Reprinted from MEDICARE
ADVANTAGE NEWS, biweekly news and business strategies about Medicare
Advantage plans, product design, marketing, enrollment, market expansions, CMS
audits, and countless federal initiatives in MA and Medicaid managed
care.
By Lauren
Flynn Kelly, Managing Editor
August 24, 2017 Volume 23 Issue 16
The opioid crisis reached a new level of concern this month when
President Donald Trump responded to recommendations from a White House panel
chaired by New Jersey Gov. Chris Christie (R) to declare it a national
emergency. As the number of opioid-related deaths surged from 19,000 in 2014 to
22,000 in 2015, insurers and pharmacy benefit managers (PBMs) have in the last
couple of years been rolling out comprehensive opioid management programs for a
variety of patient populations. But addressing this issue in an elderly
population demands a nuanced approach as well as adherence to numerous Medicare
program requirements, and Medicare Advantage and Part D sponsors are likely to
adopt more prudent policies within CMS guidelines in the coming years.
“Typically, there are less members on higher doses in the Medicare
population than we see in other populations. [But] there tends to be a higher percentage
of chronic treatment among those on therapy,” remarks Mesfin Tegenu, R.Ph.,
president of PerformRx, LLC, a wholly owned PBM
subsidiary of the AmeriHealth Caritas Family of Companies that recently
unveiled a Medicare-specific strategy as part of its broader opioid management
solution for 2018. “The biggest difference in managing the programs for
Medicare populations is making sure that we follow all the CMS guidelines. Our
programs are designed to meet all the requirements.”
MAOs Tighten Opioid Management
CMS in 2013 signaled its heightened expectations for Part D
sponsors to address opioid overuse when it began issuing reports through the
Overutilization Monitoring System (OMS) that identify Medicare beneficiaries
with potential opioid or acetaminophen overutilization issues. Plans are
expected to address the overuse through various improved drug utilization
review controls (MAN 9/12/13, p. 5). That policy resulted
in a 61% drop in the number of Part D enrollees identified as potentially very
high risk opioid overutilizers from 2011 through 2016 (see "Table: OMS Part D Potential Opioid Overutilization Rates"
below).
But the launch of the OMS focused on members with the highest risk
of adverse events, and CMS has encouraged plans to develop and refine their own
internal criteria. The overuse criteria initially used in the OMS was for
opioids with a cumulative daily morphine equivalent dose (MED) exceeding 120 mg
for at least 90 days with more than three prescribers and more than three
pharmacies contributing to their opioid claims during the most recent 12
months. CMS in the final 2018 Call Letter for MA and Part D plans revised that
criteria by shortening the measurement period to six months and established
that a patient’s average daily MED must exceed 90 mg for any duration and the
beneficiary must have received opioids from more than three prescribers and
more than three pharmacies or from more than five prescribers regardless of the
number of opioid-dispensing pharmacies. Beneficiaries with cancer or in hospice
will continue to be excluded from the review criteria.
Beginning in 2017, sponsors were expected to implement additional
hard or soft formulary-level safety edits for opioids based on a specified
cumulative MED. CMS for 2018 had proposed the implementation of only hard
edits, but after receiving numerous comments expressing concerns about access,
member disruption, operations and other issues impacting plans and prescribers,
the agency opted to not finalize that proposal and instead recommended that
sponsors continue using thresholds of greater than 90 mg MED for soft edits and
200 mg MED or more for hard edits as per 2017 guidance.
Tegenu tells AIS Health that PerformRx’s internal criteria for
identifying potentially impacted beneficiaries is stricter than what CMS has
outlined, which often results in the PBM identifying potential overutilizers
before they are flagged in OMS reports. For 2018, PerformRx has designed a
protocol to support its Part D clients that includes three key features:
·
New starts exceeding
a 200 mg MED will be stopped at the point of sale (hard edit) for prior
authorizations. Exceptions will
be made in situations such as cancer diagnoses and hospice care.
·
Selected high-potency
opioids will require a coverage determination.
·
Prior to 2018,
PerformRx will contact potentially impacted beneficiaries who are in plans that choose to implement the protocol
to determine dose appropriateness and potentially change prescribing patterns,
thereby minimizing the impact when the edit becomes effective.
Tegenu says the Medicare-specific strategy was established in
response to concerns about rising opioid misuse among an elderly population as
well as the CMS recommendations. “We had seen instances where patients with a
lower MED were not being captured by the criteria outlined by CMS,” he
explains. “Through our own impact reports, we determined that it would be
beneficial to drop the MED count to 90 Morphine Milligram Equivalents (MME) for
our Opioid Management Program (OMP) to capture members earlier on.”
