Deaths Related to Drug Poisoning in England and Wales: 2011

Deaths related to drug poisoning and misuse by cause of death, sex, age and substances involved in the death.

This is not the latest release. View latest release

This is an accredited National Statistic. Click for information about types of official statistics.

Contact:
Email Vanessa Fearn

Release date:
29 August 2012

Next release:
28 August 2013

1. Key findings

  • There were 1,772 male and 880 female drug poisoning deaths (involving both legal and illegal drugs) registered in 2011, a 6 per cent decrease since 2010 for males and a 3 per cent increase for females

  • In 2011 the drug poisoning mortality rate was 63.8 deaths per million population for males and 29.9 deaths per million population for females, both were unchanged compared with 2010

  • The number of male drug misuse deaths decreased by 14 per cent from 1,382 in 2010 to 1,192 in 2011; female deaths increased by 3 per cent from 402 in 2010 to 413 in 2011

  • The male mortality rate from drug misuse decreased significantly between 2010 and 2011 (from 50.8 to 43.4 deaths per million population), but remained stable for females (14.4 deaths per million population in 2011)

  • Deaths involving heroin/morphine decreased by 25 per cent compared with 2010, but they were still the substances most commonly involved in drug poisoning deaths (596 deaths in 2011)

  • The highest mortality rate from drug misuse was in 30 to 39-year-olds (110.0 and 30.2 deaths per million population for males and females respectively)

Back to table of contents

2. Summary

This bulletin presents the latest figures from the Office for National Statistics (ONS) on deaths related to drug poisoning (involving both legal and illegal drugs) and drug misuse (involving illegal drugs) in England and Wales for the last five years. Data (183.5 Kb Excel sheet) from 1993 are available to download from the website, and are discussed in the commentary to provide context to the latest (2011) data. Figures are presented by cause of death, sex, age and substance(s) involved in the death.

The 2011 mortality rates presented in Figures 1 to 5 are provisional as they are based on population projections rather than population estimates. Revised mortality rates for 2002 to 2011, calculated using census-based mid-year population estimates, will be published in next year’s bulletin (see Background note 13).

Table 1 shows that there were 2,652 drug poisoning deaths registered in 2011, and as in previous years, the majority of these deaths were in males. There were 1,772 male deaths from drug poisoning in 2011, a decrease of 6 per cent since 2010, and the lowest since 2006. The equivalent number of female deaths rose to 880, an increase of 3 per cent since 2010, and the highest since 2004. In 2011 there were 1,605 drug misuse deaths. The number of male deaths decreased by 14 per cent from 1,382 in 2010 to 1,192 in 2011. However over the same period the number of female deaths rose by 3 per cent from 402 to 413.

Back to table of contents

3. Introduction

Drug use and drug dependence are known causes of premature mortality, with drug poisoning accounting for nearly one in eight deaths among people in their 20s and 30s in 2011 (see Background note 7). Drug-related deaths occur in a variety of circumstances, each with different social and policy implications. Consequently, there is considerable political, media and public interest in these figures.

This bulletin covers accidents and suicides involving drug poisonings, as well as deaths from drug abuse and drug dependence, but not other adverse effects of drugs (for example anaphylactic shock). Drug poisoning deaths involve a broad spectrum of substances, including legal and illegal drugs, prescription drugs (either prescribed to the deceased or obtained by other means) and over-the-counter medications. Some of these deaths may also be the result of complications of drug abuse, such as deep vein thrombosis or septicaemia resulting from intravenous drug use, rather than an acute drug overdose.

Almost all drug-related deaths are certified by a coroner, and due to the length of time it takes to hold an inquest, about half of drug-related deaths registered in 2011 will have actually occurred prior to 2011 – see section ‘Impact of registration delays on drug-related deaths’ below for more information.

Policy context

In December 2010 the Coalition Government launched a new drug strategy entitled 'Reducing demand, restricting supply, building recovery: supporting people to live a drug-free life' (Home Office, 2010). This strategy highlights preventing drug-related deaths as one of the key outcomes that recovery-oriented services should be focused on.

