Robertson Charlene M T, Howarth Tanis M, Bork Dietlind L R, Dinu Irina A
Section of Neurosciences, Department of Pediatrics, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Canada.
Pediatrics. 2009 May;123(5):e797-807. doi: 10.1542/peds.2008-2531.
We present population-based, childhood prevalence rates of and neonatal risk factors for permanent hearing loss among extremely premature infants.
By using an inception-cohort, longitudinal study design for 1974-2003, we studied permanent hearing loss among 1279 survivors with gestational age of < or =28 weeks and birth weight of <1250 g (mortality rate: 42.7%; lost to follow-up monitoring: 4.7%) Newborn hearing screening, performed by experienced pediatric audiologists, used click-evoked auditory brainstem response testing after 1975. Survivors underwent repeated behavioral audiologic testing and multidisciplinary follow-up monitoring. Permanent hearing loss was defined as mild/moderate (26-70 dB hearing level), severe/profound (71 to >90 dB hearing level), delayed-onset (diagnosed after previously normal hearing), or progressive (increase in loss of > or =15 dB hearing level). Permanent hearing loss rates were established at 3 years of age, with newborn, infant, and >5-year final hearing outcomes being recorded. Risk factors were compared for children with and without hearing loss, odds ratios were calculated, and prediction performance was determined through area under the curve analysis.
Forty (3.1%) of 1279 survivors 3 years of age had permanent hearing loss and 24 (1.9%) had severe/profound loss, with no changes over time. Bilateral delayed-onset loss occurred for 4 children (10%) and progressive loss for 11 children (28%). One child had auditory neuropathy, and 29 (73%) had multiple disabilities. Prolonged oxygen use, gastrointestinal surgery, patent ductus arteriosus ligation, and low socioeconomic index yielded good prediction of permanent hearing loss; oxygen use was the most significant predictor of severe/profound loss.
Permanent hearing loss remains an adverse outcome of extreme prematurity, complicated by significant delayed-onset and progressive loss. Prolonged supplemental oxygen use is a marker for predicting permanent hearing loss; this requires detailed analysis of the pathophysiologic features, to reduce the prevalence of permanent hearing loss.
我们呈现了基于人群的极早早产儿永久性听力损失的儿童患病率及新生儿风险因素。
采用1974 - 2003年起始队列纵向研究设计,我们研究了1279名孕周≤28周且出生体重<1250克的存活者中的永久性听力损失情况(死亡率:42.7%;失访监测率:4.7%)。1975年后,由经验丰富的儿科听力学家进行新生儿听力筛查,采用短声诱发听觉脑干反应测试。存活者接受了多次行为听力测试和多学科随访监测。永久性听力损失定义为轻度/中度(听力水平26 - 70分贝)、重度/极重度(听力水平71至>90分贝)、迟发性(先前听力正常后被诊断)或进行性(听力损失增加≥15分贝)。在3岁时确定永久性听力损失发生率,并记录新生儿、婴儿及5岁以上的最终听力结果。比较有听力损失和无听力损失儿童的风险因素,计算比值比,并通过曲线下面积分析确定预测性能。
1279名3岁存活者中有40名(3.1%)患有永久性听力损失,24名(1.9%)患有重度/极重度听力损失,且随时间无变化。4名儿童(10%)出现双侧迟发性听力损失,11名儿童(28%)出现进行性听力损失。1名儿童患有听觉神经病,29名(73%)患有多种残疾。长时间吸氧、胃肠道手术、动脉导管未闭结扎术和低社会经济指数对永久性听力损失有较好的预测作用;吸氧是重度/极重度听力损失的最显著预测因素。
永久性听力损失仍然是极早早产的不良后果,伴有显著的迟发性和进行性听力损失。长时间使用补充氧气是预测永久性听力损失的一个指标;这需要对病理生理特征进行详细分析,以降低永久性听力损失的患病率。