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Hidden caring, hidden carers? Exploring the experience of carers for people with long-term conditions

机译:隐藏的关怀,隐藏的关怀?为有长期病情的人探索照顾者的经验

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Informal carers make a significant contribution to illness management in communities, but many struggle to access support and remain hidden carers'. We aimed to explore how carers of people with common long-term conditions (LTCs, such as coronary heart disease or kidney disease) conceptualised their caring, and whether they struggled to identify themselves with the term carer' or access for support. We conducted semi-structured interviews with 19 informal carers of people with LTCs recruited from local support groups. Topic guides were designed to encourage participants to provide their retrospective accounts of identifying as a carer or struggling to do so. Data were analysed using the constant comparative method. The study was designed collaboratively with a patient and public involvement (PPI) partner, and we consulted with a PPI steering group of people with lived experience of caring during the study. Results showed how participants drew on comparisons with those caring for more dependent relatives in explaining their reluctance to define themselves as a carer, and resisted adopting the label due to concerns that it would threaten the identity of the cared-for person. The data were interpreted in terms of types of work' undertaken to manage LTCs, and revealed that carers of patients with LTCs appear to primarily engage in biographical and emotional support, which may be more difficult to conceptualise as legitimate caring work'. Participants indicated that health professionals may be in a unique position to validate their role as carers and encourage support seeking. The study suggests how the greater focus on self-management of LTCs in the community must be complemented by recognition of this group as potentially hidden carers', who support the patient to minimise the impact the illness has on their lives and consequently may minimise their own caring role, with negative implications for support seeking.
机译:非正式护理人员为社区的疾病管理做出了重要贡献,但是许多人都在努力获得支持并仍然是隐藏的护理人员。我们的目的是探讨患有长期常见病(冠心病或肾脏疾病等长期病患)的护理人员如何概念化其护理,以及他们是否难以用“护理人员”一词或寻求支持来证明自己。我们对从当地支持小组招募的19名LTC的非正式护理人员进行了半结构化访谈。主题指南旨在鼓励参与者提供回顾性的陈述,以证明自己是照料者或挣扎于照料者。使用常数比较法分析数据。这项研究是与患者和公众参与(PPI)的合作伙伴共同设计的,我们咨询了在研究过程中具有丰富护理经验的PPI指导小组。结果表明,参加者如何与照顾更多依赖亲属的人进行比较,以解释他们不愿意将自己定义为照顾者,并且由于担心威胁被照顾者的身份而拒绝采用该标签。这些数据是根据管理LTC的工作类型来解释的,并揭示了LTC患者的看护者似乎主要从事传记和情感支持,这可能更难以概念化为合法的看护工作。与会者指出,卫生专业人员可能处于独特地位,以验证其作为护理人员的作用并鼓励寻求支持。该研究表明,必须通过将这一群体确认为潜在的隐性护理者,来补充社区对LTC自我管理的更多关注,这些人支持患者最大程度地减少疾病对其生活的影响,从而可能最小化他们自己的生活。关怀角色,对寻求支持有负面影响。

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