Zum Hauptinhalt springen

Persistent treatment resistance in genetic generalized epilepsy: A long-term outcome study in a tertiary epilepsy center.

Cerulli Irelli, E ; Morano, A ; et al.
In: Epilepsia, Jg. 61 (2020-11-01), Heft 11, S. 2452-2460
Online academicJournal

Titel:
Persistent treatment resistance in genetic generalized epilepsy: A long-term outcome study in a tertiary epilepsy center.
Autor/in / Beteiligte Person: Cerulli Irelli, E ; Morano, A ; Barone, FA ; Fisco, G ; Fanella, M ; Orlando, B ; Fattouch, J ; Manfredi, M ; Giallonardo, AT ; Di Bonaventura, C
Link:
Zeitschrift: Epilepsia, Jg. 61 (2020-11-01), Heft 11, S. 2452-2460
Veröffentlichung: Malden, MA : Blackwell Science ; <i>Original Publication</i>: Copenhagen : Munskgaard, 2020
Medientyp: academicJournal
ISSN: 1528-1167 (electronic)
DOI: 10.1111/epi.16708
Schlagwort:
  • Adult
  • Anticonvulsants pharmacology
  • Cohort Studies
  • Drug Resistant Epilepsy drug therapy
  • Drug Resistant Epilepsy genetics
  • Drug Resistant Epilepsy physiopathology
  • Electroencephalography trends
  • Epilepsy, Generalized physiopathology
  • Female
  • Humans
  • Longitudinal Studies
  • Male
  • Middle Aged
  • Myoclonic Epilepsy, Juvenile drug therapy
  • Myoclonic Epilepsy, Juvenile genetics
  • Myoclonic Epilepsy, Juvenile physiopathology
  • Retrospective Studies
  • Time Factors
  • Treatment Outcome
  • Valproic Acid pharmacology
  • Anticonvulsants therapeutic use
  • Electroencephalography drug effects
  • Epilepsy, Generalized drug therapy
  • Epilepsy, Generalized genetics
  • Valproic Acid therapeutic use
Sonstiges:
  • Nachgewiesen in: MEDLINE
  • Sprachen: English
  • Publication Type: Journal Article; Observational Study
  • Language: English
  • [Epilepsia] 2020 Nov; Vol. 61 (11), pp. 2452-2460. <i>Date of Electronic Publication: </i>2020 Oct 14.
  • MeSH Terms: Anticonvulsants / *therapeutic use ; Electroencephalography / *drug effects ; Epilepsy, Generalized / *drug therapy ; Epilepsy, Generalized / *genetics ; Valproic Acid / *therapeutic use ; Adult ; Anticonvulsants / pharmacology ; Cohort Studies ; Drug Resistant Epilepsy / drug therapy ; Drug Resistant Epilepsy / genetics ; Drug Resistant Epilepsy / physiopathology ; Electroencephalography / trends ; Epilepsy, Generalized / physiopathology ; Female ; Humans ; Longitudinal Studies ; Male ; Middle Aged ; Myoclonic Epilepsy, Juvenile / drug therapy ; Myoclonic Epilepsy, Juvenile / genetics ; Myoclonic Epilepsy, Juvenile / physiopathology ; Retrospective Studies ; Time Factors ; Treatment Outcome ; Valproic Acid / pharmacology
  • References: Mullen SA, Berkovic SF. Genetic generalized epilepsies. Epilepsia. 2018;59:1148–53. ; Jallon P, Latour P. Epidemiology of idiopathic generalized epilepsies. Epilepsia. 2005;46:10–4. ; Semah F, Picot M‐C, Adam C, Broglin D, Arzimanoglou A, Bazin B, et al. Is the underlying cause of epilepsy a major prognostic factor for recurrence? Neurology. 1998;51:1256–62. ; Mohanraj R, Brodie MJ. Outcomes of newly diagnosed idiopathic generalized epilepsy syndromes in a non‐pediatric setting. Acta Neurol Scand. 2007;115:204–8. ; Berg AT, Shinnar S, Levy SR, Testa FM, Smith‐Rapaport S, Beckerman B, et al. Two‐year remission and subsequent relapse in children with newly diagnosed epilepsy. Epilepsia. 2001;42:553–62. ; Seneviratne U, Cook M, D’Souza W. The prognosis of idiopathic generalized epilepsy. Epilepsia. 2012;53:2079–90. ; Szaflarski JP. Can EEG predict outcomes in genetic generalized epilepsies? Clin Neurophysiol. 2014;125:215–6. ; Geithner J, Schneider F, Wang Z, Berneiser J, Herzer R, Kessler C, et al. Predictors for long‐term seizure outcome in juvenile myoclonic epilepsy: 25–63 years of follow‐up. Epilepsia. 