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Canadian Journal of Anesthesia 54:223-226 (2007)
© Canadian Anesthesiologists' Society, 2007

Case Reports/Case Series

Case report: Use of two balloon-tipped catheters during thoracoscopic repair of a type C tracheoesophageal fistula in a neonate

[Présentation de cas : Utilisation de deux cathéters à ballonnet pendant la réparation thoracoscopique d’une fistule trachéo-oesophagienne de type C chez un nouveau-né.]

Anthony M.-H. Ho, MS MD FRCPC FCCP, Joyce C.P. Wong, MBChB FANZCA, Po T. Chui, MBBS FANZCA and Manoj K. Karmakar, MD FRCA

From the Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, NT, Hong Kong, SAR, PRC.

Address correspondence to: Dr. Anthony Ho, Department of Anaesthesia and Intensive Care, Prince of Wales Hospital, Shatin, NT, Hong Kong SAR. Phone: 852 2632 2735; Fax: 852 2637 2422; E-mail: hoamh{at}cuhk.edu.hk


    Abstract
 TOP
 Abstract
 Introduction
 Case report
 Discussion
 References
 
Purpose: To describe a novel airway management technique for thoracoscopic repair of a type C tracheoesophageal fistula (TEF) in a neonate.

Clinical features: A full-term neonate with a type C TEF presented for thoracoscopic repair. The fistula was at the level of the carina, making its isolation from positive pressure ventilation using traditional techniques difficult. In addition, non-ventilation of the right lung was required. The use of two Fogarty type balloon-tipped embolectomy catheters placed alongside the endotracheal tube successfully achieved the goal of blocking ventilation of the fistula and the right lung. The use of fibreoptic bronchoscopy greatly facilitated placement of the blockers. The patient made an uneventful recovery.

Conclusion: Placing two balloon-tipped blockers, one in the TEF and the other in the right mainstem bronchus, is a viable technique for thoracoscopic fistula repair when the fistula is at or very close to the level of the carina.


    Introduction
 TOP
 Abstract
 Introduction
 Case report
 Discussion
 References
 
MINIMALLY invasive surgical techniques are being used increasingly for the repair of tracheoesophageal fistula (TEF) in neonates. Traditional repair through a right dorsolateral thoracotomy has major disadvantages, including a large scar, significant postoperative pain, and a high degree of scoliosis and shoulder girdle weakness later in development.1 An advantage of minimally invasive surgery is superior visualization of the fistula and the surrounding anatomy through the thoracoscope.2 However, this new approach poses extra challenges to the anesthesiologist because of the requirement for collapsing a lung during the thorascopic repair. Thus, the anesthesiologist needs to isolate not just the TEF, but also a mainstem bronchus during the procedure. When the TEF is not too proximal to the carina, it can be isolated by the endotracheal tube (ETT).35 However, 11% of TEF are either at or below the carina.6 When the TEF is very near or at the carina, this approach becomes impossible and unreliable, and use of a balloon-tipped embolectomy catheter to block the fistula during open TEF repair has been described.7,8 The use of a balloon-tipped catheter to achieve single-lung ventilation is a well-established technique.9 With the consent of the patient’s mother for publication, we herein describe a thoracoscopic TEF repair in which airway management involved the use of two balloon-tipped catheters to block the TEF and the right mainstem bronchus simultaneously.


    Case report
 TOP
 Abstract
 Introduction
 Case report
 Discussion
 References
 
A full-term baby girl was born with type C TEF (esophageal atresia with distal fistula communicating between the distal esophagus/stomach and the lower trachea). Her birth weight was 2400 g. Other congenital abnormalities included patent foramen ovale and ductus arteriosus, both with left to right shunt, and horseshoe kidneys. She did not have any known vertebral, anal, or limb abnormalities.

Corrective surgery was undertaken on day two. Preoperatively, SpO2 was 94% on room air, she was tachypneic with a mild fever for which she received antibiotics, but vital signs were otherwise stable. Relevant blood work was unremarkable. Routine intraoperative monitors were attached; however, attempts to establish an arterial line failed. The in situ Replogle tube was placed on gentle continuous suction. Prior to induction, atropine 0.1 mg iv was given. General anesthesia was induced with up to 4% sevoflurane (end-tidal) in 100% O2 with the child in a slight reverse Trendelenberg position. Spontaneous respiration was maintained. After spraying the larynx and trachea with lidocaine 10% (total approximately 15 mg), fibreoptic bronchoscopy (Olympus LF-P 1.8 mm, Tokyo, Japan) was performed to discover that the TEF was at the carina (FigureGo). The fibrescope was withdrawn and the trachea was intubated with a 4 Fr Fogarty arterial embolectomy catheter (Applied Medical Technology, Inc, Cleveland, OH, USA) with its tip slightly bent so that the balloon was facing posteriorly. Next inserted was an uncuffed internal diameter 3 mm ETT. Under fibreoptic bronchoscopy through the ETT lumen, the TEF was intubated successfully with the Fogarty catheter tip on the first attempt (FigureGo), and the balloon was inflated just enough so that it appeared to completely occlude the fistula. The approximate inflation volume was 0.2 mL of saline. The ETT was then removed, and another 4 Fr Fogarty catheter with the tip slightly bent towards the right was passed into the trachea followed by reintubation with the same ETT. The second Fogarty catheter tip was then positioned in the right mainstem bronchus with the aid of fibreoptic bronchoscopy, again through the ETT lumen (FigureGo). Inflation of the second catheter balloon with approximately 0.2 mL of saline resulted in satisfactory isolation of the right lung. The child was then paralyzed and controlled ventilation was started. The balloon pressures were not measured. There was no gas leak around the in situ ETT and the catheters at a peak ventilatory pressure of 20 cm H2O.


