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Keith Hawton a Centre
for Suicide Research, University of Oxford Department of Psychiatry,
Warneford Hospital, Headington, Oxford OX3 7JX, b Centre for
Statistics in Medicine, Institute of Health Sciences, Headington,
Oxford OX3 7LF Correspondence to: K Hawton keith.hawton{at}psych.ox.ac.uk
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Abstract |
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Objectives:
To examine the incidence of suicides due
to co-proxamol compared with tricyclic antidepressants and paracetamol, and to compare fatality rates for self poisonings with these drugs.
Design:
Analysis of routinely collected national and local data on suicides and self poisonings.
Setting:
Records of suicides in England and Wales
1997-9; non-fatal self poisonings in Oxford District 1997-9.
Data sources:
Office for National Statistics and
Oxford monitoring system for attempted suicide.
Main outcome measures:
Incidence of suicides with
co-proxamol or tricyclic antidepressants or paracetamol. Ratios of
fatal to non-fatal self poisonings.
Results:
Co-proxamol alone accounted for 5% of all suicides. Of 4162 drug related suicides, 18% (766) involved
co-proxamol alone, 22% (927) tricyclic antidepressants alone, and 9%
(368) paracetamol alone. A higher proportion of suicides in the 10-24 year age group were due to co-proxamol than in the other age groups. The odds of dying after overdose with co-proxamol was 2.3 times (95%
confidence interval 2.1 to 2.5) that for tricyclic antidepressants and
28.1 times (24.9 to 32.9) that for paracetamol.
Conclusions:
Self poisoning with co-proxamol is
particularly dangerous and contributes substantially to drug related
suicides. Restricting availability of co-proxamol could have an
important role in suicide prevention.
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What is already known on this topic
Restricting availability of specific means of suicide can reduce deaths What this study adds
The risk of death associated with co-proxamol overdose seems to be higher than for either tricyclic antidepressants or paracetamol |
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Introduction |
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Restriction of availability of means for suicide is a key strategy for prevention of suicide. 1 2 This approach has been shown to be effective by the reduction in deaths after recent UK legislation that reduced pack sizes of analgesics3 and previous restriction of prescribing toxic sedatives.4
Co-proxamol is a prescription only analgesic that combines paracetamol and dextropropoxyphene. Respiratory depression and consequent death may occur with overdose due to ingestion of excessive dextropropoxyphene. 5 6 Concern about the number of such deaths was expressed in the BMJ as long ago as 1980.7
We compared the numbers of suicides from poisoning with co-proxamol,
paracetamol, and tricyclic antidepressants (these being relatively
common methods in poisoning suicides) in England and Wales. We also
compared fatal and non-fatal self poisonings to estimate the relative
fatality of overdoses with these three drugs.
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Methods |
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Mortality data
We obtained data from the Office for
National Statistics on deaths in people aged 10 years and over in
England and Wales for 1997-9. We considered those deaths that involved drugs and medicines in which a verdict of suicide (international classification of diseases, ninth revision, codes E950.0-E959.5) or
undetermined cause (codes E980.0-E989.5) was recorded. Deaths involving
co-proxamol, paracetamol, or tricyclic antidepressants were identified
by searching for all variants of description of these drugs in the
textual fields for cause of death.
Non-fatal self poisonings
Non-fatal self poisonings with
co-proxamol, paracetamol or tricyclic antidepressants alone for 1997-9 were identified through the Oxford monitoring system for attempted suicide.8 This records all presentations to the general
hospital in Oxford of deliberate self harm. The comprehensiveness and
reliability of the data has previously been shown.9 The
pattern of drugs used for self poisoning in the Oxford area is similar
to that seen elsewhere.10
Statistical analyses
We used Poisson regression to compute
estimates, confidence intervals, and comparison of death rates and
presentation rates according to drug, age, and sex. Odds ratios for the
relative lethality of different drugs were calculated by computing
ratios of relative death rates to relative non-fatal presentation
rates. Confidence intervals for relative lethality were calculated with
Monte Carlo methods. We used Stata release 7.0 (StataCorp, College
Station, TX, USA) for the analyses.
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Results |
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In England and Wales in 1997-9, 15 299 deaths were recorded as suicides or open verdicts. Of these, 4162 (27%) were drug related (such as self poisoning). There were more drug related deaths in men than in women, although a higher proportion of women who killed themselves did so by self poisoning (1835/3762 (49%) v 2327/11 537 (20%) in men).
