Literature DB >> 33472335

Staging model for amyotrophic lateral sclerosis in Singapore.

Yuan Teck Tay1, Josiah Y H Chai2, Kamilah Bte Shekh Jabin2, Kexin Ang2.   

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.

Entities:  

Keywords:  Amyotrophic lateral sclerosis; motor neuron disease; neurodegenerative disease; prognosis; staging model

Mesh:

Year:  2022        PMID: 33472335      PMCID: PMC9578121          DOI: 10.11622/smedj.2021001

Source DB:  PubMed          Journal:  Singapore Med J        ISSN: 0037-5675            Impact factor:   3.331


  13 in total

Review 1.  El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis.

Authors:  B R Brooks; R G Miller; M Swash; T L Munsat
Journal:  Amyotroph Lateral Scler Other Motor Neuron Disord       Date:  2000-12

2.  Early diagnosis of amyotrophic lateral sclerosis mimic syndromes: pros and cons of current clinical diagnostic criteria.

Authors:  Elena Cortés-Vicente; Jesús Pradas; Juan Marín-Lahoz; Noemi De Luna; Jordi Clarimón; Janina Turon-Sans; Ellen Gelpí; Jordi Díaz-Manera; Isabel Illa; Ricard Rojas-Garcia
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2017-04-25       Impact factor: 4.092

3.  Percutaneous endoscopic gastrostomy, body weight loss and survival in amyotrophic lateral sclerosis: a population-based registry study.

Authors:  Antonio Fasano; Nicola Fini; Diana Ferraro; Laura Ferri; Marco Vinceti; Jessica Mandrioli
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2017-01-11       Impact factor: 4.092

4.  Initiation of non-invasive ventilation in amyotrophic lateral sclerosis and clinical practice guidelines: Single-centre, retrospective, descriptive study in a national reference centre.

Authors:  Marjolaine Georges; Jean-Louis Golmard; Claudia Llontop; Amr Shoukri; François Salachas; Thomas Similowski; Capucine Morelot-Panzini; Jésus Gonzalez-Bermejo
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2016-12-15       Impact factor: 4.092

Review 5.  Advance care planning in motor neuron disease: A systematic review.

Authors:  Leigh Murray; Phyllis N Butow
Journal:  Palliat Support Care       Date:  2015-10-14

Review 6.  Management and therapeutic perspectives in amyotrophic lateral sclerosis.

Authors:  Stéphane Mathis; Philippe Couratier; Adrien Julian; Jean-Michel Vallat; Philippe Corcia; Gwendal Le Masson
Journal:  Expert Rev Neurother       Date:  2016-09-20       Impact factor: 4.618

7.  Riluzole and amyotrophic lateral sclerosis survival: a population-based study in southern Italy.

Authors:  S Zoccolella; E Beghi; G Palagano; A Fraddosio; V Guerra; V Samarelli; V Lepore; I L Simone; P Lamberti; L Serlenga; G Logroscino
Journal:  Eur J Neurol       Date:  2007-03       Impact factor: 6.089

Review 8.  Global epidemiology of amyotrophic lateral sclerosis: a systematic review of the published literature.

Authors:  A Chiò; G Logroscino; B J Traynor; J Collins; J C Simeone; L A Goldstein; L A White
Journal:  Neuroepidemiology       Date:  2013-07-11       Impact factor: 3.282

9.  The Amyotrophic Lateral Sclerosis Functional Rating Scale. Assessment of activities of daily living in patients with amyotrophic lateral sclerosis. The ALS CNTF treatment study (ACTS) phase I-II Study Group.

Authors: 
Journal:  Arch Neurol       Date:  1996-02

Review 10.  Quantifying disease progression in amyotrophic lateral sclerosis.

Authors:  Neil G Simon; Martin R Turner; Steve Vucic; Ammar Al-Chalabi; Jeremy Shefner; Catherine Lomen-Hoerth; Matthew C Kiernan
Journal:  Ann Neurol       Date:  2014-09-30       Impact factor: 10.422

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