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280<br />

Neuropathy – diabetic<br />

DAVID CLINE<br />

n Agents<br />

n Opioids<br />

n Tricyclic antidepressants<br />

n SSRIs<br />

n Selective serotonin–norepinephrine reuptake inhibitors<br />

n Anticonvulsants<br />

n Local anesthetics<br />

n Evidence<br />

Treatment decisions regarding diabetic neuropathy (DN) can be based upon<br />

useful evidence. Many agents have been assessed for therapy of DN pain, and<br />

many have some role in relief of symptoms. The breadth of therapeutic<br />

options is fortunate, given the often-refractory nature of the pain. The difficulty<br />

of controlling DN is ameliorated by the availability of several nonpharmacologic<br />

approaches (e.g. transcutaneous electrical nerve stimulator<br />

[TENS] units) that can improve pain relief provided by drug therapy. 1,2<br />

Although their side effects may relegate them to second-line use, the<br />

opioids do help in DN. Data from RCTs have demonstrated the utility of<br />

controlled-release oxycodone (starting dose 10 mg PO BID, with up-titration<br />

to a maximum of 60 mg daily). 3<br />

The opioid tramadol, which has additional (monoamine-related) mechanisms<br />

of analgesia, has particular utility in DN. Data from RCTs show that one<br />

in four patients achieves significant pain relief; analgesic benefit lasts for<br />

months. 4 Up-titration may be necessary. One RCT found that the average<br />

daily dose of tramadol required for significant relief of DN was 210 mg. 5<br />

As noted in other chapters of this text, the tricyclic antidepressants (TCAs)<br />

are among the most consistently effective therapy for neuropathic pain.<br />

Systematic review of studies including patients with DN (among others)

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