首页 > 最新文献

Epilepsy research and treatment最新文献

英文 中文
Temporal lobe epilepsy after refractory status epilepticus: an illustrative case and review of the literature. 难治性癫痫持续状态后颞叶癫痫:一例说明性病例及文献回顾。
Pub Date : 2012-01-01 Epub Date: 2012-04-10 DOI: 10.1155/2012/209701
J Gordon Boyd, Derek B Debicki, G Bryan Young

New onset refractory status epilepticus (NORSE) is a relatively newly defined disease entity, where otherwise healthy individuals develop unrelenting seizures that do not respond to conventional anticonvulsant therapy and may require months of therapy with anesthetic drugs. We have described a case of NORSE who subsequently developed mesial temporal lobe sclerosis (MTS) and recurrent temporal lobe seizures. We discuss the possible pathophysiological mechanisms by which refractory seizures may contribute to the development of temporal lobe epilepsy (TLE).

新发难治性癫痫持续状态(NORSE)是一种相对较新定义的疾病实体,在这种疾病中,原本健康的个体出现持续发作,对常规抗惊厥药物治疗无效,可能需要数月的麻醉药物治疗。我们描述了一个挪威人谁随后发展为内侧颞叶硬化(MTS)和反复颞叶癫痫发作的情况。我们讨论了难治性癫痫可能导致颞叶癫痫(TLE)发展的病理生理机制。
{"title":"Temporal lobe epilepsy after refractory status epilepticus: an illustrative case and review of the literature.","authors":"J Gordon Boyd,&nbsp;Derek B Debicki,&nbsp;G Bryan Young","doi":"10.1155/2012/209701","DOIUrl":"https://doi.org/10.1155/2012/209701","url":null,"abstract":"<p><p>New onset refractory status epilepticus (NORSE) is a relatively newly defined disease entity, where otherwise healthy individuals develop unrelenting seizures that do not respond to conventional anticonvulsant therapy and may require months of therapy with anesthetic drugs. We have described a case of NORSE who subsequently developed mesial temporal lobe sclerosis (MTS) and recurrent temporal lobe seizures. We discuss the possible pathophysiological mechanisms by which refractory seizures may contribute to the development of temporal lobe epilepsy (TLE).</p>","PeriodicalId":72948,"journal":{"name":"Epilepsy research and treatment","volume":" ","pages":"209701"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2012/209701","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30885725","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Neuropsychology in temporal lobe epilepsy: influences from cognitive neuroscience and functional neuroimaging. 颞叶癫痫的神经心理学:认知神经科学和功能神经影像学的影响。
Pub Date : 2012-01-01 Epub Date: 2012-01-30 DOI: 10.1155/2012/925238
Mary Pat McAndrews, Melanie Cohn

Neuropsychologists assist in diagnosis (i.e., localization of dysfunction) and in prediction (i.e., how cognition may change following surgery) in individuals being considered for temporal lobe surgery. The current practice includes behavioural testing as well as mapping function via stimulation, inactivation, and (more recently) functional imaging. These methods have been providing valuable information in surgical planning for 60 years. Here, we discuss current assessment strategies and highlight how they are evolving, particularly with respect to integrating recent advances in cognitive neuroscience.

