Pediatric Tracheotomy and Decannulation


Key Points

  • Because of the advances in medical care, rates of pediatric tracheotomy have recently declined.

  • The process of obtaining informed consent prior to surgery requires that families understand expectations for tracheostomy management and the potential for decannulation.

  • Prior to discharging a child with a tracheostomy from the hospital, families should have all routine and emergency supplies readily available.

  • Caring for a child with a tracheostomy is taxing on families. Although the experience can be meaningful and manageable, it often stresses families and can reduce quality of life (QOL) for the caregivers.

  • Tracheotomy complications may occur early, within the first 7 days after surgery, or late, occurring any time after.

  • Prior to decannulation, children should undergo laryngoscopy and bronchoscopy to evaluate the airway. Most protocols include hospital observation while patients are capped overnight and after extubation. The role of sleep studies prior to decannulation is somewhat controversial.

  • The presence of a tracheocutaneous fistula (TCF) after decannulation should heighten suspicion for upper or lower airway obstruction, which should be investigated prior to closure of the fistula.

Introduction and History

Tracheotomy was first credited to Asclepiades, c.100 BCE, in an ultimately unsuccessful attempt at saving a life. Paul d’Egine reported the first successful tracheotomy more than a century and a half later. The procedure was extended to treat severe respiratory infections by Armand Trousseau in the 1800s, and Chevalier Jackson eventually formalized and popularized the surgery in the 1900s. Almost 5000 tracheotomies are performed annually on children in the United States. Because of advances in pediatric critical care and a reduction in infectious sources of airway obstruction, the incidence of pediatric tracheotomy has recently declined. Notably, although little has changed over the last few decades in terms of surgical technique or tracheotomy hardware, the indications for tracheotomy in children have significantly shifted. Because of the increasing survival of children with long-term respiratory needs, there has been a trend toward longer-lasting tracheotomies, which necessitate prolonged care by pediatric otolaryngology and other disciplines. This chapter reviews the entire course of care for pediatric tracheotomy from successful presurgical selection to eventual decannulation.

Indications

The declining rate of pediatric tracheotomy , is at least partly caused by technologic and medical advances. Vaccination programs targeting Haemophilus influenzae have reduced the incidence of epiglottitis and consequently the frequency of emergent tracheotomy for infectious airway compromise. The ubiquity of flexible and rigid fiberoptic laryngoscopes has allowed for less invasive intubation, obviating the need for tracheotomy to secure difficult airways. Consequently even less experienced centers may be able to manage patients with craniofacial anomalies such as micrognathia and Pierre Robin sequence without a surgical airway. Additionally, the widespread use of low-pressure cuffed endotracheal tubes (ETTs), which allow for longer periods of intubation in premature infants, has reduced rates of subglottic stenosis. Yet the indications for tracheotomy have remained largely unchanged ( Box 32.1 ).

BOX 32.1
Surgical Indications for Tracheotomy

Airway Obstruction

  • Pierre Robin sequence/retrognathia

  • Severe obstructive sleep apnea

  • Bilateral vocal fold paralysis

  • Laryngotracheal stenosis

  • Microstomia

  • Bilateral choanal atresia

Prolonged Ventilation

  • Bronchopulmonary dysplasia

  • Neuromuscular disorders: muscular dystrophy, spinal muscular atrophy, spinal cord injury

  • Traumatic brain injuries or hypoxic encephalopathy

  • Central hypoventilation

  • Tracheobronchomalacia

  • Congenital cardiac anomalies

Pulmonary Toilet

  • Chronic aspiration

  • Vocal fold paralysis

  • Neurologic impairment

  • Spinal cord injury

  • Laryngeal cleft

  • Esophageal obstruction/dysmotility

The goal of tracheotomy is to allow safe respiration or ventilation while bypassing the glottis. Indications include the need for prolonged ventilation, laryngotracheal or upper airway obstruction, pulmonary toilet and suctioning, and facilitating ventilator weaning in patients who are unable to tolerate extubation. As infectious and craniofacial indications have become less common, a greater proportion of tracheotomies are performed for prolonged ventilation and congenital disorders. Previously fatal neurologic and neuromuscular conditions can now be meaningfully palliated or treated. Many patients with chromosomal anomalies that were previously considered fatal can live well into adulthood if early airway obstruction is alleviated. A 1999 study demonstrated that 34% of children who underwent tracheotomy had otherwise normal airways, and according to the author’s experience, this proportion may actually be higher at some centers. Children with chronic conditions may be given the option of a tracheotomy, whereas in the past they would have been offered only end-of-life care to ease a quick demise. Improved survival and quality of life (QOL) for chronic conditions will only increase the need for tracheotomy over time and its prolonged management in children.

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