Main Article Content

Abstract

Importance: The effects of COVID-19 on the neurological system warrants recognition in our paediatric population. The long-term effects on development should be closely monitored, especially if autoimmunity is suspected. 


Objective: To present paediatric cases of unusual neuroinflammatory conditions encountered during the COVID-19 pandemic in Trinidad & Tobago.


Design: Observational cross-sectional study.


Setting: Hospital – Eric Williams Medical Sciences Complex.


Participants: Inpatient encounters involving paediatric patients (aged 0-16 years) and hospitalized for neurological complaints during the period June 2020 – August 2021.


Exposure: COVID-19/SARS-CoV-2 virus


Main Outcomes: Age, gender, ethnicity, diagnosis, radiological findings, blood and CSF findings, COVID-19 status, treatment, outcomes and other systems involved.


Results: Twenty (20) patients (aged 4-months-old to 15-years-old) had documented neurological involvement. 50% (n=10) had a diagnosis of ADEM/ADS/AHNE; 45% had a diagnosis of either CNS vasculitis (n=3), autoimmune encephalitis (n=3) or GBS (n=3); 5% (n=1) had a diagnosis of acute COVID-19 encephalitis. 70% (n=14) were of African descent. The youngest age group (0-4 years) (n=11) constituted more males (82%) while the eldest age group (10-15 years) (n=3) were all females. Neuroimaging findings were corpus callosal lesions; deep white matter T2 hyperintensities; cerebellar involvement; area postrema and brainstem/C-spine involvement; microhaemorrhages and necrotizing/haemorrhagic lesions (peripheral/central). 70% of patients (n=14) were either SARS-CoV-2 PCR positive or COVID-19 antibodies positive. 40% (n=8) had other systemic inflammatory involvement – Of this specific cohort, 62.5% (n=5) had cardiac involvement (myocarditis, coronary arteries dilatation, valve regurgitation) and 37.5% (n=3) had pancreatic involvement (autoimmune pancreatitis, type 1 diabetes mellitus). Treatment modalities for CNS manifestations (n=17) were clinically based – 24% (n=4) 3rd line treatment, 29% (n=5) 2nd line treatment, 41% (n=7) 1st line treatment and 6% (n=1) requiring no treatment. All 3 patients with a diagnosis of GBS responded appropriately to IVIG. Outcomes were worse in patients with a diagnosis of autoimmune encephalitis and positive ANA.


Conclusion/Relevance: There has been an upsurge in neuro-inflammatory cases since the COVID-19 pandemic began. The range of neuroradiological diagnoses and other systemic involvement (including meeting criteria for PIMS/MIS-C) alludes to a neuroinflammatory mechanism. Effects on long-term sequelae and developmental outcomes are concerning, however, at this early stage, still unknown.

Keywords

ADEM COVID-19 GBS AHNE Demyelinating disorders Neuro-inflammatory

Article Details

How to Cite
Shukla, V., Maharaj , P., Singh , V. A., Akan, L., Solomon , N., Ramroop , R., … Fernandes, M. (2024). Unusual neurological manifestations in children during the COVID-19 pandemic: a cross-sectional study in Trinidad & Tobago. Journal of the International Child Neurology Association, 1(1). https://doi.org/10.17724/jicna.2024.252
Share |

