A comparative study of psychosocial development in children who receive cochlear implants. (November 2013)

• Record Type: Journal Article
• Authors: Warner-Czyz, Andrea D; Loy, Betty; Roland, Peter S; Tobey, Emily A
• Is Part Of: Cochlear implants international. Volume 14:Number 5(2013)
• Page Start: 266
• Page End: 275
• Publication Date: 2013-11
• Subjects: Cochlear implant -- Quality of life -- Children -- Hearing loss; Cochlear implants -- Periodicals; 617.882
• DOI: 10.1179/1754762812Y.0000000021
• Languages: English
• ISSNs: 1467-0100

Abstract

Abstract : Objectives: This study assessed self-reported quality of life of children with a cochlear implant (CI), comparing results with two published reports from the past decade. Methods: Participants included 33 pediatric CI recipients with a mean age of 10.12 years (SD = 3.59), mean implantation age of 1.36 years (SD = 0.46), and mean CI experience of 6.23 years (SD = 1.75). Children in all three studies completed a self-report quality-of-life questionnaire that included seven benefit and six problem items, rated on a 5-point Likert scale. Results: Outcomes revealed agreement across studies in overall benefit and problem ratings. Environmental awareness and frustration reduction were the most and least positively rated outcomes, respectively. Items contributing to overall ratings differed across studies. Current CI recipients rated speech production, making new friends, and understanding speech more positively and taking extra care of the device more negatively than previous generations of pediatric CI users. Discussion: Overall, benefits outweigh problems of the device, according to children using CI. Differences in issues motivating self-report ratings reflect changes in CI candidacy, technology, and social participation over the past decade. These findings emphasize the need for clinicians to address not only communication needs, but also quality-of-life issues to optimize outcomes in children using CI.