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

被引:46
作者
Hogden, Anne [1 ]
Greenfield, David [1 ]
Nugus, Peter [1 ]
Kiernan, Matthew C. [2 ,3 ]
机构
[1] Univ New S Wales, Ctr Clin Governance Res, Australian Inst Hlth Innovat, Sydney, NSW 2052, Australia
[2] Univ New S Wales, Prince Wales Clin Sch, Sydney, NSW 2052, Australia
[3] Neurosci Res Australia, Sydney, NSW, Australia
关键词
motor neuron disease; carer experience; patient-centered care; health literacy; health care triad; barriers and facilitators; MOTOR-NEURON DISEASE; NONINVASIVE VENTILATION; BEHAVIORAL-CHANGES; FAMILY CARERS; CANCER CARE; PATIENT; PEOPLE; COMPANIONS; CAREGIVERS; BURDEN;
D O I
10.2147/PPA.S40783
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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.
引用
收藏
页码:171 / 181
页数:11
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