A study of disability profile and burden in caregivers of stable schizophrenia patients

IF 0.4 Q4 PSYCHIATRY Neuropsychiatria i Neuropsychologia Pub Date : 2020-01-01 DOI:10.5114/nan.2020.101293
N. Modi, R. Mehta, P. Chaudhary, K. Dave
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引用次数: 3

Abstract

Introduction: Schizophrenia is one of the most devastating disorders, leading to long-term and progressive disability in numerous individuals. Disability reflects an interaction between features of a person’s body and of the society. In all treatments, family psycho-education is also very important as disability of schizophrenia leads to burden upon family members. Caregiver burden can be either objective or subjective. Objective burdens are behavioural phenomena: disruption of the social activities and financial difficulties. Subjective burdens comprise emotional strain on caregivers. Due to the chronic nature of the disease and the disability, patients with schizophrenia as a group need most care in social and economic areas. Aim of the study: To assess the level of burden in caregivers of stable schizophrenia patients and their relation with degree of disability in schizophrenia patients. It was a cross-sectional and observation study. Material and methods: The study was carried out with 154 stable patients of International Classification of Di-seases diagnosed schizophrenia and their primary caregivers. The patients were evaluated on the Indian Disability Evaluation and Assessment Scale (IDEAS) and Positive and Negative Syndrome Scale (PANSS), and the Burden Assessment Schedule (BAS) was used for their primary caregiver. Results: Two thirds of schizophrenia patients who were stable on medication for at least 6 months and diagnosed with schizophrenia for at least 2 years had mild (70.12%) and the rest had moderate disability (29.87%). Greater burden of care was experienced with increasing age. Conclusions: Caregivers’ burden has a direct correlation with overall disability. Deficiency in interaction, communication and employment leads to more burden of care, but not a deficiency in self-care.
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稳定型精神分裂症患者护理人员残疾状况及负担的研究
精神分裂症是最具破坏性的疾病之一,在许多个体中导致长期和进行性残疾。残疾反映了一个人的身体特征和社会特征之间的相互作用。在所有治疗中,家庭心理教育也是非常重要的,因为精神分裂症的残疾会给家庭成员带来负担。照顾者的负担可以是客观的,也可以是主观的。客观负担是行为现象:社会活动中断和财政困难。主观负担包括照顾者的情绪压力。由于精神分裂症的慢性性质和残疾,精神分裂症患者作为一个群体最需要社会和经济领域的照顾。目的:探讨稳定型精神分裂症患者照护者的负担水平及其与精神分裂症患者残疾程度的关系。这是一项横断面观察研究。材料和方法:研究对象为154例经国际疾病分类诊断为精神分裂症的稳定患者及其主要照顾者。采用印度残疾评估量表(IDEAS)和阳性与阴性综合征量表(PANSS)对患者进行评估,对其主要照顾者采用负担评估量表(BAS)。结果:在服药稳定6个月以上、诊断为精神分裂症至少2年的精神分裂症患者中,三分之二为轻度残疾(70.12%),其余为中度残疾(29.87%)。随着年龄的增长,照顾的负担也越来越重。结论:照顾者负担与整体失能有直接关系。缺乏互动、沟通和就业导致照顾负担加重,但不缺乏自我照顾。
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来源期刊
CiteScore
0.80
自引率
20.00%
发文量
15
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