Figure 1
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FIGURE The patient had a large tracheoesophageal fistula at the level of the carina (left panel). The fistula was intubated by a balloon-tipped catheter (middle panel). The fistula and the right mainstem bronchus were intubated by balloon-tipped catheters (right panel).

 
The baby was turned into a semi-prone position, right side up. The right endobronchial blocker was inflated after an exhalation pause. Surgically, a camera port was inserted at the fourth intercostal space at the posterior axillary line. Two additional ports, one 5 mm above and another below, were also inserted at the anterior axillary line. Carbon dioxide insufflation at 5 mmHg was induced for thoracoscopic division of the fistula and anastomosis of the two esophageal stumps. After the anastomosis, a 10-Fr chest drain was inserted and the right lung was re-inflated. One-lung ventilation lasted just over four hours. The child at times needed hand ventilation with 100% O2 to maintain SpO2 > 88%. Surgery took longer than expected because of difficulties with the anastomosis, but was otherwise uneventful.

Postoperatively, the child was treated with antibiotics for pneumonia and intermittent iv boluses of fentanyl for analgesia and sedation. Her trachea was extubated on postoperative day six upon resolution of the pneumonia. She was discharged to a peripheral hospital on postoperative day 12. Subsequent recovery was uneventful, as evaluated during multiple visits to clinic up to one year later.


    Discussion
 TOP
 Abstract
 Introduction
 Case report
 Discussion
 References
 
We have described the use of two embolectomy catheters to simultaneously isolate the right mainstem bronchus and a TEF that existed at the level of the carina. This approach afforded a "quiet" lung that did not require the surgeons to create an extra port for lung retraction. This approach greatly facilitated surgery and minimized trauma to the right lung.

Formulation of the airway management plan was possible after the airway anatomy was delineated with fibreoptic bronchoscopy. Once a two-blocker technique was chosen, the TEF blocker was the first to be inserted. As reported by others,7 and due to the downward direction of the tracheo-distal esophageal/ gastric fistula, this task was not time-consuming. Because the ETT was too small to accommodate a Fogarty catheter and a fibrescope, both blockers had to be outside of the ETT. The ETT thus was inserted twice: after the fistula blocker was placed, and after the endobronchial blocker was inserted. The accurate positioning of both blockers required bronchoscopy through the ETT lumen. One concern which arose was whether the presence of two blockers and an ETT would create excessive pressure on the tracheal mucosa. We were unable to objectively investigate this aspect, but noted that the child had no clinical evidence of tracheo-malacia or stenosis on multiple follow-up visits. Bearing in mind that the cross-section of the neonatal trachea has a partial oval shape, it was thought that the stems of the blockers would migrate into the gaps between the tracheal mucosa and the ETT. Others have not reported this potential problem with the use of a single blocker and an ETT.7,8

The disadvantages of bronchial blockers include the possibility of retrograde migration of either blocker into the tracheal lumen, resulting in partial or complete airway obstruction; and insufficient blockade of the mainstem bronchus leading to partial ventilation of the collapsed lung; and bronchial rupture.10

One alternative technique of blocking the TEF and the right mainstem bronchus simultaneously is to deliberately slide the ETT into the left mainstem bronchus.11,12 This simple approach is sometimes effective.13 However, differences in the diameters of either mainstem bronchus and the trachea may result in an ETT that fits a mainstem bronchus well but is too small for the trachea, or one that fits the latter but is too large for the former. This might predispose to left bronchial edema. In one report, left upper lobe collapse also highlighted the low margin of safety in deliberate endobronchial ETT placement in neonates to achieve one-lung ventilation.11 Another disadvantage stems from the not uncommon occurrence of desaturation during one-lung ventilation in TEF repair.14 As such, intraoperatively, the ETT may need to be retracted several times to ventilate both lungs. Subsequent repositioning of the ETT tip back into the left mainstem bronchus requires fibreoptic bronchoscopy, which may be hazardous and cumbersome in a semiprone neonate, made even more difficult by the clutter of sterile drapes separating the small distance between the operative field and the patient’s mouth.