神经心理学家协助诊断(即,功能障碍的定位)和预测(即,认知如何在手术后改变)的个体考虑进行颞叶手术。目前的做法包括行为测试,以及通过刺激、失活和(最近的)功能成像来绘制功能。60年来,这些方法一直为外科手术计划提供有价值的信息。在这里,我们讨论了当前的评估策略,并强调了它们是如何发展的,特别是在整合认知神经科学的最新进展方面。
{"title":"Neuropsychology in temporal lobe epilepsy: influences from cognitive neuroscience and functional neuroimaging.","authors":"Mary Pat McAndrews,&nbsp;Melanie Cohn","doi":"10.1155/2012/925238","DOIUrl":"https://doi.org/10.1155/2012/925238","url":null,"abstract":"<p><p>Neuropsychologists assist in diagnosis (i.e., localization of dysfunction) and in prediction (i.e., how cognition may change following surgery) in individuals being considered for temporal lobe surgery. The current practice includes behavioural testing as well as mapping function via stimulation, inactivation, and (more recently) functional imaging. These methods have been providing valuable information in surgical planning for 60 years. Here, we discuss current assessment strategies and highlight how they are evolving, particularly with respect to integrating recent advances in cognitive neuroscience.</p>","PeriodicalId":72948,"journal":{"name":"Epilepsy research and treatment","volume":" ","pages":"925238"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2012/925238","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30888602","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 47
Epileptic encephalopathy. 癫痫性脑病。
Pub Date : 2012-01-01 Epub Date: 2012-12-31 DOI: 10.1155/2012/460256
Nicola Specchio, Marina Trivisano, Rod C Scott, Colin Ferrie
Epileptic encephalopathies are conditions in which epileptic activity itself is postulated to contribute to severe cognitive and behavioural impairments above and beyond what might be expected from the underlying pathology alone. The term has been used in two ways: (1) as a generic classification term for epilepsies with severe cognitive and be-havioural outcomes and (2) as a pathophysiological process. We argue that the term is not synonymous with " severe epileptic syndrome ". Epileptic encephalopathy can complicate many different epileptic conditions. In some it is an almost constant feature (e.g., Lennox-Gastaut syndrome), in others expected but not invariable (e.g., West syndrome) whilst in yet others it may or may not occur with almost equal frequency (e.g., Doose syndrome). Epileptic encephalopathy very occasionally complicates otherwise benign epilepsies (e.g., benign rolandic epilepsy). Epileptic encephalopathy is a dynamic condition that may persist over time causing increasingly severe functional effects or else it may improve and remit, either spontaneously or with treatment which suppresses the proposed causative epileptic activity. Fundamental to the concept of epileptic encephalopathy is that the cognitive and other problems which characterise it result from epileptic activity, rather than being a consequence of any underling cerebral pathology (whether genetic, structural, metabolic inflammatory, etc.) which may itself be causing the epilepsy. However, all spontaneous epileptic phenomena in humans are a function of some kind of brain disease (genetic through to structural) and therefore it is likely that all cognitive impairments in children with epilepsy are at least in part a function of aetiology. When a brain disorder gives rise to both epilepsy and cog-nitive and behavioural problems, it should not be classed as an epileptic encephalopathy, but rather as an " epileptogenic encephalopathy ". The crucial difference being that the cogni-tive and behavioural problems are not a consequence of the epilepsy, but of the cerebral pathology. However, in epilepto-genic encephalopathies seizures may aggravate cognitive and behavioural problems and thus treatment of seizures may improve outcomes. Some disorders, mostly genetically determined and char-acterised by the onset of seizures in the first months of life and with developmental stagnation are best considered as " early onset epilepsies with encephalopathy " rather than epileptic encephalopathy. Both the epilepsy and the enceph-alopathy appear to be symptoms of a known or unknown genetic defect and there is no evidence that epileptic activity is primarily responsible for the developmental stagnation. Examples of this include disorders associated with CDKL5, …
{"title":"Epileptic encephalopathy.","authors":"Nicola Specchio,&nbsp;Marina Trivisano,&nbsp;Rod C Scott,&nbsp;Colin Ferrie","doi":"10.1155/2012/460256","DOIUrl":"https://doi.org/10.1155/2012/460256","url":null,"abstract":"Epileptic encephalopathies are conditions in which epileptic activity itself is postulated to contribute to severe cognitive and behavioural impairments above and beyond what might be expected from the underlying pathology alone. The term has been used in two ways: (1) as a generic classification term for epilepsies with severe cognitive and be-havioural outcomes and (2) as a pathophysiological process. We argue that the term is not synonymous with \" severe epileptic syndrome \". Epileptic encephalopathy can complicate many different epileptic conditions. In some it is an almost constant feature (e.g., Lennox-Gastaut