Patterns of drug use change over time. For instance, in recent years people have been taking new psychoactive substances, including so-called legal highs. In response to this, the 2010 drug strategy outlined the Government’s plan to introduce a system of temporary 12-month bans on newly emerging substances. The Advisory Council on the Misuse of Drugs (ACMD) can then evaluate the harm caused by the substance and advise whether there should be a permanent ban.

Uses made of this data

The figures contained in this statistical bulletin are used by a range of public bodies, such as the National Treatment Agency for Substance Misuse (NTA), the Department of Health (DH) and the Welsh Government to evaluate the effectiveness of various drug strategies. For example, the NTA is linking ONS data on drug-related deaths with data from the National Drug Treatment Monitoring System (NDTMS), to investigate the timing of drug-related deaths in relation to treatment history. This research will also examine risk factors associated with these deaths and carry out area-based comparisons.

The European Monitoring Centre for Drugs and Drug Addiction (EMCDDA) combines data for England and Wales from the ONS drug poisoning database with data from Scotland and Northern Ireland to publish UK figures, allowing comparisons to be made with other European countries. The latest EMCDDA report shows that the drug-related mortality rate in the UK was the fifth highest in Europe (EMCDDA, 2012). However, caution should be applied when making international comparisons, because of differences in definitions and the quality of reporting.

ONS drug poisoning data are also used by academic researchers. For example, analysis of this data by the Centre for Suicide Research at the University of Oxford revealed that there was a major reduction in deaths involving co-proxamol following its withdrawal in 2005, with no evidence of an increase in deaths involving other analgesics, apart from oxycodone (Hawton et al, 2012). Updated data on deaths involving co-proxamol and other analgesics are shown below in Table 3.

Back to table of contents

4. ICD coding changes implemented in 2011

ONS use the International Classification of Diseases, Tenth Revision (ICD-10, WHO, 2010) to code all conditions and events mentioned on the death certificate. The ICD contains a general principle and a range of selection and modification rules that are used to ascertain a causal sequence and consistently assign an underlying cause of death from the conditions recorded on the death certificate. The underlying cause is defined by the World Health Organisation (WHO) as:

  • the disease or injury that initiated the train of events directly leading to death

  • the circumstances of the accident or violence that produced the fatal injury

In January 2011, ONS introduced a new version of ICD-10 (version 2010), which replaced the version introduced in 2001 (version 2001.2). This means that figures for 2011 will not be directly comparable with figures for 2001 to 2010.

To understand the impact of the introduction of ICD-10 v2010 on mortality statistics, ONS carried out a bridge coding study in which a sample of deaths that had previously been coded using v2001.2 were then independently recoded using the new version of ICD-10 (Office for National Statistics, 2011).

However, not all of the information provided by coroners at registration was available to use when recoding deaths, so the bridge coding study results for drug-related deaths should be treated with caution.

The impact of the new version of ICD-10 on drug-related deaths figures was not reported in the bridge coding study. However, new analysis presented below shows that the number of deaths coded as mental and behavioural disorders due to drug use (ICD-10 codes F11–F16 and F18–F19) decreased by 84 per cent in v2010, compared with v2001.2.

This decrease is due to these deaths being allocated to accidental poisonings by drugs (ICD-10 code X40–X44), which consequently increased by 44 per cent. The new version of ICD-10 caused very little change in the number of deaths being coded as intentional self-poisoning by drugs, or poisoning by drugs, undetermined intent.

The number of deaths from assault by drugs are very small and there were no deaths from this cause in the bridge coded sample, so the impact of the ICD coding change could not be examined.

The changes in the number of deaths coded to mental and behavioural disorders due to drug use and accidental poisonings by drugs are due to changes in the ICD selection rule 3, which states that:

  • if a condition selected by the general principle or by rules 1 or 2 is obviously a direct consequence of another reported condition, whether in part I or part II of the death certificate, select this as the underlying cause

In ICD-10 v2001.2, if both accidental poisoning by drugs (ICD-10 codes X40–X44) and drug dependence (ICD-10 codes F11.2, F12.2, F13.2, F14.2, F15.2, F16.2, F18.2 and F19.2) were mentioned on the death certificate, and accidental poisoning had been selected as the tentative underlying cause, then this would be considered a direct consequence of the drug dependence. Therefore selection rule 3 meant that the drug dependence would be chosen as the underlying cause.

