Pre-intervention morphologic and functional echocardiographic characteristics of neonates with critical left heart obstruction: a Congenital Heart Surgeons Society (CHSS) inception cohort study.

Journal Article

Aims

The aims of this study were to provide a detailed descriptive analysis of pre-intervention morphologic and functional echocardiographic parameters in a large, unselected, multicentre cohort of neonates diagnosed with critical left heart obstruction and to compare echocardiographic features between the different subtypes of left-sided lesions.

Methods and results

Pre-intervention echocardiograms for 651 patients from 19 Congenital Heart Surgeons' Society (CHSS) institutions were reviewed in a core lab according to a standardized protocol including >150 morphologic and functional variables. The four most common subtypes of lesions were: aortic atresia (AA)/mitral atresia (MA) (29% of patients), AA/mitral stenosis (MS) (20%), aortic stenosis (AS)/MS (26%), and isolated AS (iAS) (18%). Only 17% of patients with AS/MS had an apex-forming left ventricle, compared with 0% of those with AA/MA and AA/MS (P < 0.0001). Aortic arch hypoplasia and coarctation were common across all four groups, while those with AA/MA and AA/MS had the smallest ascending aorta diameters. Flow in the ascending aorta was retrograde in 43% and 10% of the patients with AS/MS and iAS, respectively. The right ventricle was apex forming in 100% of patients with AA/MA and AA/MS, 96% with AS/MS and 70% with iAS (P < 0.0001). Moderate to severe tricuspid regurgitation was present in 13% of all patients.

Conclusion

This large multi-institutional study generates insight into the distribution of the functional and morphologic spectrum in patients with critical left-sided heart disease and identifies differences in these functional and morphologic characteristics between the main anatomic subtypes of critical left heart obstruction.

Full Text

Duke Authors

Cited Authors

  • Slieker, MG; Meza, JM; Devlin, PJ; Burch, PT; Karamlou, T; DeCampli, WM; McCrindle, BW; Williams, WG; Morgan, CT; Fleishman, CE; Mertens, L

Published Date

  • June 2019

Published In

Volume / Issue

  • 20 / 6

Start / End Page

  • 658 - 667

PubMed ID

  • 30339206

Pubmed Central ID

  • 30339206

Electronic International Standard Serial Number (EISSN)

  • 2047-2412

International Standard Serial Number (ISSN)

  • 2047-2404

Digital Object Identifier (DOI)

  • 10.1093/ehjci/jey141

Language

  • eng