syndrome), in others expected but not invariable (e.g., West syndrome) whilst in yet others it may or may not occur with almost equal frequency (e.g., Doose syndrome). Epileptic encephalopathy very occasionally complicates otherwise benign epilepsies (e.g., benign rolandic epilepsy). Epileptic encephalopathy is a dynamic condition that may persist over time causing increasingly severe functional effects or else it may improve and remit, either spontaneously or with treatment which suppresses the proposed causative epileptic activity. Fundamental to the concept of epileptic encephalopathy is that the cognitive and other problems which characterise it result from epileptic activity, rather than being a consequence of any underling cerebral pathology (whether genetic, structural, metabolic inflammatory, etc.) which may itself be causing the epilepsy. However, all spontaneous epileptic phenomena in humans are a function of some kind of brain disease (genetic through to structural) and therefore it is likely that all cognitive impairments in children with epilepsy are at least in part a function of aetiology. When a brain disorder gives rise to both epilepsy and cog-nitive and behavioural problems, it should not be classed as an epileptic encephalopathy, but rather as an \" epileptogenic encephalopathy \". The crucial difference being that the cogni-tive and behavioural problems are not a consequence of the epilepsy, but of the cerebral pathology. However, in epilepto-genic encephalopathies seizures may aggravate cognitive and behavioural problems and thus treatment of seizures may improve outcomes. Some disorders, mostly genetically determined and char-acterised by the onset of seizures in the first months of life and with developmental stagnation are best considered as \" early onset epilepsies with encephalopathy \" rather than epileptic encephalopathy. Both the epilepsy and the enceph-alopathy appear to be symptoms of a known or unknown genetic defect and there is no evidence that epileptic activity is primarily responsible for the developmental stagnation. Examples of this include disorders associated with CDKL5, …","PeriodicalId":72948,"journal":{"name":"Epilepsy research and treatment","volume":" ","pages":"460256"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2012/460256","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31180587","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Epileptic encephalopathies in adults and childhood. 成人和儿童的癫痫性脑病。
Pub Date : 2012-01-01 Epub Date: 2012-09-27 DOI: 10.1155/2012/205131
Zekiye Kural, Ali Fahir Ozer
Epileptic encephalopathies are motor-mental retardations or cognitive disorders secondary to epileptic seizures or epileptiform activities. Encephalopaties due to brain damage, medications, or systemic diseases are generally not in the scope of this definition, but they may rarely accompany the condition. Appropriate differential diagnosis of epileptic seizures as well as subclinical electroencephalographic discharges are crucial for management of seizures and epileptiform discharges and relative regression of cognitive deterioration in long-term followup. Proper antiepileptic drug, hormonal treatment, or i.v. immunoglobulin choice play major role in prognosis. In this paper, we evaluated the current treatment approaches by reviewing clinical electrophysiological characteristics of epileptic encephalopathies.
癫痫性脑病是继发于癫痫发作或癫痫样活动的运动智力迟钝或认知障碍。由于脑损伤、药物治疗或全身性疾病引起的脑外科手术通常不在此定义的范围内,但它们可能很少伴随该病症。在长期随访中,癫痫发作和亚临床脑电图放电的适当鉴别诊断对于癫痫发作和癫痫样放电的管理以及认知退化的相对回归至关重要。正确的抗癫痫药物、激素治疗或静脉注射免疫球蛋白是影响预后的主要因素。本文通过综述癫痫性脑病的临床电生理特点,对目前的治疗方法进行评价。
{"title":"Epileptic encephalopathies in adults and childhood.","authors":"Zekiye Kural,&nbsp;Ali Fahir Ozer","doi":"10.1155/2012/205131","DOIUrl":"https://doi.org/10.1155/2012/205131","url":null,"abstract":"Epileptic encephalopathies are motor-mental retardations or cognitive disorders secondary to epileptic seizures or epileptiform activities. Encephalopaties due to brain damage, medications, or systemic diseases are generally not in the scope of this definition, but they may rarely accompany the condition. Appropriate differential diagnosis of epileptic seizures as well as subclinical electroencephalographic discharges are crucial for management of seizures and epileptiform discharges and relative regression of cognitive deterioration in long-term followup. Proper antiepileptic drug, hormonal treatment, or i.v. immunoglobulin choice play major role in prognosis. In this paper, we evaluated the current treatment approaches by reviewing clinical electrophysiological characteristics of epileptic encephalopathies.","PeriodicalId":72948,"journal":{"name":"Epilepsy research and treatment","volume":" ","pages":"205131"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2012/205131","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30969655","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Temporal lobe epilepsy in children. 儿童颞叶癫痫。
Pub Date : 2012-01-01 Epub Date: 2011-10-20 DOI: 10.1155/2012/849540
Katherine C Nickels, Lily C Wong-Kisiel, Brian D Moseley, Elaine C Wirrell

