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Cardiac Findings in the Fetus with Cerebral Arteriovenous Malformation Are Associated with Adverse Outcome
Max E Godfrey1, Wayne Tworetzky, Donna Morash
1Department of Cardiology, Children's Hospital Boston, Boston Mass., USA.
Insights
Fetal cerebral arteriovenous malformations (CAVMs) strain the fetal heart, particularly right-sided structures. Increased right heart dilation and dysfunction in fetuses with CAVMs are linked to poorer survival outcomes.
Area of Science:
- Cardiology
- Fetal Medicine
- Neurology
Background:
- Fetal cerebral arteriovenous malformations (CAVMs) are complex vascular anomalies.
- The cardiac sequelae of CAVMs are not well understood.
- Assessing cardiac impact is crucial for managing these high-risk pregnancies.
Purpose of the Study:
- To evaluate cardiac structure and function in fetuses diagnosed with CAVMs.
- To determine the association between cardiac findings and fetal/neonatal outcomes.
Main Methods:
- Retrospective analysis of fetal echocardiograms in 11 fetuses with CAVMs.
- Comparison of cardiac parameters with a control group.
- Correlation of cardiac findings with survival and neonatal demise.
Main Results:
- Fetuses with CAVMs commonly showed dilated superior vena cava and right atrium, reduced middle cerebral artery pulsatility index, tricuspid regurgitation, and right ventricular (RV) dysfunction.
- Nonsurvivors exhibited a larger tricuspid valve z-score and RV dysfunction.
- Higher indexed cardiac output was observed in nonsurvivors compared to controls.
Conclusions:
- CAVMs induce a significant volume load on the fetal circulation.
- Right heart dilation and dysfunction are key indicators of poor prognosis in fetuses with CAVMs.
- Early identification of cardiac changes is vital for risk stratification.
Objectives:
To assess cardiac sequelae of fetal cerebral arteriovenous malformations (CAVMs) and evaluate any association with outcomes.
Methods:
We retrospectively analyzed cardiac structure and function in fetuses with CAVMs who underwent fetal echocardiography (October 1999 to August 2015, n = 11), and compared them with normal controls.
Results:
The median gestational age was 36 weeks (range 18-38). Common abnormal findings included dilated superior vena cava (100%) and right atrium (82%), reduced middle cerebral artery pulsatility index (86%), tricuspid regurgitation (82%), and right ventricular (RV) dysfunction (64%). Hydrops was present in 1 fetus, who did not survive. The median cardiothoracic ratio (CTR) was 0.36 (0.29-0.45, n = 10); the median combined cardiac output indexed to estimated fetal weight (iCCO) was 565 ml/kg/min (379-1,565, n = 7). Of the 11 fetuses, 1 patient elected for termination, and 5 suffered neonatal demise. Comparing survivors (n = 5) and nonsurvivors (n = 6), a larger tricuspid valve (TV) z-score (p = 0.009) and RV dysfunction (p = 0.015) were associated with nonsurvival, and nonsurvivors had a higher iCCO than controls (990 vs. 550 ml/kg/min, p = 0.035). A larger difference between the TV and mitral valve z-scores (surrogate for RV dilation, p = 0.052), and CTR >0.38 (p = 0.0762) tended towards nonsurvival.
Conclusion:
CAVMs impose volume load on the fetal circulation, mainly affecting right heart structures. Increased right heart dilation and dysfunction are associated with nonsurvival.
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