Literature DB >> 27816330

Men with Duchenne muscular dystrophy and end of life planning.

David Abbott1, Helen Prescott2, Karen Forbes3, James Fraser4, Anirban Majumdar4.   

Abstract

There is very limited evidence about the views of men with Duchenne muscular dystrophy (DMD) and end of life issues including death and dying. Studies have shown the physiological and psychological benefits of talking about and planning for end of life. Despite policy documents and guidance in the UK about end of life planning, there is consensus on the need for improvement. The study reported here is a qualitative one with 15 men with DMD (aged 20-45 years). Participants could not recall any significant conversations with clinicians about end of life and assumed that clinicians were reluctant to discuss the issue. The men in the study wanted to be given proactive cues that they could bring up topics such as death and dying and wanted to have these conversations with clinicians who combined expert knowledge about the condition as well as good listening skills. Topics of interest to participants included likely nature and place of death; practical planning for funerals and wills; and sources of information and support. Emotional or psychological support to think about end of life was not routinely offered and participants found it very difficult to discuss these issues with family members. The study suggests that more could be done to encourage clinicians, men with Duchenne, family members and the wider NMD community to pay attention to end of life planning issues and the associated need for emotional support and high quality interactions between patients and clinicians.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Death; Duchenne muscular dystrophy; End of life; Neuromuscular disease; Palliative care

Mesh:

Year:  2016        PMID: 27816330     DOI: 10.1016/j.nmd.2016.09.022

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  10 in total

1.  Achieving Life Milestones in Duchenne/Becker Muscular Dystrophy: A Retrospective Analysis.

Authors:  Andrew Donaldson; Debra Guntrum; Emma Ciafaloni; Jeffrey Statland
Journal:  Neurol Clin Pract       Date:  2021-08

2.  A comprehensive qualitative framework for health-related quality of life in Duchenne muscular dystrophy.

Authors:  Philip A Powell; Jill Carlton
Journal:  Qual Life Res       Date:  2022-09-01       Impact factor: 3.440

3.  Development of a New Quality of Life Measure for Duchenne Muscular Dystrophy Using Mixed Methods: The DMD-QoL.

Authors:  Philip A Powell; Jill Carlton; Donna Rowen; Fleur Chandler; Michela Guglieri; John E Brazier
Journal:  Neurology       Date:  2021-03-30       Impact factor: 9.910

Review 4.  Lifetime Care of Duchenne Muscular Dystrophy.

Authors:  Erin W MacKintosh; Maida L Chen; Joshua O Benditt
Journal:  Sleep Med Clin       Date:  2020-10-05

Review 5.  The adult multidisciplinary respiratory neuromuscular clinic.

Authors:  Neeraj M Shah; Patrick B Murphy; Georgios Kaltsakas
Journal:  Breathe (Sheff)       Date:  2020-09

6.  Adult North Star Network (ANSN): Consensus Guideline For The Standard Of Care Of Adults With Duchenne Muscular Dystrophy.

Authors:  R Quinlivan; B Messer; P Murphy; R Astin; R Mukherjee; J Khan; A Emmanuel; S C Wong; R Kulshresha; T Willis; J Pattni; D Willis; A Morgan; K Savvatis; R Keen; J Bourke; C Marini Bettolo; C Hewamadduma
Journal:  J Neuromuscul Dis       Date:  2021

7.  Enhancing human aspects of care with young people with muscular dystrophy: An evaluation of a participatory qualitative study with clinicians.

Authors:  Jenny Setchell; Donya Mosleh; Laura McAdam; Patricia Thille; Thomas Abrams; Hugh J McMillan; Bhavnita Mistry; Barbara E Gibson
Journal:  PLoS One       Date:  2022-02-25       Impact factor: 3.240

Review 8.  Duchenne and Becker muscular dystrophy in adolescents: current perspectives.

Authors:  Jennifer G Andrews; Richard A Wahl
Journal:  Adolesc Health Med Ther       Date:  2018-03-15

9.  Transition from Childhood to Adulthood in Patients with Duchenne Muscular Dystrophy.

Authors:  Eliza Wasilewska; Sylwia Małgorzewicz; Agnieszka Sobierajska-Rek; Joanna Jabłońska-Brudło; Lucyna Górska; Karolina Śledzińska; Joanna Bautembach-Minkowska; Jolanta Wierzba
Journal:  Medicina (Kaunas)       Date:  2020-08-24       Impact factor: 2.430

Review 10.  Advance Care Planning in Neurodegenerative Disorders: A Scoping Review.

Authors:  Andrea Giordano; Ludovica De Panfilis; Marta Perin; Laura Servidio; Marta Cascioli; Maria Grazia Grasso; Alessandra Lugaresi; Eugenio Pucci; Simone Veronese; Alessandra Solari
Journal:  Int J Environ Res Public Health       Date:  2022-01-12       Impact factor: 3.390

  10 in total

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