Semin Neurol
DOI: 10.1055/a-2538-3354
Review Article

Disconnection Methods in the Surgical Treatment of Epilepsy

Runze Yang
1   Section of Neurosurgery, Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada
,
2   Department of Neurosurgery, University of Tsukuba Hospital, Tsukuba, Japan
,
Julia Jacobs
3   Section of Neurology, Department of Pediatrics, University of Calgary, Calgary, Alberta, Canada
4   Alberta Children's Hospital and Research Institute, University of Calgary, Calgary, Alberta, Canada
,
Walter Hader
1   Section of Neurosurgery, Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada
4   Alberta Children's Hospital and Research Institute, University of Calgary, Calgary, Alberta, Canada
› Institutsangaben
Funding None.

Abstract

Disconnection procedures in epilepsy surgery have become an important tool for the management of multifocal drug-resistant epilepsy. In this chapter, we will review their indications, describe the technical procedures, and review outcome data in the literature. Among the curative approaches, anterior quadrant disconnection, posterior quadrant (PQ) disconnection, and functional hemispherectomy can be performed for patients whose epileptic focus resides in one hemisphere or one quadrant. Seizure freedom rates from these procedures range from 50 to 81% for anterior quadrant disconnections, 50 to 92% for PQ disconnections, and 43 to 93% for hemispherectomy. Although typically performed in the pediatric population, data suggest that carefully selected adult patients could also benefit from a disconnection procedure. Of the palliative approaches, corpus callosotomy has been shown to be effective for drop attacks, resulting in significant improvement in seizure frequency, severity, and quality of life. Minimally invasive alternatives to standard open corpus callosotomies with laser interstitial thermal therapy (LITT) have been proposed. Overall, surgical disconnection procedures are an effective way of treating multifocal epilepsy, with good outcomes that can improve the quality of life for these patients.



Publikationsverlauf

Artikel online veröffentlicht:
10. März 2025

© 2025. Thieme. All rights reserved.

Thieme Medical Publishers, Inc.
333 Seventh Avenue, 18th Floor, New York, NY 10001, USA

