Pediatric Subglottic Stenosis Surgery

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Pediatric Subglottic Stenosis Surgery

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Subglottic stenosis (SGS) is a narrowing of the subglottic airway (see the image below). The subglottis is defined as the airway directly below the level of the vocal folds and encased in the cricoid cartilage. The subglottic airway is the narrowest area of the airway because it is encased in a complete, nonexpandable, and nonpliable ring.  In contrast, the trachea has a posterior membranous section, and the larynx has a posterior muscular section.

The term SGS implies a narrowing of the subglottic airway that is either congenital or acquired in etiology, though the term is applied to both congenital lesions of the cricoid ring and acquired SGS.

Acquired SGS is the most common acquired anomaly of the larynx in children and the most common abnormality requiring tracheotomy in children younger than 1 year. Correction of this abnormality requires expanding the lumen of the cricoid area to increase airflow and decrease obstructive breathing. Surgical correction of SGS has been performed with various techniques over the years.

Early in the 20th century, acquired SGS was usually related to trauma or infection from syphilis, tuberculosis, typhoid fever, or diphtheria. Often, the treatment itself for SGS at this time, a tracheostomy, led to further damage to the airway  

The incidence of acquired SGS increased in the late 1960s through the 1970s, after McDonald and Stocks introduced long-term intubation as a treatment method for neonates in need of prolonged ventilation. [1] The increased incidence of SGS focused new attention on the pediatric larynx, as well as the need for development of novel treatment modalities.

The exact pathophysiology of congenital SGS is unknown, though there is a known association of SGS with syndromes such as Down syndrome.  

Acquired SGS, on the other hand, is most freqently associated with intubation or airway trauma. Mechanical trauma from an endotracheal tube, as it passes through or remains for long periods in the narrowed neonatal and subglottic airway, can lead to mucosal edema and hyperemia. These conditions then can progress to pressure necrosis of the mucosa. These changes have been observed within a few hours of intubation and may progress to expose the perichondrium of the cricoid cartilage. Infection of the perichondrium can result in a subglottic scar.

This series of events can be hastened if an oversized endotracheal tube is used. Always check for an air leak after placing an endotracheal tube because of the risk of necrosis of the mucosa, even in short surgical procedures. Usually, the pressure of the air leak should be less than 20 cm H2O, so that no additional pressure necrosis occurs in the mucosa of the subglottis.

The exact etiology of congenital SGS is unknown.

The etiology of acquired SGS is related to trauma of the subglottic mucosa. Injury can be caused by infection or mechanical trauma, usually from endotracheal intubation but also from blunt, penetrating, or other trauma. Historically, acquired SGS has been related to infections such as tuberculosis and diphtheria. Over the past 40 years, the condition has typically been related to mechanical trauma.

Factors implicated in the development of SGS include the size of the endotracheal tube relative to the child’s larynx, the duration of intubation, the motion of the tube, and repeated intubations. Additional factors that affect wound healing include systemic illness, malnutrition, anemia, and hypoxia. [2]

Local bacterial infection may play an important role in the development of SGS. Gastroesophageal reflux (GER) may play an adjuvant role in the development of SGS because it causes the subglottis to be continually bathed in acid, which irritates and inflames the area and prevents it from correctly healing. A systemic or gastrointestinal (GI) allergy may cause the airway to be more reactive, creating a greater chance of developing stenosis.

No known frequency has been reported for congenital SGS; the incidence of acquired SGS has greatly decreased over the past 40 years. In the late 1960s, when endotracheal intubation and long-term ventilation for premature infants began, the incidence of acquired SGS was as high as 24% in patients who required such care. In the 1970s and 1980s, estimates of the incidence of SGS were 1-8%.

In 2000, Choi reported that the incidence of SGS had remained constant at the Children’s National Medical Center in Washington DC, accounting for approximately 1-2% of the children who had graduated from the neonatal intensive care unit (NICU). [3]

Walner reported that of 504 neonates who were admitted to the level III NICU at the University of Chicago in 1997, 281 were intubated for an average of 11 days; over a 3-year period, no patients developed SGS. [4]

International frequency is the same as that of the United States.

