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
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom