Functioning and well‐being in older children and adolescents with achondroplasia: A qualitative study. Issue 2 (13th October 2021)

• Record Type: Journal Article
• Authors: Pfeiffer, Kathryn M.; Brod, Meryl; Smith, Alden; Viuff, Dorthe; Ota, Sho; Charlton, R. Will
• Is Part Of: American journal of medical genetics. Volume 188:Issue 2(2022)
• Page Start: 454
• Page End: 462
• Publication Date: 2021-10-13
• Subjects: achondroplasia -- adolescents -- physical functioning -- quality of life -- school; Medical genetics -- Periodicals; 616.14205
• DOI: 10.1002/ajmg.a.62534
• Languages: English
• ISSNs: 1552-4825

Abstract

Abstract: The study aimed to explore how having achondroplasia affects older children and adolescents' day‐to‐day functioning and well‐being. Individual/focus group interviews were conducted with older children/adolescents between the ages of 9 to <18 years and diagnosed with achondroplasia to elicit key concepts. An adapted grounded theory approach informed the qualitative analysis of interview data. Thirty‐two children and adolescents completed interviews. Study results revealed five impact domains, including physical health, functioning, school impacts, emotional well‐being, and social well‐being. Frequently reported impacts on physical health included low stamina/tiring easily (81%) and back pain (69%). Key impacts in the functioning domain were difficulty with reaching objects or high places (84%) and walking long distances (75%). Emotional impacts included feeling different (63%), worried/scared (47%), and embarrassed/self‐conscious (47%). Impacts on social well‐being included difficulty with sports or physical play (81%) and others treating child as younger than their actual age (75%). The most frequent school impact was trouble participating in physical education (81%). A preliminary theoretical model depicting the experiences of older children/adolescents with achondroplasia was constructed based on the analysis. The preliminary theoretical model of older children and adolescents' experiences of living with achondroplasia may be used to inform future research and clinical practice.