Deaths due to self poisoning with co-proxamol
There were 766 deaths due to poisoning with co-proxamol alone
during the three year period (255 per year, 95% confidence interval
238 to 274). These comprised 18% of all drug related deaths (table 1)
and 5% of all suicides. After tricyclic antidepressants co-proxamol
was the second most common prescribed drug used for suicide. More
co-proxamol poisoning deaths occurred in men than in women (P=0.01).
Although the total numbers of deaths increased with age, the proportion
due to co-proxamol poisoning was significantly higher (24%) in 10-24 year-olds (P=0.01). In addition, there were 171 deaths in which
co-proxamol was used with another drug.
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Comparison with deaths due to tricyclic antidepressants and
paracetamol
There were an average 309 (289 to 330) deaths per year due to
tricyclic antidepressants alone. These deaths comprised 22% of all
drug related suicides, significantly more than for co-proxamol alone
(P<0.001). Compared with men, women were more likely to use tricyclics
than co-proxamol (P=0.02). Use of tricyclics was similar across age
groups (P=0.07). In 270 deaths tricyclics were taken with other drugs.
An average 123 (110 to 136) deaths per year were due to paracetamol alone, and this comprised 9% of all drug related deaths (table 1). Compared with men, women were more likely to use paracetamol that co-proxamol (P=0.02), and its use increased more clearly with age (P<0.001). In 128 deaths paracetamol was taken with other drugs.
Fatal and non-fatal self poisonings
Table 2 gives details of annual numbers of non-fatal self
poisonings. Non-fatal tricyclic antidepressant and paracetamol
overdoses presented 2.7 (2.1 to 3.6) times and 13.5 (10.7 to 17.0)
times more frequently than non-fatal co-proxamol overdoses,
respectively.
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Comparison of ratios of death and non-fatal presentations suggests that the odds that an overdose will be fatal with co-proxamol is 2.3 (2.1 to 2.5) times higher than for tricyclic overdoses and 28.1 (24.9 to 32.9) times higher than for paracetamol overdoses.
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Discussion |
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In England and Wales co-proxamol is the second most common prescribed drug that people use to commit suicide and is used as the sole method in 18% of all drug related suicides for 1997-9 and 5% of all total suicides. Comparison with non-fatal poisonings indicates that overdoses of co-proxamol are more likely to result in death than overdoses with tricyclic antidepressant or paracetamol. Death can result from an overdose with relatively few tablets, especially when alcohol is also taken. 5 6 Given earlier concerns about deaths from poisoning with to co-proxamol 5 7 the absence of specific initiatives to try to reduce them is surprising and should now be addressed.1
Factors to be considered in tackling this problem are that co-proxamol is a prescription only drug, patients with pain already have an increased risk of suicide, 11 12 the risk of self poisoning is not restricted to the person for whom the drug is prescribed,13 and, as with paracetamol,14 availability within a household may be an influential factor, especially in impulsive overdoses. Also, while co-proxamol is regarded as an important analgesic, 15 16 a systematic review has shown that it is no more effective than paracetamol for short term relief of pain.17
Reducing the availability of drugs used for suicide can result in a
reductions in deaths,
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and availability of co-proxamol should be restricted. Clinicians must be informed about the risks of
overdose of co-proxamol, both for their patients and others in the
household, and large quantities should not be prescribed without good
reason. Patients should be instructed to dispose of unwanted supplies.
Finally, clinicians should consider whether there are other equally
effective but less dangerous methods of pain relief, such as combining
a safer analgesic with an opiate while maximal relief is required.
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Acknowledgments |
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We thank Alan Baker of the Office for National Statistics, and Liz Bale, Alison Bond, and the staff of the Department of Psychological Medicine, John Radcliffe Hospital.
Contributors: KH initiated the study, SS coordinated the data collection, and JD conducted the statistical analyses. All authors contributed to the study design, interpretation of the results, and preparation of the report. KH is guarantor for the study.
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Footnotes |
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Funding: South East Region NHSE Research and Development Committee. KH is also supported by Oxfordshire Mental Healthcare NHS Trust. The guarantor accepts full responsibility for the conduct of the study, had access to the data, and controlled the decision to publish.
Competing interests: None declared.
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References |
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(Accepted 5 March 2003)
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