Prevalence and risk factors of hearing loss in high-risk neonates at a tertiary care hospital in Mumbai

Monalisa Pradhan, B. Bhaisara, S. Shinde
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Abstract

Background: The present study was conducted to assess the prevalence of hearing loss using measurements of otoacoustic emission (OAE) in newborns admitted to NICU and to determine the risk factors predictive of hearing impairment in these newborns. Methods: This was a Prospective observational study conducted among 220 newborns admitted to the NICU over 18 months. Ethical clearance was obtained from the IEC. The sample size was obtained by the universal sampling technique. All candidates underwent hearing assessment in a sound-treated room in the department using a distortion product OAEs (DPOAE) test at the time of discharge.  Babies who did not pass the initial screening underwent another OAE test within one month after being discharged. If they failed the test again, they were referred to an otologist for BERA. Results: Of the 226 neonates included in the study, 40 cases (17.7%) failed the initial screening. 29 cases (12.8%) failed the second OAE screening and were subjected to BERA. Risk factors included asphyxia (p≤0.001), mechanical ventilation (p<0.0004), history of ototoxic medication (p=0.004), neonates with hyperbilirubinemia requiring exchange transfusion (p=0.005), low Apgar scores (p≤0.001). Conclusions: A two-stage OAE hearing screening can be a suitable method for early detection of hearing impairment in newborns. This method has shown high prevalence of hearing loss among high-risk neonates but needs to be confirmed with diagnostic BERA. It is crucial to have universal hearing screening to detect the large number of hearing-impaired neonates in the newborn population of our country, including those who are not considered at risk.
孟买一家三级医院高危新生儿听力损失的发生率和风险因素
研究背景本研究旨在通过测量新生儿重症监护室(NICU)新生儿的耳声发射(OAE)来评估听力损失的发生率,并确定预测这些新生儿听力受损的风险因素。研究方法这是一项前瞻性观察研究,研究对象是新生儿重症监护室在 18 个月内收治的 220 名新生儿。研究获得了 IEC 的伦理许可。样本量通过普遍抽样技术获得。所有候选者在出院时都在科室的声音处理室中接受了听力评估,使用的是失真产物 OAEs(DPOAE)测试。 未通过初筛的婴儿在出院后一个月内再次接受 OAE 测试。如果再次未能通过测试,则转诊至耳科医生进行 BERA 检查。结果:在纳入研究的 226 名新生儿中,有 40 例(17.7%)未能通过初筛。29例(12.8%)未能通过第二次OAE筛查,并接受了BERA检查。风险因素包括窒息(p≤0.001)、机械通气(p<0.0004)、耳毒性药物史(p=0.004)、需要交换输血的高胆红素血症新生儿(p=0.005)、低Apgar评分(p≤0.001)。结论两阶段 OAE 听力筛查是早期发现新生儿听力障碍的合适方法。这种方法在高危新生儿中显示出听力损失的高患病率,但需要通过诊断性 BERA 加以确认。在我国的新生儿群体中,包括那些不被认为是高危人群的新生儿在内,要发现大量听力受损的新生儿,就必须普及听力筛查。
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