Showing posts with label teleprescribing. Show all posts
Showing posts with label teleprescribing. Show all posts

Monday, March 3, 2025

One in 10 Patients Starts Buprenorphine Treatment for OUD via Telehealth

One in 10 buprenorphine initiations is provided via telehealth, and about 20% of those involved no in-person visit within two years prior or 30 days after, according to a study in today’s JAMA Network Open.

“Our findings suggest that telehealth initiation of buprenorphine without a prior in-person visit is an important pathway for accessing this lifesaving treatment for adults with opioid use disorder,” lead investigator Beth McGinty, Ph.D., M.S., of Weill Cornell Medicine, told Psychiatric News. “The pending final rule on telehealth would support this access, and given that we know buprenorphine reduces risk of opioid overdose by 50%, it would save lives.”

The Drug Enforcement Administration issued a final rule in the waning days of the Biden administration that would allow a clinician to teleprescribe up to six months of buprenorphine without an in-person visit as long as the clinician reviewed the prescription drug monitoring program for the state where the patient resides. The rule had been scheduled to take effect in mid-February, but the Trump administration issued an executive order pausing all federal rules not yet in effect, pending further review.

McGinty and colleagues used IQVIA data to assess buprenorphine initiations from March 2020 through November 2022. The researchers included physicians who continuously practiced from 2018 to 2022 and who had treated at least one patient with opioid use disorder. They measured their proportion of telehealth initiations that had no in-person visit with the prescribing clinician within two years prior, and no in-person visit within two years prior or 30 days after.

During the study timeframe, about 10% of the 228,598 total buprenorphine initiations were via telehealth, involving 3,950 clinicians and 21,220 patients. Among these telehealth initiations, 28% had no in-person visit with the prescribing clinician in the prior two years, while 20% had no in-person visit with the prescriber two years prior or 30 days after. The proportion of telehealth initiations with no in-person visit before or after was higher among behavioral health physicians (27% of all telehealth initiations) than primary care physicians (15%) and nurse practitioners or physician assistants (22%).

“In-person visit requirements can impede access due to limited in-person provider appointment availability and other barriers, such as transportation,” McGinty said. “Additional research is needed to compare the effectiveness of telehealth buprenorphine initiations with and without in-person visits to determine if six months is the ‘right’ duration and to consider … whether fully remote telehealth models with no in-person visits are able to deliver comparably safe and effective care.”

For related information, see the Psychiatric News article “New Rules Allow Telehealth Prescribing, but ‘Special Registration’ Proposal May Create Barriers to Care.”

(Image: Getty Images/iStock/pe-art)




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Thursday, January 16, 2025

New Federal Rules Boost Telehealth Flexibility When Treating OUD

As part of a flurry of end-of-term activity, the Drug Enforcement Administration (DEA) along with the U.S. Department of Health and Human Services (HHS) has finalized two rules that permanently expand some telehealth prescribing options and proposed a third rule that would create a new special registration for telehealth prescribing.

Expansion of Buprenorphine Treatment via Telemedicine Encounter

This final rule authorizes registered clinicians to prescribe controlled substances in Schedules III to V for the treatment of opioid use disorder (OUD) via a telemedicine appointment or an audio-only visit, without first seeing the patient in person.

APA has long advocated for a permanent extension to the telemedicine prescribing flexibility that was allowed during the COVID-19 public health emergency and later extended three times. This flexibility prevents lapses of care and expands access to OUD treatment to patients who might not have transportation or a psychiatrist in their area.

“This final rule is a huge win for our patients and colleagues, and key components were directly shaped by feedback from APA and allied organizations,” said Lief Fenno, M.D., Ph.D, assistant professor of neuroscience and psychiatry at the Mulva Clinic for the Neurosciences at the University of Texas at Austin. “The rule reduces the potential for gaps in treatment, lowers barriers to access, and expands the use of life-saving buprenorphine.”

Continuity of Care via Telemedicine for Veterans Affairs Patients

DEA and HHS yesterday also issued a final rule that applies only to VA patients who have previously received an in-person medical evaluation with a VA practitioner. For such patients, the final rule authorizes a different VA practitioner to prescribe Schedule II-V controlled substances via telemedicine, without being limited to a 30-day supply.

The rule stipulates that prescribing VA clinicians must first review the patient’s VA internal prescription database and prescription drug monitoring program (PDMP) data prior to prescribing controlled substances via telemedicine. If unavailable, clinicians are limited to providing a seven-day supply via telehealth.

Both rules take effect 30 days from their date of publication in the Federal Register, which is expected this week.

Special Registration Proposed for Telehealth Controlled Substances Prescribing

The DEA also proposed a new rule to establish three types of special registrations to allow for prescribing and dispensing of controlled substances by registered practitioners and online telemedicine platforms. The separation would mean that only specialized clinicians, such as psychiatrists, neurologists, and board-certified mid-level practitioners (hospice nurses), can prescribe Schedule II substances, while those without this “advanced registration” can prescribe Schedules III-V.

The proposed rule also makes heightened changes to prescriptions, recordkeeping, and reporting. For example, three years after implementation of the rule, clinicians must perform a nationwide PDMP check prior to prescribing controlled substances. For the first three years, clinicians must perform a PDMP check for the patient’s location, clinician’s location, and states with reciprocity agreements.

Public comments about this proposed rule will be due within 60 days after publication in the Federal Register, which is expected this week.

For related information, see the Psychiatric News article “APA Members Urge Congress to Protect Telehealth Access.”

(Image: Getty Images/iStock/Drazen Zigic)




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