Advisory Panel Targets Rising Medicare Drug Costs In Its Latest Report To Congress

2016-06-15 | Kaiser Health News

Congress should move to slow spending in Medicare’s drug benefit by adopting a package of changes that could save billions, but would also add costs to insurers and have mixed effects on enrollees, an independent advisory commission said Wednesday.

In its June report to Congress, the Medicare Payment Advisory Commission warned that rising drug costs and other factors have helped drive Medicare Part D spending up nearly 60 percent from 2007 to 2014.

The commission recommends an interrelated set of proposals it estimates could save at least $10 billion over five years, partly by encouraging more use of generic drugs and also by creating incentives for insurers to negotiate better prices from drug makers. While MedPAC recommendations are considered influential, most experts don’t expect Congress to pursue those changes during an election year.

The proposals would:

  • Sharply reduce or even eliminate the copayments that about 12 million low-income Medicare enrollees pay for generic drugs — to encourage the use of the lower-cost medications.
  • Create an annual out-of-pocket spending cap for higher-income enrollees that is similar to one already in place for low-income beneficiaries. After enrollees hit the cap, Medicare would cover 100 percent of the cost of their medications.
  • Make it harder to reach that annual cap by not allowing a drug discount given by manufacturers to count toward the enrollees’ out-of-pocket maximum.
  • Require insurers to pay 80 percent of drug costs, up from the current 20 percent, after patients hit the out-of-pocket maximum.

While patient groups like the idea of reducing generic copayments for low-income enrollees and setting an annual cap, they fear that the proposal would mean patients will remain in what is called the coverage gap or “doughnut hole” for longer periods. While in that doughnut hole, enrollees pay a higher percentage of drug costs. MedPAC estimates that its proposal would mean about half of beneficiaries whose drug spending is enough to hit this gap would remain in it longer, paying about $1,000 more each as a result.

“We’re pleased that some of the recommendations would protect beneficiaries from the rising cost of medications … but we have concerns that fewer beneficiaries would benefit from the out-of-pocket maximum,” said Stacy Sanders, federal policy director for the Medicare Rights Center.

This year, the doughnut hole occurs after patients and their insurers combined have spent $3,310 on covered drugs. In the coverage gap, enrollees must pay a larger share of the cost of their drugs until catastrophic coverage kicks in. That happens when spending hits $4,850 and the enrollee then pays 5 percent of the cost of their drugs. While 5 percent isn’t much when a low-cost generic is taken, it can be substantial for expensive drugs, such as many used for hepatitis, cancer, multiple sclerosis and some forms of arthritis.

The Affordable Care Act gradually phases out the coverage gap by requiring drug makers to give enrollees discounts. This year, the discount is 50 percent of the cost of the drug. Even though enrollees are not paying that discounted amount out of their own pockets, the ACA allowed the dollar value to count toward the $4,850 threshold for catastrophic coverage to begin. Since the ACA took effect, the number of Medicare Part D enrollees who reach the catastrophic coverage level has grown from 400,000 in 2010 to 700,000 by 2013, according to MedPAC. That costs Medicare and taxpayers more because the program pays 80 percent of the costs for drugs after enrollees go through the coverage gap.

Under the commission’s proposal, enrollees would no longer be allowed to count those drug maker discounts toward the total, meaning it would take longer to hit the out-of-pocket cap. Indeed, about half of enrollees might not reach the threshold in a given year and not benefit from the 100 percent coverage, notes the report.

“For many people, this will actually increase spending,” said Caroline Pearson of consulting firm Avalere in Washington, D.C., which is in the process of analyzing the financial impacts of the MedPAC proposals. “While our results aren’t finalized yet, our generalized finding is that a small number of beneficiaries would save a lot of money … but a lot would spend more.”

Other elements of the proposal would affect insurers. MedPAC recommends insurers shoulder more of the cost of prescriptions after enrollees exit the doughnut hole. That would encourage insurers to try to keep enrollees from hitting the coverage gap’s upper limit by getting them to choose lower-cost drugs or by driving harder bargains with drug makers, said Mark Miller, executive director of the commission.

“A good portion of that payment is because beneficiaries are either using more expensive drugs or the prices of their drugs are going up relatively aggressively,” said Miller. “We’re trying to say … you’re going to want to negotiate as tough prices as you can.”

MedPAC says the proposals are needed because rising drug prices and other factors helped drive spending in the program to $73 billion in 2014 — and more high-cost drugs will hit the market soon. Without action, the rising costs could drive up program costs and probably premiums for enrollees, MedPAC said.

When MedPAC adopted its recommendations unanimously this spring, they drew mixed reviews and many comments from the drug industry, consumer groups and insurers. All groups found elements they liked in the plans and parts they opposed.

Little change was seen in the final version released to Congress.

“PhRMA remains concerned about the sweeping recommendations MedPAC approved in April and opposes changes to Medicare Part D that taken together could harm beneficiaries by eroding coverage and protections for many of the most vulnerable enrollees in the program,” said Allyson Funk, spokeswoman for the drug industry’s trade group PhRMA.

Some proposals have been rejected before, but the report could spark discussion under a new administration and Congress in 2017.

“Once MedPAC makes a recommendation, it gives it legitimacy,” said Sanders. “In future years, we could see the proposals as a starting point for some legislation.”

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