SROM (oral morphine) an add on medication for the treatment of opioid dependence: risks & benefits. Gabriele Fischer. Medical University Vienna



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Transcription:

ATHS Biarritz oct 1 th, 2015 SROM (oral morphine) an add on medication for the treatment of opioid dependence: risks & benefits Gabriele Fischer gabriele.fischer@meduniwien.ac.at Medical University Vienna

Conflict of Interest Reckitt Benckiser/Shering Plough/ Indivior Nepp/Mundipharma Lannacher/GL Pharma Travel support, payment for presentations, clinical research studies

Main considerations Pharmacological medication Efficacy of medication Retention Reduced consumption of drug of dependence Safety Spectrum of side effects Low diversion risk Quality of life

Diversification possibilities for therapist and patient preferences ABSTINENCE Naltrexone ER implant Naltrexone ER i.m. Life without opioids Naltrexone p.o. Methadone HD Buprenophine HD s.l. Life without illicit opioids Buprenorphine/Naloxon (Suboxone) s.l./film Methadone LD L-Methadone = Polamidon Slow release oral morphine p.o. (SROM) SROM with naloxone p.o. Burenorphine i.m. Heroin p.o. Morphine i.v. Search for a safe high Heroin inhalable and i.v. HARM

Percentage of patients Opioid Medication Distribution across Europe 100% 90% 80% 70% 60% 50% 40% 30% 20% 10% 0% 90 80 70 60 50 40 30 20 10 0 France Finland Greece Sweden Norway Italy Portugal Austria Denmark UK 1. Qrtl. 2. Qrtl. 3. Qrtl. 4. Qrtl. SROM Methadone Subutex/Generic Bupe Suboxone Ost West Nord Germany Belgium Switz. Luxembourg Spain

Morphinuse in kg /Mio. Inhabitant (1994 2004) Austria, Denmark, Great Britain 120 100 80 60 40 20 1994 1995 1996 1997 1998 1999 2000 2001 2002 2003 2004 0 Österreich Dänemark GB

Morphinsulphate- capsules SROM slow release oral morphine Morphinhydrochloride- tablets

Slow-release oral morphine Formulated for a longer half-life than standard morphine, enabling use for once-daily maintenance Suitable for patients responding poorly to methadone Mitchell et al, DAD, 2003;... Oral slow-release for maintenance...

Mitchell T, White J, Somodyi A, Bochner F; Addiction 99: 940-946; 2004 18 methadone maintained patients Transfer & at least over 4 weeks stable dosing on SROM Dose Ratio: METHADONE: SROM 1:4.6 with mean SROM dosis: 350 mg. Results: SROM was associated with improved social functioning, weight loss, fewer and less troublesome side-effects. Greater drug liking, reduced heroin craving, an enhanced sense of feeling normal - the majority (78 %) preferred SROM (78%) over methadone (22%)

SR-morphine vs methadone in pregnancy Fischer et al., 1999; Addiction 94 (2), 231-239 Both are safe and well tolerated Prevention of preterm delivery - healthy neonates Both induce a NAS - no difference in intensity and duration of NAS But: Significant lower concomitant consumption of heroin and benzodiazepines in SR-morphine-group Limitations: SR-morphine was given twice a day in contrast to methadone once a day Use of phenobarbiturates in the treatment of NAS - mean duration of NAS treatment 16 days

2005 Ratio: Methadone - SROM: 1: 7.75

Comparative Study of the Effectiveness of Slow-Release Morphine Capsules and Methadone Oral Solution for Opioid Maintenance Therapy Eder H., Jagsch R., Kraigher D., Primorac A., Fischer G.: Addiction 100:1101-1109 (2005) 1 7 15 weeks SR-morphine SR-morphine screening -3 0 days methadone cross- over methadone Double-blind, doubledummy 5* 12* * driving simulating performance

Demographical data Sample: 64 patients with opioid dependence (DSM IV 304.0) double-blind, double-dummy A (SR Morphine/ Methadone) B (Methadone/ SR Morphine) n=32 n=32 Sex age (years) Age of first injecting heroin Duration of opioid dependence (months) Heroin use in the last 30 days 5f (15.6%) 29.5 ( 7.5) [19; 57] 21.8 ( 5.0) [15; 35] 64.2 (52.7) [6; 180] 25.7 ( 8.4) [15; 30] 3f (9.4%) 27.9 ( 5.6) [19; 38] 21.4 ( 4.7) [15; 30] 60.2 (49.2) [6; 192] 22.5 (12.2) [11; 30] n.sign. n.sign. n.sign. n.sign. n.sign.

week00 week01 week02 week03 week04 week05 week06 week07 crossover week09 week10 week11 week12 week13 week14 Retention percentage Retention rate 100 90 80 70 60 50 40 30 20 10 0 A (Mo/Me) 81.3% B (Me/Mo) 90.6%

Test1 Test3 Test5 Test7 Test9 Test11 Test13 Test15 Test17 Test19 Test21 Test23 Test25 Test27 Test29 Test31 Number Injection sites 5 4 3 )A (Mo/Me 2 )B (Me/Mo 1 0

Score List of complaints 35 30 25 20 15 A (Mo/Me) B (Me/Mo) 10 5 0 pre week 5 week 12 Time p=.001, group n.sign., interaction time*group p<.001

Score Beck Depression Inventory 20 18 16 14 12 10 8 A (Mo/Me) B (Me/Mo) 6 4 2 0 pre week 5 week 12 Time p=.001, group n.sign., interaction time*group p<.001

Score Stait/Trait Anxiety Inventory 48 46 44 42 A (Mo/Me) B (Me/Mo) 40 38 36 pre week 5 week 12 Time p=.008, group n.sign., interaction time*group p<.003

Results Methadone - SROM: 1: 7.75 methadone (mean): 85 mg SR- morphine (mean): 680 mg High retentionrate in both treatment groups - no significant difference (84% SR morphine vs 88% methadone) in a 15 weeks study duration with daily attendance Significant reduction in injection sites (p<0.001) No significant differences in concomitant consumption of benzodiazepines and cocaine between the groups, however a time effect is significant for cocaine (p<0.001) Significant better clinical well-being on SR morphine maintenance (p<0.001) Discussion: future SR morphine/naloxone (?)

