Continuing Education Activity
Upper airway obstruction is defined as occlusion or narrowing of the airways leading to compromise in ventilation. Obstruction can vary from acute to chronic, from congenital to acquired, and in many cases, can be fatal if left untreated. This activity examines the etiology, assessment, treatment, management, and patient education pertaining to upper airway obstruction.
- Identify the etiology of upper airway obstruction.
- Review signs and symptoms that would indicate emergent intervention for upper airway obstruction.
- Outline the treatment and management options available for upper airway obstruction
- SUmmarize interprofessional team strategies for improving care coordination and communication to advance diagnosis and treatment of upper airway obstruction and improve outcomes.
The upper airway consists of the nasal cavities, oral cavity, pharynx, and larynx. The pharynx is further subdivided into the nasopharynx, oropharynx, and hypopharynx. The larynx is divided into three regions, dependent on their relationship to the vocal cords (glottis). These areas are the supraglottis, glottis, and subglottis. The supraglottis consists of the epiglottis, the arytenoids, the aryepiglottic folds, the false cords, and the ventricles. The subglottis is the subregion just below the free edge of the vocal cords to the inferior margin of the cricoid. The narrowest part of an adult airway is the glottis. The narrowest part of a pediatric airway is the cricoid. Upper airway obstruction varies from narrowing to partial or complete occlusion of any of these anatomic structures, potentially leading to a compromise in ventilation. Given the urgency related to this issue, it is crucial that healthcare professionals fully understand and appreciate the signs and symptoms that indicate upper airway obstruction.
When forming a differential diagnosis for upper airway obstruction, it is important to determine the level at which the obstruction is occurring. A vital clinical sign is noisy breathing, which can be described as 'stertor' or 'stridor'. ‘Stertor’ is noisy breathing which occurs above the larynx. ‘Stridor’ is noisy breathing that occurs at the level of the larynx or below. Stridor can be further subdivided as inspiratory (level of the supraglottis), expiratory (level of the glottis), and biphasic (level of the subglottis or trachea).
Upper airway obstruction can be partial or complete. A partial obstruction can be chronic or acute, therefore it is crucial to take a good history and perform an efficient and comprehensive exam to determine the etiology of the obstruction and therefore the urgency of subsequent management. Left untreated, upper airway obstruction can have significant long-term or fatal effects.
It helps classify the causes of upper airway obstruction by the type of noisy breathing they can cause, i.e., stertor or stridor.
A blockage can cause stertor at the level of the oral or nasal cavities or the level of the oropharynx or nasopharynx. Causes of a blockage at this level can be classified as congenital or acquired. Congenital causes of the nasal cavity or nasopharyngeal airway obstruction can cause symptoms soon after birth. Neonatal anatomy dictates that newborns are obligate nasal breathers for the first few months of life. This ensures that they can breathe and feed simultaneously. Pyriform aperture stenosis and bilateral choanal atresia are rare but important causes of upper airway obstruction at this level.
Bilateral choanal atresia will cause immediate upper airway obstruction and distress at birth, which is relieved by crying, as this facilitates breathing via the oral cavity. Acquired causes of nasal or nasopharyngeal obstruction include nasal turbinate hypertrophy secondary to allergic rhinitis, nasal polyposis, and nasal foreign bodies, septal deviation, or adenoidal hypertrophy. Congenital causes of upper airway obstruction at the level of the oral cavity include retrognathia (either isolated or associated with Pierre Robin Sequence), glossoptosis, macroglossia, and lymphovascular malformation. Acquired causes at this level include angioedema, Ludwig angina (floor of mouth abscess secondary to dental infection), oral cavity or oropharyngeal cancer (squamous cell carcinoma most common, also consider lymphoma of tonsils), tonsillar hypertrophy, and parapharyngeal/retropharyngeal/peri-tonsillar abscess. Potential traumatic causes include penetrating neck injury, burns, or caustic injury, all of which can cause edema.
