奇纳
遗传咨询
心理信息
医学
基因检测
梅德林
家庭医学
临床心理学
精神科
遗传学
内科学
心理干预
政治学
生物
法学
作者
Tasha Wainstein,Sheila K. Marshall,Colin J.D. Ross,Alice Virani,Jehannine Austin,Alison M. Elliott,Bartha Maria Knoppers,Larry D. Lynd,Alivia Dey,Shelin Adam,Nick Bansback,Patricia Birch,Lorne A. Clarke,Nick Dragojlovic,Jan M. Friedman,Deborah Lambert,Daryl Pullman,Wyeth W. Wasserman,Ma’n H. Zawati
出处
期刊:JAMA Pediatrics
[American Medical Association]
日期:2021-11-22
卷期号:176 (2): 185-185
被引量:7
标识
DOI:10.1001/jamapediatrics.2021.4290
摘要
The number of adolescents who are diagnosed with a genetic disorder is increasing as genome sequencing becomes the standard of clinical diagnostic testing. However, the experience of receiving a diagnosis of a genetic condition has not been extensively studied in adolescents.To identify how adolescents with a genetic condition engage with genetic or genomic counseling services as well as interpret, adapt to, and experience their diagnosis.A literature search of MEDLINE, Embase, CINAHL, and PsycINFO was undertaken. Articles (primary literature, knowledge syntheses, and gray literature) in English that investigated the experiences of adolescents between 10 and 19 years of age who received genetic or genomic counseling were included. Data were extracted from 45 eligible articles and analyzed descriptively.A total of 45 studies were included, most of which were quantitative in nature (21 of 45 [47%]) and conducted in the US (n = 13), followed by the UK (n = 8), Australia (n = 8), and Canada (n = 6). A total of 29 distinct monogenic disorders were investigated. Sample sizes ranged from 1 to 930, with a median of 23 participants, and the year of publication ranged from 1977 to 2019. Included studies addressed all aspects of genetic counseling, but a preponderance of articles assessed knowledge about genetic conditions (n = 17) and challenges of communication within families (n = 16). Fewer articles addressed the experiences of adolescents adapting to their genetic conditions (n = 8) and the genetic counseling process (n = 4). Only 1 study addressed any aspect of genetic counseling in relation to genome sequencing.This scoping review found that most of the included studies focused on adolescents' knowledge about their genetic condition and communication about genetic risks, whereas fewer studies explored their adaptation to the condition and the genetic counseling process. A systematic reconsideration of the genetic counseling process may be undertaken to provide an evidence-informed health care service that is tailored to the needs of this adolescent population.
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