Screening for Developmental Delays in Pediatric Cochlea Implant Candidates and Recipients.

IF 1.9 3区 医学 Q3 CLINICAL NEUROLOGY
Mallory Warrick, Sophie Sherman, Kaylene King, Angela LaRosa, Theodore R McRackan, Patty Coker-Bolt, Kara C Schvartz-Leyzac
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引用次数: 0

Abstract

Objective: Conduct a pilot clinical improvement project to effectively screen children with hearing loss for developmental delays. Children with hearing loss and cochlear implants (CIs) are at risk for additional developmental delays; however, screening to aid in early identification and referral for developmental delays is not routinely performed at CI centers. It is important to consider all aspects of child development to maximize CI outcomes and access to language.

Study design: Caregivers of 31 children completed the Ages and Stages Questionnaire (ASQ) and the Sensory Profile-2 (SP2), which are standardized questionnaires that assess developmental milestones in areas of communication, gross motor, fine motor, problem solving, personal-social, and sensory integration.

Setting: Participants were prospectively evaluated at a CI center in a tertiary medical center.

Patients: Participants included children, aged ≤5 years old with bilateral hearing loss who use CIs or who were CI candidates, and their families.

Main outcome measures: Scores on ASQ and SP2 questionnaires.

Results: Thirty-one children were screened, and approximately 40 to 50% screened positive for risk of developmental delay in areas excluding communication and received referrals for evaluations in occupational therapy (n = 16; 51.6%), physical therapy (n = 13; 41.9%), and developmental pediatrics (n = 13; 41.9%). Of children referred and seen for evaluations, six were diagnosed with developmental delays in at least one developmental area beyond the communication domains.

Conclusions: Routine screening in children with significant hearing loss can successfully detect developmental delays, which may go unnoticed. This proactive approach enables timely and comprehensive treatment for developmental delays beyond those solely related to communication.

筛查小儿耳蜗植入候选者和接受者的发育迟缓。
目标:开展临床改进试点项目,有效筛查听力损失儿童的发育迟缓。听力损失和植入人工耳蜗(CI)的儿童有可能出现额外的发育迟缓;然而,CI 中心并未常规开展筛查,以帮助早期识别和转诊发育迟缓的儿童。为了最大限度地提高 CI 的效果和语言能力,必须考虑到儿童发展的各个方面:研究设计:31 名儿童的照顾者填写了年龄与阶段问卷 (ASQ) 和感官特征-2 (SP2),这两份标准化问卷用于评估儿童在沟通、粗大运动、精细运动、解决问题、个人社交和感觉统合等方面的发育里程碑:参与者在一家三级医疗中心的 CI 中心接受前瞻性评估:参与者包括使用 CI 或 CI 候选者的 5 岁以下双侧听力损失儿童及其家人:主要结果测量:ASQ 和 SP2 问卷得分:31名儿童接受了筛查,约40%至50%的筛查结果呈阳性,显示他们在除沟通以外的领域存在发育迟缓的风险,并接受了职业疗法(16人;51.6%)、物理疗法(13人;41.9%)和发育儿科(13人;41.9%)的转诊评估。在转诊并接受评估的儿童中,有 6 名儿童被诊断出在沟通领域之外的至少一个发育领域存在发育迟缓:结论:对有严重听力损失的儿童进行常规筛查,可以成功发现可能被忽视的发育迟缓。这种积极主动的方法能够及时、全面地治疗发育迟缓,而不仅仅是与沟通有关的发育迟缓。
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来源期刊
Otology & Neurotology
Otology & Neurotology 医学-耳鼻喉科学
CiteScore
3.80
自引率
14.30%
发文量
509
审稿时长
3-6 weeks
期刊介绍: ​​​​​Otology & Neurotology publishes original articles relating to both clinical and basic science aspects of otology, neurotology, and cranial base surgery. As the foremost journal in its field, it has become the favored place for publishing the best of new science relating to the human ear and its diseases. The broadly international character of its contributing authors, editorial board, and readership provides the Journal its decidedly global perspective.
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