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DOI: 10.1590/0004-282X-ANP-2021-0226
Treatment-related fluctuations in Guillain-Barré syndrome: clinical features and predictors of recurrence
Fluctuaciones relacionadas al tratamiento en el Síndrome de Guillain-Barré: características clínicas y predictores de recurrencia
ABSTRACT
Background: A treatment-related fluctuation (TRF) in a patient with Guillain-Barré syndrome (GBS) is defined as clinical deterioration within two months of symptom onset following previous stabilization or improvements with treatment. Objective: To investigate the clinical characteristics and factors that could increase the risk of relapse of GBS in patients with and without TRFs. Methods: Retrospective review of medical records of patients (>18 years) with GBS evaluated between January/2006 and July/2019. Demographic and clinical characteristics, ancillary studies, treatment received, and the clinical course of patients with and without TRFs were analyzed. Results: Overall, 124 cases of GBS were included; seven (5.6%) presented TRFs. GBS-TRF cases were triggered more frequently by infectious mononucleosis (28.57 vs. 8.55%; p=0.01). GBS-TRF were initially treated with plasmapheresis more frequently than those without TRF (14.29 vs. 1.70%; p=0.0349). Combined treatment (71.43 vs. 4.27%; p<0.001) and corticosteroids (42.86 vs. 1.71%; p<0.001) were more commonly used in the GBS-TRF group. GBS-TRF patients presented a higher median initial disability score (4 vs. 2; p=0.01). Conclusions: Patients with GBS triggered by infectious mononucleosis and a high degree of initial disability have higher chances of developing TRFs. Although patients with TRF were treated with plasmapheresis more often, the total number was too low to suggest a link between plasma exchange and TRF.
RESUMEN
Antecedentes: Una fluctuación relacionada al tratamiento (FRT) en un paciente con síndrome de Guillain-Barré (SGB) se define como un deterioro clínico dentro de los dos meses posteriores al inicio de los síntomas después de una estabilización previa o mejoría con el tratamiento. Objetivo: Investigar las características clínicas y los factores que podrían incrementar el riesgo de recaída, comparando pacientes con SGB, con y sin FRT. Métodos: Revisión retrospectiva de historias clínicas de pacientes (>18 años) con SGB evaluados entre enero/2006 y julio/2019. Se analizaron las características demográficas y clínicas, los estudios complementarios, el tratamiento recibido y la evolución clínica de los pacientes con y sin FRT. Resultados: Se incluyeron 124 casos de SGB en el total; 7 (5,6%) presentaron FRT. Los casos de SGB con FRT se desencadenaron con mayor frecuencia por mononucleosis infecciosa (28,57 vs. 8,55%; p=0,01). Los casos de SGB con FRT se trataron inicialmente con plasmaféresis con más frecuencia que aquellos sin FRT (14,29 vs. 1,70%; p=0,0349). El tratamiento combinado (71,43 vs. 4,27%; p<0,001) y los corticosteroides (42,86 vs. 1,71%; p<0,001) se utilizaron con mayor frecuencia en el grupo de SGB con FRT. Los pacientes con FRT presentaron una escala de discapacidad inicial mediana más alta (4 vs. 2; p=0,01). Conclusiones: Aquellos SGB desencadenados por mononucleosis infecciosa y un alto grado de discapacidad inicial tienen una mayor probabilidad de desarrollar FRT. Aunque los pacientes con FRT fueron tratados con plasmaféresis con mayor frecuencia, el número total fue demasiado bajo para sugerir un vínculo entre la plasmaféresis y FRT.
Keywords:
Cytomegalovirus - Herpesvirus 4, Human - Guillain-Barré Syndrome - Infectious MononucleosisPalabras claves:
Citomegalovirus - Herpesvirus Humano 4 - Síndrome de Guillain-Barré - Mononucleosis InfecciosaAuthors’ contributions:
LA: collected the data, conceived and designed the analysis, wrote the paper; JIC: collected the data; PB, VB: performed the analysis; FB: conceived and designed the analysis.
