Opioid Induced Hyperalgesia Jill Mosby MD June 18
Opioid Induced Hyperalgesia Jill Mosby, MD June 18 th 2008
History OIH n 1880: Rossbach “When dependence on opioids finally becomes an illness of itself, opposite effects like restlessness, sleep disturbance, hyperesthesia, neuralgia, and irritability become manifest” 2
History OIH Six decades later Himmelsbach described opioid abstinence syndrome: “aching in bones, joints, muscles is probably the most common withdrawal symptom” 2
Definitions Analgesia n absence of sense of pain Nociceptive n Causing pain Agonist n a chemical substance capable of activating a receptor to induce a full or partial pharmacological response Antagonist n a drug that counteracts the effects of another drug
More definitions TOLERANCE n Exposure to a drug induces changes that cause decreased response to drug’s effects over time n Can develop quickly or slowly n Cross tolerance can occur (ie: with opioids) SENSITIZATION § A form of nonassociative learning characterized by an increase in responsiveness upon repeated exposure to a stimulus
Standard Risks of Opioid n Physical dependence Tolerance Addiction Overdose Typical side effects n ? Opioid Induced Hyperalgesia n n
Opioid Induced Hyperalgesia n n n Enhanced pain response to a noxious stimulus Evidence for changes/ source in spinal cord and brain AKA: Opioid Neurotoxicity
Types of OIH n n n Maintenance therapy and withdrawal (MW) Very high dose, or escalating dose (HD) Ultra-low dose (LD)
Early evidence OIH: MW Rodent Studies Summery § § § Rodents: mice, rats, guinea pigs > 75 studies since 1970’s Multiple opioids (Morphine, Fentanyl, Heroin, experimental) § § Multiple routes (IT/SQ/IV/PO/IP) Time frame of OIH: hours, days, or longer § Pain threshold measured: Mechanical, Electrical or Thermal stimuli This must not be one of the experimental rats…it’s too happy!
Rat studies: during opioid exposure Vanderah et al, J Neurosc 2001 Angst (chart)
Rats: Persistent hyperalgesia Celerier et al, J Neurosc 2001 Angst (chart)
Rats: Persistent hyperalgesia Celerier et al, J Neurosc 2001 Angst (chart)
Celerier et al, J Neurosc 2001
Acute hyperalgesia after isolated exposure Celerier et al, Anes 2000
Mechanisms studied OIH-MW n n n Opioid receptors: Mu receptor NMDA antagonist (ketamine, MK-801) NMDA activation PKC inhibition IT glutamate/ substance P Spinal EAA (increase in chronic opioid use) IT Cyclooxygenase inhibitors (NSAID) Spinal dynophin Spinal cytokines IT GM 1 ganglioside Dorsal horn Fos-C Hemoxygenase & nitric oxide synthase inhibitors ↑ ↓ ↑ ↑ ? ? ↓
Evidence for MW in humans § § § Human studies former opioid addicts Maintained on methadone vs. no maintenance Show increased sensitivity to some types of pain Test Threshold CPP ---- Tolerance MM 42% ↓ PP No change ---- EP No change ---- CPP ---- MM 53% ↓ CPP ---- MM 56% ↓ CPP/ EP MM 43% ↓ No change MM 74% ↓ MM 15% ↓ CPP/ EP MM 34% ↓ No change MM 76% ↓ No change
OIH: MW n n n Surgery pts, volunteer High vs. low/no opioid dose intraop Increased postop pain, opioid use in pts received high dose C/S* TAH Col Opioid use HD 60%↑ HD vs. LD/None 120% ↑ HD 85% ↑ HD ND Postop Pain HD vs. LD/None 30% ↑ HD 50% ↑ HD ND ND Gyn Angst Anesth 2006
Chronic Pain Patients n n n 6 Pts chronic back pain >6 months Started on LA morphine ↓ Tolerance & Threshold of CPP Pain scores ↓ 30% Secondary outcomes not changed Angst J Pain 2006
OIH: MW n n Human volunteers Capsaicin-heat for mechanical pain Pain ↓ remifentanil Pain & allodynia ↑ after infusion Wood, Anesth Analg
Clinical significance of MW n n n Argues acute & chronic opioid use may have new risk: OIH (MW) Opioids may worsen initial pain & ↑ sensitivity to other sources of pain Query NMDA antagonists future role help prevent OIH
OIH: LD Animal Studies n n n Animal studies opioid 1000 x lower normal dose: OIH to mechanical & thermal Locally injected LD→hyperalgesia Normal dose→antinociceptic Both reversed with antagonist Theory: LD opioid trigger excitatory signaling cascade
