Brivaracetam in the treatment of focal and idiopathic generalized epilepsies and of status epilepticus

被引:49
|
作者
Strzelczyk, Adam [1 ,2 ,3 ,4 ]
Klein, Karl Martin [1 ,2 ,3 ,4 ]
Willems, Laurent M. [1 ,2 ]
Rosenow, Felix [1 ,2 ,3 ,4 ]
Bauer, Sebastian [1 ,2 ,3 ,4 ]
机构
[1] Goethe Univ Frankfurt, Epilepsy Ctr Frankfurt Rhine Main, D-60528 Frankfurt, Germany
[2] Goethe Univ Frankfurt, Dept Neurol, D-60528 Frankfurt, Germany
[3] Univ Marburg, Epilepsy Ctr Hessen, Marburg, Germany
[4] Univ Marburg, Dept Neurol, Marburg, Germany
关键词
Brivaracetam; myoclonus; epilepsy; seizure; PARTIAL-ONSET SEIZURES; SYNAPTIC VESICLE PROTEIN; PLACEBO-CONTROLLED TRIAL; DRUG-RESISTANT EPILEPSY; ADVERSE EVENT PROFILE; QUALITY-OF-LIFE; ADJUNCTIVE BRIVARACETAM; DOUBLE-BLIND; SV2A LIGAND; CNS PHARMACODYNAMICS;
D O I
10.1586/17512433.2016.1156529
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Brivaracetam is the latest approved antiepileptic drug in focal epilepsy and exhibits high affinity as SV2A-ligand. More than two thousand patients have received brivaracetam within randomized placebo-controlled trials. Significant median seizure reduction rates of 30.5% to 53.1% for 50mg/d, 32.5% to 37.2% for 100mg/d and 35.6% for 200mg/d were reported. Likewise, 50% responder rates were 32.7% to 55.8% for 50mg/d, 36% to 38.9% for 100mg/d and 37.8% for 200mg/d. Overall, brivaracetam is well tolerated. The main adverse events are fatigue, dizziness, and somnolence. Immediate switch from levetiracetam to brivaracetam at a conversion ratio between 10:1 to 15:1 is feasible, and might alleviate the behavioral side effects associated with levetiracetam. Brivaracetam has the potential to perform as an important, possibly broad-spectrum AED, initially in patients with drug-refractory epilepsies. Its intravenous formulation may be a new and desirable alternative for status epilepticus, but there is so far no experience in these patients.
引用
收藏
页码:637 / 645
页数:9
相关论文
共 50 条
  • [1] Perampanel in the treatment of focal and idiopathic generalized epilepsies and of status epilepticus
    Strzelczyk, Adam
    Willems, Laurent M.
    Willig, Sophia
    Rosenow, Felix
    Bauer, Sebastian
    EXPERT REVIEW OF CLINICAL PHARMACOLOGY, 2015, 8 (06) : 733 - 740
  • [2] Use of brivaracetam in genetic generalized epilepsies and for acute, intravenous treatment of absence status epilepticus
    Strzelczyk, Adam
    Kay, Lara
    Bauer, Sebastian
    Inunisch, Ilka
    Klein, Karl Martin
    Knake, Susanne
    Kowski, Alexander
    Kunz, Rhina
    Kurlemann, Gerhard
    Langenbruch, Lisa
    Moeddel, Gabriel
    Mueller-Schlueter, Karen
    Reif, Philipp S.
    Schubert-Bast, Susanne
    Steinhoff, Bernhard J.
    Steinig, Isabel
    Willems, Laurent M.
    Von Podewils, Felix
    Rosenow, Felix
    EPILEPSIA, 2018, 59 (08) : 1549 - 1556
  • [3] Familial aggregation of status epilepticus in generalized and focal epilepsies
    Weisenberg, Judith L. Z.
    Fitzgerald, Robert T.
    Constantino, John N.
    Winawer, Melodie R.
    Thio, Liu Lin
    NEUROLOGY, 2020, 95 (15) : E2140 - E2149
  • [4] Are Idiopathic Generalized Epilepsies Focal?
    Szaflarski, Jerzy P.
    EPILEPSY CURRENTS, 2016, 16 (04) : 242 - 244
  • [5] Idiopathic generalized epilepsies imitating focal epilepsies
    Ferrie, CD
    EPILEPSIA, 2005, 46 : 91 - 95
  • [6] FOCAL ASPECTS IN IDIOPATHIC GENERALIZED EPILEPSIES
    Ferrie, C.
    EPILEPSIA, 2010, 51 : 187 - 188
  • [7] GENERALIZED ASPECTS IN IDIOPATHIC FOCAL EPILEPSIES
    Fusco, L.
    EPILEPSIA, 2010, 51 : 187 - 187
  • [8] Focal seizure symptoms in idiopathic generalized epilepsies
    Seneviratne, Udaya
    Woo, Jia J.
    Boston, Ray C.
    Cook, Mark
    D'Souza, Wendyl
    NEUROLOGY, 2015, 85 (07) : 589 - 595
  • [9] FOCAL SEIZURE SYMPTOMS IN IDIOPATHIC GENERALIZED EPILEPSIES Response
    Seneviratne, Udaya
    Cook, Mark
    D'Souza, Wendyl
    NEUROLOGY, 2016, 86 (08) : 792 - 792
  • [10] Electroencephalographic generalized features in idiopathic childhood focal epilepsies
    Yum, Mi-Sun
    Ko, Tae-Sung
    Lee, Eun Hye
    Jeong, Min-Hee
    SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2010, 19 (04): : 222 - 225