Literature DB >> 28681543

Supportive care needs of patients with amyotrophic lateral sclerosis/motor neuron disease and their caregivers: A scoping review.

Juyeon Oh1,2, Jung A Kim1.   

Abstract

AIMS AND
OBJECTIVES: To identify the supportive care needs of amyotrophic lateral sclerosis/motor neuron disease patients and their caregivers, categorise and summarise them into a Supportive Care Needs Framework and identify gaps in literature.
BACKGROUND: Little is known about the supportive care needs of amyotrophic lateral sclerosis/motor neuron disease patients and their caregivers, and this subject has not previously been systemically reviewed.
DESIGN: Scoping review.
METHODS: We conducted a scoping review from the MEDLINE, EMBASE, CINAHL and Cochrane databases for the period January 2000-July 2016, using the following inclusion criteria: (i) written in English only, (ii) published in peer-reviewed journals, (iii) at least part of the research considered the supportive care needs perspective of amyotrophic lateral sclerosis/motor neuron disease patients or their caregivers and (iv) the population sample included patients of amyotrophic lateral sclerosis/motor neuron disease or their caregivers.
RESULTS: Thirty-seven articles were included. Our review shows that amyotrophic lateral sclerosis/motor neuron disease patients and their caregivers' supportive care needs were mentioned across all seven domains of the Supportive Care Needs Framework. Most common were practical needs (n = 24), followed by Informational needs (n = 19), Social needs (n = 18), Psychological needs (n = 16), Physical needs (n = 15), Emotional needs (n = 13) and Spiritual needs (n = 8).
CONCLUSION: From the perspectives of amyotrophic lateral sclerosis/motor neuron disease patients and their caregivers, there is a significant need for more practical, social, informational, psychological, physical, emotional and spiritual support. RELEVANCE TO CLINICAL PRACTICE: The Supportive Care Needs Framework has potential utility in the development of patient-centred support services or healthcare policies and serves as an important base for further studies; especially, specific examples of each supportive care needs domain can guide in clinical settings when healthcare professionals provide multidisciplinary care to amyotrophic lateral sclerosis/motor neuron disease patients and individualised care.
© 2017 John Wiley & Sons Ltd.

Entities:  

Keywords:  amyotrophic lateral sclerosis; caregiver; health service needs; motor neuron disease; review; scoping review; supportive care

Mesh:

Year:  2017        PMID: 28681543     DOI: 10.1111/jocn.13945

Source DB:  PubMed          Journal:  J Clin Nurs        ISSN: 0962-1067            Impact factor:   3.036


  8 in total

1.  Supportive care needs of patients with rare chronic diseases: multi-method, cross-sectional study.

Authors:  Miram K Depping; Natalie Uhlenbusch; Yskert von Kodolitsch; Hans F E Klose; Victor-Felix Mautner; Bernd Löwe
Journal:  Orphanet J Rare Dis       Date:  2021-01-22       Impact factor: 4.123

2.  Use of a modular ontology and a semantic annotation tool to describe the care pathway of patients with amyotrophic lateral sclerosis in a coordination network.

Authors:  Sonia Cardoso; Pierre Meneton; Xavier Aimé; Vincent Meininger; David Grabli; Gilles Guezennec; Jean Charlet
Journal:  PLoS One       Date:  2021-01-06       Impact factor: 3.240

3.  Caregivers' View of Socio-Medical Care in the Terminal Phase of Amyotrophic Lateral Sclerosis-How Can We Improve Holistic Care in ALS?

Authors:  Katharina Linse; Elisa Aust; René Günther; Andreas Hermann
Journal:  J Clin Med       Date:  2022-01-04       Impact factor: 4.241

4.  Supportive needs of informal caregivers of people with amyotrophic lateral sclerosis in Switzerland: a qualitative study.

Authors:  Christopher Poppe; Kathi Schweikert; Tanja Krones; Tenzin Wangmo
Journal:  Palliat Care Soc Pract       Date:  2022-02-28

5.  "Walking a tightrope": A grounded theory approach to informal caregiving for amyotrophic lateral sclerosis.

Authors:  Christopher Poppe; Martine Verwey; Tenzin Wangmo
Journal:  Health Soc Care Community       Date:  2021-10-31

6.  Alleviation of Psychological Distress and the Improvement of Quality of Life in Patients With Amyotrophic Lateral Sclerosis: Adaptation of a Short-Term Psychotherapeutic Intervention.

Authors:  Moritz Caspar Franz Oberstadt; Peter Esser; Joseph Classen; Anja Mehnert
Journal:  Front Neurol       Date:  2018-04-16       Impact factor: 4.003

7.  The experiences of, and need for, palliative care for people with motor neurone disease and their informal caregivers: A qualitative systematic review.

Authors:  Kate Flemming; Victoria Turner; Samantha Bolsher; Bill Hulme; Elizabeth McHugh; Ian Watt
Journal:  Palliat Med       Date:  2020-04-14       Impact factor: 4.762

Review 8.  Support Needs and Interventions for Family Caregivers of Patients with Amyotrophic Lateral Sclerosis (ALS): A Narrative Review with Report of Telemedicine Experiences at the Time of COVID-19 Pandemic.

Authors:  Giulia D'Alvano; Daniela Buonanno; Carla Passaniti; Manuela De Stefano; Luigi Lavorgna; Gioacchino Tedeschi; Mattia Siciliano; Francesca Trojsi
Journal:  Brain Sci       Date:  2021-12-30
  8 in total

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