The temporal lobe is a common focus for epilepsy. Temporal lobe epilepsy in infants and children differs from the relatively homogeneous syndrome seen in adults in several important clinical and pathological ways. Seizure semiology varies by age, and the ictal EEG pattern may be less clear cut than what is seen in adults. Additionally, the occurrence of intractable seizures in the developing brain may impact neurocognitive function remote from the temporal area. While many children will respond favorably to medical therapy, those with focal imaging abnormalities including cortical dysplasia, hippocampal sclerosis, or low-grade tumors are likely to be intractable. Expedient workup and surgical intervention in these medically intractable cases are needed to maximize long-term developmental outcome.

颞叶是癫痫的常见病灶。婴幼儿颞叶癫痫在临床和病理上与成人相对单一的综合征有几大不同。不同年龄段的癫痫发作半定型不尽相同,发作性脑电图模式也可能不如成人清晰。此外,在发育中的大脑中出现难治性癫痫发作可能会影响颞区以外的神经认知功能。虽然许多患儿对药物治疗反应良好,但那些有局灶性影像异常(包括皮质发育不良、海马硬化或低级别肿瘤)的患儿很可能是难治性的。对于这些药物治疗难以奏效的病例,需要进行快速检查和手术干预,以最大限度地提高长期发育效果。
{"title":"Temporal lobe epilepsy in children.","authors":"Katherine C Nickels, Lily C Wong-Kisiel, Brian D Moseley, Elaine C Wirrell","doi":"10.1155/2012/849540","DOIUrl":"10.1155/2012/849540","url":null,"abstract":"<p><p>The temporal lobe is a common focus for epilepsy. Temporal lobe epilepsy in infants and children differs from the relatively homogeneous syndrome seen in adults in several important clinical and pathological ways. Seizure semiology varies by age, and the ictal EEG pattern may be less clear cut than what is seen in adults. Additionally, the occurrence of intractable seizures in the developing brain may impact neurocognitive function remote from the temporal area. While many children will respond favorably to medical therapy, those with focal imaging abnormalities including cortical dysplasia, hippocampal sclerosis, or low-grade tumors are likely to be intractable. Expedient workup and surgical intervention in these medically intractable cases are needed to maximize long-term developmental outcome.</p>","PeriodicalId":72948,"journal":{"name":"Epilepsy research and treatment","volume":" ","pages":"849540"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3420576/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30889206","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Neocortical temporal lobe epilepsy. 新皮质颞叶癫痫。
Pub Date : 2012-01-01 Epub Date: 2012-07-16 DOI: 10.1155/2012/103160
Eduard Bercovici, Balagobal Santosh Kumar, Seyed M Mirsattari

Complex partial seizures (CPSs) can present with various semiologies, while mesial temporal lobe epilepsy (mTLE) is a well-recognized cause of CPS, neocortical temporal lobe epilepsy (nTLE) albeit being less common is increasingly recognized as separate disease entity. Differentiating the two remains a challenge for epileptologists as many symptoms overlap due to reciprocal connections between the neocortical and the mesial temporal regions. Various studies have attempted to correctly localize the seizure focus in nTLE as patients with this disorder may benefit from surgery. While earlier work predicted poor outcomes in this population, recent work challenges those ideas yielding good outcomes in part due to better localization using improved anatomical and functional techniques. This paper provides a comprehensive review of the diagnostic workup, particularly the application of recent advances in electroencephalography and functional brain imaging, in neocortical temporal lobe epilepsy.

