42 U.S.C. § 280g–15
(a)
In general— The
Secretary is authorized to award demonstration grants to
States for the development, implementation, and evaluation of alternatives to current tort litigation for resolving disputes over injuries allegedly caused by
health care providers or
health care organizations. In awarding such grants, the
Secretary shall ensure the diversity of the alternatives so funded.
(c)
Conditions for demonstration grants—
(1)
Requirements— Each
State desiring a grant under
subsection (a) shall develop an alternative to current tort litigation
that—
(B)
promotes a reduction of health care errors by encouraging the collection and analysis of patient safety data related to disputes resolved under
subparagraph (A) by organizations that engage in efforts to improve patient safety and the quality of health care.
(2)
Alternative to current tort litigation— Each
State desiring a grant under
subsection (a) shall demonstrate how the proposed alternative described in
paragraph (1)(A)—
(A)
makes the medical liability system more reliable by increasing the availability of prompt and fair resolution of disputes;
(B)
encourages the efficient resolution of disputes;
(C)
encourages the disclosure of health care errors;
(D)
enhances patient safety by detecting, analyzing, and helping to reduce medical errors and adverse events;
(E)
improves access to liability insurance;
(F)
fully informs patients about the differences in the alternative and current tort litigation;
(G)
provides patients the ability to opt out of or voluntarily withdraw from participating in the alternative at any time and to pursue other options, including litigation, outside the alternative;
(H)
would not conflict with
State law at the time of the application in a way that would prohibit the adoption of an alternative to current tort litigation; and
(I)
would not limit or curtail a patient’s existing legal rights, ability to file a
claim in or access a
State’s legal system, or otherwise abrogate a patient’s ability to file a medical malpractice
claim.
(3)
Sources of compensation— Each
State desiring a grant under
subsection (a) shall identify the sources from and methods by which compensation would be paid for
claims resolved under the proposed alternative to current tort litigation, which may include public or private funding sources, or a combination of such sources. Funding methods shall to the extent practicable provide financial incentives for activities that improve patient safety.
(4)
Scope—
(A)
In general— Each
State desiring a grant under
subsection (a) shall establish a scope of jurisdiction (such as Statewide, designated geographic region, a designated area of health care practice, or a designated group of
health care providers or
health care organizations) for the proposed alternative to current tort litigation that is sufficient to evaluate the effects of the alternative. No scope of jurisdiction shall be established under this paragraph that is based on a health care payer or patient population.
(B)
Notification of patients— A
State shall demonstrate how patients would be notified that they are receiving
health care services that fall within such scope, and the process by which they may opt out of or voluntarily withdraw from participating in the alternative. The decision of the patient whether to participate or continue participating in the alternative process shall be made at any time and shall not be limited in any way.
(5)
Preference in awarding demonstration grants— In awarding grants under
subsection (a), the
Secretary shall give preference to
States—
(B)
that make proposals that are likely to enhance patient safety by detecting, analyzing, and helping to reduce medical errors and adverse events; and
(C)
that make proposals that are likely to improve access to liability insurance.
(d)
Application—
(1)
In general— Each
State desiring a grant under
subsection (a) shall submit to the
Secretary an application, at such time, in such manner, and containing such information as the
Secretary may require.
(2)
Review panel—
(A)
In general— In reviewing applications under
paragraph (1), the
Secretary shall consult with a review
panel composed of relevant experts appointed by the Comptroller General.
(B)
Composition—
(i)
Nominations— The Comptroller General shall solicit nominations from the public for individuals to serve on the review
panel.
(ii)
Appointment— The Comptroller General shall appoint, at least 9 but not more than 13, highly qualified and knowledgeable individuals to serve on the review
panel and shall ensure that the following entities receive fair representation on such
panel:
(IV)
Medical malpractice insurers.
(VI)
Patient safety experts.
(C)
Chairperson— The Comptroller General shall designate a member of the review
panel to be the chairperson of the review
panel.
(D)
Availability of information— The
Secretary shall make available to the review
panel such information, personnel, and administrative
services and assistance as the review
panel may reasonably require to carry out its duties.
(E)
Information from agencies— The review
panel may request directly from any department or agency of the
United States any information that such
panel considers necessary to carry out its duties. To the extent consistent with applicable laws and
regulations, the head of such department or agency shall furnish the requested information to the review
panel.
(e)
Reports—
(1)
By State— Each
State receiving a grant under
subsection (a) shall submit to the
Secretary an annual report evaluating the effectiveness of activities funded with grants awarded under such subsection. Such report shall, at a minimum, include the impact of the activities funded on patient safety and on the availability and price of medical liability insurance.
(2)
By Secretary— The
Secretary shall submit to Congress an annual compendium of the reports submitted under
paragraph (1) and an analysis of the activities funded under
subsection (a) that examines any differences that result from such activities in terms of the quality of care, number and nature of medical errors, medical resources used, length of time for dispute resolution, and the availability and price of liability insurance.
(f)
Technical assistance—
(2)
Requirements— Technical assistance under
paragraph (1) shall
include—
(A)
guidance on non-economic
damages, including the consideration of individual facts and circumstances in determining appropriate payment, guidance on identifying avoidable injuries, and guidance on disclosure to patients of health care errors and adverse events; and
(B)
the development, in consultation with
States, of common definitions, formats, and data collection infrastructure for
States receiving grants under this section to use in reporting to facilitate aggregation and analysis of data both within and between
States.
