Doyle Karen Jo, Kong Ying Yee, Strobel Karen, Dallaire Patricia, Ray R Mark
University of California Davis Medical Center, Sacramento, California, USA.
Otol Neurotol. 2004 May;25(3):318-22. doi: 10.1097/00129492-200405000-00020.
The specific aims of the research are to determine whether newborn ears with persistent middle ear effusion at age 30 to 48 hours are more likely to develop chronic otitis media with effusion over the first year of life when compared with ears without persistent middle ear effusion. The hypothesis is that neonates with middle ear effusion persisting to 30 to 48 hours are more likely to develop chronic otitis media with effusion.
Prospective, case-control design. Loupe-magnified pneumatic otoscopy performed at the time of newborn hearing screening determined presence or absence of effusion. Infants enrolled in the study returned for outpatient examinations.
University medical center well-baby nursery and out-patient audiology clinic.
From 454 neonates, 14 experimental subjects with neonatal middle ear effusions and 15 control subjects free of neonatal effusion were recruited for the study and followed-up for 1 year.
Outpatient study tests included transient-evoked otoacoustic emissions, tympanometry, pneumatic otoscopy, and visual reinforcement audiometry (starting at age 6 months), at 3, 6, 9, and 12 months of age. Experimental (neonatal effusion) infants were followed-up starting at age 1 month. Infants found at any follow-up examination to have effusion on otoscopy were followed-up and tested 1 month later.
Chronic otitis media with effusion defined as hypomobile or immobile tympanic membrane on pneumatic otoscopy in one or both ears for three consecutive monthly examinations. Hearing loss defined as greater than 25-dB hearing loss visual reinforcement audiometry thresholds.
Eight experimental infants (58%) and three control infants (20%) developed chronic otitis media with effusion (p < 0.04). The average number of effusions was 1.27 for control and 4.14 for experimental infants (average number of effusions for each group at 3-, 6-, 9-, and 12-month visits). Warbled tone and speech visual reinforcement audiometry thresholds averaged 3 dB worse in the experimental group, but these differences were not statistically significant. For the control group, mean visual reinforcement audiometry thresholds never exceeded 25 dB hearing loss. For the experimental group, mean visual reinforcement audiometry thresholds exceeded 25 dB hearing loss at 1,000, 2,000, and 4,000 Hz at 9 months.
A majority of infants with persistent neonatal middle ear effusion found by pneumatic otoscopy at 30 to 48 hours will develop chronic otitis media with effusion during the first year of life. However, chronic otitis media with effusion is common in all infants (20% of controls), a time during which infants are examined and tested frequently.
本研究的具体目的是确定出生30至48小时时存在持续性中耳积液的新生儿耳朵,与没有持续性中耳积液的耳朵相比,在出生后的第一年内是否更有可能发展为慢性分泌性中耳炎。假设是中耳积液持续到30至48小时的新生儿更有可能发展为慢性分泌性中耳炎。
前瞻性病例对照设计。在新生儿听力筛查时进行头戴放大镜的鼓气耳镜检查,以确定是否存在积液。纳入研究的婴儿返回门诊进行检查。
大学医学中心的健康婴儿托儿所和门诊听力诊所。
从454名新生儿中,招募了14名患有新生儿中耳积液的实验对象和15名无新生儿积液的对照对象进行研究,并随访1年。
门诊研究测试包括瞬态诱发耳声发射、鼓室图、鼓气耳镜检查和视觉强化听力测试(从6个月大开始),在3、6、9和12个月大时进行。实验性(新生儿积液)婴儿从1个月大开始随访。在任何一次随访检查中发现耳镜检查有积液的婴儿,1个月后进行随访和测试。
慢性分泌性中耳炎定义为连续三个月的门诊检查中,一只或两只耳朵在鼓气耳镜检查时鼓膜活动度降低或固定。听力损失定义为视觉强化听力测试阈值大于25分贝的听力损失。
8名实验性婴儿(58%)和3名对照婴儿(20%)发展为慢性分泌性中耳炎(p<0.04)。对照组的平均积液次数为1.27次,实验性婴儿为4.14次(每组在3、6、9和12个月随访时的平均积液次数)。实验性组的啭音和言语视觉强化听力测试阈值平均差3分贝,但这些差异无统计学意义。对于对照组,平均视觉强化听力测试阈值从未超过25分贝的听力损失。对于实验性组,在9个月时,1000、2000和4000赫兹处的平均视觉强化听力测试阈值超过了25分贝的听力损失。
在出生30至48小时时通过鼓气耳镜检查发现有持续性新生儿中耳积液的大多数婴儿,在出生后的第一年内将发展为慢性分泌性中耳炎。然而,慢性分泌性中耳炎在所有婴儿中都很常见(对照组的20%),在此期间婴儿会经常接受检查和测试。