The Palliative Care Information Needs of Patients with Amyotrophic Lateral Sclerosis and their Informal Caregivers: A Scoping Review

被引:15
作者
Gillespie, Jacqueline [1 ]
Przybylak-Brouillard, Antoine [2 ]
Watt, Christine L. [3 ,4 ]
机构
[1] Trillium Hlth Partners, Div Palliat Care, Mississauga, ON, Canada
[2] McGill Univ, Inst Hlth Sci Educ, Montreal, PQ, Canada
[3] Univ Ottawa, Div Palliat Care, Dept Med, Ottawa, ON, Canada
[4] Bruyere Res Inst, Ottawa, ON, Canada
关键词
Amyotrophic lateral sclerosis; palliative care; information needs; thematic synthesis; MOTOR-NEURON DISEASE; FAMILY CARERS; MECHANICAL VENTILATION; DECISION-MAKING; ALS PATIENTS; EXPERIENCES; PEOPLE; PREFERENCES; MANAGEMENT; SERVICES;
D O I
10.1016/j.jpainsymman.2021.03.008
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Context. Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disease, associated with impaired quality of life for patients and caregivers. As treatment is largely supportive, early involvement of palliative care (PC) is recommended as standard of care. Despite this, literature surrounding PC information needs is limited. Objectives. To explore the PC information needs of patients with ALS and their caregivers and identify gaps in the literature. Methods. A scoping review using MEDLINE, EMBASE, CINAHL and PsycINFO databases (2000-2019) was conducted. Articles examining PC information needs as stated by ALS patients and/or current/bereaved caregivers were included. Studies examining other diagnoses and those focused on healthcare workers were excluded. Thematic synthesis was used to summarize and identify prevalent domains and themes in the literature. Results. 581 articles underwent primary screening, with thirty-two ultimately included (26 original articles, six reviews). Fourteen examined information needs of both patients and caregivers, 13 caregivers only, 5 patients only. The most common PC information needs were as follows: for patients, disease course/prognosis (n = 10), general disease information (n = 9), decision-making (n = 7) and symptoms (n = 6); for caregivers, services and resources (n = 15), disease course/prognosis (n = 14), general disease information (n = 13) and skills (n = 10). There was substantial variability in information needs, both between patients and caregivers and among members of the same group. Conclusion. ALS patients and caregivers have unique and varying PC information needs. Future research should better characterize these needs to improve patient and caregiver quality of life. The delivery of information must be tailored to individual patient or caregiver preferences. (C) 2021 American Academy of Hospice and Palliative Medicine. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:848 / 862
页数:15
相关论文
共 58 条
  • [1] Alankaya N., 2015, HLTH SCI J, V4, P1
  • [2] Breathlessness in motor neurone disease: a review of the current strategies and gaps in the evidence
    Alcroft, Peter
    [J]. CURRENT OPINION IN SUPPORTIVE AND PALLIATIVE CARE, 2014, 8 (03) : 213 - 217
  • [3] EFNS guidelines on the Clinical Management of Amyotrophic Lateral Sclerosis (MALS) - revised report of an EFNS task force
    Andersen, Peter M.
    Abrahams, Sharon
    Borasio, Gian D.
    de Carvalho, Mamede
    Chio, Adriano
    Van Damme, Philip
    Hardiman, Orla
    Kollewe, Katja
    Morrison, Karen E.
    Petri, Susanne
    Pradat, Pierre-Francois
    Silani, Vincenzo
    Tomik, Barbara
    Wasner, Maria
    Weber, Markus
    [J]. EUROPEAN JOURNAL OF NEUROLOGY, 2012, 19 (03) : 360 - E24
  • [4] Who cares for the bereaved? A national survey of family caregivers of people with motor neurone disease
    Aoun, Samar M.
    Cafarella, Paul A.
    Rumbold, Bruce
    Thomas, Geoff
    Hogden, Anne
    Jiang, Leanne
    Gregory, Sonia
    Kissane, David W.
    [J]. AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2021, 22 (1-2) : 12 - 22
  • [5] Grief, depression, and anxiety in bereaved caregivers of people with motor neurone disease: a population-based national study
    Aoun, Samar M.
    Kissane, David W.
    Cafarella, Paul A.
    Rumbold, Bruce
    Hogden, Anne
    Jiang, Leanne
    Bear, Natasha
    [J]. AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2020, 21 (7-8) : 593 - 605
  • [6] Identifying and addressing the support needs of family caregivers of people with motor neurone disease using the Carer Support Needs Assessment Tool
    Aoun, Samar M.
    Deas, Kathleen
    Kristjanson, Linda J.
    Kissane, David W.
    [J]. PALLIATIVE & SUPPORTIVE CARE, 2017, 15 (01) : 32 - 43
  • [7] Motor Neurone Disease family carers' experiences of caring, palliative care and bereavement: An exploratory qualitative study
    Aoun, Samar M.
    Connors, Sianne Lee
    Priddis, Lynn
    Breen, Lauren J.
    Colyer, Sue
    [J]. PALLIATIVE MEDICINE, 2012, 26 (06) : 842 - 850
  • [8] Optimizing the noninvasive ventilation pathway for patients with amyotrophic lateral sclerosis/motor neuron disease: a systematic review
    Baxter, Susan Kathryn
    Johnson, Maxine
    Clowes, Mark
    O'brien, David
    Norman, Paul
    Stavroulakis, Theocharis
    Bianchi, Stephen
    Elliott, Mark
    Mcdermott, Christopher
    Hobson, Esther
    [J]. AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2019, 20 (7-8) : 461 - 472
  • [9] Palliative care in amyotrophic lateral sclerosis: a review of current international guidelines and initiatives
    Bede, Peter
    Oliver, David
    Stodart, James
    van den Berg, Leonard
    Simmons, Zachary
    Brannagain, Doiminic O.
    Borasio, Gian Domenico
    Hardiman, Orla
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2011, 82 (04) : 413 - 418
  • [10] The End-of-Life Experiences of People with Motor Neuron Disease: Family Carers' Perspectives
    Bentley, Brenda
    O'Connor, Moira
    [J]. JOURNAL OF PALLIATIVE MEDICINE, 2016, 19 (08) : 857 - 862