(Circulation. 2006;113:1401-1405.)
© 2006 American Heart Association, Inc.
Congenital Heart Disease |
From the Department of Cardiology (K.M., D.B.M., J.C.L., G.R.M., S.D.C., A.C.M., J.E.L., E.N.M., W.T.), Childrens Hospital, and Harvard Medical School, Boston, Mass, and the Department of Obstetrics and Gynecology (K.M.), University of Oulu, Oulu, Finland.
Correspondence to Wayne Tworetzky, MD, Department of Cardiology, Childrens Hospital, 300 Longwood Ave, Boston, MA 02115. E-mail wayne.tworetzky{at}cardio.chboston.org
Received September 14, 2005; revision received January 3, 2006; accepted January 13, 2006.
Background Fetal aortic valvuloplasty may prevent progression of aortic stenosis (AS) to hypoplastic left heart syndrome (HLHS). Predicting which fetuses with AS will develop HLHS is essential to optimize patient selection for fetal intervention. The aim of this study was to define echocardiographic features associated with progression of midgestation fetal AS to HLHS.
Methods and Results Fetal echocardiograms were reviewed from 43 fetuses diagnosed with AS and normal left ventricular (LV) length at
30 weeks gestation. Of 23 live-born patients with available follow-up data, 17 had HLHS and 6 had a biventricular circulation. At the time of diagnosis, LV length, mitral valve, aortic valve, and ascending aortic diameter Z-scores did not differ between fetuses that ultimately developed HLHS and those that maintained a biventricular circulation postnatally. However, all of the fetuses that progressed to HLHS had retrograde flow in the transverse aortic arch (TAA), 88% had left-to-right flow across the foramen ovale, 91% had monophasic mitral inflow, and 94% had significant LV dysfunction. In contrast, all 6 fetuses with a biventricular circulation postnatally had antegrade flow in the TAA, biphasic mitral inflow, and normal LV function. With advancing gestation, growth arrest of left heart structures became evident in fetuses developing HLHS.
Conclusions In midgestation fetuses with AS and normal LV length, reversed flow in the TAA and foramen ovale, monophasic mitral inflow, and LV dysfunction are predictive of progression to HLHS. These physiological features may help refine patient selection for fetal intervention to prevent the progression of AS to HLHS.
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