z-logo
Premium
Palliative care services in families of males with duchenne muscular dystrophy
Author(s) -
Arias Rebeca,
Andrews Jennifer,
Pandya Shree,
Pettit Kathleen,
Trout Christina,
Apkon Susan,
Karwoski Jane,
Cunniff Christopher,
Matthews Dennis,
Miller Timothy,
Davis Melinda F.,
Meaney F. John
Publication year - 2011
Publication title -
muscle and nerve
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.025
H-Index - 145
eISSN - 1097-4598
pISSN - 0148-639X
DOI - 10.1002/mus.22005
Subject(s) - respite care , palliative care , receipt , psychosocial , medicine , duchenne muscular dystrophy , family medicine , nursing , psychiatry , world wide web , computer science
: 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. Muscle Nerve 44: 93–101, 2011

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom