19. Severe prognostic factors in children with Guillain – Barre syndrome

Vu Thu Phuong, Cao Vu Hung, Do Thanh Huong

Main Article Content

Abstract

We conducted a survey research on 127 children with Guillain - Barre syndrome at the National Children's Hospital from 7/2018 to 6/2023 to investigate severe prognosis factors associated with this condition. The mean age was 6.14 ± 0.37 years old (16 months - 16 years old), male/female ratio was 2.1/1. There were 13 patients in the severe group requiring mechanical ventilation, including 1 death (0.8%). 62.2% had pre - infectious factors, common were fever 36.2%, respiratory infections 31.1%, digestive disorders 7.1%. Cytoalbuminologic dissociation was found in 72% of patients, 2 common types of electromyography were demyelination and axonal degeneration for 31.7% and 41.3%. Prognosis of severe disease were pre - infection with fever, short day of presentation, oropharyngeal weakness at onset, low muscle strength score at admission, autonomic dysfunction, cranial nerve palsy, respiratory failure, fever during treatment, increased leucocyte count, increased C - reactive protein and increased neutrophil lymphocyte ratio. Clinical symptoms of Guillain - Barre syndrome in children are various and atypical thus it is necessary to combine clinical and laboratory studies to fully evaluate the severe prognostic factors of the disease. Peripheral blood count and C - reactive protein testing should be indicated in patients with clinical findings suggestive of severe disease.


Methods: A survey research on 127 children with Guillain - Barre syndrome at the National Children's Hospital from 7/2018 to 6/2023.


Results: Analysis of a total of 127 children, the male/female ratio was 2.1/1, the mean age was 6.14 ± 0.37 years old (16 months - 16 years old). 62.2% had antecedent illness, common were respiratory infections 31.1%, fever 36.2%, digestive disorders 7.1%. There are 13/127 patients in the severe group (Hughes >4 points) requiring mechanical ventilation, including 1 death (0.8%). Some factors related to the prognosis of severe disease: pre - infection with fever (p = 0.015), short day of presentation (p = 0.0001), oropharyngeal weakness at onset (p = 0.013), low MRC score at admission (p = 0.003), autonomic dysfunction (p = 0.0001), cranial nerve palsy (p = 0.026), respiratory failure ( p = 0.0001), fever during treatment (p = 0.0001), increased leucocyte count (p = 0.008), increased CRP (C - reactive protein) (p = 0.004), increased NLR (Neutrophil lymphocyte ratio) (p = 0.009).


Conclusions: Clinical symptoms of Guillain - Barre syndrome in children are various and atypical. Prognostic factors for severe disease include pre - infection with fever, short time of presentation, oropharyngeal weakness at onset, low MRC score at admission, autonomic dysfunction, cranial nerve palsy, respiratory failure and fever during treatment, increased leukocytes count, increased CRP and increased NLR. It is necessary to combine clinical and laboratory studies to fully evaluate the severe prognostic factors of the disease. Peripheral blood count and CRP testing should be indicated in patients with clinical findings suggestive of severe disease.

Article Details

References

1. Hughes RA, Cornblath DR. Guillain-Barré syndrome. The Lancet. 2005; 366(9497): 1653-1666. doi:10.1016/S0140-6736(05)67665-9.
2. Asbury AK, Cornblath DR. Assessment of current diagnostic criteria for Guillain-Barré syndrome. Ann Neurol. 1990; 27 Suppl: S21-24. doi:10.1002/ana.410270707.
3. Korinthenberg R, Schessl J, Kirschner J. Clinical presentation and course of childhood Guillain-Barré syndrome: a prospective multicentre study. Neuropediatrics. 2007; 38(1): 10-17. doi:10.1055/s-2007-981686.
4. Evans OB, Vedanarayanan V. Guillain-Barré syndrome. Pediatr Rev. 1997; 18(1): 10-16. doi:10.1542/pir.18-1-10
5. Hughes RA, Newsom-Davis JM, Perkin GD,et al. Controlled trial prednisolone in acute polyneuropathy. Lancet Lond Engl. 1978; 2(8093): 750-753. doi:10.1016/s0140-6736(78)92644-2.
6. McMillan HJ, Kang PB. Pediatric Electromyography: Concepts and Clinical Applications. Springer; 2017.
7. Moosmann J, Krusemark A, Dittrich S, et al. Age- and sex-specific pediatric reference intervals for neutrophil-to-lymphocyte ratio, lymphocyte-to-monocyte ratio, and platelet-to-lymphocyte ratio. Int J Lab Hematol. 2022; 44(2): 296-301. doi:10.1111/ijlh.13768.
8. Levison LS, Thomsen RW, Markvardsen LK,et al. Pediatric Guillain-Barré Syndrome in a 30-Year Nationwide Cohort. Pediatr Neurol. 2020; 107: 57-63. doi:10.1016/j.pediatrneurol.2020.01.017.
9. Singh S, Gupta N, Gupta AM,et al. Clinical profile and predictors for outcome in children presenting with Guillain–Barré syndrome. J Fam Med Prim Care. 2020; 9(10): 5316-5319. doi:10.4103/jfmpc.jfmpc_951_20.
10. Ruts L, Drenthen J, Jongen JLM, et al. Pain in Guillain-Barre syndrome: a long-term follow-up study. Neurology. 2010; 75(16): 1439-1447. doi:10.1212/WNL.0b013e3181f88345.
11. Lee JH, Sung IY, Rew IS. Clinical presentation and prognosis of childhood Guillain-Barré syndrome. J Paediatr Child Health. 2008; 44(7-8): 449-454. doi:10.1111/j.1440-1754.2008.01325.x.
12. Tiwari I, Alam A, Kanta C, et al. Clinical Profile and Predictors of Mechanical Ventilation in Guillain-Barre Syndrome in North Indian Children. J Child Neurol. 2021; 36(6): 453-460. doi:10.1177/0883073820978020.
13. Ethemoglu O, Calik M. Effect of serum inflammatory markers on the prognosis of adult and pediatric patients with Guillain-Barré syndrome. Neuropsychiatr Dis Treat. 2018; 14:1255-1260. doi:10.2147/NDT.S162896.
14. Barzegar M, Toopchizadeh V, Golalizadeh D,et al. A Predictive Model for Respiratory Failure and Determining the Risk Factors of Prolonged Mechanical Ventilation in Children with Guillain-Barre Syndrome. Iran J Child Neurol. 2020; 14(3): 33-46.
15. Li C, Sun RD, Feng L,et al. Risk factors associated with the need for mechanical ventilation in children with Guillain-Barré syndrome. Zhongguo Dang Dai Er Ke Za Zhi Chin J Contemp Pediatr. 2021; 23(9): 922-926. doi:10.7499/j.issn.1008-8830.2106003.