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Usefulness of Postnatal Echocardiograms in Patients with Omphaloceles Who Previously Had a Normal Fetal Echocardiogram.
Clark, Michael; Aldrink, Jennifer H; Richards, Bernadette; Corbitt, Rebecca; Stiver, Corey; Cua, Clifford L.
Afiliação
  • Clark M; Nationwide Children's Hospital, Columbus, OH, 43205, USA.
  • Aldrink JH; Nationwide Children's Hospital, Columbus, OH, 43205, USA.
  • Richards B; Nationwide Children's Hospital, Columbus, OH, 43205, USA.
  • Corbitt R; Nationwide Children's Hospital, Columbus, OH, 43205, USA.
  • Stiver C; Nationwide Children's Hospital, Columbus, OH, 43205, USA.
  • Cua CL; Nationwide Children's Hospital, Columbus, OH, 43205, USA. clcua@hotmail.com.
Cardiol Ther ; 11(1): 155-161, 2022 Mar.
Article em En | MEDLINE | ID: mdl-34727327
ABSTRACT

INTRODUCTION:

Neonates with omphaloceles routinely have a transthoracic echocardiogram (TTE) performed due to a high association with congenital heart defects (CHD). The utility of a TTE in these patients with a normal fetal echocardiogram is unknown. The primary objective of this study was to determine whether a critical CHD diagnosis was missed in patients with an omphalocele who had a normal fetal echocardiogram. The secondary objective of the study was to determine whether any CHD diagnosis was missed postnatally when a fetal echocardiogram was read as normal.

METHODS:

A retrospective chart review was performed of patients with omphaloceles born between January 1, 2008, and June 30, 2020. Patients were included if they had a fetal echocardiogram that was read as normal and had a postnatal echocardiogram performed. Baseline demographics, postnatal data echocardiographic findings, and hospital course were collected. Critical CHD was defined as CHD requiring neonatal cardiac intervention.

RESULTS:

Fifty-six fetal echocardiograms on patients with omphaloceles were performed, of which 24 patients met the inclusion criteria. No patient was diagnosed with a critical CHD postnatally (negative predictive value [NPV] = 100%). Two patients were diagnosed with ventricular septal defects (VSD) postnatally (NPV = 91.7%). One of the VSDs required closure with a patch at 4 months of life, while the other, a small muscular VSD, closed spontaneously within the first year of life. Both patients had a murmur on exam during their initial hospital stay. The patient that required surgery also had an abnormal electrocardiogram and chest X-ray. There were no mortalities due to cardiac causes in these patients.

CONCLUSION:

Critical CHD was not missed on any patient with an omphalocele who had a normal fetal echocardiogram. All other patients with omphaloceles who had CHD diagnosed postnatally had an abnormal clinical finding on postnatal evaluation. The routine performance of a postnatal TTE in patients with an omphalocele who had a normal fetal echocardiogram may not be needed in those with a normal clinical workup. Further studies evaluating echocardiographic imaging recommendations are needed to maximize care and optimize resource allocation in this complex patient population.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Prognostic_studies Idioma: En Revista: Cardiol Ther Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Prognostic_studies Idioma: En Revista: Cardiol Ther Ano de publicação: 2022 Tipo de documento: Article