Evidence map›Paper›PMID 36265326›Full record

ArticleThe International journal on drug policy2022

Methadone and buprenorphine-related deaths among people prescribed and not prescribed Opioid Agonist Therapy during the COVID-19 pandemic in England.

D Aldabergenov, L Reynolds, J Scott, M J Kelleher, J Strang, C S Copeland, N J Kalk

Open access · hybridAbstract read
In one paragraph

Article in The International journal on drug policy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 3 pooled it
5.4field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 3 syntheses or guidelines pooled it, 28 citations in OpenAlex.

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  15. Eliminate the buprenorphine DEA X waiver: Justification using a policy analysis approach.Journal of nursing scholarship : an official publication of Sigma Theta Tau International Honor Society of Nursing · 2023
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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

7 authors at 2 institutions in 1 country.

D AldabergenovCentre for Pharmaceutical Medicine Research, Institute of Pharmaceutical Sciences, King's College London, London, United Kingdom.
L ReynoldsCentre for Pharmaceutical Medicine Research, Institute of Pharmaceutical Sciences, King's College London, London, United Kingdom.
J ScottDepartment of Pharmacy and Pharmacology, University of Bath, Bath, United Kingdom.
M J KelleherSouth London and Maudsley NHS Foundation Trust, London, United Kingdom; National Addictions Centre, Institute of Psychology, Psychiatry and Neuroscience, King's College London, London, United Kingdom.
J StrangSouth London and Maudsley NHS Foundation Trust, London, United Kingdom; National Addictions Centre, Institute of Psychology, Psychiatry and Neuroscience, King's College London, London, United Kingdom.
C S CopelandCentre for Pharmaceutical Medicine Research, Institute of Pharmaceutical Sciences, King's College London, London, United Kingdom.
N J KalkSouth London and Maudsley NHS Foundation Trust, London, United Kingdom; National Addictions Centre, Institute of Psychology, Psychiatry and Neuroscience, King's College London, London, United Kingdom. Electronic address: Nicola.kalk@kcl.ac.uk.
King's College London · GBUniversity of Bath · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe coronavirus pandemic resulted in many changes which had the potential to impact mortality related to opioid agonist therapy (OAT; methadone, buprenorphine), including changes in the prescribing and dispensing of OAT and patterns of drug availability and use. We aimed to assess the impact of the first lockdown (initiated March 23rd 2020) on methadone- and buprenorphine-related deaths in England in people both prescribed and not prescribed OAT using data from the National Programme on Substance Abuse Deaths.

methodsThis was a retrospective post-mortem toxicology study of OAT-related deaths which occurred in the 3-month period March 23rd to June 22nd in the years 2016-2020. Provisional data regarding numbers accessing treatment for opioid use disorder was provided by the National Drug Treatment Monitoring System.

resultsWe found a 64% increase in methadone-related deaths in March to June 2020 compared to March to June 2019 (2019 n = 96; 2020 projected n = 157). There were increases in the mortality rate of both in-treatment decedents (22% increase; 2019 n = 45; an exponential smoothing model of the 2016-19 trend [α=0.5] predicted 44 deaths in 2020, 55 were reported) and decedents not prescribed methadone (74% increase; 2019 n = 46; 2016-19 trend predicted 43 deaths in 2020, 80 were reported). There was no increase in buprenorphine-related deaths (2019 n = 9/529; 2020 n = 11/566). There were no changes in the numbers of deaths where other opioids or multiple substances were detected, or in methadone levels detected. Numbers of people accessing treatment for opioid use disorder in 2020 did not decrease relative to previous years (p >0.05).

conclusionsMethadone-related deaths in non-prescribed individuals, but not prescribed individuals, increased considerably above the annual trend forecast for 2020 during the first COVID-19 lockdown in England. Further studies are thus needed to understand this difference.

Indexed as

BuprenorphineCOVID-19Opioid-Related DisordersAnalgesics, OpioidCommunicable Disease ControlHumansMethadoneOpiate Substitution TreatmentPandemicsRetrospective StudiesAnalgesics, OpioidBuprenorphineMethadoneBuprenorphineCOVID-19Drug-related deathMethadoneMortalityOpioid agonist therapy

Identifiers

PMID36265326
PMCPMC9531664
OpenAlexW4301394218

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.