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Published on: September 8, 2023
Evaluation of the aorta in infants with simple or complex coarctation of the aorta using CT angiography
Hui-Jun Xiao1, A-Lai Zhan1, Qing-Wen Huang1
1Department of Radiology, Zhangzhou Affiliated Hospital of Fujian Medical University, Zhangzhou, China.
Insights
Infants with coarctation of the aorta (CoA) face risks of ascending aortic dilatation. The degree of coarctation is a key predictor, identifiable through computed tomography angiography (CTA).
Area of Science:
- Cardiology
- Pediatric Cardiology
- Medical Imaging
Background:
- Coarctation of the aorta (CoA) is a congenital heart defect.
- Ascending aortic dilatation is a potential complication in infants with CoA.
- Computed tomography angiography (CTA) is a valuable tool for cardiac imaging.
Purpose of the Study:
- To assess aortic dilatation in infants with coarctation of the aorta (CoA).
- To identify factors related to aortic dilatation in infants with CoA.
- To evaluate the utility of CTA in identifying aortic dilatation risk in infants with CoA.
Main Methods:
- Retrospective analysis of clinical data from 52 infant patients with CoA diagnosed by CTA.
- Measurement of aortic diameters at six levels, standardized as Z scores.
- Logistic regression analysis to determine predictors of ascending aortic dilatation.
Main Results:
- Ascending aortic dilatation was observed in infants with both simple and complex CoA.
- Infants with complex CoA showed more aortic arch hypoplasia compared to simple CoA.
- Increased degree of coarctation (CDR value) was an independent predictor of ascending aortic dilatation.
Conclusions:
- Infants with CoA, both simple and complex, are at risk for ascending aortic dilatation.
- The degree of coarctation is a significant factor influencing ascending aortic dilatation.
- CTA can effectively identify the risk of aortic dilatation in infants with CoA.
Objective:
To assess aortic dilatation and determine its related factors in infants with coarctation of the aorta (CoA) by using computed tomography angiography (CTA).
Methods:
The clinical data of 55 infantile patients with CoA diagnosed by CTA were analyzed retrospectively. Aortic diameters were measured at six different levels and standardized as Z scores based on the square root of body surface area. The results of simple and complex CoA were compared. Univariate and multivariate logistic regression were used to analyze the effects of sex, age, hypertension, degree of coarctation, CoA type, bicuspid aortic valve (BAV), and other factors related to aortic dilatation.
Results:
In total, 52 infant patients with CoA were analyzed, including 22 cases of simple CoA and 30 cases of complex CoA. The ascending aorta of the infants in the simple CoA group and the complex CoA group were dilated to different degrees, but the difference was not statistically significant (50.00% vs. 73.33%, P = 0.084, and 2.05 ± 0.40 vs. 2.22 ± 0.43 P = 0.143). The infants in the complex CoA group had more aortic arch hypoplasia than those in the simple CoA group (33.33% vs. 9.09%, P = 0.042). Compared to the ventricular septal defect (VSD) group, the Z score of the ascending aorta in the CoA group was significantly higher than that in the VSD group (P = 0.023 and P = 0.000). A logistic retrospective analysis found that an increased degree of coarctation (CDR value) was an independent predictor of ascending aortic dilatation (adjusted OR = 0.002; P = 0.034).
Conclusion:
Infants with simple or complex CoA are at risk of ascending aortic dilatation, and the factors of ascending aortic dilatation depend on the degree of coarctation. The risk of aortic dilatation in infants with CoA can be identified by CTA.
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