Parents' perspectives on the dilemmas with intervention for infants with auditory neuropathy spectrum disorder : A qualitative study
OBJECTIVE: This paper explores parental experiences of choices surrounding auditory management and language and communication development for infants and children with auditory neuropathy spectrum disorder (ANSD) in the light of the heterogeneity of condition, a poor evidence base for best outcomes in relation to management options, and the scarcity of data rooted in parent and family experience.
DESIGN: Qualitative narrative study.
STUDY SAMPLE: Twenty-five parents of 21 children (aged four months to six years) identified with ANSD through the newborn hearing screening programme.
RESULTS: Families identify barriers to early management due to conflicting expert opinions and ANSD-specific challenges with diagnosis and prognosis in infants, and share their accounts on their own evaluations of intervention benefit in their children.
CONCLUSIONS: The results are of relevance to the clinicians and other professionals involved in early intervention, management, and support of infants with ANSD.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2015 |
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Erschienen: |
2015 |
Enthalten in: |
Zur Gesamtaufnahme - volume:54 |
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Enthalten in: |
International journal of audiology - 54(2015), 8 vom: 23. Aug., Seite 552-8 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Uus, Kai [VerfasserIn] |
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Links: |
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Themen: |
Auditory neuropathy spectrum disorder |
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Anmerkungen: |
Date Completed 14.04.2016 Date Revised 08.04.2022 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.3109/14992027.2015.1020970 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM247593621 |
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520 | |a OBJECTIVE: This paper explores parental experiences of choices surrounding auditory management and language and communication development for infants and children with auditory neuropathy spectrum disorder (ANSD) in the light of the heterogeneity of condition, a poor evidence base for best outcomes in relation to management options, and the scarcity of data rooted in parent and family experience | ||
520 | |a DESIGN: Qualitative narrative study | ||
520 | |a STUDY SAMPLE: Twenty-five parents of 21 children (aged four months to six years) identified with ANSD through the newborn hearing screening programme | ||
520 | |a RESULTS: Families identify barriers to early management due to conflicting expert opinions and ANSD-specific challenges with diagnosis and prognosis in infants, and share their accounts on their own evaluations of intervention benefit in their children | ||
520 | |a CONCLUSIONS: The results are of relevance to the clinicians and other professionals involved in early intervention, management, and support of infants with ANSD | ||
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