A very common cause of stertor in children is adenotonsillar hypertrophy. This can lead to obstructive sleep apnea (OSA). Symptoms of OSA in children include snoring/stertor, frequent night awakenings, hyperactivity, poor concentration in school, and enuresis. It is important to perform sleep studies in children with a history suggestive of obstructive sleep apnea and concurrent craniofacial abnormalities or complex medical histories to determine the severity of their OSA. In a sleep study, apnea and hypopnea events are recorded. These are reported as the 'Apnea-Hypopnea Index' (AHI). The AHI correlates to the sum of the number of apneas and hypopneas per hour during sleep. Apnea is defined as the cessation of airflow for greater than or equal to ten seconds, and hypopnea is classified as a reduction in respiratory effort with greater than 4% oxygen desaturation. A sleep study result showing an apnea-hypopnea index above one is abnormal in a child.
Adults also experience OSA. However, OSA in adults has a different grading system for severity. Less than five events in an hour are normal, five to fifteen demonstrates mild sleep apnea, fifteen to thirty events correlate with moderate OSA, and anything above thirty is severe.
Stridor is a high-pitched sound associated with obstruction at the level of the larynx. Congenital causes include laryngomalacia, unilateral or bilateral vocal cord palsy, laryngeal web, subglottic stenosis, subglottic hemangioma, or tracheomalacia. Acquired causes in childhood include recurrent respiratory papillomatosis (RRP), vocal cord palsy, subglottic stenosis secondary to intubation, epiglottitis, tracheobronchitis/croup, and inhaled foreign body. It is worth noting that subglottic stenosis or subglottic hemangioma can present like croup, as they both can cause a ‘barking cough.’ It is common for patients with these causes of stridor to be treated on multiple occasions in the Emergency Department prior to being referred to an otorhinolaryngologist or pulmonologist for further evaluation. Such evaluation includes direct micro laryngoscopy and bronchoscopy.
Colloquially known as "choking," foreign body aspiration is an emergency that is more frequently encountered in children than in adults. Commonly aspirated materials in children include peanuts, buttons, and beads. One study showed that the majority of inhaled foreign bodies amongst their cohort were organic material. Objects such as button batteries are especially dangerous, causing not only airway obstruction but also caustic injury.
Laryngomalacia is a common but usually not life-threatening form of upper airway obstruction affecting mostly neonates and can become evident within the first year of life. It is due to a relative immaturity and laxity of the laryngeal framework, which improves over time as the child grows. Laryngomalacia causes high-pitched inspiratory stridor and can be associated with feeding difficulties and failure to thrive.
Stridor in adults is usually worrying, as it can be a sign of laryngeal cancer. Adults with sudden onset stridor should be evaluated urgently, as it may signify a rapidly progressing airway emergency. Other causes of stridor in an adult include infectious causes such as epiglottitis or supraglottis, which may be caused by bacteria, fungi, or mycobacteria. Unusual causes of stridor in an adult include immunologic and auto-immune diseases such as Behcet’s disease, granulomatous polyangiitis, sarcoidosis, and amyloidosis. Acquired subglottic stenosis following prolonged intubation or trauma is also worth considering, especially in the case of biphasic stridor.
Bilateral vocal cord palsy is an uncommon but recognized cause of stridor. Airway burns are important causes of upper airway edema and inflammation, which may cause upper airway obstruction. Any patient following exposure to the fumes from a fire should be assessed, and anyone with singed nasal hairs and edema of the oral cavity should have a flexible nasendoscopy where possible and may need emergency intubation.
External compression of the trachea can occur as a congenital or acquired process. Some neonates are born with a vascular ring or aortic anomalies causing tracheal compression. In adults, a slow-growing thyroid goiter can cause tracheal compression, as can other cancers of the head and neck might impinge the larynx or trachea.
Epidemiology for upper airway obstruction varies as much as the etiological causes of this disorder varies. The following are a few of the most common causes of upper airway obstruction, and their respective statistics.
