Congenitally deaf children's care trajectories in the context of universal neonatal hearing screening: a qualitative study of the parental experiences
The objective of this study is to examine the early care trajectories of congenitally deaf children from a parental perspective, starting with universal neonatal hearing screenings. The analysis using a three-dimensional care trajectory concept is aimed at developing a basic typology of postscreening care trajectories. Children with severe/profound hearing loss, registered in the Flanders' (Belgium) universal neonatal hearing screening program, born between 1999 and 2001. Thematic content analysis of qualitative data collected retrospectively from participant's parents. Two basic types of care... Mehr ...
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Dokumenttyp: | journalarticle |
Erscheinungsdatum: | 2011 |
Schlagwörter: | Social Sciences / EXPECTATIONS / SERVICES / NEWBORN / LANGUAGE / FLANDERS / OUTCOMES / SURGERY / FAMILIES / DISTRESS / PEDIATRIC COCHLEAR IMPLANTATION |
Sprache: | Englisch |
Permalink: | https://search.fid-benelux.de/Record/base-28648056 |
Datenquelle: | BASE; Originalkatalog |
Powered By: | BASE |
Link(s) : | https://biblio.ugent.be/publication/2130820 |