Key result
Two decades of experience with fetal aortic valvuloplasty have documented the safety of in utero intervention for fetuses with evolving hypoplastic left heart syndrome.
Why the study?
Initial attempts at fetal aortic valvuloplasty were unsuccessful and carried high morbidity and mortality, prompting the adoption of refined techniques to document safety and understand the impact of in utero intervention on evolving HLHS.
Over two decades, fetal cardiac intervention for aortic stenosis and evolving HLHS has been refined to improve safety and understanding of its impact on cardiac development.
Supports safety of fetal aortic valvuloplasty; leaves open need for randomized efficacy trials in evolving HLHS.
Fetal cardiac intervention was first proposed in the early 1990s to impact cardiac development and survival of fetuses with fetal aortic stenosis and evolving hypoplastic left heart syndrome (HLHS). Although initial attempts of fetal aortic valvuloplasty were unsuccessful and carried a high rate of morbidity and mortality, our collaborative group at the Brigham and Women's Hospital and Boston Children's Hospital have reinvigorated the procedure using improvements in imaging, anesthesia, balloon catheters, and surgical techniques. Two decades of experience have now allowed us to document the safety of in utero intervention and to achieve a better understanding of the impact of midgestation intervention on developing HLHS. Research into underlying genetics, predictive biomarkers, and ways to incorporate stem cell technology will hopefully allow us to further refine the procedure to most benefit children with this historically lethal disease.
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Guseh et al. (2019) conducted a review in Fetal aortic stenosis and evolving hypoplastic left heart syndrome (HLHS). Fetal cardiac intervention (fetal aortic valvuloplasty) was evaluated. Two decades of experience with fetal aortic valvuloplasty have documented the safety of in utero intervention for fetuses with evolving hypoplastic left heart syndrome.
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