Visits to Emergency Departments for choking incidents in children were studied by the Centers for Disease Control and Prevention (CDC) in 2000. They reported that 160 children aged 14 years or less died of choking incidents. The number of visits for non-fatal choking incidents was around 17,537 that year.
It is widely recognized that surgery for adenotonsillar hypertrophy is a common procedure. Quoted rates for these procedures vary from country to country and have been documented as anywhere between 19 per 10,000 children and 118 per 10,000 children. In adults, obstructive sleep apnea has been reported as affecting 26% of the adult population of the United States.
Head and neck cancers account for in excess of 650,000 cases and 330,000 deaths each year worldwide. Head and Neck cancer accounts for 3% of all malignancies recorded in the United States. Men are more often affected than women, at a rate of 2 to 1 versus 4 to 1.
When considering the pathophysiology of upper airway obstruction, it is imperative to understand the variations between adult and pediatric upper airway anatomy. Children have larger heads and a larger occiput, causing hyperflexion of the airway when lying flat and supine.
Children also have a larger tongue and smaller mandible compared with adults. Their epiglottis is floppy and can obscure the view of the larynx on laryngoscopy at intubation. A pediatric larynx sits higher than in adults and is shaped like a funnel. The cricoid is at C4 level at birth, dropping eventually to the C6 level at around age ten. Therefore, a cricothyroidotomy is not a viable procedure in a child younger than 10. Also, pediatric supraglottic cartilages are softer and more distensible than that of adults, leading at times to dynamic collapse, which is seen in laryngomalacia. It is crucial to remember also that babies are obligate nasal breathers from birth for the first few months of life. In terms of the lower airway physiology, children consume more oxygen at rest than adults, as their resting metabolic demand is 2 to 3 times that of an adult. They also have a lower functional residual capacity, which translates to a more precipitous onset of hypoxemia and hypercarbia during apnea.
Due to Poseuille’s Law, a small decrease in the diameter of a child’s airway can have a devastating effect. This can be caused by edema, stenosis, foreign body, or even mucus. Babies from 36 weeks onwards have mature alveoli; however, these continue to develop with septation and microvascular maturation from birth until around 8 years of age. Therefore, the surface area for gas exchange is less in pediatric patients.
The most narrow region of the adult airway is at the level of the glottis. Given that the most common cause of upper airway obstruction in adults is OSA, it is important to understand the physiologic processes involved in this presentation. These patients are often obese. They usually have an element of pharyngeal collapse, which can also be associated with retrognathia and underlying conditions such as hypertension and diabetes mellitus.
History and Physical
In children, a history will need to be elicited from a parent or primary caregiver. For example, OSA questions will be addressed to the adult accompanying the child and focus on inquiries involving a history of snoring with apneic episodes and either tiredness or hyperactivity the following day. Children with OSA due to adenotonsillar hypertrophy are described as ‘mouth-breathers’ by parents. As previously mentioned, children can have various symptoms suggestive of OSA, such as hyperactivity and enuresis.
For adults with OSA, history can be slightly different. These patients complain of frequently waking at night and feeling unrefreshed the next day despite having spent the full night in bed. They often have a high BMI and complain of hypersomnolence. Their cohabitants will often complain that they snore.
It is crucial to identify a patient with acute upper airway obstruction. Respiratory distress can quickly lead to respiratory failure without appropriate management. An urgent and comprehensive assessment of ABC’s (airway, breathing, and circulation) must be performed while also ensuring the patient is in a safe environment. Approaches differ depending on the patient's presentation.
Every effort should be made to complete an efficient ENT examination in patients at risk of upper airway obstruction, where safe and possible. Often, history and examination can take place simultaneously.
As with all patients, a general examination of body habitus, facial features (paying close attention to any syndromic features), and respiratory effort should take place as part of the comprehensive exam. Mental status should be noted. Any signs of tobacco use or signs of drug or alcohol intoxication or dependence should be assessed.
