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Validation and adjustment of modified Erasmus GBS outcome score in Bangladesh

OBJECTIVE: We have assessed and improved the performance of the modified Erasmus GBS Outcome Score (mEGOS) among patients with Guillain‐Barré syndrome (GBS) from Bangladesh. METHODS: Validation cohort consisted of patients with GBS from two prospective cohort studies in Bangladesh. Poor outcome was...

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Autores principales: Papri, Nowshin, Doets, Alex Y., Mohammad, Quazi D., Endtz, Hubert P., Lingsma, Hester F., Jacobs, Bart C., Islam, Zhahirul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380155/
https://www.ncbi.nlm.nih.gov/pubmed/35908170
http://dx.doi.org/10.1002/acn3.51627
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author Papri, Nowshin
Doets, Alex Y.
Mohammad, Quazi D.
Endtz, Hubert P.
Lingsma, Hester F.
Jacobs, Bart C.
Islam, Zhahirul
author_facet Papri, Nowshin
Doets, Alex Y.
Mohammad, Quazi D.
Endtz, Hubert P.
Lingsma, Hester F.
Jacobs, Bart C.
Islam, Zhahirul
author_sort Papri, Nowshin
collection PubMed
description OBJECTIVE: We have assessed and improved the performance of the modified Erasmus GBS Outcome Score (mEGOS) among patients with Guillain‐Barré syndrome (GBS) from Bangladesh. METHODS: Validation cohort consisted of patients with GBS from two prospective cohort studies in Bangladesh. Poor outcome was defined as being unable to walk independently at week 4 and week 26. We excluded patients able to walk independently, patients who died within the first week, or with missing GBS disability scores. Performance of mEGOS at entry and week 1 was determined based on the discriminative ability (ability to differentiate between patients able and unable to walk independently; measured using the area under the receiver operating characteristic curves [AUC]) and calibration (observed probability versus predicted probability of poor outcome). RESULTS: A total of 506 patients aged ≥6‐year‐old were enrolled, with 471 and 366 patients included in mEGOS validation analysis at entry and week 1, respectively. The AUC values for predicting poor outcome (1) at week 4 were 0.69 (mEGOS entry) and 0.78 (mEGOS week 1) and (2) at week 26 were 0.67 (mEGOS entry) and 0.70 (mEGOS week 1). Mean predicted probabilities of poor outcome corresponded with observed outcomes except for the probability of poor outcome at week 4 which was overestimated by mEGOS week 1. This was resolved by updating the model intercept. INTERPRETATION: The mEGOS shows valid outcome predictions among patients with GBS from Bangladesh. The model can aid the identification of patients at high risk of poor outcome and help to adequately allocate healthcare resources in low‐resource settings.
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spelling pubmed-93801552022-08-19 Validation and adjustment of modified Erasmus GBS outcome score in Bangladesh Papri, Nowshin Doets, Alex Y. Mohammad, Quazi D. Endtz, Hubert P. Lingsma, Hester F. Jacobs, Bart C. Islam, Zhahirul Ann Clin Transl Neurol Research Articles OBJECTIVE: We have assessed and improved the performance of the modified Erasmus GBS Outcome Score (mEGOS) among patients with Guillain‐Barré syndrome (GBS) from Bangladesh. METHODS: Validation cohort consisted of patients with GBS from two prospective cohort studies in Bangladesh. Poor outcome was defined as being unable to walk independently at week 4 and week 26. We excluded patients able to walk independently, patients who died within the first week, or with missing GBS disability scores. Performance of mEGOS at entry and week 1 was determined based on the discriminative ability (ability to differentiate between patients able and unable to walk independently; measured using the area under the receiver operating characteristic curves [AUC]) and calibration (observed probability versus predicted probability of poor outcome). RESULTS: A total of 506 patients aged ≥6‐year‐old were enrolled, with 471 and 366 patients included in mEGOS validation analysis at entry and week 1, respectively. The AUC values for predicting poor outcome (1) at week 4 were 0.69 (mEGOS entry) and 0.78 (mEGOS week 1) and (2) at week 26 were 0.67 (mEGOS entry) and 0.70 (mEGOS week 1). Mean predicted probabilities of poor outcome corresponded with observed outcomes except for the probability of poor outcome at week 4 which was overestimated by mEGOS week 1. This was resolved by updating the model intercept. INTERPRETATION: The mEGOS shows valid outcome predictions among patients with GBS from Bangladesh. The model can aid the identification of patients at high risk of poor outcome and help to adequately allocate healthcare resources in low‐resource settings. John Wiley and Sons Inc. 2022-07-30 /pmc/articles/PMC9380155/ /pubmed/35908170 http://dx.doi.org/10.1002/acn3.51627 Text en © 2022 International Centre for Diarrhoeal Disease Research, Bangladesh. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Papri, Nowshin
Doets, Alex Y.
Mohammad, Quazi D.
Endtz, Hubert P.
Lingsma, Hester F.
Jacobs, Bart C.
Islam, Zhahirul
Validation and adjustment of modified Erasmus GBS outcome score in Bangladesh
title Validation and adjustment of modified Erasmus GBS outcome score in Bangladesh
title_full Validation and adjustment of modified Erasmus GBS outcome score in Bangladesh
title_fullStr Validation and adjustment of modified Erasmus GBS outcome score in Bangladesh
title_full_unstemmed Validation and adjustment of modified Erasmus GBS outcome score in Bangladesh
title_short Validation and adjustment of modified Erasmus GBS outcome score in Bangladesh
title_sort validation and adjustment of modified erasmus gbs outcome score in bangladesh
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380155/
https://www.ncbi.nlm.nih.gov/pubmed/35908170
http://dx.doi.org/10.1002/acn3.51627
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