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Pediatric Surgery—Tracheoesophageal Fistula

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Pediatric Surgery—Tracheoesophageal Fistula

Concept

Common cause of respiratory distress in the infant.

Several variants:

(A) esophageal atresia and distal TEF (most common) (B) atresia without fistula

(C) H-type TEF

(D) atresia with proximal and distal TEF

Approximately 50% of infants will have other congenital defects (VACTERL—vertebral, anorectal, cardiovascular, TEF, renal, limb) and you need to rule these in/out prior to operation.

Way Question May be Asked?

“Called to NICU to evaluate a newborn who is small for his gestational age that had an episode of choking and desaturation with his first two feedings. What do you want to do?” Should consider any newborn with respiratory dis- tress. Key is that problems are associated with feeding.

Most should be identified preterm by U/S.

How to Answer?

History

Maternal polyhydramnios

Respiratory distress with first feeding (choking, cough- ing, regurgitation)

Desaturation with eating

Physical Exam

Can’t place NGT

Small for gestational age infant

Scaphoid abdomen (if atresia without TEF)

Imperforate anus or limb abnormalities Cardiac exam

Diagnostic Tests

“Babygram”

air in GI tract rules out atresia without TEF r/o duodenal atresia, vertebral anomalies 0.5 cc barium down NGT (identify blunt pouch) Pre-op echo to r/o cardiac anomalies (affects anesthesia

management)

Renal U/S before or after repair

Surgical Treatment

(1) NGT in pouch (2) Elevate head of bed (3) abx if pneumonia

(4) OR in first 24 h for repair:

(a) extrapleural approach/right thoracotomy (b) divide fistula

(c) close trachea

(d) end to end esophageal anastomosis (e) gastrotomy for early post-op feeding (f) leave drain next to esophageal anastomosis (g) alternative is gastrotomy only and spit fistula

in neck and delay repair until one year old (colon interposition →usually in cases of atresia without TEF)

Common Curveballs

Post-op complication:

Leak Stricture

Recurrent fistula Reflux

94

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Will enter pleura during extrapleural approach

Will be associated anomalies (Down syndrome, valvu- lar defect, etc.)

Won’t be able to perform primary end to end anasto- mosis because of long “gap”

Pt will present with H-type fistula (repeated episodes of pneumonia in infancy)

Scenario will switch to management of associated imperforate anus

Strikeouts

Not making the diagnosis

Not knowing most common type/how to repair most common type

Not ruling other associated anomalies pre-op (espe- cially cardiac!)

Not trying to place NGT (alternatively, continuing to try to advance when meet resistance)

Not placing G-tube at operation

Strikeouts 95

Part 2.qxd 10/19/05 2:52 AM Page 95

Riferimenti

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