Staging model for amyotrophic lateral sclerosis in Singapore

Introduction: A clinical-based staging model would guide physicians in the prompt management of the evolving symptoms and functional needs of patients with amyotrophic lateral sclerosis (ALS). Methods: We aimed to delineate the clinical trajectory of ALS in Singapore and test the degree of congruity...

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Main Authors: Yuan Teck Tay, Josiah YH Chai, Kamilah Bte Shekh Jabin, Kexin Ang
Format: Article
Language:English
Published: Wolters Kluwer – Medknow Publications 2022-07-01
Series:Singapore Medical Journal
Subjects:
Online Access:https://journals.lww.com/10.11622/smedj.2021001
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author Yuan Teck Tay
Josiah YH Chai
Kamilah Bte Shekh Jabin
Kexin Ang
author_facet Yuan Teck Tay
Josiah YH Chai
Kamilah Bte Shekh Jabin
Kexin Ang
author_sort Yuan Teck Tay
collection DOAJ
description Introduction: A clinical-based staging model would guide physicians in the prompt management of the evolving symptoms and functional needs of patients with amyotrophic lateral sclerosis (ALS). Methods: We aimed to delineate the clinical trajectory of ALS in Singapore and test the degree of congruity of King’s College staging for ALS (King’s staging) among Singapore patients. In this retrospective cohort study, clinical milestones used for staging were identical to King’s staging: stage 1 corresponded to symptom onset; stage 2A corresponded to diagnosis; stage 2B corresponded to two central nervous system (CNS) regions; stage 3B corresponded to three CNS regions; stage 4A corresponded to requirement of supportive enteric feeding; and stage 4B corresponded to requirement of non-invasive ventilation, of which bulbar, diaphragmatic, upper and lower limb pyramidal involvements each constituted one CNS region. Standardised timings from disease onset (0) to death (1) among Singapore patients with ALS were measured. Results: 46 patients with ALS were reviewed. Results were largely congruous with King’s staging. Results for patients with limb-onset. ALS were: diagnosis (0.35); two CNS region involvement (0.42); three CNS region involvement (0.63); diaphragmatic involvement (0.81); and bulbar involvement (0.73). Results for patients with bulbar-onset. ALS were: diagnosis (0.14); two CNS region involvement (0.28); three CNS region involvement (0.42); diaphragmatic involvement (0.62); and bulbar involvement (0.67). Conclusion: King’s staging can be used to model ALS trajectory in Singapore due to the large degree of congruity seen. Easily remembered and accessible knowledge of ALS staging will allow prompt management of the evolving needs of patients with ALS.
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spelling doaj-art-fb72bb5176354df2b3bdd186fd2dc3a02025-02-10T05:20:38ZengWolters Kluwer – Medknow PublicationsSingapore Medical Journal0037-56752737-59352022-07-0163737137510.11622/smedj.2021001Staging model for amyotrophic lateral sclerosis in SingaporeYuan Teck TayJosiah YH ChaiKamilah Bte Shekh JabinKexin AngIntroduction: A clinical-based staging model would guide physicians in the prompt management of the evolving symptoms and functional needs of patients with amyotrophic lateral sclerosis (ALS). Methods: We aimed to delineate the clinical trajectory of ALS in Singapore and test the degree of congruity of King’s College staging for ALS (King’s staging) among Singapore patients. In this retrospective cohort study, clinical milestones used for staging were identical to King’s staging: stage 1 corresponded to symptom onset; stage 2A corresponded to diagnosis; stage 2B corresponded to two central nervous system (CNS) regions; stage 3B corresponded to three CNS regions; stage 4A corresponded to requirement of supportive enteric feeding; and stage 4B corresponded to requirement of non-invasive ventilation, of which bulbar, diaphragmatic, upper and lower limb pyramidal involvements each constituted one CNS region. Standardised timings from disease onset (0) to death (1) among Singapore patients with ALS were measured. Results: 46 patients with ALS were reviewed. Results were largely congruous with King’s staging. Results for patients with limb-onset. ALS were: diagnosis (0.35); two CNS region involvement (0.42); three CNS region involvement (0.63); diaphragmatic involvement (0.81); and bulbar involvement (0.73). Results for patients with bulbar-onset. ALS were: diagnosis (0.14); two CNS region involvement (0.28); three CNS region involvement (0.42); diaphragmatic involvement (0.62); and bulbar involvement (0.67). Conclusion: King’s staging can be used to model ALS trajectory in Singapore due to the large degree of congruity seen. Easily remembered and accessible knowledge of ALS staging will allow prompt management of the evolving needs of patients with ALS.https://journals.lww.com/10.11622/smedj.2021001amyotrophic lateral sclerosismotor neuron diseaseneurodegenerative diseaseprognosisstaging model
spellingShingle Yuan Teck Tay
Josiah YH Chai
Kamilah Bte Shekh Jabin
Kexin Ang
Staging model for amyotrophic lateral sclerosis in Singapore
Singapore Medical Journal
amyotrophic lateral sclerosis
motor neuron disease
neurodegenerative disease
prognosis
staging model
title Staging model for amyotrophic lateral sclerosis in Singapore
title_full Staging model for amyotrophic lateral sclerosis in Singapore
title_fullStr Staging model for amyotrophic lateral sclerosis in Singapore
title_full_unstemmed Staging model for amyotrophic lateral sclerosis in Singapore
title_short Staging model for amyotrophic lateral sclerosis in Singapore
title_sort staging model for amyotrophic lateral sclerosis in singapore
topic amyotrophic lateral sclerosis
motor neuron disease
neurodegenerative disease
prognosis
staging model
url https://journals.lww.com/10.11622/smedj.2021001
work_keys_str_mv AT yuantecktay stagingmodelforamyotrophiclateralsclerosisinsingapore
AT josiahyhchai stagingmodelforamyotrophiclateralsclerosisinsingapore
AT kamilahbteshekhjabin stagingmodelforamyotrophiclateralsclerosisinsingapore
AT kexinang stagingmodelforamyotrophiclateralsclerosisinsingapore