The impact of communication on healthcare involvement for people living with motor neurone disease and their carers: A longitudinal qualitative study

被引:3
|
作者
Paynter, Camille [1 ]
Mathers, Susan [2 ,3 ]
Gregory, Heidi [2 ,4 ]
Vogel, Adam P. [1 ,5 ]
Cruice, Madeline [6 ]
机构
[1] Univ Melbourne, Dept Audiol & Speech Pathol, Melbourne, Vic, Australia
[2] Calvary Hlth Care Bethlehem, Melbourne, Vic, Australia
[3] Monash Univ, Sch Clin Sci, Melbourne, Vic, Australia
[4] Monash Univ, Eastern Hlth Clin Sch, Melbourne, Vic, Australia
[5] Redenlab, Melbourne, Vic, Australia
[6] City Univ London, London, England
基金
英国医学研究理事会;
关键词
dysarthria; longitudinal; progressive neurological disorders; qualitative; AMYOTROPHIC-LATERAL-SCLEROSIS; DECISION-MAKING; EXPERIENCES; DYSARTHRIA; ALS;
D O I
10.1111/1460-6984.12757
中图分类号
R36 [病理学]; R76 [耳鼻咽喉科学];
学科分类号
100104 ; 100213 ;
摘要
Background Communication and cognitive impairments are known barriers to shared decision-making. Most people diagnosed with motor neurone disease (MND) will develop a motor speech impairment over the disease course. Some will develop cognitive, linguistic or behavioural disturbance. Despite this, the impact of communication and cognitive impairment on personal healthcare decision-making in MND is not well known. Aims This exploratory, longitudinal study aimed to capture the perspectives of people living with MND (plwMND) and family members on managing their healthcare with, or in anticipation of, a communication impairment. Methods & Procedures Semi-structured interviews and functional assessments were conducted with plwMND and family members over one to three time points between December 2017 and January 2020. Participants were recruited from a specialist MND clinic using a maximum variation sampling approach. Interview transcripts were analysed using trajectory data analysis: a matrix-based approach for thematic analysis of longitudinal data. The study was underpinned by interpretive descriptive methodology. Outcomes & Results A total of 19 plwMND with a range of MND phenotypes and 15 family members were recruited. Disease progression and participant withdrawal resulted in attrition, however 12 plwMND and seven family members participated at all three time points. Consistent cognitive screening was not feasible, which limited the opportunity to explore the impact of cognitive change. An overarching theme 'Communicating takes effort' was identified and illustrates the efforts required to compensate for, or circumnavigate, impairments to maintain involvement in healthcare. Assistance from family and accommodation from healthcare professionals (HCPs) was needed for ongoing engagement. Where plwMND were dependent on alternative communication devices, this assistance was essential and primarily carried out by family members. Despite these efforts, the quality, quantity and accuracy of communication were sometimes compromised. Participants equated good communication with receiving good healthcare, and some expressed anxiety in the anticipation of being unable to express their needs to healthcare workers. Conclusion & Implications Communication impairment has a direct impact on healthcare involvement. This study demonstrates the effort required by plwMND and their carers to maintain or maximize ongoing involvement. This effort may not always be visible to HCPs. This information may prompt clinicians to consider the best ways to conduct clinical consultations to accommodate patients' abilities. Compromised communication experiences can be moderated by accommodations and support from HCPs and appropriate adjustments in the health system. Asking patients about their communication preferences and needs, allowing extra time and conducting multidisciplinary sessions are examples of such support. What this paper adds What is already known on this subject? Communication and cognitive impairments are known contributors to negative health outcomes and barriers to shared decision-making generally. The existing literature in decision-making in MND does not address the specific impact of these impairments on personal healthcare involvement for plwMND and their carers. What this paper adds to existing knowledge? This paper reports the findings of a research project that interviewed 19 plwMND and 15 carers on one to three occasions over a 26-month period to obtain their perspectives of the impact of communication on healthcare involvement. Whilst a priori the intention was to look at both communicative and cognitive decline, only the former was achieved. The effort and often 'invisible' activity undertaken to manage or maintain involvement in healthcare is identified. Communication impairment requires support and accommodation, otherwise healthcare involvement can be compromised. Results show participants may associate effective communication with good healthcare. What are the potential or actual clinical implications of the work? Clinicians may wish to use these insights from plwMND and their carers to guide adjustments to their professional practice to maximize healthcare involvement for their patients. Tailored education for different healthcare groups is needed to improve understanding of MND-related communication impairments and supportive strategies so that involvement in healthcare is not compromised.