New horizon: sustained release morphine as agonist treatment George Woody Addiction, 2005; 100: 1758-1759

Maintenance treatment with SROM appears to be a clinically useful alternative treatment in subjects not tolerating methadone or with inadequate withdrawal suppression. Addiction, 103, 1837-1846 (2008). Methadone / SR morphine ratio 1:8

Beck, et al. (2014). Addiction, 109 (4), 617-626.

11 weeks (1week adjustment + 10 weeks treatment 11 weeks (1week adjustment + 10 weeks treatment 11 weeks (1week adjustment + 10 weeks treatment 11 weeks (1week adjustment + 10 weeks treatment

11 weeks (1week adjustment + 10 weeks treatment 11 weeks (1week adjustment + 10 weeks treatment 11 weeks (1week adjustment + 10 weeks treatment 11 weeks (1week adjustment + 10 weeks treatment During treatment phase flexible dosing permitted

11 weeks (1week adjustment + 10 weeks treatment 11 weeks (1week adjustment + 10 weeks treatment 11 weeks (1week adjustment + 10 weeks treatment Mean SROM Dose/day 791 ± 233 mg 11 weeks (1week adjustment + 10 weeks treatment Mean METH Dose/day 103 ± 30 mg Transfer METH to SROM relation 1 : 7,7 ± 1.3 SROM to METH relation 7,5 ± 2.4 :1 Around 10% of patients needed dose adjustement

Results Retention: no sign difference between groups or conditions Rentention Methadone SROM Retention Group 1 88,0% 88,7% Retention group 2 91,1% 82,1% Women had sign lower retention than men (p = 0,03) No sign. assoziation between retention and psychiatric co-morbidity (p = 0.06) Urintoxicology: sign. difference (p = 0,05) But: non-inferiority frame of 10% Non-inferiority SROM confirmed Urintoxikology Methadone SROM Pos urinetoxicology heroin 0,15% 0,20% No sign difference in urintoxikology positive for benzodiazepines, cannabis, cocaine Beck, et al. (2014). Addiction, 109(4), 617-626.

Key EQUATOR publications Methods Fischer G, Stöver H. HARCP 2012;14(3):5 70. Results Goulão J, Stöver H. HARCP 2012;14(4):7 22. Dale-Perera A, et al. HARCP 2012;14(4):23 38. Fischer G, et al. HARCP 2012;14(4):39 50. Stöver H. HARCP 2012;14(4):51 64. Benyamina A, Stöver H. HARCP 2012;14(4):65 80. Full questionnaires are published as appendices to the methods paper

What is EQUATOR? Project Improve survey 1 Project Access EQUATOR analysis Extension to new countries Original study in Germany 1 Adaptation of Project Improve survey in 10+ EU countries Combined analysis of first 10 country surveys in EU Belgium, Netherlands, and Switzerland Treatment experts from across the world participated as advisors or collaborators in the implementation of the survey EQUATOR: European Quality Audit of Opioid Treatment 1. Stöver H. Eur Addict Res 2011;17:44 54

EQUATOR: General recruitment procedures Physicians (treating) Identified by research collaborators, official lists or internet research Telephone or face-to-face interviews, ~60 questions Patients (currently in OMT) Recruited via physicians, treatment/user groups or drug support centres Self-completion questionnaire or face-toface interviews, ~50 questions Opioid users (currently out of OMT)* *Many users had past treatment experience Recruited via treatment/user groups or drug support centres Self-completion questionnaire or face-toface interviews, ~50 questions

Austria: SROM is associated with a high risk of injectable misuse More than half of patients on SROM reported injecting their OMT compared with only 17% of patients on buprenorphine and 7% on buprenorphine naloxone (p<0.01 SROM vs other options) SROM: slow-release oral morphine

Oral morphine/naloxone medication trial

FUTURE EudraCT Number:2011-005903-34 Sponsor's Protocol Code Number: KKSMUW2011-09 National Competent Authority:Austria - BASG Clinical Trial Type:EEA CTA Trial Status:Ongoing Date on which this record was first entered in the EudraCT database:2012-03-29

Suboxone R Buprenorphine : Naloxone (4:1)

Buprenorphine diversion and injection in Melbourne, Australia: An emerging issue? Jenkinson RA et al.; Addiction (2005) 100; 197-205 Setting: Syringe & needle exchange programme in Melbourne Patients: 156 current IDU Results: 37% reporting injection of bup during lifetime, 33% within the last 6 months. 47% reported to have bup obtained illicitly Buprenorphine injection was associated with: Injection of other drugs Buprenorphine maintenance Injection-related health problems Involvement in crime Conclusion: Monitoring & Education in addiction medicine

% of respondents willing to purchase the substance at a particular price: Street price in for 8mg Respondents were willing to pay significantly (p<0.0001) higher street price for buprenorphine than for the combinating product 89% were willing to pay 25 for 8mg buprenorphine only 3% would pay that for 8mg buprenorphine-naloxone

Thank you for your attention Edvard Munch (1918-1919) Women With Poppies