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CENTERS FOR MEDICARE &
MEDICAID SERVICES (CMS)
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Special
Edition – Wednesday, September 2, 2020
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CMS Advancing Seniors’ Access to Cutting-edge
Therapies and Technology in Medicare Hospital Rule
Finalized policy changes expand new
technology add-on payment pathway for certain antimicrobials
On September 2, CMS issued the FY 2021
Medicare Hospital Inpatient Prospective Payment System and Long Term Acute
Care Hospital (LTCH) final rule, which includes important provisions designed
to ensure access to potentially life-saving diagnostics and therapies for
hospitalized Medicare beneficiaries. The changes will affect approximately
3,200 acute care hospitals and approximately 360 LTCHs. CMS estimates that
total Medicare spending on acute care inpatient hospital services will
increase by about $3.5 billion in FY 2021, or 2.7 percent.
“President Trump is committed to ensuring
that seniors on Medicare have access to the latest life-saving diagnostics
and therapies,” said CMS Administrator Seema Verma. “This rule is another
critical step in our effort to modernize the program and strip away
bureaucratic barriers between our seniors and the latest innovative
treatments.”
CMS’ rule creates a new Medicare Severity
Diagnostic Related Group (MS-DRG) that provides a predictable payment to help
adequately compensate hospitals for administering Chimeric Antigen Receptor
(CAR) T-cell therapies. The current FDA-approved CAR-T-cell cancer therapies
use a patient’s genetically modified immune cells to treat specific types of
cancer.
Also in the final rule, CMS approved a record
number of 24 New Technology Add-on Payments (NTAPs), which is an additional
payment to hospitals for cases involving eligible new and relatively high
cost technologies. Last year, to remove barriers to innovation, CMS
established alternative streamlined pathways for FDA Breakthrough Devices and
FDA Qualified Infectious Disease Products (QIDPs) to qualify for NTAPs. Among
CMS’ approval of these 24 additional NTAPs are two technologies for new
medical devices that are part of the FDA’s Breakthrough Devices Program and
six technologies that received FDA QIDP designation. This will provide
additional Medicare payment for these technologies while real-world evidence
is emerging, giving Medicare beneficiaries timely access to the latest
innovations.
CMS is also expanding the add-on payment
alternative pathway for antimicrobial products approved under FDA’s Limited
Population Pathway for Antibacterial and Antifungal Drugs (LPAD pathway),
which encourages the development of safe and effective drug products that
address unmet needs of patients with serious bacterial and fungal infections.
Specifically, an antibacterial or antifungal drug approved under the LPAD pathway
is used to treat a serious or life-threatening infection in a limited
population of patients with unmet needs.
CMS is also taking steps to ensure that the
Medicare Fee-for-Service (FFS) program adopts pricing strategies based on
real world market forces. Medicare generally pays hospitals a rate that is
weighted by the relative cost of providing certain services based on a
patient's diagnosis. These weights are currently based in large part on the
charges that hospitals report to the federal government, which often have
little relevancy to the actual rates paid by insurance companies. Hospitals
are already required to report these negotiated rates as part of the Trump
Administration’s efforts to promote price transparency, and CMS is now
finalizing a requirement for hospitals to report to CMS the median rate
negotiated with Medicare Advantage Organizations for inpatient services to
use instead of the charge based data. CMS will begin to collect this data in
2021 and will use it in the methodology for calculating inpatient hospital
payments beginning in 2024. These provisions will introduce the influences of
market competition into hospital payment and help advance CMS's goal of
utilizing market- based pricing strategies in the Medicare FFS program.
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