Palliative care services in families of males with Duchenne muscular dystrophy. Academic Article uri icon

Overview

abstract

  • INTRODUCTION: Palliative care services that address physical pain and emotional, psychosocial, and spiritual needs may benefit individuals with Duchenne muscular dystrophy (DMD). METHODS: The objective of this study was to describe the palliative care services that families of males with DMD report they receive. A questionnaire was administered to families of males with DMD born prior to January 1, 1982. Thirty-four families responded. RESULTS: Most families (85%) had never heard the term palliative care. Only attendant care and skilled nursing services showed much usage, with 44% and 50% indicating receipt of these services, respectively. Receipt of other services was reported less frequently: pastoral care (27%); respite care (18%); pain management (12%); and hospice care (6%). Only 8 respondents (25%) reported having any type of directive document in place. CONCLUSION: The data suggest a need for improved awareness of palliative care and related services among families of young men with DMD.

publication date

  • July 1, 2011

Research

keywords

  • Caregivers
  • Health Knowledge, Attitudes, Practice
  • Muscular Dystrophy, Duchenne
  • Palliative Care

Identity

Scopus Document Identifier

  • 79959322121

Digital Object Identifier (DOI)

  • 10.1002/mus.22005

PubMed ID

  • 21674523

Additional Document Info

volume

  • 44

issue

  • 1