Diseases
Pediatric Diseases and Neuromuscular Disorders
Key Concepts
Overview of common pediatric diseases and neuromuscular disorders.
Important to understand the clinical presentation, diagnosis, and management of these conditions.
Upper Airway Obstruction
Epiglottitis
Age Range: 2-6 years old.
Onset: Sudden within 6-8 hours.
Cause: Bacterial infection (Haemophilus influenzae).
Clinical Features:
Sore throat and hoarseness
Drooling due to difficulty swallowing (dysphagia)
High fever and tachypnea
Inspiratory stridor, jaw jutted forward, retractions, tripod position
Diagnosis:
Clinical presentation and lateral neck X-ray showing “thumb sign”.
Management:
Airway maintenance in upright position
Intubation if necessary
Administer antibiotics and humidified oxygen if not severe.
Laryngotracheobronchitis (Croup)
Age Range: 6 months - 6 years old.
Onset: 2-3 days.
Cause: Viral (often parainfluenza virus, RSV).
Clinical Features:
Barking cough, inspiratory stridor
Hoarseness and use of accessory muscles for breathing
Mild fever, tachypnea, tachycardia
Diagnosis:
Throat and blood cultures, AP neck X-ray with “steeple sign”.
Management:
Administer cool aerosol with O2, racemic epinephrine, corticosteroids, and ensure rest.
Lower Airway Disorders
Foreign Body Aspiration
Age Range: 6 months - 3 years old.
Onset: Immediate after inhalation.
Presentation:
Violent coughing, dyspnea, cyanosis
May develop fever if not removed, unilateral wheezing
Diagnosis:
Chest X-ray showing air trapping and hyperinflation.
Management:
Emergency oxygen therapy, bronchoscopy for viewing/removal, corticosteroids.
Acute Bronchiolitis
Age: < 1 year old.
Cause: Respiratory Syncytial Virus (RSV).
Diagnosis:
Clinical signs (coryza, cough, wheezing) and viral culture.
Management:
Monitor for apnea and hypoxia, use of ribavirin, suctioning, albuterol, and oxygen therapy.
Neuromuscular Disorders
Duchenne Muscular Dystrophy (DMD)
X-linked genetic disorder affecting primarily boys.
Signs and Symptoms:
Late walkers,