
Supreme Court Rules That Hospitals Serving the Poor Ineligible for Medicare Increases
The Supreme Court ruled 7-2 on April 29 that hospitals that serve large numbers of poor people are not eligible for higher Medicare payments from the government.
Justice Amy Coney Barrett wrote the majority
Acknowledging the statute governing the Medicare program is 'notoriously complex,' Barrett wrote that the hospitals' flawed interpretation of the law improperly increases 'the amount of funding a hospital may receive.'
'We must respect the formula that Congress prescribed,' she said.
Justice Ketanji Brown Jackson filed a dissenting opinion that was joined by Justice Sonia Sotomayor. Jackson wrote that the majority's interpretation of the law 'will deprive hospitals serving the neediest among us of critical federal funds that Congress plainly attempted to provide.'
Advocate Christ Medical Center in Oak Lawn, Illinois, is the lead petitioner, and U.S. Department of Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. is the respondent.
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At issue was how HHS calculates Medicare payments to 'disproportionate share hospitals,' or DSH hospitals, so named because they serve a 'disproportionate share' of low-income persons. Medicare provides health insurance to the elderly and disabled.
More than 200 hospitals challenged the government's funding methodology, saying it violated federal law. Washington-based U.S. District Judge Tanya Chutkan upheld the formula on June 8, 2022.
Meanwhile, in a separate case, the Supreme Court
On Sept. 1, 2023, the U.S. Court of Appeals for the District of Columbia Circuit
The hospitals
Because treating low-income patients often costs more, a federal law known as 42 U.S. Code Section 1395ww was enacted to reimburse DSH hospitals.
A hospital receives larger payments partly based on how many days it gives inpatient care to senior or disabled low-income patients, 'measured as those who 'were entitled to benefits under part A of [Medicare] and were entitled to supplementary security income [SSI] benefits,'' according to a
Supplemental security income benefits are given to the blind, disabled, and needy elderly.
In Empire, the Supreme Court found that 'entitled to [Medicare part A] benefits' encompasses 'all those qualifying for the [Medicare] program,' regardless of whether Medicare covered the hospital stay, but did not resolve the issue of whether 'entitled to [supplementary security income] benefits' covers everyone who qualifies under the [supplementary security income] program, the brief said.
Although HHS's position was that only patients who took in a supplementary security income cash payment during the month of their hospital stay are 'entitled to benefits,' the phrase should 'mean the same thing for Medicare part A and [supplementary security income], such that it includes all who meet basic program-eligibility criteria, whether or not benefits are actually received,' the brief said.
In the new opinion, Barrett wrote that Section 1395ww lays out how to calculate how much the government pays a DSH hospital for treating low-income Medicare patients.
Barrett wrote that the percentage comes from adding two fractions: the Medicare fraction and the Medicaid fraction. Medicaid is a joint federal–state program that offers health insurance coverage to low-income Americans.
She wrote that the numerator of the Medicare fraction counts how many patient days can be attributed to Medicare patients who were 'entitled to benefits under [Medicare] part A' and were 'entitled to supplementary security income benefits … under subchapter XVI,' according to Section 1395ww. Subchapter XVI provides rules for the supplementary security income program.
In math, a numerator is the number above the line in a fraction that shows how many parts of the denominator, or the number below the line, are taken. For example, in the fraction 2/3, two is the numerator and three is the denominator.
In Empire, the court held the phrase ''entitled to [Medicare Part A] benefits'' includes 'all those qualifying for the program, regardless of whether they are receiving Medicare payments for part or all of a hospital stay,' Barrett wrote.
'We did not decide, however, what it means to be 'entitled to supplementary security income benefits … under subchapter XVI.''
'Today, we hold that a person is entitled to such benefits when she is eligible to receive a cash payment during the month of her hospitalization,' she wrote.
HHS interprets the statutory text to reference patients who are 'entitled to receive [supplemental security income] benefits during the month' in which they were in the hospital. However, the hospitals argue the phrase covers 'all patients enrolled in the [supplemental security income] system at the time of their hospitalizations, even if those patients were not entitled to a [supplemental security income] payment during that month,' Barrett wrote.
This approach 'sweeps more people into the numerator of the Medicare fraction, thereby increasing the amount of funding a hospital may receive.'
