Preciado Diego A, Lawson Louise, Madden Colm, Myer David, Ngo Chris, Bradshaw John K, Choo Daniel I, Greinwald John H
Center for Hearing and Deafness Research (CHDR) and the Division of Pediatric Otolaryngology,Cincinnati, Ohio 45229-3039, USA.
Otol Neurotol. 2005 Jul;26(4):610-5. doi: 10.1097/01.mao.0000178133.89353.1d.
To determine whether a stepwise diagnostic paradigm is more diagnostically efficient and cost-effective than a simultaneous testing approach in the evaluation of idiopathic pediatric sensorineural hearing loss (SNHL).
Prospective prevalence study.
Tertiary referral children's hospital.
Consecutive children (n = 150) presenting with idiopathic SNHL in the last 2 years.
All children were evaluated with full diagnostic evaluations including GJB2 screens, temporal bone computed tomography scans, and laboratory investigations.
Overall, 12.0% of patients had biallelic mutations in the GJB2 gene, whereas 30% of patients had an abnormality on temporal bone scan. Laboratory testing did not reveal the SNHL etiology in any patient. While maintaining diagnostic accuracy, significant cost savings were inferred by using a sequential diagnostic algorithm. Our data show children with severe to profound SNHL should first be tested with a GJB2 screen, as opposed to those with milder SNHL, who should undergo imaging as the initial testing step. In patients with initially positive GJB2 or imaging screens, logistic regression analysis significantly predicted negative results on further testing.
A stepwise diagnostic paradigm tailored to the level of the hearing loss in children with bilateral SNHL is more diagnostically efficient and cost effective than the more commonly used full, simultaneous testing approach. Laboratory investigation should not be routine but based on clinical history.
确定在评估特发性小儿感音神经性听力损失(SNHL)时,逐步诊断模式是否比同时检测方法在诊断效率和成本效益方面更高。
前瞻性患病率研究。
三级转诊儿童医院。
过去2年中连续出现特发性SNHL的儿童(n = 150)。
所有儿童均接受了全面的诊断评估,包括GJB2筛查、颞骨计算机断层扫描和实验室检查。
1)按SNHL类别划分的GJB2筛查、影像学检查和实验室检查结果的诊断率;2)比较序贯检测方法与同时检测方法的成本分析。
总体而言,12.0%的患者在GJB2基因中有双等位基因突变,而30%的患者颞骨扫描有异常。实验室检查未在任何患者中揭示SNHL的病因。在保持诊断准确性的同时,使用序贯诊断算法可显著节省成本。我们的数据显示,重度至极重度SNHL的儿童应首先进行GJB2筛查,而轻度SNHL的儿童则应以影像学检查作为初始检测步骤。在GJB2或影像学筛查最初呈阳性的患者中,逻辑回归分析显著预测进一步检测结果为阴性。
针对双侧SNHL儿童听力损失程度量身定制的逐步诊断模式,比更常用的全面同时检测方法在诊断效率和成本效益方面更高。实验室检查不应作为常规检查,而应基于临床病史。