Neuropediatrics 2023; 54(03): 197-205
DOI: 10.1055/s-0043-1761922
Original Article

Focality in Febrile Seizures: A Retrospective Assessment Using Arterial Spin Labeling MRI

1   Department of Pediatrics, Gyeongsang National University of Hospital, Jinju, South Korea
2   Gyeongsang National University College of Medicine, Institute of Health Science, Jinju, South Korea
,
Young-Soo Kim
2   Gyeongsang National University College of Medicine, Institute of Health Science, Jinju, South Korea
3   Department of Neurology, Gyeongsang National University of Hospital, Jinju, South Korea
,
Dae-Seob Choi
2   Gyeongsang National University College of Medicine, Institute of Health Science, Jinju, South Korea
4   Department of Radiology, Gyeongsang National University of Hospital, Jinju, South Korea
› Author Affiliations
Funding This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

Abstract

Purpose Defining focality of febrile seizures (FS) in clinical practice remains controversial. We investigated focality issues in FS with a postictal arterial spin labeling (ASL) sequence.

Methods We retrospectively reviewed 77 children (median: 19.0 months, range: 15.0–33.0 months) who consecutively visited our emergency room for FS and underwent brain magnetic resonance imaging (MRI), including the ASL sequence, within 24 hours of seizure onset. ASL data were visually analyzed to assess perfusion changes. Factors related to the perfusion changes were investigated.

Results The mean time to ASL acquisition was 7.0 (interquartile range: 4.0–11.0) hours. The most common seizure classification was unknown-onset seizures (n = 37, 48%), followed by focal-onset (n = 26, 34%) and generalized-onset seizures (n = 14, 18%). Perfusion changes were observed in 43 (57%) patients: most were hypoperfusion (n = 35, 83%). The temporal regions were the most common location of perfusion changes (n = 26, 60%); the majority of these were distributed in the unilateral hemisphere. Perfusion changes were independently associated with seizure classification (focal-onset seizures, adjusted odds ratio [aOR]: 9.6, p = 0.01; unknown-onset seizures aOR: 10.4, p < 0.01), and prolonged seizures (aOR: 3.1, p = 0.04), but not with other factors (age, sex, time to MRI acquisition, previous FS, repeated FS within 24 hour, family history of FS, structural abnormality on MRI, and developmental delay). The focality scale of seizure semiology positively correlated with perfusion changes (R = 0.334, p < 0.01).

Conclusion Focality in FS may be common, and its primary origin might be the temporal regions. ASL can be useful for assessing focality in FS, particularly when seizure onset is unknown.

Authors' Contributions

J.S.Y. and D.S.C. helped in study conception and design, J.S.Y. contributed to data collection and draft manuscript preparation, J.S.Y., Y.S.K., and D.S.C. helped in analysis and interpretation of results. All authors read and approved the final manuscript.