 
  • References

  • 1 Wiebe S, Blume WT, Girvin JP, Eliasziw M. Effectiveness and Efficiency of Surgery for Temporal Lobe Epilepsy Study Group. A randomized, controlled trial of surgery for temporal-lobe epilepsy. N Engl J Med 2001; 345 (05) 311-318
  • 2 Dwivedi R, Ramanujam B, Chandra PS. et al. Surgery for drug-resistant epilepsy in children. N Engl J Med 2017; 377 (17) 1639-1647
  • 3 Hwang JK, Kim DS. From resection to disconnection for seizure control in pediatric epilepsy children. J Korean Neurosurg Soc 2019; 62 (03) 336-343
  • 4 Chen JS, Harris WB, Wu KJ. et al. Comparison of hemispheric surgery techniques for pediatric drug-resistant epilepsy: an individual patient data meta-analysis. Neurology 2023; 101 (04) e410-e424
  • 5 De Ribaupierre S, Delalande O. Hemispherotomy and other disconnective techniques. Neurosurg Focus 2008; 25 (03) E14
  • 6 Griessenauer CJ, Salam S, Hendrix P. et al. Hemispherectomy for treatment of refractory epilepsy in the pediatric age group: a systematic review. J Neurosurg Pediatr 2015; 15 (01) 34-44
  • 7 Rasmussen T. Hemispherectomy for seizures revisited. Can J Neurol Sci 1983; 10 (02) 71-78
  • 8 Delalande O, Bulteau C, Dellatolas G. et al. Vertical parasagittal hemispherotomy: surgical procedures and clinical long-term outcomes in a population of 83 children. Neurosurgery 2007; 60 (2 suppl 1): ONS19-ONS32 , discussion ONS32
  • 9 Villemure JG, Mascott CR. Peri-insular hemispherotomy: surgical principles and anatomy. Neurosurgery 1995; 37 (05) 975-981
  • 10 Karagianni MD, Brotis AG, Tasiou A. et al. Hemispherotomy revised: a complication overview and a systematic review meta-analysis. Brain Spine 2023; 3: 101766
  • 11 Chugani HT, Asano E, Juhász C, Kumar A, Kupsky WJ, Sood S. “Subtotal” hemispherectomy in children with intractable focal epilepsy. Epilepsia 2014; 55 (12) 1926-1933
  • 12 Benifla M, Otsubo H, Ochi A, Snead III OC, Rutka JT. Multiple subpial transections in pediatric epilepsy: indications and outcomes. Childs Nerv Syst 2006; 22 (08) 992-998
  • 13 Morrell F, Kanner AM, de Toledo-Morrell L, Hoeppner T, Whisler WW. Multiple subpial transection. Adv Neurol 1999; 81: 259-270
  • 14 Sawhney IM, Robertson IJ, Polkey CE, Binnie CD, Elwes RD. Multiple subpial transection: a review of 21 cases. J Neurol Neurosurg Psychiatry 1995; 58 (03) 344-349
  • 15 Hufnagel A, Zentner J, Fernandez G, Wolf HK, Schramm J, Elger CE. Multiple subpial transection for control of epileptic seizures: effectiveness and safety. Epilepsia 1997; 38 (06) 678-688
  • 16 Cloppenborg T, May TW, Blümcke I. et al. Differences in pediatric and adult epilepsy surgery: A comparison at one center from 1990 to 2014. Epilepsia 2019; 60 (02) 233-245
  • 17 Harvey AS, Cross JH, Shinnar S, Mathern GW. ILAE Pediatric Epilepsy Surgery Survey Taskforce. Defining the spectrum of international practice in pediatric epilepsy surgery patients. Epilepsia 2008; 49 (01) 146-155
  • 18 Ukishiro K, Osawa SI, Iwasaki M. et al. Complete corpus callosotomy brings worthwhile seizure reduction in both pediatric and adult patients. Neurosurgery 2025; 96: 410-415
  • 19 Wu X, Ou S, Zhang H. et al. Long-term follow-up seizure outcomes after corpus callosotomy: a systematic review with meta-analysis. Brain Behav 2023; 13 (04) e2964
  • 20 Chan AY, Rolston JD, Lee B, Vadera S, Englot DJ. Rates and predictors of seizure outcome after corpus callosotomy for drug-resistant epilepsy: a meta-analysis. J Neurosurg 2018; 130 (04) 1193-1202
  • 21 Baumgartner JE, Ajmal FQ, Baumgartner ME. et al. Palliation for catastrophic nonlocalizing epilepsy: a retrospective case series of complete corpus callosotomy at a single institution. J Neurosurg Pediatr 2023; 32 (05) 553-561
  • 22 Liang S, Zhang S, Hu X. et al. Anterior corpus callosotomy in school-aged children with Lennox-Gastaut syndrome: a prospective study. Eur J Paediatr Neurol 2014; 18 (06) 670-676
