TEF/EA: The less talked about issues
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Transcript TEF/EA: The less talked about issues
Alyssa Brzenski MD
May 2, 2012
Overview
Background
Pre-repair bronchoscopy
Thorascopic repair
To extubate or not?
Esophageal atresia – treatment of long-gap esophageal
atresia
Complications following TEF/EA repair
Case 1
Called to do a case in the NICU. The patient is a 2 day old
26 week neonate with a distended abdomen. He under
went an ex-lap yesterday for NEC with free-air and
resection of part of the small bowel and primary
anastamosis. Over the last few hours, progressive
abdominal distention with free air seen again on X-ray.
The surgeon gains adequate exposure of the abdomen and
can not find any area of bowel perforation, but notes that
the stomach is enlarged and seems to be increasing in a
rhythmic cycle, perhaps with the ventilator.
Case 2
5 month old term infant presenting for definitive
repair of EA. Initially, taken to the operating room at
an OSH on DOL 1 for repair of TEF. On exposure, the
gap was noted to be 4cm and thought to be too
lengthy for closure. Fistula was ligated, cervical
esophagoscopy was created and g-tube placed.
Plan today to perform esophageal anastamosis with lap
assisted gastric pull-through via a cervical approach.
Background
TEF/EA associated with
1:2,500-4,000 live births
30% of which the neonate is premature
Few cases diagnosed prenatally
May present with inability to pass an OGT
Background
Co-morbidities
Waterson Classification
Spitz Classification
Pre-repair Bronchoscopy
The Evidence behind the pre-repair
Bronch
May change the operative management (changed
operative approach in 57% with 31% being crucial
changes)
Bronchoscopy can
Define the fistula location
Determine unusual characteristics of the fistula(double
fistula or trifurcation)
Determine presence of tracheobronchitis (surgery
contraindicated)
Locate the aortic arch
Influence anesthetic management
Thorascopic vs. Open Repair
Thorascopic vs. Open Repair
Reduces Musculocutaneous sequelae
32% of patients have significant musculocutaeous
sequelae
24% with winged scapula
20% asymmetry of chest wall 2/2 atrophic serratus
anterior
18% developed thoracic scoliosis
Better visualization
Reduced Pain Post-operatively
Patient Position
Anesthesia for Thorascopic
Rarely need lung isolation as operative lung
compressed by CO2 insufflation (5mmHg)
Can be associated with mild desaturation requiring
100% O2 or mild hand ventilation.
Some centers using HFOV for these repairs to
minimize the movement of the operative side
(MAP 14-24, Hz=10-14, delta P=20-27, FiO2 adjusted to
Sat of 92%)
EtCO2 will be falsely low due to compression of the
lung and CO2 insufflation.
Anesthetic Considerations
Routine ASA monitors +/- A-line
Maintence of spontaneous ventilation during
induction
Classic teaching that paralysis can be given after fistula
ligated
Balanced anesthetic +/- epidural for post-op pain
management
May have difficulty with hypercapnia or difficulty
ventilating
Fistula Management
Extubate or Not?
Must consider pre-op lung disease and other
comorbidities
Spontaneous ventilation decreases the stress placed on
the suture line
Risk of injury to the repaired fistula with re-intubation
Long-gap Esophageal Atresia
Defined as Greater than 3cm between the esophageal
ends
Ideal to use the patient’s own esophagus
Excess tension on the esophageal anastamosis is
associated with increased complications and worse
outcome
Surgical Options
Primary anastamosis at time of initial repair
Serial staged dilation with bougie followed by
esophageal anastamosis
External tension with sutures, magnets, etc to
lengthen esophagus following by esophageal
anastamosis
Esophageal replacement with gastric pullthrough,
colonic graft or jejunal graft
Gastric Pullthrough
Gastric Pullthrough
Free up the stomach via laparoscopy
Cervical approach to bring down the cervical
esophagoscopy (spit fistula), followed by creating a
track in the mediastinum to approach the two ends of
the esophagus
Anesthetic Concerns of Gastric
Pullthrough
Lengthy procedure
Capnothorax or Capnomediastinum when surgeon
taking down the stomach
Can have difficulty ventilating during the
esophagoscopy take down and esophageal
mediastinum due to large dilators compressing a small
airway
Bleeding– Need adequate IV access
Complications following TEF/EA
Repair
Anastomotic leak
Recurrent esophageal fistula
Esophageal strictures
GERD/Esophageal dismotility
Tracheomalacia/ Pulmonary Issues
Musculocutaneous disturbances
Anastomotic leak
Early complication occurring in 17% of patients
Typically will resolve spontaneously without oral feeds or
with pleural drainage
Case reports of glycopyrolate and atropine used to
minimize secretions
Major leaks may require cervical esophagostomy and
gastrostomy with delayed definitive repair
Esophageal strictures and recurrent fistula are more likely
to follow
Recurrent TEF
Recurrent Esophageal Fistula
Serious complication affecting 5-20% of patients
Open thoracotomy associated with morbidity and
mortality rates of 10-22%
Endoscopic Closure preferred
Presents with cough, choking, or cyanosis with
feeding, or recurrent pneumonia
Endoscopic Closure of RTEF
Closure can be obtained with de-epitheliazation of the
fistula, application of tissue adhesives
De-epitheliazation of the fistula
Application of tissue adhesives(Tissel, dermabond, etc)
Combination of both
Highest overall and first time success with
combination treatment(93.3 and 66.7% respectively)
Likely will need repeat procedures– first time success
28.6% with tissue adhesives and 50% for deepitheliazation
De-epithelithalization
Fibrin Glue
Endoscopic Closure of RTEF
Performed with Rigid Bronch
Possibility of inability to ventilate if
aspiration of a Fibrin Plug
Occlusion of the trachea with the glue
Esophageal Strictures
Occurs in 6-40% of patients
More common with
Gap >2.5cm
EA/TEF type A, C, D
Non-absorbable sutures
Presents with dysphagia, poor feeding, and emesis
Treated with Esophageal dilation
Improves with time
Esophageal Dysmotility
Esophageal peristalsis is abnormal in 75-100% of
patients with EA/TEF
Small discoordinate contractions lead to increased risk
for esophageal obstructions
Improves with time as 65% of kids will be admitted
with GI sx in the first 10 years of their life, but only 3%
of patients will be admitted after 18 years of age
GERD
Occurs in 35-58% of TEF/EA children
Due to intrinsic motor dysfunction of the esophagus as
well as possible anastomotic tension
56% of patients with GERD respond to medical
therapy
13-25% of patients will require a Nissen fundoplication
However, attempts are made to avoid fundoplication
due to risk of severe dysphagia following given
dyskinetic esophagus
Respiratory Complications
Present in 46% of patients following EA/TEF repair
74% GERD
13% with tracheomalacia
13% with recurrent TEF
Tracheomalacia
Present in 75% of pathologic specimens in patients
with EA/TEF
Clinically significant in 10-20%
Usually found at or just above the level of the original
EA/TEF
Presents with brassy cough, stridor, and dyspnea with
feeds
Treatment usually medical
Bibliography
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recurrent tracheoesophageal fistula in children. International Journal of Pediatric Otolaryngology.
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Atzori P et al. Preoperative tracheobroncoscopy in newborns with esophageal atresia. Journal of Peds
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