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Stapleford-Athens 2011 International Addiction Conference Further Experience with Ambulatory Benzodiazepine detox. Dr George O’Neil email@drgeorgeoneil.com Fresh Start Recovery Programme Perth, Western Australia. History of Flumazenil treatment for benzodiazepine addiction.
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Stapleford-Athens 2011International Addiction Conference Further Experience with Ambulatory Benzodiazepine detox Dr George O’Neil email@drgeorgeoneil.com Fresh Start Recovery Programme Perth, Western Australia
History of Flumazenil treatment for benzodiazepine addiction • 1961: Hollister, L.E., Motzenbecker, F.P. & Degan, R.O. (1961) Withdrawal reactions from chlordiazepoxide ('Librium'). Psychopharmacologia, 2, 63-68. • 1982: McNicholas, L.F. & Martin (1982) The effect of a benzodiazepine antagonist, R015-1788, in diazepam dependent rats. Life Science. Vol 31, (8); 731-737. • 1991: Savic, I., Widen, L, & Stone-Elander, S. (1991) Feasibility of reversing benzodiazepine tolerance with flumazenil. Lancet 337: 133-137 • 1992: Lader, M.H. & Morton S.V. (1992) A pilot study of the effects of flumazenil on symptoms persisting after benzodiazepine withdrawal. Journal of Psycopharmacology 6(3);357-363.3 email@drgeorgeoneil.com
History - continued • 1996: Gerra, G. et al (1996) Intravenous flumazenil following prolonged exposure to lormetazepam in humans: lack of precipitated withdrawal. International Clinical Psychopharmacology, Jun;11(2):81-8 • IV flumazenil following prolonged exposure to lormetazepam • 2002:Gerra, G. Zaimovic, A., Giusti, F., Moi, G. & Brewer, C (2002) Intravenous flumazenil versus oxazepam tapering in the treatment of benzodiazepine withdrawal: a randomized, placebo-controled study. Addiction Biology, 7(4):385-95 • 50 patients 20 flumazenil. 20 oxazepam taper; 10 placebo • Demonstrated flumazenil efficiency at reversing benzo effects and withdrawal symptoms. • 2004: Pericic, D. et al (2004) Chronic exposure of cells expressing recombinant GABBA receptors to benzodiazepine antagonist flumazenil enhances the maximum number of benzodiazepine binding sites. Life Science, Vol 76 (3):303-317 • Prolonged occupancy of benzo receptors by benzos leads to uncoupling of the allosteric linkages to the GABBA receptor. • Result - Tolerance/ craving for benzos, Flumazenil – recouples receptor function • Resets tone. Tolerance & cravings decrease. email@drgeorgeoneil.com
Background • Gerra et al (2002) demonstrated that flumazenil was efficient at reversing the effects of benzodiazepine and withdrawal symptoms. • In 2006, we reported IV flumazenil infusions in 29 benzodiazepine dependent patients email@drgeorgeoneil.com
Experience with flumazenil infusions • Melbourne • 2005-2008 IV only • 2009-2011 (SC only) • 4 day (In Patient only) • Perth • 2005-2008 IV only (usually 4 days) • 2009-2011 SC only (4-30 days) • out patient with carer after first 2 days. email@drgeorgeoneil.com
Flumazenil 12mg/30ml filtered infusion system email@drgeorgeoneil.com
Jon Currie, Melbourne Blood Levels email@drgeorgeoneil.com
Perth Flumazenil Work • Continuous infusion of 100-400µg/hr causes some detox symptoms in the first 6hrs with relief of anxiety and aggression during the infusion. • Subcutaneous infusion have proven more reliable in more than 100 patients compared to 100 managed by IV infusion • Patients were noted to have a return of anxiety when the infusion stoped and so the infusion is now continued up to 30 days email@drgeorgeoneil.com
Flumazenil reducing cravings for Benzodiazepines Hood, S., O’Neil, G & Hulse, G. (2009) The role of flumazenil in the treatment of benzodiazepine dependence: physiological and psychological profiles. Journal of Psychopharmacology, 23(4);401-409 email@drgeorgeoneil.com
Perth Flumazenil Work cont. • Perth is the first city to allow the patients home providing a carer remains with them after the first 1-2 days of infusion. • Research work is continuing; • Flumazenil implants • Flumazenil injections 7-28 days • Flumazenil patches email@drgeorgeoneil.com