Children in respiratory distress may show increased work of breathing via the use of accessory muscles. They also can present with nasal flaring, tracheal tug, intercostal and subcostal recession, and grunting. If respiratory failure is reached, there is shallow breathing, bradycardia, and altered mental status. It is worth noting that altered mental status in an infant often presents as listlessness. Stranger anxiety is a normal developmental sign in babies aged 9 - 18 months, and the absence of this behavior is a worrying sign in a sick child. It is also very worrying if a small child does not resist some elements of examination and treatment, such as placement of a needle or intravenous cannula. A particular case of critical upper airway obstruction in children can occur as a result of epiglottitis. In suspected epiglottitis of a child, they will classically present with a short history of sore throat, with a muffled voice, and drooling. In advanced cases, the patient may be in the tripod position, which is a body placement that stents the upper airway open. If epiglottitis is the likely diagnosis, there should be no attempt to examine the oropharynx, as it may upset the child and cause devastating laryngospasm.
Tachypnea and a feeling of shortness of breath, including failure to complete sentences, can signal respiratory distress in adults. In recurrent respiratory papillomatosis, an adult may present with chronic dysphonia and shortness of breath, which may progress to stridor. They may present with acute respiratory distress; however, in this scenario, they will have acute on chronic symptoms.
It is important to assess for septal deviation, hypertrophy of the nasal turbinates, or nasal polyposis during anterior rhinoscopy. A quick test to prove choanal patency can be performed by asking the patient to exhale nasally onto a cold metal spatula (‘nasal misting test’).
The oral cavity should also be thoroughly examined, paying close attention to any signs of micrognathia, edema of the lips, trismus, floor of mouth or tongue edema, tumor or palatal fullness with uvular deviation, as in the case of a peri-tonsillar abscess.
A cardiorespiratory examination should take place when appropriate. Basic vital signs, i.e., pulse, respiratory rate, blood pressure, and O2 saturation, should occur initially as part of the ABCs of assessment. Any noisy breathing and quality of the breathing, including dysphonia, should be noted.
Following a basic history and exam, some investigations are necessary to diagnose the common and urgent causes of upper airway obstruction.
No comprehensive ENT examination is complete without flexible nasendoscopy/ laryngoscopy to assess the pharynx and larynx dynamically. This can help diagnose turbinate inflammation, septal deviation, adenoidal hypertrophy, Waldeyer’s ring hypertrophy, or laryngeal/hypopharyngeal pathology. It is particularly useful when assessing the dynamic function of the larynx. A dynamic assessment is essential when assessing vocal cord movement and relatively common conditions affecting the larynx, such as laryngomalacia in children. It can also diagnose a laryngeal tumor in adults.
Oxygen saturations are an essential first step in assessing a patient with airway obstruction, as it can act as a marker for the severity of their obstruction.
Imaging studies help delineate the affected anatomical area and can also aid in the diagnosis of the cause of obstruction. Ultrasound or MRI are the imaging modalities of choice in children, as they do not involve radiation. However, a general anesthetic is usually needed for a young child to tolerate an MRI. Therefore CT is used in situations that are time-sensitive or in cases that may need surgical intervention, such as a retropharyngeal abscess or a possible inhaled foreign body. If a child with a possible inhaled foreign body is stable, inspiratory, and expiratory, chest radiographs can aid in diagnosis. For example, if there is a foreign body partially obstructing the left main bronchus, there may be hyperlucency of the left lung due to hyperinflation secondary to the ball-valve effect of the foreign body.
To formally assess OSA, a sleep study or polysomnography should be performed. The important results of a sleep study are the patient’s oxygen nadir and the apnea-hypopnea index (AHI). The AHI averages the number of apneic and hypopneic episodes that occur per hour. An AHI of anything above 1 is abnormal in a child, and there is a grading system of severity for increasing numbers of AHI in adults.
