Title II — Extensions and Other Provisions
II Extensions and Other Provisions
A Medicare Extensions
Sec. 202 Medicare payment for therapy services
“(iii) With respect to services furnished during the period beginning on the date of enactment of the SGR Repeal and Medicare Beneficiary Access Act of 2013, and ending on December 31, 2014, the provisions of this paragraph shall only apply to the extent necessary to carry out the manual medical review process under this subparagraph.”
“(aa) Medical review of outpatient therapy services
“(1) In general
“(A) Process for medical review—The Secretary shall implement a process for the medical review (as described in paragraph (2)) of outpatient therapy services (as defined in paragraph (10)) and, subject to paragraph (12), apply such process to such services furnished on or after January 1, 2015, focusing on services identified under subparagraph (B).
“(B) Identification of services for review—Under the process, the Secretary shall identify services for medical review, using such factors as the Secretary determines appropriate, which may include the following:
“(i) Services furnished by a therapy provider (as defined in paragraph (10)) whose pattern of billing is higher compared to peers.
“(ii) Services furnished by a therapy provider who, in a prior period, has a high claims denial percentage or is least compliant with other applicable requirements under this title.
“(iii) Services furnished by a therapy provider that is newly enrolled under this title.
“(iv) Services furnished by a therapy provider who has questionable billing practices, such as billing medically unlikely units of services in a day.
“(v) Services furnished to treat a type of medical condition.
“(vi) Services identified by use of the standardized data elements required to be reported under section 1834(p).
“(vii) Services furnished by a single therapy provider or a group that includes a therapy provider identified by factors described in this subparagraph.
“(viii) Other services as determined appropriate by the Secretary.
“(2) Medical review
“(A) Prior authorization medical review
“(i) In general—Subject to the succeeding provisions of this subparagraph, the Secretary shall use prior authorization medical review for outpatient therapy services furnished to an individual above one or more thresholds established by the Secretary, such as a dollar threshold or a threshold based on factors such as the type of outpatient therapy service or setting.
“(ii) Ending application of prior authorization for a therapy provider—The Secretary shall end the application of prior authorization medical review to outpatient therapy services furnished by a therapy provider if the Secretary determines that the provider has a low denial rate under such prior authorization. The Secretary may subsequently reapply prior authorization medical review to such therapy provider if the Secretary determines it to be appropriate.
“(iii) Prior authorization of multiple services—The Secretary shall, where practicable, provide for prior authorization medical review for multiple services at a single time, such as services in a therapy plan of care described in section 1861(p)(2).
“(B) Other types of medical review—The Secretary may use pre-payment review or post-payment review for services identified under paragraph (1)(B) that are not subject to prior authorization medical review under subparagraph (A).
“(C) Limitation for law enforcement activities—The Secretary may determine that medical review under this subsection does not apply in the case where fraud may be involved.
“(3) Review contractors—The Secretary shall conduct prior authorization medical review of outpatient therapy services under this subsection using medicare administrative contractors (as described in section 1874A) or other review contractors (other than contractors under section 1893(h) or contractors paid on a contingent basis).
“(4) No payment without prior authorization—With respect to an outpatient therapy service for which prior authorization medical review under this subsection applies, no payment shall be made under this part for the service unless a prior authorization determination is made, in advance of furnishing such service, that such service would meet the applicable requirements of section 1862(a)(1)(A).
“(5) Submission of information—A therapy provider may submit the information necessary for medical review by fax, by mail, or by electronic means. The Secretary shall make available the electronic means described in the preceding sentence as soon as practicable, but not later than 24 months after the date of enactment of this subsection.
“(6) Timeliness—The Secretary shall make a prior authorization determination under this subsection within 10 business days of the date of the Secretary’s receipt of medical documentation needed to make such determination or the Secretary shall be deemed to have found the services to meet the applicable requirements of section 1862(a)(1)(A).
“(7) Construction—With respect to an outpatient therapy service that has been affirmed by medical review under this subsection, nothing in this subsection shall be construed to preclude the subsequent denial of a claim for such service that does not meet other applicable requirements under this Act.
“(8) Beneficiary protections—With respect to services furnished on or after January 1, 2015, where payment may not be made as a result of application of medical review under this subsection, section 1879 shall apply in the same manner as such section applies to a denial that is made by reason of section 1862(a)(1).
“(9) Implementation
“(A) Authority—The Secretary may implement the provisions of this subsection by interim final rule with comment period.
“(B) Administration—Chapter 35 of title 44, United States Code, shall not apply to medical review under this subsection.
“(10) Definitions—For purposes of this subsection:
“(A) Outpatient therapy services—The term outpatient therapy services means the following services for which payment is made under section 1848, 1834(g), or 1834(k):
“(i) Physical therapy services of the type described in section 1861(p).
“(ii) Speech-language pathology services of the type described in such section though the application of section 1861(ll)(2).
“(iii) Occupational therapy services of the type described in section 1861(p) through the operation of section 1861(g).
“(B) Therapy provider—The term therapy provider means a provider of services (as defined in section 1861(u)) or a supplier (as defined in section 1861(d)) who submits a claim for outpatient therapy services.
“(11) Funding—For purposes of implementing this subsection, the Secretary shall provide for the transfer, from the Federal Supplementary Medical Insurance Trust Fund under section 1841, of $35,000,000 to the Centers for Medicare & Medicaid Services Program Management Account for each fiscal year (beginning with fiscal year 2014). Amounts transferred under this paragraph shall remain available until expended.
“(12) Scaling back
“(A) Periodic determinations—Beginning with 2017, and every two years thereafter, the Secretary shall—
“(i) make a determination of the improper payment rate for outpatient therapy services for a 12-month period; and
“(ii) make such determination publicly available.
“(B) Scaling back—If the improper payment rate for outpatient therapy services determined for a 12-month period under subparagraph (A) is 50 percent or less of the Medicare fee-for-service improper payment rate for such period, the Secretary shall—
“(i) reduce the amount and extent of medical review conducted for a prospective year under the process established in this subsection; and
“(ii) return an appropriate portion of the funding provided for such year under paragraph (11).”
“(p) Collection of standardized data elements for outpatient therapy services
“(1) Standardized data elements
“(A) In general—Not later than 6 months after the date of enactment of this subsection, the Secretary shall post on the Internet website of the Centers for Medicare & Medicaid Services a draft list of standardized data elements for individuals receiving outpatient therapy services.
“(B) Domains—Such standardized data elements shall include information with respect to the following domains, as determined appropriate by the Secretary:
“(i) Demographic information.
“(ii) Diagnosis.
“(iii) Severity.
“(iv) Affected body structures and functions.
“(v) Limitations with activities of daily living and participation.
“(vi) Functional status.
“(vii) Other domains determined to be appropriate by the Secretary.
“(C) Solicitation of input—The Secretary shall accept comments from stakeholders through the date that is 60 days after the date the Secretary posts the draft list of standardized data elements pursuant to subparagraph (A). In seeking such comments, the Secretary shall use one or more mechanisms to solicit input from stakeholders that may include use of open door forums, town hall meetings, requests for information, or other mechanisms determined appropriate by the Secretary.
“(D) Operational list of standardized data elements—Not later than 120 days after the end of the comment period described in subparagraph (C), the Secretary, taking into account such comments, shall post on the Internet website of the Centers for Medicare & Medicaid Services an operational list of standardized data elements.
“(E) Subsequent revisions—Subsequent revisions to the operational list of standardized data elements shall be made through rulemaking. Such revisions may be based on experience and input from stakeholders.
“(2) System to report standardized data elements
“(A) In general—Not later than 18 months after the date the Secretary posts the operational list of standardized data elements pursuant to paragraph (1)(D), the Secretary shall develop and implement an electronic system (which may be a web portal) for therapy providers to report the standardized data elements for individuals with respect to outpatient therapy services.
“(B) Consultation—The Secretary shall seek comments from stakeholders regarding the best way to report the standardized data elements.
“(3) Reporting
“(A) Frequency of reporting—The Secretary shall specify the frequency of reporting standardized data elements. The Secretary shall seek comments from stakeholders regarding the frequency of the reporting of such data elements.
