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Chronic nonmalignant pain: How to ‘turn down’ its physiologic triggers

Current Psychiatry. 2008 August;07(08):19-36
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Ease suffering by managing psychiatric and social factors that heighten pain awareness.

Benzodiazepines have been used short-term to mitigate muscle spasm pain as in fibromyalgia, phantom limb pain, and restless legs syndrome.36,37 Long-term benzodiazepine use can lead to low activity levels, high use of ambulatory medical services, and high disability levels, however.38 if required for muscle spasm or restless legs syndrome, benzodiazepines may best be confined to short-term use.

Antipsychotics. Limited studies have evaluated antipsychotics’ efficacy for chronic pain.39,40 Some have been found to be useful in neuropathic pain.40 Antipsychotics are seldom used to treat pain because of limited efficacy data, potential side effects, and an abundance of alternate agents. Because risks—most notably extrapyramidal side effects and tardive dyskinesia—appear to outweigh analgesic efficacy, I would confine antipsychotics to pain patients with delirium or psychosis. Antipsychotics’ potential role in treating refractory pain might warrant further investigation.40

Stimulants may reduce sedation, dysphoria, and cognitive inefficiency that can accompany opioid use.

Table 4

Uses of psychotropics in patients with chronic pain

Class/drugUsesLimitations
AntidepressantsNeuropathic pain, tension and migraine headache, FM, functional GI disorders, pain comorbid with depression/anxietyNE/5-HT reuptake inhibitors are most effective for analgesia; side effects (TCAs may be least tolerable); drug interactions
AnticonvulsantsNeuropathic pain, migraine headache, central pain, phantom limb painSide effects (sedation, motor and GI effects, rash); drug interactions
BenzodiazepinesMuscle relaxation, restless legs syndrome, anxiety, insomniaAbuse/dependence potential; sedation
LithiumCluster headache prophylaxisNot effective for episodic cluster headache; risk of toxicity if dehydration occurs or with certain drug combinations
StimulantsOpioid analgesia augmentation, opioid-induced fatigue and sedationAbuse/dependence potential; overstimulation, anorexia, insomnia
StimulantsOpioid analgesia augmentation, opioid-induced fatigue and sedationAbuse/dependence potential; overstimulation, anorexia, insomnia
AntipsychoticsNeuropathic pain, migraine, cancer pain, deliriumLimited data; risks such as EPS and TD may outweigh benefi ts
EPS: extrapyramidal symptoms; FM: fibromyalgia; GI: gastrointestinal; NE: norepinephrine; 5-HT: serotonin; TCAs: tricyclic antidepressants; TD: tardive dyskinesia
Source: Adapted from reference 3

Table 5

Psychotropics approved for managing pain

DrugIndication
CarbamazepineTrigeminal neuralgia
DivalproexMigraine prophylaxis
DuloxetineDiabetic neuropathy
GabapentinPostherpetic neuralgia
PregabalinPostherpetic neuralgia, diabetic neuropathy, fibromyalgia
Source: Adapted from reference 3
Related resource
  • International Association for the Study of Pain. www.iasp-pain.org.
  • Leo RJ. Clinical manual of pain management in psychiatry. Washington, DC: American Psychiatric Publishing; 2007.
  • Loeser JD, Butler SH, Chapman CR, Turk DC. Bonica’s management of pain. 3rd ed. Philadelphia, PA: Lippincott, Williams & Wilkins; 2001.
Drug brand names
  • Acetaminophen/hydrocodone • Lortab, others
  • Amitriptyline • Elavil, Endep
  • Carbamazepine • Tegretol
  • Divalproex • Depakote
  • Duloxetine • Cymbalta
  • Fentanyl transdermal • Duragesic
  • Gabapentin • Neurontin
  • Lithium • Eskalith, Lithobid
  • Pregabalin • Lyrica
Disclosure

Dr. Leo reports no financial relationship with any company whose products are mentioned in this article or with manufacturers of competing products.