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1.
Acta Neurol Scand ; 138(3): 259-262, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29633241

ABSTRACT

BACKGROUND: Nearly 10 years after its introduction into the market, the significance of lacosamide in genetic generalized epilepsies is still unclear. Its new mode of action may qualify lacosamide as a therapeutic agent in this entity, but only a limited number of cases have been published so far. AIM: To describe the efficacy of lacosamide as treatment in a patient with the absence status epilepticus. METHOD: We report on a 28-year-old woman with genetic generalized epilepsy who suffered recurrent absence status epilepticus during video-EEG-monitoring. After treatment failure of first- and second-line medication, lacosamide was administered. The outcome in this patient was evaluated, and a systematic literature review was performed for the use of lacosamide in the absence status epilepticus. RESULTS: After application of 400 mg lacosamide intravenously, the absence status epilepticus terminated within 30 minutes. No further seizures or epileptiform discharges reoccurred until the end of video-EEG-Monitoring 3 days later. CONCLUSIONS: The role of lacosamide as a therapeutic option in patients with the absence status epilepticus is unclear. Only two cases have been reported so far with conflicting results. Further randomized controlled studies are required to validate the relevance of lacosamide as treatment for status epilepticus in genetic generalized and the absence epilepsy.


Subject(s)
Acetamides/therapeutic use , Anticonvulsants/therapeutic use , Epilepsy, Absence/drug therapy , Adult , Female , Humans , Lacosamide , Seizures/drug therapy
2.
Nervenarzt ; 87(10): 1086-1093, 2016 Oct.
Article in German | MEDLINE | ID: mdl-27389600

ABSTRACT

Brivaracetam is the latest antiepileptic drug to be approved for adjunctive therapy in focal epilepsy and has a high affinity as a SV2A ligand. The aim of this review article is to summarize the data from the pivotal studies in which more than 2000 patients received brivaracetam. A significant median reduction in seizures from 30.5 % to 53.1 % for 50 mg/day, from 32.5 % to 37.2 % for 100 mg/day and 35.6 % for 200 mg/day could be demonstrated. Overall brivaracetam appears to be well-tolerated, with fatigue, dizziness and somnolence being the main adverse side effects. An immediate change from levetiracetam to brivaracetam at a conversion ratio of 10:1 to 15:1 seems feasible and could alleviate behavioral side effects related to treatment with levetiracetam. A swift permeability into brain tissue and a faster onset of action compared to levetiracetam suggest that brivaracetam could be useful in emergency situations.


Subject(s)
Disorders of Excessive Somnolence/chemically induced , Dizziness/chemically induced , Epilepsies, Partial/drug therapy , Fatigue/chemically induced , Pyrrolidinones/administration & dosage , Pyrrolidinones/adverse effects , Anticonvulsants/administration & dosage , Anticonvulsants/adverse effects , Chemotherapy, Adjuvant , Disorders of Excessive Somnolence/prevention & control , Dizziness/prevention & control , Dose-Response Relationship, Drug , Epilepsies, Partial/diagnosis , Evidence-Based Medicine , Fatigue/prevention & control , Humans , Treatment Outcome
3.
Clin Exp Rheumatol ; 32(6 Suppl 86): S-88-93, 2014.
Article in English | MEDLINE | ID: mdl-25372793

ABSTRACT

OBJECTIVES: Knowledge about the nature and impact of symptoms faced by patients with systemic sclerosis (SSc) is needed to identify targets for research and treatment. The aim of this study was to assess and compare the frequency and impact on everyday activities of SSc symptoms among patients from five European countries. METHODS: European patients with SSc were invited through announcements by patient associations to complete an online survey. The survey included items assessing the frequency of 40 SSc symptoms and the impact on daily activities, if present. Chi-square tests were utilised to assess the differences in frequency and impact of symptoms across countries. RESULTS: In total, 537 patients were included from France (n=111), the Netherlands (n=229), Spain (n=61), Switzerland (n=50), and the United Kingdom (n=86). Symptoms experienced by ≥ 70% of patients in all countries were fatigue, Raynaud's phenomenon, joint pain, and muscle pain. Twenty symptoms were experienced by ≥ 50% of patients in all countries. Thirty symptoms had an impact on daily activities in ≥ 50% of patients who reported that the symptom was present in all countries. There were significant differences among countries in the prevalence of 17 out of 40 symptoms. Furthermore, in 24 out of 40 symptoms significant differences in the proportion of patients reporting impact of a specific symptom on everyday activities were observed. CONCLUSIONS: European patients with SSc experience a broad range of symptoms that have an impact on everyday activities. International research initiatives should target common SSc symptoms cooperatively. Further research is needed to better understand the differences in SSc symptoms among countries.


Subject(s)
Activities of Daily Living , Mobility Limitation , Scleroderma, Diffuse/physiopathology , Scleroderma, Limited/physiopathology , Aged , Arthralgia/etiology , Cost of Illness , Fatigue/etiology , Female , France , Humans , Male , Middle Aged , Myalgia/etiology , Netherlands , Raynaud Disease/etiology , Scleroderma, Diffuse/complications , Scleroderma, Limited/complications , Scleroderma, Systemic/complications , Scleroderma, Systemic/physiopathology , Severity of Illness Index , Spain , Surveys and Questionnaires , Switzerland , United Kingdom
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