“(B) Reporting requirement—Beginning on the date the system to report standardized data elements under this subsection is operational, no payment shall be made under this part for outpatient therapy services furnished to an individual unless a therapy provider reports the standardized data elements for such individual.
“(4) Report on new payment system for outpatient therapy services
“(A) In general—Not later than 18 months after the date described in paragraph (3)(B), the Secretary shall submit to Congress a report on the design of a new payment system for outpatient therapy services. The report shall include an analysis of the standardized data elements collected and other appropriate data and information.
“(B) Features—Such report shall consider—
“(i) appropriate adjustments to payment (such as case mix and outliers);
“(ii) payments on an episode of care basis; and
“(iii) reduced payment for multiple episodes.
“(C) Consultation—The Secretary shall consult with stakeholders regarding the design of such a new payment system.
“(5) Implementation
“(A) Funding—For purposes of implementing this subsection, the Secretary shall provide for the transfer, from the Federal Supplementary Medical Insurance Trust Fund under section 1841, of $7,000,000 to the Centers for Medicare & Medicaid Services Program Management Account for each of fiscal years 2014 through 2018. Amounts transferred under this subparagraph shall remain available until expended.
“(B) Administration—Chapter 35 of title 44, United States Code, shall not apply to specification of the standardized data elements and implementation of the system to report such standardized data elements under this subsection.
“(C) Limitation—There shall be no administrative or judicial review under section 1869, section 1878, or otherwise of the specification of standardized data elements required under this subsection or the system to report such standardized data elements.
“(D) Definition of outpatient therapy services and therapy provider—In this subsection, the terms “outpatient therapy services” and therapy provider have the meaning given those term in section 1833(aa).”
“(3) Each request for payment, or bill submitted, by a therapy provider (as defined in section 1833(aa)(10)) for an outpatient therapy service (as defined in such section) furnished by a therapy assistant on or after January 1, 2015, shall include (in a form and manner specified by the Secretary) an indication that the service was furnished by a therapy assistant.”
Sec. 203 Medicare ambulance services
“(16) Submission of cost and other information
“(A) Development of data collection system—The Secretary shall develop a data collection system (which may include use of a cost survey and standardized definitions) for providers and suppliers of ambulance services to collect cost, revenue, utilization, and other information determined appropriate by the Secretary. Such system shall be designed to submit information—
“(i) needed to evaluate the appropriateness of payment rates under this subsection;
“(ii) on the utilization of capital equipment and ambulance capacity; and
“(iii) on different types of ambulance services furnished in different geographic locations, including rural areas and low population density areas described in paragraph (12).
“(B) Specification of data collection system
“(i) In general—Not later than January 1, 2015, the Secretary shall—
“(I) specify the data collection system under subparagraph (A); and
“(II) identify the providers and suppliers of ambulance services who would be required to submit the information under such data collection system.
“(ii) Respondents—Subject to subparagraph (D)(ii), the Secretary shall determine an appropriate sample of providers and suppliers of ambulance services to submit information under the data collection system each year.
“(C) Reporting of cost information—Beginning July 1, 2015, a 5 percent reduction to payments under this part shall be made for a 1-year period to a provider or supplier of ambulance services who—
“(i) is identified under subparagraph (B)(i)(II) as being required to submit the information under the data collection system; and
“(ii) does not submit such information.
“(D) Ongoing data collection
“(i) Revision of data collection system—The Secretary may revise, as the Secretary determines appropriate, the data collection system. The Secretary shall consult with providers and suppliers of ambulance services when revising such system.
“(ii) Subsequent data collection—In order to continue to evaluate the appropriateness of payment rates under this subsection, the Secretary shall require providers and suppliers of ambulance services to submit information for years after 2015 as the Secretary determines appropriate, but in no case less often than once every 3 years.
“(E) Consultation—The Secretary shall consult with stakeholders in carrying out the development of the system and collection of information under this paragraph, including the activities described in subparagraphs (A) and (D). Such consultation shall include the use of requests for information and other mechanisms determined appropriate by the Secretary.
“(F) Administration—Chapter 35 of title 44, United States Code, shall not apply to the collection of information required under this subsection.
“(G) Limitations on review—There shall be no administrative or judicial review under section 1869, section 1878, or otherwise of the data collection system or identification of respondents under this paragraph.
“(H) Funding for implementation—For purposes of carrying out subparagraph (A), the Secretary shall provide for the transfer, from the Federal Supplementary Medical Insurance Trust Fund under section 1841, of $1,000,000 to the Centers for Medicare & Medicaid Services Program Management Account for fiscal year 2014. Amounts transferred under this subparagraph shall remain available until expended.”
Sec. 204 Revision of the Medicare-dependent hospital (MDH) program
Sec. 205 Revision of Medicare inpatient hospital payment adjustment for low-volume hospitals
Sec. 206 Specialized Medicare Advantage plans for special needs individuals
“(A) In general—Subject to subparagraphs (B) and (C), in the case”
“(B) Application to dual SNPs—Subparagraph (A) shall only apply to a specialized MA plan for special needs individuals described in subsection (b)(6)(B)(ii) for periods before January 1, 2021.
“(C) Application to severe or disabling chronic condition SNPs—Subparagraph (A) shall only apply to a specialized MA plan for special needs individuals described in subsection (b)(6)(B)(iii) for periods before January 1, 2018.”
“(F) The plan meets the requirements applicable under paragraph (8).”
“(8) Increased integration of dual SNPs
“(A) Designated contact—The Secretary, acting through the Federal Coordinated Health Care Office (Medicare-Medicaid Coordination Office) established under section 2602 of the Patient Protection and Affordable Care Act (in this paragraph referred to as the “MMCO”), shall serve as a dedicated point of contact for States to address misalignments that arise with the integration of specialized MA plans for special needs individuals described in subsection (b)(6)(B)(ii) under this paragraph. Consistent with such role, the MMCO shall—
“(i) establish a uniform process for disseminating to State Medicaid agencies information under this title impacting contracts between such agencies and such plans under this subsection; and
“(ii) establish basic resources for States interested in exploring such plans as a platform for integration.
“(B) Unified appeals process
“(i) In general—Not later than April 1, 2015, the Secretary shall establish procedures unifying the appeals procedures under sections 1852(g), 1902(a)(3), and 1902(a)(5) for items and services provided by specialized MA plans for special needs individuals described in subsection (b)(6)(B)(ii) under this title and title XIX. The Secretary shall solicit comment in developing such procedures from States, plans, beneficiary representatives, and other relevant stakeholders.
“(ii) Procedures—To the extent compatible with a unified process, the procedures established under clause (i) shall—
“(I) adopt the most protective provisions for the enrollee under current law, including continuation of benefits under title XIX pending appeal if an appeal is filed in a timely manner;
“(II) take into account differences in State plans under title XIX;
“(III) be easily navigable by an enrollee; and
“(IV) include the elements described in clause (iii).
“(iii) Elements described—The following elements are described in this clause:
“(I) Single notification of all applicable appeal rights under this title and title XIX.
“(II) Notices written in plain language and available in a language and format that is accessible to the enrollee.
“(III) Unified timeframes for internal and external appeals processes, such as an individual's filing of appeals, a plan’s acknowledgment and resolution of appeals, and notification of appeals decisions.
“(IV) Mechanisms to allow the plan to track and resolve grievances.
“(C) Requirement for unified appeals
“(i) In general—For 2016 and subsequent years, the contract of a specialized MA plan for special needs individuals described in subsection (b)(6)(B)(ii) with a State Medicaid agency under this subsection shall require the use of unified appeals procedures as described in subparagraph (B).
“(ii) Consideration of application for other SNPs—The Secretary shall consider applying the unified appeals process described in subparagraph (B) to specialized MA plans for special needs individuals described in subsection (b)(6)(B)(i) and subsection (b)(6)(B)(iii).
