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Clinical Presentation and Outcome of Congenital Thoracic Malformations in Children Beyond Neonatal Period

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Objective: To describe the clinical spectrum of presentation and outcome of children with congenital thoracic malformations beyond neonatal age. Methodology: Cross sectional study conducted at inpatient department of National institute of child health from Jan-Dec 2021. All patients hospitalized in study duration with diagnosis of congenital thoracic formations from 1 month till 12 years of age were enrolled. History, examination, laboratory tests, treatment and outcome were recorded. Results: Total 44 children were enrolled with mean age of 7.7+10.8 months. Common congenital thoracic malformations were congenital diaphragmatic hernia 24(54.5%), congenital cystic adenomatoid malformation 6(13.6%), congenital lobar emphysema5(11.4%) and eventration of diaphragm 4(9.1%). Three (6.9%) patients had associated cardiac anomalies. Surgical intervention was done in 33 (75%) patients with a postoperative survival rate of 95.4%. Conclusion: Congenital diaphragmatic hernia and cystic adenomatoid malformation are common congenital thoracic malformations that present beyond neonatal age and are associated with good postsurgical outcome. Keywords: congenital diaphragmatic hernia, congenital cystic adenomatoid malformation, beyond neonate
Title: Clinical Presentation and Outcome of Congenital Thoracic Malformations in Children Beyond Neonatal Period
Description:
Objective: To describe the clinical spectrum of presentation and outcome of children with congenital thoracic malformations beyond neonatal age.
Methodology: Cross sectional study conducted at inpatient department of National institute of child health from Jan-Dec 2021.
All patients hospitalized in study duration with diagnosis of congenital thoracic formations from 1 month till 12 years of age were enrolled.
History, examination, laboratory tests, treatment and outcome were recorded.
Results: Total 44 children were enrolled with mean age of 7.
7+10.
8 months.
Common congenital thoracic malformations were congenital diaphragmatic hernia 24(54.
5%), congenital cystic adenomatoid malformation 6(13.
6%), congenital lobar emphysema5(11.
4%) and eventration of diaphragm 4(9.
1%).
Three (6.
9%) patients had associated cardiac anomalies.
Surgical intervention was done in 33 (75%) patients with a postoperative survival rate of 95.
4%.
Conclusion: Congenital diaphragmatic hernia and cystic adenomatoid malformation are common congenital thoracic malformations that present beyond neonatal age and are associated with good postsurgical outcome.
Keywords: congenital diaphragmatic hernia, congenital cystic adenomatoid malformation, beyond neonate.

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