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Cohort study of informal carers of first-time stroke survivors: profile of health and social changes in the first year of caregiving.

机译:首次卒中幸存者非正式护理人员的队列研究:护理第一年的健康和社会变化情况。

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摘要

Informal carers underpin community care policies. An initial cohort of 105 informal live-in carers of new stroke patients from the South Coast of England was followed up before discharge, six weeks after discharge and 15 months after stroke with face-to-face interviews assessing physical and psychological health, and social wellbeing. The carer cohort was compared to a cohort of 50 matched non-carers over the same time period. Carer distress was common (37-54%), started early on in the care-giving experience and continued until 15 months after stroke. Carers were 2.5 times as likely as non-carers to have significant psychological distress. Presence of early distress predicted 90% of those significantly distressed 15 months after stroke. Female carers were likely to develop distress earlier than male carers and in anticipation of the care-giving situation. Male carers developed similar levels of distress but only once the care-giving situation became reality. Further research is needed to establish ways to screen for psychological distress early after onset of caregiving, to find ways to tailor proven support interventions to the individual carer, and to evaluate the effect of early detection and support provision on later carer distress.
机译:非正式照顾者是社区护理政策的基础。在出院前,出院后六周和中风后15个月,对来自英格兰南海岸的105名新的中风患者的非正式住家护理人员进行了初始队列随访,并进行了面对面的访谈,评估了他们的身心健康和社交福利。将护理者队列与同一时期内50个匹配的非护理者队列进行了比较。护理人员的困扰很普遍(37-54%),从护理经历的早期开始,一直持续到中风后15个月。照顾者遭受严重心理困扰的可能性是非照顾者的2.5倍。早期困扰的存在预示着中风后15个月严重困扰的人群中有90%会出现这种情况。女性护理人员可能比男性护理人员更早患病,并且预料到护理情况。男性护理人员的痛苦程度相似,但只有在护理情况变为现实之后。需要进行进一步的研究,以建立在照护开始后早期筛查心理困扰的方法,找到方法以针对个体护理者量身定制行之有效的支持干预措施,并评估早期发现和提供支持对以后护理者困扰的影响。

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