“(D) Requirement for full integration for certain dual SNPs
“(i) Requirement—Subject to the succeeding provisions of this subparagraph, for 2018 and subsequent years, a specialized MA plan for special needs individuals described in subsection (b)(6)(B)(ii) shall—
“(I) integrate all benefits under this title and title XIX; and
“(II) meet the requirements of a fully integrated plan described in section 1853(a)(1)(B)(iv)(II) (other than the requirement that the plan have similar average levels of frailty, as determined by the Secretary, as the PACE program), including with respect to long-term care services or behavioral health services to the extent State law permits capitation of those services under such plan.
“(ii) Initial sanctions for failure to meet requirement for 2018 or 2019—For each of 2018 and 2019, if the Secretary determines that a plan has failed to meet the requirement described in clause (i), the Secretary shall impose one of the following on the plan:
“(I) A reduction in payments under this part.
“(II) Closing enrollment in the plan.
“(III) Sanctioning the plan in accordance with section 1857(g).
“(IV) Other reasonable action (other than the sanction described in clause (iii)) the Secretary determines appropriate.
“(iii) Sanctions for failure to meet requirement for 2020 and subsequent years—For 2020 and subsequent years, if the Secretary determines that a plan has failed to meet the requirement described in clause (i), the plan shall be deemed to no longer meet the definition of a specialized MA plan for special needs individuals described in subsection (b)(6)(B)(ii).
“(iv) Limitation—This subparagraph shall not apply to a specialized MA plan for special needs individuals described in subsection (b)(6)(B)(ii) that only enrolls individuals for whom the only medical assistance to which the individuals are entitled under the State plan is medicare cost sharing described in section 1905(p)(3)(A)(ii).”
“(6) To act as a designated contact for States under subsection (f)(8)(A) of section 1859 of the Social Security Act (42 U.S.C. 1395w–28) with respect to the integration of specialized MA plans for special needs individuals described in subsection (b)(6)(B)(ii) of such section.”
“(A) In general—Subject to subparagraph (B), the requirements”
“(B) Improvements to care management requirements for severe or disabling chronic condition SNPs—For 2016 and subsequent years, in the case of a specialized MA plan for special needs individuals described in subsection (b)(6)(B)(iii), the requirements described in this paragraph include the following:
“(i) The interdisciplinary team under subparagraph (A)(ii)(III) includes a team of providers with demonstrated expertise, including training in an applicable specialty, in treating individuals similar to the targeted population of the plan.
“(ii) Requirements developed by the Secretary to provide face-to-face encounters with individuals enrolled in the plan.
“(iii) As part of the model of care under clause (i) of subparagraph (A), the results of the initial assessment and annual reassessment under clause (ii)(I) of such subparagraph of each individual enrolled in the plan are addressed in the individual’s individualized care plan under clause (ii)(II) of such subparagraph.
“(iv) As part of the annual evaluation and approval of such model of care, the Secretary shall take into account whether the plan fulfilled the previous year’s goals (as required under the model of care).
“(v) The Secretary shall establish a minimum benchmark for each element of the model of care of a plan. The Secretary shall only approve a plan's model of care under this paragraph if each element of the model of care meets the minimum benchmark applicable under the preceding sentence.”
“(6) Changes to quality ratings of SNPs
“(A) Emphasis on improvement across SNPs—Subject to subparagraph (B), beginning in plan year 2016, in the case of a specialized MA plan for special needs individuals, the Secretary shall increase the emphasis on the plan’s improvement or decline in performance when determining the star rating of the plan under this subsection for the year as follows:
“(i) At least 25 percent, but not more than 33 percent, of the total star rating of the plan shall be based on improvement or decline in performance.
“(ii) Improvement or decline in performance under this subparagraph shall be measured based on net change in the individual star rating measures of the plan, with appropriate weight given to specific individual star ratings measures, such as readmission rates, as determined by the Secretary.
“(iii) The Secretary shall make an appropriate adjustment to the improvement rating of a plan under this subparagraph if the plan has achieved a 5-star rating or the highest rating possible overall or for an individual measure in order to ensure that the plan is not punished in cases where it is not possible to improve.
“(B) No application to certain plans—Subparagraph (A) shall not apply, with respect to a year, to a specialized MA plan for special needs individuals that has a rating that does not exceed two-and-one-half stars.
“(C) Quality Measurement at the Plan Level
“(i) In general—The Secretary may require reporting for and apply under this subsection quality measures at the plan level for specialized MA plan for special needs individuals instead of at the contract level.
“(ii) Consideration—The Secretary shall take into consideration the minimum number of enrollees in a specialized MA plan for special needs individuals in order to determine if a valid measurement of quality at the plan level is possible under clause (i).
“(iii) Application—If the Secretary applies quality measurement at the plan level under this subparagraph—
“(I) such quality measurement shall include Medicare Health Outcomes Survey (HOS), Healthcare Effectiveness Data and Information Set (HEDIS), and Consumer Assessment of Healthcare Providers and Systems (CAHPS) measures; and
“(II) payment and other administrative actions linked to quality measurement (including the 5-star rating system under this subsection) shall be applied at the plan level in accordance with this subparagraph.”
Sec. 207 Reasonable cost reimbursement contracts
“(iv) In the case of an eligible organization that is offering a reasonable cost reimbursement contract that may no longer be extended or renewed because of the application of clause (ii)—
“(I) notwithstanding such clause, such contract may be extended or renewed for one last reasonable cost reimbursement contract year;
“(II) the organization may not enroll any new enrollees under such contract during such last reasonable cost reimbursement contract year; and
“(III) on a date determined by the Secretary prior to the beginning of such last reasonable cost reimbursement contract year, the organization shall provide notice to the Secretary as to whether or not the organization will apply to have the contract converted over and offered as a Medicare Advantage plan under part C for the year following such last reasonable cost reimbursement contract year.
“(v) If an eligible organization that is offering a reasonable cost reimbursement contract that is extended or renewed pursuant to clause (iv) provides the notice described in clause (iv)(III) that the contract will be converted—
“(I) the deemed enrollment under section 1851(c)(4) shall apply; and
“(II) the special rule for quality increases under 1853(o)(3)(A)(iv) shall apply.”
“(4) Deemed enrollment relating to converted reasonable cost reimbursement contracts
“(A) In general—On the first day of the annual, coordinated election period under subsection (e)(3) for plan years beginning on or after January 1, 2016, an MA eligible individual described in clause (i) or (ii) of subparagraph (B) is deemed to have elected to receive benefits under this title through an applicable MA plan (and shall be enrolled in such plan) beginning with such plan year, if—
“(i) the individual is enrolled in a reasonable cost reimbursement contract under section 1876(h) in the previous plan year;
“(ii) such reasonable cost reimbursement contract was extended or renewed for one last reasonable cost reimbursement contract year pursuant to section 1876(h)(5)(C)(iv);
“(iii) the eligible organization that is offering such reasonable cost reimbursement contract provided the notice described in subclause (III) of such section that the contract was to be converted;
“(iv) the applicable MA plan—
“(I) is the plan that was converted from the reasonable cost reimbursement contract described in clause (iii);
“(II) is offered by the same entity (or an organization affiliated with such entity) that entered into such contract; and
“(III) is offered in the service area where the individual resides;
“(v) the amount of the MA monthly basic beneficiary premium for such applicable MA plan with respect to the plan year does not exceed monthly premiums under such reasonable cost reimbursement contract for the previous plan year by more than 10 percent;
“(vi) the applicable MA plan provides benefits, premiums, and access to providers that are comparable to the benefits, premiums, and access to providers under such reasonable cost reimbursement contract for the previous plan year; and
“(vii) the applicable MA plan—
“(I) allows enrollees transitioning from the converted reasonable cost contract to such plan to maintain current providers and course of treatment at the time of enrollment for at least 90 days after enrollment; and
“(II) during such period, pays non-contracting providers for items and services furnished to the enrollee an amount that is not less than the amount of payment applicable for those items and services under the original medicare fee-for-service program under parts A and B.
“(B) MA eligible individuals described
“(i) Without prescription drug coverage—An MA eligible individual described in this clause, with respect to a plan year, is an MA eligible individual who is enrolled in a reasonable cost reimbursement contract under section 1876(h) in the previous plan year and who does not, for such previous plan year, receive any prescription drug coverage under part D, including coverage under section 1860D–22.