However, 'Congress made a specific choice: For purposes of the Medicare fraction, an individual is 'entitled to [SSI] benefits' when she is eligible to receive an [supplemental security income] cash payment during the month of her hospitalization. We must respect the formula that Congress prescribed,' Barrett wrote.
The Supreme Court affirmed the ruling of the U.S. Court of Appeals for the D.C. Circuit.
In her dissent, Jackson wrote the majority's interpretation of the DSH formula reflects 'a fundamental misunderstanding of how [the supplemental security income] cash-benefit program works.'
It is 'wholly irrelevant' whether an 'individual actually received a cash payment under the [supplemental security income] program during the month of their hospitalization.'
'The majority's interpretation both ignores this critical context and endorses an interpretation of the Medicare formula that arbitrarily undercounts a hospital's low-income patients,' Jackson wrote.
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Sanofi Media RelationsSandrine Guendoul | +33 6 25 09 14 25 | Berland | +1 215 432 0234 | Léo Le Bourhis | +33 6 75 06 43 81 | Victor Rouault | +33 6 70 93 71 40 | Timothy Gilbert | +1 516 521 2929 | Ubaldi | +33 6 30 19 66 46 | Sanofi Investor RelationsThomas Kudsk Larsen |+ 44 7545 513 693 | Alizé Kaisserian | + 33 6 47 04 12 11 | Felix Lauscher | + 1 908 612 7239 | Keita Browne | +1 781 249 1766 | Nathalie Pham | +33 7 85 93 30 17 | Elgoutni| + 1 617 710 3587 | Thibaud Châtelet | +33 6 80 80 89 90 | Li | +33 6 84 00 90 72 | Blueprint Medicines Media Relations & Investor RelationsJim Baker | +1 617 844 8236 | media@ Cohen | +1 857 209 3147 | ir@ Sanofi forward-looking statementsThis communication contains forward-looking statements that are subject to risks, uncertainties and other factors that could cause actual results to differ materially from those implied by the forward-looking statements. Forward-looking statements are statements that are not historical facts and may include projections and estimates and their underlying assumptions, statements regarding plans, objectives, intentions and expectations with respect to future financial results, events, operations, services, product development and potential, and statements regarding future performance. Forward-looking statements are generally identified by the words 'expects', 'anticipates', 'believes', 'intends', 'estimates', 'plans', 'will be' and similar expressions. Although Sanofi's management believes that the expectations reflected in such forward-looking statements are reasonable, investors are cautioned that forward-looking information and statements are subject to various risks and uncertainties, many of which are difficult to predict and generally beyond the control of Sanofi, that could cause actual results and developments to differ materially from those expressed in, or implied or projected by, the forward-looking information and statements. These risks and uncertainties include among other things, unexpected regulatory actions or delays, or government regulation generally, that could affect the availability or commercial potential of the product, or the fact that the product may not be commercially successful, and risks related to Sanofi's and Blueprint's ability to complete the acquisition on the proposed terms or on the proposed timeline or at all, including the receipt of required regulatory approvals, the risk that the conditions to the closing of the transaction may not be satisfied, the possibility that competing offers will be made, the risks that the milestones related to the contingent value right will not be achieved, the risk of securityholder litigation relating to the proposed acquisition, including resulting expense or delays, other risks associated with executing business combination transactions, such as the risk that the businesses will not be integrated successfully, that such integration may be more difficult, time-consuming or costly than expected or that the expected benefits of the acquisition will not be realized, risks related to future opportunities and plans for the combined company, including uncertainty of the expected financial performance and results of the combined company following completion of the proposed acquisition, disruption from the proposed acquisition making it more difficult to conduct business as usual or to maintain relationships with customers, employees, manufacturers, suppliers or patient groups, and the possibility that, if the combined company does not achieve the perceived benefits of the proposed acquisition as rapidly or to the extent anticipated by financial analysts or investors, the market price of Sanofi's shares could decline, as well as other risks related to Sanofi's and Blueprint's respective businesses, including the ability to grow sales and revenues from existing products and to develop, commercialize or market new products, competition, including potential generic competition, the uncertainties inherent in research and development, including future clinical data and analysis, regulatory obligations and oversight by regulatory authorities, such as the FDA or the EMA, including decisions of such authorities regarding