In 1996, a report from France also described no incidence of SGS in the neonatal population who were intubated with very small endotracheal tubes (2.5 mm internal diameter) in attempts to prevent trauma to the airway.

SGS is observed more often in premature infants because they may require mechanical ventilation for other system or pulmonary problems secondary to their prematurity. The mechanical ventilation can result in airway trauma and, potentially, SGS.

Equal sex distribution is noted. No racial predilection is noted.

The symptoms and prognosis of SGS can be highly variable, mostly depending on the severity of the SGS.  Difficulty in breathing and exercise intolerance can occur with mild, moderate, or severe SGS.  In moderate-to-severe cases of SGS, respiratory insufficiency can lead to failure to thrive, acute life threatening events (ALTE), and even death.

The outcome of laryngotracheal reconstruction depends on its grade and the procedure performed. Most authors report success rates of 80-90% when the patient has undergone successful preoperative evaluation and when the appropriate operation has been performed (see the images below).

The presence of acute or chronic respiratory illness, GER, or a reactive larynx may decrease the success rate. Choi and Zalzal showed that age can affect success rates; scars are more likely to recur in children younger than 2 years than in others. [5] Success is more likely with localized SGS than with extensive SGS. [6]

Zalzal noted that in any child with voice abnormalities before surgery, those abnormalities persisted after surgery. [7] Subglottic pressure is required to produce a strong voice. If the narrowed subglottic airway is expanded, subglottic airflow and pressure increase, and the voice usually is stronger (see the images below). Voice therapy may help relieve nonsevere glottic stenosis over time.

The voice of a patient with SGS, especially those who require reconstruction, may never return to its preoperative state, because the following are possible:

Because reconstructive techniques have improved over the past few decades, the focus of attention in patients with SGS who require reconstruction has switched from decannulation to decannulation with improved voice outcome.

Avelino et al reported a 100% success rate with balloon laryngoplasty in children with acute subglottic stenosis, though they found the procedure to be less successful in chronic subglottic stenosis. [8]  Factors that predicted a good outcome were as follows:

Teaching parents life-saving maneuvers for a child with a tracheotomy or airway stent following laryngotracheal reconstruction is critical. It is also important to teach parents cardiopulmonary resuscitation (CPR) before their child leaves the hospital.

For further information, see Subglottic Stenosis in Children. For patient education resources, see Bronchoscopy.

McDonald IH, Stocks JG. Prolonged nasotracheal intubation. A review of its development in a paediatric hospital. Br J Anaesth. 1965 Mar. 37:161-73. [Medline].

Rao A, Starritt N, Park J, Kubba H, Clement A. Subglottic stenosis and socio-economic deprivation: a 6-year review of the Scottish National Service for Paediatric Complex Airway Reconstruction. Int J Pediatr Otorhinolaryngol. 2013 Jul. 77(7):1132-4. [Medline].

Choi SS, Zalzal GH. Changing trends in neonatal subglottic stenosis. Otolaryngol Head Neck Surg. 2000 Jan. 122(1):61-3. [Medline].

Walner DL, Loewen MS, Kimura RE. Neonatal subglottic stenosis–incidence and trends. Laryngoscope. 2001 Jan. 111(1):48-51. [Medline].

Choi SS, Zalzal GH. Pitfalls in laryngotracheal reconstruction. Arch Otolaryngol Head Neck Surg. 1999 Jun. 125(6):650-3. [Medline].

Morita K, Yokoi A, Bitoh Y, Fukuzawa H, Okata Y, Iwade T, et al. Severe acquired subglottic stenosis in children: analysis of clinical features and surgical outcomes based on the range of stenosis. Pediatr Surg Int. 2015 Oct. 31 (10):943-7. [Medline].

