Bonino Angela Yarnell, Goodwich Sara F, Mood Deborah
Department of Hearing and Speech Sciences and Vanderbilt Kennedy Center, Vanderbilt University Medical Center, Nashville, TN.
Department of Biomedical Engineering, Vanderbilt University, Nashville, TN.
Am J Audiol. 2025 Mar 3;34(1):60-71. doi: 10.1044/2024_AJA-24-00118. Epub 2024 Dec 3.
We aim to determine the prevalence and characteristics of developmental disabilities among the clinical population of children who receive hearing health care in the United States.
Using electronic health records of 131,709 children (0-18 years), we identified those with a diagnosis of attention deficit/hyperactivity disorder, autism spectrum disorder, vision differences, cerebral palsy, chromosomal abnormalities, delayed milestones, Down syndrome, or intellectual disability. We determined prevalence, age of first audiology encounter, age of diagnosis for the developmental disability, and hearing status based on the specific disability and the number of diagnoses. Binomial and multinomial logistic regressions were performed.
One in four children had a diagnosed developmental disability. The most common disabilities were delayed milestones (11.3%), vision differences (7.4%), attention-deficit/hyperactivity disorder (6.6%), and autism spectrum disorder (6.2%). Half of the children with developmental disabilities had at least one diagnosis before their first audiology encounter. Children with developmental disabilities were more likely to have a reduced hearing or an unknown hearing status than children without developmental diagnoses. For children with reduced hearing, those with developmental disabilities had higher rates of bilateral configurations and poorer hearing severity levels.
Developmental disabilities are common among children who seek hearing health care. Moreover, developmental disabilities often co-occur with reduced hearing. Further research and advocacy efforts are critical for creating clinical practices that are inclusive of, and equitable for, children with complex and diverse developmental profiles.
我们旨在确定在美国接受听力保健的儿童临床群体中发育障碍的患病率和特征。
利用131,709名儿童(0至18岁)的电子健康记录,我们识别出那些被诊断患有注意力缺陷/多动障碍、自闭症谱系障碍、视力差异、脑瘫、染色体异常、发育迟缓、唐氏综合征或智力残疾的儿童。我们根据特定残疾情况和诊断数量确定了患病率、首次听力检查年龄、发育障碍诊断年龄以及听力状况。进行了二项式和多项逻辑回归分析。
四分之一的儿童被诊断患有发育障碍。最常见的残疾是发育迟缓(11.3%)、视力差异(7.4%)、注意力缺陷/多动障碍(6.6%)和自闭症谱系障碍(6.2%)。一半患有发育障碍的儿童在首次听力检查之前至少有一项诊断。与没有发育障碍诊断的儿童相比,患有发育障碍的儿童听力下降或听力状况不明的可能性更大。对于听力下降的儿童,患有发育障碍者双侧听力配置的比例更高,听力严重程度更差。
发育障碍在寻求听力保健服务的儿童中很常见。此外,发育障碍常与听力下降同时出现。进一步的研究和宣传工作对于建立包容并公平对待具有复杂多样发育特征儿童的临床实践至关重要。