“(ii) With prescription drug coverage—An MA eligible individual described in this clause, with respect to a plan year, is an MA eligible individual who is enrolled in a reasonable cost reimbursement contract under section 1876(h) in the previous plan year and who, for such previous plan year, receives prescription drug coverage under part D—
“(I) through such contract; or
“(II) through a prescription drug plan, if the sponsor of such plan is the same entity (or an organization affiliated with such entity) that entered into such contract.
“(C) Applicable MA plan defined—In this paragraph, the term “applicable MA plan” means, in the case of an individual described in—
“(i) subparagraph (B)(i), an MA plan that is not an MA–PD plan; and
“(ii) subparagraph (B)(ii), an MA–PD plan.
“(D) Identification of deemed individuals—Not later than 30 days before the first day of the annual, coordinated election period under subsection (e)(3) for plan years beginning on or after January 1, 2016, the Secretary shall identify the individuals who will be subject to deemed elections under subparagraph (A) on the first day of such period.”
“(F) Special period for certain deemed elections
“(i) In general—At any time during the period beginning after the last day of the annual, coordinated election period under paragraph (3) in which an individual is deemed to have elected to enroll in an MA plan or MA–PD plan under subsection (c)(4) and ending on the last day of February of the first plan year for which the individual is enrolled in such plan, such individual may change the election under subsection (a)(1) (including changing the MA plan or MA–PD plan in which the individual is enrolled).
“(ii) Limitation of one change—An individual may exercise the right under clause (i) only once during the applicable period described in such clause. The limitation under this clause shall not apply to changes in elections effected during an annual, coordinated election period under paragraph (3) or during a special enrollment period under paragraph (4).”
“(ii) Notification related to certain deemed elections—The Secretary shall, not later than 15 days prior to the first day of the annual, coordinated election period under subsection (e)(3) of a year, mail to any individual identified by the Secretary under subsection (c)(4)(D) for such year—
“(I) a notification that such individual will, on such day, be deemed to have made an election to receive benefits under this title through an MA plan or MA–PD plan (and shall be enrolled in such plan) for the next plan year under subsection (c)(4)(A), but that the individual may make a different election during the annual, coordinated election period for such year;
“(II) the information described in subparagraph (A);
“(III) a description of the differences between such MA plan or MA–PD plan and the reasonable cost reimbursement contract in which the individual was most recently enrolled with respect to benefits covered under such plans, including cost-sharing, premiums, drug coverage, and provider networks; and
“(IV) information about the special period for elections under subsection (e)(2)(F).”
“(iv) Special rule for first 2 plan years for plans that were converted from a reasonable cost reimbursement contract—In applying paragraph (1) for the first 2 plan years under this part in the case of a plan that is a new MA plan (as defined in clause (iii)(II)) to which deemed enrollment applies under section 1851(e)(4), the Secretary shall use the star rating that applied to the converted reasonable cost reimbursement contract for the year preceding the first plan year for such plan under this part.”
Sec. 208 Quality measure endorsement and selection
“1890A Contract with an entity regarding input on the selection of measures
“(a) Contract
“(1) In general—For purposes of activities conducted under this Act, the Secretary shall identify and have in effect a contract with an entity that meets the requirements described in subsection (c). Such contract shall provide that the entity will perform the duties described in subsection (b).
“(2) Timing for first contract—The first contract under paragraph (1) shall begin on October 1, 2014.
“(3) Period of contract—A contract under paragraph (1) shall be for a period of 3 years (except as may be renewed after a subsequent bidding process).
“(4) Competitive procedures—Competitive procedures (as defined in section 4(5) of the Office of Federal Procurement Policy Act (41 U.S.C. 403(5))) shall be used to enter into a contract under paragraph (1).
“(b) Duties—The duties described in this subsection are the following:
“(c) Requirements described—The requirements described in this subsection are the following:
“(1) Private nonprofit, board membership, membership fees, and not a measure developer—The requirements described in paragraphs (1), (2), (7), and (8) of section 1890(c).
“(2) Experience—The entity has at least 4 years of experience working with quality and efficiency measures.”
“(4) Facilitation to better coordinate and align public and private sector use of quality measures
“(A) In general—The entity shall facilitate increased coordination and alignment between the public and private sector with respect to quality and efficiency measures.
“(B) Reports—The entity shall prepare and make available to the public annual reports on its findings under this paragraph. Such public availability shall include posting each report on the Internet website of the entity.
“(5) Gap analysis—The entity shall conduct an ongoing analysis of—
“(A) gaps in endorsed quality and efficiency measures, which shall include measures that are within priority areas identified by the Secretary under the national strategy established under section 399HH of the Public Health Service Act; and
“(B) areas where quality measures are unavailable or inadequate to identify or address such gaps.
“(6) Annual report to congress and the Secretary; Secretarial publication and comment
“(A) Annual report—By not later than March 1 of each year, the entity shall submit to Congress and the Secretary a report containing—
“(i) a description of—
“(I) the recommendations made under paragraph (1);
“(II) the matters described in clauses (i) and (ii) of paragraph (2)(A);
“(III) the results of the analysis under paragraph (5); and
“(IV) the performance by the entity of the duties required under the contract entered into with the Secretary under subsection (a); and
“(ii) any other items determined appropriate by the Secretary.
“(B) Secretarial review and publication of annual report—Not later than 6 months after receiving a report under subparagraph (A) for a year, the Secretary shall—
“(i) review such report; and
“(ii) publish such report in the Federal Register, together with any comments of the Secretary on such report.”
“(E) Input—In providing the input described in subparagraph (A), the multi-stakeholder groups—
“(i) shall include a detailed description of the rationale for each recommendation made by the multi-stakeholder group, including in areas relating to—
“(I) the expected impact that implementing the measure will have on individuals;
“(II) the burden on providers of services and suppliers;
“(III) the expected influence over the behavior of providers of services and suppliers;
“(IV) the applicability of a measure for more than one setting or program; and
“(V) other areas determined in consultation with the Secretary; and
“(ii) may consider whether it is appropriate to provide separate recommendations with respect to measures for internal use, public reporting, and payment provisions.
“(F) Equal representation—In convening multi-stakeholder groups pursuant to this paragraph, the entity shall, to the extent feasible, make every effort to ensure such groups are balanced across stakeholders.”
“(3) Facilitation to better coordinate and align public and private sector use of quality measures
“(A) In general—The entity shall facilitate increased coordination and alignment between the public and private sector with respect to quality and efficiency measures.
“(B) Reports—The entity shall prepare and make available to the public annual reports on its findings under this paragraph. Such public availability shall include posting each report on the Internet website of the entity.
“(4) Annual report to congress and the Secretary; secretarial publication and comment
“(A) Annual report—By not later than March 1 of each year, the entity shall submit to Congress and the Secretary a report containing—
“(i) a description of—
“(I) the coordination of quality initiatives under this Act with quality initiatives implemented by other payers;
“(II) areas in which evidence is insufficient to support endorsement of quality measures in priority areas identified by the Secretary under the national strategy established under section 399HH of the Public Health Service Act and where targeted research may address such gaps; and
“(III) the performance by the entity of the duties required under the contract entered into with the Secretary under subsection (a); and
“(ii) any other items determined appropriate by the Secretary.
“(B) Secretarial review and publication of annual report—Not later than 6 months after receiving a report under subparagraph (A) for a year, the Secretary shall—
“(i) review such report; and
“(ii) publish such report in the Federal Register, together with any comments of the Secretary on such report.”
“(8) Not a measure developer—The entity is not a measure developer.”
“(2) Public availability of measures considered for selection—Subject to paragraph (4), not later than October 1 or December 31 of each year, the Secretary shall make available to the public a list of quality and efficiency measures described in section 1890A(b)(2)(B) that the Secretary is considering under this title. The Secretary shall provide for an appropriate balance of the number of measures to be made available by each such date in a year.
“(3) Transmission of multi-stakeholder input
“(A) In general—Subject to paragraph (4), not later than the applicable date described in subparagraph (B) of each year, the entity with a contract under section 1890A shall, pursuant to subsection (b)(3) of such section, transmit to the Secretary the input of multi-stakeholder groups described in paragraph (1).