Zalzal GH, Loomis SR, Derkay CS, et al. Vocal quality of decannulated children following laryngeal reconstruction. Laryngoscope. 1991 Apr. 101(4 Pt 1):425-9. [Medline].

Avelino M, Maunsell R, Jubé Wastowski I. Predicting outcomes of balloon laryngoplasty in children with subglottic stenosis. Int J Pediatr Otorhinolaryngol. 2015 Apr. 79 (4):532-6. [Medline].

Zdanski C, Davis S, Hong Y, Miao D, Quammen C, Mitran S, et al. Quantitative assessment of the upper airway in infants and children with subglottic stenosis. Laryngoscope. 2016 May. 126 (5):1225-31. [Medline]. [Full Text].

Walner DL, Stern Y, Gerber ME. Gastroesophageal reflux in patients with subglottic stenosis. Arch Otolaryngol Head Neck Surg. 1998 May. 124(5):551-5. [Medline].

Cotton RT. Management of subglottic stenosis. Otolaryngol Clin North Am. 2000 Feb. 33(1):111-30. [Medline].

Chen C, Ni WH, Tian TL, Xu ZM. The outcomes of endoscopic management in young children with subglottic stenosis. Int J Pediatr Otorhinolaryngol. 2017 Aug. 99:141-145. [Medline].

Edmondson NE, Bent J 3rd. Serial intralesional steroid injection combined with balloon dilation as an alternative to open repair of subglottic stenosis. Int J Pediatr Otorhinolaryngol. 2010 Sep. 74(9):1078-81. [Medline].

Maresh A, Preciado DA, O’Connell AP, Zalzal GH. A comparative analysis of open surgery vs endoscopic balloon dilation for pediatric subglottic stenosis. JAMA Otolaryngol Head Neck Surg. 2014 Oct. 140 (10):901-5. [Medline].

Sharma SD, Gupta SL, Wyatt M, Albert D, Hartley B. Safe balloon sizing for endoscopic dilatation of subglottic stenosis in children. J Laryngol Otol. 2017 Mar. 131 (3):268-272. [Medline].

Cotton RT, Seid AB. Management of the extubation problem in the premature child. Anterior cricoid split as an alternative to tracheotomy. Ann Otol Rhinol Laryngol. 1980 Nov-Dec. 89(6 Pt 1):508-11. [Medline].

Okamoto M, Nishijima E, Yokoi A, Nakao M, Bitoh Y, Arai H. Strategy for surgical treatment of congenital subglottic stenosis in children. Pediatr Surg Int. 2012 Nov. 28(11):1115-8. [Medline]. [Full Text].

O’Connor TE, Bilish D, Choy D, Vijayasekaran S. Laryngotracheoplasty to avoid tracheostomy in neonatal and infant subglottic stenosis. Otolaryngol Head Neck Surg. 2011 Mar. 144(3):435-9. [Medline].

Preciado D. A randomized study of suprastomal stents in laryngotracheoplasty surgery for grade III subglottic stenosis in children. Laryngoscope. 2014 Jan. 124 (1):207-13. [Medline].

Seid AB, Pransky SM, Kearns DB. One-stage laryngotracheoplasty. Arch Otolaryngol Head Neck Surg. 1991 Apr. 117(4):408-10. [Medline].

Rothschild MA, Cotcamp D, Cotton RT. Postoperative medical management in single-stage laryngotracheoplasty. Arch Otolaryngol Head Neck Surg. 1995 Oct. 121(10):1175-9. [Medline].

Lusk RP, Gray S, Muntz HR. Single-stage laryngotracheal reconstruction. Arch Otolaryngol Head Neck Surg. 1991 Feb. 117(2):171-3. [Medline].

Zalzal GH. Rib cartilage grafts for the treatment of posterior glottic and subglottic stenosis in children. Ann Otol Rhinol Laryngol. 1988 Sep-Oct. 97(5 Pt 1):506-11. [Medline].

Richardson MA, Inglis AF Jr. A comparison of anterior cricoid split with and without costal cartilage graft for acquired subglottic stenosis. Int J Pediatr Otorhinolaryngol. 1991 Sep. 22(2):187-93. [Medline].

