A National Academies panel on Thursday urged radical changes in state and federal law to improve treatment and prevention of opioid use disorder, which in turn would cut the nation’s infectious disease burden.
The committee’s 10 members — comprising academics, medical
professionals, epidemiologists, nurses, and health policy specialists —
recommended scrapping mandatory waivers for buprenorphine prescribers;
eliminating prior authorization requirements for buprenorphine and all
FDA-approved treatments for opioid use disorder; and allowing methadone
treatment to be delivered in primary care settings.
The committee held that one reason for the “unprecedented number of
HIV and viral hepatitis outbreaks” is that substance use disorder
treatment is siloed from delivery of other medical care.
Also, “well-intentioned policies” such as increasing reliance on
prescription drug monitoring programs, intended to curb access to
prescription opioids, have had unintended consequences — sometimes
driving people to illicit injected drugs such as heroin.
As the number of people who inject drugs increased, so did the risk of infectious disease.
The good news is that preventing and treating opioid use disorders can improve infectious disease outcomes, the authors noted.
For instance, patients with a co-occurring opioid use disorder and
HIV will be better at complying with their HIV medication regimens if
their treatment plan also includes medication for opioid use disorder.
“In this way removing barriers for opioid use disorder treatment is,
in itself, a process to improve prevention, and treatment for infectious
disease,” the report said.
Moreover, when substance use disorder and infectious disease services
are better coordinated, co-located or, ideally, fully integrated,
healthcare becomes “simpler, more accessible and patient centered.”
End DATA Waiver, Prior Authorization
One of the report’s most dramatic recommendations is to eliminate
state-level prior authorization requirements for buprenorphine. The
authors say this additional step delays access to evidence-based care
for patients with opioid use disorder and increases the risk of
infectious disease due to patients’ continued drug use.
To put federal teeth into such a policy, the Centers for Medicare
& Medicaid Services should withhold approval of any requests for
Medicaid state plan amendments from states that maintain prior
authorization requirements, the report said.
A federal law enacted two decades ago mandates that providers seeking
permission to prescribe buprenorphine complete an 8- to 24-hour
training course. But the committee said this waiver “poses a barrier for
some providers.”
For that reason, the committee recommended that Congress amend the legislation to drop that requirement.
In speaking with clinician prescribers, the report’s authors found
that many believed the mandated training was “inadequate and clinically
irrelevant.”
For that reason, the committee recommended that any organizations
that currently offer training should examine its curriculum and its
usefulness and “provide newly trained providers with greater access to
experienced peers.”
Another recommendation: the Substance Abuse and Mental Health
Services Administration (SAMHSA) should offer additional funds and
grants aimed at “expand[ing] mentorship networks for providers.”
Additionally, the report called on Congress to eliminate the cap on the number of patients that prescribers can serve.
The report also addressed barriers to methadone treatment for opioid
use disorder. It recommended federal legislation to let clinicians
provide the drug in primary care settings. As the law now stands,
methadone can only be prescribed for addiction treatment in certain
licensed and regulated facilities — i.e., dedicated opioid treatment
programs.
Conversely, the committee noted that with 1,600 opioid treatment
programs across the country in 2018 serving 380,000 patients each year,
it’s a mistake — a “missed opportunity” — that such programs do not
frequently offer testing and treatment for infectious disease.
The committee therefore suggested that the Department of Health and
Human Services consider instituting “universal, opt-out-testing and
connection to treatment for infectious diseases,” particularly in
methadone-based opioid treatment programs.
But on the thorny issue of 42 CFR Part 2,
often known simply as “Part Two” — the federal rule that defines the
right of access among different stakeholders to patients’ records from
substance use disorder treatment programs — the committee mostly punted.
The report suggested that SAMHSA either align Part Two with the
Health Insurance Portability and Accountability Act or “alter the
definition of which specific service programs” are encompassed in Part
Two.
“[T]here is significant debate about whether and how changing this
regulation would jeopardize patient privacy or allow providers to
deliver more coordinated, effective care,” the authors noted.
SAMHSA should “formally engage with patients, advocacy groups, the
general public, and legal experts” to weigh the pros and cons of wider
data sharing, the report concluded.
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