pain and its treatment in psychiatric practice (2) (1)
TRANSCRIPT
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A D O N I S S F E RA , M D
CHRONIC PAIN IN PSYCHIATRIC PRACTICE
DEFINITION OF ACUTE AND CHRONIC PAIN, NOCICEPTIVE AND NEUROPATHIC PAIN, PERIPHERAL AND CENTRAL SENSITIZATION, PAIN AND MOOD, PHARMACOLOGY OF PAIN, CHRONIC PAIN SYNDROMES
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RIVER OF PAIN
Acheron was known as the river of pain, and was one of the five rivers of the Greek underworld.
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THE HISTORY OF MEDICINE IS THE HISTORY OF PAIN
• Asclepius, the god of medicine attending to a patient in pain
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MORPHEUS AND HIS ELIXIR
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TWO PARALLEL HISTORIES: ACUTE AND CHRONIC PAIN
Acute Pain Chronic Pain
Physiological: protective (survival benefit)
Pathological: non-protective (no survival benefit)
Causes external: obvious Causes internal: obscure
Tissue damage: resolution within days/weeks
CNS changes: may not resolve
Attended by physicians (illness) Attended by clergy (suffering)
Symptom of illness Existential: a social phenomenon
The demon is outside The demon is within
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CHRONIC PAIN: A WAY OF LIFE
• Headaches, backaches, pain in amputated limbs, causalgias and neuralgias have always existed, but the sufferers were not always considered “ill”.
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“A WAY OF LIFE” IN OUR SOCIETY
• Destitution, Poverty, Homelessness affect health, yet are not being addressed by medical science (a way of life).
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MEDICALIZATION OF CHRONIC PAIN
• In March of 1899 Felix Hoffman discovered Aspirin.
• Aspirin was more than a drug – it changed the way of thinking about chronic pain.
• Pain and suffering became medicalized (medical model applied).
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A CULTURE OF PAIN AND PAINKILLERS
• In 2005 more than 10 million Americans were abusing prescription medications – which is more than the combined number of people abusing cocaine, heroin, hallucinogens and inhalants.
• Prescription painkiller overdoses killed nearly 15,000 people in the US in 2008 (three times the 4,000 people killed by these drugs in1999).
Scott M. Fishman, MD; Responsible opioid prescribing a physician’s guide; Waterford Life Sciences, 2007
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A “PERFECT STORM” OF CONTROVERSY
*War on pain *War on drugs
• Physicians are being enlisted on both fronts:
-combating pain
-reducing the risk of diversion, abuse and addiction.
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PHARMACOVIGILENCE
• The science of detecting, understanding and preventing adverse effects or any other drug related problem.
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PAIN: DEFINITION
• “An unpleasant sensory and emotional experience associated with actual or potential tissue damage or described in terms of such damage” (International Association for the Study of Pain (IASP).
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PAIN - A LEARNED EXPERIENCE
• Each individual “learns” pain through experiences related to injury in early life.
To hear about pain is to have doubt; to experiencepain is to have certainty. (Elaine Scarry: The Body in Pain)
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PAIN THAT IS PRONE TO BECOME CHRONIC
• Type: post-op, post trauma, post-herpes
• Neuropathic component: nerve injury
• Disability and compensation
• Inadequate analgesia
• Prolonged pain before surgery
• Repeated surgeries
• Radiation or chemotherapy
• Psychiatric vulnerabilities
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CLASSIFICATION OF CHRONIC PAIN
Inflammation or mechanical damage
Classic examples-osteoarthritis-rheumatoid arthritis
Damage or entrapment of peripheral nerves
Classic examples-diabetic peripheral neuropathic pain-post-herpetic neuralgia
Central disturbance in pain processing
Classic examples-fibromyalgia-IBS-headaches-LBP-TMJ disorder-Chronic pelvic pain
Perpheral (nociceptive)
Neuropathic Central (non-nociceptive)
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ALLODYNIA AND HYPERALGESIA
Allodinia = Pain evoked by innocuous stimuli.
Hyperalgesia = exaggerated pain produced by mildly painful stimuli.
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NOCICEPTION (THE AFFERENTS)
-A beta fibers respond only to non-noxious stimuli-A delta and C fibers respond to noxious mechanical, heat, and chemical stimuli.
Stephen M. Stahl;Stahl’s Essential Psychopharmacology; Third Edition;Cambridge University Press 2008
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NOCICEPTION AND NEUROPATHY
1. Sensory Pathway =information about the location and intensity of the painful stimulus (spinothalamic tract).
2. Emotional Pathway =affective component of the pain experience (spinobulbar tract).
Combined data from these pathways = human subjective experience of pain.
