42 U.S.C. § 299b–37: Dissemination and…

Summary

The Office of Communication and Knowledge Transfer at AHRQ (the “Office”) must widely share research from the Patient-Centered Outcomes Research Institute (the “Institute”) and other government-funded studies about which treatments work best. The Office must make easy-to-use tools and a public database that collect evidence from government, private, nonprofit, and academic sources for doctors, patients, providers, payers, policymakers, and health IT vendors. Shared materials must note who did the research, the methods used, limits of the studies, and how results may apply to different groups. Those materials must not be treated as rules for payment, coverage, or treatment. The Office must help health IT systems add new findings into clinical decision tools and get feedback from clinicians, patients, vendors, associations, and health plans. AHRQ, with NIH, must run grants to train researchers in accepted comparative-effectiveness methods (meeting the standards in section 1320e(d)(9)). The Secretary must coordinate federal programs to build linked data networks, registries, and use of electronic health records for this research. Federal agencies may enter agreements and accept funds to support this research if their laws allow.

Title 42, §299b–37

The Public Health and Welfare, Source: USLM XML via OLRC

(a)In general

(1)Dissemination

The Office of Communication and Knowledge Transfer (referred to in this section as the “Office”) at the Agency for Healthcare Research and Quality (or any other relevant office designated by Agency for Healthcare Research and Quality), in consultation with the National Institutes of Health, shall broadly disseminate the research findings that are published by the Patient Centered Outcomes Research Institute established under section 1320e(b) of this title (referred to in this section as the “Institute”) and other government-funded research relevant to comparative clinical effectiveness research. The Office shall create informational tools that organize and disseminate research findings for physicians, health care providers, patients, payers, and policy makers. The Office shall also develop a publicly available resource database that collects and contains government-funded evidence and research from public, private, not-for profit, and academic sources.

(2)Requirements

The Office shall provide for the dissemination of the Institute’s research findings and government-funded research relevant to comparative clinical effectiveness research to physicians, health care providers, patients, vendors of health information technology focused on clinical decision support, appropriate professional associations, and Federal and private health plans. Materials, forums, and media used to disseminate the findings, informational tools, and resource databases shall—

(A)include a description of considerations for specific subpopulations, the research methodology, and the limitations of the research, and the names of the entities, agencies, instrumentalities, and individuals who conducted any research which was published by the Institute; and

(B)not be construed as mandates, guidelines, or recommendations for payment, coverage, or treatment.

(b)Incorporation of research findings

The Office, in consultation with relevant medical and clinical associations, shall assist users of health information technology focused on clinical decision support to promote the timely incorporation of research findings disseminated under subsection (a) into clinical practices and to promote the ease of use of such incorporation.

(c)Feedback

The Office shall establish a process to receive feedback from physicians, health care providers, patients, and vendors of health information technology focused on clinical decision support, appropriate professional associations, and Federal and private health plans about the value of the information disseminated and the assistance provided under this section.

(d)Rule of construction

Nothing in this section shall preclude the Institute from making its research findings publicly available as required under section 1320e(d)(8) of this title.

(e)Training of researchers

The Agency for Health Care Research and Quality, in consultation with the National Institutes of Health, shall build capacity for comparative clinical effectiveness research by establishing a grant program that provides for the training of researchers in the methods used to conduct such research, including systematic reviews of existing research and primary research such as clinical trials. At a minimum, such training shall be in methods that meet the methodological standards adopted under section 1320e(d)(9) of this title.

(f)Building data for research

The Secretary shall provide for the coordination of relevant Federal health programs to build data capacity for comparative clinical effectiveness research, including the development and use of clinical registries and health outcomes research data networks, in order to develop and maintain a comprehensive, interoperable data network to collect, link, and analyze data on outcomes and effectiveness from multiple sources, including electronic health records.

(g)Authority to contract with the Institute

Agencies and instrumentalities of the Federal Government may enter into agreements with the Institute, and accept and retain funds, for the conduct and support of research described in this part, provided that the research to be conducted or supported under such agreements is authorized under the governing statutes of such agencies and instrumentalities.

Editorial Notes

Prior Provisions

A prior section 937 of act July 1, 1944, was renumbered section 947 and is classified to section 299c–6 of this title.

§299b–37 Dissemination and Building Capacity for Research

Summary

Title 42, §299b–37

Notes & Related Subsidiaries

Editorial Notes

Prior Provisions

Citations & Metadata