Klassen Samantha, Dufault Brenden, Salman Michael S
College of Medicine, Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.
George and Fay Yee Center for Healthcare Innovation, College of Medicine, Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada.
Cerebellum. 2017 Apr;16(2):348-357. doi: 10.1007/s12311-016-0810-0.
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.
慢性共济失调是儿童相对常见的症状。慢性共济失调的病因众多,难以及时做出诊断。我们推测,通过对慢性共济失调儿科患者的临床特征进行系统分析,可以提高诊断过程的效率。我们的目标是提高慢性共济失调儿科患者诊断过程的效率。回顾性地从几个医院数据库中确定了一组184例年龄在0至16岁之间、于1991年至2008年期间在温尼伯儿童医院接受治疗的慢性共济失调患者。从医院病历中提取临床细节。使用单变量分析在更常见的疾病之间比较数据,以确定可能提高诊断过程效率的相关临床特征。然后进行潜在类别分析,以检测临床特征的独特模式,并确定这些模式是否与慢性共济失调诊断相关。根据统计标准和临床知识,选择了两个各有三个类别的模型以实现最佳拟合。每个类别代表一种特定的症状表现模式或其他临床特征。这三个类别对应于一份合理且较短的可能诊断清单。例如,发育迟缓与肌张力减退与天使综合征的相关性最强。症状表现的特定模式或其他临床特征可能有助于对慢性共济失调儿科患者进行初步评估和诊断。这可能会提高诊断过程的效率。