Hirono N, Kobayashi H, Mori E
Department of Clinical Neurosciences, Hyogo Institute for Aging Brain and Cognitive Disorders, Saishoko, Japan.
No To Shinkei. 1998 Jun;50(6):561-7.
Dementia patients need assistance or supervision in their daily activities. This often places a major burden on their caregivers. The caregiver burden is reportedly a critical determinant for negative caregiving outcomes. However, in Japan, no study evaluating the burden experienced by caregivers for patients with established dementia diagnosis with a standardized instrument has been carried out. The Zarit Caregiver Burden Interview (ZBI) is a standardized, validated, reliable tool for assessment of the burden of caregivers for dementia patients, and has been used in many studies in North America. In this study, we arranged a Japanese version of the ZBI and applied it to caregivers who were caring dementia patients. After examining the reliability and validity of this version, we then studied a relationship between patients' impairments and caregivers' burden.
Subjects were 117 dementia patients. Diagnosis of dementia was made through extensive examinations including MRI and PET/SPECT of the brain and based on appropriate clinical diagnostic criteria of each disorder, which included Alzheimer's disease (n = 76), frontotemporal dementia (n = 10), vascular dementia (n = 11), progressive supranuclear palsy (n = 3), corticobasal degeneration (n = 5), dementia with Lewy bodies (n = 11), and normal pressure hydrocephalus (n = 1). The patients included 80 women and 37 men; the mean age was 72.3 +/- 7.7 (SD) years. Trained nurses interviewed a principal caregiver of each patient by using the ZBI. The caregivers included the patients' spouses (n = 62), offsprings (n = 17), offspring's spouses (n = 37), and sibling (n = 1). Cognitive, functional, and neuropsychiatric impairments and severity of dementia were assessed with standardized instruments of the Mini-Mental State Examination (MMSE), Hyogo Activities of Daily Living Scale (HADLS), Neuropsychiatric Inventory (NPI), and Clinical Dementia Rating (CDR), respectively.
The mean total ZBI score was 28.6 +/- 15.3 (SD), the Personal strain (PS) score was 17.4 +/- 8.9, and Role strain (RS) score was 6.5 +/- 5.7. All three scores had high Cronbach's alpha coefficients (Total: 0.88, PS: 0.78, RS: 0.80) and had high Pearson's correlation coefficients with a single global rating of burden (Total: 0.69, PS: 0.65, RS: 0.60). All ZBI scores were significantly correlated with MMSE, CDR, HADLS, and NPI scores. A stepwise regression analysis revealed only the HADLS score and NPI score as significant predictors of ZBI scores.
This Japanese version of the ZBI has a sufficient reliability and validity comparable to those reported for the original version. Our results suggested that the patients' functional and neuropsychiatric impairments were main patient's factors to increase the caregiver's burden.
痴呆患者在日常活动中需要协助或监督。这往往给他们的照料者带来沉重负担。据报道,照料者负担是负面照料结果的关键决定因素。然而,在日本,尚未有研究使用标准化工具评估已确诊痴呆患者的照料者所经历的负担。 Zarit照料者负担访谈(ZBI)是一种用于评估痴呆患者照料者负担的标准化、经过验证且可靠的工具,已在北美的许多研究中使用。在本研究中,我们编制了ZBI的日文版,并将其应用于照料痴呆患者的照料者。在检验了该版本的信度和效度后,我们接着研究了患者的损伤与照料者负担之间的关系。
研究对象为117例痴呆患者。通过包括脑部MRI和PET/SPECT在内的广泛检查,并依据每种疾病的适当临床诊断标准做出痴呆诊断,其中包括阿尔茨海默病(n = 76)、额颞叶痴呆(n = 10)、血管性痴呆(n = 11)、进行性核上性麻痹(n = 3)、皮质基底节变性(n = 5)、路易体痴呆(n = 11)和正常压力脑积水(n = 1)。患者包括80名女性和37名男性;平均年龄为72.3±7.7(标准差)岁。经过培训的护士使用ZBI对每位患者的主要照料者进行访谈。照料者包括患者的配偶(n = 62)、子女(n = 17)、子女的配偶(n = 37)和兄弟姐妹(n = 1)。分别使用简易精神状态检查表(MMSE)、兵库日常生活活动量表(HADLS)、神经精神科问卷(NPI)和临床痴呆评定量表(CDR)等标准化工具评估认知、功能和神经精神损伤以及痴呆的严重程度。
ZBI总分的平均值为28.6±15.3(标准差),个人压力(PS)得分为17.4±8.9,角色压力(RS)得分为6.5±5.7。所有这三个得分都具有较高的克朗巴哈α系数(总分:0.88,PS:0.78,RS:0.80),并且与单一整体负担评定具有较高的皮尔逊相关系数(总分:0.69,PS:0.65,RS:0.60)。所有ZBI得分均与MMSE、CDR、HADLS和NPI得分显著相关。逐步回归分析显示,只有HADLS得分和NPI得分是ZBI得分的显著预测因素。
这个ZBI的日文版具有与原始版本相当的足够信度和效度。我们的结果表明,患者的功能和神经精神损伤是增加照料者负担的主要患者因素。