Literature DB >> 27743907

Parental Reflections on the Diagnostic Process for Duchenne Muscular Dystrophy: A Qualitative Study.

Roxanna M Bendixen, Amy Houtrow.   

Abstract

PURPOSE: Duchenne muscular dystrophy (DMD) is a rare neuromuscular disease with no known cure. We sought to update over 30 years of research reporting on the diagnostic delays in DMD.
METHODS: Through personal interviews, this study qualitatively explored parents' experiences regarding receipt of the DMD diagnosis and the guidance for care provided. Thematic analysis identified themes and provided answers to the research questions being addressed.
RESULTS: Four themes emerged: (a) Dismissive illustrates little consideration of parent concern in the diagnostic process; (b) Limited Knowledge describes misunderstandings about clinical signs, recommended screenings, and testing to achieve a diagnosis of DMD; (c) Careless Delivery reports on the manner in which the diagnosis was given; and (d) Lack of Guidance describes the follow-up that occurred after the diagnosis.
CONCLUSION: Despite marked medical progress over the past several decades, substantial barriers to arriving at the diagnosis of DMD and the provision of care guidance remain.
Copyright © 2016 National Association of Pediatric Nurse Practitioners. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Clinical decision-making; delayed diagnosis; neuromuscular disorder; parent-report; rare disease

Mesh:

Year:  2016        PMID: 27743907      PMCID: PMC5389929          DOI: 10.1016/j.pedhc.2016.09.002

Source DB:  PubMed          Journal:  J Pediatr Health Care        ISSN: 0891-5245            Impact factor:   1.812


  20 in total

1.  Quality of life in Duchenne muscular dystrophy: the subjective impact on children and parents.

Authors:  Ilaria Baiardini; Carlo Minetti; Simona Bonifacino; Anna Porcu; Catherine Klersy; Paolo Petralia; Sara Balestracci; Filippo Tarchino; Stefania Parodi; Giorgio Walter Canonica; Fulvio Braido
Journal:  J Child Neurol       Date:  2011-04-11       Impact factor: 1.987

2.  Diagnostic delay in Duchenne's muscular dystrophy.

Authors:  D E Crisp; F A Ziter; P F Bray
Journal:  JAMA       Date:  1982 Jan 22-29       Impact factor: 56.272

3.  Patient- and family-centered care and the pediatrician's role.

Authors: 
Journal:  Pediatrics       Date:  2012-01-30       Impact factor: 7.124

4.  Disparities in the diagnostic process of Duchenne and Becker muscular dystrophy.

Authors:  Caleb Holtzer; F John Meaney; Jennifer Andrews; Emma Ciafaloni; Deborah J Fox; Katherine A James; Zhenqiang Lu; Lisa Miller; Shree Pandya; Lijing Ouyang; Christopher Cunniff
Journal:  Genet Med       Date:  2011-11       Impact factor: 8.822

5.  Motor delays: early identification and evaluation.

Authors:  Garey H Noritz; Nancy A Murphy
Journal:  Pediatrics       Date:  2013-05-27       Impact factor: 7.124

6.  Diagnosis of Duchenne muscular dystrophy: parents' experiences and satisfaction.

Authors:  J M Green; F E Murton
Journal:  Child Care Health Dev       Date:  1996-03       Impact factor: 2.508

Review 7.  Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management.

Authors:  Katharine Bushby; Richard Finkel; David J Birnkrant; Laura E Case; Paula R Clemens; Linda Cripe; Ajay Kaul; Kathi Kinnett; Craig McDonald; Shree Pandya; James Poysky; Frederic Shapiro; Jean Tomezsko; Carolyn Constantin
Journal:  Lancet Neurol       Date:  2009-11-27       Impact factor: 44.182

Review 8.  Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care.

Authors:  Katharine Bushby; Richard Finkel; David J Birnkrant; Laura E Case; Paula R Clemens; Linda Cripe; Ajay Kaul; Kathi Kinnett; Craig McDonald; Shree Pandya; James Poysky; Frederic Shapiro; Jean Tomezsko; Carolyn Constantin
Journal:  Lancet Neurol       Date:  2009-11-27       Impact factor: 44.182

9.  Improving recognition of Duchenne muscular dystrophy: a retrospective case note review.

Authors:  Henriette J A van Ruiten; Volker Straub; Kate Bushby; Michela Guglieri
Journal:  Arch Dis Child       Date:  2014-09-03       Impact factor: 3.791

Review 10.  The importance of genetic diagnosis for Duchenne muscular dystrophy.

Authors:  Annemieke Aartsma-Rus; Ieke B Ginjaar; Kate Bushby
Journal:  J Med Genet       Date:  2016-01-11       Impact factor: 6.318

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  3 in total

1.  Early diagnosis of ataxia telangiectasia in the neonatal phase: a parents' perspective.

Authors:  M H D Schoenaker; M Blom; M C de Vries; C M R Weemaes; M van der Burg; M A A P Willemsen
Journal:  Eur J Pediatr       Date:  2019-11-11       Impact factor: 3.183

2.  Communicating the Spinal Muscular Atrophy diagnosis to children and the principle of autonomy.

Authors:  Isabella Araujo Mota Fernandes; Renata Oliveira Almeida Menezes; Guilhermina Rego
Journal:  BMC Pediatr       Date:  2022-08-17       Impact factor: 2.567

Review 3.  EMPATIA: A Guide for Communicating the Diagnosis of Neuromuscular Diseases.

Authors:  Isabella Araujo Mota Fernandes; Renata Oliveira Almeida Menezes; Guilhermina Rego
Journal:  Int J Environ Res Public Health       Date:  2022-08-09       Impact factor: 4.614

  3 in total

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