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  • The Internet Journal of Pharmacology
  • Volume 1
  • Number 1

Original Article

Anti-epileptic Drugs For Pain Management

A Burton

Keywords

anti-epileptic medication, chronic pain, medicine, pain, pain management, palliative care, symptom control

Citation

A Burton. Anti-epileptic Drugs For Pain Management. The Internet Journal of Pharmacology. 2000 Volume 1 Number 1.

Abstract

Antiepileptic drugs (AED's) depress abnormal neuronal discharges and raise the threshold for neural impulse propagation. They have been found to have therapeutic efficacy in neuropathic pain states. Carbamazepine(CZ) and phenytoin (PT) were the drugs of choice for treating trigeminal neuralgia for 40 plus years. These two agents have been largely replaced due to the introduction of many newer, better-tolerated, and safer antiepileptic drugs.

 

Clinical Use/Mechanism of Action/Side Effects:

There has been an explosion in the number of available AEDs. Many studies are ongoing to evaluate their efficacy in neuropathic pain states. Only CZ, PT, gabapentin (GB), and lamotrigine (LT) have been evaluated in double blind trials. (4,5,6)

Some tenets of use are common in all of these medications. Initial dosing should be done at a low dose administered at bedtime, increased slowly up to a therapeutic level over 4 to 8 weeks. These medications do not have a ceiling dose, but are usually more effective at higher doses. Clinically the dose should be titrated upwards until side effects are encountered, then back down a small amount. The pain relief obtained is gradual with most agreeing that an adequate trial of an AED for pain should last 4-8 weeks at therapeutic doses prior to calling a medication ineffective.

A brief summary of clinical uses, mechanism of action, and side effects will be presented for the following AEDs.

Conclusion

AED’s depress abnormal neuronal discharges and raise the threshold for neural impulse propagation. They have been found to have therapeutic efficacy in neuropathic pain states. The older AED’s have been largely replaced due to the introduction of many newer, better-tolerated, and safer antiepileptic drugs. (3) The AED of choice for different painful states has not yet been determined, nor has an algorithm of use been developed for the newer agents.

References

1. Hunter JC, Gogas KR, Hedley LR, etal. The effect of novel anti-epileptic drugs in rats with an experimental peripheral neuropathy. J Pharmacol Exp Ther 1995;273:878-86.
2. Nicol CF. A four year double blind study of tegretol in facial pain. Headache 1969;9:54-7.
3. White HS. Comparative anticonvulsant and mechanistic profile of the established and newer antiepileptic drugs. Epilepsia 1999;40 Suppl 5:S2-10.
4. Backonja M, BeydounA, Edwards KR, et al. Gabapentin for the symptomatic treatment of painful neuropathy in patients with diabetes mellitis: a randomized clinical trial. JAMA 1998;280:1837-42.
5. Rowbotham M, Harden N, Stacey B, Podolnick P, Magnus-Miller L. Gabapentin for the treatment of post-herpetic neuralgia: a randomized clinical trial. JAMA 1998;280:1837-42.
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9. Saudek CD, Werns S, Reidenberg MM. Phenytoin in the treatment of diabetic symmetrical polyneuropathy. Clin Pharmacol Ther 1977; 22:196-9.
10. Ghose K and Niven B. Prophylactic sodium valproate therapy in patients with drug resistant migraine. Methods Exp Clin Pharmacol 1998; 20(4):353-9.
11. Candis MM, Susan GL, Carol PS. Effects of gabapentin compared to amitryptiline on pain in diabetic neuropathy. Diabetes 1998;47:A374.
12. McCleane GJ. Lamotrigine in the management of neuropathic pain: a review of the literature. Clin Jnl Pain 2000; 16:321-326.
13. Perucc E, BialerM. The clinical pharmacokinetics of the newer antiepileptic drugs. Focus on topiramate, zonisamaide, and tiagibine. Clin Pharmcokinet 31:29-46.
14. Remillard G. Oxcarbezepine in the treatment of trigeminal neuralgia. Epilepsia 1994;35 (S3):S28-29.
15. Mellick GA. Hemifacial spasm, successful treatment with felbamate. J Pain Sympt Manage 1995:10:392-5.
16. Leppik IE. Zonisamide. Epilepsia 1999;40 (S5):S23-9.

Author Information

Allen W Burton, MD, Associate Professor of Anesthesiology, Critical, and Palliative Care
Section Chief of Pain Management, Anesthesiology, Critical, and Palliative Care, University of Texas MD Anderson Cancer Center

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