复杂部分性癫痫发作(CPSs)可表现为各种不同的症状,颞叶中叶癫痫(mTLE)是CPS的公认病因,而新皮质颞叶癫痫(nTLE)虽然不太常见,但已逐渐被认为是一种独立的疾病实体。由于新皮质和颞叶中叶之间的相互联系,许多症状会重叠,因此如何区分这两种疾病仍然是癫痫专家面临的一项挑战。各种研究都试图正确定位nTLE的发作病灶,因为这种疾病的患者可能会从手术中获益。虽然早期的研究预测这类患者的治疗效果不佳,但近期的研究对这些观点提出了挑战,并取得了良好的治疗效果,部分原因是利用改进的解剖学和功能学技术进行了更好的定位。本文全面回顾了新皮质颞叶癫痫的诊断工作,特别是脑电图和脑功能成像的最新进展。
{"title":"Neocortical temporal lobe epilepsy.","authors":"Eduard Bercovici, Balagobal Santosh Kumar, Seyed M Mirsattari","doi":"10.1155/2012/103160","DOIUrl":"10.1155/2012/103160","url":null,"abstract":"<p><p>Complex partial seizures (CPSs) can present with various semiologies, while mesial temporal lobe epilepsy (mTLE) is a well-recognized cause of CPS, neocortical temporal lobe epilepsy (nTLE) albeit being less common is increasingly recognized as separate disease entity. Differentiating the two remains a challenge for epileptologists as many symptoms overlap due to reciprocal connections between the neocortical and the mesial temporal regions. Various studies have attempted to correctly localize the seizure focus in nTLE as patients with this disorder may benefit from surgery. While earlier work predicted poor outcomes in this population, recent work challenges those ideas yielding good outcomes in part due to better localization using improved anatomical and functional techniques. This paper provides a comprehensive review of the diagnostic workup, particularly the application of recent advances in electroencephalography and functional brain imaging, in neocortical temporal lobe epilepsy.</p>","PeriodicalId":72948,"journal":{"name":"Epilepsy research and treatment","volume":" ","pages":"103160"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3420667/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30884560","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A seizure care pathway in the emergency department: preliminary quality and safety improvements. 急诊科癫痫发作护理路径:初步质量和安全改进。
Pub Date : 2012-01-01 Epub Date: 2012-05-29 DOI: 10.1155/2012/273175
Parameswaran M Iyer, Patricia H McNamara, Margaret Fitzgerald, Liam Smyth, Christopher Dardis, Tania Jawad, Patrick K Plunkett, Colin P Doherty

Aim. To evaluate the utility of a seizure care pathway for seizure presentations to the emergency department (ED) in order to safely avoid unnecessary admission and to provide early diagnostic and therapeutic guidance and minimize length of stay in those admitted. Methods. 3 studies were conducted, 2 baseline audits and a 12-month intervention study and prospective data was collected over a 12-month period (Nov 2008-09). Results. Use of the Pathway resulted in a reduction in the number of epilepsy related admissions from 341 in 2004 to 276 in 2009 (P = 0.0006); a reduction in the median length of stay of those admittedfrom 4-5 days in the baseline audits to 2 days in the intervention study (P ≤ 0.001); an improvement in time to diagnostic investigations such as CT brain, MRI brain and Electroencephalography (P ≤ 0.001, P ≤ 0.048, P ≤ 0.001); a reduction in readmission rates from 45.1% to 8.9% (P ≤ 0.001); and an improvement in follow-up times from a median of 16 weeks to 5 weeks (P < 0.001). From a safety perspective there were no deaths in the early discharged group after 12 months follow-up. Conclusion. The burden of seizure related admissions through the ED can be improved in a safe and effective manner by the provision of a seizure care pathway.

