Objective: To characterize differences in the prenatal diagnosis of
birth defects (BDs) associated with singleton and multiple pregnancies.
Design: An observational study conducted using data from a BDs
surveillance system. Setting: Eastern China. Population: A total of
54,572 babies with BDs, born in 90 hospitals located in 30 regions of
Zhejiang Province between 2012 and 2018. Methods: BDs were diagnosed by
obstetricians using ultra sonographic, genetic tests et al., on the
basis of the ICD 10th Revision (Q00–Q99). Main outcome measures:
Differences in incidence and characteristics of BDs associated with
singleton and multiple pregnancies. Multivariate logistic regression
models were constructed to characterize relationships between the
prenatal diagnosis of BDs and multiple pregnancies, with adjustment for
covariates. Results: Totals of 49,872 singletons and 3,324 multiple
pregnancies with BDs were analyzed. The mean incidences of BD for single
and multiple pregnancies were 26.29 and 109.99 per 1,000 births,
respectively (χ2=7600, P<0.001). After adjustment for
covariates, BDs associated with multiple pregnancies were less likely to
be diagnosed prenatally (adjusted OR: 0.36, 95% CI: 0.32–0.40); as
were congenital heart defects, congenital hydrocephalus, cleft lip with
cleft palate, congenital talipes equinovarus, cleft lip without cleft
palate, limb reduction defects, congenital diaphragmatic hernia, trisomy
21 syndrome, congenital malformation of the urinary system, and other
chromosomal malformation, compared with singletons with BDs.
Conclusions: Multiple pregnancy is associated with a significantly
higher risk of BD, but a significantly lower prenatal diagnosis rate.
Therefore, the healthcare of women with multiple pregnancy and their
fetuses should be strengthened.