新生儿听力筛查——最新进展
Screening of the hearing of newborns - Update.
作者信息
Schnell-Inderst Petra, Kunze Silke, Hessel Franz, Grill Eva, Siebert Uwe, Nickisch Andreas, von Voß Hubertus, Wasem Jürgen
机构信息
Alfried Krupp von Bohlen und Halbach-Stiftungslehrstuhl für Medizinmanagement der Universität Duisburg-Essen, Campus Essen, Essen, Deutschland.
出版信息
GMS Health Technol Assess. 2006 Nov 27;2:Doc20.
INTRODUCTION
Permanent congenital bilateral hearing loss (CHL) of moderate or greater degree (≥40 dB HL) is a rare disease, with a prevalence of about 1 to 3 per 1000 births. However, it is one of the most frequent congenital diseases. Reliance on physician observation and parental recognition has not been successful in the past in detecting significant hearing loss in the first year of life. With this strategy significant hearing losses have been detected in the second year of life. With two objective technologies based on physiologic response to sound, otoacoustic emissions (OAE) and auditory brainstem response (ABR) hearing screening in the first days of life is made possible.
OBJECTIVES
The objective of this health technology assessment report is to update the evaluation on clinical effectiveness and cost-effectiveness of newborn hearing screening programs. Universal newborn hearing screening (UHNS) (i), selective screening of high risk newborns (ii), and the absence of a systematic screening program are compared for age at identification and age at hearing aid fitting of children with hearing loss. Secondly the potential benefits of early intervention are analysed. Costs and cost-effectiveness of newborn hearing screening programs are determined. This report is intended to make a contribution to the decision making whether and under which conditions a newborn hearing screening program should be reimbursed by the statutory sickness funds in Germany.
METHODS
This health technology assessment report updates a former health technology assessment (Kunze et al. 2004 [1]). A systematic review of the literature was conducted, based on a documented search and selection of the literature using predefined inclusion and exclusion criteria and a documented extraction and appraisal of the included studies. To assess the cost-effectiveness of the different screening strategies in Germany the decision analytic Markov state model which had been developed in our former health technology assessment report was updated.
RESULTS
Universal newborn hearing screening programs are able to substantially reduce the age at identification and the age at intervention of children with CHL to six months of age in the German health care setting. High coverage rates, low fail rates and - if tracking systems are implemented - high follow-up-rates to diagnostic evaluation for test positives were achieved. New publications on potential benefits of early intervention could not be retrieved. For a final assessment of cost-effectiveness of newborn hearing screening evidence based long-term data are lacking. Decision analytic models with lifelong time horizon assuming that early detection results in improved language abilities and lower educational costs and higher life time productivity showed a potential of UNHS for long term cost savings compared to selective screening and no screening. For the short-term cost-effectiveness with a time horizon up to diagnostic evaluation more evidence based data are available. The average costs per case diagnosed range from 16,000 EURO to 33,600 EURO in Germany and hence are comparable to the cost of other implemented newborn screening programs. Empirical data for cost of selective screening in the German health care setting are lacking. Our decision analytic model shows that selective screening is more cost-effective but detects only 50% of all cases of congenital hearing loss.
DISCUSSION
There is good evidence that UNHS-Programs with appropriate quality management can reduce the age at start of intervention below six months. Up to now there is no indication of considerable negative consequences of screening for children with false positive test results and their parents. However, it is more difficult to prove the efficacy of early intervention to improve long-term outcomes. Randomized clinical trials of the efficacy of early intervention for children with CHL hearing losses are inappropriate because of ethical reasons. Prospective cohort studies with long-term outcomes of rare diseases are costly, take a long time and simultaneously substantial benefits of early intervention for language development seem likely.
CONCLUSIONS
A UNHS-Program should be implemented in Germany and be reimbursed by the statutory sickness funds. To achieve high coverage and because of better conditions for obtaining low false positive rates UNHS should be performed in hospital after birth. For outpatient deliveries additionally screening measures in an outpatient setting must be provided.
引言
永久性先天性双侧听力损失(CHL),中度或更严重程度(≥40 dB HL)是一种罕见疾病,每1000例出生中患病率约为1至3例。然而,它是最常见的先天性疾病之一。过去,依靠医生观察和家长识别在一岁内未能成功检测出严重听力损失。采用这种策略,严重听力损失往往在第二年才被发现。基于声音生理反应的两种客观技术,耳声发射(OAE)和听觉脑干反应(ABR)使得在出生后几天内进行听力筛查成为可能。
目的
本卫生技术评估报告的目的是更新对新生儿听力筛查项目临床有效性和成本效益的评估。比较普遍新生儿听力筛查(UHNS)(i)、高危新生儿选择性筛查(ii)以及缺乏系统筛查项目这三种情况,看其对听力损失儿童的识别年龄和佩戴助听器年龄的影响。其次,分析早期干预的潜在益处。确定新生儿听力筛查项目的成本和成本效益。本报告旨在为德国法定疾病基金是否以及在何种条件下应报销新生儿听力筛查项目的决策提供参考。
方法
本卫生技术评估报告更新了之前的一份卫生技术评估报告(Kunze等人,2004年[1])。基于预先定义的纳入和排除标准,通过文献记录检索和选择,以及对纳入研究的文献记录提取和评估,进行了系统的文献综述。为评估德国不同筛查策略的成本效益,更新了我们之前卫生技术评估报告中开发的决策分析马尔可夫状态模型。
结果
在德国医疗环境中,普遍新生儿听力筛查项目能够大幅降低CHL儿童的识别年龄和干预年龄至六个月。实现了高覆盖率、低失败率,并且如果实施追踪系统,对检测呈阳性者进行诊断评估的高随访率。未检索到关于早期干预潜在益处的新出版物。对于新生儿听力筛查成本效益的最终评估,缺乏基于证据的长期数据。假设早期检测能提高语言能力、降低教育成本并提高终身生产力的具有终身时间跨度的决策分析模型表明,与选择性筛查和不筛查相比,普遍新生儿听力筛查有长期节省成本的潜力。对于直至诊断评估的短期成本效益,有更多基于证据的数据。在德国,每例确诊病例的平均成本在16,000欧元至33,600欧元之间,因此与其他已实施的新生儿筛查项目成本相当。德国医疗环境中选择性筛查成本的实证数据缺乏。我们的决策分析模型表明,选择性筛查更具成本效益,但只能检测出所有先天性听力损失病例的50%。
讨论
有充分证据表明,具备适当质量管理的普遍新生儿听力筛查项目能够将干预开始年龄降低至六个月以下。到目前为止,没有迹象表明对检测呈假阳性结果的儿童及其家长进行筛查会产生相当大的负面影响。然而,要证明早期干预改善长期结果的疗效则更为困难。由于伦理原因,对CHL听力损失儿童进行早期干预疗效的随机临床试验不合适。对罕见疾病长期结果进行前瞻性队列研究成本高昂、耗时久,同时早期干预对语言发展的显著益处似乎很可能存在。
结论
德国应实施普遍新生儿听力筛查项目并由法定疾病基金报销。为实现高覆盖率且因获得低假阳性率的条件更好,普遍新生儿听力筛查应在出生后在医院进行。对于门诊分娩,还必须在门诊环境中提供额外的筛查措施。