Publication History
Received: 11 June 2021
Accepted: 05 August 2021
Article published online:
06 February 2023
© 2022. Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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References
- 1 Osterman PO, Fagius J, Säfwenberg J, Wikström B. Early relapse of acute inflammatory polyradiculoneuropathy after successful treatment with plasma exchange. Acta Neurol Scand 1988; Apr; 77 (04) 273-277 https://doi.org/10.1111/j.1600-0404.1988.tb05909.x
- 2 Ropper AH, Albers JW, Addison R. Limited relapse in Guillain-Barré syndrome after plasma exchange. Arch Neurol 1988; Mar; 45 (03) 314-315 https://doi.org/10.1001/archneur.1988.00520270096026
- 3 Kleyweg RP, Van der Meche FG. Treatment related fluctuations in Guillain-Barre syndrome after high-dose immunoglobulins or plasma-exchange. J Neurol Neurosurg Psychiatry 1991; Nov; 54 (11) 957-960 https://doi.org/10.1136/jnnp.54.11.957
- 4 Visser LH, Van der Meché FGA, Meulstee J, Van Doorn PA. Dutch Guillain-Barré study group. Risk factors for treatment related clinical fluctuations in Guillain-Barre syndrome. J Neurol Neurosurg Psychiatry 1998; Feb; 64 (02) 242-244 https://doi.org/10.1136/jnnp.64.2.242
- 5 Ruts L, van Koningsveld R, van Doorn PA. Distinguishing acute-onset CIDP from Guillain-Barré syndrome with treatment related fluctuations. Neurology 2005; Jul; 65 (01) 138-140 https://doi.org/10.1212/01.wnl.0000167549.09664.b8
- 6 Ruts L, Drenthen J, Jacobs BC, Van Doorn PA. Distinguishing acute-onset CIDP from fluctuating Guillain-Barre syndrome: a prospective study. Neurology 2010; May; 74 (21) 1680-1686 https://doi.org/10.1212/WNL.0b013e3181e07d14
- 7 Verboon C Doets AY, Galassi G Davidson A, Waheed W Péréon Y, Monges S. Current treatment practice of Guillain-Barré syndrome. Neurology 2019; Jul; 93 (01) e59-e76 https://doi.org/10.1212/WNL.20210226202102267719
- 8 Doets AY, Verboon C, van den Berg B, Harbo T, Cornblath DR, Willison HJ. et al. Regional variation of Guillain-Barré syndrome. Brain 2018; Oct; 141 (10) 2866-2877 https://doi.org/10.1093/brain/awy232
- 9 Kimura J. Electrodiagnosis in diseases of nerve and muscle: principles and practice. 4. Oxford: Oxford University Press; 2001. https://doi.org/10.1093/med/9780199738687.001.0001
- 10 Hadden RD, Cornblath DR, Hughes RA, Zielasek HP, Toyka KV, Swan AV. Electrophysiological classification of Guillain-Barré syndrome: clinical associations and outcome: Plasma Exchange/Sandoglobulin Guillain-Barré Syndrome Trial Group. Ann Neurol 1998; Nov; 44 (05) 780-788 https://doi.org/10.1002/ana.410440512
- 11 Hughes RA, Newsom-Davis JM, Perkin GD, Pierce JM. Controlled trial of prednisolone in acute polyneuropathy. Lancet 1978; Oct; 2(8093) 750-753 https://doi.org/10.1016/s0140-6736(78)92644-2
- 12 Hadden RDM, Karch H, Hartung HP, Zielasek J, Weissbrich B, Schubert J. et al. Preceding infections, immune factors, and outcome in Guillain-Barré syndrome. Neurology 2001; Mar; 56 (06) 758-765 https://doi.org/10.1212/wnl.56.6.758
- 13 Chevret S, Hughes RA, Annane D. Plasma exchange for Guillain-Barré syndrome. Cochrane Database Syst Rev 2002; (02) CD001798-CD001798 https://doi.org/10.1002/14651858.CD001798
- 14 Hughes RA, Swan AV, van Doorn PA. Intravenous immunoglobulin for Guillain-Barré syndrome. Cochrane Database Syst Rev 2012; Jul; (07) CD002063-CD002063 https://doi.org/10.1002/14651858.CD002063.pub5
- 15 Plasma Exchange/Sandoglobulin Guillain-Barre Syndrome Trial Group. Randomised trial of plasma exchange, intravenous immunoglobulin, and combined treatments in Guillain-Barre syndrome. Lancet 1997; Jan; 349(9047) 225-230
- 16 Walgaard C, Jacobs BC, Lingsma HF, Steyerberg DR, van Doorn PA. Second IVIg course in Guillain-Barré syndrome patients with poor prognosis (SID-GBS trial): protocol for a double-blind randomized, placebo-controlled clinical trial. J Peripher Nerv Syst 2018; Dec; 23 (04) 210-215 https://doi.org/10.1111/jns.12286
- 17 Verboon C, van Doorn PA, Jacobs BC. Treatment dilemmas in Guillain-Barré syndrome. J Neurol Neurosurg Psychiatry 2017; Apr; 88 (04) 346-352 https://doi.org/10.1136/jnnp-2016-314862
- 18 van der Meché FG, Schmitz PI. A randomized trial comparing intravenous immune globulin and plasma exchange in Guillain-Barre syndrome: Dutch Guillain-Barre Study Group. N Engl J Med 1992; Apr; 326 (17) 1123-1129 https://doi.org/10.1056/NEJM199204233261705
- 19 Hughes RA, Brassington R, Gunn AA, van Doorn PA. Corticosteroids for Guillain-Barré syndrome. Cochrane Database Syst Rev 2016; Oct; 10 (10) CD001446-CD001446 https://doi.org/10.1002/14651858.CD001446.pub5