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INSULAR CORTEX – WHERE PAIN BECOMES SUFFERING
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VON ECONOMO NEURONS (VEN): INSULA AND ACC
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THE PHYSIOLOGY OF INSULAR CORTEX
The insulae are believed to be involved in:• emotion • pain• empathy• perception, • self-awareness, • cognitive functioning, • interpersonal experience.
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EMPATHY IS PAIN … SORT OF
VEN in Insula and Anterior Cingulate Cortex (ACC) are activated when subjects evaluate painful stimuli and when empathizing with others who experience physical pain.
The Neural Basis of Empathy;Annual Review of Neuroscience,Vol. 35: 1-23 (Volume publication date July 2012);DOI: 10.1146/annurev-neuro-062111-150536
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VON ECONOMO NEURON DISCOVERED IN THE INSULA OF MACAQUE MONKEYS
• Published on June 4, 2012: A scientist from the Max Planck Institute discovered that von Economo neuron (VEN) is also found in the insula of macaque monkeys
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PERIPHERAL SENSITIZATION (PRIMARY HYPERALGESIA)
SENSITIZING SOUP
• Hydrogen ions• Noradrenaline• Bradykinin• Histamine• Potassium ions• Prostaglandins• Purines• Cytokines• Serotonin• Nerve growth factor• neuropeptides
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PERIPHERAL SENSITIZATION LEADS TO CENTRAL SENSITIZATION
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CENTRAL SENSITIZATION (SECONDARY HYPERALGESIA)
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PAIN BEGETS MORE PAIN (OVERACTIVE ASCENDING PATHWAYS)
Long term potentiation (LTP) is perpetuated by pain and leads to strengthened synapses.
These stronger synapses are able to:recruit subliminal inputs.
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CAUSES OF SENSITIZATION?
When a nerve is severed, the distal portion degenerates and dies.
The proximal portion sprouts trying to reach the previous target tissue.
The sprouts lack guidance and form tangeled neuromas.
Neuromas generate ectopic activity and heightened sensitivity to mechanical, thermal and chemical stimuli.
Stephen M. Stahl;Stahl’s Essential Psychopharmacology; Third Edition;Cambridge University Press 2008
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EPHAPTIC CROSS-TALK
Disruption to myelination may also allow cross-talk between neurons(ephaptic cross- talk).
The electrical activity in an A beta fiber neuroma can electrically stimulate activity in a C fiber.
Repetitive firing of one neuron can stimulate activity in the neighboring neurons(hyperalgesia and allodynia).
Stephen M. Stahl;Stahl’s Essential Psychopharmacology; Third Edition;Cambridge University Press 2008
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FUNCTIONAL SOMATIC SYNDROMES (FSS)
• Fibromyalgia• Irritable bowel syndrome• Chronic Fatigue Syndrom• Temporomandibular Joint Disorder• Interstitial cystitis
Patients with one FSS often suffer from one or moreother FSS as well as psychiatric comorbidity.
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THE COMPLEX RELATIONSHIP BETWEEN PAIN AND DEPRESSION
• The overlap between pain and depression ranges from 30% - 60%
• Depression may lower pain threshold (depressed people fell more pain)
• Pain may precipitate depression
• Patients with chronic pain are at higher risk of developing depression
• Pain and depression may be considered integrated.
Gallagher RM, Verma S. Semin; Clin Neuropsychiatry 1999; 4 :203-220;Von Korff M, Simon G; Br J Psychiatry.1996;168 (sup 30):101-103
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PAIN PATIENTS IN PSYCHIATRIC PRACTICE
Psychiatrist: Somatization d/o
Rheumatologist: fibromyalgia
Neurologist: chronic fatigue syndrome/myalgic encephalomyelitis
Patient: “multiple chemicalsensitivities”
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WAR ON PAIN (FRONTS)
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SNRI DRUGS APPROVED FOR CHRONIC PAIN
Duloxetine Milnacipran
60 mg once daily; higher doses increase SEs without increasing efficacy in pain disorders
30-200 mg/day in 2 doses
Approved for multiple neuropathic pain disorders
Approved for fibromyalgia
SEs include nausea, dry mouth; can cause urinary retention, rare activation of suicidality, rare hepatotoxicity
SEs: nausea, constipation, sweating, urologic complaints, urinary hesitancy, dose-dependent increase in blood pressure; can cause rare activation of suicidality
Metabolized by CYP 450 2D6 Few known adverse pharmacokinetic drug interactions
Not for use with Thioridazine, MAOIs, or patients with uncontrolled narrow angle glaucoma or hepatic impairment
Not for use with MAOIs, or patients with uncontrolled narrow angle glaucoma or hepatic impairment
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OTHER SNRI DRUGS
Venlafaxine Desvenlafaxine
75-225 mg once daily 50 mg once daily
Clinical efficacy in reducing chronic pain Clinical efficacy in reducing chronic pain
SEs include headaches, insomnia, nausea, sweating, dose dependent increase in BP, rare activation of suicidality
SEs include insomnia, nausea, constipation, sweating, increase in BP, rare activation of suicidality.