Treatment / Management
As mentioned, the initial step in airway obstruction management is ‘ABC,’ i.e., Airway, Breathing, Circulation. An oxygen saturation monitor should be placed, and oxygen by mask should be initiated. In a stable patient in the acute setting, there may be time to perform imaging studies, initiate antibiotic treatment, etc. In the unstable patient in the acute setting, it is crucial to efficiently assess the patient while also taking a quick history/collateral history. Outside the hospital setting, an ambulance should be called. If choking is suspected, the Heimlich maneuver should be performed. In the unconscious patient's case, a pulse check should be performed, and the patient managed as per Basic Life Support Protocols (BLS) while waiting for an ambulance. In the case of acute airway obstruction in a hospital setting, a code should be called, and the Airway Team and the Medical Team involved in the management of cardiorespiratory arrest should be called immediately. The nearest healthcare professionals should initiate the BLS algorithm.
Pediatric Inhaled Foreign Body
In the case of suspected inhaled foreign body in children, if the child is in respiratory distress and is unstable, the patient should be moved to the Operating Room (OR) immediately, and the most senior Pediatric ENT and Anesthesiology team members should be involved as soon as possible. A direct microlaryngoscopy and bronchoscopy should be performed to remove the foreign body. The child should be placed supine with a shoulder roll to aid in the extension of the neck. Inhaled Sevoflurane and oxygen can be used for the induction and maintenance of general anesthesia. It is usually preferable to maintain spontaneous respiration. Occasionally, teams will use total intravenous anesthesia (TIVA) to maintain anesthesia. In this case, propofol with or without remifentanil is used for good airway reflex suppression and quick emergence from anesthesia. Once asleep, a tooth guard or moist gauze (if the patient has no teeth) is used, and a laryngoscope is inserted for a view of the larynx. Lidocaine is sprayed on the vocal cords (e.g., 4% lidocaine is 0.1 ml per kg). An appropriately sized bronchoscope with a zero degree Hopkin’s rod endoscope is inserted to view the trachea. If a foreign body is found, optical grasping forceps can be used for retrieval.
Management of Acute Upper Airway Obstruction in Adults
Awake Fibreoptic Intubation
In adults, there will often be different presentations requiring intervention. In the case of upper airway obstruction at the level of the oral cavity or oropharynx, it is important to secure an airway if impending airway obstruction is anticipated. For example, in the case of Ludwig’s angina, i.e., a bacterial infection of the oral cavity, causing tongue and floor of mouth edema, it may be possible to perform awake fibreoptic intubation. In this scenario, the providing physician slides an endotracheal tube (ETT) onto a flexible endoscope. The nose is decongested, and the scope is passed to the level of the glottis while the patient is sitting upright. Lidocaine is inserted through the side port of the scope and onto the cords to anesthetize them to avoid laryngospasm. When this has worked, the scope is passed through the level of the vocal cords, and the ETT is then pushed down past the cords using the Seldinger technique. The patient is then given a general anesthetic, and the dental abscess is drained. The patient will likely need to be sedated for one to two days to allow the edema to settle prior to pulling the ETT.
In such cases where intubation would be considered difficult or impossible, a cricothyroidotomy is a very quick procedure that can be performed in adults in cases of a true emergency. While the patient is lying supine, the operator holds the larynx in place, makes a vertical incision between the thyroid and cricoid cartilage, and inserts a blunt instrument such as a hemostat through the cricothyroid membrane. This takes some force. It is helpful to insert a bougie with a lumen at this point and then railroad a small, i.e., size six, ETT over this to secure the airway.
Tracheostomy is sometimes necessary in upper airway obstruction cases where intubation is anticipated to be very difficult or impossible. This can be performed under local anesthetic. If time allows, it should be performed in the OR with experienced staff and with anesthesiology involved. Before the procedure, it is helpful to administer at least 5 to 10 ml of nebulized 1% Lidocaine. In the OR, the patient should have oxygen via face mask or nasal prongs and be comfortable in a supine position, or sometimes semi-recumbent if in respiratory distress. Occasionally the anesthesiologist may administer medication, for example, ketamine, to reduce anxiety without suppressing the respiratory drive. A solution of 1% lidocaine can be injected directly into the larynx via the cricothyroid membrane, and position in the airway can be confirmed by drawing air back into the syringe before injecting. A tracheostomy is then performed under local anesthesia using the usual steps.