(3)
Use of common definitions, formats, and data collection infrastructure— States not receiving grants under this section may also use the common definitions, formats, and data collection infrastructure developed under
paragraph (2)(B).
(g)
Evaluation—
(1)
In general— The
Secretary, in consultation with the review
panel established under
subsection (d)(2), shall enter into a contract with an appropriate research organization to conduct an overall evaluation of the effectiveness of grants awarded under
subsection (a) and to annually prepare and submit a report to Congress. Such an evaluation shall begin not later than 18 months following the date of implementation of the first
program funded by a grant under
subsection (a).
(2)
Contents— The evaluation under
paragraph (1) shall
include—
(E)
a comparison, with regard to the measures described in
paragraph (3),
of—
(ii)
States that enacted, prior to March 23, 2010, any cap on non-economic
damages; and
(iii)
States that have enacted, prior to March 23, 2010, a requirement that the
complainant obtain an opinion regarding the merit of the
claim, although the substance of such opinion may have no bearing on whether the
complainant may proceed with a case.
(3)
Measures— The evaluations under
paragraph (2) shall analyze and make comparisons on the basis
of—
(B)
the nature and number of
claims in which tort litigation was pursued despite the existence of an alternative under
subsection (a);
(C)
the disposition of disputes and
claims, including the length of time and estimated costs to all parties;
(D)
the medical liability environment;
(F)
patient safety in terms of detecting, analyzing, and helping to reduce medical errors and adverse events;
(H)
impact on utilization of medical
services, appropriately adjusted for risk.
(4)
Funding— The
Secretary shall reserve 5 percent of the amount appropriated in each fiscal year under
subsection (k) to carry out this subsection.
(h)
MedPAC and MACPAC reports—
(1)
MedPAC— The Medicare Payment Advisory
Commission shall conduct an independent review of the alternatives to current tort litigation that are implemented under grants under
subsection (a) to determine the impact of such alternatives on the Medicare
program under title XVIII of the Social Security Act
[42 U.S.C. 1395 et seq.], and its
beneficiaries.
(2)
MACPAC— The Medicaid and CHIP Payment and Access
Commission shall conduct an independent review of the alternatives to current tort litigation that are implemented under grants under
subsection (a) to determine the impact of such alternatives on the Medicaid or CHIP
programs under titles XIX and XXI of the Social Security Act
[42 U.S.C. 1396 et seq., 1397aa et seq.], and their
beneficiaries.
(3)
Reports— Not later than December 31, 2016, the Medicare Payment Advisory
Commission and the Medicaid and CHIP Payment and Access
Commission shall each submit to Congress a report that includes the findings and recommendations of each respective
Commission based on independent reviews conducted under paragraphs
(1) and
(2), including an analysis of the impact of the alternatives reviewed on the efficiency and effectiveness of the respective
programs.
(i)
Option to provide for initial planning grants— Of the
funds appropriated pursuant to
subsection (k), the
Secretary may use a portion not to exceed $500,000 per
State to provide planning grants to such
States for the development of
demonstration project applications meeting the criteria described in
subsection (c). In selecting
States to receive such planning grants, the
Secretary shall give preference to those
States in which
State law at the time of the application would not prohibit the adoption of an alternative to current tort litigation.
(j)
Definitions— In this section:
(1)
Health care services— The term “health care services” means any
services provided by a
health care provider, or by any individual working under the supervision of a
health care provider, that relate
to—
(A)
the diagnosis, prevention, or
treatment of any human disease or impairment; or
(B)
the assessment of the health of human beings.
(2)
Health care organization— The term “health care organization” means any individual or entity which is obligated to provide, pay for, or administer health benefits under any
health plan.
(3)
Health care provider— The term “health care provider” means any individual or entity—
(B)
required to be so licensed, registered, or certified but that is exempted by other statute or regulation.
(k)
Authorization of appropriations— There are authorized to be appropriated to carry out this section, $50,000,000 for the 5-fiscal year period beginning with fiscal year 2011.
(l)
Current State efforts to establish alternative to tort litigation— Nothing in this section shall be construed to limit any prior, current, or future efforts of any
State to establish any alternative to tort litigation.
(m)
Rule of construction— Nothing in this section shall be construed as limiting
states’
1 authority over or responsibility for their
state1 justice systems.
Notes, amendments, and revision history
(July 1, 1944, ch. 373, title III, § 399V–4, as added Pub. L. 111–148, title X, § 10607, Mar. 23, 2010, 124 Stat. 1009; amended Pub. L. 114–301, § 3(d), Dec. 16, 2016, 130 Stat. 1515.)
Editorial Notes
References in Text
The Social Security Act, referred to in subsec. (h)(1), (2), is act Aug. 14, 1935, ch. 531, 49 Stat. 620. Titles XVIII, XIX, and XXI of the Act are classified generally to subchapters XVIII (§ 1395 et seq.), XIX (§ 1396 et seq.), and XXI (§ 1397aa et seq.), respectively, of chapter 7 of this title. For complete classification of this Act to the Code, see section 1305 of this title and Tables.
Amendments
2016—Subsec. (d)(2)(C). Pub. L. 114–301, § 3(d)(1), substituted “shall designate a member of the review panel to” for “, or an individual within the Government Accountability Office designated by the Comptroller General, shall”.
Subsec. (d)(2)(D). Pub. L. 114–301, § 3(d)(2), substituted “Secretary” for “Comptroller General”.