期刊文献+

Eiehavioral Symptoms in Motor Neuron Disease and Their Negative Impact on Caregiver Burden 被引量:1

Eiehavioral Symptoms in Motor Neuron Disease and Their Negative Impact on Caregiver Burden
原文传递
导出
摘要 Background: The spectrum of abnormal behaviors in amyotrophic lateral sclerosis/motor neuron disease (ALS/MND) has been described, but its practical meaning, namely its impact on caregiver burden, has not been clearly documented in Chinese population. This study aimed to assess the distribution of abnormal behaviors in Chinese population, and to analyze the relationship between behavior changes and caregivcr burden. Methods: Sixty-five patients with ALS/MND have been consecutively enrolled into registry platform of Peking Union Medical College Hospital. An investigation was performed to these patients and their caregivers using the revised ALS function rating scale, Frontal Behavioral Inventory-ALS version, the Frontal Assessment Battery, and the Caregiver Burden Inventory. Results: Twenty-eight (43.1%) patients displayed abnormal behaviors of varying degrees, with one fulfilling the diagnostic criteria of frontotemporal lobe degeneration. Irritability, logopenia, and inflexibility ranked top 3 of abnormal behavior list. Correlation analysis revealed that the degree of behavioral change and frontal cognitive status were significantly associated with caregiver burden, with more extensive impact from disinhibitive behaviors. Analysis of covariance analysis showed that after associated factors were corrected, caregivers of patients with moderate to severe behavior change reported significantly heavier developmental burden, physical burden, and total burden than those with no behavioral change. Conclusions: Nettrobehavioral symptoms could present in around 40% of Chinese patients with ALS/MND, and the distribution of these behaviors was also unique. Besides, abnormal behaviors were highly related to caregivers' burden. Background: The spectrum of abnormal behaviors in amyotrophic lateral sclerosis/motor neuron disease (ALS/MND) has been described, but its practical meaning, namely its impact on caregiver burden, has not been clearly documented in Chinese population. This study aimed to assess the distribution of abnormal behaviors in Chinese population, and to analyze the relationship between behavior changes and caregivcr burden. Methods: Sixty-five patients with ALS/MND have been consecutively enrolled into registry platform of Peking Union Medical College Hospital. An investigation was performed to these patients and their caregivers using the revised ALS function rating scale, Frontal Behavioral Inventory-ALS version, the Frontal Assessment Battery, and the Caregiver Burden Inventory. Results: Twenty-eight (43.1%) patients displayed abnormal behaviors of varying degrees, with one fulfilling the diagnostic criteria of frontotemporal lobe degeneration. Irritability, logopenia, and inflexibility ranked top 3 of abnormal behavior list. Correlation analysis revealed that the degree of behavioral change and frontal cognitive status were significantly associated with caregiver burden, with more extensive impact from disinhibitive behaviors. Analysis of covariance analysis showed that after associated factors were corrected, caregivers of patients with moderate to severe behavior change reported significantly heavier developmental burden, physical burden, and total burden than those with no behavioral change. Conclusions: Nettrobehavioral symptoms could present in around 40% of Chinese patients with ALS/MND, and the distribution of these behaviors was also unique. Besides, abnormal behaviors were highly related to caregivers' burden.
出处 《Chinese Medical Journal》 SCIE CAS CSCD 2015年第17期2295-2300,共6页 中华医学杂志(英文版)
关键词 Amyotrophic Lateral Sclerosis Behavioral Symptoms Caregiver Burden Motor Neuron Disease Amyotrophic Lateral Sclerosis Behavioral Symptoms Caregiver Burden Motor Neuron Disease
  • 相关文献

参考文献1

二级参考文献5

  • 1Lillo P, Garcin B, Hornberger M, Bak TH, Hodges JR.Neurobehavioral features in frontotemporal dementia with amyotrophic lateral sclerosis. Arch Neuro12010, 67: 826-830. 被引量:1
  • 2Olojugba C, de Silva R, Kartsounis LD, Royan L, Carter J. De Clerambault's syndrome (erotomania) as a presenting feature of fronto-temporal dementia and motor neurone disease (FTD- MND). Behav Neuro12007, 18: 193-195. 被引量:1
  • 3Woollacott IOC., Mead S. The C9ORF72 expansion mutation: gene structure, phenotypic and diagnostic issues. Acta Neurophathol 2014, 127:319-322. 被引量:1
  • 4Fahey C, Byrne S, McLaughlin R, Kenna K, Shatunov A, Donohoe G, et al. Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample. Neurobiol Aging 2014, 35: 1510. 被引量:1
  • 5Zou ZY, Li XG, Liu MS, Cui LY. Screening for C9orf72 repeat expansions in Chinese amyotrophic lateral sclerosis patients. NeurobiolAging 2013, 34:1710. 被引量:1

同被引文献3

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部