Literature DB >> 25052401

Fetal aortic valvuloplasty for evolving hypoplastic left heart syndrome: postnatal outcomes of the first 100 patients.

Lindsay R Freud1, Doff B McElhinney2, Audrey C Marshall2, Gerald R Marx2, Kevin G Friedman2, Pedro J del Nido2, Sitaram M Emani2, Terra Lafranchi2, Virginia Silva2, Louise E Wilkins-Haug2, Carol B Benson2, James E Lock2, Wayne Tworetzky2.   

Abstract

BACKGROUND: Fetal aortic valvuloplasty can be performed for severe midgestation aortic stenosis in an attempt to prevent progression to hypoplastic left heart syndrome (HLHS). A subset of patients has achieved a biventricular (BV) circulation after fetal aortic valvuloplasty. The postnatal outcomes and survival of the BV patients, in comparison with those managed as HLHS, have not been reported. METHODS AND
RESULTS: We included 100 patients who underwent fetal aortic valvuloplasty for severe midgestation aortic stenosis with evolving HLHS from March 2000 to January 2013. Patients were categorized based on postnatal management as BV or HLHS. Clinical records were reviewed. Eighty-eight fetuses were live-born, and 38 had a BV circulation (31 from birth, 7 converted after initial univentricular palliation). Left-sided structures, namely aortic and mitral valve sizes and left ventricular volume, were significantly larger in the BV group at the time of birth (P<0.01). After a median follow-up of 5.4 years, freedom from cardiac death among all BV patients was 96±4% at 5 years and 84±12% at 10 years, which was better than HLHS patients (log-rank P=0.04). There was no cardiac mortality in patients with a BV circulation from birth. All but 1 of the BV patients required postnatal intervention; 42% underwent aortic or mitral valve replacement. On the most recent echocardiogram, the median left ventricular end-diastolic volume z score was +1.7 (range, -1.3 to +8.2), and 80% had normal ejection fraction.
CONCLUSIONS: Short- and intermediate-term survival among patients who underwent fetal aortic valvuloplasty and achieved a BV circulation postnatally is encouraging. However, morbidity still exists, and ongoing assessment is warranted.
© 2014 American Heart Association, Inc.

Entities:  

Keywords:  aortic valve stenosis; balloon valvuloplasty; fetal heart; heart defects, congenital; hypoplastic left heart syndrome; pediatrics; treatment outcome

Mesh:

Year:  2014        PMID: 25052401      PMCID: PMC4299861          DOI: 10.1161/CIRCULATIONAHA.114.009032

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


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5.  Staged left ventricular recruitment after single-ventricle palliation in patients with borderline left heart hypoplasia.

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9.  Neurodevelopmental Outcome in Children after Fetal Cardiac Intervention for Aortic Stenosis with Evolving Hypoplastic Left Heart Syndrome.

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