Short-term results in infants with multiple left heart obstructive lesions.


Journal

Congenital heart disease
ISSN: 1747-0803
Titre abrégé: Congenit Heart Dis
Pays: United States
ID NLM: 101256510

Informations de publication

Date de publication:
Nov 2019
Historique:
received: 26 04 2019
revised: 05 06 2019
accepted: 16 07 2019
pubmed: 7 9 2019
medline: 1 7 2020
entrez: 7 9 2019
Statut: ppublish

Résumé

Deciding on a surgical pathway for neonates with ≥2 left heart obstructive lesions is complex. Predictors of the successful biventricular (2V) repair in these patients are poorly defined. The goal of our study was to identify patients who underwent the 2V repair and assess anatomic and echocardiographic predictors of success. Infants born between July 2015 and August 2017 with ≥2 left heart obstructive lesions with no prior interventions were identified (n = 19). Patients with aortic or mitral valve (MV) atresia and critical aortic stenosis were excluded. Initial echocardiograms were reviewed for aortic, MV, tricuspid valve annulus size, and left (LV) and right (RV) ventricle diastolic longitudinal dimensions. The valve morphology and presence of a ventricular septal defect (VSD) and coarctation were assessed. Clinical outcomes included successful 2V repair, complications, and repeat interventions or surgeries. Failed 2V repair was defined as a takedown to single ventricle (1V) physiology, cardiac transplantation, or death. For 2V repair, 14/19 patients were selected and for 1V, 5/19 patients were selected. Initial surgical procedures of the 2V group were simple coarctation repair (5), complex coarctation/arch reconstruction +/- septal defect closure (6), hybrid stage 1 (2), and none (1). Three of the 2V patients required reintervention in the first 90 days. The LV to RV diastolic longitudinal ratio >0.75 and mitral/tricuspid ratio of <0.8 were observed in 13/14 of the 2V patients. The LV:RV ratio and the aortic valve z score were significantly larger in the 2V group compared to the 1V group. All patients in the 1V group had a nonapex forming LV. There was no mortality with follow-up to three years of age. This study showed excellent short-term and midterm surgical results in the 2V population. The LV:RV diastolic longitudinal ratio may be a useful tool in the risk stratification of a successful 2V repair even in cases with a small MV.

Identifiants

pubmed: 31489778
doi: 10.1111/chd.12829
doi:

Types de publication

Comparative Study Journal Article

Langues

eng

Pagination

1193-1198

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Références

de Leval MR. The Fontan circulation: what have we learned? What to expect? Pediatr Cardiol. 1998;19:316-320.
Bolling SF, Iannettoni MD, Dick M, Rosenthal A, Bove EL. Shone’s anomaly: operative results and late outcome. Ann Thorac Surg. 1990;49:887-893.
Brauner RA, Laks H, Drinkwater DC, Scholl F, McCaffery S. Multiple left heart obstructions (Shone’s anomaly) with mitral valve involvement: long-term surgical outcome. Ann Thorac Surg. 1997;64:721-729.
Fedderly RT. Left ventricular outflow obstruction. Pediatr Clin N Am. 1999;46:369-384.
Rhodes LA, Colan SD, Perry SB, Jonas RA, Sanders SP. Predictors of survival in neonates with critical aortic stenosis. Circulation. 1991;84:2325-2335.
Schwartz ML, Gauvreau K, Geva T. Predictors of outcome of biventricular repair in infants with multiple left heart obstructive lesions. Circulation. 2001;104(6):682-687.
Tani LY, Minich LL, Pagotto LT, Shaddy RE, McGough EC, Hawkins JA. Left heart hypoplasia and neonatal aortic arch obstruction: is the Rhodes left ventricular adequacy score applicable? J Thorac Cardiovasc Surg. 1999;118(1):81-86.
Brown JW, Ruzmetov M, Vijay P, et al. Operative results and outcomes in children with Shone’s anomaly. Ann Thorac Surg. 2005;79(4):1358-1365.
St Louis JD, Bannan NM, Lutin WA, Wiles HB. Surgical strategies and outcomes in patients with Shone complex: a retrospective review. Ann Thorac Surg. 2007;84(4):1357-1362.
Freud LR, McElhinney DB, Marshall AC, et al. Fetal aortic valvuloplasty for evolving hypoplastic left heart syndrome: postnatal outcomes of the first 100 patients. Circulation. 2014;130(8):638-645.
Chung ML, Lee BS, Kim E-R, et al. Impact of fetal echocardiography on trends in disease patterns and outcomes of congenital heart disease in a neonatal intensive care unit. Neonatalogy. 2010;98(1):41-46.
Mart CR, Eckhauser AW. Development of an echocardiographic scoring system to predict biventricular repair in neonatal hypoplastic left heart complex. Pediatr Cardiol. 2014;35(8):1456-1466.

Auteurs

Jeremy M Steele (JM)

The Heart Institute, Cincinnati Children's Hospital, Cincinnati, Ohio.
Department of Pediatric Cardiology, Cleveland Clinic Children's, Cleveland, Ohio.

Rukmini Komarlu (R)

Department of Pediatric Cardiology, Cleveland Clinic Children's, Cleveland, Ohio.

Sarah Worley (S)

Quantitative Sciences Department, Cleveland Clinic Foundation, Cleveland, Ohio.

Tarek Alsaied (T)

The Heart Institute, Cincinnati Children's Hospital, Cincinnati, Ohio.

Christopher Statile (C)

The Heart Institute, Cincinnati Children's Hospital, Cincinnati, Ohio.

Francine G Erenberg (FG)

Department of Pediatric Cardiology, Cleveland Clinic Children's, Cleveland, Ohio.

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