引用
收藏
页码:1318 / 1333
页数:16
相关论文
共 50 条
  • [1] How people living with motor neurone disease and their carers experience healthcare decision making: a qualitative exploration
    Paynter, C.
    Mathers, S.
    Gregory, H.
    Vogel, A. P.
    Cruice, M.
    DISABILITY AND REHABILITATION, 2022, 44 (13) : 3095 - 3103
  • [2] Using the Concept of Health Literacy to Understand How People Living with Motor Neurone Disease and Carers Engage in Healthcare: A Longitudinal Qualitative Study
    Paynter, Camille
    Mathers, Susan
    Gregory, Heidi
    Vogel, Adam P.
    Cruice, Madeline
    HEALTHCARE, 2022, 10 (08)
  • [3] Palliative care for patients with motor neurone disease and their bereaved carers: a qualitative study
    Mc Veigh, Clare
    Donaghy, Colette
    Mc Laughlin, Briege
    Dick, Alison
    Kaur, Kiran
    Mc Conville, John
    Watson, Max
    BMC PALLIATIVE CARE, 2019, 18 (1)
  • [4] Palliative care for patients with motor neurone disease and their bereaved carers: a qualitative study
    Clare Mc Veigh
    Colette Donaghy
    Briege Mc Laughlin
    Alison Dick
    Kiran Kaur
    John Mc Conville
    Max Watson
    BMC Palliative Care, 18
  • [5] Navigating an emotional journey: A qualitative study of the emotional experiences of family carers currently supporting people living with motor neurone disease
    Trucco, Ana Paula
    Mioshi, Eneida
    Kishita, Naoko
    Barry, Caroline
    Backhouse, Tamara
    PALLIATIVE & SUPPORTIVE CARE, 2024, 22 (05) : 1191 - 1197
  • [6] The meaning of living with uncertainty for people with motor neurone disease
    Harris, Denise Andrea
    Jack, Kirsten
    Wibberley, Christopher
    JOURNAL OF CLINICAL NURSING, 2018, 27 (9-10) : 2062 - 2071
  • [7] Healthcare professionals' accounts of challenges in managing motor neurone disease in primary healthcare: a qualitative study
    Lerum, Sverre Vigeland
    Solbraekke, Kari Nyheim
    Frich, Jan C.
    HEALTH & SOCIAL CARE IN THE COMMUNITY, 2017, 25 (04) : 1355 - 1363
  • [8] The need for support services for family carers of people with motor neurone disease (MND): views of current and former family caregivers a qualitative study
    O'Brien, Mary R.
    Whitehead, Bridget
    Jack, Barbara A.
    Mitchell, J. Douglas
    DISABILITY AND REHABILITATION, 2012, 34 (03) : 247 - 256
  • [9] Voice banking for people living with motor neurone disease: Views and expectations
    Cave, Richard
    Bloch, Steven
    INTERNATIONAL JOURNAL OF LANGUAGE & COMMUNICATION DISORDERS, 2021, 56 (01) : 116 - 129
  • [10] Expanding Qualitative Interviewing for Studies Involving Adults With Different Communication Needs: Reflections on Research With People Living With Motor Neurone Disease
    Wilson, Eleanor
    Turner, Nicola
    INTERNATIONAL JOURNAL OF QUALITATIVE METHODS, 2024, 23