Impact of demographic, clinical and psychological variables of patients and caregivers on the perception of burden among the family caregivers of patients with cancer

Badii Amamou, S. Fathallah, Dhekra Ammar, A. Mhalla, F. Zaafrane, L. Gaha
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引用次数: 2

Abstract

The study aims were to assess the level of burden among caregivers of patients diagnosed with cancer and to examine patient and caregiver variables associated with high levels of burden. A descriptive cross sectional study was performed at the Psychiatric Department in the University Hospital of Monastir, Tunisia. The study included a total of 138 dyads of patients and their corresponding family caregivers. The dyads were convoked then examined. The data were assembled using questionnaires elaborated by the research team and caregiver burden was measured with the Zarit Burden Interview. Patients completed the Hospital Anxiety and Depression Scale and the KATZ Index of Activities of Daily Living. About one third of the caregivers experienced high levels of burden. The scores at the Zarit Burden Interview ranged from 15 to 70 and mean score was 48.7 (SD =18.2). This negative outcome of caregiving was found to be related to both patients’ and caregivers’ variables. Statistically, the factors associated to high levels of burden among family caregivers that are linked to the patient’s profile were: male gender, age between 61 and 70 years old, having other medical morbidities, necessitating pre and post-operative chemotherapy, having intermediate to high levels of anxious or depressive symptoms and a severe functional impairment. Caregivers who helped their patients to accomplish many daily activities were found to be high-burdened. The caregiver variables that were found to be related to high levels of burden among caregivers were: male gender, age between 40 and 59 years old, employed full-time status, being the child of the patient, having another member of the family needing daily care, caregiving period more than one year, and not resorting to a professional healthcare at home. The current study demonstrates the importance of a systematic assessment and early intervention procedures needed in order to detect vulnerable caregivers.
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患者和照顾者的人口学、临床和心理变量对癌症患者家庭照顾者负担感知的影响
这项研究的目的是评估癌症患者护理人员的负担水平,并检查与高负担水平相关的患者和护理人员变量。在突尼斯莫纳斯提尔大学医院精神科进行了一项描述性横断面研究。该研究共包括138对患者及其相应的家庭照顾者。二人组被召集起来,然后被检查。数据采用研究小组编制的问卷收集,并采用Zarit负担访谈法测量照顾者负担。患者完成医院焦虑抑郁量表和日常生活活动KATZ指数。大约三分之一的照顾者承受着很高的负担。Zarit Burden Interview的得分范围为15 ~ 70分,平均得分为48.7分(SD =18.2)。研究发现,护理的负面结果与患者和护理者的变量有关。从统计上看,与家庭照顾者的高负担相关的因素与患者的情况有关:男性,年龄在61至70岁之间,有其他疾病,需要术前和术后化疗,有中高水平的焦虑或抑郁症状以及严重的功能损伤。帮助病人完成许多日常活动的护理人员被发现负担沉重。研究发现,与护理人员高负担水平相关的护理人员变量为:男性、年龄在40至59岁之间、全职工作、是患者的子女、有其他家庭成员需要日常护理、护理时间超过一年、没有在家中求助于专业医疗保健。目前的研究证明了系统评估和早期干预程序的重要性,以便发现弱势照顾者。
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