Hearing Research Unit for Children, Division of Audiology, School of Health & Rehabilitation Sciences, The University of Queensland, Brisbane, 4072, Australia; Children's Health Queensland Hospital and Health Service, Child and Youth Community Health Service, 10 Chapel Street, Nundah, Queensland, 4012, Australia.
Children's Health Queensland Hospital and Health Service, Child and Youth Community Health Service, 10 Chapel Street, Nundah, Queensland, 4012, Australia.
Int J Pediatr Otorhinolaryngol. 2023 Aug;171:111630. doi: 10.1016/j.ijporl.2023.111630. Epub 2023 Jun 12.
Infants diagnosed with a conductive hearing loss (CHL) are at increased risk of developmental delays. Using a sample of infants diagnosed with CHL through UNHS, this study aimed to investigate the relationship between specific demographic or clinical characteristics and 1) occasions of service to reach a hearing diagnosis and 2) the profile of CHL.
Retrospective analysis was conducted for all infants with CHL born between 01/01/2007 and 31/12/2018 who had received UNHS. Chi squared analysis was conducted on data from 1208 records.
Infants with ≥1 risk factor for hearing loss were more likely to attend more than three occasions of service. Infants who were bilateral refer/medical exclusion, Torres Strait Islander, had ≥1 risk factors for hearing loss or were born pre-term had greater proportions of bilateral CHL than unilateral CHL. Mild to moderate was the most frequent degree of CHL, although a unilateral or bilateral CHL did not have an association with the severity of CHL. Compared to other risk factors, infants with a syndrome had greater proportions of bilateral than unilateral CHL. Risk factors of craniofacial abnormality, prolonged ventilation, or syndrome had greater proportions of mild to moderate CHL than moderate or greater. On average, infants were diagnosed with a CHL at 37.29 weeks of age.
These findings highlight the relationship between clinical/demographic characteristics and occasions of service to diagnose CHL in children, including the CHL profile. An understanding of this relationship may help clinicians to better plan, assess and manage infants diagnosed with a CHL through UNHS.
患有传导性听力损失(CHL)的婴儿发生发育迟缓的风险增加。本研究通过 UNHS 对诊断为 CHL 的婴儿进行样本分析,旨在调查特定的人口统计学或临床特征与 1)达到听力诊断的服务次数和 2)CHL 特征之间的关系。
对 2007 年 1 月 1 日至 2018 年 12 月 31 日期间通过 UNHS 接受检查的所有患有 CHL 的婴儿进行回顾性分析。对 1208 份记录的数据进行卡方分析。
患有≥1 种听力损失危险因素的婴儿更有可能接受三次以上的服务。双侧转诊/医学排除、托雷斯海峡岛民、有≥1 种听力损失危险因素或早产的婴儿双侧 CHL 的比例高于单侧 CHL。轻度至中度是最常见的 CHL 程度,尽管单侧或双侧 CHL 与 CHL 的严重程度无关。与其他危险因素相比,患有综合征的婴儿双侧 CHL 的比例更高。颅面畸形、延长通气或综合征的危险因素中,轻度至中度 CHL 的比例高于中度或更严重的 CHL。平均而言,婴儿在 37.29 周龄时被诊断为 CHL。
这些发现强调了临床/人口统计学特征与通过 UNHS 诊断 CHL 的儿童服务次数之间的关系,包括 CHL 特征。了解这种关系可能有助于临床医生更好地规划、评估和管理通过 UNHS 诊断为 CHL 的婴儿。