However, in ICD-10 v2010, this causal sequence is no longer valid, so even if both accidental poisoning and drug dependence are mentioned, the underlying cause will normally be the accidental poisoning. More information about the bridge coding study can be found on the ONS website.

Back to table of contents

11. Heroin and morphine

Over half (57 per cent) of all deaths related to drug poisoning involved an opiate drug. In 2011, as in previous years, the most commonly mentioned opiates were heroin and/or morphine, which were involved in 596 deaths (see Background note 8). For males, heroin/morphine was involved in more deaths than any other substance.

However, the mortality rate for males has fallen sharply in the last two years, down from 27.9 deaths per million population in 2009 to 17.1 in 2011. This is a 39 per cent fall and is the lowest rate since 1997. The corresponding rate in females was much lower at 4.5 deaths per million population in 2011, and has not changed significantly since 1997, when the rate was 2.2 deaths per million population.

Evidence suggests that from October 2010 there has been a ‘heroin drought’ in the UK, with shortages in the availability of heroin continuing in some areas in 2011/12. This heroin drought has resulted in typical street heroin purity falling from 46 per cent in September 2009 to around 32 per cent in September 2010, and down again to 19 per cent in July to September 2011 (SOCA, 2011 and 2012 and Simonson and Daly, 2011).

Drugs workers were concerned that the heroin drought may result in more drug-related deaths, as users who had developed a reduced tolerance could overdose if they used a high quality batch of heroin (Simonson and Daly, 2011). However, ONS data show the opposite trend with deaths involving heroin falling in recent years.

Results from the British Crime Survey (Home Office, 2011) suggest there was a significant decline in the proportion of 16 to 59-year-olds reporting use of heroin in the last month between 2009/10 and 2010/11. Moreover, the NTA (2012) report that the number of adults newly entering treatment for heroin and crack use has fallen by 15 per cent in two years.

They suggest that this decline is probably due to reduced demand rather than any shortfall in services. These factors may explain the decline in deaths involving heroin/morphine that has been seen over the last couple of years.

Back to table of contents

12. Methadone

In 2011 there were 486 deaths involving methadone (an opiate substance used to treat heroin addiction, which is sometimes abused). The male mortality rate for deaths involving methadone increased significantly from 9.9 deaths per million population in 2010 to 13.5 in 2011. This is a 36 per cent increase and is the highest rate since 1997. The equivalent rate for females increased slightly in 2011 to 4.3 deaths per million population.

The increase in deaths involving methadone correlates with findings from the British Crime Survey (Home Office, 2011) showing the proportion of 16 to 59-year-olds using methadone in the last year increased significantly in 2010/11. In addition, the latest Druglink Street Drug Trends Survey (Daly and Simonson, 2011) found there had been an increase in the use of methadone (and other substances) by primary heroin users, possibly as a result of the heroin drought.

Back to table of contents

13. Cocaine

There were 112 deaths involving cocaine in 2011. The male mortality rate was 3.2 deaths per million population in 2011, which continues a significant downward trend since the peak in 2008. The equivalent rates for females were lower than for males, rising slightly from 0.7 deaths per million population in 2010 to 0.9 in 2011 (see Background note 9).

Back to table of contents

14. Other recreational drugs

Over the past few years a number of new drugs have been controlled under the Misuse of Drugs Act 1971, including synthetic cannabinoid receptor agonists (for example, ‘spice’), gamma-hydroxybutyrate (GHB) and its precursor gamma-butyrolactone (GBL), piperazines (benzylpiperazine – BZP and trifluoromethylphenylpiperazine – TFMPP), cathinones such as mephedrone, and pipradrols such as desoxypipradrol.

The number of deaths involving so-called ‘legal highs’ are low compared with the number of deaths from heroin/morphine, and have been relatively stable over the last few years (see Background notes 10 and 11). Deaths involving cannabis were also very low (seven deaths in 2011) and usually involved more than one substance.

Back to table of contents

15. Benzodiazepines

There were 293 drug poisoning deaths involving benzodiazepines in 2011. Mortality rates in males have increased significantly from an all-time low of 4.5 deaths per million population in 2006 to an all-time high of 8.0 deaths per million population in 2011.

