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Fetal major cardiac defects and placental dysfunction at 11-13 weeks' gestation.
Fantasia, I; Kasapoglu, D; Kasapoglu, T; Syngelaki, A; Akolekar, R; Nicolaides, K H.
Afiliação
  • Fantasia I; Harris Birthright Research Centre for Fetal Medicine, King's College Hospital, London, UK.
  • Kasapoglu D; Harris Birthright Research Centre for Fetal Medicine, King's College Hospital, London, UK.
  • Kasapoglu T; Harris Birthright Research Centre for Fetal Medicine, King's College Hospital, London, UK.
  • Syngelaki A; Harris Birthright Research Centre for Fetal Medicine, King's College Hospital, London, UK.
  • Akolekar R; Harris Birthright Research Centre for Fetal Medicine, King's College Hospital, London, UK.
  • Nicolaides KH; Department of Fetal Medicine, Medway Maritime Hospital, Gillingham, UK.
Ultrasound Obstet Gynecol ; 51(2): 194-198, 2018 02.
Article em En | MEDLINE | ID: mdl-28833651
ABSTRACT

OBJECTIVE:

To investigate the relationship between fetal major cardiac defects and markers of placental perfusion and function.

METHODS:

This was a prospective screening study in singleton pregnancies at 11-13 weeks' gestation. Uterine artery pulsatility index (UtA-PI), serum pregnancy-associated plasma protein-A (PAPP-A) and placental growth factor (PlGF) were measured and the values were converted into multiples of the normal median (MoM). Median MoM values in fetuses with isolated major cardiac defects were compared with those in fetuses without major defects.

RESULTS:

The 50 094 singleton pregnancies fulfilling the entry criteria included 49 898 pregnancies with normal cardiac anatomy and 196 (0.39%) with major congenital cardiac defects 73 (37.2%) with conotruncal defects, 63 (32.1%) with left ventricular outflow tract defects and 60 (30.6%) with valvular defects. In the group with cardiac defects, compared with controls, there was lower median PAPP-A MoM (0.81 vs 1.00, P < 0.0001) and PlGF MoM (0.78 vs 1.00, P < 0.0001) but no significant difference in UtA-PI MoM (1.01 vs 1.00, P = 0.162).

CONCLUSION:

In pregnancies with isolated fetal major cardiac defects, there is evidence of placental dysfunction in the absence of impaired placental perfusion. Copyright © 2017 ISUOG. Published by John Wiley & Sons Ltd.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Placentárias / Fluxo Pulsátil / Ultrassonografia Pré-Natal / Artéria Uterina / Sofrimento Fetal / Coração Fetal / Cardiopatias Congênitas Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Ultrasound Obstet Gynecol Assunto da revista: DIAGNOSTICO POR IMAGEM / GINECOLOGIA / OBSTETRICIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Placentárias / Fluxo Pulsátil / Ultrassonografia Pré-Natal / Artéria Uterina / Sofrimento Fetal / Coração Fetal / Cardiopatias Congênitas Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Ultrasound Obstet Gynecol Assunto da revista: DIAGNOSTICO POR IMAGEM / GINECOLOGIA / OBSTETRICIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Reino Unido