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Airway obstruction

Last updated: April 14, 2025

Summarytoggle arrow icon

An upper airway or central airway obstruction can be rapidly fatal. Stridor is a common clinical feature of airway obstruction and is a red flag for respiratory failure and difficult airway management. Patients with respiratory distress or signs of respiratory failure require immediate airway management, respiratory support, and/or treatment of rapidly reversible causes of airway obstruction. Upper airway obstruction is often managed with endotracheal intubation. Central airway obstruction may require rigid bronchoscopy, flexible bronchoscopy, and/or endobronchial intubation. Advanced evaluation and diagnostic testing are done only after securing the airway and/or excluding life-threatening causes of airway obstruction. Airway obstruction may be caused by infectious, inflammatory, or structural changes in the airway and/or neuromuscular conditions that reduce airway patency. Airway obstruction is diagnosed clinically, but airway endoscopy and imaging may be necessary to determine the specific etiology. Definitive treatment is based on the underlying cause.

Distal airway obstruction involving bronchioles and/or alveoli usually manifests with wheezing, and the causes and progression vary from those of upper and central airway obstruction. The approach and management of wheezing are discussed separately.

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Definitionstoggle arrow icon

Upper airway [1][2]

Lower airway [1][2][3][4]

Definitions of the beginning of the lower airway vary and range from the epiglottis to the distal larynx. The central airway begins with the trachea.

Central airway [3]

Obstruction of the upper airway or central airway is a medical emergency that can cause respiratory failure and death.

Distal airway [5]

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Initial managementtoggle arrow icon

Stridor is a risk factor for a difficult airway.

Avoid unnecessary procedures that may increase agitation and worsen turbulent airflow, especially in children. [6]

Consider transporting stable patients to the operating room for intubation.

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Etiologytoggle arrow icon

Use age to help narrow potential diagnoses. Laryngomalacia and vocal fold immobility (e.g., vocal cord paralysis) are common in infants; foreign body aspiration and croup are common in young children. [7]

Infectious [4][6]

Acute

Chronic

Allergic or inflammatory [4][6]

Acute

Chronic

Structural [6]

Acute

Chronic

Neuromuscular impairment

Systemic conditions that impair airway protective reflexes may also decrease airway patency.

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Clinical featurestoggle arrow icon

Clinical features of partial airway obstruction [8]

Clinical features of complete airway obstruction [8]

Clinical features of central airway obstruction [3][4]

Central airway obstruction is easy to misdiagnose because it is less common than other lower airway diseases (e.g., asthma) but has similar clinical features. [4]

Stridor [9]

Stridor is a harsh, high-pitched vibratory breath sound produced by upper airway obstruction.

Although stridor is a key clinical feature of airway obstruction, it does not always occur.

Stertor [10][11]

Wheezing

Differentiating wheezing from expiratory stridor is difficult. Wheezing is a musical sound produced primarily during expiration, whereas expiratory stridor is typically a single harsh, high-pitched expiratory sound. [12]

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Clinical evaluationtoggle arrow icon

A focused history and physical examination can narrow potential diagnoses and facilitate the choice of diagnostic testing. [6][9]

Focused history

Focused physical examination

Do not assume decreasing stridor is a reassuring sign. Respiratory failure due to decreased airflow may be imminent. [10]

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Diagnosistoggle arrow icon

Airway obstruction is diagnosed clinically; the suspected etiology and the patient's clinical status guide the choice of diagnostic testing. [9][10]

Airway endoscopy

Direct visualization of the airway can provide a definitive diagnosis. Endoscopy may also be used for definitive management (e.g., removal of a foreign body or excision of an airway mass).

Perform a diagnostic bronchoscopy in all patients with symptomatic central airway obstruction. [13]

Imaging [6][9]

Imaging can be helpful to assess for anatomical abnormalities, foreign bodies, or infection (e.g., abscesses).

A CT should be obtained in all patients with suspected central airway obstruction. [3][4][13]

Ensure the airway is protected or an airway specialist is immediately available when obtaining imaging. Sedation and/or supine position may cause complete airway obstruction. [6]

Laboratory studies [6][14]

Routine testing is not recommended for airway obstruction, but studies may confirm the etiology and guide management.

Pulmonary function testing (PFTs) [3][4]

Do not obtain spirometry and PFTs in patients with respiratory distress or advanced disease; these tests may lead to acute respiratory failure. [3]

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Infectious causestoggle arrow icon

Infectious causes of airway obstruction [10]
Etiology Cause Characteristic clinical features Diagnostics Management

Croup [14]

  • Onset: 12–48 hours
  • Appearance: well-appearing
  • Cough: barking
  • Voice: hoarse
  • Difficulty swallowing/drooling: absent
Epiglottitis [15]
Diphtheria [6][16]
Bacterial tracheitis [6][17]
Retropharyngeal abscess [15]
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Allergic or inflammatory causestoggle arrow icon

Allergic or inflammatory causes of airway obstruction [10]
Etiology Characteristic clinical features Diagnostics Management
Spasmodic croup [18]
  • Barking cough
  • Hoarse voice
  • Nightly symptoms that resolve during the day

Angioedema [19]

Anaphylaxis [20]
Inhalation injury [21][22]
Autoimmune disease [4]
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Structural causestoggle arrow icon

Acquired

Acquired structural causes of airway obstruction [10]
Etiology Characteristic clinical features Diagnostics Management
FBA [6][23]
Blood, vomit, and/or liquid aspiration [24][25]
Tumor
OSA [26]
Postextubation laryngeal edema [27][28]
Laryngotracheal stenosis [29][30]

Congenital

Congenital structural causes of airway obstruction
Distinguishing clinical features Diagnosis Management
Airway malacias [31]
Syndromes with craniofacial abnormalities
Congenital macroglossia
  • Clinical evaluation
  • Imaging for underlying causes
Choanal atresia
  • Failure of nasal catheter passage
  • CT scan of nasal passages
Mass
  • Clinical evaluation
  • Head and neck imaging (e.g., CT, MRI)
  • Chest imaging (e.g., CT, MRI)
Vascular ring
  • Stridor
  • Feeding difficulty
  • Persistent respiratory symptoms
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Neuromuscular causestoggle arrow icon

Neuromuscular causes of airway obstruction [10]
Etiology Characteristic clinical features Diagnostics Management
AMS and coma
Neuromuscular weakness involving the airway

Laryngospasm [32]

Vocal cord paralysis [33][34]
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Acute management checklist for airway obstructiontoggle arrow icon

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Dispositiontoggle arrow icon

Disposition is based on etiology and severity of symptoms. Consider admission for patients with: [6][10]

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Treatmenttoggle arrow icon

Follow the initial management of airway obstruction for all patients. Further management is based on the specific cause of the obstruction.

Upper airway obstruction treatment [1]

Complete airway obstruction can recur immediately after endotracheal tube removal. Be prepared for reintubation when extubating patients with airway obstruction.

Central airway obstruction treatment [3][4][13]

Therapeutic bronchoscopy

Surgery

  • Tumor resection
  • Resection of the stenotic portion of the airway

Adjunct treatment

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