“(B) Applicable date described—The applicable date described in this subparagraph for a year is—
“(i) February 1 with respect to quality and efficiency measures made available under paragraph (2) by October 1 of the preceding year; and
“(ii) April 1 with respect to quality and efficiency measures made available under paragraph (2) by December 31 of the preceding year.”
“(4) Limited process for additional multi-stakeholder input—In addition to the Secretary making measures publically available pursuant to the dates described in paragraph (2) and multi-stakeholder groups transmitting the input pursuant to the applicable dates described in paragraph (3)—
“(A) the Secretary may, at times that do not meet the time requirements described in paragraph (2), make available to the public a limited number of quality and efficiency measures described in section 1890A(b)(2) that the Secretary is considering under this title; and
“(B) if the Secretary uses the authority under subparagraph (A), the entity with a contract under section 1890A shall, pursuant to section 1890A(b)(3), transmit to the Secretary on a timely basis the input from a multi-stakeholder group described in paragraph (1) with respect to such measures.”
“(7) Concordance rates—For each year (beginning with 2015), the Secretary shall include a list of concordance rates for each type of provider of services and supplier in the annual final rule applicable to such type of provider or supplier.”
“(C) take into consideration the benefits of the alignment of measures between the public and private sector.”
“(g) Funding
“(1) In general—For purposes of carrying out this section (other than subsections (e) and (f)) and sections 1890 and 1890A, the Secretary shall provide for the transfer, from the Federal Hospital Insurance Trust Fund under section 1817 and the Federal Supplementary Medical Insurance Trust Fund under section 1841, in such proportion as the Secretary determines appropriate, to the Centers for Medicare & Medicaid Services Program Management Account of $25,000,000 for each of fiscal years 2015 through 2017.
“(2) Availability—Amounts transferred under paragraph (1) shall remain available until expended.”
Sec. 209 Permanent extension of funding outreach and assistance for low-income programs
B Medicaid and Other Extensions
Sec. 211 Qualifying individual program
“(a) Applicable FMAP—With respect to assistance described in section 1902(a)(10)(E)(iv) furnished in a State, the Federal medical assistance percentage shall be equal to 100 percent.”
Sec. 212 Transitional Medical Assistance
“(6) Opt-out option for States that expand adult coverage and provide 12-month continuous eligibility under Medicaid and CHIP
“(A) In general—In the case of a State described in subparagraph (B), the State may elect through a State plan amendment to have this section and sections 408(a)(11)(A), 1902(a)(52), 1902(e)(1), and 1931(c)(2) not apply to the State.
“(B) State described—A State is described in this subparagraph if the State is one of the 50 States or the District of Columbia and—
“(i) has elected to provide medical assistance to individuals under subclause (VIII) of section 1902(a)(10)(A)(i);
“(ii) has elected under section 1902(e)(12)(A) the option to provide continuous eligibility for a 12-month period for individuals under 19 years of age;
“(iii) has elected under section 1902(e)(12)(B) the option to provide continuous eligibility for a 12-month period for all categories of individuals described in that section; and
“(iv) has elected to apply section 1902(e)(12)(A) to the State child health plan under title XXI.”
“(C) If a State has made an election under section 1925(a)(6), subparagraph (A) and section 1925 shall not apply to the State.”
“(B) At the option of the State, the plan may provide that an individual who is determined to be eligible for benefits under a State plan approved under this title under any of the following eligibility categories, or who is redetermined to be eligible for such benefits under any of such categories, shall be considered to meet the eligibility requirements met on the date of application and shall remain eligible for those benefits until the end of the 12–month period following the date of the determination or redetermination of eligibility:
“(i) Section 1902(a)(10)(A)(i)(VIII).
“(ii) Section 1931.”
“(E) Section 1902(e)(12)(A) (relating to the State option for 12-month continuous eligibility and enrollment).”
“(3) Opt-out option for States that expand adult coverage and provide 12-month continuous eligibility under Medicaid and CHIP
“(A) In general—In the case of a State described in subparagraph (B), the State may elect through a State plan amendment to have paragraphs (1) and (2) of this subsection and sections 408(a)(11), 1902(a)(52), 1902(e)(1), and 1925 not apply to the State.
“(B) State described—A State is described in this subparagraph if the State is one of the 50 States or the District of Columbia and—
“(i) has elected to provide medical assistance to individuals under subclause (VIII) of section 1902(a)(10)(A)(i);
“(ii) has elected under section 1902(e)(12)(A) the option to provide continuous eligibility for a 12-month period for individuals under 19 years of age;
“(iii) has elected under section 1902(e)(12)(B) the option to provide continuous eligibility for a 12-month period for all categories of individuals described in that section; and
“(iv) has elected to apply section 1902(e)(12)(A) to the State child health plan under title XXI.”
“(C) States that expand adult coverage and elect to opt-out of transitional coverage
“(i) In general—For purposes of determining compliance with the requirements of paragraph (2), a State which exercises the option under sections 1925(a)(6) and 1931(c)(3) to provide no transitional medical assistance or other extended eligibility (as applicable) shall not, as a result of exercising such option, be considered to have in effect eligibility standards, methodologies, or procedures described in clause (ii) that are more restrictive than the standards, methodologies, or procedures in effect under the State plan or under a waiver of the plan on the date of enactment of the Patient Protection and Affordable Care Act.
“(ii) Standards, methodologies, or procedures described—The eligibility standards, methodologies, or procedures described in this clause are those standards, methodologies, or procedures applicable to determining the eligibility for medical assistance of any child under 19 years of age (or such higher age as the State may have elected).”
Sec. 213 Express lane eligibility
Sec. 214 Pediatric quality measures
Sec. 215 Special diabetes programs
C Human Services Extensions
Sec. 221 Abstinence education grants
Sec. 222 Personal responsibility education program
Sec. 223 Family-to-family health information centers
“(iv) $6,000,000 for each of fiscal years 2014 through 2018.”
Sec. 224 Health workforce demonstration project for low-income individuals
D Program Integrity
Sec. 231 Reducing improper Medicare payments
“(G) Improper payment outreach and education program—Having in place an improper payment outreach and education program described in subsection (h).”
“(h) Improper payment outreach and education program
“(1) In general—In order to reduce improper payments under this title, each medicare administrative contractor shall establish and have in place an improper payment outreach and education program under which the contractor, through outreach, education, training, and technical assistance activities, shall provide providers of services and suppliers located in the region covered by the contract under this section with the information described in paragraph (3). The activities described in the preceding sentence shall be conducted on a regular basis.
“(2) Forms of outreach, education, training, and technical assistance activities—The outreach, education, training, and technical assistance activities under a payment outreach and education program shall be carried out through any of the following:
“(A) Emails and other electronic communications.
“(B) Webinars.
“(C) Telephone calls.
“(D) In-person training.
“(E) Other forms of communications determined appropriate by the Secretary.
“(3) Information to be provided through activities—The information to be provided to providers of services and suppliers under a payment outreach and education program shall include all of the following information:
“(A) A list of the provider’s or supplier's most frequent and expensive payment errors over the last quarter.
“(B) Specific instructions regarding how to correct or avoid such errors in the future.
“(C) A notice of all new topics that have been approved by the Secretary for audits conducted by recovery audit contractors under section 1893(h).
“(D) Specific instructions to prevent future issues related to such new audits.
“(E) Other information determined appropriate by the Secretary.
“(4) Error rate reduction training
“(A) In general—The activities under a payment outreach and education program shall include error rate reduction training.
“(B) Requirements
“(i) In general—The training described in subparagraph (A) shall—
“(I) be provided at least annually; and
“(II) focus on reducing the improper payments described in paragraph (5).
“(C) Invitation—A medicare administrative contractor shall ensure that all providers of services and suppliers located in the region covered by the contract under this section are invited to attend the training described in subparagraph (A) either in person or online.
