TY - JOUR
T1 - Predicting Outcome in Guillain-Barré Syndrome International Validation of the Modified Erasmus GBS Outcome Score
AU - the IGOS Consortium
AU - Doets, Alex Y.
AU - Lingsma, Hester F.
AU - Walgaard, Christa
AU - Islam, Badrul
AU - Papri, Nowshin
AU - Davidson, Amy
AU - Yamagishi, Yuko
AU - Kusunoki, Susumu
AU - Dimachkie, Mazen M.
AU - Waheed, Waqar
AU - Kolb, Noah
AU - Islam, Zhahirul
AU - Mohammad, Quazi Deen
AU - Harbo, Thomas
AU - Sindrup, Soren H.
AU - Chavada, Govindsinh
AU - Willison, Hugh J.
AU - Casasnovas, Carlos
AU - Bateman, Kathleen
AU - Miller, James A.L.
AU - van den Berg, Bianca
AU - Verboon, Christine
AU - Roodbol, Joyce
AU - Leonhard, Sonja E.
AU - Benedetti, Luana
AU - Kuwabara, Satoshi
AU - van den Bergh, Peter
AU - Monges, Soledad
AU - Marfia, Girolama A.
AU - Shahrizaila, Nortina
AU - Galassi, Giuliana
AU - Péréon, Yann
AU - Bürmann, Jan
AU - Kuitwaard, Krista
AU - Kleyweg, Ruud P.
AU - Marchesoni, Cintia
AU - Sedano Tous, María J.
AU - Querol, Luis
AU - Illa, Isabel
AU - Wang, Yuzhong
AU - Nobile-Orazio, Eduardo
AU - Rinaldi, Simon
AU - Schenone, Angelo
AU - Pardo, Julio
AU - Vermeij, Frederique H.
AU - Lehmann, Helmar C.
AU - Granit, Volkan
AU - Cavaletti, Guido
AU - Gutiérrez-Gutiérrez, Gerardo
AU - Silvestri, Nicholas J.
N1 - Publisher Copyright:
© 2022 Lippincott Williams and Wilkins. All rights reserved.
PY - 2022/2/1
Y1 - 2022/2/1
N2 - Background and Objectives The clinical course and outcome of the Guillain-Barré syndrome (GBS) are diverse and vary among regions. The modified Erasmus GBS Outcome Score (mEGOS), developed with data from Dutch patients, is a clinical model that predicts the risk of walking inability in patients with GBS. The study objective was to validate the mEGOS in the International GBS Outcome Study (IGOS) cohort and to improve its performance and region specificity. Methods We used prospective data from the first 1,500 patients included in IGOS, aged ≥6 years and unable to walk independently. We evaluated whether the mEGOS at entry and week 1 could predict the inability to walk unaided at 4 and 26 weeks in the full cohort and in regional subgroups, using 2 measures for model performance: (1) discrimination: area under the receiver operating characteristic curve (AUC) and (2) calibration: observed vs predicted probability of being unable to walk independently. To improve the model predictions, we recalibrated the model containing the overall mEGOS score, without changing the individual predictive factors. Finally, we assessed the predictive ability of the individual factors. Results For validation of mEGOS at entry, 809 patients were eligible (Europe/North America [n = 677], Asia [n = 76], other [n = 56]), and 671 for validation of mEGOS at week 1 (Europe/North America [n = 563], Asia [n = 65], other [n = 43]). AUC values were >0.7 in all regional subgroups. In the Europe/North America subgroup, observed outcomes were worse than predicted; in Asia, observed outcomes were better than predicted. Recalibration improved model accuracy and enabled the development of a region-specific version for Europe/North America (mEGOS-Eu/NA). Similar to the original mEGOS, severe limb weakness and higher age were the predominant predictors of poor outcome in the IGOS cohort. Discussion mEGOS is a validated tool to predict the inability to walk unaided at 4 and 26 weeks in patients with GBS, also in countries outside the Netherlands. We developed a region-specific version of mEGOS for patients from Europe/North America. Classification of Evidence This study provides Class II evidence that the mEGOS accurately predicts the inability to walk unaided at 4 and 26 weeks in patients with GBS.
AB - Background and Objectives The clinical course and outcome of the Guillain-Barré syndrome (GBS) are diverse and vary among regions. The modified Erasmus GBS Outcome Score (mEGOS), developed with data from Dutch patients, is a clinical model that predicts the risk of walking inability in patients with GBS. The study objective was to validate the mEGOS in the International GBS Outcome Study (IGOS) cohort and to improve its performance and region specificity. Methods We used prospective data from the first 1,500 patients included in IGOS, aged ≥6 years and unable to walk independently. We evaluated whether the mEGOS at entry and week 1 could predict the inability to walk unaided at 4 and 26 weeks in the full cohort and in regional subgroups, using 2 measures for model performance: (1) discrimination: area under the receiver operating characteristic curve (AUC) and (2) calibration: observed vs predicted probability of being unable to walk independently. To improve the model predictions, we recalibrated the model containing the overall mEGOS score, without changing the individual predictive factors. Finally, we assessed the predictive ability of the individual factors. Results For validation of mEGOS at entry, 809 patients were eligible (Europe/North America [n = 677], Asia [n = 76], other [n = 56]), and 671 for validation of mEGOS at week 1 (Europe/North America [n = 563], Asia [n = 65], other [n = 43]). AUC values were >0.7 in all regional subgroups. In the Europe/North America subgroup, observed outcomes were worse than predicted; in Asia, observed outcomes were better than predicted. Recalibration improved model accuracy and enabled the development of a region-specific version for Europe/North America (mEGOS-Eu/NA). Similar to the original mEGOS, severe limb weakness and higher age were the predominant predictors of poor outcome in the IGOS cohort. Discussion mEGOS is a validated tool to predict the inability to walk unaided at 4 and 26 weeks in patients with GBS, also in countries outside the Netherlands. We developed a region-specific version of mEGOS for patients from Europe/North America. Classification of Evidence This study provides Class II evidence that the mEGOS accurately predicts the inability to walk unaided at 4 and 26 weeks in patients with GBS.
UR - https://www.scopus.com/pages/publications/85124464881
U2 - 10.1212/WNL.0000000000013139
DO - 10.1212/WNL.0000000000013139
M3 - Article
C2 - 34937789
AN - SCOPUS:85124464881
SN - 0028-3878
VL - 98
SP - E518-E532
JO - Neurology
JF - Neurology
IS - 5
ER -