Evidence map›Paper›PMID 32840386›Full record

ArticleClinical toxicology (Philadelphia, Pa.)2021

Trends in hydrocodone combination product exposures reported to California Poison Control System (CPCS) following DEA rescheduling.

Alice Wu, Christine Phan, Kim Chi Nguyen, Melvin Quindoy, Justin Lewis, Dorie E Apollonio

Open access · greenAbstract read
In one paragraph

Article in Clinical toxicology (Philadelphia, Pa.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 28% of its field
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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 2 institutions in 1 country.

Alice WuClinical Pharmacy, University of California, San Francisco, San Francisco, CA, USA.
Christine PhanClinical Pharmacy, University of California, San Francisco, San Francisco, CA, USA.
Kim Chi NguyenClinical Pharmacy, University of California, San Francisco, San Francisco, CA, USA.
Melvin QuindoyClinical Pharmacy, University of California, San Francisco, San Francisco, CA, USA.
Justin LewisCalifornia Poison Control System - Sacramento Division, University of California Davis Medical Center, Sacramento, CA, USA.
Dorie E ApollonioClinical Pharmacy, University of California, San Francisco, San Francisco, CA, USA.ORCID https://orcid.org/0000-0003-4694-0826
University of California, San Francisco · USUniversity of California Davis Medical Center · US

Funding

Linking local variation in marijuana and opioid policies to health outcomesR21DA046051 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI APOLLONIO, DOROTHY ELINOR, RAMO, DANIELLE E · 2019 to 2020
$442k
NIDA NIH HHS R21 DA046051
6 · The paper itself

Abstract

contextOn October 6, 2014, the United States Drug Enforcement Administration (DEA) implemented a regulatory change for hydrocodone combination products (HCPs), moving them from Schedule III to II, in an effort to decrease drug overdoses. Existing research suggests this regulatory action reduced HCP prescribing and dispensing; however, there is limited research assessing its possible effects on overdoses and accidental exposures.

objectiveTo analyze the changes in opioid exposures reported to the California Poison Control System (CPCS) before and after DEA rescheduling of HCPs.

methodsWe collected monthly exposure data reported to CPCS from 2012 to 2019 and conducted interrupted time series analyses to assess changes in exposures after rescheduling for HCPs, tramadol, oxycodone, morphine, codeine, fentanyl, and heroin. Additional analyses were done to assess any changes in exposures resulting in severe outcomes (moderate or major health effects). For HCPs, we also conducted logistic regressions to identify characteristics of exposures resulting in severe outcomes before and after rescheduling.

resultsOverall monthly opioid exposures reported to CPCS decreased after DEA rescheduling of HCPs. These decreases were significant for HCP, tramadol, and morphine ( DISCUSSION: The DEA rescheduling of HCPs was associated with a significant decrease in HCP exposures and prescription opioid exposures overall, but was associated with increased fentanyl and heroin exposures. While other initiatives may have contributed to this decrease, our findings suggest that rescheduling may be a useful regulatory strategy to reduce drug exposures.

conclusionDEA rescheduling of HCPs was associated with a significant reduction in prescription opioid exposures, suggesting that rescheduling high-risk drugs may be an effective strategy to improve public health.

Indexed as

CaliforniaCodeineDrug and Narcotic ControlDrug OverdoseDrug PrescriptionsFentanylHeroinHumansHydrocodoneInterrupted Time Series AnalysisMorphineOxycodonePoison Control CentersTramadolCodeineFentanylHeroinHydrocodoneMorphineOxycodoneTramadolanalgesicsdrug and narcotic controldrug overdoseHydrocodoneopioidpublic health

Identifiers

PMID32840386
PMCPMC7996450
OpenAlexW3081316225

What OpenQuestion holds

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Registered trials

None linked

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.