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Stridor
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Stridor
, Inspiratory Stridor, Biphasic Stridor
See Also
Pediatric Airway Obstruction Causes
Wheezing
Stertor
Definitions
Stridor
Audible, high pitched sound during respiration
Results from partial obstruction of the upper airway (
Larynx
, trachea) with luminal narrowing
Epidemiology
Most common in younger children
Airway diameter reduction of 25% results in a cross-sectional airway reduction of 50% (see above)
Pathophysiology
Turbulent air flow in a partially obstructed upper airway results in a high pitched sound
Location of obstruction determines inspiratory or biphasic timing
Obstruction above the glottis results in Inspiratory Stridor
Obstruction at or immediately below the glottis results in both inspiratory and expiratory Stridor (Biphasic Stridor)
A child's small airways are impacted most significantly by even relatively small partial obstructions (Poiseuille's Law)
Infant: Airway edema of 1 mm reduces a 2 mm radius airway to 1 mm
Resistance to flow increases by 16 fold (Resistance = 1/r^4)
Adult: Airway edema of 1 mm reduces a 5 mm radius airway to 4 mm
Resistance to flow increases by 2-4 fold
Airway Radius By Age at Cricoid Cartilage
Age 0 to 1 year: 3 mm
Age 1 to 2 years: 3.75 mm
Age 2 to 4 years: 4 mm
Age 4 to 5 years: 4.5 mm
Precautions
See
Awake Nasotracheal Intubation
Maintain airway and consider differential diagnosis
Stridor becomes more quiet as airway narrowing becomes severe
Ready all airway management equipment (RSI, intubation, failed airway)
Do not distress a child with suspected partial airway obstruction (e.g. croup)
Avoid unnecessary procedures (e.g. delay
Intravenous Access
until stable)
Position child as they are most comfortable
History
Pediatric
Past Medical History
Prenatal and birth history (e.g. prematurity)
Immunization
history (e.g.
DTaP
, HIB,
Prevnar
)
Gene
tic disorders
Down Syndrome
(supraglottic stenosis)
VATER Syndrome or VACERTL Syndrome (
Tracheomalacia
, tracheoesophageal fistula)
Pallister-Hall Syndrome (laryngeal cleft)
CHARGE Syndrome
(
Cranial Nerve
palsy)
Medical history
Surgical history
Prior intubations
History of Present Illness
Stridor and associated respiratory symptom history (e.g. onset, frequency, progression, recurrence)
Recent illness (e.g.
Upper Respiratory Infection
, fever, cough or congestion)
Contagious contacts
Possible foreign body exposures
Exam
Precautions
Avoid agitating patient (best respiratory effort is when patient is calm)
Involve parent with calming measures (e.g. exam in parent's lap)
Monitoring
Full
Vital Sign
s including
Respiratory Rate
,
Temperature
Pulse Oximetry
End-Tidal CO2
(if hypercapnea suspected)
Stridor
Timing during inspiration, expiration or both (Biphasic Stridor)
Respiratory Distress
Nasal flaring
Intercostal retractions
Accessory
Muscle
use
Tachypnea
Grunting
Tripod positioning
Cardiopulmonary decompensation
Cyanosis
Hypoxia
Altered Mental Status
Head and Neck
Micrognathia
Cutaneous
Hemangioma
s
Neck Mass
es including lymphatic malformations
Imaging
Soft Tissue Neck XRay (including lateral neck) Findings
Steeple sign (croup)
Thumbprint (
Epiglottitis
)
Wide retropharyngeal space (retropharyngeal space)
Chest XRay
Findings
Radiopaque Foreign Body
Subglottic cyst
Tracheal stenosis
CT Neck or
Chest
Avoid in
Unstable Patient
s (ensure stable airway)
Avoid in young patients (see
CT-associated Radiation Exposure
)
Evaluate for masses, abscess, foreign bodies
MRI (stable patients)
Vascular abnormalities
Causes
By Age
Age <1 year (infants)
Laryngomalacia
(60%)
Croup
Vocal Cord Paralysis
Subglottic Stenosis
Airway
Hemangioma
Vascular Ring
s or slings
Age 1-3 years (toddlers)
Croup
Retropharyngeal Abscess
Epiglottitis
Foreign Body Aspiration
Age 4-18 years
Peritonsillar Abscess
Vocal Cord Dysfunction
Anaphylaxis
Hereditary Angioedema
Causes
Congenital
Choanal Atresia
Maxillofacial dysplasia
Vascular anomalies (e.g.
Vascular Ring
)
Laryngeal or tracheal abnormalities
Laryngomalacia
Tracheomalacia
Bronchomalacia
Subglottic Stenosis
(esp. post-intubation)
Causes
Inflammatory or Infectious
See
Pediatric Airway Obstruction Causes
Laryngotracheal Bronchitis
(
Croup
)
Epiglottitis
Bacterial Tracheitis
Tonsillitis
Diphtheria
Oropharyngeal deep space infection
Peritonsillar Abscess
Retropharyngeal Abscess
Causes
Neoplasm
Airway Papilloma
Airway
Hemangioma
(subglottic
Hemangioma
)
Causes
Neurogenic
Vocal Cord Paralysis
Vocal Cord Dysfunction
Aspiration
Causes
Trauma
Foreign Body Aspiration
Facial Fracture
Mandibular
Fracture
Laryngeal Fracture
Subglottic Stenosis
Causes
Allergy
Spasmodic Croup
Angioneurotic edema
Management
Do not distress a patient with Stridor (risk of worsening obstruction, see precautions above)
Avoid painful procedures, until immediate
Advanced Airway
management is available if needed
Emergent management
See
Rapid Cardiopulmonary Asessment in Children
See
ABC Management
See
Emergency Airway Management
See
Advanced Airway
See
Respiratory Distress in the Newborn
See
Newborn Resuscitation
Consult otolaryngology or
Anesthesia
emergently as needed
Advanced Airway
Indications
Severe Stridor (esp. quiet Stridor, rapid onset)
Persistent refractory respiratory distress or
Hypoxia
Precautions
Use an
Endotracheal Tube
that is 1-2 sizes smaller than estimated for size
Most experienced in
Advanced Airway
should perform procedure
Ideally perform in controlled environment (e.g. OR) by otolaryngology or anesthesiology
Evaluate and treat specific conditions
See
Croup
See
Laryngeal Foreign Body
See
Angioedema
Awake
Fiber
optic
Nasolaryngoscopy
May identify Stridor source
References
Dahan, Campbell and Melville (2020) Crit Dec Emerg Med 34(11): 3-10
Mehta and Eliason (2024) Crit Dec Emerg Med 38(6): 27-35
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