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Expiratory Wheezing
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Expiratory Wheezing
, Expiratory Wheeze, Wheeze, Wheezing
See Also
Stridor
Noisy Breathing
Pathophysiology
Airway wall fluttering results from flow limitation
Expiration typically occurs passively with elastic recoil of the chest wall
Obstruction to outflow requires active expulsion of air
Resulting positive intrapleural pressure worsens the obstruction
Wheezing is more common in children than adults
Inflammation of a child's smaller
Bronchi
has a greater impact on airway resistance
Obstruction is more likely in a child's airway due to less chest elastic recoil
A child's compliant airway walls collapse more easily under negative pressure
Causes
Infants
Acute
RSV or other
Bronchiolitis
(most common cause in infants)
Asthma Exacerbation
Other respiratory infection (
Acute Bronchitis
,
Pneumonia
)
Foreign Body Aspiration
(uncommon under age 1 year)
Chronic or Recurrent: Common
Asthma
Gastroesophageal Reflux
Chronic or Recurrent: Uncommon or Rare
Aspiration Pneumonitis
Anomalous innominate artery
Anomalous left common
Carotid Artery
Bronchopulmonary Dysplasia
Bronchomalacia
Choanal Atresia
Congenital Lobar
Emphysema
Congestive Heart Failure
Cystic Fibrosis
or ciliary
Dyskinesia
Double aortic arch
Diaphragmatic Hernia
Extrinsic compression by tumor (
Neuroblastoma
)
Hemosiderosis
Tracheal Stenosis
Tracheomalacia
Tracheoesophageal Fistula
Vascular Ring
Visceral larval migrans
Causes
Children and Adolescents
Acute
Asthma Exacerbation
(most common cause in children)
RSV or other
Bronchiolitis
Acute Bronchitis
Pneumonia
Foreign Body Aspiration
(uncommon after preschool age, if no
Developmental Delay
)
Chronic or Recurrent: Common
Asthma
Allergic Rhinitis
Gastroesophageal Reflux
disease
Obstructive Sleep Apnea
(adenoid hypertrophy, also with craniofacial abnormalities)
Chronic or Recurrent: Uncommon or rare
a1-antitrypsin Deficiency
Aspergillosis
Cystic Fibrosis
Ciliary Dysmotility Syndrome
Sarcoidosis
Tumors or
Lymph Node
compression
Vocal Cord Dysfunction
History
Onset
Onset as an infant: Congenital cause
Sudden onset:
Foreign Body Aspiration
Winter onset with upper respiratory symptoms and with cluster of cases
Respiratory Syncytial Virus
(fall to spring)
Croup
(fall and winter)
Human
Metapneumovirus
(winter to spring)
Pattern
Seasonal pattern
Asthma
Allergic Rhinitis
Persistent or recurrent respiratory illnesses with Wheezing
Cystic Fibrosis
Bronchopulmonary Dysplasia
Laryngomalacia
Immunodeficiency
(e.g. Primary ciliary
Dyskinesia
,
Agammaglobulinemia
)
Associated cough
Cough
After feeding:
Gastroesophageal Reflux
Dry, nighttime cough
Gastroesophageal Reflux
Allergic Rhinitis
Asthma
Obstructive Sleep Apnea
Modifying Factors
Wheezing after feeding
Gastroesophageal Reflux
(most common)
Tracheoesophageal fistula
Laryngeal cleft
Positional change
Tracheomalacia
Great Vessel
anomalies
Signs
Gene
ral: Signs of chronic systemic illness (e.g.
Cystic Fibrosis
,
Immunodeficiency
)
Observe for ill, wan, tired appearance
Review growth charts for fall in
Growth Velocity
Wheezing Intensity
Wheezing in infant heard without stethoscope suggests
Congenital Anomaly
Wheezing Modifying maneuvers
Worse with neck flexion and better with extension suggests
Vascular Ring
Severity: Asseess for outpatient versus inpatient management
Observe for critical or ominous signs
Altered Mental Status
Diaphoresis
Observe for respiratory distress
Neck or intercostal retractions
Tachypnea
Grunting (
Auto-PEEP
)
Imaging
Chest XRay
Consider inspiratory and expiratory films (detects airway foreign bodies)
Evaluation
Full
Vital Sign
s including
Oxygen Saturation
,
Respiratory Rate
and
Peak Flow
s (if possible)
V-Q Mismatch in
Asthma
or
Bronchiolitis
is typically mild to moderate
Severe V-Q Mismatch with significant
Hypoxemia
(
O2 Sat
<90%) suggests other underlying cause
Example:
Pneumonia
Consider specific testing or empiric therapy in common conditions
Asthma
(e.g.
Spirometry
)
Allergic Rhinitis
(e.g.
Allergy Test
ing)
Gastroesophageal Reflux
(e.g. barium swallow)
Consider testing for uncommon conditions
Cystic Fibrosis
(e.g.
Sweat Chloride
)
Immunodeficiency
(e.g. Serum
Immunoglobulin
s)
References
Claudius and Brown (2017) Crit Dec Emerg Med 31(12): 13-20
Majoewsky (2012) EM:Rap-C3 2(5):2
Bush (2007) Prim Care Respir J 16:7-15 [PubMed]
Martinati (1995) Allergy 50:701-10 [PubMed]
Weiss (2008) Am Fam Physician 77: 1109-14 [PubMed]
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