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capitol hill report: AAN RECOMMENDS MORE TRANSPARENCY IN MEDICARE ADVANTAGE

April 8, 2024

Issue in Focus

Building on a slate of recently finalized reforms impacting Medicare Advantage (MA), the AAN submitted a robust set of recommendations to the Centers for Medicare and Medicaid Services (CMS) in response to a request for information concerning the need for further transparency within the MA program.

The AAN’s recommendations include a call for the agency to expand on existing transparency requirements surrounding prior authorization and to require plans to disaggregate and publicly disclose relevant prior authorization data at the service level. The AAN also urged the agency to require additional transparency surrounding the use of artificial intelligence tools in the coverage determination process to ensure that care is not being inappropriately denied and that such tools do not exacerbate discrimination and bias.

Further, the AAN recommended that the agency reinstate the ban on step therapy for Part B drugs in MA, and absent such a decision, to release further data concerning the impact of step therapy policies on patient access to care.

Before the release of this critical request for information, CMS finalized two crucial rules that fundamentally reform how MA plans may implement utilization management policies including prior authorization.

The first rule was finalized in April 2023. Consistent with the AAN’s long-standing recommendations, it places crucial mandates on MA plans, most notably that beneficiaries must receive the same access to care as they would in traditional Medicare. Under this rule, MA prior authorization policies cannot be more restrictive than existing Medicare Fee for Service coverage policies. The rule also mandates that MA plans’ use of prior authorization may not function to delay or discourage clinically appropriate care and that MA plans must use widely accepted treatment guidelines and clinical literature when creating internal coverage criteria. Further, MA plans are also required to implement a 90-day authorization transition period when a patient transitions between payers into an MA plan during which an ongoing course of care cannot be subject to prior authorization. Lastly, denial reviews are required to be conducted by a professional with expertise in the relevant field of medicine.

The second rule, finalized in January 2024, was also consistent with AAN advocacy and recommendations. Applying to MA, Medicaid, and payers offering plans in the federally facilitated exchanges, it serves to develop the data sharing infrastructure needed to operationalize electronic prior authorization and requires the development of a standardized electronic prior authorization application. These requirements must be implemented by January 1, 2027. The rule also requires impacted payers to share specific reasons for denials and mandates that payers make decisions on prior authorization requests on a set timeframe—within seven calendar days for standard requests and within 72 hours for urgent ones. Further, this rule requires additional reporting of critical metrics that will allow patients, providers, researchers, and policymakers to better understand how plans are utilizing prior authorization. These operational or process-related policies were finalized with a compliance date starting January 1, 2026, and the initial set of metrics must be reported by March 31, 2026.

The AAN recognizes the specific impact that utilization management policies implemented by MA plans are having on beneficiary access to high-quality neurologic care. The AAN is committed to working with CMS to strengthen the MA program by ensuring that care is not inappropriately denied or delayed and that MA beneficiaries maintain robust access to neurologic care.

 

Latest Advocacy News

AAN Submits Comments on Generic Drug Shortages
On April 3, the AAN submitted comments in response to a request for information from the Federal Trade Commission (FTC) and US Department of Health and Human Services (HHS) regarding the root cause of generic drug shortages. Specifically, the RFI requests comment on the impact on the drug supply chain of the competition and contracting practices of Group Purchasing Organizations (GPOs) and drug wholesalers. The comments convey concerns regarding shortages and encourage the agencies to investigate other causes of disruptions to the supply chain.

AAN Supports Colorado Prior Authorization Reform Bill
On April 3, the AAN submitted a letter to the Colorado State Legislature in support of HB24-1149, the Prior Authorization Requirements Alternatives bill, ahead of a Senate Committee on Health & Human Services hearing. If passed, this bill would mandate private utilization review organizations to adopt a program aimed at reducing or eliminating prior authorization requirements in a way that reduces administrative burdens for qualified providers and their patients, among other reforms.

AAN Supports Massachusetts Parkinson’s Disease Research Registry
The AAN submitted a letter in March showing its support for a Massachusetts bill that would establish a Parkinson’s disease research registry. The bill, S.1344/H.3614, would allow for data collection on people diagnosed with Parkinson’s disease in the state. The registry would help provide more accurate prevalence data, identify high-risk groups, support patient contact studies, and serve as a valuable resource for the research community. Other states including California and Washington have Parkinson's disease registries, helping to expand current knowledge of the disease and accelerate research for improved therapeutics and treatments.

 

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