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Dynamics of Nerve Conduction Studies in Patients With Guillain–Barré Syndrome

  • Samuel Arends*
  • , Laura de Koning
  • , Judith Drenthen
  • , IGOS Consortium
  • , Mahova Zhu
  • , Peter Y.K. van den Bergh
  • , Robert M. Hadden
  • , Nortina Shahrizaila
  • , Ricardo C. Reisin
  • , Satoshi Kuwabara
  • , Senda Ajroud-Driss
  • , Giovanni Antonini
  • , Claudia Balducci
  • , Fabio A. Barroso
  • , Thomas Brannagan
  • , Jan Buermann
  • , Carlos Casasnovas
  • , Guido Cavaletti
  • , Chi Chao Chao
  • , Ulrich Dillmann
  • Mazen Dimachkie, Giuliana Galassi, Gerardo Gutiérrez-Gutiérrez, Thomas Harbo, Sung Tsang Hsieh, Badrul Islam, Hans Katzberg, Lynette Kiers, Giorgia Mataluni, Julio Pardo, Yann Peréon, Yusuf Rajabally, Mark Stettner, Camiel Verhamme, Bart C. Jacobs, Amy Davidson, Alex Doets, Pieter van Doorn, Chris Fokke, Badrul Islam, Zhahirul Islam, Rinske van Koningsveld, Krista Kuitwaard, Linda Luijten, Farah Pelouto, Johnny P.A. Samijn, Robin C.M. Thomma, Frederique H. Vermeij, Leo H. Visser, Christa Walgaard, Marieke van Woerkom
*Corresponding author for this work
  • Cliniques Universitaires Saint-Luc
  • King’s College Hospital
  • University of Malaya
  • Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia
  • Chiba University Hospital
  • Northwestern University
  • University of Rome La Sapienza
  • Azienda Ospedaliera San Gerardo Monza
  • Columbia University
  • Saarland University
  • University Hospital Bellvitge
  • National Taiwan University
  • University of Kansas
  • University of Modena and Reggio Emilia
  • Hospital Universitario Infanta Sofía
  • Universidad Europea de Madrid
  • Aarhus University Hospital
  • University of Toronto
  • Royal Melbourne Hospital
  • University of Rome Tor Vergata
  • Complejo Hospitalario Universitario de Santiago
  • CHU de Nantes
  • Aston University
  • University of Duisburg-Essen
  • Amsterdam UMC

Research output: Contribution to journalArticleAcademicpeer-review

2 Citations (Scopus)
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Abstract

Introduction/Aims: The value of electrodiagnostic subtyping of Guillain–Barré syndrome (GBS) is still debated. This study aimed to determine the diagnostic yield, timing, and changes of the electrodiagnostic subtyping in patients with GBS in serial nerve conduction studies (NCS). Methods: Data were extracted from the International GBS Outcome Study (IGOS) database. Serial NCS were available for 469 patients. For the serial NCS analysis, the intervals between the first and second study were defined as ≥ 7 and ≤ 42 days after onset of weakness. All NCS were classified according to the electrodiagnostic criteria sets of Hadden et al. and Rajabally et al. Results: In NCS conducted within 3 days of onset of weakness, an axonal or demyelinating subtype could be demonstrated in 58.4% (Hadden) and 52.1% (Rajabally). NCS performed at a later timepoint demonstrated a similar yield of axonal and demyelinating subtypes. In patients with motor-sensory and motor GBS, the electrodiagnostic subtype changed on serial NCS in 37.8% (Hadden) and 44.7% (Rajabally). As the subtypes changed in multiple and opposite directions, the total proportion of axonal and demyelinating subtypes remained stable across time points. In patients with motor GBS, both axonal and demyelinating subtypes were found. Discussion: This study demonstrates the highly dynamic disease course of GBS. The role of NCS remains to support the clinical diagnosis of GBS and should be performed as quickly as possible after onset of weakness. If these early NCS are non-diagnostic, repeating the study should be considered. Electrodiagnostic subtyping offers no additional value.

Original languageEnglish
Pages (from-to)832-842
Number of pages11
JournalMuscle and Nerve
Volume73
Issue number5
Early online date8 Feb 2026
DOIs
Publication statusPublished - May 2026

Bibliographical note

Publisher Copyright:
© 2026 The Author(s). Muscle & Nerve published by Wiley Periodicals LLC.

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