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What are the roles of carers in decision-making for amyotrophic lateral sclerosis multidisciplinary care?

机译:护理人员在肌萎缩性侧索硬化多学科护理决策中的作用是什么?

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摘要

Purpose: Family carers of patients with amyotrophic lateral sclerosis (ALS) are presumed to have frequent involvement in decision-making for symptom management and quality of life. To better understand and improve decision-making, we investigated the range and extent of carer participation in decision-making. By focusing on the perspectives of ALS support carers, the study aimed to explore carer participation in decision-making, to identify carer roles, and determine the facilitators and barriers to carer participation in decision-making for ALS multidisciplinary care. Participants and methods: An exploratory, in-depth study was conducted with eight carers of ALS patients from two specialized ALS multidisciplinary clinics. Carers participated in semi-structured interviews that were audio recorded and transcribed then coded and analyzed for emergent themes. Results: Carers made a significant contribution to ALS decision-making. Their roles were: promoting the patient voice, promoting patient health literacy, and providing emotional support and logistical assistance. Facilitators of carer participation in decision-making were perceived to be: health professional endorsement of patients' decision-making style; access to credible information sources; evidence-based information from the ALS clinic, ALS support association, and health practitioners; supportive relationships with family and friends; spiritual faith; ease of contact with ALS services; and availability of physical and practical support for carers. Barriers to carer participation included: changes to patient communication and cognition; conflict between respect for patients' independence and patients' best interest; communication breakdown between patient, carer, and service providers; the confronting nature of disease information; credibility of Internet sites; carer coping strategies; lack of support for the carer; and the burden of care. Conclusion: Carers enhance ALS patient-centered care through their participation in decision-making. They collaborate with patients and health professionals to form a decision-making triad within specialized multidisciplinary ALS clinical care. Nevertheless, health professional engagement with carers as collaborative partners is acknowledged to be a significant challenge.
机译:目的:假定患有肌萎缩性侧索硬化症(ALS)患者的家庭护理人员经常参与症状管理和生活质量的决策。为了更好地理解和改善决策,我们调查了护理人员参与决策的范围和程度。通过关注ALS支持护理人员的观点,该研究旨在探索护理人员参与决策,确定护理人员角色,并确定护理人员参与ALS多学科护理决策的促进因素和障碍。参与者和方法:对来自两家专门的ALS多学科诊所的8名ALS患者的护理人员进行了探索性深入研究。护老者参加了半结构化访谈,这些访谈被录音和转录,然后进行编码和分析以发现紧急主题。结果:护理人员为ALS决策做出了重大贡献。他们的作用是:提高患者的声音,提高患者的健康素养以及提供情感支持和后勤援助。护理人员参与决策的促进者被认为是:卫生专业人士对患者决策风格的认可;获得可靠的信息来源; ALS诊所,ALS支持协会和卫生从业人员提供的基于证据的信息;与家人和朋友的支持性关系;精神信仰;易于与ALS服务联系;以及提供给护理人员的实际和实际支持。护理人员参与的障碍包括:患者沟通和认知的改变;尊重患者独立性与患者最大利益之间的冲突;患者,护理人员和服务提供商之间的通信故障;疾病信息的对立性质;互联网站点的信誉;照顾者应对策略;缺乏照顾者的支持;和护理负担。结论:护理人员通过参与决策来增强ALS以患者为中心的护理。他们与患者和卫生专业人员合作,组成专业的多学科ALS临床护理中的决策三元组。尽管如此,与护理人员作为合作伙伴的卫生专业人员互动仍被认为是一项重大挑战。

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