Equivalent mortality rates in females were significantly lower than in males at 2.6 deaths per million population in 2011, and have fallen slightly since 2010. Diazepam was the most common type of benzodiazepine mentioned on deaths certificates in 2011, and was involved in 179 deaths.

This increase in male deaths is consistent with a recent survey that suggested illicit diazepam use has continued to rise, almost certainly as a result of the heroin drought (Daly and Simonson, 2011). However, the role of diazepam and other benzodiazepines in drug-related deaths is unclear, as more than 9 out of 10 deaths involving benzodiazepines also mentioned another drug.

Back to table of contents

16. Antidepressants

There were 393 deaths involving antidepressants in 2011. Mortality rates were similar in males and females in 2011 (7.1 and 6.7 deaths per million population respectively), and have not changed significantly since 2010. There were 200 deaths involving tricyclic antidepressants (TCAs) in 2011, and the majority of these deaths involved amitriptyline (133 deaths in 2011).

Although TCAs are still involved in more deaths than other types of antidepressant, the number of deaths from TCA poisoning have been relatively stable since 2006 and are much lower than their peak of 490 deaths in 1998.

Deaths involving Selective Serotonin Re-uptake Inhibitors (SSRIs) have been steadily increasing, although the number of deaths were down slightly to 127 in 2011, from a peak of 136 in 2010. The majority of these deaths involve the SSRI citalopram (84 deaths in 2011).

Studies show that SSRIs are less toxic in overdose than TCAs (Hawton et al, 2010), but SSRIs are prescribed more frequently. Moreover, in the last five years prescriptions for SSRIs have increased more rapidly than prescriptions for TCAs (NHS Information Centre, 2008 and 2012), which may explain the rise in deaths involving SSRIs.

In 2011 deaths involving ‘other antidepressants’ (British National Formulary section 4.3.4, BMA and Royal Pharmaceutical Society, 2012) such as venlafaxine and mirtazapine, reached a record high, at 84 deaths. National Institute for Health and Clinical Excellence guidelines (NICE, 2009) suggest that these drugs should not be used as a first-line treatment for depression, and should only be prescribed to people who have not responded to SSRIs.

Venlafaxine in particular is associated with a greater risk of death from overdose. Therefore prescriptions for ‘other antidepressants’ accounted for only 16 per cent of all antidepressant prescriptions in 2011. However, prescriptions for this type of antidepressant are increasing more quickly than SSRIs or TCAs (NHS Information Centre, 2008 and 2012), which may partly explain the rise in deaths.

Back to table of contents

17. Antipsychotics

The number of deaths involving antipsychotic medication reached a record high of 104 deaths in 2011, which is a 20 per cent increase since 2010. The antipsychotics most commonly involved in deaths are quetiapine and olanzapine. More detailed analysis of the data showed that about half of deaths involving antipsychotics are accidents and half are suicides.

Back to table of contents

18. Paracetamol and other analgesics

There were 207 deaths involving paracetamol and its compounds in 2011. The mortality rates for males and females were similar, and both increased slightly between 2010 and 2011. During this period the male mortality rate increased from 3.0 to 3.1 deaths per million population. In females, the equivalent rate went up from 3.4 to 3.6 deaths per million population.

Deaths involving paracetamol not from a compound dropped slightly in 2011, so the small increase in overall paracetamol deaths is the result of an increase in deaths involving paracetamol compounds such as co-codamol (paracetamol and codeine), co-dydramol (paracetamol and dihydrocodeine) and co-proxamol (paracetamol and dextropropoxyphene).

Although deaths involving paracetamol increased slightly between 2010 and 2011, overall there has been a declining trend since the peak in 1997. This decline is largely because of a fall in deaths mentioning co-proxamol, which fell dramatically from 388 deaths in 1999 to 18 deaths in 2011 (up slightly from 13 deaths in 2010). This can be explained by the withdrawal of co-proxamol in 2005 (Hawton et al, 2012).

Despite the decrease in deaths involving co-proxamol Hawton et al (2012) suggested that there was little observed change in deaths involving other analgesics. However, Hawton’s analysis was restricted to deaths mentioning only one substance (see Reference Table 6b (183.5 Kb Excel sheet) ), and when deaths mentioning more than one substance are included, deaths involving some types of analgesics have increased.

