Table 1.
Available pharmacotherapy for neuropathic pain
| Drug | Mechanisms of action | NNT* (range) | Adverse effects | Precautions and contraindications |
|---|---|---|---|---|
| Tricyclic antidepressants | ||||
|
| ||||
| Nortriptyline, desipramine, amitriptyline, clomipramine and imipramine | Monoamine reuptake inhibition, sodium channel blockade and anticholinergic effects | 3.6 (3–4.4) | Somnolence, anticholinergic effects and weight gain | • Cardiac disease, glaucoma, prostatic adenoma and seizure • High doses should be avoided in adults >65 years of age and in those with amyloidosis |
|
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| Serotonin-noradrenaline reuptake inhibitors | ||||
|
| ||||
| Duloxetine | Serotonin and noradrenaline reuptake inhibition | 6.4 (5.2–8.2) | Nausea, abdominal pain and constipation | • Hepatic disorder and hypertension • Use of tramadol |
|
| ||||
| Venlafaxine | Serotonin and noradrenaline reuptake inhibition | 6.4 (5.2–8.2) | Nausea and hypertension at high doses | • Cardiac disease and hypertension • Use of tramadol |
|
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| Calcium channel α2δ ligands | ||||
|
| ||||
| Gabapentin, extended-released gabapentin and enacarbil, and pregabalin | Act on the α2δ subunit of voltage-gated calcium channels, which decrease central sensitization | • 6.3 (5–8.4 for gabapentin) • 8.3 (6.2–13 for extended-released gabapentin and enacarbil) • 7.7 (6.5–9.4 for pregabalin) |
Sedation, dizziness, peripheral oedema and weight gain | Reduce dose in patients with renal insufficiency |
|
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| Topical lidocaine | ||||
|
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| Lidocaine 5% plaster | Sodium channel blockade | Not reported | Local erythema, itching and rash | None |
|
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| Capsaicin high-concentration patch (8%) | Transient receptor potential cation channel subfamily V member 1 agonist | 10.6 (7.4–19) | Pain, erythema, itching and rare cases of high blood pressure (initial increase in pain) | No overall impairment of sensory evaluation after repeated applications and caution should be taken in progressive neuropathy |
|
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| Opioids | ||||
|
| ||||
| Tramadol | μ-Receptor agonist and monoamine reuptake inhibition | 4.7 (3.6–6.7) | Nausea, vomiting, constipation, dizziness and somnolence | History of substance abuse, suicide risk and use of antidepressant in elderly patients |
|
| ||||
| Morphine and oxycodone | μ-Opioid receptor agonists; oxycodone might also cause κ-opioid receptor antagonism | 4.3 (3.4–5.8) | Nausea, vomiting, constipation, dizziness and somnolence | History of substance abuse, suicide risk and risk of misuse in the long term |
|
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| Neurotoxin | ||||
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| Botulinum toxin A | Acetylcholine release inhibitor and neuromuscular-blocking agent; potential effects on mechanotransduction and central effects in neuropathic pain | 1.9 (1.5–2.4) | Pain at injection site | Known hypersensitivity and infection of the painful area |
Number needed to treat (NNT) for 50% pain relief represents the number of patients necessary to treat to obtain one responder more than the comparison treatment, typically placebo101.