Relative toxicity of analgesics commonly used for intentional self-poisoning: A study of case fatality based on fatal and non-fatal overdoses.


Journal

Journal of affective disorders
ISSN: 1573-2517
Titre abrégé: J Affect Disord
Pays: Netherlands
ID NLM: 7906073

Informations de publication

Date de publication:
01 03 2019
Historique:
received: 20 09 2018
revised: 21 12 2018
accepted: 04 01 2019
pubmed: 12 1 2019
medline: 18 4 2019
entrez: 12 1 2019
Statut: ppublish

Résumé

Analgesics are used most frequently in fatal and non-fatal medicinal self-poisonings. Knowledge about their relative toxicity in overdose is important for clinicians and regulatory agencies. Using data for 2005-2012 we investigated case fatality (number of suicides relative to number of non-fatal self-poisonings) of paracetamol, aspirin, codeine, dihydrocodeine, tramadol, paracetamol with codeine (co-codamol), paracetamol with dihydrocodeine (co-dydramol), ibuprofen and co-proxamol (paracetamol plus dextropropoxyphene; withdrawn in the UK in 2008 due to high toxicity). Data on suicides obtained from the Office for National Statistics and on non-fatal self-poisonings from the Multicentre Study of Self-harm in England. Case fatality was estimated for each drug, using paracetamol as the reference category. Compared to paracetamol and based on single drug deaths the case fatality index of dihydrocodeine was considerably elevated (odds ratio (OR) 12.81, 95% Confidence Interval (CI) 10.19-16.12). Case fatality indices for tramadol (OR 4.05, 95% CI 3.38-4.85) and codeine (OR 2.21, 95% CI 1.81-2.70) were also significantly higher than for paracetamol. The results when multiple drug deaths were included produced similar results. The relative toxicity of co-proxamol far exceeded that of the other analgesics. Data on fatal self-poisonings were based on national data, whereas those for non-fatal poisonings were based on local data. Dihydrocodeine and tramadol are particularly toxic in overdose and codeine is also relatively toxic. They should be prescribed with caution, particularly to individuals at risk of self-harm.

Sections du résumé

BACKGROUND
Analgesics are used most frequently in fatal and non-fatal medicinal self-poisonings. Knowledge about their relative toxicity in overdose is important for clinicians and regulatory agencies.
METHODS
Using data for 2005-2012 we investigated case fatality (number of suicides relative to number of non-fatal self-poisonings) of paracetamol, aspirin, codeine, dihydrocodeine, tramadol, paracetamol with codeine (co-codamol), paracetamol with dihydrocodeine (co-dydramol), ibuprofen and co-proxamol (paracetamol plus dextropropoxyphene; withdrawn in the UK in 2008 due to high toxicity). Data on suicides obtained from the Office for National Statistics and on non-fatal self-poisonings from the Multicentre Study of Self-harm in England. Case fatality was estimated for each drug, using paracetamol as the reference category.
RESULTS
Compared to paracetamol and based on single drug deaths the case fatality index of dihydrocodeine was considerably elevated (odds ratio (OR) 12.81, 95% Confidence Interval (CI) 10.19-16.12). Case fatality indices for tramadol (OR 4.05, 95% CI 3.38-4.85) and codeine (OR 2.21, 95% CI 1.81-2.70) were also significantly higher than for paracetamol. The results when multiple drug deaths were included produced similar results. The relative toxicity of co-proxamol far exceeded that of the other analgesics.
LIMITATIONS
Data on fatal self-poisonings were based on national data, whereas those for non-fatal poisonings were based on local data.
CONCLUSIONS
Dihydrocodeine and tramadol are particularly toxic in overdose and codeine is also relatively toxic. They should be prescribed with caution, particularly to individuals at risk of self-harm.

Identifiants

pubmed: 30634113
pii: S0165-0327(18)32135-9
doi: 10.1016/j.jad.2019.01.002
pii:
doi:

Substances chimiques

Analgesics 0
Drug Combinations 0
acetaminophen, codeine drug combination 0
Acetaminophen 362O9ITL9D
acetaminophen, dextropropoxyphene, drug combination 39400-85-6
dihydrocodeine N9I9HDB855
Dextropropoxyphene S2F83W92TK
Codeine UX6OWY2V7J

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

814-819

Subventions

Organisme : Department of Health
ID : RP-PG-0610-10026
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019. Published by Elsevier B.V.

Auteurs

Keith Hawton (K)

Department of Psychiatry, University of Oxford, UK; Oxford Health NHS Foundation Trust, Oxford, UK. Electronic address: keith.hawton@psych.ox.ac.uk.

Anne Ferrey (A)

Department of Psychiatry, University of Oxford, UK.

Deborah Casey (D)

Department of Psychiatry, University of Oxford, UK.

Claudia Wells (C)

Office for National Statistics, UK.

Alice Fuller (A)

Nuffield Department of Primary Care Health Sciences, University of Oxford, UK.

Clare Bankhead (C)

Nuffield Department of Primary Care Health Sciences, University of Oxford, UK.

Caroline Clements (C)

Manchester Academic Health Sciences Centre, University of Manchester, UK.

Jennifer Ness (J)

Centre for Self-harm and Suicide Prevention Research, Derbyshire Healthcare NHS Foundation Trust, UK.

David Gunnell (D)

School of Social and Community Medicine, University of Bristol, UK.

Navneet Kapur (N)

Manchester Academic Health Sciences Centre, University of Manchester, UK; Greater Manchester Mental Health NHS Foundation Trust, UK.

Galit Geulayov (G)

Department of Psychiatry, University of Oxford, UK.

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Classifications MeSH