Evidence map›Paper›PMID 39452808›Full record

ReviewPharmacy (Basel, Switzerland)2024

Clinical Outcomes of Benzodiazepine Prescribing for People Receiving Opioid Agonist Treatment: A Systematic Review of the Evidence.

Catriona Matheson, Chris Vucic, Josh Dumbrell, Roy Robertson, Trina Ritchie, Clare Duncan, Karthigayan Kessavalou, Caroline Woolston, Joe Schofield

Abstract readReview
In one paragraph

Review in Pharmacy (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

9 authors.

Catriona MathesonFaculty of Applied Social Science, University of Stirling, Stirling FK9 4LA, UK.
Chris VucicFaculty of Applied Social Science, University of Stirling, Stirling FK9 4LA, UK.
Josh DumbrellFaculty of Applied Social Science, University of Stirling, Stirling FK9 4LA, UK.
Roy RobertsonThe Usher Institute, BioQuarter, Little France, Edinburgh EH16 4UX, UK.ORCID 0000-0001-8237-816X
Trina RitchieGlasgow Alcohol and Drug Recovery Services, NHS Greater Glasgow and Clyde, Glasgow G1 1DH, UK.ORCID 0000-0002-5409-700X
Clare DuncanNHS Ayrshire and Arran, 35 Lister Street, Crosshouse Hospital, Kilmarnock KA2 0BE, UK.
Karthigayan KessavalouNHS Ayrshire and Arran, 35 Lister Street, Crosshouse Hospital, Kilmarnock KA2 0BE, UK.
Caroline WoolstonNHS Ayrshire and Arran, 35 Lister Street, Crosshouse Hospital, Kilmarnock KA2 0BE, UK.
Joe SchofieldSchool of Medicine, University of St Andrews, St Andrews KY16 9TF, UK.ORCID 0000-0002-1307-2375

Funding

Scottish Drug Death Taskforce RF15 BENZORT
6 · The paper itself

Abstract

Many countries are experiencing an increased use of unregulated benzodiazepines in combination with opioids and other drugs, which contributes to drug-related harm. This descriptive review identifies and synthesises the outcomes of studies co-prescribing benzodiazepines and opioids. A systematic review was undertaken in Medline, CINAHL, PsychInfo, Embase, and the Cochrane databases covering publications from 1 January 1991 to 18 November 2021. Inclusion criteria were peer reviewed, English language studies of adults prescribed opioid agonist treatment (OAT) and a concurrent benzodiazepine, and reporting outcome data. Of the 4370 titles screened, 18 papers were included. The main outcomes identified covered all-cause mortality (ACM) (n = 5); overdose death (n = 3); retention in treatment (n = 7); and hospitalisation/emergency department encounters (n = 2). Other outcomes included QTc interval, cognitive function, illicit drug use, and mental health. The prescription of benzodiazepines alongside OAT increased the ACM by 75-90%, while evidence on overdose death was less robust but indicative of increased risk (40-334%). There was an indicative positive effect on treatment retention, with increased retention in those prescribed a benzodiazepine with OAT compared to those not prescribed or taking non-prescribed benzodiazepines. In conclusion, methodologically robust epidemiological studies found increased ACM and overdose death but possibly improved retention. However confounders (e.g., psychiatric comorbidity) exist, so a trial is recommended.

Indexed as

addictionbenzodiazepine prescriptionclinical decision-makingclinical outcomesdrug overdoseillicit drug usemortalityopioid agonist treatmentopioid replacement treatmentstreet benzodiazepines

Identifiers

PMID39452808
PMCPMC11511121

What OpenQuestion holds

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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 OpenQuestion graph.