anticonvulsant
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Introduction
See specific agent
Indications
- prevention & treatment of seizures
- also used for treatment of:[7]
- akathisia, attention-deficit hyperactivity disorder, pain, trigeminal neuralgia, glossopharyngeal neuralgia, neuropathic pain, postoperative pain, post herpetic neuralgia, migraine prophylaxis, anxiety, panic disorder, alcoholic withdrawal syndrome, delirium tremens, ischemic heart disease, menopause, hot flash, essential tremor, head injury, amnesia, depression, bipolar disorder, mania, tetanus, muscle spasms, infantile spasms. restless legs syndrome
- used in narcoanalysis, general anesthesia, neurosurgery, sedation[7]
Dosage
- generics may differ in bioavailability by as much as 20%
- use same manufacturer from month to month[10]
- consider tapering of dosage if
- seizure-free for 2-5 years
- not juvenile myoclonic epilepsy
- history of difficulty in seizure control
- risk factors for epilepsy
Adverse effects
- suicide, 2-fold risk of suicidal behavior or ideation compared to patients receiving placebo
- withdrawal effects with abrupt discontinuation[3]
- Stevens-Johnson syndrome -> toxic epidermal necrolysis
- major congenital malformations range from 2.0-4.2% vs 2.2% in unexposed group[4]
- probably not associated with increased risk for miscarriage or stillbirth [9]
- may increase bone catabolism (supplement vitamin D & calcium)[10]
- osteopenia & osteoporosis less with lamotrigine or levetiracetam than carbamazepine, phenytoin, valproate, phenobarbital[10]
- association between epilepsy & cardiovascular events in elderly largely due to enzyme-inducing anticonvulsants [16]
- strong enzyme-inducing anticonvulsants include:
- weak enzyme-inducing anticonvulsants include:
- of the cardiovascular events, strong enzyme-inducing anticonvulsant appear to have the largest effect on myocardial infarction (59%)[16]
Drug interactions
- some antibiotics, antihistamines, antipsychotics & analgesics can lower the seizure threshold & interact negatively with anticonvulsants (see drugs causing seizures)[10]
- anticonvulsants may increase statin clearance[10]
- drug interaction(s) anticonvulsants with anti-bacterial agents
- drug interaction(s) anticonvulsants with statins
Notes
- change in pill color may be associated with non-compliance, especially in patients with anticonvulsants[5]
- lamotrigine, levetiracetam, topiramate, valproate & zonisamide are broad spectrum agents that may be used to treat both generalized & partial seizures[10]
- among anticonvulsants used as monotherapy in poststroke epilepsy, lamotrigine is associated with the lowest risk for mortality, valproate the highest[15]
More general terms
More specific terms
- amobarbital (Amytal)
- brivaracetam (Briviact)
- carbamazepine; CBZ (Tegretol, Atretol, Eiptol, Carbatrol, Equetro)
- cenobamate (Xcopri)
- clonazepam (Klonopin)
- diazepam (Vallium, Diastat)
- eslicarbazepine acetate (Aptiom)
- ethosuximide (Zarontin)
- ethotoin; 3-ethyl-5-phenyl-2,4-imidazolidinedione (Peganone)
- ezogabine (Potiga, retigabine)
- felbamate (Felbatol)
- fosphenytoin (Cerebyx)
- gabapentinoid; GABA analog
- ganaxolone (Ztalmy)
- lacosamide (Vimpat, erlosamide, harkoseride)
- lamotrigine (Lamictal, Lamictal ODT, Lamictal XR)
- levetiracetam (Keppra, Etiracetam, Spritam)
- mephenytoin; methoin; methylphenylethylhydantoin (Mesantoin)
- methsuximide (Celontin, Kapseal)
- oxcarbazepine (Trileptal)
- paramethadione; paradione
- perampanel (Fycompa)
- phenacemide; phenylacetylurea; phenurone; cetylureum
- phenobarbital; PB; PHB (Luminal, Barbita, Solfoton)
- phensuximide (Milontin)
- phenylethylmalonamide (PEMA)
- phenytoin; diphenylhydantoin; PTN (Dilantin, Dephenylan, Antilepsin)
- primidone; desoxyphenobarbital (Primaclone, Mysoline)
- rufinamide (Banzel, Inovelon, Xilep)
- stiripentol (Diacomit)
- sulthiame; trolone; sulphenyltame; sulthiamine; (Ospolot)
- tiagabine (Gabitril)
- topiramate (Topamax, Qudexy XR, Trokendi XR)
- trimethadione (Tridione)
- valproic acid; n-dipropylacetic acid (Depakene, Depakote, Divalproex, Mylproin, Valontin, Stavzor)
