Treatment of fetal circular shunt with non-steroidal anti-inflammatory drugs
Insights
Transplacental non-steroidal anti-inflammatory drugs (NSAIDs) effectively constricted the ductus arteriosus in fetuses with Ebstein's anomaly and circular shunt. This treatment improved fetal hemodynamics, prolonged pregnancies, and increased neonatal survival rates.
Area of Science:
- Fetal Medicine
- Cardiology
- Pharmacology
Background:
- Circular shunt (CS) is a critical prenatal condition characterized by abnormal blood flow from the aorta to the left ventricle via the ductus arteriosus.
- CS commonly occurs in fetuses with severe Ebstein's anomaly (EA), leading to significant hemodynamic compromise.
Observation:
- This study investigated the use of transplacental non-steroidal anti-inflammatory drugs (NSAIDs) to induce ductal constriction in fetuses with EA/CS.
- Treatment was initiated between 26 and 34 weeks' gestation.
Findings:
- 75% of treated fetuses (3 out of 4) showed sustained ductal constriction and improved hemodynamics.
- Pregnancies were prolonged by 3-7 weeks, allowing for elective delivery.
- All successfully treated neonates survived after surgical correction of the CS.
Implications:
- Transplacental NSAID therapy offers a novel approach to manage fetal CS, potentially preventing in-utero demise.
- Early initiation of treatment may prevent fetal hypoperfusion and subsequent brain injury.
- This strategy can prolong gestation, improving neonatal outcomes and surgical eligibility.
Abstract:
A circular shunt (CS) is a life-threatening condition involving massive shunting of systemic arterial blood via the ductus arteriosus to the left ventricle without traversing the lungs. In the prenatal setting, it occurs mainly in fetuses with severe forms of Ebstein's anomaly (EA) owing to unrestricted ductal flow and significant pulmonary and tricuspid regurgitation. We aimed to improve the fetal hemodynamics and chances of survival of affected fetuses by inducing ductal constriction using transplacental non-steroidal anti-inflammatory drugs (NSAIDs). Following initiation of treatment between 26 and 34 weeks' gestation, three (75%) of four fetuses with EA/CS responded with sustained ductal constriction and improved hemodynamic function, which allowed continuation of pregnancy for 3-7 weeks and elective delivery. All successfully treated cases underwent neonatal surgery immediately after birth to eliminate the CS and survived. This included two neonates that underwent single-ventricle palliation surgery that required postoperative extracorporeal membrane oxygenation and hemofiltration for transient respiratory and renal failure. The one case that did not respond to treatment with NSAIDs was delivered prematurely for progressive fetal compromise and died shortly after birth. Transplacental treatment with NSAIDs represents a novel approach to controlling fetal CS, avoiding in-utero death and prolonging the pregnancy to a more advanced gestational age, thereby potentially increasing the chances of neonatal survival. This treatment should be considered and initiated at an early stage of systemic steal to prevent brain injury due to hypoperfusion. Copyright © 2018 ISUOG. Published by John Wiley & Sons Ltd.
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