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先天性心脏病合并右心室发育不良婴儿的 CT 定量测量右心室初始尺寸。

Quantification of Initial Right Ventricular Dimensions by Computed Tomography in Infants with Congenital Heart Disease and a Hypoplastic Right Ventricle.

机构信息

Department of Radiology and Research Institute of Radiology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.

出版信息

Korean J Radiol. 2020 Feb;21(2):203-209. doi: 10.3348/kjr.2019.0662.

Abstract

OBJECTIVE

To demonstrate the feasibility of using cardiothoracic CT for quantification of the initial right ventricle (RV) dimensions in infants with congenital heart disease (CHD) and a hypoplastic RV and to compare these measurements with those obtained in a control group with CHD without a hypoplastic RV.

MATERIALS AND METHODS

Initial RV dimensions, including RV volumes, RV/left ventricle (LV) volume ratios, atrioventricular valve annulus diameter ratios, and RV/LV length ratios based on CT data, were collected from 57 infants with CHD and a hypoplastic RV (hypoplastic RV group; age range, 1 day to 6 months) and 33 infants with tetralogy of Fallot (control group; age range, 1 day to 6 months) and compared between the 2 groups. The type of final surgery was also evaluated in the hypoplastic RV group over a follow-up period of 3-8 years.

RESULTS

The RV and LV volumes and lengths were successfully quantified in all 90 patients. The tricuspid valve annulus diameter could not be measured in cases showing muscular tricuspid atresia and double-inlet LV. The initial RV dimensions quantified by CT were significantly lower for the hypoplastic RV group than for the control group ( < 0.001). The types of final surgery performed in the hypoplastic RV group were univentricular repair in 46 patients, biventricular repair in 4 patients, or an indeterminate surgery in 7 patients.

CONCLUSION

Initial RV dimensions in infants with CHD and a hypoplastic RV can be quantified by CT and are substantially smaller than those in infants with tetralogy of Fallot.

摘要

目的

展示使用心胸 CT 定量评估先天性心脏病(CHD)伴右心室(RV)发育不良婴儿初始 RV 尺寸的可行性,并与不伴 RV 发育不良的 CHD 对照组进行比较。

材料与方法

收集 57 例 RV 发育不良的 CHD 婴儿(RV 发育不良组;年龄 1 天至 6 个月)和 33 例法洛四联症婴儿(对照组;年龄 1 天至 6 个月)的 CT 数据,得出初始 RV 尺寸,包括 RV 容积、RV/LV 容积比、房室瓣环直径比和 RV/LV 长度比,并进行比较。在 3 至 8 年的随访期间,还对 RV 发育不良组的最终手术类型进行了评估。

结果

90 例患者的 RV 和 LV 容积和长度均可成功定量。肌性三尖瓣闭锁和双入口左心室无法测量三尖瓣环直径。RV 发育不良组的初始 RV 尺寸明显小于对照组(<0.001)。RV 发育不良组最终手术类型为单心室修复 46 例,双心室修复 4 例,不确定手术 7 例。

结论

CHD 伴 RV 发育不良婴儿的初始 RV 尺寸可通过 CT 定量,且明显小于法洛四联症婴儿。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65df/6992442/17d91d1c8e9a/kjr-21-203-g001.jpg

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