References

  1. Alison Knows. Children with acute COVID-19 most likely to have CNS imaging abnormalities. The Brown University Child & Adolescent Psychopharmacology Update March 2021
  2. Acute Disseminated Encephalomyelitis - NORD (National Organization for Rare Disorders) (rarediseases.org)
  3. Dubey D, Pittock SJ, Kelly CR, McKeon A, Lopez-Chiriboga AS, Lennon VA, et al. Autoimmune encephalitis epidemiology and a comparison to infectious encephalitis. Ann Neurol. 2018;83(1):166–77
  4. https://cso.gov.tt/subjects/population-and-vital-statistics/population/
  5. Hinds A et al. Caribbean Public Health Agency
  6. Lee YJ et al. Acute disseminated encephalomyelitis in children: differential diagnosis from multiple sclerosis on the basis of clinical course. Korean J Pediatr 2011;54(6):234-240
  7. Bunyan RF, Tang J, Weinshenker B. Acute demyelinating disorders: emergencies and management. Review Neurol Clin. 2012 Feb;30(1):285-307, ix-x
  8. Mullaguri N, Sivakumar S, Battineni A, Anand S, Vanderwerf J. COVID-19 Related Acute Hemorrhagic Necrotizing Encephalitis: A Report of Two Cases and Literature Review. Cureus 2021 Apr 1;13(4):e14236
  9. Graus F, Titulaer MJ, Balu R, Benseler S, et al. A clinical approach to diagnosis of autoimmune encephalitis. Lancet Neurol. 2016 April ; 15(4): 391–404
  10. Rice CM, Scolding NJ. The diagnosis of primary central nervous system vasculitis. Pract Neurol 2020;20:109–115
  11. Chaudhuri A, Kennedy PGE. Diagnosis and treatment of viral encephalitis. Postgrad Med J 2002;78:575–583
  12. Leonhard SE, Mandarakas MR, Gondim FAA, Bateman K, Ferreira MLB, Cornblath DR, et al. Diagnosis and management of Guillain–Barré syndrome in ten steps. Nat Rev Neurol. 2019 Nov;15(11):671-683
  13. RCPCH Guidance - COVID-19 paediatric multisystem inflammatory syndrome (1 May 2020)
  14. Pagana KD, Pagana TJ, Pagana TN. Mosby’s Diagnostic & Laboratory Test Reference. 14th ed. St. Louis, Mo: Elsevier; 2019
  15. Michael O’Sullivan, Andrew McLean-Tooke, Richard Loh. Antinuclear Antibody Test. Australian Family Physician. Volume 42, Issue 10, October 2013
  16. Clinical Practice Guidelines : CSF interpretation (rch.org.au)
  17. Innovita 2019-nCoV Ab Test (Colloidal Gold) - Instructions for Use (fda.gov)
  18. Trinidad And Tobago Population 2021 (Demographics, Maps, Graphs) (worldpopulationreview.com)
  19. Vladimir N. Uversky, Fatma Elrashdy, Abdullah Aljadawi, Syed Moasfar Ali, Rizwan Hasan Khan, Elrashdy M. Redwan. Severe acute respiratory syndrome coronavirus 2 infection reaches the human nervous system: How? J Neurosci Res. 2021 Mar;99(3):750-777.
  20. Hodel J, Darchis C, Outteryck O, et al. Punctate pattern: a promising imaging marker for the diagnosis of natalizumab-associated PML. Neurology 2016;86:1516–23.
  21. Monteil V, Kwon H, Prado P, et al. Inhibition of SARS-CoV-2 infections in engineered human tissues using clinical-grade soluble human ACE2. Cell 2020;181:905–913.e7.
  22. Gao Z, Zhang H, Liu C, Dong K. Autoantibodies in COVID-19: frequency and function. Autoimmunity Reviews 20 (2021) 10275.
  23. Yuki N, Hartung HP. Guillain-Barré syndrome. N Engl J Med. 2012;366(24):2294-2304.
  24. Kreye J, Reincke SM, Prüss H. Do cross-reactive antibodies cause neuropathology in COVID-19? Nat Rev Immunol. 2020;20(11):645-646.
  25. Lindan CE, Mankad K, Ram D, et al; ASPNR PECOBIG Collaborator Group. Neuroimaging manifestations in children with SARS-CoV-2 infection: a multinational, multicentre collaborative study. Lancet Child Adolesc Health. 2020;S2352-4642(20)30362-X.
  26. Lindan CE, Mankad K, Ram D, et al; ASPNR PECOBIG Collaborator Group. Neuroimaging manifestations in children with SARS-CoV-2 infection: a multinational, multicentre collaborative study. Lancet Child Adolesc Health. 2020;S2352-4642(20)30362-X.
  27. Abdel-Mannan O, Eyre M, Löbel U, et al. Neurologic and radiographic findings associated with COVID-19 infection in children.JAMA Neurol. 2020.
  28. Lin J, Lawson EC, Verma S, Peterson RB, Sidhu R. Cytotoxic lesion of the corpus callosum in an adolescent with multisystem inflammatory syndrome and SARS-CoV-2 infection. AJNR Am J Neuroradiol. 2020;41(11):2017-2019.
  29. Stéphane Kremer, François Lersy , Mathieu Anheim, Hamid Merdji, Maleka Schenck et al. Neurologic and neuroimaging findings in patients with COVID-19: A retrospective multicenter study. Neurology. 2020 Sep 29;95(13):e1868-e1882.
  30. Rasmussen C, Niculescu I, Patel S, Krishnan A. COVID-19 and involvement of the corpus callosum: potential effect of the cytokine storm? AJNR Am J Neuroradiol. 2020;41(9):1625-1628.
  31. Moonis G, Filippi CG, Kirsch CFE, et al. The spectrum of neuroimaging findings on CT and MRI in adults with coronavirus disease (COVID-19). AJR Am J Roentgenol. 2020.
  32. Radmanesh A, Derman A, Lui YW, et al. COVID-19-associated diffuse leukoencephalopathy and microhemorrhages. Radiology. 2020;297(1):E223-E227.
  33. Kim MG, Stein AA, Overby P, et al. Fatal cerebral edema in a child with COVID-19. Pediatr Neurol. 2021;114:77-78. doi:10.1016/j.pediatrneurol.2020.10.005.
  34. Piliero PJ, Brody J, Zamani A, Deresiewicz RL. Eastern equine encephalitis presenting as focal neuroradiographic abnormalities: case report and review. Clin Infect Dis. 1994;18(6):985-988.
  35. Wendell LC, Potter NS, Roth JL, Salloway SP, Thompson BB. Successful management of severe neuroinvasive eastern equine encephalitis. Neurocrit Care. 2013;19(1):111-115. doi:10.1007/s12028-013-9822-5.
  36. Krishnan P, Glenn OA, Samuel MC, et al. Acute fulminant cerebral edema: a newly recognized phenotype in children with suspected encephalitis. J Pediatric Infect Dis Soc. 2020;piaa063.
  37. Agarwal S, Conway J, Nguyen V, et al. Serial Imaging of virus-associated necrotizing disseminated acute leukoencephalopathy (VANDAL) in COVID-19. AJNR Am J Neuroradiol. 2021;42(2):279-284.
  38. Abdel-Mannan O, Eyre M, Löbel U, Bamford A, Eltze C, Hameed B, Hemingway C, Hacohen Y. Neurologic and Radiographic Findings Associated With COVID-19 Infection in Children. JAMA Neurol. 2020 Nov; 77(11): 1–6
  39. Vepa A, Bae JP, Ahmed F, Pareek M, Khunti K. COVID-19 and ethnicity: A novel pathophysiological role for inflammation. Diabetes Metab Syndr. Sep-Oct 2020;14(5):1043-1051
  40. Kerri L. LaRovere, Becky J. Riggs, Tina Y. Poussaint et al. Neurologic Involvement in Children and Adolescents Hospitalized in the United States for COVID-19 or Multisystem Inflammatory Syndrome. JAMA Neurol. 2021;78(5):536-547. doi:10.1001/jamaneurol.2021.0504

Similar Articles

1 2 3 4 5 6 7 > >> 

You may also start an advanced similarity search for this article.