Fetal laser ablation of feeding artery of cystic lung lesions with systemic arterial blood supply
ABSTRACT Objective To assess the effectiveness of laser surgery in fetuses with a cystic lung lesion with systemic arterial blood supply (hybrid lung lesion) at risk of perinatal death. Methods A cohort of five consecutive fetuses with a large hybrid lung lesion associated with hydrops and/or pleura...
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Veröffentlicht in: | Ultrasound in obstetrics & gynecology 2017-06, Vol.49 (6), p.744-750 |
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Zusammenfassung: | ABSTRACT
Objective
To assess the effectiveness of laser surgery in fetuses with a cystic lung lesion with systemic arterial blood supply (hybrid lung lesion) at risk of perinatal death.
Methods
A cohort of five consecutive fetuses with a large hybrid lung lesion associated with hydrops and/or pleural effusion with severe lung compression was selected for percutaneous ultrasound‐guided fetal laser ablation of the feeding artery (FLAFA) before 32 weeks' gestation in a single tertiary national referral center in Queretaro, Mexico. The primary outcomes were survival and need for postnatal surgery.
Results
FLAFA was performed successfully in all cases at a median gestational age of 24.9 (range, 24.4–31.7) weeks. After fetal intervention, dimensions in both lungs increased and fluid effusions resolved in all cases. All cases were delivered liveborn at term at a median gestational age of 39.6 (range, 38.0–39.7) weeks, without respiratory morbidity or need for oxygen support, resulting in perinatal survival of 100%. During follow‐up, three (60%) cases showed progressive regression of the entire lung mass and did not require postnatal surgery, whereas in two (40%) cases a progressive decrease in size of the mass was observed but a cystic portion of the lung mass persisted and postnatal lobectomy was required.
Conclusion
In fetuses with large hybrid lung lesions at risk of perinatal death, FLAFA is feasible and could improve survival and decrease the need for postnatal surgery. Copyright © 2016 ISUOG. Published by John Wiley & Sons Ltd. |
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ISSN: | 0960-7692 1469-0705 |
DOI: | 10.1002/uog.16011 |