{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,8,30]],"date-time":"2025-08-30T16:22:30Z","timestamp":1756570950766,"version":"3.40.5"},"reference-count":25,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2022,8,24]],"date-time":"2022-08-24T00:00:00Z","timestamp":1661299200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["J Paediatrics Child Health"],"published-print":{"date-parts":[[2022,12]]},"abstract":"<jats:sec><jats:title>Background<\/jats:title><jats:p>Guillain\u2013Barre syndrome (GBS) is the commonest cause of acute flaccid paralysis in children. There is a paucity of studies that assess the long\u2010term outcome of paediatric GBS.<\/jats:p><\/jats:sec><jats:sec><jats:title>Aim<\/jats:title><jats:p>To assess the frequency of neurological sequelae and the new\u2010onset symptoms in the long\u2010term follow\u2010up of paediatric GBS and to identify the risk factors associated with them.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>This longitudinal study involved 78 children with GBS treated between January 2015 and 2021. The parents of those children were contacted to visit the hospital for a detailed neurological examination and to look for new\u2010onset symptoms after the initial treatment for GBS.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Of the 78 children, acute inflammatory demyelinating polyradiculoneuropathy, acute motor axonal neuropathy, and acute motor\u2010sensory axonal neuropathy variants were observed in 30 (38.5%), 27 (34.6%) and 11 (14.1%) children, respectively. The median (interquartile range (IQR)) duration of follow\u2010up was 3 (2, 4.5) years. The median (IQR) time to independent ambulation was 30 (13.5, 105) days. The neurological sequelae were found in 22 (28.2%) children. GBS disability score at admission (odds ratio (OR)\u00a0=\u00a04.6; 95% confidence interval (CI): 1.1\u201319.8;<jats:italic>P<\/jats:italic>\u00a0=\u00a00.04) and axonal variant of GBS (OR\u00a0=\u00a04.1; 95% CI: 1.5\u201320.8;<jats:italic>P<\/jats:italic>\u00a0=\u00a00.04) were found to be independent predictors of neurologic sequelae. A total of 28 children experienced new\u2010onset symptoms after GBS, with frequent falls while running and fatigue being the predominant symptoms. Those children with demyelinating variant achieved independent ambulation earlier than the axonal group on survival analysis (log\u2010rank<jats:italic>P<\/jats:italic>value\u00a0=\u00a00.04).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>The presence of neurological sequelae and new\u2010onset symptoms were found in 28.2 and 35% of the GBS children, respectively. High GBS disability score at admission and axonal variant of GBS were independent predictors of neurological sequelae. Knowledge about these would help in devising a plan for rehabilitation.<\/jats:p><\/jats:sec>","DOI":"10.1111\/jpc.16185","type":"journal-article","created":{"date-parts":[[2022,8,24]],"date-time":"2022-08-24T10:38:59Z","timestamp":1661337539000},"page":"2211-2217","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["Assessment of neurological sequelae and new\u2010onset symptoms in the long\u2010term follow\u2010up of paediatric Guillain\u2013Barre syndrome: A longitudinal study from India"],"prefix":"10.1111","volume":"58","author":[{"given":"Kiruthiga","family":"Sugumar","sequence":"first","affiliation":[{"name":"Department of Pediatrics Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER) Pondicherry India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Aakash C","family":"Chidambaram","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER) Pondicherry India"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1070-0070","authenticated-orcid":false,"given":"Dhandapany","family":"Gunasekaran","sequence":"additional","affiliation":[{"name":"Department of Pediatrics Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER) Pondicherry India"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2022,8,24]]},"reference":[{"key":"e_1_2_7_2_1","doi-asserted-by":"publisher","DOI":"10.1007\/s00415-017-8429-8"},{"key":"e_1_2_7_3_1","doi-asserted-by":"publisher","DOI":"10.1542\/pir.2017-0189"},{"key":"e_1_2_7_4_1","doi-asserted-by":"publisher","DOI":"10.1002\/ana.410270707"},{"key":"e_1_2_7_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/S1474-4422(07)70130-8"},{"key":"e_1_2_7_6_1","doi-asserted-by":"publisher","DOI":"10.1002\/mus.880141111"},{"key":"e_1_2_7_7_1","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.53.8.1648"},{"key":"e_1_2_7_8_1","doi-asserted-by":"publisher","DOI":"10.1001\/archneur.1989.00520460115022"},{"key":"e_1_2_7_9_1","doi-asserted-by":"publisher","DOI":"10.4103\/0028-3886.86549"},{"key":"e_1_2_7_10_1","doi-asserted-by":"publisher","DOI":"10.1007\/s13312-021-2302-7"},{"key":"e_1_2_7_11_1","doi-asserted-by":"publisher","DOI":"10.4103\/0972-2327.132662"},{"key":"e_1_2_7_12_1","doi-asserted-by":"publisher","DOI":"10.1055\/s-2007-981686"},{"key":"e_1_2_7_13_1","doi-asserted-by":"publisher","DOI":"10.1002\/mus.26706"},{"key":"e_1_2_7_14_1","doi-asserted-by":"crossref","first-page":"24","DOI":"10.4103\/0972-2327.144274","article-title":"Pediatric Guillain\u2010Barr\u00e9 syndrome: Indicators for a severe course","volume":"18","author":"Varkal MA","year":"2015","journal-title":"Ann. 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