Suppr超能文献

使用马尔可夫模型评估新生儿听力障碍早期筛查策略的成本效益

Estimated cost-effectiveness of early screening strategies for newborn hearing impairment using a Markov model.

作者信息

Wen Cheng, Wang Xiaomo, Shu JunTao, Ruan Yu, Xie Jinge, Cheng Xiaohua, Qi Beier, En Hui, Qin Gang, Huang Lihui, Han Demin

机构信息

Department of Otolaryngology-Head and Neck Surgery, Beijing Tongren Hospital, Capital Medical University, Beijing, China.

Beijing Institute of Otolaryngology, Beijing, China.

出版信息

Front Public Health. 2025 May 23;13:1498860. doi: 10.3389/fpubh.2025.1498860. eCollection 2025.

Abstract

BACKGROUND

Decision-making on how to conduct the concurrent hearing and genetic screening of newborns lacks a health economics basis. To estimate the cost-effectiveness of different newborn hearing screening strategy is necessary.

METHODS

A decision tree for a simulated cohort population of 9.56 million newborns was developed: (1) Only universal newborn hearing screening (UNHS); (2) Targeted deafness genetic screening; (3) Concurrent hearing and genetic screening. Markov model was used to evaluate the lifetime horizon (78 years). Cost values were estimated based on medical expenses at Beijing Tongren Hospital and previous studies based on a health system perspective. Health state utility values were represented by Quality-adjusted Life Years (QALYs), costs and utilities were discounted at a rate of 3%. The Incremental Cost-effectiveness Ratio (ICER) was analyzed, along with one-way sensitivity analysis and probability sensitivity analysis.

RESULTS

Compared with only UNHS strategy, the ICER of targeted screening strategy is $ 181.9/QALY, the ICER of concurrent screening is $ 1,563.45/QALY at the discounted rate of 3%. UNHS confirms 21,098 cases of hearing loss, of which 18,666 patients receive early hearing intervention. Concurrent screening confirms 34,244 cases of hearing loss, 26,000 of which receive early hearing intervention. Additionally, 27,036 cases of ototoxicity deafness are avoided. Reducing the cost of genetic screening could enhance the cost-effectiveness of both concurrent screening strategy and targeted genetic screening strategies. At a willingness to pay threshold of 1 time the per capita GDP, at $12,741, the probability of the concurrent screening strategy being cost-effective was 57.6%; at a willingness to pay is three times the per capita GDP, at $38,223, the probability of the concurrent screening strategy being cost-effective was 59.10%.

CONCLUSION

Both the targeted screening and concurrent screening strategy exhibit good cost-effectiveness compared with only UNHS strategy. The targeted screening strategy is preferable when the willingness to pay is between $181.90/QALY and $1,563.45/QALY, whereas the concurrent screening strategy becomes the preferred choice when the willingness to pay exceeds $1,563.45/QALY.

摘要

背景

关于如何进行新生儿听力同步筛查和基因筛查的决策缺乏卫生经济学依据。因此,有必要评估不同新生儿听力筛查策略的成本效益。

方法

针对956万新生儿的模拟队列人群建立了决策树:(1)仅进行普遍新生儿听力筛查(UNHS);(2)进行针对性耳聋基因筛查;(3)进行听力和基因同步筛查。采用马尔可夫模型评估终身范围(78岁)。成本值根据北京同仁医院的医疗费用及以往基于卫生系统视角的研究进行估算。健康状态效用值用质量调整生命年(QALYs)表示,成本和效用按3%的贴现率进行贴现。分析增量成本效益比(ICER),并进行单向敏感性分析和概率敏感性分析。

结果

与仅采用UNHS策略相比,在3%的贴现率下,针对性筛查策略的ICER为每QALY 181.9美元,同步筛查的ICER为每QALY 1563.45美元。UNHS确诊21098例听力损失病例,其中18666例患者接受了早期听力干预。同步筛查确诊34244例听力损失病例,其中26000例接受了早期听力干预。此外,避免了27036例耳毒性耳聋病例。降低基因筛查成本可提高同步筛查策略和针对性基因筛查策略的成本效益。在支付意愿阈值为1倍人均GDP(12741美元)时,同步筛查策略具有成本效益的概率为57.6%;在支付意愿为3倍人均GDP(38223美元)时,同步筛查策略具有成本效益的概率为59.10%。

结论

与仅采用UNHS策略相比,针对性筛查和同步筛查策略均显示出良好的成本效益。当支付意愿在每QALY 181.90美元至1563.45美元之间时,针对性筛查策略更可取;而当支付意愿超过每QALY 1563.45美元时,同步筛查策略成为首选。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13c0/12141332/9f02dcae3110/fpubh-13-1498860-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验