  • 23 Aum DJ, Reynolds RA, McEvoy S. et al. Surgical outcomes of open and laser interstitial thermal therapy approaches for corpus callosotomy in pediatric epilepsy. Epilepsia 2023; 64 (09) 2274-2285
  • 24 Roland JL, Akbari SHA, Salehi A, Smyth MD. Corpus callosotomy performed with laser interstitial thermal therapy. J Neurosurg 2019; 134 (01) 314-322
  • 25 Graham D, Tisdall MM, Gill D. Corpus callosotomy outcomes in pediatric patients: A systematic review. Epilepsia 2016; 57 (07) 1053-1068
  • 26 Maehara T, Shimizu H. Surgical outcome of corpus callosotomy in patients with drop attacks. Epilepsia 2001; 42 (01) 67-71
  • 27 Rathore C, Abraham M, Rao RM, George A, Sankara Sarma P, Radhakrishnan K. Outcome after corpus callosotomy in children with injurious drop attacks and severe mental retardation. Brain Dev 2007; 29 (09) 577-585
  • 28 Chourasia N, Stone SSD, Tsuboyama M. et al. Influence of extent and age at corpus callosotomy on seizure outcomes. A single center experience. Epilepsia Open 2023; 8 (04) 1596-1601
  • 29 Frigeri T, Paglioli E, Soder RB. et al. Control of drop attacks with selective posterior callosotomy: anatomical and prognostic data. Epilepsy Res 2021; 171: 106544
  • 30 Paglioli E, Martins WA, Azambuja N. et al. Selective posterior callosotomy for drop attacks: a new approach sparing prefrontal connectivity. Neurology 2016; 87 (19) 1968-1974
  • 31 Jea A, Vachhrajani S, Widjaja E. et al. Corpus callosotomy in children and the disconnection syndromes: a review. Childs Nerv Syst 2008; 24 (06) 685-692
  • 32 Baud MO, Perneger T, Rácz A. et al. European trends in epilepsy surgery. Neurology 2018; 91 (02) e96-e106
  • 33 Cossu G, Lebon S, Seeck M. et al. Periinsular anterior quadrantotomy: technical note. J Neurosurg Pediatr 2018; 21 (02) 124-132
  • 34 Liu X, Zhu Y, Liu Q. et al. Clinical characteristics and surgical outcomes in children with mild malformation of cortical development and oligodendroglial hyperplasia in epilepsy. Epilepsia Open 2023; 8 (03) 898-911
  • 35 Wang Y, Liu Q, Yu H. et al. Frontal disconnection for treating mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE) in the frontal lobe. J Vis Exp 2024;210
  • 36 Cossu G, González-López P, Pralong E, Kalser J, Messerer M, Daniel RT. Unilateral prefrontal lobotomy for epilepsy: technique and surgical anatomy. Neurosurg Focus 2020; 48 (04) E10
  • 37 Scavarda D, Cavalcante T, Trébuchon A. et al. Tailored suprainsular partial hemispherotomy: a new functional disconnection technique for stroke-induced refractory epilepsy. J Neurosurg Pediatr 2018; 22 (06) 601-609
  • 38 Weil AG, Lewis EC, Ibrahim GM. et al. Hemispherectomy Outcome Prediction Scale: development and validation of a seizure freedom prediction tool. Epilepsia 2021; 62 (05) 1064-1073
  • 39 Tamura GA, Appendino JP, Ho A, Scantlebury M, Jacobs-Levan J, Hader W. An anterior quadrant disconnection, as a subtotal modification of a periinsular hemispherotomy, was effective in seizure control for pediatric intractable frontoparietal epilepsy associated with early ischemic stroke or hypoxic-ischemic encephalopathy. ISPN 2024: 50th Annual Meeting of the International Society for Pediatric Neurosurgery. Childs Nerv Syst 2024; 40: 3367-3469
  • 40 Kamalboor H, Alhindi H, Alotaibi F, Althubaiti I, Alkhateeb M. Frontal disconnection surgery for drug-resistant epilepsy: outcome in a series of 16 patients. Epilepsia Open 2020; 5 (03) 475-486
  • 41 Wang Y, Wang R, Liu Q. et al. Disconnection surgery in pediatric epilepsy: a single center's experience with 185 cases. Neurosurgery 2023; 93 (06) 1251-1258
  • 42 Elsharkawy AE, Alabbasi AH, Pannek H. et al. Outcome of frontal lobe epilepsy surgery in adults. Epilepsy Res 2008; 81 (2-3): 97-106
