Kochhar Sanimar S, Chadda Rakesh K, Sood Mamta, Bhargava Rachna
Clinical Psychology, All India Institute of Medical Sciences, New Delhi, New Delhi, IND.
Psychiatry, Amrita Hospital, Faridabad, IND.
Cureus. 2024 Aug 8;16(8):e66448. doi: 10.7759/cureus.66448. eCollection 2024 Aug.
Schizophrenia is a severe mental illness that greatly impacts the real-world functioning of patients. In India, caregivers are primarily responsible for their patients and function as their support system, often taking treatment decisions on their behalf. However, they may have insufficient knowledge of the illness, which can have a negative impact on their roles as effective caregivers. The knowledge of schizophrenia and its associations among caregivers has received very little research attention.
To examine the knowledge of mental illness and its socio-demographic and psychosocial associations among caregivers of patients with schizophrenia. The objectives were to assess the knowledge of mental illness and its treatment in caregivers of patients with schizophrenia, to assess the socio-demographic and clinical associations of this knowledge, and to assess the caregivers' psychosocial variables associated with this knowledge.
This cross-sectional observational data was taken from a larger study carried out between August 2018 and January 2021 at an urban tertiary care hospital in the capital city of India. One hundred fifty-eight patients with schizophrenia and their caregivers (n=158) were taken using purposive sampling. Knowledge of Mental Illness Scale was used to evaluate the knowledge and understanding of the illness and its treatment among caregivers. Caregivers coming to this institution in New Delhi were also assessed with respect to their demographic variables, caregiving experience, family functioning, coping strategies, available social support, psychological distress, quality of life, and spiritual, religious, and personal beliefs. The assessment also included demographic and clinical variables of the patients.
Caregivers possessed relatively greater knowledge regarding the medication being taken (52.5%), its side effects (38%), and the diagnosis (36.1%). However, their knowledge was poorer with respect to the meaning and implications of the diagnosis (21.5%) and the purpose of the medication (10.1%). In multivariate regression analysis of these five domains with socio-demographic, clinical, and psychosocial variables; the knowledge of the diagnosis was associated with a family history of psychiatric illness in a second-degree relative, the total duration of treatment, and stigma in caregivers. The meaning of the diagnosis was associated with the environmental domain of quality of life and positive symptoms of the patient. Knowledge of medication was associated with the number of patient hospitalizations, caregivers supervising medications, caregiver age, and the total duration of illness. Knowledge of the purpose of medication was associated with the total duration of illness and patient positive symptoms. Knowledge of medication side effects was associated with the roles domain of family functioning, positive caregiving experience, patient negative symptoms, and the acceptance/redefinition domain of coping.
A range of associations were examined in this study. Correct knowledge of schizophrenia is necessary to promote timely help-seeking, preventing a longer duration of untreated psychosis and a poor prognosis. In research, knowledge of illness is a construct with immense potential applicability. In patient care, this knowledge may help caregivers participate in treatment planning, improve patient functioning, and support their patients toward better functional outcomes.
精神分裂症是一种严重的精神疾病,对患者的现实世界功能有极大影响。在印度,照顾者主要负责照顾患者并充当他们的支持系统,常常代表患者做出治疗决策。然而,他们可能对该疾病了解不足,这可能对他们作为有效照顾者的角色产生负面影响。关于照顾者对精神分裂症及其关联因素的了解,相关研究关注甚少。
考察精神分裂症患者照顾者对精神疾病的了解及其社会人口学和心理社会关联因素。目标包括评估精神分裂症患者照顾者对精神疾病及其治疗的了解,评估这种了解的社会人口学和临床关联因素,以及评估与这种了解相关的照顾者心理社会变量。
本横断面观察数据取自2018年8月至2021年1月在印度首都一家城市三级护理医院开展的一项更大规模研究。采用目的抽样法选取了158例精神分裂症患者及其照顾者(n = 158)。使用精神疾病知识量表评估照顾者对疾病及其治疗的了解和认识。还对来到新德里这家机构的照顾者的人口统计学变量、照顾经历、家庭功能、应对策略、可得的社会支持、心理困扰、生活质量以及精神、宗教和个人信仰进行了评估。评估还包括患者的人口统计学和临床变量。
照顾者对所服用药物(52.5%)、其副作用(38%)和诊断(36.1%)的了解相对较多。然而,他们对诊断的意义和影响(21.5%)以及药物的用途(10.1%)的了解较差。在对这五个领域与社会人口学、临床和心理社会变量进行的多变量回归分析中;对诊断的了解与二级亲属的精神疾病家族史、治疗总时长以及照顾者的污名化有关。诊断的意义与生活质量的环境领域以及患者的阳性症状有关。对药物的了解与患者住院次数、监督用药的照顾者、照顾者年龄以及疾病总时长有关。对药物用途的了解与疾病总时长和患者阳性症状有关。对药物副作用的了解与家庭功能的角色领域、积极的照顾经历、患者阴性症状以及应对的接受/重新定义领域有关。
本研究考察了一系列关联因素。正确了解精神分裂症对于促进及时寻求帮助、防止未治疗精神病的持续时间延长和预后不良至关重要。在研究中,对疾病的了解是一个具有巨大潜在适用性的概念。在患者护理中,这种了解可能有助于照顾者参与治疗计划、改善患者功能,并支持患者实现更好的功能结局。