Most notably, the number of deaths mentioning tramadol (a synthetic opioid analgesic) have increased steadily from the first recorded death in 1996 to 154 deaths in 2011. This increase in deaths may be partly explained by a 42 per cent increase in prescriptions for tramadol over the last five years (NHS Information Centre, 2008 and 2012).

In addition, there is evidence that recreational use of tramadol increased over the last year (Daly and Simonson, 2011). It is interesting to note that, unlike most other opioid analgesics, tramadol is not controlled under the Misuse of Drugs Act 1971.

Back to table of contents

20. Comparisons with the rest of the UK

Figures on drug-related deaths in Scotland are available on the National Records of Scotland website.

Figures for Northern Ireland are available on the Northern Ireland Statistics and Research Agency website.

Figures for Europe are available on the European Monitoring Centre for Drugs and Drug Addiction (EMCDDA) website.

Figures for other countries may not be comparable with figures presented above for England and Wales, due to differences in data collection methods and in the death registration system.

Back to table of contents

22 .Data tables

A back series of data (183.5 Kb Excel sheet) on deaths related to drug poisoning in England and Wales between 1993 and 2011 are available to download in a Microsoft Excel workbook from the ONS website. The workbook contains the following tables:

  • Table 1 – Number of deaths from drug-related poisoning and drug misuse, by sex and country, England and Wales, 1993–2011

  • Table 2 – Number of deaths from drug-related poisoning by sex and underlying cause, England and Wales, 1993–2011

  • Table 3 – Number of deaths related to. drug misuse by sex and underlying cause, England and Wales, 1993–2011

  • Table 4 – Number of deaths from drug-related poisoning by sex and age, England and Wales, 1993–2011

  • Table 5 – Number of deaths related to drug misuse by sex and age, England and Wales, 1993–2011

  • Table 6a – Number of drug-related deaths where selected substances were mentioned on the death certificate, England and Wales, 1993–2011

  • Table 6b – Number of drug-related deaths where selected substances were mentioned without other drugs, England and Wales, 1993–2011

  • Table 6c – Number of drug-related deaths where selected substances were mentioned with alcohol, England and Wales, 1993–2011

  • Table 7 – Number of deaths from drug-related poisoning and drug misuse, by year of occurrence, England and Wales, 1993–2011

  • Figure 1 – Age-standardised mortality rates for deaths related to drug poisoning and drug misuse, by sex, England and Wales, 1993–2011

  • Figure 2 – Age-specific mortality rates for deaths related to drug misuse, males, England and Wales, 1993–2011

  • Figure 3 – Age-specific mortality rates for deaths related to drug misuse, females, England and Wales, 1993–2011

  • Figure 4 – Age-standardised mortality rates for selected substances, males, England and Wales 1993–2011

  • Figure 5 – Age-standardised mortality rates for selected substances, females, England and Wales 1993–2011

  • Figure 6 – Average registration delay for all drug poisoning deaths and deaths related to drug misuse, by sex, England and Wales, deaths registered in 1993–2011

  • Annotated example showing how estimated death occurrences in Table 7 are calculated

Back to table of contents

23 .References

  1. The Advisory Council on the Misuse of Drugs (2000) Reducing drug related deaths, Home Office: London

  2. BMA and Royal Pharmaceutical Society (2012) ‘British National Formulary 63’, BMJ Group and Pharmaceutical Press. Accessed on 03 August 2012

  3. Christophersen O, Rooney C and Kelly S (1998) ‘Drug related deaths: methods and trends’, Population Trends 93, 29–37. Accessed on 17 August 2012

  4. Daly M and Simonson P (2011) ‘Street drug trends survey 2011: The ketamine zone’, Druglink November/December 2011, 26(6), 6-9. Accessed on 27 July 2012

  5. Department of Health (2001) ‘The Government Response to the Advisory Council on the Misuse of Drugs Report into Drug Related Deaths’. Accessed on 31 July 2012

  6. The European Monitoring Centre for Drugs and Drug Addiction (2012) ‘Statistical Bulletin 2012: Drug-related deaths and mortality’. Accessed on 27 July 2012

