ICARS ATAXIA PDF

Toll-Free U. From high-quality clinical care and groundbreaking research to community programs that improve quality of life, philanthropic support drives our mission and vision. The ICARS was developed to quantify the level of impairment as a result of ataxia as related to hereditary ataxias. Instrument Details. Depends on proficiency of administrator and amount of involvement of patient. Do you see an error or have a suggestion for this instrument summary?

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Clinicians require scientifically rigorous, clinically meaningful rating scales to evaluate the health impact of disease and treatment that cannot be measured using conventional laboratory instruments. Two assumptions of its measurement model were tested: the legitimacy of reporting ICARS scores in FRDA, and the acceptability, reliability, and validity of total and subscale scores.

Seventy-seven people with FRDA were assessed. The posture and gait disturbances subscale also performed well. The other three subscales did not pass standard criteria for tests of scaling assumptions, reliability, and validity. However, the extent to which this score quantifies the true extent of FRDA remains uncertain as our validity testing was limited, partly by the lack of appropriate validating measures.

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Save Cancel. Create a file for external citation management software Create file Cancel. Full-text links Cite Favorites. Abstract Clinicians require scientifically rigorous, clinically meaningful rating scales to evaluate the health impact of disease and treatment that cannot be measured using conventional laboratory instruments.

Mov Disord. PMID: Reliability and validity of the International Cooperative Ataxia Rating Scale: a study in spinocerebellar ataxia patients. Storey E, et al.

J Neurochem. PMID: Review. Systematic review of the psychometric properties of balance measures for cerebellar ataxia. Winser SJ, et al. Clin Rehabil. Epub Jun Show more similar articles See all similar articles. Rummey C, et al. Neurol Genet. Paap BK, et al. Mov Disord Clin Pract. Walton MK, et al. Value Health. Epub Aug Rating disease progression of Friedreich's ataxia by the International Cooperative Ataxia Rating Scale: analysis of a patient database.

Metz G, et al. Common data elements for clinical research in Friedreich's ataxia. Lynch DR, et al. Epub Dec Show more "Cited by" articles See all "Cited by" articles.

Publication types Comparative Study Actions. Research Support, Non-U. Gov't Actions. Validation Study Actions.

MeSH terms Adolescent Actions. Adult Actions. Child Actions. Disability Evaluation Actions. Female Actions. Humans Actions. Male Actions. Middle Aged Actions. Models, Statistical Actions.

Reproducibility of Results Actions. Sensitivity and Specificity Actions. Sickness Impact Profile Actions. Full-text links [x] Wiley. Copy Download.

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International Cooperative Ataxia Rating Scale

The scale is scored out of with 19 items and 4 subscales of postural and gait disturbances, limb ataxia, dysarthria , and oculomotor disorders. Higher scores indicate higher levels of impairment. The ICARS has been validated for use in patients with focal cerebellar lesions [1] and hereditary spinocerebellar and Friedrich's ataxia. From Wikipedia, the free encyclopedia. International Cooperative Ataxia Rating Scale Purpose quantification of impairment due to cerebellar ataxia The International Cooperative Ataxia Rating Scale ICARS is an outcome measure that was created in by the Committee of the World Federation of Neurology with the goal of standardizing the quantification of impairment due to cerebellar ataxia. Subscale Items Weight Postural and gait disturbances 7 34 12 for gait, 22 for stance Limb ataxia 7 52 Dysarthria 2 8 Oculomotor disorders 3 6 The ICARS has been validated for use in patients with focal cerebellar lesions [1] and hereditary spinocerebellar and Friedrich's ataxia. Nov

ARTICLE 108 UCMJ PDF

Development of a Brief Ataxia Rating Scale (BARS) Based on a Modified Form of the ICARS

Clinicians require scientifically rigorous, clinically meaningful rating scales to evaluate the health impact of disease and treatment that cannot be measured using conventional laboratory instruments. Two assumptions of its measurement model were tested: the legitimacy of reporting ICARS scores in FRDA, and the acceptability, reliability, and validity of total and subscale scores. Seventy-seven people with FRDA were assessed. The posture and gait disturbances subscale also performed well.

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