Chapters 191-209 Pediatrics Flashcards

1
Q

Describe the types of TE fistulas.

A

Type A: no esphogeal communication with the trachea; 2 blind ends
Type B: Communication with the upper part of the esophageal segment to the trachea
Type C: Communication with the the lower part of the esophageal segment to the trachea– accounts for 90% of all TEF
Type D: both upper and lower esophageal segments connecting to the trachea
Type E: No atresia, esophagus is in continuity, but does have abnormal connection to trachea
Type F: Esophageal stenosis without connection to the trachea

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2
Q

How might an infant present that has Type C TEF?

A

excessive drooling, cyanosis, coughing relieved by suctioning, clinician unable to pass catheter into stomach,

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3
Q

What radiology imaging would you get to confirm suspicion of TEF?

A

Xray- curled catheter in upper esophageal pouch with air bubble in stomach

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4
Q

What other abnormalites are common with TEF?

A

prematurity, heart disease, midline defects

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5
Q

What are some considerations for type of ETT to use in intubating a fetus with TEF?

A

If has Murphey’s eye, make sure it is facing anterior OR cut it off all together

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6
Q

What would be the steps you would use for induction of anesthesia for patient with TEF?

A

Rapid sequence or awake intubation with inhalation agents; AVOID NO2. Perform R mainstem intubation and then pull back until have B breath sounds. Continue spontaneous breath sounds until fistula has been ligated.

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7
Q

How will you do 1 lung ventilation for thorascopy for TEF repair?

A

Fogarty catheter into right mainstem bronchus by bronchoscopy will allow for one-lung ventilation OR left side intubation.

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8
Q

What are postoperative complications after TEF repair?

A

Avoid aggressive suctioning to stay about from anastomosis site.

Most patients will have swallowing problems, 70% have GERD, stricture of esophagus is common

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9
Q

What are the main differences between omphalocele and gastroschisis?

A

Omphalocele-75% have other congenital defects- often cardiac defects (VSD most common); is midline

Gastroschisis- not midline (usually right), normal umbilical cord, rarely associated with other congenital abnormalities

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10
Q

What is BeckWith-Wiedemann syndrome?

A

omphalocele, organomegaly, macroglossia and hypoglycemia

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11
Q

Where can omphaloceles be located and what abnormalities are associated with these other locations?

A

Epigastric- cardiac and lung abnormalities

Hypogastric- exstrophy of the bladder and other GU abnormalities

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12
Q

What are preoperative considerations for patients with omphalocele OR gastroschisis?

A

Exposed viscera in bag- helps with heat and fluid loss

- monitor and replace electrolytes, glucose and fluid losses

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13
Q

What is your anesthetia induction strategy for omphalocele/gastroschisis?

A

GETA with controlled ventilation by RSI

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14
Q

What do you want to watch for during omphalocele/gastroschisis surgery?

A

Elevated abdominal pressures, high peak airway pressures, IVC compression===circulatory stasis in lower extremities

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