whether and when to approve any drug, device or biological application that may be filed for any product candidates as well as decisions regarding labelling and other matters that could affect the availability or commercial potential of any product candidates, the absence of a guarantee that any product candidates, if approved, will be commercially successful, the future approval and commercial success of therapeutic alternatives, Sanofi's ability to benefit from external growth opportunities, to complete related transactions and/or obtain regulatory clearances, risks associated with intellectual property and any related pending or future litigation and the ultimate outcome of such litigation, trends in exchange rates and prevailing interest rates, volatile economic and market conditions, cost containment initiatives and subsequent changes thereto, and the impact that global crises may have on us, our customers, suppliers, vendors, and other business partners, and the financial condition of any one of them, as well as on our employees and on the global economy as a whole. While the list of factors presented here is representative, no list should be considered a statement of all potential risks, uncertainties or assumptions that could have a material adverse effect on companies' consolidated financial condition or results of operations. The foregoing factors should be read in conjunction with the risks and cautionary statements discussed or identified in the public filings with the U.S. Securities and Exchange Commission (the 'SEC') and the Autorité des marchés financiers made by Sanofi, including those listed under 'Risk Factors' and 'Cautionary Statement Regarding Forward-Looking Statements' in Sanofi's annual report on Form 20-F for the year ended December 31, 2024 and its other filings with the SEC and the current reports on Form 8-K, quarterly reports on Form 10-Q and annual reports on Form 10-K and other filings with the SEC filed by Blueprint. The forward-looking statements speak only as of the date hereof and, other than as required by applicable law, Sanofi and Blueprint do not undertake any obligation to update or revise any forward-looking information or statements. Blueprint forward-looking statementsThis communication contains forward-looking statements regarding, among other things, the proposed acquisition of Blueprint by Sanofi, the expected timetable for completing the transaction, and Blueprint's future financial or operating performance. Blueprint generally identifies forward-looking statements by terminology such as 'aim,' 'may,' 'will,' 'could,' 'would,' 'should,' 'expect,' 'plan,' 'anticipate,' 'intend,' 'believe,' 'estimate,' 'predict,' 'project,' 'opportunity,' 'contemplate,' 'potential,' 'continue,' 'target' or the negative of these terms or other similar words, although not all forward-looking statements contain such terms. All statements that are not statements of historical facts are, or may be deemed to be, forward-looking statements. These forward-looking statements are only predictions, and such statements are based on current expectations and projections about future events and trends as well as the beliefs and assumptions of management. Forward-looking statements are subject to a number of risks and uncertainties, many of which involve factors or circumstances that are beyond Blueprint's control. Actual results could differ materially from those stated or implied in forward-looking statements due to a number of factors, including but not limited to: (i) risks associated with the timing of the closing of the proposed transaction, including the risks that a condition to closing would not be satisfied within the expected timeframe or at all or that the closing of the proposed transaction will not occur; (ii) uncertainties as to how many of Blueprint's stockholders will tender their shares in the offer; (iii) the possibility that a governmental entity may prohibit, delay or refuse to grant approval for the consummation of the transaction; (iv) the possibility that competing offers will be made; (v) the occurrence of any event, change or other circumstance that could give rise to the termination of the transaction; (vi) the outcome of any legal proceedings that may be instituted against the parties and others related to the merger agreement; (vii) unanticipated difficulties or expenditures relating to the proposed transaction, the response of business partners and competitors to the announcement of the proposed transaction, and/or potential difficulties in employee retention as a result of the announcement and pendency of the proposed transaction; (viii) risks related to non-achievement of the CVR milestones and that holders of the CVRs will not receive payments in respect of the CVRs; (ix) the risk that the marketing and sale of AYVAKIT/ AYVAKYT or any future approved drugs may be unsuccessful or less successful than anticipated, or that AYVAKIT/ AYVAKYT may not gain market acceptance by physicians, patients, third-party payors and others in the medical community; (x) the risk that the market opportunities for AYVAKIT/ AYVAKYT or Blueprint's drug candidates are smaller than Blueprint estimates or that any approval that