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How long does it take for epilepsy to become intractable? A prospective investigation
Anne T Berg1, Barbara G Vickrey, Francine M Testa
1Department of Biology, Northern Illinois University, DeKalb, 60115, USA. atberg@niu.edu
Insights
Epilepsy intractability can be delayed, particularly in focal epilepsy, often following a period of remission. This understanding is crucial for timely surgical referrals in complex epilepsy cases.
Area of Science:
- Neurology
- Pediatric Epilepsy Research
Background:
- Epilepsy intractability is a significant challenge in pediatric care.
- Understanding the temporal course of epilepsy intractability is crucial for effective management and treatment strategies.
Purpose of the Study:
- To prospectively investigate the timing of epilepsy intractability onset in children.
- To identify factors influencing the delayed onset of intractable epilepsy, particularly in different epilepsy syndromes.
Main Methods:
- Prospective cohort study of 613 children with epilepsy, followed for a median of 9.7 years.
- Epilepsy syndromes were categorized (focal, idiopathic, catastrophic, other).
- Intractability defined by drug failure and seizure frequency criteria; delayed intractability set at ≥3 years post-diagnosis.
Main Results:
- 13.8% (stringent) and 23.2% (two-drug) met intractability definitions.
- Delayed intractability occurred in 31.3% (stringent) and 27.5% (two-drug) of cases.
- Focal epilepsy showed significantly higher rates of delayed intractability compared to catastrophic epilepsy (p < 0.003).
- Quiescent periods preceded delayed intractability in 65.4-74.3% of cases.
Conclusions:
- Intractable epilepsy, especially focal epilepsy, can have a delayed onset.
- A period of remission often precedes the development of intractability.
- These findings may explain long delays in surgical referral for treatable epilepsies.
Objective:
To determine prospectively when in the course of epilepsy intractability becomes apparent.
Methods:
Data are from a prospective cohort of 613 children followed for a median of 9.7 years. Epilepsy syndromes were grouped: focal, idiopathic, catastrophic, and other. Intractability was defined in two ways: (1) 2 drugs failed, 1 seizure/month, on average, for 18 months (stringent), and (2) failure of 2 drugs. Delayed intractability was defined as 3 or more years after epilepsy diagnosis.
Results:
Eighty-three children (13.8%) met the stringent and 142 (23.2%) met the two-drug definition. Intractability depended on syndrome (p < 0.0001): 26 (31.3%) children meeting stringent and 39 (27.5%) meeting the 2-drug definition had delayed intractability. Intractability was delayed more often in focal than catastrophic epilepsy (stringent: 46.2 vs 14.3%, p = 0.003; two-drug: 40.3 vs 2.2%, p
Interpretation:
Intractable epilepsy may be delayed, especially in focal epilepsy. It often is preceded by a quiescent period, followed by further remissions. These findings help explain why surgically treatable epilepsies may take 20 years or longer before referral to surgery.
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