的目标。评估癫痫发作护理途径在急诊科(ED)的实用性,以安全避免不必要的入院,并提供早期诊断和治疗指导,最大限度地缩短住院时间。方法:进行了3项研究,2项基线审计和1项为期12个月的干预研究,并收集了12个月(2008年11月- 2009年11月)的前瞻性数据。结果。该途径的使用使癫痫相关入院人数从2004年的341人减少到2009年的276人(P = 0.0006);入院患者的中位住院时间从基线审计中的4-5天减少到干预研究中的2天(P≤0.001);CT脑、MRI脑和脑电图等诊断检查的时间缩短(P≤0.001,P≤0.048,P≤0.001);再入院率从45.1%降至8.9% (P≤0.001);随访时间中位数从16周缩短至5周(P < 0.001)。从安全性的角度来看,在12个月的随访后,早期出院组没有死亡。结论。通过急诊科提供癫痫治疗途径,可以以安全有效的方式改善癫痫相关入院的负担。
{"title":"A seizure care pathway in the emergency department: preliminary quality and safety improvements.","authors":"Parameswaran M Iyer,&nbsp;Patricia H McNamara,&nbsp;Margaret Fitzgerald,&nbsp;Liam Smyth,&nbsp;Christopher Dardis,&nbsp;Tania Jawad,&nbsp;Patrick K Plunkett,&nbsp;Colin P Doherty","doi":"10.1155/2012/273175","DOIUrl":"https://doi.org/10.1155/2012/273175","url":null,"abstract":"<p><p>Aim. To evaluate the utility of a seizure care pathway for seizure presentations to the emergency department (ED) in order to safely avoid unnecessary admission and to provide early diagnostic and therapeutic guidance and minimize length of stay in those admitted. Methods. 3 studies were conducted, 2 baseline audits and a 12-month intervention study and prospective data was collected over a 12-month period (Nov 2008-09). Results. Use of the Pathway resulted in a reduction in the number of epilepsy related admissions from 341 in 2004 to 276 in 2009 (P = 0.0006); a reduction in the median length of stay of those admittedfrom 4-5 days in the baseline audits to 2 days in the intervention study (P ≤ 0.001); an improvement in time to diagnostic investigations such as CT brain, MRI brain and Electroencephalography (P ≤ 0.001, P ≤ 0.048, P ≤ 0.001); a reduction in readmission rates from 45.1% to 8.9% (P ≤ 0.001); and an improvement in follow-up times from a median of 16 weeks to 5 weeks (P < 0.001). From a safety perspective there were no deaths in the early discharged group after 12 months follow-up. Conclusion. The burden of seizure related admissions through the ED can be improved in a safe and effective manner by the provision of a seizure care pathway.</p>","PeriodicalId":72948,"journal":{"name":"Epilepsy research and treatment","volume":" ","pages":"273175"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2012/273175","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30884562","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 17
Postoperative neuropsychological outcome in patients with mesial temporal lobe epilepsy in Argentina. 阿根廷内侧颞叶癫痫患者术后神经心理预后分析。
Pub Date : 2012-01-01 Epub Date: 2011-11-22 DOI: 10.1155/2012/370351
Silvia Oddo, Patricia Solis, Damian Consalvo, Eduardo Seoane, Brenda Giagante, Luciana D'Alessio, Silvia Kochen

The aim of the present study is to compare pre- and postsurgical neuropsychological outcome in individuals suffering from mesial temporal lobe epilepsy (mTLE), in order to evaluate prognosis. The selected thirty-five patients had medically mTLE and had undergone an anterior temporal lobectomy (ATL). Neuropsychological evaluation was performed in three different stages: before ATL, 6 months after resection, and a year afterwards. Neuropsychological protocol evaluated attention, verbal memory, visual memory, executive function, language, intelligence, and handedness. There was a significant improvement (P = 0.030) in the group with visual memory deficit after surgery, whereas no changes were observed across patients with verbal memory deficit. No changes were observed in language after surgery. Executive function showed significant improvement 6 months after surgery (P = 0.035). Postoperative outcome of cognitive impairments depends on baseline neuropsychological status of the patients with TLE. In our case series, deficits found in patients with mTLE after ATL did not result in a subjective complaint.

