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基于年龄的基因组筛查:儿科医疗服务提供者对实施的看法。

Age-Based Genomic Screening: Pediatric Providers' Perspectives on Implementation.

作者信息

Waltz Margaret, Foreman Ann Katherine M, Gibson Rebecca A, Schilling Samantha, Milko Laura V, Phillips Rachel, O'Daniel Julianne M, Giric Stefanija, Foss Kimberly, Branch Elizabeth K, DeJong Neal A, Hernandez Michelle L, Powell Bradford C, Berg Jonathan S, Cadigan R Jean, Roberts Megan C

机构信息

Center for Bioethics and Department of Social Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

出版信息

Public Health Genomics. 2025;28(1):180-189. doi: 10.1159/000545839. Epub 2025 Apr 21.

Abstract

INTRODUCTION

As genomic technologies and therapies advance, paired with increasing clinical knowledge and declining sequencing cost, the scope of DNA-based preventive pediatric screening is expected to expand. Age-Based Genomic Screening (ABGS) is an approach that proposes to integrate targeted genomic sequencing for highly actionable genetic conditions into routine well-child care at specific time points aligned with optimal interventions. Prior to the clinical implementation of ABGS in pediatric primary care, however, it is necessary to investigate the factors that may affect its adoption.

METHODS

We conducted 20 interviews with providers from 11 clinics across North Carolina. Interviews lasted approximately 45 min, and rapid qualitative analysis was conducted using an analytic matrix.

RESULTS

Interviewees stated that, in general, implementation of ABGS would be feasible but identified several barriers, including providers' potential discomfort discussing genomic screening and returning results as well as broader concerns about the potential to exacerbate health disparities. Providers also noted potential challenges affecting interest from patients and families, such as caregiver anxiety while awaiting results, patient apprehension regarding invasive sample collection methods (like blood draws), and a general lack of trust in government and medical institutions.

CONCLUSION

While ABGS was viewed as feasible, the identified barriers emphasize the importance of piloting this approach, particularly in terms of potential exacerbation of health disparities. These findings are useful to guide early development and assessment of efforts like ABGS and may also be applicable to broader integration of genomic screening into primary care.

摘要

引言

随着基因组技术和疗法的进步,加之临床知识的不断增加以及测序成本的下降,基于DNA的预防性儿科筛查范围有望扩大。基于年龄的基因组筛查(ABGS)是一种方法,它提议将针对高度可干预遗传疾病的靶向基因组测序整合到与最佳干预措施相匹配的特定时间点的常规儿童健康保健中。然而,在儿科初级保健中临床实施ABGS之前,有必要调查可能影响其采用的因素。

方法

我们对北卡罗来纳州11家诊所的医疗服务提供者进行了20次访谈。访谈持续约45分钟,并使用分析矩阵进行快速定性分析。

结果

受访者表示,总体而言,实施ABGS是可行的,但也指出了几个障碍,包括医疗服务提供者在讨论基因组筛查和反馈结果时可能会感到不适,以及对可能加剧健康差距的更广泛担忧。医疗服务提供者还指出了影响患者和家庭兴趣的潜在挑战,例如照顾者在等待结果时的焦虑、患者对侵入性样本采集方法(如抽血)的担忧,以及对政府和医疗机构普遍缺乏信任。

结论

虽然ABGS被认为是可行的,但所确定的障碍强调了试行这种方法的重要性,特别是在可能加剧健康差距方面。这些发现有助于指导ABGS等早期开发和评估工作,也可能适用于将基因组筛查更广泛地整合到初级保健中。

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Well-Child Visit Adherence.健康儿童体检依从性。
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