Neonatal Surgery
|
Reviewed by Charge Nurse - Newborn and Carl Kuschel and Mr Philip Morreau (Surgery) |
| April 2005 |
Gastroschisis and omphalocoele are congenital defects of abdominal wall that result in a portion of the intestinal contents remaining outside the abdominal cavity. These defects occur with an incidence of 1:6000 births. An omphalocoele is a defect in the umbilicus, with herniation of intestine as well as other viscera. The viscera are covered with a peritoneal sac, unless the sac has ruptured. If the defect is <5cm in diameter a primary repair is usually done. If the defect is >10cm then a staged repair is done.
In contrast, gastroschisis occurs as a defect in the abdominal wall lateral and to the right of the umbilicus, and no peritoneal sac covers the exposed bowel.
Other intestinal abnormalities are common (malrotation is nearly universal in omphalocoele; intestinal atresias are found with both defects but occur in up to 10% of gastroschisis). Extra-intestinal anomalies are common with omphalocoele, with congenital cardiac disease occurring in up to 20% of babies. Trisomy 13 and 18 occur in up to 10% of fetuses with omphalocoele. Other conditions associated with omphalocoele include Beckwith-Wiedemann syndrome (omphalocoele, macroglossia, and hypoglycaemia) and the pentalogy of Cantrell (epigastric omphalocoele, defects of the diaphragm, heart, pericardium, and sternum).
Preoperative Care
| Step | Action |
|
1 |
Follow standard pre-operative care guidelines. |
|
2 |
The bowel needs to be protected from injury. |
|
3 |
Wrap the exposed
bowel in Gladwrap (ordinary
supermarket Gladwrap – does not need to be sterile).
|
|
4 |
Support the intestines to
prevent occlusion of the blood supply by kinking.
|
| 5 |
Fluids management: The eviscerated bowel loses large
volumes of fluid.
|
| 6 | Observe peripheral perfusion, warmth and colour. |
| 7 | Record urine output. Renal failure can easily occur due to dehydration or if the bowel to be replaced into the abdominal cavity causes raised intra-abdominal pressure, resulting in circulation to the kidneys being compromised. |
| 8 |
Monitor blood glucoses levels
|
| 9 |
Nasogastric Tube:
|
| 10 | Medical staff will inform the surgeons when the baby is on its way or as soon as baby is delivered. The earlier they are informed the better. |
Postoperative Care
Follow the steps below to ensure safety of baby postoperatively.
|
Steps |
Action |
|
1 |
Follow standard steps for postoperative care. |
| 2 | Ensure baby is nursed in a supine position. |
| 3 | Fluid balance is
maintained.
|
| 4 | The orogastric tube remains on free drainage, and is also aspirated 2-4 hourly. Aspirate losses should be replaced intravenously as prescribed (0.9% NaCl with 10mmol KCl/500ml). |
| 5 | Administer volume expander as prescribed. |
| 6 | Accurately measure and record urine output - 6 hourly total urinalysis with every nappy change |
| 7 | Observe for metabolic acidosis (low pH <7.3, normal pCO2, raised base deficit >-5). |
| 8 | Observe for respiratory compromise due to increased bowel returned into peritoneal cavity causing increased pressure on the diaphragm. |
| 9 | Observe for signs of inferior
vena cava compression.
If possible do not use legs for intravenous cannulation as inferior vena cava flow is reduced. |
| 10 | Observe wound/suture line for:
|
| 11 | Introduce oral feeding on surgeon’s orders (usually when gastric aspirates are clear and minimal amount). |
Follow the steps below to ensure the silastic pouch is cared for in correct manner.
|
Steps |
Action |
|
1 |
Support the silastic pouch by cotton tape tied to the top of the bag and tied to top of radiant heat table, keeping tension firm. |
| 2 | Ensure that 2 nurses are present when the baby is weighed or x-rayed. One nurse holds the silastic bag in place (upright and correct tension); the other nurse holds the baby. |
| 3 | The surgeon reduces the pouch daily, lowering the bowel into the abdominal cavity and gradually reducing the size of the defect. The length of time for complete closure will depend on the defect. |
Follow the steps below for the care of omphalocoele.
|
Steps |
Action |
|
1 |
Swab the omphalocoele 4 hourly with 70% ethanol alcohol or as per the surgeons instructions. |
| 2 | Observe for Eschar (scab) formation which then peels off, leaving granulation tissue forming over the defect (it takes 2-6 months for skin to grow over). |
| 3 | Observe for any signs of infection. |
| 4 | Administer antibiotics only when baby has an infection, as prescribed. Prophylactic antibiotics are sometimes used |
| 5 | Ensure comfort of the baby is maintained. Carefully support omphalocoele with folded up napkins when baby is lying on their side. |
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