Literature DB >> 27352287

Can Latent Class Analysis Be Used to Improve the Diagnostic Process in Pediatric Patients with Chronic Ataxia?

Samantha Klassen1, Brenden Dufault2, Michael S Salman3,4.   

Abstract

Chronic ataxia is a relatively common symptom in children. There are numerous causes of chronic ataxia, making it difficult to derive a diagnosis in a timely manner. We hypothesized that the efficiency of the diagnostic process can be improved with systematic analysis of clinical features in pediatric patients with chronic ataxia. Our aim was to improve the efficiency of the diagnostic process in pediatric patients with chronic ataxia. A cohort of 184 patients, aged 0-16 years with chronic ataxia who received medical care at Winnipeg Children's Hospital during 1991-2008, was ascertained retrospectively from several hospital databases. Clinical details were extracted from hospital charts. The data were compared among the more common diseases using univariate analysis to identify pertinent clinical features that could potentially improve the efficiency of the diagnostic process. Latent class analysis was then conducted to detect unique patterns of clinical features and to determine whether these patterns could be associated with chronic ataxia diagnoses. Two models each with three classes were chosen based on statistical criteria and clinical knowledge for best fit. Each class represented a specific pattern of presenting symptoms or other clinical features. The three classes corresponded to a plausible and shorter list of possible diagnoses. For example, developmental delay and hypotonia correlated best with Angelman syndrome. Specific patterns of presenting symptoms or other clinical features can potentially aid in the initial assessment and diagnosis of pediatric patients with chronic ataxia. This will likely improve the efficiency of the diagnostic process.

Entities:  

Keywords:  Ataxia; Latent class analysis

Mesh:

Year:  2017        PMID: 27352287     DOI: 10.1007/s12311-016-0810-0

Source DB:  PubMed          Journal:  Cerebellum        ISSN: 1473-4222            Impact factor:   3.847


  26 in total

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2.  Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients.

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4.  Ethnicity and geographic distribution of pediatric chronic ataxia in Manitoba.

Authors:  Michael S Salman; Shaheen Masood; Meghan Azad; Bernard N Chodirker
Journal:  Can J Neurol Sci       Date:  2014-01       Impact factor: 2.104

5.  Social economic costs and health-related quality of life in patients with degenerative cerebellar ataxia in Spain.

Authors:  Julio López-Bastida; Lilisbeth Perestelo-Pérez; Fernando Montón-Alvarez; Pedro Serrano-Aguilar
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6.  The epidemiology of intermittent and chronic ataxia in children in Manitoba, Canada.

Authors:  Michael S Salman; Esther J Lee; Anindita Tjahjadi; Bernard N Chodirker
Journal:  Dev Med Child Neurol       Date:  2013-02-07       Impact factor: 5.449

7.  Clinical spectrum of episodic ataxia type 2.

Authors:  J Jen; G W Kim; R W Baloh
Journal:  Neurology       Date:  2004-01-13       Impact factor: 9.910

8.  Cerebellar hypoplasia: differential diagnosis and diagnostic approach.

Authors:  Andrea Poretti; Eugen Boltshauser; Dan Doherty
Journal:  Am J Med Genet C Semin Med Genet       Date:  2014-05-16       Impact factor: 3.908

Review 9.  Clinical and genetic aspects of Angelman syndrome.

Authors:  Charles A Williams; Daniel J Driscoll; Aditi I Dagli
Journal:  Genet Med       Date:  2010-07       Impact factor: 8.822

Review 10.  Autosomal recessive cerebellar ataxias.

Authors:  Francesc Palau; Carmen Espinós
Journal:  Orphanet J Rare Dis       Date:  2006-11-17       Impact factor: 4.123

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