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Guillain-Barré syndrome in children - High occurrence of Miller Fisher syndrome in East Asian region.
Chiu, Annie Ting Gee; Chan, Ricky Wing Ki; Yau, Maggie Lo Yee; Yuen, Angus Chi Lap; Lam, Alva King Fai; Lau, Shirley Wai Yin; Lau, Alan Ming Chung; Fung, Sharon Tsui Hang; Ma, Kam Hung; Lau, Christine Wai Ling; Yau, Man Mut; Ko, Chun Hung; Tsui, Kwing Wan; Ma, Che Kwan; Tai, Shuk Mui; Yau, Eric Kin Cheong; Fung, Eva; Wu, Shun Ping; Kwong, Karen Ling; Chan, Sophelia Hoi Shan.
Afiliação
  • Chiu ATG; Neurology Team, Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, Hong Kong Special Administrative Region; Neurology Team, Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong Special Administrative Region.
  • Chan RWK; Neurology Team, Department of Paediatrics and Adolescent Medicine, Princess Margaret Hospital, Hong Kong Special Administrative Region.
  • Yau MLY; Neurology Team, Department of Paediatrics, Prince of Wales Hospital, Hong Kong Special Administrative Region.
  • Yuen ACL; Neurology Team, Department of Paediatrics and Adolescent Medicine, Tuen Mun Hospital, Hong Kong Special Administrative Region.
  • Lam AKF; Neurology Team, Department of Paediatrics, Queen Elizabeth Hospital, Hong Kong Special Administrative Region.
  • Lau SWY; Neurology Team, Department of Paediatrics and Adolescent Medicine, Pamela Youde Nethersole Eastern Hospital, Hong Kong Special Administrative Region.
  • Lau AMC; Neurology Team, Department of Paediatrics and Adolescent Medicine, United Christian Hospital, Hong Kong Special Administrative Region.
  • Fung STH; Neurology Team, Department of Paediatrics and Adolescent Medicine, Kwong Wah Hospital, Hong Kong Special Administrative Region.
  • Ma KH; Neurology Team, Department of Paediatrics and Adolescent Medicine, Alice Ho Miu Ling Nethersole Hospital, Hong Kong Special Administrative Region.
  • Lau CWL; Neurology Team, Department of Paediatrics and Adolescent Medicine, Caritas Medical Centre, Hong Kong Special Administrative Region.
  • Yau MM; Neurology Team, Department of Paediatrics and Adolescent Medicine, Tseung Kwan O Hospital, Hong Kong Special Administrative Region.
  • Ko CH; Neurology Team, Department of Paediatrics and Adolescent Medicine, Caritas Medical Centre, Hong Kong Special Administrative Region.
  • Tsui KW; Neurology Team, Department of Paediatrics and Adolescent Medicine, Alice Ho Miu Ling Nethersole Hospital, Hong Kong Special Administrative Region.
  • Ma CK; Neurology Team, Department of Paediatrics and Adolescent Medicine, United Christian Hospital, Hong Kong Special Administrative Region.
  • Tai SM; Neurology Team, Department of Paediatrics and Adolescent Medicine, Pamela Youde Nethersole Eastern Hospital, Hong Kong Special Administrative Region.
  • Yau EKC; Neurology Team, Department of Paediatrics and Adolescent Medicine, Princess Margaret Hospital, Hong Kong Special Administrative Region.
  • Fung E; Neurology Team, Department of Paediatrics, Prince of Wales Hospital, Hong Kong Special Administrative Region.
  • Wu SP; Neurology Team, Department of Paediatrics, Queen Elizabeth Hospital, Hong Kong Special Administrative Region.
  • Kwong KL; Neurology Team, Department of Paediatrics and Adolescent Medicine, Tuen Mun Hospital, Hong Kong Special Administrative Region.
  • Chan SHS; Neurology Team, Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, Hong Kong Special Administrative Region; Neurology Team, Department of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong Special Administrative Region. Electronic address: sophehs@hku.hk
Brain Dev ; 44(10): 715-724, 2022 Nov.
Article em En | MEDLINE | ID: mdl-35906115
ABSTRACT

BACKGROUND:

Guillain-Barré syndrome (GBS) is a rare acquired immune-mediated polyneuropathy. Updated population-based data concerning paediatric GBS is needed.

METHODS:

Paediatric patients aged below 18 years diagnosed with GBS between 2009 and 2018 in all 11 paediatric departments in Hong Kong were identified from the Hong Kong Hospital Authority Clinical Data Analysis and Reporting System. The collected data from medical health records were reviewed by paediatric neurologist from each department. Estimated incidence of paediatric GBS was calculated. We also compared our findings with other paediatric GBS studies in Asia.

RESULTS:

63 subjects of paediatric GBS were identified, giving an estimated annual incidence of 0.62 per 100,000 population. Half of the subjects had acute inflammatory demyelinating polyneuropathy (AIDP) (n = 31; 49.2%), one quarter had Miller Fisher Syndrome (MFS) (n = 16; 25.4%), one-fifth had axonal types of GBS (n = 12; 19.0%), and four were unclassified. Paediatric subjects with axonal subtypes of GBS compared to the other 2 subtypes, had significantly higher intensive care unit (ICU) admission rates (p = 0.001) and longest length of stay (p = 0.009). With immunomodulating therapy, complete recovery was highest in those with MFS (100%), followed by AIDP (87.1%) and axonal GBS (75%). Our study also confirms a higher MFS rate for paediatric GBS in East Asia region and our study has the highest MFS rate (25.4%).

CONCLUSION:

Our population-based 10-year paediatric GBS study provides updated evidence on estimated incidence, healthcare burden and motor outcome of each subtype of paediatric GBS and confirmed a higher occurrence of paediatric MFS in East Asia.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Miller Fisher / Síndrome de Guillain-Barré Tipo de estudo: Diagnostic_studies / Incidence_studies / Prognostic_studies Limite: Aged / Child / Humans País/Região como assunto: Asia Idioma: En Revista: Brain Dev Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Miller Fisher / Síndrome de Guillain-Barré Tipo de estudo: Diagnostic_studies / Incidence_studies / Prognostic_studies Limite: Aged / Child / Humans País/Região como assunto: Asia Idioma: En Revista: Brain Dev Ano de publicação: 2022 Tipo de documento: Article