Prolonged infusions • Detox symptoms in first 6 hours usually. • Detox symptoms usually settle but in high benzo users can continue for days. • Anxiety may return when infusion stops but the return of anxiety is decreased with long infusions. • Anxiety control, cognitive depression and depression symptoms all improve with length of the infusion. email@drgeorgeoneil.com
In Vitro Release of FLU/PLA/PLGA tablets email@drgeorgeoneil.com
Perth Flumazenil Infusions Aug 2010 • 100+ IV infusions balloon driven • Patients became irritable whenever the infusion was stop by a blocked IV site • On one occasion a patient fitted • 100+ Subcutaneous infusions • No obstructions to flow occurred and outpatient management became practical email@drgeorgeoneil.com
Drug use Before & After Naltrexone & Flumazenil (Hood, 2009) email@drgeorgeoneil.com
Flumazenil Reducing Anxiety (Hood, 2009) email@drgeorgeoneil.com
Flumazenil infusions the future • Subcutaneous has replaced IV • Nasal may be useful for symptom control. • Transdermal experiments are continuing. • Implant delivery; trial protocols are developed. • Use in benzo addiction is well demonstrated. • Use in alcohol, amphetamine and other addictions is less well established. email@drgeorgeoneil.com
Karolinska Institute 2010 • In aggressive patients flumazenil decreases the existing aggression • In the control group, flumazenil increases aggression and alertness • The dose delivery method of large bolus intermittent doses may have caused aggression in the controls where it is my belief that a continuous low dose infusion might have increased alertness without increasing aggression. Saxon, L., Borg, S. & Hiltunen, A.J. (2010) Reduction of aggression during benzodiazepine withdrawal: Effects of flumazenil. Pharmacology, Biochemistry and Behaviour, 96, 148-151 email@drgeorgeoneil.com
Croatia 2008, Molecular & Neuropharmacology • They confirm up-regulation of GABAA receptors may be from; • Growth of new receptors via synthesis of receptor proteins confirmed with their experiments during prolonged flumazenil exposure or • Via flumazenil causing the correction of uncoupling of non sensitive GABAA receptors so that they return to full sensitivity (uncoupling of receptors follows exposure to benzodiazepines) Jazvinscak, M. et al (2008) The role of transcriptional and translational mechanisms in flumazenil-induced up-regulation of recombinant GABAA receptors. Neuroscience Research, 61;234-241 email@drgeorgeoneil.com
GABAA Receptor email@drgeorgeoneil.com
Case Study – Female Aged 30 • Childhood terror • PTSD diagnosed at 15 • Anxiety led to 20 years benzo and 10 years opiate addiction • Total of 35 admissions for benzo overdoses requiring ventilation occurred email@drgeorgeoneil.com
Case Study – Female Aged 30 cont. • Presenting medications: • 200 x 2mg/day Xanax (alprazolam) • 50 x 5mg/day Valium (diazepam) • 50 x 5mg/day Mogadon (nitrazepam) • 1600 mg/day Seroquel (quetiapine: atypical antipsychotic) • 80/day Panadeine Forte (co-codamol: each tablet paracetamol 500 mg + codeine phosphate 30 mg) • Naltrexone implants to control the opiate disorder • Flumazenil infusions to control the GABAA system anxiety disorder email@drgeorgeoneil.com
Heart rate patterns following Valium at midday and flumazenil at 6.15pm Flumazenil (antagonist) Valium (agonist) Heart rate (bpm) email@drgeorgeoneil.com
Case Study – female aged 50 • PTSD following presence at 9/11 • Stilnox addiction (agonist at benzo receptor) followed sleep disturbance • Culminating in 20 tab/day Stilnox (zolpidem) • Treated with flumazenil infusions to upregulate (re-sensitise) the benzo receptors damaged by chronic stress from PTSD and Stilnox email@drgeorgeoneil.com
Contact Information • Dr George O’Neil • Email: email@drgeorgeoneil.com • Phone +61 893881991 • Perth (GMT+8) 6-8am or 7-11pm • London (GMT) 10-12pm or 11am-3pm • New York (GMT-5) 5-7pm or 6-10am • Los Angeles (GMT-8) 2-4pm email@drgeorgeoneil.com