  7. Hawton K, Bergen H, Simkin S, Cooper J, Waters K, Gunnell D and N Kapur (2010) ‘Toxicity of antidepressants: rates of suicide relative to prescribing and non-fatal overdose’, The British Journal of Psychiatry 196, 354-358. Accessed on 17 August 2012

  8. Hawton K, Bergen H, Simkin S, Wells C, Kapur N and Gunnell D (2012) ‘Six-Year Follow-Up of Impact of Co-proxamol Withdrawal in England and Wales on Prescribing and Deaths: Time-Series Study’, PLOS Medicine. Accessed on 31 July 2012

  9. Home Office (2010) ‘Drug Strategy 2010 – Reducing demand, restricting supply, building recovery: supporting people to live a drug-free life’. Accessed on 31 July 2012.

  10. Home Office (2011) ‘Drug Misuse Declared: Findings from the 2010/11 British Crime Survey, England and Wales’. Accessed on 27 July 2012

  11. The Misuse of Drugs Act (1971) The Stationary Office Ltd. Accessed on 31 July 2012

  12. NHS Information Centre for Health and Social Care (2008) ‘Prescription Cost Analysis: England 2007’. Accessed on 16 August 2012

  13. NHS Information Centre for Health and Social Care (2012) ‘Prescription Cost Analysis: England 2011’. Accessed on 16 August 2012.

  14. National Institute for Health and Clinical Excellence – NICE (2009) ‘Quick reference guide: Depression’. Accessed on 31 July 2012

  15. NTA (2012) ‘Drug treatment in England: the road to recovery’. Accessed on 31 July 2012

  16. Office for National Statistics (2002) ‘Report: Deaths related to drug poisoning: results for England and Wales, 1993 to 2000’, Health Statistics Quarterly 13, 76–82. Accessed on 16 August 2012.

  17. Office for National Statistics (2011) ‘Results of the ICD-10 v2010 bridge coding study, England and Wales, 2009’. Accessed on 21 August 2012

  18. Simonson P and Daly M (2011) ‘The Great Heroin Crash’, Druglink, March/April 2011, 6-7. Accessed on 31 July 2012

  19. SOCA (2011) ‘Serious Organised Crime Agency Annual Report and Accounts 2010/11’. Accessed on 31 July 2012

  20. SOCA (2012) ‘Serious Organised Crime Agency Annual Report and Accounts 2011/12’. Accessed on 31 July 2012

  21. World Health Organisation – WHO (2010) International Statistical Classification of Diseases and Related Health Problems, volumes 1, 2 and 3 (Tenth Revision). WHO: Geneva. Accessed on 16 August 2012

Back to table of contents

24 .Background notes

  1. Quality information

    Further information about the quality of drug-related deaths data can be found in the Quality and Methodology Information (QMI) paper.

  2. Mortality metadata

    Information about the underlying mortality data, including details on how the data is collected and coded are available in the mortality metadata.

  3. Drug poisoning database

    The figures presented in this bulletin have been produced using a special database of deaths related to drug poisoning, which has been developed to facilitate research into these deaths and to aid the identification of specific substances involved. The database is extracted from the national mortality database for England and Wales. Deaths are included if the underlying cause of death is regarded as drug-related, according to the National Statistics definition. More information on this definition and issues relating to the interpretation of drug-related deaths data can be found in Christophersen et al (1998).

  4. Almost all deaths on the drug poisoning database had a coroner’s inquest. For each death the database includes information about the causes of death and substances involved in addition to other information about the deceased. For each death the database of drug related poisonings includes:

    • the ICD codes for underlying cause of death and other causes mentioned on the death certificate
    • every mention of a substance recorded by the coroner in the cause of death section or elsewhere on the coroner's certificate after inquest (Form 99(REV))
    • an indicator to show if alcohol is mentioned. This includes a wide variety of scenarios ranging from evidence of alcohol consumption around the time of death (for example an empty vodka bottle found at the scene or alcohol found after toxicology tests) to long-term alcohol abuse and cirrhosis of the liver.
    • other information recorded at death registration such as age, sex, marital status, occupation and place of usual residence.
  5. Definition of a drug-related death