OIH: LD in Humans n n n 1940’s study biphasic response to morphine in 7/57 former addicts. Mild hyperalgesia to heat at low dose, analgesia at high dose. 1979 study showed LD opioid & antagonist had improved post op pain, but was not confirmed repeat studies No controlled studies in humans
OIH: HD in Animal studies n n IT morphine 10 x normal: scratching/ biting/ aversion to touch, not resolved with naloxone IT strychnine: allodynic/ hyperalgesic Spinal cord EP studies: HD opioids act similar to IT Strychnine IT injected Glycine: attenuates allodynia
OIH: HD in Animal Studies § 33 opioid related structures studied, characteristic of chemicals produce allodynia/ hyperalgesia: • Phenantrene structure • • Hydrogen at position 14 Ether bond One or no methyl group on nitrogen Free 3 -OH position ro glucuronide/sulfate conjugate
OIH: HD in humans n n n Nine case reports pts with allodynia 22 pts, 8 had myoclonus Most patients morphine Routes: PO, IV, IT Reducing dose opioid or rotation resolved/ reduced sx in 21/22 pts This is the OIH that is seen clinically in palliative care, ? Rad-Onc
OIH: HD Clinical Picture n n n n Severe allodynia Intractable, escalating pain on HD/ED opioid < 50% myoclonus (? ), more at rest Delirium, mental status changes Increased doses caused ↑ pain Can lead to sz, coma, death Reducing dose or rotating opioid reversed sx in almost all patients
Culprit Medications n *Morphine is most common • most used opioid n n *Dilaudid Oxycodone Less often fentanyl or methadone * I have seen clinically this year
Mechanism HD n n n Phenantrene structure linked NMDA linked, with effects on excitatory signals in CNS ? Metabolites of opioid (Morphine-3 glucuronide), this is less discussed in literature
Phenantrene ring
Barriers to Treatment n n n Clinicians often do not know about, recognize, or understand OIH Family/ patients understanding: How can my Morphine do harm? Both groups need education
Management of HD n n n Pain controlled/ mild: ↓ opioid dose Uncontrolled pain: ↓ dose + adjuvant OR rotate to non-phenantrene opioid Benzodiazapines Fluids Educate Davis M, Walsh D
Bottom Line n n n Future of pain control will be greatly influenced by this area of research Peripheral nerves, spinal cord & CNS all involved in OIH Chronic pain could be worsened by acute and ongoing opioid therapy
Bottom Line (cont’d) n n For Patients with resistant/ escalating pain, hyperalgesia should be considered OIH (HD) treat with decreased opioid dose or rotation to another opioid I hope this has given some insight into some of the challenges in treating pain I hope this helps you recognize OIH (HD)
Questions to ponder § Opioid tolerance & hyperalgesia linked? n Worsening chronic non-malignant pain? n n Are there genetic differences that cause OIH MW & HD? What is on horizon to help HD OIH? Ketamine like medication?
Bibliography 1) 2) 3) 4) Angst MA, Clark JD: Opioid induced hyperalgesia. Anesth 2006; 104: 570 -87 Mercandante S, Ferrera P, et al: Hyperalgesia: an emerging Iatrogenic Syndrome. J Pain and Sympt Management 2003; 2: 769 -775 Davis MP, Shaiova LA, Angst MS: When opioids cause pain. 2007; 25: 44974498 Chang G, Chen L, Mao J: Opioid tolerance and hyperalgesia. 2007; 91: 199 -211
Bibliography 5) 6) 7) 8) 9) Ballantyne JC, et all: Opioid Induced Hyperalgesia. Pain: Clinical Updates 2008; 16: 1 -4 Celerier E, Rivat C, et al: Long-lasting Hyperalgesia Induced by Fentanyl in Rats. Anesth 2001; 92: 465 -72 Celerier E, Laulin JP, et al: Progressive Enhancement of Delayed Hyperalgesia Induced by Repeated Heroin Administration: a Sensitization Process. J Neurosc 2001; 21: 4074 -80 Chu LF, Clark DJ, et al: Opioid Tolerance and Hyperalgesia in Chronic Pain Patients after one month of oral morphine therapy: a preliminary prospective study. J Pain 2006; 7: 43 -48 Hood DD, Curry R, Eisenach JC: Intravenous remifentanyl produces withdrawal hyperalgesia in volunteers with capsaicin-induced hyperalgesia. Anesth Analg 2003; 97: 810 -5
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