UPPER AIRWAY OBSTRUCTION
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Poiseuille’s law
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Q=ΔPπr48ηl; r = Radius of airway
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Flow (Q) is proportional to the radius to the fourth power; incremental changes in the radius cause exponential decreases in airflow
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Bernoulli’s principle
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Increased airflow results in a decrease in pressure
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Narrowed airway → Increased airflow speed → Decreased intraluminal pressure (vacuum) → Further collapse of walls of lumen
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Stridor – high-speed airflow through collapsed tissues causes vibration and a resonance, resulting in a sound
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Physical obstruction of the airway is associated with noise on inspiration or expiration, depending on the site and nature of the lesion
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Stridor is not only audible, but also visible
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Examiner should be able to visualize site of obstruction while noise is being made
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Requires adequate instrumentation techniques of the airway
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Isolated tachypnea (i.e., without stridor) is not a sign of airway obstruction
SYMPTOMS BY SUBSITE SEE TABLE 20-1
Symptoms by Subsite
Subsite | Hallmark Symptoms |
Nasal | Mouth breathing, snoring |
Acute respiratory distress in neonates – obligate nasal breathers | |
Pharynx | Snoring, stertor (pharyngeal resonance, similar to snoring), retractions |
Supraglottis | Pure inspiratory stridor, dysphagia in infants, retractions, pectus excavatum |
Glottis | Biphasic stridor, retractions, hoarseness |
Subglottis | Inspiratory or biphasic stridor, retractions, barking cough, recurrent croup |
Trachea | Expiratory stridor, barking cough, poor secretion clearance |
LESIONS AND TREATMENTS BY SUBSITE
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Piriform aperture stenosis
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Bony narrowing of the anterior nasal vestibule in neonates; results in airway-related respiratory distress and feeding problems
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Diagnosed by computerized tomography (CT) scan showing <8 mm patency between nasal processes of maxillary bone
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Can be associated with holoprosencephaly (central incisor) or choanal atresia
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Treatment: sublabial approach to nasal vestibule with high-powered drill reduction of nasal process of maxillary bone
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Choanal atresia/stenosis
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Incomplete or uncannulated opening from the nose to the nasopharynx in neonates; results in airway-related respiratory distress
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CHARGE syndrome (coloboma, heart defects, atresia choanae, growth retardation, genital abnormalities, and ear abnormalities)
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May go undiagnosed if unilateral
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Treatment: transnasal or transpalatal resection of posterior obstructive tissues
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Adenotonsillar disease
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Most common cause of obstructive sleep apnea (OSA) in children
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Diagnosed by direct visualization on exam and attended nocturnal polysomnogram
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Treatment: adenotonsillectomy adequately treats >80% of patients with pharyngeal airway obstruction
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Pharyngomalacia
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Poor pharyngeal muscle tone, results in collapse of tissues and obstruction with stertor
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Treatment: noninvasive positive pressure ventilation (continuous or bilevel)
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Glossoptosis/macroglossia (Figure 20-1)
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Tongue and tongue base obstruction of the airway
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Pierre-Robin’s sequence, Down’s syndrome, lingual tonsil hypertrophy, isolated micrognathia, Ludwig’s angina (anterior floor of mouth abscess)
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Treatment: alleviate obstruction by resection, advancement, or bypass (i.e., tracheotomy)
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Pharyngeal obstruction results primarily in sleep apnea symptoms
FIGURE 20-1
Glossoptosis causing upper airway obstruction. Note how the base of the tongue compresses the epiglottis against the posterior pharynx.


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