Blueprint obtains may be based on a narrower definition of the patient population that Blueprint anticipates; (xi) the risk of delay of any current or planned clinical trials or the development of Blueprint's current or future drug candidates, including but not limited to BLU-808 and elenestinib; (xii) risks related to Blueprint's ability to successfully demonstrate the safety and efficacy of its drug candidates and gain approval of its drug candidates on a timely basis, if at all; (xiii) preclinical and clinical results for Blueprint's drug candidates may not support further development of such drug candidates either as monotherapies or in combination with other agents or may impact the anticipated timing of data or regulatory submissions; (xiv) the timing of the initiation of clinical trials and trial cohorts at clinical trial sites and patient enrollment rates may be delayed or slower than anticipated; (xv) actions of regulatory agencies may affect Blueprint's approved drugs or its current or future drug candidates, including affecting the initiation, timing and progress of clinical trials, as well as the pricing of its drug candidates; (xvi) risks related to Blueprint's ability to obtain, maintain and enforce patent and other intellectual property protection for its products and current or future drug candidates it is developing; (xvii) the success of Blueprint's current and future collaborations, financing arrangements, partnerships or licensing and other arrangements; (xviii) risks related to Blueprint's liquidity and financial position and the accuracy of its estimates of revenues, expenses, cash burn, and capital requirements; and (xix) those risks detailed in Blueprint's most recent Annual Report on Form 10-K and subsequent reports filed with the SEC, as well as other documents that may be filed by Blueprint from time to time with the SEC. Blueprint cannot assure you that the events and circumstances reflected in the forward-looking statements will be achieved or occur, and actual results could differ materially from those projected in the forward-looking statements. The forward-looking statements made in this communication relate only to events as of the date on which the statements are made. Blueprint undertakes no obligation to update any forward-looking statement to reflect events or circumstances after the date on which the statement is made or to reflect the occurrence of unanticipated events. Additional information for US shareholders and where to find itThe tender offer for the outstanding shares of Blueprint Medicines Corporation common stock ('Blueprint') referenced in this communication has not yet commenced. This communication is for informational purposes only and is neither an offer to purchase nor a solicitation of an offer to sell shares of Blueprint, nor is it a substitute for the tender offer materials that Sanofi and its acquisition subsidiary will file with the U.S. Securities and Exchange Commission (the 'SEC') upon commencement of the tender offer. At the time the tender offer is commenced, Sanofi and its acquisition subsidiary will file tender offer materials on Schedule TO, and Blueprint will file a Solicitation/Recommendation Statement on Schedule 14D-9 with the SEC with respect to the tender offer. The tender offer materials (including an Offer to Purchase, a related Letter of Transmittal and certain other tender offer documents) and the Solicitation/Recommendation Statement will contain important information. HOLDERS OF SHARES OF BLUEPRINT ARE URGED TO READ THESE DOCUMENTS WHEN THEY BECOME AVAILABLE BECAUSE THEY WILL CONTAIN IMPORTANT INFORMATION THAT BLUEPRINT STOCKHOLDERS SHOULD CONSIDER BEFORE MAKING ANY DECISION REGARDING TENDERING THEIR SHARES. The Offer to Purchase, the related Letter of Transmittal and certain other tender offer documents, as well as the Solicitation/Recommendation Statement, will be made available to all holders of shares of Blueprint at no expense to them. The tender offer materials and the Solicitation/Recommendation Statement will be made available for free at the SEC's web site at Additional copies may be obtained for free by contacting Sanofi's Investor Relations Team at or on Sanofi's website at In addition to the Offer to Purchase, the related Letter of Transmittal and certain other tender offer documents, as well as the Solicitation/Recommendation Statement, Sanofi files annual and special reports and other information with the SEC and Blueprint files annual, quarterly and special reports and other information with the SEC. You may read and copy any reports or other information filed by Sanofi and Blueprint at the SEC public reference room at 100 F. Street, N.E., Washington D.C. 20549. Please call the Commission at 1-800-SEC-0330 for further information on the public reference room. Sanofi's and Blueprint's filings with the SEC are also available to the public from commercial document-retrieval services and at the website maintained by the SEC at Trademarks Blueprint Medicines, AYVAKIT, AYVAKYT and associated logos are trademarks of Blueprint Medicines Press_ReleaseError in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data
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