Literature DB >> 24674229

Developing an information leaflet on 22q11.2 deletion syndrome for parents to use with professionals during healthcare encounters.

Honor Nicholl1, Carmel Doyle, Thelma Begley, Maryanne Murphy, Anne Lawlor, Helen Malone.   

Abstract

PURPOSE: The purpose of this project was to gather parents' expertise to inform an educational leaflet for parents to share with professionals caring for children with 22q11.2 deletion syndrome (22q11.2 DS). DESIGN AND METHODS: A mixed-method design was adopted. Data were collected by one focus group interview (n = 8) and questionnaires with 92 other parents of children with 22q11.2 DS.
RESULTS: Quantitative and qualitative responses informed the development of an information leaflet. PRACTICE IMPLICATIONS: Parents are well positioned to assist in development of information leaflets that can minimize "repeated storytelling" during professional encounters.
© 2014, Wiley Periodicals, Inc.

Entities:  

Keywords:  22q11.2 deletion syndrome; information leaflet; parent; rare disorder; research

Mesh:

Year:  2014        PMID: 24674229     DOI: 10.1111/jspn.12078

Source DB:  PubMed          Journal:  J Spec Pediatr Nurs        ISSN: 1539-0136            Impact factor:   1.260


  1 in total

1.  Internet Use by Parents of Children With Rare Conditions: Findings From a Study on Parents' Web Information Needs.

Authors:  Honor Nicholl; Catherine Tracey; Thelma Begley; Carole King; Aileen M Lynch
Journal:  J Med Internet Res       Date:  2017-02-28       Impact factor: 5.428

  1 in total

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