Clinical characteristics of heterotaxy syndrome with congenital heart defects: A ten-year single-center experience

Aim: Congenital heart defects (CHDs) are a major component of heterotaxy syndrome (HS), contributing significantly to high morbidity and mortality. The anatomical variability, surgical complexity, and poor prognosis of HS-associated CHDs present major clinical challenges. Material and Methods: We retrospectively reviewed 292 patients diagnosed with HS and CHDs at The First Hospital of Tsinghua University between January 2014 and December 2023. Demographic information and cardiac imaging data were collected to analyze the spectrum of cardiac malformations, spleen anatomy, sex distribution, and the frequency and distribution of major structural abnormalities. Results: The cohort included 292 patients (mean age 6.8±8.7 years), with females accounting for 40.8%. Dextrocardia was present in 50%. The asplenia type was most common (42.8%), followed by unisplenia (41.8%) and polysplenia (15.4%). The most frequent cardiac malformations were single ventricle (61.9%), conotruncal anomalies (54.5%), and pulmonary stenosis (42.8%). The overall incidence of anomalous pulmonary venous connection was 7.8%, with total anomalous pulmonary venous connection (TAPVC) accounting for 6.8%. Gender analysis revealed a significantly higher proportion of males in the asplenia group (66.4% vs. 33.6%, P<0.05) and in the unisplenia group (59.0% vs. 41.0%, P<0.05). Although females were more frequent in the polysplenia group (57.8% vs. 42.2%), the difference was not statistically significant (P>0.05). Conclusion: HS with CHDs presents with complex and diverse anatomical abnormalities and is associated with challenging management and poor prognosis. This ten-year single-center study provides a comprehensive overview of the clinical spectrum of HS-associated CHDs and reveals significant sex differences among patients with asplenia, unisplenia, and polysplenia. These findings may contribute to clinical classification, preoperative assessment, and individualized management strategies.

Authors

Publication Details

Journal
Azerbaijan Journal of Cardiovascular Surgery
Published
2025-01-01
DOI
https://doi.org/10.5455/azjcvs.2025.06.09
Primary Topic
Congenital Heart Disease Studies
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Clinical characteristics of heterotaxy syndrome with congenital heart defects: A ten-year single-center experience

Lianyi Wang, Xiujie Tang, Qingyu Wu, Mengqi Zhao
Azerbaijan Journal of Cardiovascular Surgery
Congenital Heart Disease Studies
article

Clinical characteristics of heterotaxy syndrome with congenital heart defects: A ten-year single-center experience

Lianyi Wang, Xiujie Tang, Qingyu Wu, Mengqi Zhao
article en

Abstract

Aim: Congenital heart defects (CHDs) are a major component of heterotaxy syndrome (HS), contributing significantly to high morbidity and mortality. The anatomical variability, surgical complexity, and poor prognosis of HS-associated CHDs present major clinical challenges. Material and Methods: We retrospectively reviewed 292 patients diagnosed with HS and CHDs at The First Hospital of Tsinghua University between January 2014 and December 2023. Demographic information and cardiac imaging data were collected to analyze the spectrum of cardiac malformations, spleen anatomy, sex distribution, and the frequency and distribution of major structural abnormalities. Results: The cohort included 292 patients (mean age 6.8±8.7 years), with females accounting for 40.8%. Dextrocardia was present in 50%. The asplenia type was most common (42.8%), followed by unisplenia (41.8%) and polysplenia (15.4%). The most frequent cardiac malformations were single ventricle (61.9%), conotruncal anomalies (54.5%), and pulmonary stenosis (42.8%). The overall incidence of anomalous pulmonary venous connection was 7.8%, with total anomalous pulmonary venous connection (TAPVC) accounting for 6.8%. Gender analysis revealed a significantly higher proportion of males in the asplenia group (66.4% vs. 33.6%, P<0.05) and in the unisplenia group (59.0% vs. 41.0%, P<0.05). Although females were more frequent in the polysplenia group (57.8% vs. 42.2%), the difference was not statistically significant (P>0.05). Conclusion: HS with CHDs presents with complex and diverse anatomical abnormalities and is associated with challenging management and poor prognosis. This ten-year single-center study provides a comprehensive overview of the clinical spectrum of HS-associated CHDs and reveals significant sex differences among patients with asplenia, unisplenia, and polysplenia. These findings may contribute to clinical classification, preoperative assessment, and individualized management strategies.

Azerbaijan Journal of Cardiovascular SurgeryVol. 6(2)
Openalex Percentile: Top 74%
Congenital Heart Disease Studies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Clinical characteristics of heterotaxy syndrome with congenital heart defects: A ten-year single-center experience — Lianyi Wang, Xiujie Tang, et al. · Azerbaijan Journal of Cardiovascular Surgery (2025) | TGRS Research Map | TGRS