Copyright Dr Andrew Dean Pain Classification and Opioid Physiology A Review.

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Presentation transcript:

Copyright Dr Andrew Dean Pain Classification and Opioid Physiology A Review

Copyright Dr Andrew Dean Analgesic Ladder Non-Opioid Non-Opioid + Adjuvant Analgesic Weak Opioid Weak Opioid + Adjuvant Analgesic Strong Opioid Strong Opioid + Adjuvant Analgesic

Copyright Dr Andrew Dean Visceral Pain Pain from abdominal & thoracic viscera Deep, squeezing, pressure. Poorly localised. Sometimes referred. Liver, pancreas, lung Mechanisms of Pain

Copyright Dr Andrew Dean Mechanisms of Pain Somatic Pain ‘Nociceptive’ Pain from nerve endings in tissues & bones Aching, gnawing. Well localised. eg Bone Metastases

Copyright Dr Andrew Dean Neuropathic Pain Pain from nerve irritation/damage. Flashing, sharp, electric, burning. Often follows nerve pathway. Plexus pain. Mechanisms of Pain

Copyright Dr Andrew Dean Pain Pathway Receptors Cortico-Spinal Peripheral Nerve Spino-thalamic 5HTNA

Copyright Dr Andrew Dean Synapse Spinal Nerve Peripheral Nerve Synaptic Cleft

Copyright Dr Andrew Dean Synapse Impulse Depolarisation

Copyright Dr Andrew Dean The Busy Gate Cortico-Spinal Sympathetic Spinothalamic Other

Copyright Dr Andrew Dean Opioid Receptors Mu Ca

Copyright Dr Andrew Dean Receptors Mu K/Ca To Spino- thalamic tract Excitatory receptors Inhibitory receptors

Copyright Dr Andrew Dean Opioid Response Opioid level Opioid Dose % opioid receptor binding 100%

Copyright Dr Andrew Dean Opioid Response Opioid level Opioid Dose % opioid receptor binding 100% Maximum opioid analgesia Side Effects

Copyright Dr Andrew Dean Opioid Receptor Sites Receptors Cortico-Spinal Peripheral Nerve Spino-thalamic 5HTNA

Copyright Dr Andrew Dean Peripheral Action of Morphine Mu K/Ca Nociceptor Inflammatory cell

Copyright Dr Andrew Dean Pain wind up

Copyright Dr Andrew Dean Receptors and Channels  AMPA  Short depolarisation  “Fast”  Sharp, pricking pain  NMDA  Enhance depolarisation  Greater response to stimulus  Response outlasts stimulus

Copyright Dr Andrew Dean Receptors Mu K/Ca To Spino- thalamic tract Excitatory Receptors AMPA

Copyright Dr Andrew Dean NMDA feedback K/Ca To Spino- thalamic tract NMDA receptors NMDA receptors

Copyright Dr Andrew Dean Receptor responses Impulses AMPANMDA Stimulus Time

Copyright Dr Andrew Dean Receptor co-operation AMPA NK 1-2 NMDA C-fibre response Stimulus number

Copyright Dr Andrew Dean NMDA Antagonists Very weak  Paracetamol Weak  Some NSAID’s  Methadone  Pethidine  Valproate  Amantidine

Copyright Dr Andrew Dean NMDA Antagonists Moderate  Ketamine  Dextromethorphan Strong  Experimental  Lethal

Copyright Dr Andrew Dean Opioid Response Opioid level Opioid Dose % opioid receptor binding

Copyright Dr Andrew Dean Opioid Receptor Sites Receptors Cortico-Spinal Peripheral Nerve Spino-thalamic 5HTNA

Copyright Dr Andrew Dean Receptors Mu K/Ca To Spino- thalamic tract Excitatory Receptors AMPA

Copyright Dr Andrew Dean Sodium Channels K/Ca To Spino- thalamic tract

Copyright Dr Andrew Dean Receptors K/Ca To Spino- thalamic tract 3. Receptors next to synapse bind opioids which stop chemical transmission of impulse Inhibitory receptors 1. Cell body receives electrical impulse producing Mu receptor 2. Mu receptors migrate down nerve cell membrane

Copyright Dr Andrew Dean Sodium Channel Blockers Valproate Gabapentin Carbamazepine

Copyright Dr Andrew Dean Pain Pathway Receptors Cortico-Spinal Peripheral Nerve Spino-thalamic 5HTNA

Copyright Dr Andrew Dean Paracetamol Receptors Cortico-Spinal Peripheral Nerve Spino-thalamic 5HTNA Paracetamol acts here

Copyright Dr Andrew Dean NSAID’s Receptors Cortico-Spinal Peripheral Nerve Spino-thalamic 5HTNA NSAIDs acts here

Copyright Dr Andrew Dean Morphine Receptors Cortico-Spinal Peripheral Nerve Spino-thalamic 5HTNA Morphine acts here 5% 25% 70%

Copyright Dr Andrew Dean Dorsal Horn

Copyright Dr Andrew Dean Dorsal Horn

Copyright Dr Andrew Dean Neuropathic Pain Has many mechanisms Therefore illogical to expect one drug to work every time Often need combination therapy

Copyright Dr Andrew Dean Pain Pathway Receptors Cortico-Spinal Peripheral Nerve Spino-thalamic 5HTNA

Copyright Dr Andrew Dean Opioid Receptors Mu Ca

Copyright Dr Andrew Dean Opioid Response Opioid level Opioid Dose % opioid receptor binding

Copyright Dr Andrew Dean Side Effect Threshold Opioid level Opioid Dose High threshold

Copyright Dr Andrew Dean Side Effect Threshold Opioid level Opioid Dose Low threshold

Copyright Dr Andrew Dean Methadone Potent Mu agonist NMDA receptor activity No active metabolites

Copyright Dr Andrew Dean Methadone Formulation –Oral liquid, tablets –Injection, SC, IM, IV Not predicable –Large inter-individual variation –1-2 hours onset, lasts 6-12 hours –t 1/2 <120 hrs, Steady state 2-10 days.

Copyright Dr Andrew Dean Methadone Formulation –Oral liquid, tablets –Injection, SC, IM, IV Not predicable –Large inter-individual variation –1-2 hours onset, lasts 6-12 hours –t 1/2 <120 hrs, Steady state 2-10 days.

Copyright Dr Andrew Dean Opioid level Opioid Dose Side Effect Threshold Morphine side effect threshold Methadone side effect threshold

Copyright Dr Andrew Dean Methadone Study Retrospective Case study - 68 patients Morphine side effects Co-analgesics unchanged Opioid changed to methadone

Copyright Dr Andrew Dean Methadone Study Pain Types n Somatic28 n Neuropathic 2 n Visceral11 n SV 3 n SN22 n SVN 1

Copyright Dr Andrew Dean Methadone Study Side Effects Confusion20 Drowsiness34 Hallucinations13 Nausea24 Pruritis 2

Copyright Dr Andrew Dean Methadone Study Case study - 68 patients n Resolution of adverse effects in 56 (82%) n Side effects same or changed in 12

Copyright Dr Andrew Dean Morphine/Methadone Conversion Average = 6.34

Copyright Dr Andrew Dean Methadone Study Ratios Neuropathic Pain Ratio 7.06 Non-Neuropathic Pain Ratio 5.78 Does this reflect NMDA antagonism?

Copyright Dr Andrew Dean Dose Regimen bd57 tds11

Copyright Dr Andrew Dean Methadone Study Conclusions Methadone is a suitable alternative to morphine for cancer pain Suggested ratio n Suggested regimen n May be better for neuropathic pain 6:1 bd n Consider threshold theory