Health and Economic Outcomes for Newborn Screening

描述(由申请人提供)：最近筛查技术的增强使得新生儿能够在几乎不增加检测成本的情况下对许多其他疾病进行筛查。与此同时，关于新生儿筛查可以检测到的疾病的长期结果的信息很少。卫生资源和服务管理局授权部长的新生儿和儿童遗传性疾病咨询委员会，利用系统审查程序评估提名列入建议的新生儿统一筛查小组的新情况。有几种情况已被提名，但不建议进行统一筛查，主要是因为缺乏证据。这一研究项目将以新生儿和儿童遗传性疾病咨询委员会的名义进行的证据审查为基础。由于技术和伦理方面的挑战，不能在这一领域使用传统的临床试验，该研究项目将使用计算机建模来模拟新生儿筛查计划的临床试验，而不是不筛查(临床鉴定)。通过将来自系统审查的信息、已公布和未公布的数据以及专家意见结合起来，我们将预测新生儿筛查可以发现的疾病的长期健康和经济结果。这项研究还将对新生儿筛查计划的公众价值进行调查。该项目团队将包括来自广泛学科的研究人员，他们在新生儿筛查计划的证据合成和政策分析以及临床专业知识方面拥有丰富的专业知识。这项研究的研究问题将由一个咨询委员会指导，该委员会的成员代表在考虑扩大新生儿筛查计划时的许多相关观点。这项拟议的研究项目侧重于秘书的新生儿和儿童遗传性疾病咨询委员会确定的证据差距，并侧重于儿童，这是AHRQ确定的优先人群。关于健康和经济结果的结果与公众偏好数据相结合，将为新生儿筛查小组选择条件的政策决策提供必要的信息。

DESCRIPTION (provided by applicant): Recent enhancements in screening technology have allowed for newborn screening for many additional disorders with little increase in testing cost. At the same time, there is little information on long-term outcomes for conditions that can be detected by newborn screening. The Secretary's Advisory Committee on Heritable Disorders in Newborns and Children was chartered by the Health Resources and Services Administration to evaluate new conditions nominated for inclusion on the recommended uniform newborn screening panel using a systematic review process. Several conditions have been nominated but not recommended for uniform screening, primarily due to a lack of evidence. This research project will build on the evidence reviews conducted on behalf of the Advisory Committee for Heritable Disorders in Newborns and Children. Due to technical and ethical challenges that preclude the use of traditional clinical trials in this area, this research project will use computer modeling to simulate clinical trials of newborn screening programs compared to no screening (clinical identification). By combining information from systematic reviews, published and unpublished data, and expert opinion, we will project long-term health and economic outcomes for conditions that can be detected by newborn screening. This research study will also conduct a survey of public values for newborn screening programs. The project team will include investigators from a wide range of disciplines who have substantial expertise in evidence synthesis and policy analysis of newborn screening programs as well as clinical expertise. Research questions for the study will be guided by an Advisory Committee whose members represent the many relevant viewpoints when considering the expansion of newborn screening programs. This proposed research project focuses on the evidence gap identified by the Secretary's Advisory Committee on Heritable Disorders in Newborns and Children and focuses on children, an identified AHRQ priority population. Results on health and economic outcomes paired with public preference data will provide the necessary information needed for policy decisions regarding the selection of conditions for newborn screening panels.