Zalzal GH, Choi SS, Patel KM. Ideal timing of pediatric laryngotracheal reconstruction. Arch Otolaryngol Head Neck Surg. 1997 Feb. 123(2):206-8. [Medline].

Zalzal GH, Cotton RT. A new way of carving cartilage grafts to avoid prolapse into the tracheal lumen when used in subglottic reconstruction. Laryngoscope. 1986 Sep. 96(9 Pt 1):1039. [Medline].

Monnier P, Savary M, Chapuis G. Partial cricoid resection with primary tracheal anastomosis for subglottic stenosis in infants and children. Laryngoscope. 1993 Nov. 103(11 Pt 1):1273-83. [Medline].

Cotton RT, Gray SD, Miller RP. Update of the Cincinnati experience in pediatric laryngotracheal reconstruction. Laryngoscope. 1989 Nov. 99(11):1111-6. [Medline].

Stern Y, Willging JP, Cotton RT. Use of Montgomery T-tube in laryngotracheal reconstruction in children: is it safe?. Ann Otol Rhinol Laryngol. 1998 Dec. 107(12):1006-9. [Medline].

Saghebi SR, Zangi M, Tajali T, Farzanegan R, Farsad SM, Abbasidezfouli A, et al. The role of T-tubes in the management of airway stenosis. Eur J Cardiothorac Surg. 2013 May. 43(5):934-9. [Medline].

John E McClay, MD Associate Professor of Pediatric Otolaryngology, Department of Otolaryngology-Head and Neck Surgery, Children’s Hospital of Dallas, University of Texas Southwestern Medical Center

John E McClay, MD is a member of the following medical societies: American Academy of Otolaryngic Allergy, American Academy of Otolaryngology-Head and Neck Surgery, American College of Surgeons, American Medical Association

Disclosure: Nothing to disclose.

Mary L Windle, PharmD Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Nothing to disclose.

Alan D Murray, MD Pediatric Otolaryngologist, ENT for Children; Full-Time Staff, Medical City Dallas Children’s Hospital; Consulting Staff, Department of Otolaryngology, Children’s Medical Center at Dallas, Cook Children’s Medical Center; Full-Time Staff, Texas Pediatric Surgery Center, Cook Children’s Pediatric Surgery Center Plano

Alan D Murray, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Otolaryngology-Head and Neck Surgery, American Society of Pediatric Otolaryngology, Society for Ear, Nose and Throat Advances in Children, American Academy of Pediatrics, American College of Surgeons, Texas Medical Association

Disclosure: Nothing to disclose.

Ravindhra G Elluru, MD, PhD Professor, Wright State University, Boonshoft School of Medicine; Pediatric Otolaryngologist, Department of Otolaryngology, Dayton Children’s Hospital Medical Center

Ravindhra G Elluru, MD, PhD is a member of the following medical societies: American Academy of Otolaryngology-Head and Neck Surgery, American Academy of Pediatrics, American Bronchoesophagological Association, American College of Surgeons, American Medical Association, Association for Research in Otolaryngology, Society for Ear, Nose and Throat Advances in Children, Triological Society, American Society for Cell Biology

Disclosure: Nothing to disclose.

Orval Brown, MD Director of Otolaryngology Clinic, Professor, Department of Otolaryngology-Head and Neck Surgery, University of Texas Southwestern Medical Center at Dallas

Orval Brown, MD is a member of the following medical societies: American Academy of Otolaryngology-Head and Neck Surgery, American Academy of Pediatrics, American Bronchoesophagological Association, American College of Surgeons, American Medical Association, American Society of Pediatric Otolaryngology, Society for Ear, Nose and Throat Advances in Children, and Society of University Otolaryngologists-Head and Neck Surgeons

Disclosure: Nothing to disclose.

Pediatric Subglottic Stenosis Surgery

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Pediatric Subglottic Stenosis Surgery

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