Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-g7gxr Total loading time: 0 Render date: 2024-11-10T02:33:09.617Z Has data issue: false hasContentIssue false

3 - Which Antiseizure Medicines Treat Epilepsy and How Do I Pick?

Published online by Cambridge University Press:  28 January 2023

Patrick Landazuri
Affiliation:
University of Kansas Medical Centre
Nuria Lacuey Lecumberri
Affiliation:
University of Texas Health Science Center, Houston
Laura Vilella Bertran
Affiliation:
University of Texas Health Science Center, Houston
Mark Farrenburg
Affiliation:
University of Kansas Medical Centre
Samden Lhatoo
Affiliation:
University of Texas Health Science Center, Houston
Get access

Summary

Antiseizure medicines (ASMs) are medicines that reduce seizure frequency. They work by influencing cellular electrical channels like sodium or neurotransmitters like GABA. They are very effective, with 65% of patients seizure-free within the first three ASMs that they take. Unfortunately, less than 1% of people are seizure-free with ASMs after failing three ASMs. These data inform the definition of drug-resistant epilepsy, which is failing two ASMs. Newer ASMs have not been found to be more effective. Lamotrigine has been shown to be better tolerated compared to several other medications. Divalproex has been specifically shown to be most effective for generalized epilepsy, but has a challenging side effect profile, particularly in women. Side effects can be a cause of poor ASM compliance. Proactively accounting for patient factors like psychiatric comorbidity or renal impairment can lead to better tolerability and thus improved compliance. Monotherapy is typically preferred. Polytherapy can be considered in specific situations as well.

Type
Chapter
Information
Seizure and Epilepsy Care
The Pocket Epileptologist
, pp. 41 - 56
Publisher: Cambridge University Press
Print publication year: 2023