“(5) Priority—A medicare administrative contractor shall give priority to activities under the improper payment outreach and education program that will reduce improper payments for items and services that—
“(A) have the highest rate of improper payment;
“(B) have the greatest total dollar amount of improper payments;
“(C) are due to clear misapplication or misinterpretation of Medicare policies;
“(D) are clearly due to common and inadvertent clerical or administrative errors; or
“(E) are due to other types of errors that the Secretary determines could be prevented through activities under the program.
“(6) Information on improper payments from recovery audit contractors
“(A) In general—In order to assist medicare administrative contractors in carrying out improper payment outreach and education programs, the Secretary shall provide each contractor with a complete list of improper payments identified by recovery audit contractors under section 1893(h) with respect to providers of services and suppliers located in the region covered by the contract under this section. Such information shall be provided on a quarterly basis.
“(B) Information—The information described in subparagraph (A) shall include the following information:
“(i) The providers of services and suppliers that have the highest rate of improper payments.
“(ii) The providers of services and suppliers that have the greatest total dollar amounts of improper payments.
“(iii) The items and services furnished in the region that have the highest rates of improper payments.
“(iv) The items and services furnished in the region that are responsible for the greatest total dollar amount of improper payments.
“(v) Other information the Secretary determines would assist the contractor in carrying out the improper payment outreach and education program.
“(C) Format of information—The information furnished to medicare administrative contractors by the Secretary under this paragraph shall be transmitted in a manner that permits the contractor to easily identify the areas of the Medicare program in which targeted outreach, education, training, and technical assistance would be most effective. In carrying out the preceding sentence, the Secretary shall ensure that—
“(i) the information with respect to improper payments made to a provider of services or supplier clearly displays the name and address of the provider or supplier, the amount of the improper payment, and any other information the Secretary determines appropriate; and
“(ii) the information is in an electronic, easily searchable database.
“(7) Communications—All communications with providers of services and suppliers under a payment outreach and education program are subject to the standards and requirements of subsection (g).
“(8) Funding—After application of paragraph (1)(C) of section 1893(h), the Secretary shall retain a portion of the amounts recovered by recovery audit contractors under such section which shall be available to the program management account of the Centers for Medicare & Medicaid Services for purposes of carrying out this subsection and to implement corrective actions to help reduce the error rate of payments under this title. The amount retained under the preceding sentence shall not exceed an amount equal to 25 percent of the amounts recovered under section 1893(h).”
“(A) In general—The Secretary”
“(B) Inclusion of certain information
“(i) In general—For reports submitted under this paragraph for 2015 or a subsequent year, each such report shall include the information described in clause (ii) with respect to each of the following categories of audits carried out by recovery audit contractors under this subsection:
“(I) Automated.
“(II) Complex.
“(III) Medical necessity review.
“(IV) Part A.
“(V) Part B.
“(VI) Durable medical equipment.
“(ii) Information described—For purposes of clause (i), the information described in this clause, with respect to a category of audit described in clause (i), is the result of all appeals for each individual level of appeals in such category.”
Sec. 232 Authority for Medicaid fraud control units to investigate and prosecute complaints of abuse and neglect of Medicaid patients in home and community-based settings
“(4)
“(A) The entity’s function includes a statewide program for the—
“(i) investigation and prosecution, or referral for prosecution or other action, of complaints of abuse or neglect of patients in health care facilities which receive payments under the State plan under this title or under a waiver of such plan;
“(ii) at the option of the entity, investigation and prosecution, or referral for prosecution or other action, of complaints of abuse or neglect of individuals in connection with any aspect of the provision of medical assistance and the activities of providers of such assistance in a home or community based setting that is paid for under the State plan under this title or under a waiver of such plan; and
“(iii) at the option of the entity, investigation and prosecution, or referral for prosecution or other action, of complaints of abuse or neglect of patients residing in board and care facilities.”
Sec. 233 Improved use of funds received by the HHS Inspector General from oversight and investigative activities
“(b) Additional use of funds by Inspector General
“(1) Collections from Medicare and Medicaid recovery actions—Notwithstanding section 3302 of title 31, United States Code, or any other provision of law affecting the crediting of collections, the Inspector General of the Department of Health and Human Services may receive and retain three percent of all amounts collected pursuant to civil debt collection actions related to false claims or frauds involving the Medicare program under title XVIII or the Medicaid program under title XIX.
“(2) Crediting—Funds received by the Inspector General under paragraph (1) shall be deposited to the credit of any appropriation available for oversight and enforcement activities of the Inspector General permitted under subsection (a), and shall remain available until expended.”
Sec. 234 Preventing and reducing improper Medicare and Medicaid expenditures
“(4) Requiring valid prescriber National Provider Identifiers on pharmacy claims
“(A) In general—For plan year 2015 and subsequent plan years, subject to subparagraph (B), the Secretary shall prohibit PDP sponsors of prescription drug plans from paying claims for prescription drugs under this part that do not include a valid prescriber National Provider Identifier.
“(B) Procedures—The Secretary shall establish procedures for determining the validity of prescriber National Provider Identifiers under subparagraph (A).
“(C) Report—Not later than January 1, 2017, the Inspector General of the Department of Health and Human Services shall submit to Congress a report on the effectiveness of the procedures established under subparagraph (B).”
“(C) Inclusion of improper payment vulnerabilities identified—For reports submitted under this paragraph for 2015 or a subsequent year, each such report shall include—
“(i) a description of—
“(I) the types and financial cost to the program under this title of improper payment vulnerabilities identified by recovery audit contractors under this subsection; and
“(II) how the Secretary is addressing such improper payment vulnerabilities; and
“(ii) an assessment of the effectiveness of changes made to payment policies and procedures under this title in order to address the vulnerabilities so identified.
“(D) Limitation—The Secretary shall ensure that each report submitted under subparagraph (A) does not include information that the Secretary determines would be sensitive or would otherwise negatively impact program integrity.”
“(10) Addressing improper payment vulnerabilities—The Secretary shall address improper payment vulnerabilities identified by recovery audit contractors under this subsection in a timely manner, prioritized based on the risk to the program under this title.”
“(12) Information comparisons and disclosures to assist in administration of the Medicare program and State health subsidy programs
“(A) Disclosure to the Administrator of the Centers for Medicare & Medicaid Services—The Administrator of the Centers for Medicare & Medicaid shall have access to the information in the National Directory of New Hires for purposes of determining the eligibility of an applicant for, or enrollee in, the Medicare program under title XVIII or an applicable State health subsidy program (as defined in section 1413(e) of the Patient Protection and Affordable Care Act (42 U.S.C. 18083(e)).
“(B) Disclosure to the Inspector General of the Department of Health and Human Services
“(i) In general—If the Inspector General of the Department of Health and Human Services transmits to the Secretary the names and social security account numbers of individuals, the Secretary shall disclose to the Inspector General information on such individuals and their employers maintained in the National Directory of New Hires.
“(ii) Use of information—The Inspector General of the Department of Health and Human Services may use information provided under clause (i) only for purposes of —
“(I) determining the eligibility of an applicant for, or enrollee in, the Medicare program under title XVIII or an applicable State health subsidy program (as defined in section 1413(e) of the Patient Protection and Affordable Care Act (42 U.S.C. 18083(e)); or
“(II) evaluating the integrity of the Medicare program or an applicable State health subsidy program (as so defined).
“(C) Disclosure to State agencies
“(i) In general—If, for purposes of determining the eligibility of an applicant for, or an enrollee in, an applicable State health subsidy program (as defined in section 1413(e) of the Patient Protection and Affordable Care Act (42 U.S.C. 18083(e)), a State agency responsible for administering such program transmits to the Secretary the names, dates of birth, and social security account numbers of individuals, the Secretary shall disclose to such State agency information on such individuals and their employers maintained in the National Directory of New Hires, subject to this subparagraph.
“(ii) Condition on disclosure by the Secretary—The Secretary shall make a disclosure under clause (i) only to the extent that the Secretary determines that the disclosure would not interfere with the effective operation of the program under this part.
“(iii) Use and disclosure of information by State agencies
“(I) In general—A State agency may not use or disclose information provided under clause (i) except for purposes of determining the eligibility of an applicant for, or an enrollee in, a program referred to in clause (i).
