McElhinney Doff B, Marshall Audrey C, Wilkins-Haug Louise E, Brown David W, Benson Carol B, Silva Virginia, Marx Gerald R, Mizrahi-Arnaud Arielle, Lock James E, Tworetzky Wayne
Department of Cardiology, Children's Hospital, Boston, MA 02115, USA.
Circulation. 2009 Oct 13;120(15):1482-90. doi: 10.1161/CIRCULATIONAHA.109.848994. Epub 2009 Sep 28.
Aortic stenosis in the midgestation fetus with a normal-sized or dilated left ventricle predictably progresses to hypoplastic left heart syndrome when associated with certain physiological findings. Prenatal balloon aortic valvuloplasty may improve left heart growth and function, possibly preventing evolution to hypoplastic left heart syndrome.
Between March 2000 and October 2008, 70 fetuses underwent attempted aortic valvuloplasty for critical aortic stenosis with evolving hypoplastic left heart syndrome. We analyzed this experience to determine factors associated with procedural and postnatal outcome. The median gestational age at intervention was 23 weeks. The procedure was technically successful in 52 fetuses (74%). Relative to 21 untreated comparison fetuses, subsequent prenatal growth of the aortic and mitral valves, but not the left ventricle, was improved after intervention. Nine pregnancies (13%) did not reach a viable term or preterm birth. Seventeen patients had a biventricular circulation postnatally, 15 from birth. Larger left heart structures and higher left ventricular pressure at the time of intervention were associated with biventricular outcome. A multivariable threshold scoring system was able to discriminate fetuses with a biventricular outcome with 100% sensitivity and modest positive predictive value.
Technically successful aortic valvuloplasty alters left heart valvar growth in fetuses with aortic stenosis and evolving hypoplastic left heart syndrome and, in a subset of cases, appeared to contribute to a biventricular outcome after birth. Fetal aortic valvuloplasty carries a risk of fetal demise. Fetuses undergoing in utero aortic valvuloplasty with an unfavorable multivariable threshold score at the time of intervention are very unlikely to achieve a biventricular circulation postnatally.
妊娠中期胎儿出现主动脉狭窄,若左心室大小正常或扩大,并伴有某些生理表现,可预测其会进展为左心发育不全综合征。产前球囊主动脉瓣成形术可能会改善左心的生长和功能,有可能防止病情发展为左心发育不全综合征。
2000年3月至2008年10月期间,70例胎儿因严重主动脉狭窄并伴有进展性左心发育不全综合征而接受了主动脉瓣成形术。我们分析了这一经验,以确定与手术及产后结局相关的因素。干预时的中位孕周为23周。52例胎儿(74%)手术在技术上成功。与21例未治疗的对照胎儿相比,干预后主动脉瓣和二尖瓣的后续产前生长得到改善,但左心室未改善。9例妊娠(13%)未足月或早产。17例患者产后为双心室循环,其中15例出生时即如此。干预时左心结构较大及左心室压力较高与双心室结局相关。一个多变量阈值评分系统能够以100%的敏感性和适度的阳性预测值区分双心室结局的胎儿。
技术上成功的主动脉瓣成形术可改变患有主动脉狭窄及进展性左心发育不全综合征胎儿的左心瓣膜生长,在一部分病例中,似乎有助于出生后实现双心室结局。胎儿主动脉瓣成形术有导致胎儿死亡的风险。干预时多变量阈值评分不利的接受宫内主动脉瓣成形术的胎儿出生后极不可能实现双心室循环。