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

Becker muscular dystrophy Duchenne muscular dystrophy caregiver survey palliative care use service utilization

Journal

SAGE open medicine
ISSN: 2050-3121
Titre abrégé: SAGE Open Med
Pays: England
ID NLM: 101624744

Informations de publication

Date de publication:
2019
Historique:
received: 07 12 2018
accepted: 06 03 2019
entrez: 5 4 2019
pubmed: 5 4 2019
medline: 5 4 2019
Statut: epublish

Résumé

Information on use of palliative care services among individuals with Duchenne and Becker muscular dystrophy is scant despite the clearly documented need. We examined associations between uptake of palliative care services by 233 males with Duchenne and Becker muscular dystrophy aged 12 and older for both caregiver and affected male characteristics using the Muscular Dystrophy Surveillance Tracking and Research Network baseline interview. Ninety-one percent of caregivers (213/233) used at least one palliative care service. Case management had the highest frequency of use (59%). Use of palliative care was more frequently associated with the characteristics of affected males, as were some individual palliative care services. Utilization of six individual services differed among Muscular Dystrophy Surveillance Tracking and Research Network sites. While research suggests that pain is a frequent problem in Duchenne and Becker muscular dystrophy, only 12.5% reported use of pain management services. Although palliative care use among families of males with Duchenne and Becker muscular dystrophy is high overall, there is much variability in use of individual services. Use of palliative care is driven by disease experience in the affected male. Many of the care recommendations for these individuals highlight the importance for early involvement of palliative care professionals.

Identifiants

pubmed: 30944724
doi: 10.1177/2050312119840518
pii: 10.1177_2050312119840518
pmc: PMC6437326
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2050312119840518

Subventions

Organisme : NCBDD CDC HHS
ID : U01 DD001041
Pays : United States

Déclaration de conflit d'intérêts

Declaration of conflicting interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

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Auteurs

Jennifer G Andrews (JG)

Department of Pediatrics, The University of Arizona, Tucson, AZ, USA.

Shree Pandya (S)

Department of Neurology and School of Medicine and Dentistry, University of Rochester, Rochester, NY, USA.

Christina Trout (C)

The University of Iowa Wellstone Muscular Dystrophy Cooperative Research Center, Iowa City, IA, USA.

Treeva Jaff (T)

Birth Defects Registry and Surveillance Section, New York State Department of Health, Albany, NY, USA.

Dennis Matthews (D)

School of Medicine, University of Colorado, Denver, CO, USA.

Christopher Cunniff (C)

Department of Pediatrics, Joan and Sanford I. Weill Medical College, Cornell University, New York, NY, USA.

F John Meaney (FJ)

Department of Pediatrics, The University of Arizona, Tucson, AZ, USA.

Classifications MeSH