New psychoactive substances – responding to emerging public health needs.
Submitting Institution
Liverpool John Moores UniversityUnit of Assessment
Allied Health Professions, Dentistry, Nursing and PharmacySummary Impact Type
PoliticalResearch Subject Area(s)
Medical and Health Sciences: Public Health and Health Services
Summary of the impact
The emergence of new psychoactive substances (NPS) in Europe over the
last decade (including
performance and image enhancing drugs), poses challenges to policy makers.
These are
substances which are frequently not controlled under law, and governments
have struggled to
address potential societal and health harms of use. We have analysed this
drugs market,
described the potential health harms of NPS, and generated evidence on
effective intervention
responses for some of these. Our findings have provided the necessary
evidence to support the
development of robust, responsive and predictive policy making at both
national and international
levels.
Underpinning research
We have undertaken a programme of research investigating the
pharmacology, forensic chemistry
and behavioural epidemiology of NPS. Our work has led to national and
European decision makers
being better informed about the most appropriate evidence based responses
to NPS.
Coinciding with the UK legal control of mephedrone in 2010, the group
began a novel programme
of research investigating the emergence of NPS in the UK drugs market [1].
Studies conducted
indicated that drugs sold under new `brand names' after the ban were
controlled drugs. In light of
several high profile deaths, characterisation of subtle differences in the
pharmacology of such
NPS, compared with `classic' illegal drugs, suggested that NPS warrant
special consideration with
regards to harm reduction strategies, medical intervention and policy
[2-3]. Our work was one of
the first to examine the ways in which the `legal highs' retail market
responded to changes in UK
drugs legislation. This is important as it provides an understanding of
how existing drugs policy (i.e.
the Misuse of Drugs Act, 1971) is unlikely to provide sufficient control
of NPS, and illustrates the
harms that users may face (health and societal) in purchasing such
products.
We have also provided some of the first pharmacological data on the
mechanism of action of a
number of NPS [2]. This work is important because legislation and
understanding of the potential
adverse health effects of these drugs have largely been based upon their
dis/similarity to existing
illegal substances (e.g. MDMA).
Grant funded activities (iTrend project; grant reference i) have
supported the analysis of a diverse
range of NPS samples and facilitated exchange of reference standards among
international
laboratories, in addition to activities including the monitoring of online
user forums and online
shops; online surveys and triangulation with field data from existing drug
monitoring networks. This
work contributes to a European wide Early Warning System on NPS which we
coordinate in the UK
(ii). We have also developed evidence based quality standards in drug
prevention that form part of
the key recommended actions that the European Commission has proposed in
response to the
increased use of NPS in the EU (iii).
We also research the use of growth hormones and anabolic steroids to
enhance bodily aesthetics,
and were the first group to publish on the self-injected tanning agent
Melanotan [4-5]. The work
also identified the extent of the market for such drugs, clinical utility,
potential health harms, and
implications for policy. Furthermore, alongside partners including Public
Health England, Health
Protection Agency and Public Health Wales (iv), we have conducted the
largest study of blood
borne viruses amongst users of these types of drugs, and were the first to
identify HIV within the
user population [5]. Our group has also undertaken research to support the
development of NICE
guidance in 2009 to examine the evidence for how needle and syringe
programmes may be
optimally configured in order to increase service coverage for users of
performance and image
enhancing drugs [6]. This client group represent the largest proportion of
new presentations to
such services but have been historically underserved.
Research group members: Professor Harry Sumnall (Professor in Substance
Use, from 2003); Dr
Simon Brandt (Reader in Bioactive Drug Chemistry, from 2005); Jim McVeigh
(Reader in
Substance Use Epidemiology, from 1998); Michael Evans-Brown (Researcher in
Emerging Drug
Issues, 2006-2012); Lisa Jones (Reader in Public Health Evidence, from
2005); Amanda Atkinson
(Researcher in Public Health, from 2008).
References to the research
Representative peer reviewed journal articles (citation
information taken from Scopus unless
otherwise stated, 20th November 2013):
1. Brandt SD, Sumnall HR, Measham F and Cole JC (2010). Analyses of
second-generation
`legal highs' in the UK. Drug Testing and Analysis, 2,
377-382. DOI: 10.1002/dta.155. Cited
91 times.
2. Baumann MH, Partilla JS, Lehner KR, Thorndike EB, Hoffmann AF, Holy M,
Rothman RB,
Goldberg SR, Lupica CR, Sitte HH, Brandt SD, Srihari RT, Cozzi NV and
Schindler CW
(2013). Powerful cocaine-like actions of 3,4-methylenedioxypyrovalerone
(MDPV), a
principal constituent of psychoactive "bath salts" products. Neuropsychopharmacology,
38,
552-62. DOI: 10.1038/npp.2012.204. Cited 8 times.
3. Sumnall HR, McVeigh J and Evans-Brown M (2011). Social, policy, and
public health
perspectives on new psychoactive substances. Drug Testing and
Analysis, 3, 515-523.
DOI: 10.1002/dta.310. Cited 10 times.
4. Evans-Brown M, Dawson RT, Chandler M and McVeigh J (2009). Use of
Melanotan I and II
in the General Public. British Medical Journal, 338, b566.
DOI:
http://dx.doi.org
10.1136/bmj.b566.
Cited 9 times (Web of Science).
5. Hope VD, McVeigh J, Marongiu A, Evans-Brown ME, Smith J, Kimergard A,
Croxford S,
Beynon CM, Parry JV, Bellis MA and Ncube F (2013). Prevalence of, and risk
factors for,
HIV, hepatitis B and C infections among men who inject image and
performance enhancing
drugs: a cross-sectional study. BMJ Open 3:e003207.