本研究的目的是比较内侧颞叶癫痫(mTLE)患者手术前后的神经心理结果,以评估预后。所选的35例医学上患有mTLE并接受了前颞叶切除术(ATL)的患者。神经心理学评估分三个不同阶段进行:ATL前、术后6个月和术后1年。神经心理学方案评估了注意力、言语记忆、视觉记忆、执行功能、语言、智力和惯用手。视觉记忆缺陷组术后有显著改善(P = 0.030),而言语记忆缺陷组术后无变化。术后未见语言变化。术后6个月执行功能明显改善(P = 0.035)。认知功能障碍的术后预后取决于TLE患者的基线神经心理状态。在我们的病例系列中,ATL后mTLE患者发现的缺陷并没有导致主观主诉。
{"title":"Postoperative neuropsychological outcome in patients with mesial temporal lobe epilepsy in Argentina.","authors":"Silvia Oddo,&nbsp;Patricia Solis,&nbsp;Damian Consalvo,&nbsp;Eduardo Seoane,&nbsp;Brenda Giagante,&nbsp;Luciana D'Alessio,&nbsp;Silvia Kochen","doi":"10.1155/2012/370351","DOIUrl":"https://doi.org/10.1155/2012/370351","url":null,"abstract":"<p><p>The aim of the present study is to compare pre- and postsurgical neuropsychological outcome in individuals suffering from mesial temporal lobe epilepsy (mTLE), in order to evaluate prognosis. The selected thirty-five patients had medically mTLE and had undergone an anterior temporal lobectomy (ATL). Neuropsychological evaluation was performed in three different stages: before ATL, 6 months after resection, and a year afterwards. Neuropsychological protocol evaluated attention, verbal memory, visual memory, executive function, language, intelligence, and handedness. There was a significant improvement (P = 0.030) in the group with visual memory deficit after surgery, whereas no changes were observed across patients with verbal memory deficit. No changes were observed in language after surgery. Executive function showed significant improvement 6 months after surgery (P = 0.035). Postoperative outcome of cognitive impairments depends on baseline neuropsychological status of the patients with TLE. In our case series, deficits found in patients with mTLE after ATL did not result in a subjective complaint.</p>","PeriodicalId":72948,"journal":{"name":"Epilepsy research and treatment","volume":" ","pages":"370351"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2012/370351","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30886654","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 19
Spontaneous EEG-Functional MRI in Mesial Temporal Lobe Epilepsy: Implications for the Neural Correlates of Consciousness. 中颞叶癫痫自发性脑电图功能MRI:意识神经相关的意义。
Pub Date : 2012-01-01 Epub Date: 2012-03-08 DOI: 10.1155/2012/385626
Zheng Wang, Loretta Norton, R Matthew Hutchison, John R Ives, Seyed M Mirsattari

The combination of electroencephalography (EEG) and functional magnetic resonance imaging (fMRI) has been shown to have great potential for providing a greater understanding of normal and diseased states in both human and animal studies. Simultaneous EEG-fMRI is particularly well suited for the study of epilepsy in that it may reveal the neurobiology of ictal and interictal epileptiform discharges and noninvasively localize epileptogenic foci. Spontaneous, coherent fluctuations of neuronal activity and the coupled hemodynamic responses have also been shown to provide diagnostic markers of disease, extending our understanding of intrinsically structured ongoing brain activity. Following a short summary of the hardware and software development of simultaneous EEG-fMRI, this paper reviews a unified framework of integrating neuronal and hemodynamic processes during epileptic seizures and discusses the role and impact of spontaneous activity in the mesial temporal lobe epilepsies with particular emphasis on the neural and physiological correlates of consciousness.

