TY - JOUR
T1 - Acute flaccid myelitis and Guillain–Barré syndrome in children
T2 - A comparative study with evaluation of diagnostic criteria
AU - the 2016 Enterovirus D68 Acute Flaccid Myelitis Working Group and the Dutch Pediatric GBS Study Group
AU - Helfferich, Jelte
AU - Roodbol, Joyce
AU - de Wit, Marie-Claire
AU - Brouwer, Oebele F.
AU - Jacobs, Bart C.
AU - Aberle, Stephan W.
AU - Popow-Kraupp, Theresia
AU - Nikolaeva-Glomb, Lubomira
AU - Rainetova, Petra
AU - Midgley, Sofie
AU - Fischer, Thea Kølsen
AU - Simonlatser, Grethel
AU - Savolainen-Kopra, Carita
AU - Lina, Bruno
AU - Schuffenecker, Isabelle
AU - Aubart, Melodie
AU - Gitiaux, Cyril
AU - Antona, Denise
AU - Eis-Hübinger, Anna Maria
AU - Buderus, Stephan
AU - Panning, Marcus
AU - Nowotny, Markus
AU - Kiechle, Lisa
AU - Böttcher, Sindy
AU - Takács, Mária
AU - Farkas, Ágnes
AU - Löve, Arthur
AU - Baldanti, Fausto
AU - Capobianchi, Maria Rosaria
AU - Valli, Maria Beatrice
AU - Esposito, Susanna
AU - Pariani, Elena
AU - Binda, Sandro
AU - Neuteboom, Rinze
AU - Pas, Suzan
AU - Benschop, Kimberley
AU - Meijer, Adam
AU - Nordbø, Svein Arne
AU - Hafstrøm, Maria
AU - Dudman, Susanne Gjeruldsen
AU - Viekilde Pfeiffer, Helle Cecilie
AU - Guiomar, Raquel
AU - Palminha, Paula
AU - Costa, Inês
AU - Dias, Andrea Sofia
AU - Tecu, Cristina
AU - Cherciu, Carmen Maria
AU - Lazarevic, Ivana
AU - Filipović-Vignjević, Svetlana
AU - Berginc, Natasa
AU - Margüello, Mónica Gozalo
AU - Cabrerizo, María
AU - García Iñiguez, Juan Pablo
AU - Castro, Sonia Perez
AU - Rodrigo, Carlos
AU - Antón, Andrés
AU - Garcia, Núria Rabella
AU - Dyrdak, Robert
AU - Albert, Jan
AU - Kramer, Rolf
AU - Stacpoole, Sybil
AU - Thomas, Rhys
AU - O'Flaherty, Niamh
AU - Drew, Richard
AU - Templeton, Kate
AU - McDougall, Catherine
AU - Eunson, Paul
AU - Chinchankar, Nandita
AU - Shetty, Jay
AU - Moore, Catherine
AU - Williams, Christopher
AU - Knoester, Marjolein
AU - Poelman, Randy
AU - van Leer-Buter, Coretta
AU - Niesters, Bert
AU - Engelen, Marc
AU - Erasmus, Corrie E.
AU - Geleijns, Karin
AU - Kotsopoulos, Irene A.W.
AU - Nicolai, Joost
AU - Niermeijer, Jikke Mien F.
AU - Niks, Erik H.
AU - Samijn, Johnny P.A.
N1 - Funding Information:
M.C.d.W. has received honoraria paid to her institution by Novartis for serving on a steering committee and presenting at a conference, and has received research funding from the Epilepsiefonds (Dutch Epilepsy Foundation), Hersenstichting, and Sophia Foundation. B.C.J. has received funding for travel from Baxter International, and has received research funding from the Netherlands Organization for Health Research and Development, Erasmus MC, Prinses Beatrix Spierfonds, Stichting Spieren voor Spieren, CSL‐Behring, Grifols, Annexon, Hansa Biopharma, and the GBS‐CIDP Foundation International. None of the other authors has any conflict of interest to disclose.