“(II) Information security—The State agency shall have in effect data security and control policies that the Secretary finds adequate to ensure the security of information obtained under clause (i) and to ensure that access to such information is restricted to authorized persons for purposes of authorized uses and disclosures.
“(III) Penalty for misuse of information—An officer or employee of the State agency who fails to comply with this clause shall be subject to the sanctions under subsection (l)(2) to the same extent as if such officer or employee were an officer or employee of the United States.
“(iv) Procedural requirements—State agencies requesting information under clause (i) shall adhere to uniform procedures established by the Secretary governing information requests and data matching under this paragraph.
“(v) Reimbursement of costs—The State agency shall reimburse the Secretary, in accordance with subsection (k)(3), for the costs incurred by the Secretary in furnishing the information requested under this subparagraph.”
“(iv) furthering the Secretary’s design, development, installation, or enhancement of an automated data system architecture—
“(I) to collect, integrate, and assess data for purposes of program integrity, program oversight, and administration, including the Medi-Medi Program; and
“(II) that improves the coordination of requests for data from States.”
E Other Provisions
Sec. 241 Commission on Improving Patient Directed Health Care
“1150C. Commission on Improving Patient Directed Health Care
“(a) Purposes—The purposes of this section are to—
“(1) provide a forum for a nationwide public debate on improving patient self-determination in health care decision-making;
“(2) identify strategies that ensure every American has the health care they want; and
“(3) provide recommendations to Congress that result from the debate.
“(b) Establishment—The Secretary shall establish an entity to be known as the Commission on Improving Patient Directed Health Care (referred to in this section as the “Commission”).
“(c) Membership
“(1) Number and appointment—The Commission shall be composed of 15 members. One member shall be the Secretary. The Comptroller General of the United States shall appoint 14 members.
“(2) Qualifications—The membership of the Commission shall include—
“(A) health care consumers impacted by decision-making in advance of a health care crisis, such as individuals of advanced age, individuals with chronic, terminal and mental illnesses, family care givers, and individuals with disabilities;
“(B) providers in settings where crucial health care decision-making occurs, such as those working in intensive care settings, emergency room departments, primary care settings, nursing homes, hospice, or palliative care settings;
“(C) payors ensuring patients get the level of care they want;
“(D) experts in advance care planning, hospice, palliative care, information technology, bioethics, aging policy, disability policy, pediatric ethics, cultural sensitivity, psychology, and health care financing;
“(E) individuals who represent culturally diverse perspectives on patient self-determination and end-of-life issues; and
“(F) members of the faith community.
“(d) Period of appointment—Members of the Commission shall be appointed for the life of the Commission. Any vacancies shall not affect the power and duties of the Commission but shall be filled in the same manner as the original appointment.
“(e) Designation of the chairperson—Not later than 15 days after the date on which all members of the Commission have been appointed, the Comptroller General shall designate the chairperson of the Commission.
“(f) Subcommittees—The Commission may establish subcommittees if doing so increases the efficiency of the Commission in completing tasks.
“(g) Duties
“(1) Hearings—Not later than 90 days after the date of designation of the chairperson under subsection (e), the Commission shall hold no fewer than 8 hearings to examine—
“(A) the current state of health care decision-making and advance care planning laws in the United States at the Federal level and across the States, as well as options for improving advance care planning tools, especially with regard to use, portability, and storage;
“(B) consumer-focused approaches that educate the American public about patient choices, care planning, and other end-of-life issues;
“(C) the use of comprehensive, patient-centered care plans by providers, the impact care plans have on health care delivery, and methods to expand the use of high quality care planning tools in both public and private health care systems;
“(D) the role of electronic medical records and other technologies in improving patient-directed health care;
“(E) innovative tools for improving patient experience with advanced illness, such as palliative care, hospice, and other models;
“(F) the role social determinants of health, such as socio-economic status, play in patient self-direction in health care;
“(G) the use of culturally-competent tools for health care decision-making;
“(H) strategies for educating providers on care planning, palliative care, hospice care, and other issues surrounding honoring patient choices;
“(I) the sociological and psychological factors that influence health care decision-making and end-of-life choices; and
“(J) the role of spirituality and religion in patient self-determination in health care.
“(2) Additional hearings—The Commission may hold additional hearings on subjects other than those listed in paragraph (1) so long as such hearings are determined necessary by the Commission in carrying out the purposes of this section. Such additional hearings do not have to be completed within the time period specified but shall not delay the other activities of the Commission under this section.
“(3) Number and location of hearings and additional hearings—The Commission shall hold no fewer than 8 hearings as indicated in paragraph (1) and in sufficient number in order to receive information that reflects—
“(A) the geographic differences throughout the United States;
“(B) diverse populations; and
“(C) a balance among urban and rural populations.
“(4) Interactive technology—The Commission may encourage public participation in hearings through interactive technology and other means as determined appropriate by the Commission.
“(5) Report to the american people on patient directed health care—Not later than 90 days after the hearings described in paragraphs (1) and (2) are completed, the Commission shall prepare and make available to health care consumers through the Internet and other appropriate public channels, a report to be entitled, “Report to the American People on Patient Directed Health Care”. Such a report shall be understandable to the general public and include—
“(A) a summary of—
“(i) the hearings described in such paragraphs;
“(ii) how the current health care system empowers and informs decision-making in advance of a health care crisis;
“(iii) factors that contribute to the provision of health care that does not adhere to patient wishes;
“(iv) the impact of care that does not follow patient choices, particularly at the end-of-life, on patients, families, providers, and the health care system;
“(v) the laws surrounding advance care planning and health care decision-making including issues of portability, use, and storage;
“(vi) consumer-focused approaches to education of the American public about patient choices, care planning, and other end-of-life issues;
“(vii) the role of care plans in health care decision-making;
“(viii) the role of providers in ensuring patients receive the care they want;
“(ix) the role of electronic medical records and other technologies in improving patient directed health care;
“(x) the impact of social determinants on patient self-direction in health care services;
“(xi) the use of culturally competent methods for health care decision-making;
“(xii) the sociological and psychological factors that influence patient self-determination; and
“(xiii) the role of spirituality and religion in health care decision-making and end-of-life care;
“(B) best practices from communities, providers, and payors that document patient wishes and provide health care that adheres to those wishes; and
“(C) information on educating providers about health care decision-making and end-of-life issues.
“(6) Interim requirements—Not later than 180 days after the date of completion of the hearings, the Commission shall prepare and make available to the public through the Internet and other appropriate public channels, an interim set of recommendations on patient self-determination in health care and ways to improve and strengthen the health care system based on the information and preferences expressed at the community meetings. There shall be a 90-day public comment period on such recommendations.
“(h) Recommendations—Not later than 120 days after the expiration of the public comment period described in subsection (g)(6), the Commission shall submit to Congress and the President a final set of recommendations. The recommendations must be comprehensive and detailed. The recommendations must contain recommendations or proposals for legislative or administrative action as the Commission deems appropriate, including proposed legislative language to carry out the recommendations or proposals.
“(i) Administration
“(1) Executive director—There shall be an Executive Director of the Commission who shall be appointed by the chairperson of the Commission in consultation with the members of the Commission.
“(2) Compensation—While serving on the business of the Commission (including travel time), a member of the Commission shall be entitled to compensation at the per diem equivalent of the rate provided for level IV of the Executive Schedule under section 5315 of title 5, United States Code, and while so serving away from home and the member’s regular place of business, a member may be allowed travel expenses, as authorized by the chairperson of the Commission. For purposes of pay and employment benefits, rights, and privileges, all personnel of the Commission shall be treated as if they were employees of the Senate.
“(3) Information from federal agencies—The Commission may secure directly from any Federal department or agency such information as the Commission considers necessary to carry out this section. Upon request of the Commission the head of such department or agency shall furnish such information.
“(4) Postal services—The Commission may use the United States mails in the same manner and under the same conditions as other departments and agencies of the Federal Government.
