The experiences of adolescents and young adults with epilepsy: A systematic review and meta-synthesis of qualitative studies

被引:6
|
作者
Bai, Nan [1 ]
Yin, Min [1 ]
Zhang, Huiyue [1 ]
Li, Zheng [1 ,2 ]
机构
[1] Lanzhou Univ, Sch Nursing, Lanzhou, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Sch Nursing, Beijing, Peoples R China
关键词
Epilepsy; Adolescents; Young adults; Qualitative studies; Systematic review; HEALTH OUTCOMES; PEOPLE; LIFE; INTERVENTION; EXPLORATION;
D O I
10.1016/j.yebeh.2023.109086
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Background: Epilepsy is one of the most common and severe chronic neurological disorders and is asso-ciated with psychosocial problems. Several qualitative studies have investigated the experiences of ado-lescents and young adults with epilepsy. However, the findings were conflicting to some extent. This study examined and synthesized qualitative research data to understand the experiences of adolescents and young adults living with epilepsy, improving the development of targeted interventions and enhanc-ing these experiences. Objective: To synthesize qualitative evidence about the experiences of adolescents and young adults suf-fering from epilepsy.Methods: This systematic review and qualitative evidence synthesis used the Joanna Briggs methodology for qualitative systematic reviews [1]. PubMed, PsychINFO, EMBASE, and Web of Science were searched for studies indexed until March 2022. Qualitative data were extracted, analyzed, and aggregated using meta-synthesis.Results: Seventeen studies were included in the review. Three distinct themes were identified: "impact of epilepsy," "emotions associated with epilepsy," and "self-management of epilepsy." The results show that adolescents and young adults with epilepsy develop different strategies to manage epilepsy and associ-ated problems.Conclusion: The results improved our understanding of the experiences of adolescents and young adults suffering from epilepsy. Several approaches are encouraged to improve these experiences and the quality of life, including granting more autonomy to affected children, providing individualized care and advice, improving public awareness of epilepsy to avoid stigma, and strengthening legal frameworks to safe-guard the rights of affected people.(c) 2023 Elsevier Inc. All rights reserved.
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页数:12
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