» Articles » PMID: 38643018

Long-term Neuropsychological Trajectories in Children with Epilepsy: Does Surgery Halt Decline?

Abstract

Neuropsychological impairments are common in children with drug-resistant epilepsy. It has been proposed that epilepsy surgery might alleviate these impairments by providing seizure freedom; however, findings from prior studies have been inconsistent. We mapped long-term neuropsychological trajectories in children before and after undergoing epilepsy surgery, to measure the impact of disease course and surgery on functioning. We performed a retrospective cohort study of 882 children who had undergone epilepsy surgery at Great Ormond Street Hospital (1990-2018). We extracted patient information and neuropsychological functioning [obtained from IQ tests (domains: full-scale IQ, verbal IQ, performance IQ, working memory and processing speed) and tests of academic attainment (reading, spelling and numeracy)] and investigated changes in functioning using regression analyses. We identified 500 children (248 females) who had undergone epilepsy surgery [median age at surgery = 11.9 years, interquartile range = (7.8, 15.0)] and neuropsychological assessment. These children showed declines in all domains of neuropsychological functioning in the time leading up to surgery (all P-values ≤0.001; e.g. βFSIQ = -1.9, SEFSIQ = 0.3, PFSIQ < 0.001). Children lost on average one to four points per year, depending on the domain considered; 27%-43% declined by ≥10 points from their first to their last preoperative assessment. At the time of presurgical evaluation, most children (46%-60%) scored one or more standard deviations below the mean (<85) on the different neuropsychological domains; 37% of these met the threshold for intellectual disability (full-scale IQ < 70). On a group level, there was no change in performance from pre- to postoperative assessment on any of the domains (all P-values ≥0.128). However, children who became seizure free through surgery showed higher postoperative neuropsychological performance (e.g. rrb-FSIQ = 0.37, P < 0.001). These children continued to demonstrate improvements in neuropsychological functioning over the course of their long-term follow-up (e.g. βFSIQ = 0.9, SEFSIQ = 0.3, PFSIQ = 0.004). Children who had discontinued antiseizure medication treatment at 1-year follow-up showed an 8- to 13-point advantage in postoperative working memory, processing speed and numeracy, and greater improvements in verbal IQ, working memory, reading and spelling (all P-values ≤0.034) over the postoperative period compared with children who were seizure free and still receiving antiseizure medication. In conclusion, by providing seizure freedom and the opportunity for antiseizure medication cessation, epilepsy surgery might not only halt but reverse the downward trajectory that children with drug-resistant epilepsy display in neuropsychological functioning. To halt this decline as soon as possible or, potentially, to prevent it from occurring in the first place, children with focal epilepsy should be considered for epilepsy surgery as early as possible after diagnosis.

Citing Articles

Longitudinal alterations in brain networks and thalamocortical connectivity in paediatric focal epilepsy: a structural connectomics pilot study.

Chari A, Piper R, Wilson-Jeffers R, Ruiz-Perez M, Seunarine K, Tahir M Brain Commun. 2025; 7(1):fcaf081.

PMID: 40040839 PMC: 11878571. DOI: 10.1093/braincomms/fcaf081.


Detection of Epileptogenic Focal Cortical Dysplasia Using Graph Neural Networks: A MELD Study.

Ripart M, Spitzer H, Williams L, Walger L, Chen A, Napolitano A JAMA Neurol. 2025; .

PMID: 39992650 PMC: 11851297. DOI: 10.1001/jamaneurol.2024.5406.


Functional resilience of the neural visual recognition system post-pediatric occipitotemporal resection.

Granovetter M, Maallo A, Ling S, Robert S, Freud E, Patterson C iScience. 2024; 27(12):111440.

PMID: 39735436 PMC: 11681899. DOI: 10.1016/j.isci.2024.111440.


Cross-sectional and longitudinal changes in category-selectivity in visual cortex following pediatric cortical resection.

Liu T, Granovetter M, Maallo A, Robert S, Fu J, Patterson C bioRxiv. 2024; .

PMID: 39713452 PMC: 11661110. DOI: 10.1101/2024.12.08.627367.


Sharper Minds: Cognitive Recovery After Epilepsy Surgery in Children.

Englot D Epilepsy Curr. 2024; 24(6):393-395.

PMID: 39540139 PMC: 11556307. DOI: 10.1177/15357597241280032.


References
1.
Helmstaedter C, Beeres K, Elger C, Kuczaty S, Schramm J, Hoppe C . Cognitive outcome of pediatric epilepsy surgery across ages and different types of surgeries: A monocentric 1-year follow-up study in 306 patients of school age. Seizure. 2019; 77:86-92. DOI: 10.1016/j.seizure.2019.07.021. View

2.
Sonoda M, Rothermel R, Carlson A, Jeong J, Lee M, Hayashi T . Naming-related spectral responses predict neuropsychological outcome after epilepsy surgery. Brain. 2022; 145(2):517-530. PMC: 9014727. DOI: 10.1093/brain/awab318. View

3.
Ramantani G, Kadish N, Mayer H, Anastasopoulos C, Wagner K, Reuner G . Frontal Lobe Epilepsy Surgery in Childhood and Adolescence: Predictors of Long-Term Seizure Freedom, Overall Cognitive and Adaptive Functioning. Neurosurgery. 2017; 83(1):93-103. DOI: 10.1093/neuros/nyx340. View

4.
Laguitton V, Desnous B, Lepine A, McGonigal A, Mancini J, Daquin G . Intellectual outcome from 1 to 5 years after epilepsy surgery in 81 children and adolescents: A longitudinal study. Seizure. 2021; 91:384-392. DOI: 10.1016/j.seizure.2021.07.010. View

5.
van Schooneveld M, Braun K . Cognitive outcome after epilepsy surgery in children. Brain Dev. 2013; 35(8):721-9. DOI: 10.1016/j.braindev.2013.01.011. View