脑电图(EEG)和功能性磁共振成像(fMRI)的结合在人类和动物研究中显示出对正常和患病状态有更大的了解的巨大潜力。同时进行的EEG-fMRI特别适合于癫痫的研究,因为它可以揭示癫痫发作和发作间期的神经生物学,并且可以无创地定位癫痫灶。自发的、连贯的神经元活动波动和耦合的血流动力学反应也被证明是疾病的诊断标志,扩展了我们对内在结构持续的大脑活动的理解。本文简要介绍了同步脑电图-功能磁共振成像(EEG-fMRI)的硬件和软件开发情况,回顾了癫痫发作期间整合神经元和血流动力学过程的统一框架,并讨论了自发性活动在内侧颞叶癫痫中的作用和影响,特别强调了意识的神经和生理相关。
{"title":"Spontaneous EEG-Functional MRI in Mesial Temporal Lobe Epilepsy: Implications for the Neural Correlates of Consciousness.","authors":"Zheng Wang,&nbsp;Loretta Norton,&nbsp;R Matthew Hutchison,&nbsp;John R Ives,&nbsp;Seyed M Mirsattari","doi":"10.1155/2012/385626","DOIUrl":"https://doi.org/10.1155/2012/385626","url":null,"abstract":"<p><p>The combination of electroencephalography (EEG) and functional magnetic resonance imaging (fMRI) has been shown to have great potential for providing a greater understanding of normal and diseased states in both human and animal studies. Simultaneous EEG-fMRI is particularly well suited for the study of epilepsy in that it may reveal the neurobiology of ictal and interictal epileptiform discharges and noninvasively localize epileptogenic foci. Spontaneous, coherent fluctuations of neuronal activity and the coupled hemodynamic responses have also been shown to provide diagnostic markers of disease, extending our understanding of intrinsically structured ongoing brain activity. Following a short summary of the hardware and software development of simultaneous EEG-fMRI, this paper reviews a unified framework of integrating neuronal and hemodynamic processes during epileptic seizures and discusses the role and impact of spontaneous activity in the mesial temporal lobe epilepsies with particular emphasis on the neural and physiological correlates of consciousness.</p>","PeriodicalId":72948,"journal":{"name":"Epilepsy research and treatment","volume":" ","pages":"385626"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2012/385626","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30886657","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Language mapping in temporal lobe epilepsy in children: special considerations. 儿童颞叶癫痫的语言映射:特殊考虑。
Pub Date : 2012-01-01 Epub Date: 2012-02-09 DOI: 10.1155/2012/837036
Sandrine de Ribaupierre, An Wang, Susan Hayman-Abello

Temporal lobe epilepsy (TLE) in children is a slightly different entity than TLE in adults not only because of its semiology and pathology but also because of the different approach to surgical treatment. Presurgical investigations for eloquent cortex, especially language, must take these differences into account. Most diagnostic tests were created for adults, and many of the assessment tools need to be adapted for children because they are not just small adults. This paper will highlight the specific challenges and solutions in mapping language in a pediatric population with TLE.

儿童颞叶癫痫(TLE)与成人颞叶癫痫(TLE)是一个略有不同的实体,不仅是因为其符号学和病理学,而且还因为不同的手术治疗方法。术前检查雄辩皮层,特别是语言,必须考虑到这些差异。大多数诊断测试是为成人创建的,许多评估工具需要适应儿童,因为他们不仅仅是小大人。本文将重点介绍在儿童TLE人群中绘制语言地图的具体挑战和解决方案。
{"title":"Language mapping in temporal lobe epilepsy in children: special considerations.","authors":"Sandrine de Ribaupierre,&nbsp;An Wang,&nbsp;Susan Hayman-Abello","doi":"10.1155/2012/837036","DOIUrl":"https://doi.org/10.1155/2012/837036","url":null,"abstract":"<p><p>Temporal lobe epilepsy (TLE) in children is a slightly different entity than TLE in adults not only because of its semiology and pathology but also because of the different approach to surgical treatment. Presurgical investigations for eloquent cortex, especially language, must take these differences into account. Most diagnostic tests were created for adults, and many of the assessment tools need to be adapted for children because they are not just small adults. This paper will highlight the specific challenges and solutions in mapping language in a pediatric population with TLE.</p>","PeriodicalId":72948,"journal":{"name":"Epilepsy research and treatment","volume":" ","pages":"837036"},"PeriodicalIF":0.0,"publicationDate":"2012-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2012/837036","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"30889205","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 19
期刊
Epilepsy research and treatment
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1