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RN Resedancy - Case Study
RN Resedancy - Case Study
RN Residency Program
Case Study
CASE
BABY 14 HRS OLD REFERED FROM OTHER HOSPITAL AS LIFE SAVING CASE. BABY IS PT 34 WEEKS , C/S ,
LBW 1.8 KG ,STABLE VITAL SIGN. WHEN THE MOTHER PRESENTED TO LABOUR THE ULTRASOUND
SHOWING POLYHYDROMONAS. THEN AFTER DELAVARY BABY HAD DISTRESS, FAILED TO INSERT
NGT/OGT TUBE AND SHOCKING WHEN SWALLWING.
Esophageal atresia
Type A: Both the top and bottom sections of the esophagus have closed ends that don’t connect .
Type B: In this rare type, the bottom section of the esophagus is closed, and the top section attaches to the
trachea.
Type C: The most common type of esophageal atresia has the lower section of the esophagus
attached to the trachea and the upper section closed.
Type D: In this rare form of esophageal atresia, both ends of the esophagus connect to the trachea.
Clinical manifestations
Signs and symptoms of esophageal atresia usually appear as soon as a baby is born.
They can include:
Bluish-colored skin when feeding.
Choking, coughing or gagging when feeding.
Foamy mucus in the mouth.
Excessive salivation
Spitting up or drooling.
Trouble breathing
Diagnostic and Test
• Esophageal atresia is rarely diagnosed during pregnancy. After birth
when the baby first tries to feed and has choking or vomiting, or when
a tube inserted in the baby’s nose or mouth cannot pass down into the
stomach.
An x-ray can confirm that the tube stops in the upper esophagus
• In rare cases, esophageal atresia is diagnosed before birth during a
prenatal ultrasound. This imaging test uses sound waves to create an
image of the fetus on a monitor. Pregnancies affected by esophageal
atresia commonly develop a build-up of amniotic fluid
called Polyhydramnios
PRE - OP
LIKE WHAT? / If your baby has to wait for surgery, they will receive nutrition
through an IV until the operation occurs.
Nursing Care Plan