Evidence map›Paper›PMID 33472335›Full record

ArticleSingapore medical journal2022

Staging model for amyotrophic lateral sclerosis in Singapore.

Yuan Teck Tay, Josiah Y H Chai, Kamilah Bte Shekh Jabin, Kexin Ang

Abstract read
In one paragraph

Article in Singapore medical journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yuan Teck TayYong Loo Lin School of Medicine, National University of Singapore, Singapore.
Josiah Y H ChaiDepartment of Neurology, Division of Nursing, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Kamilah Bte Shekh JabinDepartment of Neurology, Division of Nursing, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.
Kexin AngDepartment of Neurology, Division of Nursing, National Neuroscience Institute, Tan Tock Seng Hospital, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Amyotrophic Lateral SclerosisDisease ProgressionHumansRespiration, ArtificialRetrospective StudiesSingaporeAmyotrophic lateral sclerosismotor neuron diseaseneurodegenerative diseaseprognosisstaging model

Identifiers

PMID33472335
PMCPMC9578121

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