Management of Chronic Upper Airway Obstruction in Adults
A common cause of upper airway obstruction in adults is OSA. Aside from lifestyle modifications such as weight loss, Continuous Positive Airway Pressure (CPAP) is used to manage this condition. It has been found that nasal Positive Airway Pressure masks are more easily tolerated than orofacial masks. The use of a nasal mask can be affected by structural ENT changes such as septal deviation and inferior turbinate hypertrophy, sometimes leading to surgery to correct these obstructions. In patients with mild to moderate OSA who have difficulty adhering to CPAP therapy, alternative therapies such as oral devices can be considered. These devices either advance the mandible (i.e., mandibular repositioning splints) or position the tongue more anteriorly (i.e., tongue retaining devices). These types of appliances effectively project soft tissue anteriorly off the posterior pharyngeal wall and improve airway patency. Another such device is a hypoglossal nerve stimulator, which can sometimes be used as an adjunct in patients with moderate to severe OSA who have struggled with CPAP use.
Surgery is reserved for patients who have failed CPAP therapy and who have a treatable cause of obstruction, or as an adjunct to CPAP therapy. Occasionally, as in the case of children with adenotonsillar hypertrophy, surgery can be the primary treatment. Nasal surgeries, including septoplasty and inferior turbinate reduction, have been shown to improve CPAP tolerance in some studies compared with no surgical intervention for nasal obstruction. Uvulopalatoplasty is the most commonly performed procedure for OSA. This involves tonsillectomy if tonsils are present, shortening and tightening the soft palate, and sometimes reducing or resectioning the uvula. However, it has been shown to be successful in treating OSA in fewer than 50% of patients and is more likely to be successful in patients with mild OSA.
OSA in children is most commonly caused by adenotonsillar hypertrophy, for which surgery is performed to reduce the bulk of tonsillar and adenoidal tissue. It has been documented that a history of sleep-disordered breathing in the setting of enlarged tonsils and adenoids has resulted in adenotonsillar reduction surgery on almost the same frequency as for recurrent infections.
Congenital causes of upper airway obstruction include craniofacial syndromes that cause midfacial hypoplasia, such as Apert and Crouzon syndromes. Pierre Robin Sequence and any other conditions causing micrognathia or retrognathia can cause upper airway obstruction. Rare causes of congenital upper airway obstruction include bilateral choanal atresia or lymphovascular malformation of the tongue or neck. Congenital subglottic stenosis is rare; however, it can occur, especially in babies with Trisomy 21. Congenital laryngeal web is a very rare but important cause of upper airway obstruction in neonates.
Acquired acute pediatric causes of upper airway obstruction commonly include infectious causes such as neck abscesses or croup. An inhaled foreign body is an uncommon but important cause of acute upper airway obstruction. Less common, but worth mentioning, are burns or caustic injury to the upper airway.
The most common cause of chronic upper airway obstruction in children is adenotonsillar hypertrophy. In terms of laryngeal pathology, bilateral vocal cord palsy, subglottic hemangioma or stenosis, or recurrent respiratory papillomatosis should be considered. Acquired subglottic stenosis is possible if the child has had previous intubation, or most commonly following prolonged or repeated intubations.
In the acute setting of upper airway obstruction in adults, infectious causes are many. Ludwig’s angina, i.e., the floor of mouth bacterial infection secondary to dental infection, can cause trismus and severe edema of the tongue, which is an airway emergency. Peri-tonsillar abscess and parapharyngeal abscesses are important differentials for trismus and sore throat. Supraglottitits can also occur in adults. Recurrent respiratory papillomatosis can cause acute on chronic upper airway in adults. Laryngeal cancer can present acutely with stridor and respiratory distress. Advanced untreated cancer of the oral cavity, oropharynx, or hypopharynx also poses a risk of upper airway obstruction.