- vigabatrin (Sabril)
- zonisamide (Zonegran)
References
- ↑ Prescriber's Letter 11(12): 2004 Comparison of FDA-Approved Antiepileptic Drugs Detail-Document#: http://prescribersletter.com/(5bhgn1a4ni4cyp2tvybwfh55)/pl/ArticleDD.aspx?li=1&st=1&cs=&s=PRL&pt=3&fpt=25&dd=201213&pb=PRL (subscription needed) http://www.prescribersletter.com
- ↑ Prescriber's Letter 14(7): 2007 Generic Substitution of Antiepileptic Drugs Detail-Document#: http://prescribersletter.com/(5bhgn1a4ni4cyp2tvybwfh55)/pl/ArticleDD.aspx?li=1&st=1&cs=&s=PRL&pt=3&fpt=25&dd=230712&pb=PRL (subscription needed) http://www.prescribersletter.com
- ↑ 3.0 3.1 FDA News FDA Requires Warnings about Risk of Suicidal Thoughts and Behavior for Antiepileptic Medications Dec. 16, 2008 http://www.fda.gov/bbs/topics/NEWS/2008/NEW01927.html
- ↑ 4.0 4.1 Hernandez-Diaz S et al. Comparative safety of antiepileptic drugs during pregnancy. Neurology 2012 May 22; 78:1692. PMID: https://www.ncbi.nlm.nih.gov/pubmed/22551726
- ↑ 5.0 5.1 Kesselheim AS et al. Variations in pill appearance of antiepileptic drugs and the risk of nonadherence. Arch Intern Med 2012 Dec 31 <PubMed> PMID: https://www.ncbi.nlm.nih.gov/pubmed/23277164 <Internet> http://archinte.jamanetwork.com/article.aspx?articleid=1487287
- ↑ Arif H, Buchsbaum R, Pierro J et al Comparative effectiveness of 10 antiepileptic drugs in older adults with epilepsy. Arch Neurol. 2010 Apr;67(4):408-15 PMID: https://www.ncbi.nlm.nih.gov/pubmed/20385905
- ↑ 7.0 7.1 7.2 Deprecated Reference
- ↑ Arif H, Buchsbaum R, Weintraub D et al Comparison and predictors of rash associated with 15 antiepileptic drugs. Neurology. 2007 May 15;68(20):1701-9. PMID: https://www.ncbi.nlm.nih.gov/pubmed/17502552
- ↑ 9.0 9.1 Bech BH et al Use of antiepileptic drugs during pregnancy and risk of spontaneous abortion and stillbirth: population based cohort study. BMJ 2014;349:g5159 <PubMed> PMID: https://www.ncbi.nlm.nih.gov/pubmed/25150301 <Internet> http://www.bmj.com/content/349/bmj.g5159
- ↑ 10.0 10.1 10.2 10.3 10.4 10.5 10.6 Medical Knowledge Self Assessment Program (MKSAP) 17, 18. American College of Physicians, Philadelphia 2015, 2018.
Medical Knowledge Self Assessment Program (MKSAP) 19 Board Basics. An Enhancement to MKSAP19. American College of Physicians, Philadelphia 2022 - ↑ Glauser T, Ben-Menachem E, Bourgeois B et al Updated ILAE evidence review of antiepileptic drug efficacy and effectiveness as initial monotherapy for epileptic seizures and syndromes. Epilepsia. 2013 Mar;54(3):551-63. PMID: https://www.ncbi.nlm.nih.gov/pubmed/23350722
- ↑ Israni RK, Kasbekar N, Haynes K, Berns JS. Use of antiepileptic drugs in patients with kidney disease. Semin Dial. 2006 Sep-Oct;19(5):408-16. PMID: https://www.ncbi.nlm.nih.gov/pubmed/16970741
- ↑ 13.0 13.1 Tomson T, Battino D, Bonizzoni E, et al Comparative risk of major congenital malformations with eight different antiepileptic drugs: a prospective cohort study of the EURAP registry. Lancet Neurology. April 18, 2018 <PubMed> PMID: https://www.ncbi.nlm.nih.gov/pubmed/29680205 <Internet> http://www.thelancet.com/journals/laneur/article/PIIS1474-4422(18)30107-8/fulltext
Pennell PB Prescribing antiepileptic drugs to women of reproductive age. Lancet Neurology. April 18, 2018 <PubMed> PMID: https://www.ncbi.nlm.nih.gov/pubmed/29680207 <Internet> http://www.thelancet.com/journals/laneur/article/PIIS1474-4422(18)30154-6/fulltext - ↑ Schmidt D. Starting, Choosing, Changing, and Discontinuing Drug Treatment for Epilepsy Patients. Neurol Clin. 2016 May;34(2):363-81, viii. Review. PMID: https://www.ncbi.nlm.nih.gov/pubmed/27086984
- ↑ 15.0 15.1 Swift Yasgur B Lamotrigine Linked to Lowest Mortality Risk in Poststroke Epilepsy. Medscape. Jan 7, 2022 https://www.medscape.com/viewarticle/966285
- ↑ 16.0 16.1 16.2 Li J, Shlobin NA, Thijs RD et al Antiseizure Medications and Cardiovascular Events in Older People With Epilepsy. JAMA Neurol. 2024 Sep 30. PMID: https://www.ncbi.nlm.nih.gov/pubmed/39348143 https://jamanetwork.com/journals/jamaneurology/fullarticle/2824203