Zane J Hellmann, Linh Buu, Shahyan Rehman, Carly Thaxton, Daniel G Solomon, Robert A Cowles
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引用次数: 0
摘要
导读:我们假设腹裂新生儿中有较高的严重先天性心脏缺陷(CCHD)患病率,这导致新生儿重症监护病房(NICU)住院期间的预后较差。方法:根据美国卫生与公众服务部(HHS)的年度数据计算胃裂、脐膨出和CCHD的发生率。另外,分析了2017年至2023年间新生儿重症监护病房进入儿童健康信息系统(PHIS)的情况,以诊断由ICD-10代码识别的胃裂、脐膨出或CCHD。结果:被诊断为胃裂的新生儿比一般人群更容易同时诊断为冠心病(OR = 8.18, 95% CI 5.56-12.02)。在新生儿重症监护病房中,同时诊断为胃裂和CCHD的新生儿接受心脏手术的几率更高(OR = 12.20, 95% CI 2.36-63.08, p)。讨论:目前的研究表明,出生时患有胃裂的婴儿比一般人群更容易被诊断为CCHD。胃裂和CCHD的诊断导致在住院期间更高的心内直视手术率和死亡率。
Prevalence of Critical Congenital Heart Defects Among Neonates Born With Abdominal Wall Defects.
Introduction: We hypothesized that there is a higher prevalence of critical congenital heart defects (CCHD) among infants born with gastroschisis, which leads to worse outcomes during index neonatal intensive care unit (NICU) admission.
Methods: Rates of gastroschisis, omphalocele, and CCHD were calculated from Department of Health and Human Services (HHS) annual data on all live births in the US. Separately, NICU admissions to the Pediatric Health Information System (PHIS) between 2017 and 2023 were analyzed for diagnosis of gastroschisis, omphalocele, or CCHD, as identified by ICD-10 codes.
Results: Neonates diagnosed with gastroschisis carried a concomitant diagnosis of CCHD more frequently than the general population (OR = 8.18, 95% CI 5.56-12.02). Among NICU admissions to PHIS hospitals, neonates diagnosed with both gastroschisis and CCHD had higher rates of open cardiac surgery (OR = 12.20, 95% CI 2.36-63.08, p < 0.001) and mortality (OR = 9.56, 95% CI 1.72-53.07, p = 0.004) during index admission compared to the general NICU population.
Discussion: The current study demonstrates that infants born with gastroschisis are more likely to be diagnosed with CCHD than the general population. A diagnosis of both gastroschisis and CCHD resulted in higher rates of open cardiac surgery and mortality during index hospital admission.
期刊介绍:
Prenatal Diagnosis welcomes submissions in all aspects of prenatal diagnosis with a particular focus on areas in which molecular biology and genetics interface with prenatal care and therapy, encompassing: all aspects of fetal imaging, including sonography and magnetic resonance imaging; prenatal cytogenetics, including molecular studies and array CGH; prenatal screening studies; fetal cells and cell-free nucleic acids in maternal blood and other fluids; preimplantation genetic diagnosis (PGD); prenatal diagnosis of single gene disorders, including metabolic disorders; fetal therapy; fetal and placental development and pathology; development and evaluation of laboratory services for prenatal diagnosis; psychosocial, legal, ethical and economic aspects of prenatal diagnosis; prenatal genetic counseling