Department of Nursing, Institute of Mental Health, Woodbridge Hospital, National University of Singapore, Singapore.
J Clin Nurs. 2012 Sep;21(17-18):2410-8. doi: 10.1111/j.1365-2702.2012.04174.x.
Examined the levels of burden and the coping strategies experienced by caregivers of persons with schizophrenia in the community. It aims (1) to provide mental healthcare professionals with more information about caregiver stressors and (2) to recommend more effective community resources and support.
A caregiver's burden increases due to negative coping skills and lack of resources. However, insufficient studies of caregiver burden and coping skills accentuate the already inadequate understanding of the field. This lack of understanding often leads to frequent readmission of patients when caregivers give up their care-giving responsibilities.
Descriptive and quantitative methods.
Convenience sampling method was used at three outpatient clinics on 150 caregivers. The Burden Assessment Scale measured care-giving burden. The Family Crisis-Oriented Personal Scales examined the coping strategies.
Findings reveal that 31.3% caregivers felt distress and 33.3% found stigma upsetting. Only 14.7% sought help from healthcare workers and 49.3% were interested to know more. Nevertheless, 24.7% verbalized sufficient social support.
Results demonstrated a high burden on caregivers because of many factors such as other commitments, lack of resources, insufficient financial support, education level and ageing. This study found that long-term caregivers suffer more than short-term ones, which is contrary to Seng's study (2005). Burden increases further for those having to cope with both work and care giving at the same time.
It is critical to improve and increase services and resources to support care giving. It is also essential to educate and ensure that the people affected know how to leverage the available resources. It is important to improve and increase our services and resources. It is also essential to educate and ensure the people concerned know how to make use of them. It also essential to educate and ensure the people concerned know how to make use of them.
调查社区精神分裂症患者照顾者的负担水平和应对策略。其目的是(1)为精神卫生保健专业人员提供更多关于照顾者压力源的信息,以及(2)建议更多有效的社区资源和支持。
由于应对技能消极和资源缺乏,照顾者的负担会增加。然而,对照顾者负担和应对技能的研究不足,加重了该领域已经不足的理解。这种理解不足往往会导致当照顾者放弃照顾责任时,患者经常再次入院。
描述性和定量方法。
在三个门诊诊所采用方便抽样方法对 150 名照顾者进行研究。照顾负担量表测量照顾负担。家庭危机导向个人量表检查应对策略。
研究结果显示,31.3%的照顾者感到痛苦,33.3%的照顾者感到耻辱感困扰。只有 14.7%的人向医护人员寻求帮助,而 49.3%的人有兴趣了解更多信息。然而,24.7%的人表示有足够的社会支持。
研究结果表明,由于其他承诺、资源缺乏、财政支持不足、教育水平和年龄等诸多因素,照顾者负担沉重。这项研究发现,长期照顾者比短期照顾者承受的负担更大,这与 Seng 的研究(2005 年)相反。同时承担工作和照顾的人负担会进一步增加。
改善和增加支持照顾的服务和资源至关重要。教育和确保受影响的人了解如何利用现有资源也很重要。