Meanwhile, PerformRx for its other populations will make stricter
recommendations such as denying all opioid prescriptions exceeding a specific
quantity and day supply limit that were not written by exempt providers (e.g.,
oncologists, hospice physicians) at the point of sale and allowing only a
five-day supply of opioid therapy for less than 90 MME at the point of sale for
new starts. Tegenu says the OMP was launched in July and that 35% of its
managed Medicaid clients have already chosen to adopt it, while most of its
Part D clients have also decided to roll it out.
Highmark Addresses Pain-Depression Ties
While MA and Part D sponsors are barred from sharing specifics
about their benefit designs for 2018, several tell AIS Health they are
considering more Medicare-specific opioid strategies. Highmark Inc., which
recently received an award from the Drug Enforcement Agency for its assistance
during narcotic investigations, is looking at initiatives for MA members aimed
at addressing opioid misuse and dependence, according to a spokesperson. The
Pennsylvania-based insurer also has programs in place that target physician
prescribing patterns, and as part of providing physicians with support for
members managing pain and patients demanding these drugs, takes steps to inform
them of potential doctor and pharmacy shopping.
Additionally, Highmark is seeking to connect pain and mental
health issues commonly affecting seniors (e.g., grief-based depression) by
using a company called Quartet to scan claims data for potential behavioral
health issues, says the spokesperson. Quartet then works with the MA member’s
doctor to speed referrals into mental health therapy (bypassing long wait times)
and enhances communication between primary care physicians and therapists.
Aetna Inc., which offers numerous initiatives to address opioid misuse
across its member population, also has a multifaceted approach to addressing
the issue among Medicare beneficiaries that includes:
·
The use of formulary
and utilization management tools to promote appropriate therapy choices.Aetna Medicare’s limitations help to promote appropriate
dosing and avoid extra doses of medication, says the insurer.
·
Starting in 2017 and
continuing in 2018, Aetna Medicare will utilize soft edit messaging at the point of sale regarding high-dose opioid MED
across multiple prescriptions. This soft edit creates the alert at the point of
sale for the decision to then be made by the pharmacist in consultation with
the prescriber.
·
Aetna also has
pharmacists, technicians and investigators reviewing Aetna data for outlier
behaviors in physician
prescribing, pharmacy filling patterns and high utilization at a member level.
Likewise, western New York insurer Independent Health has
Medicare-specific strategies outside of its broader protocols, such as a soft
edit to stop a claim exceeding 120 mg MED at the point of sale that can be
resolved by the pharmacist if deemed appropriate. If the MED is 200 mg or
higher, that is a hard edit, meaning it is rejected at the point of sale and
requires prescriber documentation, which is in line with CMS guidance. When
asked about the difference between monitoring potential opioid overuse among
seniors vs. a non-Medicare population, Vice President of Pharmacy Services
Martin Burruano remarks, “It’s really the nature of the patient population,
being more sensitive to the side effects of certain drugs, especially drugs
that have many side effects such as drowsiness, dizziness, etc. So we want to
try to control that as much as we can by limiting the dosing [of opioids].”
Independent Health also conducts retrospective reviews on a
quarterly basis and has its own criteria for identifying potential
overutilizers: two different prescribers and two different pharmacies, as
opposed to CMS’s longstanding policy of three and three. Additionally, the MA
sponsor has therapeutic duplication edits in place, monitors acetaminophen
doses so that anything containing more than 4 grams a day is rejected at the
point of sale and requires the pharmacist to contact the plan, and offers
continuing education programs for providers that are specific to opioid drug
management. “We also monitor concurrent opioid and benzodiazepine use, and we
don’t block those at the point of sale because we can’t for Medicare, but we
perform retrospective reviews and then do outreach to physicians about using
that combination concurrently,” adds Burruano.
Also helping to lower opioid utilization in New York are separate
state laws that require physicians to check a central database to see if an
opioid prescription has been written for a patient by another prescriber and a
seven-day first-fill limit on narcotics. Even though the latter policy is for
non-Medicare patients, Burruano says it has flowed over to MA because it has
become part of physicians’ prescribing practices.
*Includes partial year inactive contracts; hospice and cancer
patients are excluded from utilizer and potential overutilizer counts. For
these opioid utilization comparisons, CMS used Overutilization Monitoring
System (OMS) methodology and prescription drug event (PDE) TAP Data processed
with cut-off dates in early January of the following year.
SOURCE: CMS, final 2018 Call Letter for Medicare Advantage and
Part D plans, published April 3, 2017.
https://aishealth.com/archive/nman082417-01?utm_source=Real%20Magnet&utm_medium=email&utm_campaign=117239715
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