Supplementary Material



Publication History

Received: 02 September 2022

Accepted: 29 December 2022

Article published online:
27 February 2023

© 2023. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Verity CM, Golding J. Risk of epilepsy after febrile convulsions: a national cohort study. BMJ 1991; 303 (6814): 1373-1376
  • 2 Pavlidou E, Panteliadis C. Prognostic factors for subsequent epilepsy in children with febrile seizures. Epilepsia 2013; 54 (12) 2101-2107
  • 3 Neville B, Gindner D. Febrile seizures are a syndrome of secondarily generalized hippocampal epilepsy. Dev Med Child Neurol 2010; 52 (12) 1151-1153
  • 4 Takasu M, Kubota T, Tsuji T. et al. The semiology of febrile seizures: focal features are frequent. Epilepsy Behav 2017; 73: 59-63
  • 5 Hamer HM, Wyllie E, Lüders HO, Kotagal P, Acharya J. Symptomatology of epileptic seizures in the first three years of life. Epilepsia 1999; 40 (07) 837-844
  • 6 Soldozy S, Galindo J, Snyder H. et al. Clinical utility of arterial spin labeling imaging in disorders of the nervous system. Neurosurg Focus 2019; 47 (06) E5
  • 7 Proisy M, Bruneau B, Rozel C. et al. Arterial spin labeling in clinical pediatric imaging. Diagn Interv Imaging 2016; 97 (02) 151-158
  • 8 Kim BS, Lee ST, Yun TJ. et al. Capability of arterial spin labeling MR imaging in localizing seizure focus in clinical seizure activity. Eur J Radiol 2016; 85 (07) 1295-1303
  • 9 Gaxiola-Valdez I, Singh S, Perera T, Sandy S, Li E, Federico P. Seizure onset zone localization using postictal hypoperfusion detected by arterial spin labelling MRI. Brain 2017; 140 (11) 2895-2911
  • 10 Covanis T. Typical absences. In: Roos RP, Editor-in-Chief. MedLink Neurology. San Diego: MedLink, LLC. Available at www.medlink.com. Updated: [05.28.2022]
  • 11 Fisher RS, Cross JH, French JA. et al. Operational classification of seizure types by the international league against epilepsy: position paper of the ILAE commission for classification and terminology. Epilepsia 2017; 58 (04) 522-530
  • 12 Lee SM, Kwon S, Lee YJ. Diagnostic usefulness of arterial spin labeling in MR negative children with new onset seizures. Seizure 2019; 65: 151-158
  • 13 Pasca L, Sanvito F, Ballante E. et al. Arterial spin labelling qualitative assessment in paediatric patients with MRI-negative epilepsy. Clin Radiol 2021; 76 (12) 942.e15-942.e23
  • 14 Nordli Jr DR, Bazil CW, Scheuer ML, Pedley TA. Recognition and classification of seizures in infants. Epilepsia 1997; 38 (05) 553-560
  • 15 Berg AT, Steinschneider M, Kang H, Shinnar S. Classification of complex features of febrile seizures: interrater agreement. Epilepsia 1992; 33 (04) 661-666
  • 16 Berg AT, Shinnar S. Complex febrile seizures. Epilepsia 1996; 37 (02) 126-133
  • 17 Shinnar S, Hesdorffer DC, Nordli Jr DR. et al; FEBSTAT Study Team. Phenomenology of prolonged febrile seizures: results of the FEBSTAT study. Neurology 2008; 71 (03) 170-176
  • 18 Hamelin S, Vercueil L. A simple febrile seizure with focal onset. Epileptic Disord 2014; 16 (01) 112-115
  • 19 Hirfanoglu T, Serdaroglu A, Cansu A, Bilir E, Gucuyener K. Semiological seizure classification: before and after video-EEG monitoring of seizures. Pediatr Neurol 2007; 36 (04) 231-235
  • 20 Kim TJ, Choi JW, Han M. et al. Usefulness of arterial spin labeling perfusion as an initial evaluation of status epilepticus. Sci Rep 2021; 11 (01) 24218
  • 21 Shinnar S, Berg AT, Moshe SL, Shinnar R. How long do new-onset seizures in children last?. Ann Neurol 2001; 49 (05) 659-664
  • 22 Berg AT, Shinnar S, Hauser WA. et al. A prospective study of recurrent febrile seizures. N Engl J Med 1992; 327 (16) 1122-1127
  • 23 Ingvar M. Cerebral blood flow and metabolic rate during seizures. Relationship to epileptic brain damage. Ann N Y Acad Sci 1986; 462: 194-206
  • 24 Farrell JS, Gaxiola-Valdez I, Wolff MD. et al. Postictal behavioural impairments are due to a severe prolonged hypoperfusion/hypoxia event that is COX-2 dependent. eLife 2016; 5: e19352 DOI: 10.7554/eLife.19352.
  • 25 VanLandingham KE, Heinz ER, Cavazos JE, Lewis DV. Magnetic resonance imaging evidence of hippocampal injury after prolonged focal febrile convulsions. Ann Neurol 1998; 43 (04) 413-426
  • 26 Lewis DV, Barboriak DP, MacFall JR, Provenzale JM, Mitchell TV, VanLandingham KE. Do prolonged febrile seizures produce medial temporal sclerosis? Hypotheses, MRI evidence and unanswered questions. Prog Brain Res 2002; 135: 263-278
  • 27 Weinand ME, Carter LP, Patton DD, Oommen KJ, Labiner DM, Talwar D. Long-term surface cortical cerebral blood flow monitoring in temporal lobe epilepsy. Neurosurgery 1994; 35 (04) 657-664
  • 28 Yoo HL, Choi Y-J, Moon J-H, Jo HJ, Park DW. Serial perfusion and vascular changes after a prolonged seizure. Ann Child Neurol 2021; 29 (01) 57-60
  • 29 Gonzalez S, Vasavada M, Njau S. et al. Acute changes in cerebral blood flow after single-infusion ketamine in major depression: a pilot study. Neurol Psychiatry Brain Res 2020; 38: 5-11
  • 30 Liang P, Xu Y, Lan F, Ma D, Li K. Decreased cerebral blood flow in mesial thalamus and precuneus/PCC during midazolam induced sedation assessed with ASL. Neuroinformatics 2018; 16 (3-4): 403-410