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Home Politics & Law

SAMHSA Makes Permanent Increased Access to OUD Medications

Pandemic-era opioid treatment rules to remain in place

Jeffrey A Singer by Jeffrey A Singer
February 4, 2024
in Politics & Law
0
Pandemic-era opioid treatment rules to remain in place

Alexander Grey

In March 2020, as the COVID-19 pandemic made it more difficult for people with opioid use disorder (OUD) to access daily methadone treatment at federally‐​approved opioid treatment programs (OTPs), the Substance Abuse and Mental Health Services Administration (SAMHSA) temporarily liberalized methadone take‐​home rules for OTPs, and allowed “stable” patients to take home up to a 28‐​day supply. SAMHSA also allowed patients to visit clinicians via telehealth, rather than in‐​person, to obtain buprenorphine treatment for OUD. The program was a success. Follow‐​up studies found the policy improved patient compliance and did not cause buprenorphine or methadone diversion into the black market.

In November 2021, SAMHSA announced it was extending the policy. Then, in December 2022, SAMHSA issued a Notice of Proposed Rulemaking, announcing its intention to make the policy permanent and asking interested parties to comment. I submitted this comment.

On January 31st, 2024, the Department of Health and Human Services announced SAMHSA’s eased rules are finally permanent.

Anything that makes it easier to get access to medications to treat opioid use disorder is a welcome change. Unfortunately, in another example of cops practicing medicine, the Drug Enforcement Administration is working against that goal by requiring people who want to use telehealth to access buprenorphine to see a clinician in person within 30 days to renew their buprenorphine prescriptions. This means if the patient can’t get an office appointment with the provider within 30 days, the buprenorphine treatment abruptly ends. It takes an average of 26 days to get a new appointment with a primary care provider, so there is no guarantee a new buprenorphine patient can get an appointment within the 30‐​day window. It might be even more difficult in rural or other areas with primary care provider shortages.

Even without the DEA’s interference, this new rule change is “small ball.” As Sofia Hamilton and I wrote in a recent Cato briefing paper, a more effective way to improve access to methadone treatment is by enabling primary care clinicians to prescribe it to treat patients with opioid use disorder in their offices. Clinicians in the US were doing so before 1972. Clinicians in the UK, Canada, and Australia have continued to treat their office‐​based patients with methadone for over 50 years.

The Modernizing Opioid Treatment Access Act (MOTAA), introduced in the US Senate by Senator Edward Markey (D‑MA) and co‐​sponsored by Senators Rand Paul (R‑KY), Bernie Sanders (I‑VT), Mike Braun (R‑IN), Cory Booker (D‑NJ), and Maggie Hassan (D‑NH), would expand access to methadone treatment for people with opioid use disorder (OUD) by allowing board‐​certified addiction specialists to prescribe methadone to patients in their offices or clinics.

As I wrote here, the MOTAA doesn’t go far enough. Even assuming they were all accepting new patients, there are not nearly enough board‐​certified addiction specialists to meet the needs of people with OUD. However, MOTAA takes a much bigger step to improve access to methadone treatment than SAMHSA does in its revised policy. MOTAA is the first serious attempt in many years to remove unnecessary government barriers to methadone treatment. The bill also helps to destigmatize people with OUD by treating them as suffering from a medical condition.

Reacting to the new permanently liberalized SAMHSA policy in a press release, Senator Markey stated:

“Ultimately, tethering methadone exclusively to opioid treatment programs is less about access, or health and safety, but about control, and for many investors in those programs, it is about profit. The longer we leave this antiquated system in place, the more lives we lose. We must put people first, unwind outdated laws, and treat methadone like the life‐​saving medication it is…”

I couldn’t agree more.

Source: Cato At Liberty
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Jeffrey A Singer

Jeffrey A Singer

Jeffrey A. Singer is a senior fellow at the Cato Institute and works in the Department of Health Policy Studies. He is President Emeritus and founder of Valley Surgical Clinics Ltd., the largest and oldest group private surgical practice in Arizona, and has been in private practice as a general surgeon for more than 35 years. He received his BA from Brooklyn College (City University of New York) and his MD from New York Medical College. He is a fellow of the American College of Surgeons.

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Videos

This conversation focuses on debunking myths surrounding GLP-1 medications, particularly the misinformation about their association with pancreatic cancer. The speaker emphasizes the importance of understanding clinical study designs, especially the distinction between observational studies and randomized controlled trials. The discussion highlights the need for patients to critically evaluate the sources of information regarding medication side effects and to empower themselves in their healthcare decisions.

Takeaways
GLP-1 medications are not linked to pancreatic cancer.
Peer-reviewed studies debunk misinformation about GLP-1s.
Anecdotal evidence is not reliable for general conclusions.
Observational studies have limitations in generalizability.
Understanding study design is crucial for evaluating claims.
Symptoms should be discussed in the context of clinical conditions.
Not all side effects reported are relevant to every patient.
Observational studies can provide valuable insights but are context-specific.
Patients should critically assess the relevance of studies to their own experiences.
Engagement in discussions about specific studies can enhance understanding

Chapters
00:00
Debunking GLP-1 Medication Myths
02:56
Understanding Clinical Study Designs
05:54
The Role of Observational Studies in Healthcare
Debunking Myths About GLP-1 Medications
YouTube Video DM9Do_V6_sU
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Clinical Reads

BIIB080 in Mild Alzheimer’s Disease: What a Phase 1b Exploratory Clinical Analysis Can—and Cannot—Tell Us

BIIB080 in Mild Alzheimer’s Disease: What a Phase 1b Exploratory Clinical Analysis Can—and Cannot—Tell Us

by Daily Remedy
February 15, 2026
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Can lowering tau biology translate into a clinically meaningful slowing of decline in people with early symptomatic Alzheimer’s disease? That is the practical question behind BIIB080, an intrathecal antisense therapy designed to reduce production of tau protein by targeting the tau gene transcript. In a phase 1b program originally designed for safety and dosing, investigators later examined cognitive, functional, and global outcomes as exploratory endpoints. The clinical question matters because current disease-modifying options primarily target amyloid, while tau pathology tracks...

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