The most common cause of chronic upper airway obstruction in adults is OSA. Less common but potential causes of laryngeal pathology and subsequent airway compromise are tuberculosis, sarcoidosis, granulomatosis with polyangiitis, and Behcet disease. Acquired causes of nasal or nasopharyngeal obstruction include nasal turbinate hypertrophy secondary to allergic rhinitis, nasal polyposis and nasal foreign bodies, septal deviation, or adenoidal hypertrophy.
In the acute setting, untreated upper airway obstruction causing respiratory distress can lead to respiratory failure, and ultimately cardiorespiratory arrest. Obstructive sleep apnea is the most common chronic cause of upper airway obstruction. In children, the possible consequences of untreated OSA include failure to thrive, behavioral problems such as hyperactivity, poor performance in school, and cardiovascular disease. In adults, untreated OSA can cause impaired daytime function, including somnolence, metabolic dysfunction, and an increased risk of cardiovascular disease.
If acute upper airway obstruction goes untreated, it can result in respiratory distress, which causes bradycardia and tiring of the patient, ultimately leading to loss of consciousness and cardiorespiratory arrest. If upper airway obstruction is due to foreign body aspiration, it can be acutely fatal. Smaller size foreign body can enter the lungs causing atelectasis, pneumonia, or pneumothorax.
It is important to recognize the potential complications of the most common cause of upper airway obstruction, which is OSA. Untreated OSA in children can cause cor pulmonale. Untreated OSA in adults can result in heart disease, metabolic syndrome, impaired daytime function, somnolence, metabolic dysfunction, and an increased risk of cardiovascular disease or even car accidents.
The treatment goals are to reduce side effects from OSA, improve sleep quality, and reduce the apnea-hypopnea index (AHI). This often takes a multi-disciplinary approach, frequently led by Pulmonology. Once diagnosed, first-line treatment involves weight loss and positive airway pressure use at night. Compared to no treatment, positive airway pressure such as CPAP has significantly improved disease severity, daytime somnolence, blood pressure, and motor vehicle accidents.
Specialists well-trained in airway intervention and intubation, particularly otolaryngologists, anesthesiologists, and pulmonologists, should be notified quickly in cases of impending airway demise. In acute settings, a pulmonologist can perform a flexible bronchoscopy in a child with an inhaled foreign body, which is in a distal bronchus. Moreover, rigid equipment regularly utilized by otorhinolaryngologists is very effective for more proximal foreign bodies. Cardiothoracic surgeons can also become involved in these cases where removing the foreign body via the airway is difficult, as the patient may require a thoracotomy if the foreign body is in a distal airway and cannot be removed endoscopically.
Deterrence and Patient Education
It has been shown in some studies that the majority of inhaled foreign bodies in children are organic material. In such cases, it is common that the child was eating and walking simultaneously, which carries a higher risk of food aspiration. It is important to counsel parents that children should eat while sitting down. It is also essential to closely monitor small children while they play with toys. Toys should be age-appropriate, and care should be taken to avoid easy access to small parts that may be inhaled.
Mouthing behavior is common in small babies up to 2 years of age, and care should be taken when monitoring them. Immediate recognition of an inhaled foreign body and early access to medical service is important by calling 911.
For adult patients with OSA, education about behavioral modification regarding weight loss, sleeping posture adjustment, and alcohol avoidance before bed should be practiced. The general public should also be made aware of the risk factors for the development of head and neck cancers, including smoking, excessive alcohol consumption, and HPV infection.
Enhancing Healthcare Team Outcomes
Since severe upper airway obstruction can cause death within minutes, a rapid and efficient approach is critical in suspected cases. Stridor should be recognizable by all staff, from respiratory therapists and nursing staff to physicians of all specialties. All Emergency Department and ward staff should be aware that it is imperative to contact the airway team on-call in the case of new-onset stridor in the setting of respiratory distress. In light of this, it is important for healthcare staff to regularly undergo Basic Life Support (BLS) training.