Peripheral Neuropathy e-Support


Here is a synopsis of Dr. Wolfe's article, composed by Jo Nell Wilder. If you would like to see a PDF format version of the whole article click here.

Painful Peripheral Neuropathy

Gil I.Wolfe, MD*
Richard J. Barohn, MD
Address
*Department of Neurology
University of Texas Southwestern Medical Center
5323 Harry Hines Boulevard
Dallas, TX 75390-8897, USA.
E-mail: gil.wolfe@utsouthwestern.edu
Current Treatment Options in Neurology 2002, 4:177­188
Current Science Inc. ISSN 1092-8480
Copyright © 2002 by Current Science Inc.

 

Primary care physicians, neurologists, and other specialists commonly encounter peripheral neuropathies associated with neuropathic pain. It has been estimated that neuropathic pain affects at least 2% of the US population. Painful peripheral neuropathies can be challenging to evaluate and treat. The cause of the peripheral neuropathy may remain unknown in a majority of patients, the so called idiopathic or cryptogenic sensory polyneuropathies. The inability to identify a specific etiology for the neuropathy can be frustrating for both patients and their clinicians. Of identifiable etiologies, diabetes and alcohol abuse are the most common, but there are a large number of other causes (Table 1).

Opinion statement


Table 1. Causes of painful peripheral neuropathy


Major causes of painful peripheral neuropathy
Idiopathic or cryptogenic
Diabetes
Alcohol abuse and malnutrition
HIV infection or AIDS
Post-herpetic
Other causes of painful peripheral neuropathy
Amyloidosis
Cancer
Fabry disease
Guillian-Barré syndrome
Hereditary sensory and autonomic neuropathies (HSAN)
Leprosy
Lyme disease
Medications
Metronidazole
Misonidazole
Nitrofurantoin
Suramin
Taxol
Thalidomide
2',3'-dideoxycytidine (ddC)
2',3'-dideoxyinosine (ddI)
Porphyria
Sarcoidosis
Sjögren's syndrome
Tangier disease
Toxins
Arsenic
Thallium
Vasculitis
Vitamin deficiency
Thamine
Pyridoxine (vitamin B6)
Pantothenic acid
Cobalamin (vitamin B12)
Uremia

Treatment

Topical agents

Capsaicin Capsaicin, an alkaloid extracted from chili peppers that depletes substance P from sensory nerves, has had a significant effect on neuropathic pain in a majority of studies of diabetic neuropathy. a positive effect for capsaicin.

Standard dosage 0.075% capsaicin cream is applied to the painful area three to four times daily. Contraindications Prior hypersensitivity to topical application or to hot peppers. Main drug interactions No significant interactions for topical use. Main side effects Transient burning, sneezing, coughing, and skin irritation and rash. Special points Capsaicin cream is available over-the-counter. The cream should be used in well ventilated areas, and patients should avoid rubbing their eyes after use. Nonsteroidal anti-inflammatory agents may be added if the initial burning from capsaicin is intense. This side effect usually improves over several weeks.

Special points Percutaneous electrical nerve stimulation has decreased the daily oral analgesic requirements in a number of chronic pain states. Based on current studies, it should be viewed as an adjunctive, and not primary, therapy.

Transcutaneous stimulation
Transcutaneous electrical stimulation (TENS) is widely used in neuromuscular and pain syndromes, although its efficacy is actively debated. Response to this noninvasive technique varies significantly between studies and patients.

Standard procedure Treatment with TENS units generally begins daily, with stimulation sessions lasting 30 minutes or longer. Over time, one can reduce the frequency of treatment sessions, although the analgesic effect is transient, and the procedure needs to be repeated at least every few weeks. Contraindications None. Complications Essentially none. Some patients find it difficult to tolerate the surface stimulation due to allodynia. Special points Individual adjustments of the pulse waveform, duration, frequency, and voltage are required to maximize the clinical response.

Magnetic therapy
Annual worldwide spending for magnetic devices to treat pain is estimated to be in the billions of dollars. Public acceptance of subthreshold magnetic devices is largely based on anecdotal statements, although rigorous trials are now being performed to test this alternative approach. A preliminary randomized, sham-controlled crossover study of magnetic insoles in peripheral neuropathic pain provides some basis for efficacy. However, the study was small, diabetic patients responded far better than non-diabetics, and no group was ever assigned to sham magnets for both feet at the same time, complicating the analysis. Results from a larger, double blinded, placebo-controlled study of magnetic insoles in diabetic neuropathy are pending.

Complications Essentially none. The uneven surface of some magnetic insoles may place neuropathy patients with foot ulceration or sores at risk

Neuromuscular Disorders


Contacts

E-Mail Support, Jo Nell Wilder at tcjennin@earthlink.net

WebMaster, Dwain Wilder dwain@bearmeadow.com

We extend our appreciation to the Neuropathy Association in New York City (1-800-247-6968) for their help in getting our Support Group organized, and to all the volunteers who helped with their expertise.

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