  • 43 Jeha LE, Najm I, Bingaman W, Dinner D, Widdess-Walsh P, Lüders H. Surgical outcome and prognostic factors of frontal lobe epilepsy surgery. Brain 2007; 130 (Pt 2): 574-584
  • 44 Lee JJ, Lee SK, Lee SY. et al. Frontal lobe epilepsy: clinical characteristics, surgical outcomes and diagnostic modalities. Seizure 2008; 17 (06) 514-523
  • 45 Dorfer C, Czech T, Mühlebner-Fahrngruber A. et al. Disconnective surgery in posterior quadrantic epilepsy: experience in a consecutive series of 10 patients. Neurosurg Focus 2013; 34 (06) E10
  • 46 Mohamed AR, Freeman JL, Maixner W, Bailey CA, Wrennall JA, Harvey AS. Temporoparietooccipital disconnection in children with intractable epilepsy. J Neurosurg Pediatr 2011; 7 (06) 660-670
  • 47 Yang PF, Mei Z, Lin Q. et al. Disconnective surgery in posterior quadrantic epilepsy: a series of 12 paediatric patients. Epileptic Disord 2014; 16 (03) 296-304
  • 48 Kadam R, Arimappamagan A, Bhaskara Rao M. et al. Posterior quadrant disconnection for childhood onset sub-hemispheric posterior head region epilepsy: indications in an Indian cohort and outcome. Pediatr Neurosurg 2021; 56 (06) 538-548
  • 49 Wang Y, Zhang C, Wang X. et al. Seizure and cognitive outcomes of posterior quadrantic disconnection: a series of 12 pediatric patients. Br J Neurosurg 2020; 34 (06) 677-682
  • 50 Markosian C, Dodson V, Zhang HJ, Mahalingam RS, Geller EB, Tomycz LD. Total and partial posterior quadrant disconnection for medically refractory epilepsy: a systematic review. Seizure 2021; 91: 66-71
  • 51 Nooraine J, R SK, Iyer RB, Rao RM, Raghavendra S. Posterior quadrant disconnection for refractory epilepsy: a case series. Ann Indian Acad Neurol 2014; 17 (04) 392-397
  • 52 Daniel RT, Meagher-Villemure K, Farmer JP, Andermann F, Villemure JG. Posterior quadrantic epilepsy surgery: technical variants, surgical anatomy, and case series. Epilepsia 2007; 48 (08) 1429-1437
  • 53 Davis KL, Murro AM, Park YD, Lee GP, Cohen MJ, Smith JR. Posterior quadrant epilepsy surgery: predictors of outcome. Seizure 2012; 21 (09) 722-728
  • 54 D'Agostino MD, Bastos A, Piras C. et al. Posterior quadrantic dysplasia or hemi-hemimegalencephaly: a characteristic brain malformation. Neurology 2004; 62 (12) 2214-2220
  • 55 Limpo H, Candela-Cantó S, Asensio S. et al. A multidisciplinary approach to posterior quadrant disconnective epilepsy surgery in pediatric patients. Neurochirurgie 2023; 69 (06) 101489
  • 56 Sugano H, Nakanishi H, Nakajima M. et al. Posterior quadrant disconnection surgery for Sturge-Weber syndrome. Epilepsia 2014; 55 (05) 683-689
  • 57 McKenzie K. The present status of a patient who had right cerebral hemisphere removed. JAMA 1938; 111: 168-183
  • 58 Delalande O. Hemispherotomy: a new procedure for central disconnection. Epilepsia 1992; 33: 99-100
  • 59 Schramm J, Behrens E, Entzian W. Hemispherical deafferentation: an alternative to functional hemispherectomy. Neurosurgery 1995; 36 (03) 509-515 , discussion 515–516
  • 60 Butler J, Soni A, Melvill R. Hemispherectomy for dominant hemisphere Rasmussen's Encephalitis - how late is too late?. Epilepsy Behav Rep 2024; 27: 100689
  • 61 Schusse CM, Smith K, Drees C. Outcomes after hemispherectomy in adult patients with intractable epilepsy: institutional experience and systematic review of the literature. J Neurosurg 2018; 128 (03) 853-861
  • 62 Liang S, Zhang G, Li Y. et al. Hemispherectomy in adults patients with severe unilateral epilepsy and hemiplegia. Epilepsy Res 2013; 106 (1-2): 257-263
  • 63 Mithani K, Quon JL, Breitbart S. et al. Hemispherectomy at The Hospital for Sick Children: expanded indications and lessons learned over 35 years. J Neurosurg Pediatr 2024; 34 (03) 252-259
  • 64 Marras CE, Granata T, Franzini A. et al. Hemispherotomy and functional hemispherectomy: indications and outcome. Epilepsy Res 2010; 89 (01) 104-112
