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Original Articles

Comparison of fetal echocardiogram with fetal cardiac autopsy findings in fetuses with congenital heart disease

ORCID Icon, , , , , , , , , , , , , & show all
Pages 3844-3850 | Received 28 Mar 2019, Accepted 30 Nov 2019, Published online: 12 Dec 2019
 

Abstract

Objective

Although studies have compared fetal echo results with autopsy findings, investigations that compared multiple categories of congenital heart disease (CHD) are lacking. This study, therefore, aimed to compare fetal echocardiographic diagnoses with cardiac autopsy findings and evaluate the diagnostic accuracy of fetal echocardiography (FE).

Methods

One hundred seventy-one specimens from fetuses diagnosed with CHD were collected after termination of pregnancy, and fetal autopsies were performed. FE and autopsy diagnoses were compared and the degree of their correspondence was categorized as “complete agreement” (FE results were in accordance with autopsy findings), “minor discrepancies” (autopsies verified the main FE diagnoses but added and/or revised some minor information), or “discordance” (autopsy findings were different from the primary diagnoses of FE).

Results

The “complete agreement” group accounted for 87.1% (149/171) of the total specimens. In 11.7% (20/171) of cases, autopsies disclosed new deformities and/or revised some echo results (minor discrepancies group). Minor abnormalities were frequently embodied in small septal defects and vascular malformations. A rare malformation of common pulmonary vein atresia was confirmed by autopsy in two fetuses, but both were misdiagnosed by FE (discordance group).

Conclusions

Fetal echocardiographic diagnoses were mostly consistent with autopsy findings. The diagnostic discrepancies mainly consisted of rare cases and minor abnormalities missed or misdiagnosed by FE. Autopsies may help confirm, modify, or add information to prenatal echo results. They may also help sonographers have a better understanding of the anatomic structures of CHD, especially for rare lesions, which could further improve the diagnostic accuracy and integrity of FE.

Acknowledgments

We thank Dr. Chen Zhuo and Dr. Xue Chao for their selfless help in the support of the standardization of clinical information.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This research was supported by National Key R&D Program of China [2018YFC1002300] and Beijing Municipal Administration of Hospitals Clinical medicine Development of special funding support [XMLX201604].

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