Literature DB >> 8820016

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

J M Green1, F E Murton.   

Abstract

The purpose of the study was to investigate parents' experiences of diagnosis of Duchenne muscular dystrophy. Data were collected retrospectively by postal questionnaire from the parents of 158 boys diagnosed at different times and locations and, for some, after lengthy periods of uncertainty. Most parents knew nothing about Duchenne before being given the diagnosis. There was considerable variation in parents' experiences but the only independent predictors of parents' satisfaction with how the diagnosis was given were obtaining the information that they wanted and feeling that they had understood and remembered it. What distinguishes Duchenne from, say, Down syndrome is that doctors are having to deliver a death sentence on a child. Our data show that this can be done in a way that is satisfactory to parents. What is required is empathy and sensitivity to parents' informational and emotional needs.

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Year:  1996        PMID: 8820016

Source DB:  PubMed          Journal:  Child Care Health Dev        ISSN: 0305-1862            Impact factor:   2.508


  8 in total

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

Authors:  Roxanna M Bendixen; Amy Houtrow
Journal:  J Pediatr Health Care       Date:  2016-10-12       Impact factor: 1.812

2.  A tale worth telling: the impact of the diagnosis experience on disclosure of genetic disorders.

Authors:  J Goodwin; K Schoch; V Shashi; S R Hooper; O Morad; M Zalevsky; D Gothelf; L E Campbell
Journal:  J Intellect Disabil Res       Date:  2014-07-25

3.  Delayed diagnosis in duchenne muscular dystrophy: data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet).

Authors:  Emma Ciafaloni; Deborah J Fox; Shree Pandya; Christina P Westfield; Soman Puzhankara; Paul A Romitti; Katherine D Mathews; Timothy M Miller; Dennis J Matthews; Lisa A Miller; Christopher Cunniff; Charlotte M Druschel; Richard T Moxley
Journal:  J Pediatr       Date:  2009-04-25       Impact factor: 4.406

4.  A mixed methods exploration of families' experiences of the diagnosis of childhood spinal muscular atrophy.

Authors:  Sally Lawton; Chriselle Hickerton; Alison D Archibald; Belinda J McClaren; Sylvia A Metcalfe
Journal:  Eur J Hum Genet       Date:  2014-07-30       Impact factor: 4.246

5.  Psychological and practical difficulties among parents and healthy siblings of children with Duchenne vs. Becker muscular dystrophy: an Italian comparative study.

Authors:  Lorenza Magliano; Maria Grazia D'Angelo; Giuseppe Vita; Marika Pane; Adele D'Amico; Umberto Balottin; Corrado Angelini; Roberta Battini; Luisa Politano; Melania Patalano; Alessandra Sagliocchi; Federica Civati; Erika Brighina; Gian Luca Vita; Sonia Messina; Maria Sframeli; Maria Elena Lombardo; Roberta Scalise; Giulia Colia; Maria Catteruccia; Angela Berardinelli; Maria Chiara Motta; Alessandra Gaiani; Claudio Semplicini; Luca Bello; Guja Astrea; Antonella Zaccaro; Marianna Scutifero
Journal:  Acta Myol       Date:  2014-12

6.  Burden, professional support, and social network in families of children and young adults with muscular dystrophies.

Authors:  Lorenza Magliano; Melania Patalano; Alessandra Sagliocchi; Marianna Scutifero; Antonella Zaccaro; Maria Grazia D'angelo; Federica Civati; Erika Brighina; Giuseppe Vita; Gian Luca Vita; Sonia Messina; Maria Sframeli; Marika Pane; Maria Elena Lombardo; Roberta Scalise; Adele D'amico; Giulia Colia; Michela Catteruccia; Umberto Balottin; Angela Berardinelli; Maria Chiara Motta; Corrado Angelini; Alessandra Gaiani; Claudio Semplicini; Luca Bello; Roberta Battini; Guja Astrea; Luisa Politano
Journal:  Muscle Nerve       Date:  2015-04-22       Impact factor: 3.217

Review 7.  Integrated care of muscular dystrophies in Italy. Part 2. Psychological treatments, social and welfare support, and financial costs.

Authors:  Lorenza Magliano; Marianna Scutifero; Melania Patalano; Alessandra Sagliocchi; Antonella Zaccaro; Federica Civati; Erika Brighina; Gianluca Vita; Sonia Messina; Maria Sframeli; Maria Elena Lombardo; Roberta Scalise; Giulia Colia; Maria Catteruccia; Angela Berardinelli; Maria Chiara Motta; Alessandra Gaiani; Claudio Semplicini; Luca Bello; Guja Astrea; Giulia Ricci; Maria Grazia D'Angelo; Giuseppe Vita; Marika Pane; Adele D'Amico; Umberto Balottin; Corrado Angelini; Roberta Battini; Luisa Politano
Journal:  Acta Myol       Date:  2017-06

8.  Family context in muscular dystrophies: psychosocial aspects and social integration.

Authors:  Lorenza Magliano; Luisa Politano
Journal:  Acta Myol       Date:  2016-10
  8 in total

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