Use with caution in patients with cardiac impairment
Use with caution in patients with cardiac impairment
Not for use with MAOIs or in patients with uncontrolled narrow-angle glaucoma
Not for use with MAOIs or in patients with uncontrolled narrow-angle glaucoma
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ALPHA 2 DELTA LIGANDS
Pregabalin Gabapentin
150-600 mg/day in 2-3 doses 900-1800 mg/day in 3 doses
Approved in multiple neuropathic pain disorders
Approved in postherpetic neuralgia
Most common SEs: sedation, dizziness
Most common SEs: sedation, dizziness, fatigue, ataxia, nystagmus, tremor
Enhances slow-wave sleep Enhances slow-wave sleep
Renally excreted Renally excreted
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ANTICONVULSANTS FOR CHRONIC PAIN
Carbamazepine
Oxcarbazepine
Topiramate Lamotrigine Zonisamide
1200 mg/day; start slow
1200-1400 mg/day; start slow
50-300 mg\day 100-300 mg/day
100-600 mg/day
Approved for trigeminal neuralgia; may have efficacy in other neuropathic pain disorders
Adjunct for neuropathic pain
FDA approved for migraine prophylaxis
Clinical efficacy in neuropathic pain
Some clinical efficacy in neuropathic pain and migraines
Induces P450 enzymes, may lower the levels of other drugs
Less Induction of P450 enzymes
May have efficacy in other neuropathic pain disorders.
Efficacy can wane after several weeks of use
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TRICYCLICS FOR CHRONIC PAIN
Amytriptiline Cyclobenzaprine
25-50 mg once daily 15 mg/day in 3 doses
Used for multiple pain disorders 15-30 mg/day in one dose (ER)
SEs include sedation, weight gain, anticholinergic effects, dizziness, hypotension
Muscle relaxant
Metabolized to nortriptyline by CYP 450 1A2
Not recommended for long term use
Significant drug-drug interactions SEs: sedation, dry mouth, fatigue headache
Use with caution in patients with renal or hepatic impairment
Use with caution in patients with urinary retention, angle-closure glaucoma, hepatic impairment
Can have cardiovascular effects Can have cardiovascular effects
Multiple contraindications Do not use with MAOIs
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ON THE OPIOID BORDER: PROPOXYPHENE AND TRAMADOL
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OTHER PAIN AGENTS
NSAIDs Acetaminophen Baclophen
Better for acute pain or for chronic inflammatory pain
Less effect on bleeding and renal function compared to NSAIDs
Muscle relaxant and antispastic
Warning for GI bleeding with SSRIs
Can cause hepatotoxicity at high doses
Used for trigeminal neuralgia and some other neuropathic pain conditions
Combination with lithium may cause lithium toxicity
Many psychotropics are metabolized by the same liver enzymes
Use with caution in patients with renal impairment
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OPIOIDS
• Effective for osteoarthritis, rheumatoid arthritis, musculoskeletal pain, postherpetic neuralgia, phantom limb pain, diabetic neuropathy, and chronic low back pain.
• No studies of effectiveness beyond 8 weeks
• Not effective for fibromyalgia
• Risks (dependence, tolerance, pain worsening, reduced effects of SSRIs)
Ballantyne JC, Shin NS; Clin J Pain 2008;24:469-78; Clauw. Am J Med 2009;(Suppl 12):S 3-13
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OPIOIDS FOR CHRONIC PAIN: THE TWO FACES OF JANUS
• Opioids may elicit paradoxical “pain” in both animals and humans.
• In humans hyperalgesia is noted in areas of the body different from the site of the original pain complaint.
• Methadone maintenance patients are hyperalgesic.
