Literature DB >> 35317505

Evaluation of ALSFRS-R Scale with Fuzzy Method in Amyotrophic Lateral Sclerosis.

Gizem Gül Koç1, Cansu Dağsuyu2, Ali Kokangül1, Filiz Koç3.   

Abstract

Introduction: Amyotrophic lateral sclerosis (ALS) is a disease with high morbidity and mortality that adversely affects the activities of daily living. Disease progression in ALS is characterized by loss of function in bulbar, motor, and respiratory parameters. The revised amyotrophic lateral sclerosis functional rating scale (ALSFRS-R), which consists of 12 criteria, is used to determine disease effects on each of these functions. While each criterion is equally important when calculating the total ALSFRS-R score, the importance levels of the 12 criteria may vary in clinical practice. In this classical approach, the relationships among the parameters are not considered and the effects of bulbar, spinal, and respiratory dysfunctions on a patient's activities of daily living may be different.
Methods: In this study, we aimed to evaluate ALS cases with the ALSFRS-R fuzzy method. Although each subheading in the ALSFRS-R had the same score, the disease score was determined by the fuzzy ALSFRS-R method, based on whether a subheading had priority in management of the disease. While creating the functional rating scale ALSFRS-R approach, fuzzy ALSFRS-R score values were obtained by creating fuzzy models for each main group and integrating the fuzzy model results of each main group into a separate model.
Results: In total, 50 patients with definite ALS according to the El Escorial criteria (33 men [66%] and 17 women [34%]; mean age, 58.49±10.01 years) were included in the study. When ALSFRS-R results and fuzzy ALSFRS-R results were compared, the prioritization order of 45 patients increased using the fuzzy ALSFRS-R score, while the prioritization order of five patients remained the same in both evaluations.
Conclusion: The approach obtained by using fuzzy membership functions and decision rules, formed in accordance with expert opinion, was applied to the data of 50 patients from a large-scale hospital. In total, 90% of the patients had increased prioritization when using the fuzzy ALSFRS-R scoring method. Our results showed that the fuzzy approach provided more accurate information regarding a patient's condition. Copyright:
© 2022 Turkish Neuropsychiatric Society.

Entities:  

Keywords:  Amyotrophic lateral sclerosis; functional rating scale; fuzzy

Year:  2022        PMID: 35317505      PMCID: PMC8895801          DOI: 10.29399/npa.27449

Source DB:  PubMed          Journal:  Noro Psikiyatr Ars        ISSN: 1300-0667            Impact factor:   1.339


  16 in total

1.  Spanish adaptation of the revised Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS-R).

Authors:  Teresa Salas Campos; Francisco Rodríguez-Santos; Jesus Esteban; Pilar Cordero Vázquez; Jesus S Mora Pardina; Alejandra Cano Carmona
Journal:  Amyotroph Lateral Scler       Date:  2010-10

2.  Cross-cultural adaptation and validation of als Functional Rating Scale-Revised in Portuguese language.

Authors:  Keyte Guedes; Cecília Pereira; Karina Pavan; Berenice Cataldo Oliveira Valério
Journal:  Arq Neuropsiquiatr       Date:  2010-02       Impact factor: 1.420

3.  ALSFRS and appel ALS scores: discordance with disease progression.

Authors:  Andrei Voustianiouk; Gregory Seidel; Janki Panchal; Mark Sivak; Adam Czaplinski; Albert Yen; Stanley H Appel; Dale J Lange
Journal:  Muscle Nerve       Date:  2008-05       Impact factor: 3.217

4.  The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function. BDNF ALS Study Group (Phase III).

Authors:  J M Cedarbaum; N Stambler; E Malta; C Fuller; D Hilt; B Thurmond; A Nakanishi
Journal:  J Neurol Sci       Date:  1999-10-31       Impact factor: 3.181

5.  [Study of functional rating scale for amyotrophic lateral sclerosis: revised ALSFRS(ALSFRS-R) Japanese version].

Authors:  Y Ohashi; K Tashiro; Y Itoyama; I Nakano; G Sobue; S Nakamura; S Sumino; N Yanagisawa
Journal:  No To Shinkei       Date:  2001-04

6.  Adaptation to Turkish and Reliability Study of the Revised Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS-R).

Authors:  Filiz Koç; Mehmet Balal; Turgay Demir; Z Nazan Alparslan; Yakup Sarica
Journal:  Noro Psikiyatr Ars       Date:  2016-09-01       Impact factor: 1.339

7.  Computer-aided analysis of gait rhythm fluctuations in amyotrophic lateral sclerosis.

Authors:  Yunfeng Wu; Sridhar Krishnan
Journal:  Med Biol Eng Comput       Date:  2009-08-26       Impact factor: 2.602

8.  Validation of the German version of the extended ALS functional rating scale as a patient-reported outcome measure.

Authors:  Susanne Abdulla; Stefan Vielhaber; Sonja Körner; Judith Machts; Hans-Jochen Heinze; Reinhard Dengler; Susanne Petri
Journal:  J Neurol       Date:  2013-06-05       Impact factor: 4.849

9.  Measuring function in advanced ALS: validation of ALSFRS-EX extension items.

Authors:  P Wicks; M P Massagli; C Wolf; J Heywood
Journal:  Eur J Neurol       Date:  2009-03       Impact factor: 6.089

10.  Classification of Gait Patterns in Patients with Neurodegenerative Disease Using Adaptive Neuro-Fuzzy Inference System.

Authors:  Qiang Ye; Yi Xia; Zhiming Yao
Journal:  Comput Math Methods Med       Date:  2018-09-30       Impact factor: 2.238

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