2012;53:1379–86. ; Camfield P, Camfield C. Idiopathic generalized epilepsy with generalized tonic‐clonic seizures (IGE‐GTC): a population‐based cohort with >20 year follow up for medical and social outcome. Epilepsy Behav. 2010;18:61–3. ; Geerts A, Arts WF, Stroink H, Peeters E, Brouwer O, Peters B, et al. Course and outcome of childhood epilepsy: A 15‐year follow‐up of the Dutch Study of Epilepsy in Childhood. Epilepsia. 2010;51:1189–97. ; Scheffer IE, Berkovic S, Capovilla G, Connolly MB, French J, Guilhoto L, et al. ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology. Epilepsia. 2017;58:512–21. ; Striano S, Striano P, Nocerino C, Boccella P, Bilo L, Meo R, et al. Eyelid myoclonia with absences: an overlooked epileptic syndrome? Neurophysiol Clin. 2002;32:287–96. ; Brenner RP, Atkinson R. Generalized paroxysmal fast activity: electroencephalographic and clinical features. Ann Neurol. 1982;11:386–90. ; Beghi E, Beretta S, Carone D, Zanchi C, Bianchi E, Pirovano M, et al. Prognostic patterns and predictors in epilepsy: a multicentre study (PRO‐LONG). J Neurol Neurosurg Psychiatry. 2019;90:1276–85. ; Gesche J, Khanevski M, Solberg C, Beier CP. Resistance to valproic acid as predictor of treatment resistance in genetic generalized epilepsies. Epilepsia. 2017;58:e64–e69. ; Vorderwülbecke BJ, Kowski AB, Kirschbaum A, Merkle H, Senf P, Janz D, et al. Long‐term outcome in adolescent‐onset generalized genetic epilepsies. Epilepsia. 2017;58:1244–50. ; Dragoumi P, Tzetzi O, Vargiami E, Pavlou E, Krikonis K, Kontopoulos E, et al. Clinical course and seizure outcome of idiopathic childhood epilepsy: determinants of early and long‐term prognosis. BMC Neurol. 2013;13:206. ; Ashmawi A, Hosny H, Abdelalim A, Bianchi E, Beghi E. The long‐term prognosis of newly diagnosed epilepsy in Egypt: a retrospective cohort study from an epilepsy center in Greater Cairo. Seizure. 2016;41:86–95. ; Nicolson A, Appleton RE, Chadwick DW, Smith DF. The relationship between treatment with valproate, lamotrigine, and topiramate and the prognosis of the idiopathic generalised epilepsies. J Neurol Neurosurg Psychiatry. 2004;75:75–9. ; Cerulli Irelli E, Morano A, Cocchi E, Casciato S, Fanella M, Albini M, et al. Doing without valproate in women of childbearing potential with idiopathic generalized epilepsy: Implications on seizure outcome. Epilepsia. 2020;61:107–14. ; Cerulli Irelli E, Cocchi E, Morano A, Casciato S, Fanella M, Albini M, et al. Valproate impact and sex‐dependent seizure remission in patients with Idiopathic Generalized Epilepsy. J Neurol Sci. 2020;415:116940. https://doi.org/10.1016/j.jns.2020.116940. ; Cação G, Parra J, Mannan S, Sisodiya SM, Sander JW. Juvenile myoclonic epilepsy refractory to treatment in a tertiary referral center. Epilepsy Behav. 2018;82:81–6. ; Myers KA, Scheffer IE, Berkovic SF. Genetic literacy series: genetic epilepsy with febrile seizures plus. Epileptic Disord. 2018;20:232–8. ; Bonanni P, Malcarne M, Moro F, Veggiotti P, Buti D, Ferrari AR, et al. Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations. Epilepsia. 2004;45:149–58. ; Zhang Y‐H, Burgess R, Malone JP, Glubb GC, Helbig KL, Vadlamudi L, et al. Genetic epilepsy with febrile seizures plus: refining the spectrum. Neurology. 2017;89:1210–9. ; Johannesen K, Marini C, Pfeffer S, Møller RS, Dorn T, Niturad CE, et al. Phenotypic spectrum of GABRA1: from generalized epilepsies to severe epileptic encephalopathies. Neurology. 2016;87:1140–51. ; Marini C, Porro A, Rastetter A, Dalle C, Rivolta I, Bauer D, et al. HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond. Brain. 