“(j) Detail—Not more than 5 Federal Government employees employed by the Department of Labor, 5 Federal Government employees employed by the Social Security Administration, and 10 Federal Government employees employed by the Department of Health and Human Services may be detailed to the Commission under this section without further reimbursement. Any detail of an employee shall be without interruption or loss of civil service status or privilege.
“(k) Temporary and intermittent services—The chairperson of the Commission may procure temporary and intermittent services under section 3109(b) of title 5, United States Code, at rates for individuals which do not exceed the daily equivalent of the annual rate of basic pay prescribed for level V of the Executive Schedule under section 5316 of such title.
“(l) Annual report—Not later than 1 year after the date of enactment of this Act, and annually thereafter during the existence of the Commission, the Commission shall report to Congress and make public a detailed description of the expenditures of the Commission used to carry out its duties under this section.
“(m) Sunset of commission—The Commission shall terminate on the date that is 4 years after the date on which all the members of the Commission have been appointed under subsection (c)(1) and appropriations are first made available to carry out this section.
“(n) Administration review and comments—Not later than 45 days after receiving the final recommendations of the Commission under subsection (h), the President shall submit a report to Congress which shall contain—
“(1) additional views and comments on such recommendations; and
“(2) recommendations for such legislation and administrative action as the President considers appropriate.
“(o) Required congressional action—Not later than 45 days after receiving the report submitted by the President under subsection (n), each committee of jurisdiction of Congress, the Committee on Finance of the Senate, the Committee on Health, Education, Labor, and Pensions of the Senate, the Committee on Ways and Means of the House of Representatives, the Committee on Energy and Commerce of the House of Representatives, and the Committee on Education and the Workforce of the House of Representatives, shall hold at least 1 hearing on such report and on the final recommendations of the Commission submitted under subsection (h).
“(p) Authorization of appropriations
“(1) In general—There are authorized to be appropriated to carry out this section, $3,000,000 for each of fiscal years 2014 and 2015.
“(2) Report to the American people on patient directed health care—There are authorized to be appropriated for the preparation and dissemination of the Report to the American People on Patient Directed Health Care described in subsection (g)(5), such sums as may be necessary for the fiscal year in which the report is required to be submitted.”
Sec. 242 Expansion of the definition of inpatient hospital services for certain cancer hospitals
“(B) with respect to a hospital that is described in section 1886(d)(1)(B)(v) and that, as of the date of the enactment of the SGR Repeal and Medicare Beneficiary Access Act of 2013, is located in the same building, or on the same campus, as another hospital, items and services described in paragraphs (1) and (2) furnished on or after such date of enactment by the hospital described in such section or by others under arrangements with them made by the hospital;”
Sec. 243 Quality measures for certain post-acute care providers relating to notice and transfer of patient health information and patient care preferences
Sec. 244 Criteria for medically necessary, short inpatient hospital stays
Sec. 245 Transparency of reasons for excluding additional procedures from the Medicare ambulatory surgical center (ASC) approved list
Sec. 246 Supervision in critical access hospitals
“(6) Supervision—In the case of services furnished on or after the date of the enactment of this paragraph, the level of supervision with respect to outpatient critical access hospital services shall be general supervision (as defined by the Secretary).”
Sec. 247 Requiring State licensure of bidding entities under the competitive acquisition program for certain durable medical equipment, prosthetics, orthotics, and supplies (DMEPOS)
“(G) Requiring State licensure of bidding entities—With respect to rounds of competitions beginning on or after the date of enactment of this subparagraph, the Secretary may only accept a bid from an entity for an area if the entity meets applicable State licensure requirements for such area for all items in such bid.”
Sec. 248 Recognition of attending physician assistants as attending physicians To serve hospice patients
Sec. 249 Remote patient monitoring pilot projects
Sec. 250 Community-Based Institutional Special Needs Plan Demonstration Program
Sec. 251 Applying CMMI waiver authority to PACE in order to foster innovations
Sec. 252 Improve and modernize Medicaid data systems and reporting
Sec. 253 Fairness in Medicaid supplemental needs trusts
Sec. 254 Helping Ensure Life- and Limb-Saving Access to Podiatric Physicians
“(12) subject to section 4072(e) of the Omnibus Budget Reconciliation Act of 1987, extra-depth shoes with inserts or custom molded shoes (in this paragraph referred to as “therapeutic shoes”) with inserts for an individual with diabetes, if—
“(A) the physician who is managing the individual’s diabetic condition—
“(i) documents that the individual has diabetes;
“(ii) certifies that the individual is under a comprehensive plan of care related to the individual’s diabetic condition; and
“(iii) documents agreement with the prescribing podiatrist or other qualified physician (as established by the Secretary) that it is medically necessary for the individual to have such extra-depth shoes with inserts or custom molded shoes with inserts;
“(B) the therapeutic shoes are prescribed by a podiatrist or other qualified physician (as established by the Secretary) who—
“(i) examines the individual and determines the medical necessity for the individual to receive the therapeutic shoes; and
“(ii) communicates in writing the medical necessity to the physician described in subparagraph (A) for the individual to have therapeutic shoes along with findings that the individual has peripheral neuropathy with evidence of callus formation, a history of pre-ulcerative calluses, a history of previous ulceration, foot deformity, previous amputation, or poor circulation; and
“(C) the therapeutic shoes are fitted and furnished by a podiatrist or other qualified supplier (as established by the Secretary), such as a pedorthist or orthotist, who is not the physician described in subparagraph (A) (unless the Secretary finds that the physician is the only such qualified individual in the area);”
Sec. 255 Demonstration program to improve community mental health services
Sec. 256 Annual Medicaid DSH report
“(k) Annual report to Congress
“(1) In general—Beginning January 1, 2015, and annually thereafter, the Secretary shall submit a report to Congress on the program established under this section for making payment adjustments to disproportionate share hospitals for the purpose of providing Congress with information relevant to determining an appropriate level of overall funding for such payment adjustments during and after the period in which aggregate reductions in the DSH allotments to States are required under paragraphs (7) and (8) of subsection (f).
“(2) Required report information—Except as otherwise provided, each report submitted under this subsection shall include the following:
“(A) Information and data relating to changes in the number of uninsured individuals for the most recent year for which such data are available as compared to 2013 and as compared to the Congressional Budget Office estimates of uninsured individuals made at the time of the enactment of the Patient Protection and Affordable Care Act (Public Law 111–148) and the Health Care and Education Reconciliation Act of 2010 (Public Law 111–152).
“(B) Information and data relating to the extent to which hospitals continue to incur uncompensated care costs from providing unreimbursed or under-reimbursed services to individuals who either are eligible for medical assistance under the State plan under this title or under a waiver of such plan or who have no health insurance (or other source of third party coverage) for such services.
“(C) Information and data relating to the extent to which hospitals continue to provide charity care and unreimbursed or under-reimbursed services, or otherwise incur bad debt, under the program established under this title, the State Children's Health Insurance Program established under title XXI, and State or local indigent care programs, as reported on cost reports submitted under title XVIII or such other data as the Secretary determines appropriate.
“(D) In the first report submitted under this section, a methodology for estimating the amount of unpaid patient deductibles, copayments and coinsurance incurred by hospitals for patients enrolled in qualified health plans through an American Health Benefits Exchange, using existing data and minimizing the administrative burden on hospitals to the extent possible, and in subsequent reports, data regarding such uncompensated care costs collected pursuant to such methodology.
“(E) For each State, information and data relating to the difference between the DSH allotment for the State for the fiscal year that began on October 1 of the year preceding the year in which the report is submitted and the aggregate amount of uncompensated care costs for all disproportionate share hospitals in the State.
“(F) Information and data relating to the extent to which there are certain vital hospital systems that are disproportionately experiencing high levels of uncompensated care and that have multiple other missions, such as a commitment to graduate medical education, the provision of tertiary and trauma care services, providing public health and essential community services, and providing comprehensive, coordinated care.
“(G) Such other information and data relevant to the determination of the level of funding for, and amount of, State DSH allotments as the Secretary determines appropriate
“(3) Authorization of appropriations—There is authorized to be appropriated to the Secretary for the period of fiscal years 2015 through 2109, such sums as may be necessary to carry out this subsection.”