Literature DB >> 26044770

Health services received by individuals with duchenne/becker muscular dystrophy.

Shree K Pandya1, Kim A Campbell2, Jennifer G Andrews3, F John Meaney3, Emma Ciafaloni1.   

Abstract

INTRODUCTION: Anecdotal reports from families and care providers suggest a wide variation in services received by individuals with Duchenne/Becker muscular dystrophy (DBMD).
METHODS: We documented the type and frequency of health services received by individuals with DBMD using the Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet) interview data released in June 2012. Interviews with eligible caregivers from 5 sites (Arizona, Colorado, Georgia, Iowa, and western New York) were conducted from April 2007 to March 2012.
RESULTS: Two hundred ninety-six caregivers (66% of those contactable) participated in the interview. There were significant differences among sites in the specialists seen and services received. Concurrence with cardiac recommendations was higher than that with respiratory recommendations.
CONCLUSIONS: The results of this survey support and quantify the anecdotal reports from families and care providers regarding the disparities in services received by individuals with DBMD. It remains to be determined whether these differences affect outcomes.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  Duchenne muscular dystrophy; care recommendations; caregiver interview; disparities; health services

Mesh:

Year:  2015        PMID: 26044770     DOI: 10.1002/mus.24727

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


  4 in total

1.  Muscular Dystrophy Surveillance, Tracking, and Research Network pilot: Population-based surveillance of major muscular dystrophies at four U.S. sites, 2007-2011.

Authors:  ThuyQuynh N Do; Natalie Street; Jennifer Donnelly; Melissa M Adams; Christopher Cunniff; Deborah J Fox; Richard O Weinert; Joyce Oleszek; Paul A Romitti; Christina P Westfield; Julie Bolen
Journal:  Birth Defects Res       Date:  2018-08-02       Impact factor: 2.344

Review 2.  A Review of MD STAR net's Research Contributions to Pediatric-Onset Dystrophinopathy in the United States; 2002-2017.

Authors:  Kashika M Sahay; Tiffany Smith; Kristin M Conway; Paul A Romitti; Molly M Lamb; Jennifer Andrews; Shree Pandya; Joyce Oleszek; Christopher Cunniff; Rodolfo Valdez
Journal:  J Child Neurol       Date:  2018-10-22       Impact factor: 1.987

3.  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

4.  Health Care Use of Cardiac Specialty Care in Children With Muscular Dystrophy in the United States.

Authors:  Erika J Mejia; Kimberly Y Lin; Oluwatimilehin Okunowo; Katherine A Iacobellis; Susan E Matesanz; John F Brandsema; Carol A Wittlieb-Weber; Hannah Katcoff; Heather Griffis; Jonathan B Edelson
Journal:  J Am Heart Assoc       Date:  2022-04-12       Impact factor: 6.106

  4 in total

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