section 1798.80) of Part 4 of Division 3 of the Civil Code, and the federal Health Insurance Portability and Accountability Act of 1996 (Public Law 104-191) and the federal Health Information Technology for Economic and Clinical Health Act, Title XIII of the federal American Recovery and Reinvestment Act of 2009 (Public Law 111-5), and implementing regulations.
(2) (A) All policies and protocols developed in the performance of the contract shall ensure that the privacy, security, and confidentiality of individually identifiable health information is protected. The nonprofit organization
or organizations administering the California Health Care Cost and Quality Database shall not publicly disclose any unaggregated, individually identifiable health information and shall develop a protocol for assessing the risk of reidentification stemming from public disclosure of any health information that is aggregated, individually identifiable health information.
(B) For the purposes of this paragraph, “individually identifiable health information” has the same meaning as in Section 160.103 of Title 45 of the Code of Federal Regulations.
(3) Confidentially negotiated contract terms contained in a contract between a health care service plan or insurer and a provider or supplier shall be protected in any public disclosure of data made pursuant to this section. Individually identifiable proprietary contract information included in
a contract between a health care service plan or insurer and a provider or supplier shall not be disclosed in an unaggregated format.
(e) (1) The nonprofit organization or organizations administering the California Health Care Cost and Quality Database shall receive, process, maintain, and analyze information from data sources, including, but not limited to, data received pursuant to subdivision (c), claims from private and public payers, disease and chronic condition registries, third-party surveys of quality and patient satisfaction, reviews by licensing and accrediting bodies, and local and regional public health data. Aggregated payer and provider performance on validated measures of clinical quality and patient experience, such as measures from the Healthcare Effectiveness Data and Information Set (HEDIS) and Consumer Assessment of Healthcare Providers and Systems (CAHPS), shall be collected from accrediting
organizations, including, but not limited to, the National Committee for Quality Assurance (NCQA), URAC, and the Joint Commission.
(2) The nonprofit organization or organizations administering the California Health Care Cost and Quality Database shall include in an analysis performed pursuant to paragraph (1), but shall not be limited to, to including, all of the following:
(A) Population-level data on prevention, screening, and wellness utilization.
(B) Population-level data on behavioral and medical risk factors, interventions, and outcomes.
(C) Population-level data on chronic conditions, management, and outcomes.
(D) Population-level data on trends in utilization of procedures for treatment of similar conditions to evaluate medical appropriateness.
(E) Facility and physician organization risk adjusted performance information
measures on the quality, efficiency, and outcomes of care that are aligned with national efforts, including, but not limited to, those of the National Quality Forum, related to defining cost and quality measures. Measures shall be publicly reported without risk adjustment for sociodemographic factors and shall also be risk adjusted for sociodemographic factors if peer-reviewed literature indicates an association between health outcomes and a sociodemographic factor or factors.
(F) Data that permits consideration of socioeconomic status and disparities in care due to race, ethnicity, gender,
limited English proficiency, ZIP Code, sexual orientation, and gender identity. identity, and other factors for which there is peer-reviewed evidence of a relationship between a social determinant of health and health outcomes.
(f) No later than January 1, 2019, the nonprofit organization or organizations administering the California Health Care Cost and Quality Database shall make publicly available a web-based, searchable database. The database shall include the information and analysis described in subdivision (e). The
information and analysis included in the database shall be presented in a way that facilitates comparisons of cost, quality, and satisfaction across payers, provider organizations, and other suppliers of health care services. This public database shall be regularly updated to reflect new data submissions.
(g) Implementation and ongoing administration costs of the California Health Care Cost and Quality Database shall not be paid using General Fund moneys.