Literature DB >> 30576779

Early Outcomes of Cardiac Surgery in Patients with Noonan Syndrome.

Pouya Hemmati1, Joseph A Dearani2, Richard C Daly1, Katherine S King3, Naser M Ammash4, Frank Cetta5, Hartzell V Schaff1.   

Abstract

There is a paucity of cardiac surgery outcomes data for patients with Noonan syndrome (NS). Our objective was to evaluate early results in these patients. Between January 1999 and December 2015, 29 patients (18 males, 62%) with NS underwent cardiac surgery at our institution. Mean age was 23 ± 17.9 years; 12 (41%) were under 18 years of age. Fourteen patients (48%) had prior sternotomies. The primary operations for the main diagnosis were pulmonary valve/conduit replacement/repair (n = 14, 48%), septal myectomy for obstructive hypertrophic cardiomyopathy (n = 7, 24%), aortic valve replacement/repair (n = 4, 14%), atrial septal defect (ASD) repair (n = 2, 7%), and cardiac transplantation (n = 2, 7%). Concomitant procedures were performed in 24 patients (83%), most commonly right ventricular outflow tract reconstruction (n = 13, 45%), mitral valve repair/replacement (n = 7, 24%), and ASD repair (n = 6, 21%). Mean bypass and cross-clamp times were 88.8 ± 51 minutes and 54.7 ± 67 minutes, respectively. There was 1 early death (3%). Postoperative morbidity occurred in 18 patients (62%), most commonly arrhythmias (n = 14, 48%) or respiratory insufficiency/pneumonia (n = 6, 21%). There were 2 early reoperations and 4 early readmissions. Univariate factors associated with morbidity included male gender (P = 0.03) and longer cross-clamp time (P = 0.02). Median length of hospital stay was 6 days (interquartile range 5-10.5 days). Patients with NS frequently have multiple cardiac lesions requiring a broad spectrum of operations. Early mortality is low despite procedure complexity. Although early postoperative morbidity is common, patients overall do well with reasonable hospital lengths of stay. Additional studies are needed to evaluate long-term outcomes and quality of life.
Copyright © 2018. Published by Elsevier Inc.

Entities:  

Keywords:  Congenital heart disease; Hypertrophic cardiomyopathy; Noonan Syndrome; Pulmonary stenosis; Septal myectomy

Year:  2018        PMID: 30576779     DOI: 10.1053/j.semtcvs.2018.12.004

Source DB:  PubMed          Journal:  Semin Thorac Cardiovasc Surg        ISSN: 1043-0679


  2 in total

1.  Congenital heart defects in Noonan syndrome: Diagnosis, management, and treatment.

Authors:  Léa Linglart; Bruce D Gelb
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-02-05       Impact factor: 3.908

2.  Concomitant septal myectomy and mitral valve repair in a child with Noonan syndrome.

Authors:  Toshio Doi; Daisuke Toritsuka; Akihiko Higashida; Shigeki Yokoyama; Kazuaki Fukahara; Naoki Yoshimura
Journal:  Clin Case Rep       Date:  2020-11-18
  2 in total

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