Funding Information:
The Prinses Beatrix Spierfonds funded the PhD project of J.R. on GBS in children (project number: W.OR12-04)
Publisher Copyright:
© 2021 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology.
PY - 2022/2
Y1 - 2022/2
N2 - Background and purpose: Differentiation between acute flaccid myelitis (AFM) and Guillain–Barré syndrome (GBS) can be difficult, particularly in children. Our objective was to improve the diagnostic accuracy by giving recommendations based on a comparison of clinical features and diagnostic criteria in children with AFM or GBS. Methods: A cohort of 26 children with AFM associated with enterovirus D68 was compared to a cohort of 156 children with GBS. The specificity of the Brighton criteria, used for GBS diagnosis, was evaluated in the AFM cohort and the specificity of the Centers for Disease Control and Prevention (CDC) AFM diagnostic criteria in the GBS cohort. Results: Children with AFM compared to those with GBS had a shorter interval between onset of weakness and nadir (3 vs. 8 days, p < 0.001), more often had asymmetric limb weakness (58% vs. 0%, p < 0.001), and less frequently had sensory deficits (0% vs. 40%, p < 0.001). In AFM, cerebrospinal fluid leukocyte counts were higher, whereas protein concentrations were lower. Spinal cord lesions on magnetic resonance imaging were only found in AFM patients. No GBS case fulfilled CDC criteria for definite AFM. Of the AFM cases, 8% fulfilled the Brighton criteria for GBS, when omitting the criterion of excluding an alternate diagnosis. Conclusions: Despite the overlap in clinical presentation, we found distinctive early clinical and diagnostic characteristics for differentiating AFM from GBS in children. Diagnostic criteria for AFM and GBS usually perform well, but some AFM cases may fulfill clinical diagnostic criteria for GBS. This underlines the need to perform diagnostic tests early to exclude AFM in children suspected of atypical GBS.
AB - Background and purpose: Differentiation between acute flaccid myelitis (AFM) and Guillain–Barré syndrome (GBS) can be difficult, particularly in children. Our objective was to improve the diagnostic accuracy by giving recommendations based on a comparison of clinical features and diagnostic criteria in children with AFM or GBS. Methods: A cohort of 26 children with AFM associated with enterovirus D68 was compared to a cohort of 156 children with GBS. The specificity of the Brighton criteria, used for GBS diagnosis, was evaluated in the AFM cohort and the specificity of the Centers for Disease Control and Prevention (CDC) AFM diagnostic criteria in the GBS cohort. Results: Children with AFM compared to those with GBS had a shorter interval between onset of weakness and nadir (3 vs. 8 days, p < 0.001), more often had asymmetric limb weakness (58% vs. 0%, p < 0.001), and less frequently had sensory deficits (0% vs. 40%, p < 0.001). In AFM, cerebrospinal fluid leukocyte counts were higher, whereas protein concentrations were lower. Spinal cord lesions on magnetic resonance imaging were only found in AFM patients. No GBS case fulfilled CDC criteria for definite AFM. Of the AFM cases, 8% fulfilled the Brighton criteria for GBS, when omitting the criterion of excluding an alternate diagnosis. Conclusions: Despite the overlap in clinical presentation, we found distinctive early clinical and diagnostic characteristics for differentiating AFM from GBS in children. Diagnostic criteria for AFM and GBS usually perform well, but some AFM cases may fulfill clinical diagnostic criteria for GBS. This underlines the need to perform diagnostic tests early to exclude AFM in children suspected of atypical GBS.
KW - acute flaccid myelitis
KW - Brighton criteria
KW - Guillain–Barré syndrome
UR - http://www.scopus.com/inward/record.url?scp=85123651274&partnerID=8YFLogxK
U2 - 10.1111/ene.15170
DO - 10.1111/ene.15170
M3 - Article
C2 - 34747551
AN - SCOPUS:85123651274
SN - 1351-5101
VL - 29
SP - 593
EP - 604
JO - European Journal of Neurology
JF - European Journal of Neurology
IS - 2
ER -