Научные статьиM.H.Sayidova, S.U.Pulatova2025
MODERN APPROACHES TO MANAGEMENT OF CONGENITAL ANOMALIES: A REVIEW OF SURGICAL INTERVENTIONS FOR COMMON CONGENITAL CONDITIONS LIKE CONGENITAL DIAPHRAGMATIC HERNIA AND GASTROSCHISIS
Sahir Prasenjit Telang
Журнал инноваций нового века · 2026
Аннотация
Congenital anomalies, such as congenital diaphragmatic hernia (CDH) and gastroschisis, continue to represent significant challenges in neonatal surgery. Early diagnosis and timely surgical intervention are critical to improving survival and minimizing complications. This review examines the current approaches to the surgical management of CDH and gastroschisis, focusing on advancements in surgical techniques, neonatal care, and postoperative management. Recent improvements in prenatal diagnosis, including advanced imaging technologies, and neonatal intensive care have contributed to better outcomes for affected infants. The survival rate for CDH has increased to around 80%, while gastroschisis has a survival rate of approximately 90-95%. Despite these improvements, challenges persist, particularly in managing CDH with associated pulmonary hypoplasia. Continued research into surgical techniques, innovative neonatal care, and long-term follow-up care is essential to further enhance outcomes for these patients.
Доказательный фрагмент
«Congenital anomalies, such as congenital diaphragmatic hernia (CDH) and gastroschisis, continue to represent significant challenges in neonatal surgery.»
Образец извлечения
Демо-превьюCongenital anomalies, such as congenital diaphragmatic hernia (CDH) and gastroschisis, continue to represent significant challenges in neonatal surgery. Полный текст публикации CiteX не хранит — доступ к первоисточнику открывается по DOI согласно лицензии издателя и выбранному плану.
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- Ключевые слова
- Congenital anomalies, congenital diaphragmatic hernia, prenatal diagnosis, surgical techniques., survival rates, pulmonary hypoplasia, neonatal care, surgical management, ECMO, neonatal intensive care unit (NICU), gastroschisis, Key words: Congenital anomalies, postoperative outcomes
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