  • 65 Sood S, Ilyas M, Marupudi NI. et al. Anatomical hemispherectomy revisited-outcome, blood loss, hydrocephalus, and absence of chronic hemosiderosis. Childs Nerv Syst 2019; 35 (08) 1341-1349
  • 66 Pilioneta M, Chen HH, Losito E. et al. Interhemispheric vertical hemispherotomy: technique, outcome, and pitfalls-a bicentric retrospective case series of 39 cases. Oper Neurosurg (Hagerstown) 2024; 26 (04) 413-422
  • 67 Goel K, Ghadiyaram A, Krishnakumar A. et al. Hemimegalencephaly: a systematic comparison of functional and anatomic hemispherectomy for drug-resistant epilepsy. Neurosurgery 2024; 94 (04) 666-678
  • 68 Abraham AP, Thomas MM, Mathew V. et al. EEG lateralization and seizure outcome following peri-insular hemispherotomy for pediatric hemispheric epilepsy. Childs Nerv Syst 2019; 35 (07) 1189-1195
  • 69 Arifin MT, Muttaqin Z, Hanaya R. et al. Hemispherotomy for drug-resistant epilepsy in an Indonesian population. Epilepsy Behav Rep 2019; 12: 100337
  • 70 Granata T, Matricardi S, Ragona F. et al. Hemispherotomy in Rasmussen encephalitis: long-term outcome in an Italian series of 16 patients. Epilepsy Res 2014; 108 (06) 1106-1119
  • 71 Ji T, Liu M, Wang S. et al. Seizure outcome and its prognostic predictors after hemispherotomy in children with refractory epilepsy in a chinese pediatric epileptic center. Front Neurol 2019; 10: 880
  • 72 Kumar RM, Koh S, Knupp K, Handler MH, O'Neill BR. Surgery for infants with catastrophic epilepsy: an analysis of complications and efficacy. Childs Nerv Syst 2015; 31 (09) 1479-1491
  • 73 Kwan A, Ng WH, Otsubo H. et al. Hemispherectomy for the control of intractable epilepsy in childhood: comparison of 2 surgical techniques in a single institution. Neurosurgery 2010; 67 (2, suppl operative): 429-436
  • 74 Limbrick DD, Narayan P, Powers AK. et al. Hemispherotomy: efficacy and analysis of seizure recurrence. J Neurosurg Pediatr 2009; 4 (04) 323-332
  • 75 Terra-Bustamante VC, Inuzuka LM, Fernandes RM. et al. Outcome of hemispheric surgeries for refractory epilepsy in pediatric patients. Childs Nerv Syst 2007; 23 (03) 321-326
  • 76 Torres CV, Fallah A, Ibrahim GM. et al. The role of magnetoencephalography in children undergoing hemispherectomy. J Neurosurg Pediatr 2011; 8 (06) 575-583
  • 77 Ramantani G, Bulteau C, Cserpan D. et al. Not surgical technique, but etiology, contralateral MRI, prior surgery, and side of surgery determine seizure outcome after pediatric hemispherotomy. Epilepsia 2023; 64 (05) 1214-1224
  • 78 Cossu M, Nichelatti M, De Benedictis A, Rizzi M. Commission for Epilepsy Surgery of the Italian League Against Epilepsy (LICE), The members of the Commission for Epilepsy Surgery of the Italian League Against Epilepsy (LICE) include. Lateral versus vertical hemispheric disconnection for epilepsy: a systematic review and meta-analysis. J Neurosurg 2021; 136 (06) 1627-1637
  • 79 Fallah A, Lewis E, Ibrahim GM. et al. Comparison of the real-world effectiveness of vertical versus lateral functional hemispherotomy techniques for pediatric drug-resistant epilepsy: a post hoc analysis of the HOPS study. Epilepsia 2021; 62 (11) 2707-2718
  • 80 Yates CF, Malone S, Riney K, Shah U, Wood MJ. Peri-insular hemispherotomy: a systematic review and institutional experience. Pediatr Neurosurg 2023; 58 (01) 18-28
  • 81 Ramantani G, Cserpan D, Tisdall M. et al. Determinants of functional outcome after pediatric hemispherotomy. Ann Neurol 2024; 95 (02) 377-387
  • 82 Devlin AM, Cross JH, Harkness W. et al. Clinical outcomes of hemispherectomy for epilepsy in childhood and adolescence. Brain 2003; 126 (Pt 3): 556-566
  • 83 Wang S, Liu QZ, Zhao R. et al; SWS-CC collaborations. Seizure, motor, and cognitive outcomes after epilepsy surgery for patients with Sturge-Weber syndrome: results from a multicenter study. Neurology 2024; 103 (01) e209525