儿童生活专家预测 4 至 12 岁无陪护儿童能否成功进行核磁共振成像扫描

IF 2.1 3区 医学 Q2 PEDIATRICS Pediatric Radiology Pub Date : 2024-09-18 DOI:10.1007/s00247-024-06040-1
Jennifer H. Staab, Angela C. Yoder, John T. Brinton, Nicholas V. Stence, Claire E. Simonsen, Brianne F. Newman, Keely A. Garcia, Lorna P. Browne
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引用次数: 0

摘要

背景儿童在磁共振成像(MRI)检查中的合作是一项挑战。为了确保获得高质量的图像,通常需要使用全身麻醉。在确定是否需要进行全身麻醉时,许多机构采用简单的年龄分界线。本研究旨在评估认证儿童生命专家(CCLS)提出的筛查问题能否成功预测哪些儿童可以在不使用镇静剂的情况下完成核磁共振成像检查。数据收集是质量改进计划的一部分,CCLS 通过问卷对计划接受核磁共振成像扫描的 4 至 12 岁儿童进行筛查。研究记录了家长对筛查问题的回答、CCLS关于安排核磁共振清醒扫描的建议、核磁共振扫描的开始和结束时间以及扫描成功率。利用患儿的年龄、预计扫描时间、扫描难度和家长对筛查问题的回答,建立了 CCLS 建议的预测模型。结果 在 403 名接受筛查的儿童中,有 317 人(79%)被建议在不麻醉的情况下进行核磁共振成像。参与者的中位年龄为 7 岁(IQR 4-17 岁)。总体而言,在 CCLS 推荐参加该计划的 317 名参与者中,有 309 名(97.5%)达到了首次成功完成核磁共振成像的主要结果。结论CCLS通过筛查收集的信息以及儿童的年龄、估计扫描长度和难度有助于预测哪些儿童有可能成功完成非静息磁共振成像。
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Child life specialists predict successful MRI scanning in unsedated children 4 to 12 years old

Background

It can be challenging for children to cooperate for a magnetic resonance imaging (MRI) exam. General anesthesia is often used to ensure a high-quality image. When determining the need for general anesthesia, many institutions use a simple age cutoff. Decisions on the necessity for anesthesia are often left to schedulers who lack training on determination of patient compliance.

Objective

The study aimed to evaluate whether screening questions administered by certified child life specialists (CCLS) could successfully predict which children could complete an MRI without sedation.

Materials and methods

This is a retrospective, institutional review board approved study. Data was collected as part of a quality improvement program, where a CCLS screened 4- to 12-year-old children scheduled for MRI scanning using a questionnaire. Parent responses to the screening questions, CCLS’s recommendation for scheduling the MRI awake, start and end time for the MRI scan, and scan success were recorded. A predictive model for the CCLS’s recommendation was developed using the child’s age, estimated scan length, scan difficulty, and the parent’s responses to the screening questions. The primary outcome measure was a successfully completed MRI not requiring additional imaging under anesthesia.

Results

Of the 403 screened children, 317 (79%) were recommended to attempt the MRI without anesthesia. The median age of participants was 7 (IQR 4–17) years. Overall, 309 of 317 (97.5%) participants, recommended by the CCLS for the program, met the primary outcome of successful MRI completion on their first attempt. The multivariable regression model which included clinical information about the child’s age, estimated scan length, scan difficulty, and four of the six parent screening questions had excellent performance (area under the curve = 0.89).

Conclusion

Information collected by the CCLS via screening along with the child’s age, the estimated scan length, and difficulty can help predict which children are likely to successfully complete a non-sedate MRI.

Graphical Abstract

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来源期刊
Pediatric Radiology
Pediatric Radiology 医学-核医学
CiteScore
4.40
自引率
17.40%
发文量
300
审稿时长
3-6 weeks
期刊介绍: Official Journal of the European Society of Pediatric Radiology, the Society for Pediatric Radiology and the Asian and Oceanic Society for Pediatric Radiology Pediatric Radiology informs its readers of new findings and progress in all areas of pediatric imaging and in related fields. This is achieved by a blend of original papers, complemented by reviews that set out the present state of knowledge in a particular area of the specialty or summarize specific topics in which discussion has led to clear conclusions. Advances in technology, methodology, apparatus and auxiliary equipment are presented, and modifications of standard techniques are described. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been reviewed by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in an appropriate version of the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted.
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