ArticleBMC pediatrics2016
Prediction of spontaneous closure of isolated ventricular septal defects in utero and postnatal life.
Article in BMC pediatrics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Predictive Scoring System for Spontaneous Closure of Infant Ventricular Septal Defect: The P-VSD Score.Pediatric cardiology · 2025Article
- Early Clinical Outcomes in Infants with Prenatally Diagnosed Perimembranous and Muscular Ventricular Septal Defects (VSDs).Pediatric cardiology · 2024Article
- Cardiac Axis in Early Gestation and Congenital Heart Disease.Current cardiology reviews · 2024Review
- Prenatal finding of isolated ventricular septal defect: genetic association, outcomes and counseling.Frontiers in genetics · 2024Review
- Risk factor analysis for adverse prognosis of the fetal ventricular septal defect (VSD).BMC pregnancy and childbirth · 2023Article
- Spontaneous closure of an isolated congenital perimembranous ventricular septal defect in two dogs.BMC veterinary research · 2022Article
- Should prenatal chromosomal microarray analysis be offered for isolated ventricular septal defect? A single-center retrospective study from China.Frontiers in cardiovascular medicine · 2022Article
- A review of isolated muscular ventricular septal defect.World journal of pediatrics : WJP · 2020Review
- Prediction of spontaneous closure of ventricular septal defect and guidance for clinical follow-up.Clinical cardiology · 2019Article
- An Unusual Mechanism of Closure of Muscular Ventricular Septal Defects.Case reports in pediatrics · 2017Article
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Authors and funding
9 authors.
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Abstract
backgroundVentricular septal defect (VSD) is a highly prevalent fetal congenital heart defect, which can become spontaneously closed during infancy. The current study aims to characterize fetal VSDs that were subsequently spontaneously closed in the first 2 years of life in eastern China.
methodsBetween January 2011 and December 2013, 257 fetal patients diagnosed with isolated VSD by fetal echocardiography at Nanjing Maternity and Child Health Care Hospital, China, were enrolled in the study. Subjects were divided into three groups: group 1 = persistent VSD; group 2 = closed after birth; group 3 = closed during gestation. Fetal echocardiography data, physical features at birth and follow-up outcomes for 2 years were compared to identify factors contributing to spontaneous closure (SC) of VSD. A predictive formula was applied to patients admitted to hospital in the first quarter of 2014 (n = 23) for validation.
resultsSC occurred in 42.8% patients. Birth weight (3.095 ± 0.774, 3.174 ± 0.535, 3.499 ± 0.532 kg in groups 1, 2 and 3, respectively) and defect diameter (3.422 ± 0.972, 2.426 ± 0.599, 2.292 ± 0.479 mm, in groups 1, 2 and 3, respectively) showed statistically significant differences between the three groups (P = 0.004 and P = 0.000, respectively). Receiver operating characteristic (ROC) curves identified cut-off value for the defect diameter as 2.55 mm, and logistic regression analysis identified the SC probability = (1 + exp -[-2.151 - 0.716*birth weight + 1.393*diameter])
conclusionsThe major determinants of SC of isolated VSD are birth weight and diameter of the defect. In addition, VSD location may also affect the SC incidence.
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