Literature DB >> 15237668

Outcome following, and impact of, prenatal identification of the candidates for the Norwood procedure.

Robin R Fountain-Dommer1, Scott M Bradley, Andrew M Atz, Martha R Stroud, Geoffrey A Forbus, Girish S Shirali.   

Abstract

OBJECTIVES: Our study evaluates hospital survival following prenatal identification of candidates for the Norwood procedure, and the impact of prenatal diagnosis on survival, preoperative stability, and postoperative morbidity.
METHODS: We reviewed records of all patients who were identified prenatally as candidates for the Norwood procedure, and compared them to all postnatally diagnosed patients who underwent the Norwood procedure between August 1995 and May 2002.
RESULTS: Of the 98 patients studied, 45 (46%) were diagnosed prenatally. Of these, 35 underwent the Norwood procedure, 29 (83%) of who survived. Thus, 29 of 45 (64%) patients survived from prenatal diagnosis to discharge following the Norwood procedure. Of the 53 postnatally diagnosed patients who underwent the Norwood procedure, 42 (79%) survived. Prenatal diagnosis was not associated with improvement in survival, preoperative stability, or postoperative morbidity. By multivariate analysis, ascending aortic diameter equal to or greater than 2 mm (p = 0.01), and gestational age 36 weeks or greater (p = 0.01) independently predicted survival. Based on this, patients were stratified into groups at low risk, consisting of 69 patients, and at high risk, consisting of 19 patients. Prenatal diagnosis was unassociated with improved survival in either group. Results were unchanged when the analysis was restricted to patients with hypoplasia of the left heart.
CONCLUSION: From the time of prenatal diagnosis, 64% of patients survived to discharge following the Norwood procedure. Prenatal diagnosis did not affect preoperative stability, survival or postoperative morbidity. This remained the case after stratifying patients by risk, or restricting analysis to patients with hypoplasia of the left heart. Ascending aortic diameter and gestational age independently predicted survival.

Entities:  

Mesh:

Year:  2004        PMID: 15237668     DOI: 10.1017/s1047951104001064

Source DB:  PubMed          Journal:  Cardiol Young        ISSN: 1047-9511            Impact factor:   1.093


  3 in total

1.  Hybrid Palliation for Ductal-Dependent Systemic Circulation.

Authors:  William N Evans; Alvaro Galindo; Abraham Rothman; Michael L Ciccolo; Sergio A Carrillo; Ruben J Acherman; Gary A Mayman; Kathleen A Cass; Katrinka T Kip; Carlos F Luna; Joseph M Ludwick; Robert C Rollins; William J Castillo; John A Alexander; Humberto Restrepo
Journal:  Pediatr Cardiol       Date:  2016-03-01       Impact factor: 1.655

2.  Prenatal diagnosis and risk factors for preoperative death in neonates with single right ventricle and systemic outflow obstruction: screening data from the Pediatric Heart Network Single Ventricle Reconstruction Trial(∗).

Authors:  Andrew M Atz; Thomas G Travison; Ismee A Williams; Gail D Pearson; Peter C Laussen; William T Mahle; Amanda L Cook; Joel A Kirsh; Mark Sklansky; Svetlana Khaikin; Caren Goldberg; Michele Frommelt; Catherine Krawczeski; Michael D Puchalski; Jeffrey P Jacobs; Jeanne M Baffa; Jack Rychik; Richard G Ohye
Journal:  J Thorac Cardiovasc Surg       Date:  2010-06-18       Impact factor: 5.209

3.  Chromosomal anomalies influence parental treatment decisions in relation to prenatally diagnosed congenital heart disease.

Authors:  Sinai C Zyblewski; Elizabeth G Hill; Girish Shirali; Andrew Atz; Geoffrey Forbus; Javier Gonzalez; Anthony Hlavacek
Journal:  Pediatr Cardiol       Date:  2009-08-25       Impact factor: 1.655

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.