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Journal ArticleDOI

How long does it take for partial epilepsy to become intractable

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TLDR
A substantial proportion of localization-related epilepsy may not become clearly intractable for many years after onset, especially true of epilepsy of childhood and early adolescent onset.
Abstract
Background: Much remains unknown about the natural history of intractable localization-related epilepsy, including how long it typically takes before intractability becomes evident. This information could guide the design of future studies, resolve certain discrepancies in the literature, and provide more accurate information about long-term prognosis. Methods: Individuals evaluated for resective surgery for refractory localization-related epilepsy were prospectively identified at the time of initial surgical evaluation at seven surgical centers (between 1996 and 2001). The latency time between onset of epilepsy and failure of second medication and history of remission (≥1 year seizure-free) before surgical evaluation were examined with respect to age at onset, hippocampal atrophy, febrile seizures, and surgical site. Results: In the 333 patients included in the analysis, latency time was 9.1 years (range 0 to 48) and 26% reported a prior remission before surgery. A prior remission of ≥5 years was reported by 8.5% of study participants. Younger age at onset was strongly associated with longer latency time ( p p Conclusions: A substantial proportion of localization-related epilepsy may not become clearly intractable for many years after onset. This is especially true of epilepsy of childhood and early adolescent onset. If prospective studies confirm these findings and the underlying mechanisms behind these associations become understood, this raises the possibility of considering interventions that might interrupt such a process and some day prevent some forms of epilepsy from becoming intractable.

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Citations
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Journal ArticleDOI

Early Surgical Therapy for Drug-Resistant Temporal Lobe Epilepsy: A Randomized Trial

TL;DR: Whether surgery soon after failure of 2 antiepileptic drug (AED) trials is superior to continued medical management in controlling seizures and improving quality of life (QOL) is sought and among patients with newly intractable disabling MTLE, resective surgery plus AED treatment resulted in a lower probability of seizures during year 2 of follow-up than continued AEDtreatment alone.
Book

Epilepsy in Children

TL;DR: Treatment and quality of life have improved because the syndrome-specific efficacy profile of drugs is better known, and there is heightened awareness that compounds with severe cognitive side-effects and heavy polytherapies should be avoided.
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ILAE Commission Report. Mesial temporal lobe epilepsy with hippocampal sclerosis.

TL;DR: After a long‐lasting consensus process the ILAE Commission Neurosurgery of epilepsy accepted the resulting conclusions as state‐of‐the art report on MTLE‐HS.
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Drug resistance in epilepsy : Putative neurobiologic and clinical mechanisms

TL;DR: The laboratory and clinical evidence to date supporting the drug‐transport and the drug-target hypotheses are reviewed and directions for future research are provided, to define more clearly the role of these hypotheses in the clinical spectrum of drug‐resistant epilepsy.
References
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Journal ArticleDOI

Early Identification of Refractory Epilepsy

TL;DR: Patients who have many seizures before therapy or who have an inadequate response to initial treatment with antiepileptic drugs are likely to have refractory epilepsy.
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A randomized, controlled trial of surgery for temporal-lobe epilepsy.

TL;DR: In temporal-lobe epilepsy, surgery is superior to prolonged medical therapy, and Randomized trials of surgery for epilepsy are feasible and appear to yield precise estimates of treatment effects.
Journal Article

Guidelines for epidemiologic studies on epilepsy

Prognosis
- 01 Jan 1993 - 
TL;DR: The proposed guidelines represent a consensus between epileptologists and epidemiologists and are presented in four parts: Definition of seizures and epilepsy, (b) seizure type classification, (c) risk factors; and (d) recommended measurement indexes.
Journal ArticleDOI

Characteristics of medial temporal lobe epilepsy: I. Results of history and physical examination

TL;DR: There is a very strong relationship between complicated febrile seizures during early childhood or infancy and the later development of medial temporal lobe epilepsy, which can be a progressive disease as evidenced by silent intervals and progressive elaboration of seizures.
Journal ArticleDOI

Early development of intractable epilepsy in children: a prospective study.

TL;DR: Initial seizure frequency is highly predictive of intractable epilepsy in children, and age at onset between 5 and 9 years was associated with a lowered risk of IE, and absolute number of seizures and unprovoked or febrile status epilepticus are not.
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