  6. Definition of a death related to drug misuse

    In 2000 the Advisory Council on the Misuse of Drugs published a report called ‘Reducing Drug Related Deaths’ (The Advisory Council on the Misuse of Drugs, 2000). In response to this report’s recommendations on improving the present system for collecting data on drug-related deaths, a technical working group was set up. This group, consisting of experts across government, the devolved administrations, coroners, toxicologists and drugs agencies, proposed a headline indicator for drug misuse deaths as part of the government’s action plan (Department of Health, 2001) to reduce the number of these deaths. This indicator also takes into account the information needs of the European Monitoring Centre for Drugs and Drug Addiction. The baseline year for monitoring deaths related to drug misuse was set as 1999. The definition of the headline indicator using ICD-10 is shown below. The definition using ICD-9 was published in a previous annual report (Office for National Statistics, 2002).

    Cause of death categories included in the headline indicator of drug misuse deaths (the relevant ICD-10 codes are given in brackets):

    a) Deaths where the underlying cause of death has been coded to the following categories of mental and behavioural disorders due to psychoactive substance use (excluding alcohol, tobacco and volatile solvents):

    • Opioids (F11)
    • Cannabinoids (F12)
    • Sedatives or hypnotics (F13)
    • Cocaine (F14)
    • Other stimulants, including caffeine (F15)
    • Hallucinogens (F16)
    • Multiple drug use and use of other psychoactive substances (F19)

    b) Deaths coded to the following categories and where a drug controlled under the Misuse of Drugs Act 1971 was mentioned on the death record:

    • Accidental poisoning by drugs, medicaments and biological substances (X40–X44)
    • Intentional self-poisoning by drugs, medicaments and biological substances (X60–X64)
    • Poisoning by drugs, medicaments and biological substances, undetermined intent (Y10–Y14)
    • Assault by drugs, medicaments and biological substances (X85)
    • Mental and behavioural disorders due to use of volatile solvents (F18)

    Notes

    1 Specific rules were adopted for dealing with compound analgesics which contain relatively small quantities of drugs listed under the Misuse of Drugs Act, the major ones being dextropropoxyphene, dihydrocodeine and codeine. Where these drugs are mentioned on a death record, they have been excluded from the drug misuse indicator if they are part of a compound analgesic (such as co-proxamol, co-dydramol or co-codamol) or cold remedy. Dextropropoxyphene has been excluded on all occasions, whether or not paracetamol or a compound analgesic was mentioned. This is because dextropropoxyphene is rarely, if ever, available other than as part of a paracetamol compound. However, codeine or dihydrocodeine mentioned without paracetamol or ibuprofen were included in the indicator. This is because they are routinely available and known to be abused in this form. This approach is the same as that taken by National Records of Scotland (NRS).

    2 Drugs controlled under the Misuse of Drugs Act 1971 include class A, B and C drugs.

  7. Deaths among people in their 20s and 30s

    Nearly one in eight deaths among people in their 20s and 30s were drug-related. This figure has been calculated from the number of deaths from all drug poisonings of people aged 20 to 39, (1,069 deaths) and the number of deaths from all causes in this age group (7,739 deaths) for England and Wales in 2011. The number of deaths from all causes, by sex and age is available on the ONS website.

  8. Heroin and morphine

    As heroin (diamorphine) breaks down in the body into morphine, either heroin and/or morphine may be detected at post mortem and recorded on the death certificate. Therefore a combined figure for deaths where heroin or morphine was mentioned on the death certificate is included in Table 3.

  9. Cocaine

    The figure for cocaine in Table 3 includes deaths where cocaine was taken in the form of crack cocaine. It is not possible to separately identify crack cocaine from other forms of cocaine at post mortem. Other evidence to distinguish the form of cocaine taken is rarely provided on death certificates.

  10. GHB and GBL

    The figure for GHB (gamma-hydroxybutyrate) in Table 3 includes deaths where GBL (gamma-butyrolactone) was taken. It is not possible to separately identify GBL and GHB at post mortem as GBL is rapidly converted to GHB when ingested into the human body.

  11. BZP

    Before 2009 benzylpiperazine (BZP) was being recorded simply as ‘piperazine’ and was not included in figures for BZP. This error has now been corrected and updated figures for 2008 are shown in Table 3 above.

