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Perinatal management of fetal cardiac anomalies in a specialized obstetric-pediatrics center.
Mirlesse, V; Cruz, A; Le Bidois, J; Diallo, P; Fermont, L; Kieffer, F; Magny, J F; Jacquemard, F; Levy, R; Voyer, M; Daffos, F.
Afiliação
  • Mirlesse V; Service de Médecine foetale, Institut de Puériculture, Paris, France.
Am J Perinatol ; 18(7): 363-71, 2001 Nov.
Article em En | MEDLINE | ID: mdl-11731889
ABSTRACT
Perinatal teams dealing with fetal heart disease frequently wonder which pregnancies might be terminated, and when delivery should take place in a specialized surrounding. We present a retrospective study of 229 fetuses, in which prenatal ultrasound showed a cardiac anomaly not compatible with a standard maternity ward delivery. One hundred nineteen pregnancies were terminated (group I) while 110 pregnancies led to the birth of a live baby (group II). Pathology in group I was discovered earlier than in group II (24 vs. 29.3 weeks' gestation; p <0.01), and associated malformations or chromosomal anomalies were much more frequent in group I (80/119 vs. 9/110; p <0.001). Among live born babies, three infants with transposition of the great arteries underwent Rashkind atrioseptostomy in the delivery room. With a minimum follow-up of 12 months, 69 children (63%) have undergone surgery. Among 92 survivors (1 child is lost to follow-up), 78 (71%) are asymptomatic and 14 symptomatic. Early prenatal diagnosis of fetal heart anomalies significantly facilitates prenatal work-up and perinatal care. We present the types of pathology having led to termination and define the situations in which children are at risk of perinatal hemodynamic compromise.
Assuntos
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Base de dados: MEDLINE Assunto principal: Unidade Hospitalar de Ginecologia e Obstetrícia / Aborto Eugênico / Assistência Perinatal / Cardiopatias Congênitas Idioma: En Ano de publicação: 2001 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Unidade Hospitalar de Ginecologia e Obstetrícia / Aborto Eugênico / Assistência Perinatal / Cardiopatias Congênitas Idioma: En Ano de publicação: 2001 Tipo de documento: Article