340B Court Cases
Jason Shafrin
Senior Managing Director, Center for Healthcare Economics & Policy at FTI Consulting; Adjunct Professor, University of Southern California
The Public Health Service Act (PHSA ) in 1992, created a program to allow hospitals providing care for underserved communities to be able to access discounted drugs. The program--known as the 340B Drug Pricing Program , has been described as follows:
...[The] law requires pharmaceutical manufacturers participating in the Medicaid program to enter into a second agreement with the Secretary of HHS [Health and Human Services] — called a pharmaceutical pricing agreement (PPA) — under which the manufacturer agrees to provide statutorily specified discounts on "covered outpatient drugs" purchased by government-supported facilities, known as covered entities, that are expected to serve the nation's most vulnerable patient populations.
Which types of hospitals are eligible to participate in 340B? There are 6 general types of inpatient covered entities:
There are also outpatient facilities that quality such as federally qualified health centers (FQHCs), Ryan White HIV/AIDS program grantees, Urban Indian clinics and a number of others.
A few key issues with the 340B program. First, these these drugs discounts don't just apply at the patient level when covered entities treat poor individuals, but these covered entities can also get discounted drugs when treating not only uninsured individuals but also individuals covered by Medicare and commercial insurance. For these Medicare and commercially insured individuals, covered entities get discounted drugs but are reimbursed by Medicare and commercial insurance at much higher rates.
A paper by Cole et al., (2022) however, notes that reimbursement rates for 340B covered entities changed in 2018.
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Until 2018, 340B-certified entities were reimbursed by an amount calculated as the average sales price (ASP) of the drug plus 6%. At this level of reimbursement, covered entities received substantially more than they originally paid for the drugs, and they were permitted to retain the overpayment to subsidize other clinical activities...
However, in 2018, the US Department of Health and Human Services (DHHS) determined that Part B drug reimbursements to 340B entities were so much greater than their payments for the drugs (which are often expensive oncology drugs) that this might motivate their overuse...To align reimbursements more closely with 340B drug payments, DHHS subsequently reduced the level of reimbursement from [Average Sales Price] ASP plus 6% to ASP minus 22.5%, resulting in a loss of $1.6 billion per year for 340B entities .?
The Cole paper reviews some on-going litigation related to this change. I summarize this below.
Originally posted at Healthcare Economist .?
The views expressed herein are those of the author and not necessarily the views of?FTI Consulting , Inc. , its management, its subsidiaries, its affiliates, or its other professionals.