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302 Neuropathy – phantom limb pain<br />

200 IU) is a treatment of choice for acute PLP flares. 1,12 As with other agents<br />

with which ED providers may not be familiar, quick reference for safety<br />

purposes (e.g. withholding of calcitonin in hypocalcemic patients) is necessary.<br />

For patients with hypersensitivity to fish (in whom the nasal salmon<br />

preparation is contraindicated), a human calcitonin preparation may be used.<br />

The benzodiazepines, which potentiate the spinal neuronal inhibitory<br />

effects of gamma-aminobutyric acid (GABA), may ameliorate pain from<br />

acute PLP flares. Case reports suggest that both clonazepam and midazolam<br />

are effective. 13,14 The familiarity of ED providers with safe use of midazolam<br />

makes this an attractive choice. Slow infusion of up to 3–5 mg(over<br />

10–20 min, with meticulous ventilatory monitoring), is supported by the<br />

available case series data. 14,15<br />

Midazolam is not the only procedural sedation drug with potential utility<br />

for PLP. Multiple case series reports support ketamine use for acute PLP<br />

flares. 16,17<br />

In contradistinction to their utility in other forms of neuropathic pain,<br />

antidepressants have only a limited role for acute PLP; they may be useful<br />

as an aid to chronic management. 1 The exception may be the heterocyclic<br />

antidepressant mirtazapine, for which there is open-label case series evidence<br />

suggesting reduction in PLP via central mechanisms. 18<br />

The anticonvulsants have been investigated for PLP, with mixed results.<br />

Carbamazepine is postulated to be of utility, but supporting evidence for its<br />

use in PLP is anecdotal. 19 There is stronger evidence for gabapentin prescription<br />

in PLP. Case series evidence suggests utility for gabapentin, and a<br />

clinical trial calculated that about one in four patients will achieve significant<br />

pain relief with gabapentin. 20,21 Another RCT suggested limited gabapentin<br />

efficacy. In this RCT, although over half of participants had a meaningful pain<br />

decrease during the gabapentin phase (compared with 20% in the placebo<br />

phase), no predefined efficacy endpoints were met. 22<br />

Theoraldosingofgabapentin for NP follows an advancing regimen: 300 mg<br />

HS on day one, followed by 300 mg BID on day two, then 300 mg TID on day<br />

three. The drug can then be titrated up to 1800 mg/day over two weeks.<br />

Another anticonvulsant, topiramate, is found useful in individual<br />

time-series analyses. Three out of four amputee participants receiving

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