Permanent Childhood Hearing Loss in Infants with Hypoxic Ischaemic Encephalopathy: Incidence and Risk Factors

Alpana Kulkarni
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引用次数: 1

Abstract

Objective: To study the incidence of permanent hearing loss in infants with hypoxic ischaemic encephalopathy (HIE) and the risk factors associated with hearing loss. Study design: A single centre retrospective cohort study was completed in all term and near term infants with HIE over 9 years (2010-18). Newborn screening with one/two stage protocol was carried out initially (automated otoacoustic emissions only or with automated auditory brainstem testing if baby in NICU for more than 48 hours) of all babies with HIE. Babies with Stage 2 and 3 HIE were cooled. Those who failed this protocol had diagnostic auditory brainstem testing (ABR) which identified the hearing loss as sensorineural or auditory neuropathy spectrum disorder. Aetiological investigations were done to rule out other causes of sensorineural hearing loss including MRI IAMS, cytomegalovirus and Connexin 26 testing. Results: Ninety-nine babies were eligible and 8 died. Ten out of 91 babies failed the newborn screen. Of the 10, 8 (8.8%) had permanent hearing loss. Six out of 8 babies had bilateral sensorineural hearing loss, 1 had unilateral sensorineural hearing loss and 1 had unilateral auditory neuropathy spectrum disorder. Permanent hearing loss was associated with low Apgar score at 1 and 5 min (CI 0.5, 3.9, p=0.01), persistent pulmonary hypertension (p=0.0002, CI-0.5,-0.2) and loop diuretics (CI-0.4,-0.1, p=0.0002). Permanent hearing loss was found in all grades of HIE. Conclusion: This study adds to the previous studies indicating that there is high incidence of permanent hearing loss seen in term and near term babies with HIE (cooled as well as not cooled). Further studies with larger samples are needed to study the risk factors in this cohort and compare the incidence of hearing loss in cooled versus not cooled babies. What’s new: This study confirms that permanent hearing loss of all degree and severity can occur in all grades of hypoxic ischaemic encephalopathy. It indicates that auditory neuropathy spectrum disorder can develop secondary to HIE. Association between low Apgar score at 1 and 5 min, PPHN, loop diuretics and development of permanent hearing loss is significant and needs to be explored further.
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婴儿缺氧缺血性脑病的永久性儿童听力丧失:发病率和危险因素
目的:探讨新生儿缺氧缺血性脑病(HIE)永久性听力损失的发生率及相关危险因素。研究设计:对所有9岁以上(2010- 2018年)的足月和近足月HIE婴儿进行单中心回顾性队列研究。采用一/两阶段方案对所有HIE婴儿进行新生儿筛查(仅进行自动耳声发射,如果婴儿在NICU超过48小时,则进行自动听觉脑干检测)。第2期和第3期HIE的婴儿被冷却。未通过该方案的患者进行了诊断性听觉脑干测试(ABR),该测试将听力损失确定为感觉神经或听神经病变谱系障碍。病因学调查排除感音神经性听力损失的其他原因,包括MRI、巨细胞病毒和连接蛋白26检测。结果:符合条件的婴儿99例,死亡8例。91名婴儿中有10名未能通过新生儿筛查。在这10人中,8人(8.8%)有永久性听力损失。8例患儿中6例为双侧感音神经性听力损失,1例为单侧感音神经性听力损失,1例为单侧听神经病变谱系障碍。永久性听力损失与1分钟和5分钟Apgar评分低(CI 0.5, 3.9, p=0.01)、持续性肺动脉高压(p=0.0002, CI-0.5,-0.2)和袢利尿剂(CI-0.4,-0.1, p=0.0002)相关。所有等级的HIE患者均出现永久性听力损失。结论:本研究增加了先前的研究,表明足月和近期HIE婴儿(冷却和未冷却)的永久性听力损失发生率很高。需要更大样本的进一步研究来研究这一队列中的危险因素,并比较冷却婴儿和未冷却婴儿的听力损失发生率。最新进展:这项研究证实,所有程度和严重程度的永久性听力损失都可能发生在所有级别的缺氧缺血性脑病中。提示听神经病变谱系障碍可继发于HIE。低Apgar评分在1和5分钟,PPHN,利尿剂和发展的永久性听力损失之间的关系是显著的,需要进一步探讨。
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