• The mechanisms of opioid induced hyperalgesia are unknown
Frank Porreca, PHD, University of Arizona, Tucson, Arizona
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NONPHARMACOLOGICAL TREATMENTS FOR CHRONIC PAIN
• Cognitive behavioral therapy -May work best if targeted to a specific outcome -Adherence may be an issue
• Hypnosis, relaxation, guided imagery -May reduce pain, distress
• Education -Should be combined with other treatment approaches -Education groups can be useful, but adherence may be low
• Aerobic exercise
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EVIDENCE BASED TREATMENT OF CHRONIC PAIN SYNDROMES WITH HIGH PSYCHIATRIC
CO-MORBIDITY
1. Neuropathic Pain 2. Fibromyalgia 3. Chronic Back Pain 4. Osteoarthritis
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NEUROPATHIC PAIN
• Diabetic neuropathy - 16% of persons with diabetes.
• Postherpetic neuralgia - up to 25% develop neuropathic pain following an episode of shingles.
• Spinal stenosis – 3% develop neuropathic pain
• Lumbar disc herniation - 4% develop neuropathic low back pain
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FIRST LINE DRUGS FOR NEUROPATHIC PAIN
• Gabapentin 900-3600 mg/day (Post-herpetic neuralgia)
• Pregabalin 75-600 mg/day (Diabetic Neuropathy, Post-herpetic neuralgia)
• Duloxetine 60 mg daily (Diabetic neuropathy)
• Topical Agents: Lidoderm up to 3 patches/day (Post-herpetic neuralgia)
Schatzberg A, Nemeroff C; Textbook of Psychopharmacology; The American Psychiatric Publishing, 2009
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DIAGNOSTIC CRITERIA FOR FIBROMYALGIA
American College of Rheumatology:1. Generalized pain that is both widespread (on
both the right and the left side of the body, upper and lower halves, and axial as well as proximal arms and legs) and chronic (lasting more than 3 months).
2. Multiple tender points on physical examination (located in the front and back of the neck, upper chest and back areas, iliosacral and posterior gluteal areas, elbows and knees).
Schatzberg A, Nemeroff C; Textbook of Psychopharmacology; The American Psychiatric Publishing, 2009
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FIBROMYALGIA AND ACCELERATED BRAIN GRAY MATTER LOSS
Less gray matter density in fibromyalgia patients vs. controls :
-left parahippocampal gyrus (PHG),-left and right mid/posterior cingulate gyrus (CG)-left insular cortex (IC), and -medial frontal cortex
Anil Kuchinand, P.Schweinhardt, DA Seminowitz et al.; Accelerated brain Gray Mattewr Tissue Loss in Fibromyalgia Patients: Premature Aging of the Brain, Society of Neuroscience 2007
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FIBROMYALGIA - PHARMACOLOGIC AND NON-PHARMACOLOGIC TREATMENTS
First line:• SNRIs (Duloxetine, Milnacipran)• Alpha2 Delta ligands (Pregabalin, Gabapentin)• Aerobic Exercise• CBT• Education
Second line:• TCAs• Cyclobenzaprine (chemical structure related to TCAs)• Tramadol
Schatzberg A, Nemeroff C; Textbook of Psychopharmacology; The American Psychiatric Publishing, 2009
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LOW BACK PAIN
• The most commonly prescribed medications for low back pain are:
• NSAIDs, • Muscle relaxants, • Opioid analgesics. • Benzodiazepines, systemic corticosteroids,
antidepressants and anticonvulsants are also prescribed.
• Schatzberg A, Nemeroff C; Textbook of Psychopharmacology; The American Psychiatric Publishing, 2009
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LOW BACK PAIN GENE?
A UK study, published in the Annals of Rheumatic Diseases (Sep. 24, 2012):PARK2 gene was linked to age-related degeneration of the intervertebral discs in the spine, a common cause of lower back pain.
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LIFT WITH YOUR KNEES NOT YOUR BACK
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OSTEOARTHRITIS
• Osteophyte formation
• Focus of treatment: reduction of pain, preservation of function.
• Acetaminophen• NSAID• Aerobic exercise• Opioids
• Not enough evidence for chondroitin, glucosamine and intra-articular hyaluronic acid.
• Antidepressants not studied for pain in osteoarthritis, but Katon 2007 looked at the co-morbidity of osteoarthritis with depression (antidepressants helpful) .
Schatzberg A, Nemeroff C; Textbook of Psychopharmacology; The American Psychiatric Publishing, 2009
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THANK YOU – LET’S STOP HERE