  12. Helium

    The number of deaths mentioning helium reported in this statistical bulletin is likely to be an underestimate, as some deaths involving helium have an underlying cause of death of hanging, strangulation and suffocation (ICD-10 codes X70 and Y20), and are not included in the drug poisoning database.

  13. Calculation of mortality rates

    Mortality rates are presented as deaths per million population, directly age-standardised to the European standard population. Rates based on population estimates are available for 1993 to 2010 and provisional rates based on population projections are available for 2011. Revised mortality rates for 2002 to 2011, calculated using census-based mid-year population estimates, will be published in next year’s bulletin.

  14. Confidence intervals

    Excel workbooks containing the data used to produce Figures 1 to 6 (183.5 Kb Excel sheet) are available to download from the ONS website. These tables contain both the mortality rate and the upper and lower confidence limits. These limits form a confidence interval, which is a measure of the statistical precision of an estimate and shows the range of uncertainty around the estimated figure. Calculations based on small numbers of events are often subject to random fluctuations. As a general rule, if the confidence interval around one figure overlaps with the interval around another, we cannot say with certainty that there is more than a chance difference between the two figures. Within this statistical bulletin, a difference which is described as ‘significant’, means ‘statistically significant’, assessed by examining the confidence intervals.

  15. Calculation of registration delays

    Figure 6 presents data on the length of time taken to register a death (also known as the registration delay) for drug-related deaths. This is calculated as the difference between the date each death occurred and the date it was registered, measured in days. Data where the exact date of death was unknown or the date of death was more than 25 years before date of registration or where either the date of death or date of registration was clearly recorded incorrectly (that is, the death appeared to have been registered before it occurred) were excluded from this analysis. Approximately 0.2 per cent of the data were excluded for these reasons. Analysis showed that the data was positively skewed, and contains some deaths with very long registration delays (for example, more than eight years). Therefore the average registration delay has been presented using the median value, as this is not influenced by extreme values. The median is defined as the value that is halfway through the ordered data set, below and above which there lies an equal number of data values.

  16. Revisions

    The ONS revisions policy is available on our website.

  17. Special extracts of data

    Special extracts and tabulations of drug poisoning deaths data are available to order for a charge (subject to legal frameworks, disclosure control and agreement of costs, where appropriate). Such requests or enquiries should be made to:

    Mortality Analysis Team, Health and Life Events Division
    Office for National Statistics
    Government Buildings
    Cardiff Road
    Newport
    Gwent NP10 8XG
    Tel: 01633 455341
    E-mail: mortality@ons.gov.uk

    The ONS charging policy is available on the ONS website.

  18. Health and Life Events user engagement strategy

    As a valued user of our statistics, we would welcome feedback on this release. In particular, the content, format and structure. This is in line with the Health and Life Events user engagement strategy, available to download from the ONS website. Please send feedback to the postal or e-mail address above.

  19. Pre-release access

    A list of the names of those given pre-publication access to the statistics and written commentary is available in this pre-release access list (32.3 Kb Pdf) for deaths related to drug poisoning in England and Wales in 2011. The rules and principles which govern pre-release access are featured within the Pre-release Access to Official Statistics Order 2008.

  20. National Statistics

    National Statistics are produced to high professional standards set out in the Code of Practice for Official Statistics. They undergo regular quality assurance reviews to ensure that they meet customer needs. They are produced free from any political interference.

    © Crown copyright 2012.

  21. Terms and conditions

    You may use or re-use this information (not including logos) free of charge in any format or medium, under the terms of the Open Government Licence. To view this licence, visit the National Archives website, write to: The Information Policy Team, The National Archives, Kew, London TW9 4DU, or email: psi@nationalarchives.gsi.gov.uk.

  22. Details of the policy governing the release of new data are available by visiting www.statisticsauthority.gov.uk/assessment/code-of-practice/index.html or from the Media Relations Office email: media.relations@ons.gov.uk

    These National Statistics are produced to high professional standards and released according to the arrangements approved by the UK Statistics Authority.

Back to table of contents

25 . Methodology

Contact details for this Statistical bulletin

Vanessa Fearn
vanessa.fearn@ons.gov.uk
Telephone: +44 (0)1633 455341