take-home naloxone programs: history & perspectives
TRANSCRIPT
Take-Home Naloxone programs:History & perspectives
Sibella Hare Breidahl and Professor Sir John Strang
National Addiction Centre, King’s College London, UK
Declarations (personal & institutional)
John Strang:
• NHS provider (community & in-patient); also Phoenix House, Lifeline, KCA.
• Dept of Health, NTA, Home Office, NACD, EMCDDA, WHO, UNODC, NIDA.
• Dialogue and work with pharmaceutical companies re actual or potential development of new medicines for use in the addiction treatment field (incl re naloxone products), including (past 3 years) Martindale, Indivior, MundiPharma, Braeburn/Camurus; trial product supply from iGen and Camurus.
• Lecture includes preliminary findings from work with Pharma (Mundipharma).
• SSA (Society for the Study of Addiction); UKDPC (UK Drug Policy Commission), and two Masters degrees (taught MSc and IPAS) and an Addictions MOOC.
• Work also with several charities (and received support) including Action on Addiction, and also with J Paul Getty Charitable Trust (JPGT) and Pilgrim Trust.
• The university (King’s College London) has registered intellectual property on a buccal naloxone formulation, and JS has been named in a patent registration by a Pharma company as inventor of a novel concentrated naloxone nasal spray.
Sib Hare Breidahl:• Medical student at the University of Adelaide• Previous research assistant at KCL; working on project with JS, co-sponsored by MundiPharma• Current WHO intern; Department of Mental Health and Substance Use
Naloxone over the years
First serious consideration:
Strang J, Darke S, Hall W, Farrell M & Ali R (1996) Heroin overdose: the case for take-home naloxone. British Medical Journal, 312: 1435.
*** important achievements, but so slow, so very slow ***
(1996)
0
5
10
15
20
25
30
35
40
45
Up to 1
1 up to 2
2 up to 4
4 up to 8
8 up to 13
13 up to 26
26 up to 52 >=52
Total
Exc
ess
mor
talit
y ra
tio
Time since release (weeks)
Not drug-related Drug-related deaths
Singleton et al, 2002
When? Clustering in time and space
(2009-11)
(2013)
10
(2014)
http://www.emcdda.europa.eu/news/2016/1/pr
eventing-opioid-overdose-naloxone
Naloxone Monograph from EMCDDA (European Monitoring Centre on Drugs and Drug Addiction) (2016)
(2016)
Challenges
• Routes of administration
• Having it confiscated/scared of disciplinary action from law enforcement etc
• Size, portability=> carriage rate
• Losing naloxone
• Dose titration
• Best training technique
Service usersN=327
Staff N=158
FamilyN=39
Total respondents
N=524
Have been provided naloxone
65.0% (208/320)
26.0% (39/150)
52.9% (19/36)
50.8% (266/506)
Carrying naloxone at time of survey
17.2% (36/209)
23.8% (5/21)
17.8% (41/230)
Table 3. Naloxone device preference in NXP2U study (unpublished). “Amp” = Ampoule (figure 2), “PFS” = pre-filled syringe, “NS” = Nasal spray. Percentages shown with frequencies in brackets. This study received funding from MundiPharma.
Training
Figure 2: Still from the
training video - introduction
Figure 1: Still from the training
video - intranasal naloxone
demonstration
Service usersN=327
Staff N=158
FamilyN=39No missing values
Total respondentsN=524
Which device would you be willing to use in an overdose emergency?
AMP: 38.4% (118/307)
PFS: 70.4% (216/307)
NS: 68.7% (211/307)
None: 4.9%(15/307)
AMP: 28.3% (43/152)
PFS: 70.4% (107/152)
NS: 84.9%(129/152)
None: 0.7% (1/152)
AMP: 23.0% (9/39)
PFS: 61.5% (24/39)
NS: 76.9% (30/39)
None: 0.0% (0/39)
AMP: 34.1% (170/498)
PFS: 69.7% (347/498)
NS: 74.3% (370/498)
None: 3.2% (16/498)
Which device would you be most confident using?
Amp: 12.1% (35/307)
PFS: 41.2% (128/307)
NS: 66.4% (204/307)
None: 4.6% (14/307)
Amp: 5.9% (9/152)
PFS: 32.2% (49/152)
NS: 84.9% (129/152)
None: 1.3% (2/152)
Amp: 16.2% (6/37)
PFS: 37.8%(14/37)
NS: 83.8% (31/37)
None: 0.0% (0/37)
Amp: 10.0% (50/501)
PFS: 38.1% (191/501)
NS: 55.3% (277/501)
None: 3.2% (16/501)
Table 3. Naloxone device preference (unpublished). “Amp” = Ampoule (figure 2), “PFS” = pre-filled syringe, “NS” = Nasal spray. Percentages shown with frequencies in brackets. Respondents could elect more than one answer, explaining why totals are >100%. This study received funding from MundiPharma.