Structured reporting in fetal magnetic resonance imaging with congenital diaphragmatic hernia.

IF 2.7 2区医学 Q2 GENETICS & HEREDITY

Prenatal Diagnosis Pub Date : 2024-07-01 Epub Date: 2024-05-26 DOI:10.1002/pd.6593

G Thater, A Weidner, N Rafat, O Nowak, C Otto, K Zahn, M Boettcher, S O Schönberg, T Schaible, M Weis

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引用次数: 0

Abstract

Objective: We aim to provide a template structured report of fetal Magnetic Resonance Imaging in congenital diaphragmatic hernia (CDH) that was locally validated by the CDH study group in Mannheim.

Methods: A selection of 50 fetal MRIs of patients with an isolated diaphragmatic hernia and associated radiology reports from five different senior radiologists from a single center resulted in a primary structured report, which was put into practice by using dedicated software. A questionnaire survey of the interdisciplinary CDH study group Mannheim was used to adapt the report to the clinical requirements.

Results: There was a huge variability in how deep the free text reports go into detail. The side of the hernia was named in 94% of cases. In 58%, both the lung volume and the total lung volume were reported. A comparison with the expected lung volume was reported in 66% of cases. Additional findings, such as herniated organs, were reported in 96% of cases. Overall satisfaction with the newly established structured report was high within the CDH study group with a mean of 4.7.

Conclusions: The use of the structured report of this study can optimize the interdisciplinary dialog, the standardization of report content, increase report completeness and improve quality.

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胎儿先天性膈疝磁共振成像的结构化报告。

目的：我们旨在提供先天性膈疝（CDH）胎儿磁共振成像的结构化报告模板，该模板已由曼海姆的 CDH 研究小组在当地进行了验证：方法：从 50 例孤立性膈疝患者的胎儿磁共振成像和来自一个中心的五位不同资深放射科医生的相关放射学报告中筛选出一份主要的结构化报告，并通过专用软件将其付诸实践。曼海姆 CDH 跨学科研究小组通过问卷调查使报告符合临床要求：结果：自由文本报告的详细程度存在巨大差异。94%的病例标明了疝的一侧。58%的病例同时报告了肺活量和总肺活量。66%的病例报告了与预期肺容量的比较。96%的病例报告了其他检查结果，如器官疝。CDH 研究组对新建立的结构化报告的总体满意度很高，平均为 4.7：本研究中结构化报告的使用可以优化跨学科对话、规范报告内容、增加报告完整性并提高质量。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Prenatal Diagnosis 医学-妇产科学

CiteScore

5.80

自引率

13.30%

发文量

204

审稿时长

2 months

期刊介绍： Prenatal Diagnosis welcomes submissions in all aspects of prenatal diagnosis with a particular focus on areas in which molecular biology and genetics interface with prenatal care and therapy, encompassing: all aspects of fetal imaging, including sonography and magnetic resonance imaging; prenatal cytogenetics, including molecular studies and array CGH; prenatal screening studies; fetal cells and cell-free nucleic acids in maternal blood and other fluids; preimplantation genetic diagnosis (PGD); prenatal diagnosis of single gene disorders, including metabolic disorders; fetal therapy; fetal and placental development and pathology; development and evaluation of laboratory services for prenatal diagnosis; psychosocial, legal, ethical and economic aspects of prenatal diagnosis; prenatal genetic counseling