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Diaphragmatic hernia repair - congenital
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| Diaphragmatic hernia repair - congenital |
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Definition:
A congenital (present from birth) diaphragmatic hernia is caused by a defect in which the diaphragm, the large dome-shaped muscle that separates the chest cavity from the abdomen, fails to completely develop. The condition requires immediate surgery to repair the damage caused by the defect. The incomplete diaphragm has a large hole through which the abdominal organs can pass (herniate) into the chest cavity. Most commonly the hole occurs on the left side (almost 90% of cases). This compresses the fetal lung nearest the hernia, preventing full development, and thus interferes with breathing after the infant is born. Text Continues Below
The incidence of congenital diaphragmatic hernia is approximately 1 in 2,000 births, and boys are more commonly affected. Description:
While the child is under general anesthesia, an incision is made in the upper abdomen, under the ribs. The abdominal organs are gently pulled down through the opening in the diaphragm and positioned into the abdominal cavity. The hole in the diaphragm is repaired and the incision is stitched closed. If a large defect is present, a plastic patch is used to cover the defect in the diaphragm. A tube is placed in the chest to allow air, blood, and fluid to drain so the affected lung can re-expand. This tube remains in place after surgery for a few days. Indications:
When the abdominal organs pass into the chest cavity, the lung tissue on the affected side is compressed, fails to grow normally, and is unable to expand after birth. As the child begins to breathe, cry, and swallow, air enters the intestines that are protruding into the chest. The increasing size of the intestines puts pressure on the other side of the chest, the other lung, and the heart and can quickly cause a life-threatening situation.
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