A comparison of different methods for estimating the prevalence of problematic drug misuse in Great Britain

Citation
M. Frischer et al., A comparison of different methods for estimating the prevalence of problematic drug misuse in Great Britain, ADDICTION, 96(10), 2001, pp. 1465-1476
Citations number
38
Categorie Soggetti
Public Health & Health Care Science","Clinical Psycology & Psychiatry
Journal title
ADDICTION
ISSN journal
09652140 → ACNP
Volume
96
Issue
10
Year of publication
2001
Pages
1465 - 1476
Database
ISI
SICI code
0965-2140(200110)96:10<1465:ACODMF>2.0.ZU;2-9
Abstract
Aims. The European Monitoring Centre for Drugs and Drug Addiction (EMCDDA) has produced methodological guidelines for national drug prevalence estimat ion. This paper pilots the methods to estimate prevalence for Great Britain and provides a commentary on the methods and resulting estimates. Design. Three types of methodology were used to estimate prevalence: (a) the multip le indicator (MI) method, (b) multipliers applied to (i) drug-treatment rec ords (ii) HIV estimates and (iii) mortality statistics and (c) the British/ Scottish Crime Surveys. Setting. England, Scotland and Wales. Participants. Aggregated data on people recorded on databases and respondents in househo ld surveys. Measurements. Prevalence estimates of different forms of proble matic drug use. Findings. The estimates are 161 133 (range: 120 850-241 700 ) for people at risk of mortality due to drug overdose; 161 000-169 000 for people who have ever injected drugs; 202 000 (range: 162 000-244 000) prob lem opiate users and 268 000 problem drug users (all types). Conclusions. T he multiple indicator method offers a comprehensive approach to estimating the prevalence of problematic drug use in the United Kingdom. Simple multip lier methods and household surveys also provide a range of estimates corres ponding to different types of drug use in the United Kingdom. The current s tudy suggests that previous national estimates of 100 000-200 000 were cons ervative. The new estimate of 161 000-266 000 should enable a more focused response. For further development of this method, reliable and timely estim ates of anchor points are required for specific geographical areas such as cities or Drug Action Teams (DAT), as well as routine aggregation of drug i ndicators for these areas.