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先天性膈疝修补术后患儿肺部功能和结构的评估。

Functional and structural evaluation in the lungs of children with repaired congenital diaphragmatic hernia.

机构信息

Departments of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.

Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.

出版信息

BMC Pediatr. 2021 Mar 11;21(1):120. doi: 10.1186/s12887-021-02586-3.

Abstract

BACKGROUND

To evaluate the long-term functional and structural pulmonary development in children with repaired congenital diaphragmatic hernia (CDH) and to identify the associated perinatal-neonatal risk factors.

METHODS

Children with repaired CDH through corrective surgery who were born at gestational age ≥ 35 weeks were included in this analysis. Those who were followed for at least 5 years were subjected to spirometry and chest computed tomography for evaluation of their functional and structural growth. Main bronchus diameters and lung volumes (total, left/right) were measured. According to total lung volume (TLV) relative to body surface area, children were grouped into TLV ≥ 50 group and TLV < 50 group and the associations with perinatal-neonatal factors were analyzed.

RESULTS

Of the 28 children (mean age, 6.2 ± 0.2 years) with left-sided CDH, 7 (25%) had abnormal pulmonary function, of whom 6 (87%) showed restrictive patterns. All pulmonary functions except FEF25-75% were worse than those in matched healthy control group. Worse pulmonary function was significantly associated with small head and abdominal circumferences at birth. The mean TLV was 1339.1 ± 363.9 mL and LLV/TLV was 47.9 ± 2.5 mL. Children with abnormal pulmonary function were more likely to have smaller lung volumes. In multivariate analysis, abdominal circumference at birth was significantly associated with abnormal lung volume.

CONCLUSIONS

A quarter of children with repaired CDH showed abnormal pulmonary function. Small abdominal circumference at birth was associated with abnormal pulmonary function and lower TLV. .

摘要

背景

评估修复先天性膈疝(CDH)后儿童的长期肺功能和结构发育,并确定相关围产期-新生儿风险因素。

方法

本分析纳入了通过矫正手术修复 CDH 且出生胎龄≥35 周的患儿。对至少随访 5 年的患儿进行肺功能检查和胸部计算机断层扫描,以评估其功能和结构生长情况。测量主支气管直径和肺容量(总容量、左/右)。根据总肺容量(TLV)与体表面积的比值,将患儿分为 TLV≥50 组和 TLV<50 组,并分析与围产期-新生儿因素的相关性。

结果

28 例左侧 CDH 患儿(平均年龄 6.2±0.2 岁)中,有 7 例(25%)肺功能异常,其中 6 例(87%)表现为限制性模式。除 FEF25-75%外,所有肺功能均差于匹配的健康对照组。较差的肺功能与出生时头围和腹围小显著相关。TLV 平均值为 1339.1±363.9 mL,LLV/TLV 为 47.9±2.5 mL。肺功能异常的患儿更有可能出现较小的肺容量。多变量分析显示,出生时的腹围与异常肺容量显著相关。

结论

四分之一的修复 CDH 患儿肺功能异常。出生时的腹围小与肺功能异常和较低的 TLV 相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c160/7948352/c0813c5ff074/12887_2021_2586_Fig1_HTML.jpg

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