Evidence map›Paper›PMID 32374500›Full record

ArticleBritish journal of clinical pharmacology2020

Pregabalin poisoning and rising recreational use: a retrospective observational series.

Katherine Z Isoardi, Gregory Polkinghorne, Keith Harris, Geoffrey K Isbister

Open access · greenAbstract read
In one paragraph

Article in British journal of clinical pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
5.2field-weighted citation impact, top 3% 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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 43 citations in OpenAlex.

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  14. Who prescribes quetiapine in Denmark?British journal of clinical pharmacology · 2022
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  16. Pregabalin poisoning: Evaluation of dose-toxicity relationship.British journal of clinical pharmacology · 2022
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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

4 authors at 2 institutions in 1 country.

Katherine Z IsoardiClinical Toxicology Unit, Princess Alexandra Hospital, Brisbane, Queensland, Australia.ORCID 0000-0002-1176-7923
Gregory PolkinghorneClinical Toxicology Unit, Princess Alexandra Hospital, Brisbane, Queensland, Australia.
Keith HarrisClinical Toxicology Unit, Princess Alexandra Hospital, Brisbane, Queensland, Australia.
Geoffrey K IsbisterClinical Toxicology Research Group, University of Newcastle, Newcastle, New South Wales, Australia.ORCID 0000-0003-1519-7419
The University of Queensland · AUCalvary Mater Newcastle Hospital · AU

Funding

National Health and Medical Research Council Senior Research Fellowship ID1061041NHMRC Senior Research Fellowship ID1061041
6 · The paper itself

Abstract

aimsWith rising use worldwide, pregabalin is increasingly implicated in poisoning deaths. We aimed to investigate the clinical effects and complications of pregabalin poisoning.

methodsThis is a retrospective review of patients presenting with pregabalin poisoning to two tertiary toxicology units from 1 July 2014 to 30 June 2019. Patients were identified from prospective databases maintained by both units and data were extracted from these in addition to medical records.

resultsThere were 488 presentations in 413 patients (237 [57%] male) over the five-year period. The median age was 41 years (IQR 31-50 years). Deliberate self-poisonings accounted for 342 (70%) presentations, with 121 (25%) recreational exposures. Recreational exposures increased over the period from 2 (4%) in the first year to 54 (39%) presentations in the final year. The median dose of pregabalin was 1200 mg (IQR 600-3000 mg, range 75-16 800 mg). Co-ingestions occurred in 427 (88%) presentations, with sedating agents being co-ingested in 387 (79%)-most commonly opioids and benzodiazepines in 201 (41%) and 174 (36%) presentations respectively. Coma (GCS < 9) occurred in 89 (18%) cases, with 52 (11%) patients being intubated. Only one (0.2%) of these patients had not co-ingested a sedating agent. Hypotension occurred in 26 (5%) cases, all with co-ingestants. Seizures occurred in 11 (2%) cases, 3/59 (5%) in pregabalin-only overdoses. The median length of stay was 16.5 hours (IQR 10-25 hours).

conclusionsPregabalin overdose does not cause severe toxicity, but rather mild sedation and, uncommonly, seizures. Coma is common in the presence of sedating co-ingestants. Recreational use is increasing.

Indexed as

Analgesics, OpioidDrug OverdosePoisoningPregabalinAdultBenzodiazepinesFemaleHumansMaleRetrospective StudiesAnalgesics, OpioidBenzodiazepinesPregabalindrug abuseoverdose and poisoningtoxicology

Identifiers

PMID32374500
PMCPMC7688538
OpenAlexW3022181504

What OpenQuestion 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 OpenQuestion graph.