2021
DOI: 10.1007/s00246-021-02576-3
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Congenital Heart Disease and Myelomeningocele in the Newborn: Prevalence and Mortality

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Cited by 3 publications
(3 citation statements)
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“…In the present study, conditions such as anencephaly, omphalocele, meningomyelocele, congenital heart disease (CHD), and congenital hernia were significantly associated with increased odds of neonatal mortality, aligning with existing literature that identifies these conditions as significant risk factors for neonatal mortality [23][24][25][26][27]. These associations underscore the necessity of early detection and intervention, particularly for CHD and meningomyelocele, where appropriate prenatal and postnatal management could improve survival rates [27][28][29]. Our results suggest that healthcare policies should prioritize prenatal screening protocols to facilitate early diagnosis and management of these conditions.…”
Section: Discussionsupporting
confidence: 83%
“…In the present study, conditions such as anencephaly, omphalocele, meningomyelocele, congenital heart disease (CHD), and congenital hernia were significantly associated with increased odds of neonatal mortality, aligning with existing literature that identifies these conditions as significant risk factors for neonatal mortality [23][24][25][26][27]. These associations underscore the necessity of early detection and intervention, particularly for CHD and meningomyelocele, where appropriate prenatal and postnatal management could improve survival rates [27][28][29]. Our results suggest that healthcare policies should prioritize prenatal screening protocols to facilitate early diagnosis and management of these conditions.…”
Section: Discussionsupporting
confidence: 83%
“…All institutions followed the same data collection process using a survey developed by the authors. Patients with unknown shunt status ( n = 8) and syndromal conditions that included spinal dysraphism (e.g., cloaca, cloacal exstrophy, imperforate anus, VATER syndrome, caudal regression, lipo/meningocele), genetic anomalies (e.g., trisomy 13/18, mitochondrial disorder) or cardiac anomalies (e.g., tetralogy of Fallot, severe pulmonary hypertension) were excluded [ 18 ].…”
Section: Methodsmentioning
confidence: 99%
“…79 A detailed assessment of the entire fetus to identify any additional malformations should be performed. 108 Given that up to 5% of live births affected by spina bifida also have a congenital heart defect, 109 a fetal echocardiogram is recommended. 102,110,111 Diagnostic genetic testing by way of amniocentesis should be offered.…”
Section: Prenatal Screening and Diagnosismentioning
confidence: 99%