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Works Cited

Marson, A, Burnside, G, Appleton, R et al. The SANAD II study of the effectiveness and cost-effectiveness of levetiracetam, zonisamide, or lamotrigine for newly diagnosed focal epilepsy: An open-label, non-inferiority, multicentre, phase 4, randomised controlled trial. Lancet. 2021;397(10282):1363–74.Google ScholarPubMed
Marson, AG, Al-Kharusi, AM, Alwaidh, M et al. The SANAD study of effectiveness of valproate, lamotrigine, or topiramate for generalised and unclassifiable epilepsy: An unblinded randomised controlled trial. Lancet. 2007;369(9566):1016–26.Google ScholarPubMed
Marson, A, Burnside, G, Appleton, R et al. The SANAD II study of the effectiveness and cost-effectiveness of valproate versus levetiracetam for newly diagnosed generalised and unclassifiable epilepsy: An open-label, non-inferiority, multicentre, phase 4, randomised controlled trial. Lancet. 2021;397(10282):1375–86.Google ScholarPubMed
Jiruska, P, de Curtis, M, Jefferys, JG et al. Synchronization and desynchronization in epilepsy: controversies and hypotheses. J Physiol. 2013;591(4):787–97.CrossRefGoogle ScholarPubMed
Abou-Khalil, BW. Update on antiepileptic drugs 2019. Continuum. 2019;25(2):508–36.Google ScholarPubMed
Steffens, M, Huppertz, HJ, Zentner, J, Chauzit, E, and Feuerstein, TJ. Unchanged glutamine synthetase activity and increased NMDA receptor density in epileptic human neocortex: Implications for the pathophysiology of epilepsy. Neurochem Int. 2005;47(6):379–84.Google Scholar
Chen, Z, Brodie, MJ, Liew, D, and Kwan, P. Treatment outcomes in patients with newly diagnosed epilepsy treated with established and new antiepileptic drugs: A 30-year longitudinal cohort study. JAMA Neurol. 2018;75(3):279–86.CrossRefGoogle ScholarPubMed
Tokudome, K, Okumura, T, Shimizu, S et al. Synaptic vesicle glycoprotein 2A (SV2A) regulates kindling epileptogenesis via GABAergic neurotransmission. Sci Rep. 2016;6:27420.CrossRefGoogle ScholarPubMed
Krauss, GL, Serratosa, JM, Villanueva, V et al. Randomized phase III study 306: Adjunctive perampanel for refractory partial-onset seizures. Neurology. 2012;78(18):1408–15.CrossRefGoogle ScholarPubMed
French, JA, Krauss, GL, Biton, V et al. Adjunctive perampanel for refractory partial-onset seizures: Randomized phase III study 304. Neurology. 2012;79(6):589–96.Google Scholar
Kwan, P and Brodie, MJ. Early identification of refractory epilepsy. N Engl J Med. 2000;342(5):314–19.CrossRefGoogle ScholarPubMed
Kwan, P and Brodie, MJ. Effectiveness of first antiepileptic drug. Epilepsia. 2001;42(10):1255–60.CrossRefGoogle ScholarPubMed
Brodie, MJ, Barry, SJ, Bamagous, GA, Norrie, JD and Kwan, P. Patterns of treatment response in newly diagnosed epilepsy. Neurology. 2012;78(20):1548–54.CrossRefGoogle ScholarPubMed
Kwan, P, Arzimanoglou, A, Berg, AT et al. Definition of drug resistant epilepsy: Consensus proposal by the ad hoc Task Force of the ILAE Commission on Therapeutic Strategies. Epilepsia. 2010;51(6):1069–77.Google Scholar
Marson, AG, Al-Kharusi, AM, Alwaidh, M et al. The SANAD study of effectiveness of carbamazepine, gabapentin, lamotrigine, oxcarbazepine, or topiramate for treatment of partial epilepsy: An unblinded randomised controlled trial. Lancet. 2007;369(9566):1000–15.Google ScholarPubMed
Baulac, M, Rosenow, F, Toledo, M et al. Efficacy, safety, and tolerability of lacosamide monotherapy versus controlled-release carbamazepine in patients with newly diagnosed epilepsy: A phase 3, randomised, double-blind, non-inferiority trial. Lancet Neurol. 2017;16(1):4354.CrossRefGoogle ScholarPubMed
Trinka, E, Ben-Menachem, E, Kowacs, PA et al. Efficacy and safety of eslicarbazepine acetate versus controlled-release carbamazepine monotherapy in newly diagnosed epilepsy: A phase III double-blind, randomized, parallel-group, multicenter study. Epilepsia. 2018;59(2):479–91.CrossRefGoogle ScholarPubMed
Trinka, E, Marson, AG, van Paesschen, W et al. KOMET: An unblinded, randomised, two parallel-group, stratified trial comparing the effectiveness of levetiracetam with controlled-release carbamazepine and extended-release sodium valproate as monotherapy in patients with newly diagnosed epilepsy. J Neurol Neurosurg Psychiatry. 2013;84(10):1138–47.CrossRefGoogle ScholarPubMed
Brodie, MJ, Perucca, E, Ryvlin, P, Ben-Menachem, E, and Meencke, HJ. Comparison of levetiracetam and controlled-release carbamazepine in newly diagnosed epilepsy. Neurology. 2007;68(6):402–8.CrossRefGoogle ScholarPubMed
Baulac, M, Brodie, MJ, Patten, A, Segieth, J, and Giorgi, L. Efficacy and tolerability of zonisamide versus controlled-release carbamazepine for newly diagnosed partial epilepsy: A phase 3, randomised, double-blind, non-inferiority trial. Lancet Neurol. 2012;11(7):579–88.Google Scholar
Glauser, TA, Cnaan, A, Shinnar, S et al. Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy: Initial monotherapy outcomes at 12 months. Epilepsia. 2013;54(1):141–55.CrossRefGoogle ScholarPubMed
Perucca, E, Brodie, MJ, Kwan, P, and Tomson, T. 30 years of second-generation antiseizure medications: Impact and future perspectives. Lancet Neurol. 2020;19(6):544–56.CrossRefGoogle ScholarPubMed
Manjunath, R, Davis, KL, Candrilli, SD, and Ettinger, AB. Association of antiepileptic drug nonadherence with risk of seizures in adults with epilepsy. Epilepsy Behav. 2009;14(2):372–8.Google Scholar
Alsfouk, BAA, Brodie, MJ, Walters, M, Kwan, P, and Chen, Z. Tolerability of antiseizure medications in individuals with newly diagnosed epilepsy. JAMA Neurol. 2020;77(5):574–81.CrossRefGoogle ScholarPubMed
Perucca, E and Tomson, T. The pharmacological treatment of epilepsy in adults. Lancet Neurol. 2011;10(5):446–56.CrossRefGoogle ScholarPubMed
Lezaic, N, Gore, G, Josephson, CB et al. The medical treatment of epilepsy in the elderly: A systematic review and meta-analysis. Epilepsia. 2019;60(7):1325–40.CrossRefGoogle ScholarPubMed
Werhahn, KJ, Trinka, E, Dobesberger, J et al. A randomized, double-blind comparison of antiepileptic drug treatment in the elderly with new-onset focal epilepsy. Epilepsia. 2015;56(3):450–9.CrossRefGoogle ScholarPubMed
Sabers, A. Algorithm for lamotrigine dose adjustment before, during, and after pregnancy. Acta Neurol Scand. 2012;126(1):e1e4.CrossRefGoogle Scholar
Aícua-Rapún, I, André, P, Rossetti, AO et al. Therapeutic drug monitoring of newer antiepileptic drugs: A randomized trial for dosage adjustment. Ann Neurol. 2020;87(1):22–9.CrossRefGoogle ScholarPubMed
Deckers, CL, Hekster, YA, Keyser, A et al. Monotherapy versus polytherapy for epilepsy: A multicenter double-blind randomized study. Epilepsia. 2001;42(11):1387–94.Google Scholar
Beghi, E, Gatti, G, Tonini, C et al. Adjunctive therapy versus alternative monotherapy in patients with partial epilepsy failing on a single drug: A multicentre, randomised, pragmatic controlled trial. Epilepsy Res. 2003;57(1):113.CrossRefGoogle ScholarPubMed
Abou-Khalil, B. Selecting rational drug combinations in epilepsy. CNS Drugs. 2017;31(10):835–44.CrossRefGoogle ScholarPubMed
Sarhan, EM, Walker, MC, and Selai, C. Evidence for efficacy of combination of antiepileptic drugs in treatment of epilepsy. J Neurol. Res. 2016;5(6):267–76.Google Scholar
Margolis, JM, Chu, BC, Wang, ZJ, Copher, R, and Cavazos, JE. Effectiveness of antiepileptic drug combination therapy for partial-onset seizures based on mechanisms of action. JAMA Neurol. 2014;71(8):985–93.CrossRefGoogle ScholarPubMed
Poolos, NP, Warner, LN, Humphreys, SZ, and Williams, S. Comparative efficacy of combination drug therapy in refractory epilepsy. Neurology. 2012;78(1):62–8.Google Scholar

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×