Use of a specially designed bifurcated tracheal tube for TEF repair has also been described.15 This is not a double-lumen tube, and is therefore not suitable for differential lung ventilation. Intubating the TEF with a balloon-tipped catheter pulled through a gastrostomy has also been described16 but has been criticized for its complexity.8

In summary, the need to avoid communication between the stomach and the lungs and the importance of collapsing the right lung during thoracoscopic TEF repair led to the use of two balloon-tipped embolectomy catheters placed alongside the ETT in a neonate. This appears to be a viable technique and may be considered when the TEF is too proximal to the carina to be easily blocked with an ETT.


    Footnotes
 
Financial support: Departmental and institutional resources.

This work is attributable to the Chinese University of Hong Kong and the Prince of Wales Hospital, Shatin, NT, Hong Kong SAR.

Conflict of interest: None to declare.

Accepted for publication September 11, 2006. Revision accepted November 27, 2006.


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 Introduction
 Case report
 Discussion
 References
 
1 Jaureguizar E, Vazquez J, Murcia J, Diez Pardo JA. Morbid musculoskeletal sequelae of thoracotomy for tracheoesophageal fistula. J Pediatr Surg 1985; 20: 511–4.[Medline]

2 Rothenberg SS. Thoracoscopic repair of tracheoesophageal fistula in newborns. J Pediatr Surg 2002; 37: 869–72.[Medline]

3 Salem MR, Wong AY, Lin YH, Firor HV, Bennett EJ. Prevention of gastric distension during anesthesia for newborns with tracheoesophageal fistulas. Anesthesiology 1973; 38: 82–3.[Medline]

4 Lucking-Famira KM, Schulzke S, Hammer J. Cuffed endotracheal tube for occlusion of a tracheo-oesophageal fistula in an extremely low birth-weight infant (Letter). Intensive Care Med 2004; 30: 1249.[Medline]

5 De Gabriele LC, Cooper MG, Singh S, Pitkin J. Intraoperative fibreoptic bronchoscopy during neonatal tracheo-oesophageal fistula ligation and oesophageal atresia repair. Anaesth Intensive Care 2001; 29: 284–7.[Medline]

6 Holzki J. Bronchoscopic findings and treatment in congenital tracheo-oesophageal fistula. Paediatr Anaesth 1992; 2: 297–303.

7 Reeves ST, Burt N, Smith CD. Is it time to reevaluate the airway management of tracheoesophageal fistula? Anesth Analg 1995; 81: 866–9.[Medline]

8 Filston HC, Chitwood WR Jr, Schkolne B, Blackmon LR. The Fogarty balloon catheter as an aid to management of the infant with esophageal atresia and tracheoesophageal fistula complicated by severe RDS or pneumonia. J Pediatr Surg 1982; 17: 149–51.[Medline]

9 Hammer GB. Single-lung ventilation in infants and children. Paediatr Anaesth 2004; 14: 98–102.[Medline]

10 Borchardt RA, LaQuaglia MP, McDowall RH, Wilson RS. Bronchial injury during lung isolation in a pediatric patient. Anesth Analg 1998; 87: 324–5.[Free Full Text]

11 Krosnar S, Baxter A. Thoracoscopic repair of esophageal atresia with tracheoesophageal fistula: anesthetic and intensive care management of a series of eight neonates. Paediatr Anaesth 2005; 15: 541–6.[Medline]

12 Tercan E, Sungun MB, Boyaci A, Kucukaydin M. Onelung ventilation of a preterm newborn during esophageal atresia and tracheoesophageal fistula repair. Acta Anaesthesiol Scand 2002; 46: 332–3.[Medline]

13 Baraka A, Akel S, Haroun S, Yazigi A. One-lung ventilation of the newborn with tracheoesophageal fistula. Anesth Analg 1988; 67: 189–91.[Free Full Text]

14 Kalfa N, Allal H, Raux O, et al. Tolerance of laparoscopy and thoracoscopy in neonates. Pediatrics 2005; 116: e785–91.[Abstract/Free Full Text]

15 Miyamoto Y, Kinouchi K, Taniguchi A, Kitamura S. A bifurcated tracheal tube for a neonate with tracheoesophageal fistula. Anesthesiology 2004; 100: 733–6.[Medline]

16 Bloch EC, Filston HC. A thin fiberoptic bronchoscope as an aid to occlusion of the fistula in infants with tracheoesophageal fistula. Anesth Analg 1988; 67: 791–3.[Free Full Text]





This Article
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