2020, Number 11
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Ginecol Obstet Mex 2020; 88 (11)
Prenatal diagnosis and monitoring of omphalocele
Ortegón-López AJ, Acevedo-Gallegos S, Gallardo-Gaona JM, Velázquez-Torres B, Ramírez-Calvo JA, Camarena-Cabrera D, Copado-Mendoza Y, Aguinaga-Ríos M
Language: Spanish
References: 16
Page: 756-766
PDF size: 374.88 Kb.
ABSTRACT
Objective: Determine the prevalence of omphalocele, describe its characteristics,
its relationship to other fetal defects and congenital syndromes in a third level of care
referral center.
Materials and Methods: Retrospective, retrolective, case series study, carried out
by reviewing the records of patients attended in the defects clinic of the Maternal-Fetal
Medicine Department of the Instituto Nacional de Perinatología between 2007 and
2019. Inclusion criteria: patients with prenatal diagnosis of omphalocele, with prenatal
care and termination of pregnancy at the Institute. Prevalence was calculated, characteristics
of the defect, perinatal outcomes, other related defects and coexistence of
genetic diseases were described. Descriptive statistics were used to analyze the results.
Results: Sixty-two files were reviewed and it was found that the prevalence of the
defect was 1 case per-1000 newborns in the period studied. The average age of the
mothers was 26.7 (15 to 41) years and the weeks of pregnancy at birth 35.6 (25 to
41.1). Giant omphalocele was found in 39 patients. Thirty-seven cases of omphalocele
related to other structural defects were identified; 21 of the 62 neonates died.
Conclusion: The omphalocele is a heterogeneous and multifactorial defect;
having the knowledge of its behavior, describing the characteristics of the defect,
its association with other congenital and genetic defects allows us its prenatal and
post-birth approach in an optimal way, Prenatal ultrasound is a useful tool for its
diagnosis and surveillance.
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