Literature DB >> 25611162

Need and value of case management in multidisciplinary ALS care: A qualitative study on the perspectives of patients, spousal caregivers and professionals.

Minne Bakker1, Huub Creemers, Karen Schipper, Anita Beelen, Hepke Grupstra, Frans Nollet, Tineke Abma.   

Abstract

Our objective was to explore the needs and value of case management according to patients with amyotrophic lateral sclerosis (ALS), their spousal caregivers, and health care professionals in the context of multidisciplinary ALS care. We undertook semi-structured interviews with 10 patients with ALS, their caregivers (n = 10) and their ALS health care professionals (n = 10), and held a focus group (n = 20). We transcribed the audio-taped interviews and analysed all data thematically. Participants indicated that in certain circumstances case management can have an added value. They identified factors for receptiveness to case management: adequacy of usual care, rate of disease progression, and degree of social network support and personal factors of patients and spousal caregivers. Participants valued the time for consultation, house calls and proactive approach of the case manager. Patients with ALS and caregivers appreciated emotional support, whereas professionals did not mention the importance of emotional support by the case manager. In conclusion, ALS teams can consider implementation of valued aspects of case management (accessibility, ample time, proactive approach, emotional support) in the usual multidisciplinary ALS care. Additional support might be provided to patients with rapidly progressive disease course, passive coping style and small social network.

Entities:  

Keywords:  ALS; Case management; needs; patients; qualitative study; spousal caregivers

Mesh:

Year:  2015        PMID: 25611162     DOI: 10.3109/21678421.2014.971811

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler Frontotemporal Degener        ISSN: 2167-8421            Impact factor:   4.092


  9 in total

1.  "They Are Talking About Me, but Not with Me": A Focus Group Study to Explore the Patient Perspective on Interprofessional Team Meetings in Primary Care.

Authors:  Jerôme Jean Jacques van Dongen; Maarten de Wit; Hester Wilhelmina Henrica Smeets; Esther Stoffers; Marloes Amantia van Bokhoven; Ramon Daniëls
Journal:  Patient       Date:  2017-08       Impact factor: 3.883

2.  Experiences of health services and unmet care needs of people with late-stage Parkinson's in England: A qualitative study.

Authors:  Joy Read; Sarah Cable; Charlotte Löfqvist; Susanne Iwarsson; Gergely Bartl; Anette Schrag
Journal:  PLoS One       Date:  2019-12-30       Impact factor: 3.240

3.  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

4.  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

5.  Development of Guidelines for Spouses Engaged in Home-Based Care of Persons With Motor Neuron Disease From Indian Context.

Authors:  Manjusha G Warrier; Priya Treesa Thomas; Arun Sadasivan; Saraswati Nashi; Seena Vengalil; A Nalini
Journal:  J Patient Exp       Date:  2022-02-02

6.  Assistive Robots for Patients With Amyotrophic Lateral Sclerosis: Exploratory Task-Based Evaluation Study With an Early-Stage Demonstrator.

Authors:  Robert Klebbe; Stefan Scherzinger; Cornelia Eicher
Journal:  JMIR Rehabil Assist Technol       Date:  2022-08-23

Review 7.  Amyotrophic lateral sclerosis: improving care with a multidisciplinary approach.

Authors:  Anne Hogden; Geraldine Foley; Robert D Henderson; Natalie James; Samar M Aoun
Journal:  J Multidiscip Healthc       Date:  2017-05-19

8.  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 9.  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
  9 in total

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