Literature DB >> 21674523

Palliative care services in families of males with Duchenne muscular dystrophy.

Rebeca Arias1, Jennifer Andrews, Shree Pandya, Kathleen Pettit, Christina Trout, Susan Apkon, Jane Karwoski, Christopher Cunniff, Dennis Matthews, Timothy Miller, Melinda F Davis, F John Meaney.   

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.
Copyright © 2011 Wiley Periodicals, Inc.

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Year:  2011        PMID: 21674523     DOI: 10.1002/mus.22005

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  8 in total

1.  The Spectrum of Caregiving in Palliative Care for Serious, Advanced, Rare Diseases: Key Issues and Research Directions.

Authors:  Lynn S Adams; Jeri L Miller; Patricia A Grady
Journal:  J Palliat Med       Date:  2016-06-01       Impact factor: 2.947

2.  Palliative care services in families of males with muscular dystrophy: Data from MD STARnet.

Authors:  Jennifer G Andrews; Shree Pandya; Christina Trout; Treeva Jaff; Dennis Matthews; Christopher Cunniff; F John Meaney
Journal:  SAGE Open Med       Date:  2019-03-27

3.  Characterizing Enrollment in Observational Studies of Duchenne Muscular Dystrophy by Race and Ethnicity.

Authors:  Alison M Barnard; Samuel L Riehl; Rebecca J Willcocks; Glenn A Walter; Amber M Angell; Krista Vandenborne
Journal:  J Neuromuscul Dis       Date:  2020

Review 4.  Impact of three genetic musculoskeletal diseases: a comparative synthesis of achondroplasia, Duchenne muscular dystrophy and osteogenesis imperfecta.

Authors:  Maman Joyce Dogba; Frank Rauch; Erin Douglas; Christophe Bedos
Journal:  Health Qual Life Outcomes       Date:  2014-10-25       Impact factor: 3.186

5.  Trends in incidence, prevalence, and mortality of neuromuscular disease in Ontario, Canada: A population-based retrospective cohort study (2003-2014).

Authors:  Louise Rose; Douglas McKim; David Leasa; Mika Nonoyama; Anu Tandon; Yu Qing Bai; Reshma Amin; Sherri Katz; Roger Goldstein; Andrea Gershon
Journal:  PLoS One       Date:  2019-03-26       Impact factor: 3.240

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.  Compliance to Care Guidelines for Duchenne Muscular Dystrophy.

Authors:  Hanns Lochmüller; Katharine Bushby; Erik Landfeldt; Peter Lindgren; Christopher F Bell; Claude Schmitt; Michela Guglieri; Volker Straub
Journal:  J Neuromuscul Dis       Date:  2015

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
  8 in total

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