2018;141:3160–78. ; Epi4K Consortium. De novo mutations in SLC1A2 and CACNA1A are important causes of epileptic encephalopathies. Am J Hum Genet. 2016;99:287–98. ; Lachance‐Touchette P, Martin C, Poulin C, Gravel M, Carmant L, Cossette P. Screening of GABRB3 in French‐Canadian families with idiopathic generalized epilepsy. Epilepsia. 2010;51(9):1894–7. ; Michelucci R, Rubboli G, Passarelli D, Riguzzi P, Volpi L, Parmeggiani L, et al. Electroclinical features of idiopathic generalised epilepsy with persisting absences in adult life. J Neurol Neurosurg Psychiatry. 1996;61:471–7. ; Aydin‐Özemir Z, Matur Z, Bebek N, Gürses C, Gökyiğit A, Baykan B. Long‐term follow‐up of adult patients with genetic generalized epilepsy with typical absence seizures and generalized paroxysmal fast activity in their EEG. Seizure. 2014;23:607–15. ; Guye M, Bartolomei F, Gastaut JL, Chauvel P, Dravet C. Absence epilepsy with fast rhythmic discharges during sleep: an intermediary form of generalized epilepsy? Epilepsia. 2001;42:351–6. ; Sun Y, Seneviratne U, Perucca P, Chen Z, Tan MK, O'Brien TJ, et al. Generalized polyspike train: an EEG biomarker of drug‐resistant idiopathic generalized epilepsy. Neurology. 2018;91:e1822–e1830. ; Sagi V, Kim I, Bhatt AB, Sonmezturk H, Abou‐Khalil BW, Arain AM. Generalized paroxysmal fast activity in EEG: an unrecognized EEG finding in genetic generalized epilepsy. Epilepsy Behav. 2017;76:101–4. ; Halász P. Runs of rapid spikes in sleep: a characteristic EEG expression of generalized malignant epileptic encephalopathies: a conceptual review with new pharmacological data. Epilepsy Res Suppl. 1991;2:49–71. ; Badawy RA, Macdonell RA, Berkovic SF, Newton MR, Jackson GD. Predicting seizure control: cortical excitability and antiepileptic medication. Ann Neurol. 2010;67:64–73. ; Pawley AD, Chowdhury FA, Tangwiriyasakul C, Ceronie B, Elwes RDC, Nashef L, et al. Cortical excitability correlates with seizure control and epilepsy duration in chronic epilepsy. Ann Clin Transl Neurol. 2017;4:87–97. ; Badawy RA, Jackson GD, Berkovic SF, Macdonell RA. Cortical excitability and refractory epilepsy: a three‐year longitudinal transcranial magnetic stimulation study. Int J Neural Syst. 2013;23:1250030. ; Syvertsen MR, Flogstad I, Enger U, Landmark CJ, Koht J. Antiepileptic drug withdrawal in juvenile myoclonic epilepsy. Acta Neurol Scand. 2019;139:192–8. ; Syvertsen MR, Thuve S, Stordrange BS, Brodtkorb E. Clinical heterogeneity of juvenile myoclonic epilepsy: follow‐up after an interval of more than 20 years. Seizure. 2014;23:344–8.
  • Contributed Indexing: Keywords: generalized paroxysmal fast activity; genetic generalized epilepsy; idiopathic generalized epilepsy; prognostic factors; treatment resistance
  • Substance Nomenclature: 0 (Anticonvulsants) ; 614OI1Z5WI (Valproic Acid)
  • Entry Date(s): Date Created: 20201221 Date Completed: 20210203 Latest Revision: 20210203
  • Update Code: 20240513

Klicken Sie ein Format an und speichern Sie dann die Daten oder geben Sie eine Empfänger-Adresse ein und lassen Sie sich per Email zusenden.

oder
oder

Wählen Sie das für Sie passende Zitationsformat und kopieren Sie es dann in die Zwischenablage, lassen es sich per Mail zusenden oder speichern es als PDF-Datei.

oder
oder

Bitte prüfen Sie, ob die Zitation formal korrekt ist, bevor Sie sie in einer Arbeit verwenden. Benutzen Sie gegebenenfalls den "Exportieren"-Dialog, wenn Sie ein Literaturverwaltungsprogramm verwenden und die Zitat-Angaben selbst formatieren wollen.

xs 0 - 576
sm 576 - 768
md 768 - 992
lg 992 - 1200
xl 1200 - 1366
xxl 1366 -