Evidence map›Paper›PMID 39495456›Full record

Observational studyJournal of general internal medicine2025

Fentanyl Initiation Rate Following the Requirement for Specialist Approval.

Oren Miron, Yael Wolff-Sagy, Mark Levin, Esti Lubich, Jordan Lewinski, Maya Shpunt, Wiessam Abu Ahmad, Ilya Borochov, Doron Netzer, Gil Lavie

Abstract readObservational Study
In one paragraph

Observational study in Journal of general internal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Oren MironBranch of Planning and Strategy, Clalit Health Services, Tel Aviv, Israel. Orenmir@post.bgu.ac.il.ORCID 0000-0002-7742-478X
Yael Wolff-SagyBranch of Planning and Strategy, Clalit Health Services, Tel Aviv, Israel.
Mark LevinCommunity Medical Services Division, Clalit Health Services, Tel Aviv, Israel.
Esti LubichCommunity Medical Services Division, Clalit Health Services, Tel Aviv, Israel.
Jordan LewinskiCommunity Medical Services Division, Clalit Health Services, Tel Aviv, Israel.
Maya ShpuntCommunity Medical Services Division, Clalit Health Services, Tel Aviv, Israel.
Wiessam Abu AhmadBranch of Planning and Strategy, Clalit Health Services, Tel Aviv, Israel.
Ilya BorochovCommunity Medical Services Division, Clalit Health Services, Tel Aviv, Israel.
Doron NetzerCommunity Medical Services Division, Clalit Health Services, Tel Aviv, Israel.
Gil LavieBranch of Planning and Strategy, Clalit Health Services, Tel Aviv, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHealthcare organizations attempt to address unwarranted fentanyl use, which often leads to increased risk of addiction and overdose.

objectiveTo assess the impact of a requirement for a specialist's approval on fentanyl initiation for non-oncological pain.

designA retrospective cohort study based on observational data.

participantsAll 4.4 million non-oncological members of Clalit Health Services were included, from July 20, 2021, to July 19, 2023. MAIN MEASURES: The rate of fentanyl initiation was assessed before and after the implementation of the requirement for specialist's approval, which was introduced on July 2022, and expanded 6 months later for continued use. A sub-group analysis by age group was performed, and patient characteristics and indications were assessed. We also compared total opioid dispensation in the 6th and 12th months after the implementation with the predicted rate based on pre-implementation rates. KEY

resultsFentanyl initiation rate in the year before the requirement was 711 per million capita, which decreased following the requirement by - 81% (95% CI: - 77%; - 85%). The decrease attenuated with age. The prevalence of diagnosis with substance abuse disorders at the time of fentanyl initiation decreased from 6 to 3%. In the 6th and 12th months after the requirement was implemented, the morphine milligram equivalent (MME) from dispensation of total opioids was lower than predicted based on pre-implementation rates by 7% and 26%, respectively.

conclusionsRequiring specialist approval for fentanyl initiation for non-oncological chronic pain was associated with a decrease in fentanyl prescription initiations, especially among non-elderly patients. A decrease also occurred gradually in total opioid dispensations, further decreasing following the extension of the requirement to continuous fentanyl. The requirement for specialist approval upon fentanyl initiation and continuous fentanyl may present an effective tool for limiting the use of fentanyl and total opioids in healthcare systems.

Indexed as

Analgesics, OpioidFentanylPractice Patterns, Physicians'SpecializationAdolescentAdultAgedCohort StudiesFemaleHumansMaleMiddle AgedOpioid-Related DisordersRetrospective StudiesYoung AdultAnalgesics, OpioidFentanyl

Identifiers

PMID39495456
PMCPMC12508242

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.