Intravenous lacosamide in clinical practice-Results from an independent registry

被引:19
|
作者
Lang, Nicolas [1 ]
Lange, Max [2 ]
Schmitt, Friedhelm C. [3 ]
Boes, Monika [4 ]
Weber, Yvonne [5 ]
Evers, Stefan [6 ]
Burghaus, Lothar [7 ]
Kellinghaus, Christoph [8 ]
Schubert-Bast, Susanne [9 ]
Boesel, Julian [10 ]
Lammers, Thorsten [11 ]
Sabolek, Michael [12 ]
van Baalen, Andreas [13 ]
Dziewas, Rainer [14 ]
Kraft, Andrea [15 ]
Ruf, Susanne [16 ]
Stephani, Ulrich [13 ]
机构
[1] Univ Hosp Schleswig Holstein, Dept Neurol, Kiel, Germany
[2] Univ Hosp Regensburg, Dept Neurosurg, Regensburg, Germany
[3] Univ Hosp Magdeburg, Dept Neurol, Magdeburg, Germany
[4] St Johannes Hosp, Dept Neurol, Troisdorf, Germany
[5] Univ Tubingen, Hertie Inst Clin Brain Res, Dept Neurol & Epileptol, Tubingen, Germany
[6] Lindenbrunn Hosp, Dept Neurol, Coppenbrugge, Germany
[7] Univ Hosp Cologne, Dept Neurol, Cologne, Germany
[8] Klinikum Osnabruck, Dept Neurol, Osnabruck, Germany
[9] Univ Heidelberg Hosp, Neuropediat Dept, Heidelberg, Germany
[10] Univ Heidelberg Hosp, Dept Neurol, Heidelberg, Germany
[11] Johanna Etienne Hosp, Dept Neurol, Neuss, Germany
[12] Neurol Specialist Hosp Dietenbronn, Schwendi, Germany
[13] Univ Hosp Schleswig Holstein, Dept Neuropediat, Kiel, Germany
[14] Univ Hosp Munster, Dept Neurol, Munster, Germany
[15] Martha Maria Hosp, Dept Neurol, Halle, Saale, Germany
[16] Univ Tubingen Hosp, Dept Neuropediat, Tubingen, Germany
来源
关键词
Lacosamide iv; Efficacy; Tolerability; Epilepsy; Seizure; Status epilepticus; PARTIAL-ONSET SEIZURES; NONCONVULSIVE STATUS EPILEPTICUS; RANDOMIZED CONTROLLED-TRIAL; ORAL LACOSAMIDE; ADJUNCTIVE THERAPY; EFFICACY; REPLACEMENT; CLUSTERS; ADULTS; SAFETY;
D O I
10.1016/j.seizure.2016.01.008
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: This non-interventional study was conducted to evaluate the efficacy and tolerability of intravenous lacosamide (LCM-iv) under routine conditions in daily clinical practice as a prospective registry. Methods: Patients with any type of seizure or epilepsy syndrome were recruited in 16 neurological and neuropediatric centers in Germany if the treating physician decided to administer LCM-iv for any reason. Observation time per patient was 10 days with daily documentation of LCM-iv administration, type and frequency of seizures, currently used drugs and doses, and adverse events. Treatment efficacy, tolerability, and handling of LCM-iv were assessed using a five-step scale. Results: In 119 patients treating physicians classified epilepsies as focal in 66.1% and generalized in 17.4% (16.5% unclassifiable). Most common etiologies of seizures were tumors (36.1%) and cerebrovascular diseases (21.8%). Reasons for LCM-iv treatment included preparation for surgery (25.2%), convulsive (24.4%) and non-convulsive (18.5%) status epilepticus (SE), series of seizures (16.0%), gastrointestinal causes (5.9%), and acute seizures (4.2%). The median dose of LCM-iv was 300 mg per day. In 45 of 64 patients (70.3%) with SE or series of seizures, epileptic activity ceased during observation time. Five patients showed abnormalities in ECG prior to the infusion and one patient afterwards, but during infusion no abnormalities were reported. Treating physicians rated efficacy and tolerability as very good or good in 77.6% and 93.1% of patients, respectively. Conclusions: This large and independent multicenter registry on the use of LCM-iv in clinical practice demonstrates that LCM-iv is well-tolerated and highly efficacious when given in emergency situations, including patients experiencing SE. It is advisable to perform an electrocardiogram prior to LCM-iv administration. (C) 2016 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:5 / 9
页数:5
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