DOI:10.1136/bmjopen-2013-003207.
6. Jones L, Pickering L, Sumnall H, McVeigh J and Bellis MA (2010).
Optimal provision of
needle and syringe programmes for injecting drug users: a systematic
review. International
Journal of Drug Policy, 21, 335-342. Cited 7 times.
Cited Grants
i. Internet Tools for Research in Europe on New Drugs (I-TREND):
interdisciplinary and integrated
approaches to substances, users and markets. €317,554. Funding body:
DG-Justice Drug
Prevention and Information Programme. 2013-2015. Awarded to McVeigh
(CO-PI).
ii. Contract for the provision of the UK component of a European wide
Early Warning System
(EWS) on new psychoactive substances on behalf of the UK Focal Point on
Drugs. £19,295 p.a.
Department of Health (UK). 2011-2014. Awarded to McVeigh after competitive
tender.
iii. European Drug Prevention Quality Standards. €284,507. Funding body:
EU Executive Agency
for Health and Consumers. 2008-2011. Awarded to Sumnall (PI).
iv. Public Health Impact of PIEDs in Wales. £75,000. Funding Body: Welsh
Assembly Government.
2012-2015. Awarded to McVeigh (PI).
Details of the impact
The work of the Centre for Public Health (CPH) places Liverpool John
Moores University (LJMU) in
a unique position whereby our researchers are influential in informing
national and international
policy and procedures with respect to NPS. Our work in this area has
demonstrable policy impact,
and this is likely to continue as the UK Government and the European
Commission (EC) have
indicated their intention to develop new legislation and recommendations
in this area.
Our work has been particularly influential with respect to EU policy
making. For example, as part of
coordinated EC actions developed in response to the emergence of NPS
planned actions referred
to implementation of "Minimum quality standards to improve drug
prevention, treatment and harm-reduction
services". The prevention component of this action comprises the EU Drug
Prevention
Quality Standards developed by Sumnall, which is also included in the
overall EU drugs strategy
(2013-2020) (corroborating reference 1).
The group also provides dynamic scientific responses to NPS. When an NPS
is first detected in
any EU Member State, detailed information on the manufacture, traffic,
use, and harms is sent to
the European Police Office (Europol) in The Hague, and the European
Monitoring Centre for Drugs
and Drug Addiction (EMCDDA) in Lisbon. The EMCDDA also runs a "European
Database on New
Drugs" which is a European information system and database on new drugs.
Our work regularly
contributes to this by making available important forensic data that are
shared across European
forensic providers who need to be able to identify new and unknown drugs.
The UK NPS Early
Warning System (EWS), based at LJMU and led by Atkinson and Brandt,
contributes the UK's
response to this network through collation and analysis of scientific
submissions from a wide
variety of UK providers including police, forensic science organisations,
drug workers, and
academics (corroborating reference 2). For example, forensic chemistry and
pharmacology work
published by Brandt, was included as a key analytical reference in a joint
EMCDDA-Europol risk
profile assessment of the synthetic hallucinogen drug 5-IT (April, 2013).
In October 2013, the EC
recommended an EU wide ban of this substance (Council Decision
2013/496/EU).
The EWS at LJMU also reports directly to UK policy makers (e.g.
Department of Health; Home
Office; Department for Business, Innovation & Skills), who are able to
use the evidence
synthesised to inform their own decision making. The Advisory Council on
the Misuse of Drugs Act
(1971) was established under the Misuse of Drugs Act 1971 and provides
independent advice to
the Home Secretary on drug classification and issues of drug harm. The
ACMD's Consideration of
the Novel Psychoactive Substances (`Legal Highs') report was
published in November 2011 and
makes recommendations to Government on options for controlling access and
availability of NPS,
and how harms from use may be reduced. Sumnall was appointed to the ACMD
in 2011 (one of six
academics in the 23 member panel) and contributed to the drafting of this
report, and CPH's
forensic work identifying the illegal content of products sold as `legal
highs', is cited throughout.
The better use of medicines regulatory and consumer protection mechanisms,
as suggested by
Evans-Brown et al (2011) is also recommended. Our research group has also
contributed to other
ACMD work. The ACMD's Consideration of the Anabolic Steroids
report included McVeigh and
Evans-Brown as working group co-optees. As well as contributing to the
drafting, the report was
informed by substantial elements of research produced by the team
(corroborating reference 3). As
a result of recommendations outlined in the report anabolic steroids were
placed in Class C under
the Misuse of Drugs Act 1971.
Due to changes in the demand on NSP, new guidance was required and the
research conducted
by our group informed this guidance. This has had a direct impact on how
services are
commissioned and practiced by staff within specialist services and
pharmacies (corroborating
reference 4).
Sources to corroborate the impact
1. Drug Prevention Quality Standards European Policy impact:
Corroboration:
EMCDDA Secondment European Commission, c/o DG Justice, Freedom and
Security
2. Impact of the UK-EWS
Corroboration:
Head of Action on NPS, c/o EMCDDA
3. UK Misuse of Drugs Act 1971 impact:
- ACMD (2011) Consideration of the Novel Psychoactive Substances (`Legal
Highs').
London, ACMD
- ACMD (2010) Consideration of the anabolic steroids
Corroboration:
Chair, Advisory Council on the Misuse of Drugs, c/o Home Office
4. NICE guidance:
- NICE (2009) Needle and Syringe Programmes. NICE Public Health Guidance
18. London,
NICE (2012) Hepatitis B and C — ways to promote and offer testing. NICE
Public Health
Guidance PH43. London, NICE http://guidance.nice.org.uk/PH18
Corroboration:
Associate Director, Public Health Excellence
National Institute for Health and Care Excellence