peds Flashcards

1
Q

How is the pediatric airway different from an adults?

A
  • proportionally large tongue
  • large, floppy, epiglottis
  • Cricoid cartilage is the narrowest part of ped airway
  • Kids are not little adults−Smaller airways=more resistance
    • Increased chest wall compliance
      • Less respiratory reserve
      • Can tire out quickly and suddenly
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2
Q

What is croup?

A
  • most common cauae of airway obstruction btween 6mo to 6yr
  • common in winter and fall
  • gradual onset
  • fever, sore throat, nasal congestion
  • stridor and barky cough
  • steeple sign on lateral neck radiograph
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3
Q

What is the treatment for croup?

A
  • Largely supportive
  • Hydration
  • Exposure to cool air
  • Cool mist
  • Racemic epinephrine
  • Dexamethasone
  • Heliox?
  • If intubation is necessary be cautious to avoid any trauma

−Use smaller ETT

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4
Q

What is Epiglottitis?

A
  • Life threatening infection of the larynx that results in sudden swelling of epiglottis
  • Very rare
    • H. influenza B
  • Rapid onset
  • High fever
  • Drooling with dysphagia
  • Severe respiratory distress
  • Patient prefers to sit upright in sniffing position
  • Lateral radiograph shows “Thumb Sign”
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5
Q

What is the treatment for epiglottitis

A
  • oxygen
  • intubation
    • may need needle cricothyroidotomy
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6
Q

What is tonsillitis?

A
  • Acute illness with fever and sore throat can lead to swelling of oropharyngeal tissues
  • Leads to inflammation of tonsils and adenoids
  • Streptococcal pharyngitis
  • Severe or recurring cases may need surgical removal of tonsils and adenoids
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7
Q

What is anaphylactic laryngospasm>

A
  • Pediatric allergies are becoming more prevalent
  • Severe side effect of anaphylaxis can be critical laryngospasm
  • Treat with inhaled racemic, IM or IV epinephrine
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8
Q

Foreign body aspiration

A
  • leading cause of death in mobile infants, toddlers and young children
  • signs
    • mild to severe respiratory distress
    • recurring pneumonia
    • unilateral wheezing
    • right sided aspiration more likely
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9
Q

What is treatment for foreign body aspiration?

A
  • Depends on severity of obstruction
  • Support oxygenation as needed
  • if the child is stable
    • XRAY and History to determine the size and location of the object
    • Controlled bronchoscopy in the OR to remove the object
  • if the child is unstable
    • PALS algorithm for severe airway obstruction
    • Emergent flexible bronchoscopy to remove object may be necessary
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10
Q

What is RSV?

A
  • Highly contagious
  • Most often affects infants less than one year of age
  • Newborn to 6 month olds are at risk for most serious infections
  • Infants with pre-existing conditions (BPD, CF, etc) are at higher risk
  • Infection lasts 5-10 days and peaks at 5-7 days
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11
Q

What is Bronchiolitis?

A
  • Acute viral infection causing small airway obstruction and inflammation
  • Respiratory distress
  • Tachypnea
  • Cough
  • Wheezing
  • Copious secretions
  • Apnea (Newborns and very young infants)
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12
Q

Cystic Fibrosis

A
  • Lethal autosomal recessive disease caused by a dysfunctional gene on chromosome 7
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13
Q

What does Cystic Fibrosis Transmembrane Regulator (CFTR) gene do and what happens when it dysfunctions?

A
  • Normally helps control flow of ions and substrates across cell membranes lining the airways, intestines, vas deferens, biliary tree, sweat ducts, and pancreatic ducts
  • CFTR dysfunction
  • Chloride ion cannot be transported
    • Insufficient secretion of fluid and inadequate hydration
    • Leads to thickened secretions in all affected organ systems
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14
Q

What are some treatments for CF and what are the symptoms?

A
  • increased goblet cells - increased secretions and sputum
  • secrections are dry and thick
  • airway inflammation
  • Treatments
    • VEST, Postural drainage and CPT, Acapella, Metaneb
  • Meds
    • Bronchodilators
    • Mucoltics- Dornase alfa (Pulmozyme), 7% NaCl
    • Antibiotics- Tobi
  • GI symptoms
    • pancreatic insufficiency
      • ducts can plug due to thickened pancreas secretions→ malabsorption of fat and protein
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15
Q

What is Spinal muscular atrophy (SMA)?

A
  • Autosomal recessive inherited disorder
  • Progressive destruction of the motor neurons of spinal cord and brainstem

−Results in significant muscle weakness

•Three identified types of SMA

−Type 1

−Type 2

−Type 3

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16
Q

What is Duchenne Muscular Dystrophy?

A

•Genetic disorder

−Mutation of the dystrophin gene an Important structural component of muscle tissue

•Affects cardiac, respiratory, gastrointestinal, endocrine, and nervous systems

−Male predominance (X Linked)

•Progressive, irreversible muscle weakness

  • Signs and symptoms
    • childhood-onset
    • difficulty running, climbing stairs, and standing
    • may become wheelchair bound
    • no cure, most die by 20
17
Q

What happens when a child drowns and how do we treat them?

A
  • child below surface of water → voluntary apnea→ become hypercarbic, hypoxemic and acidotic → involuntarily swallow water and inhale water into lungs → become unconscious, panic and eventually arrest
  • provide supportive care, PALS algorithm
  • attempt to correct acidosis
  • warm slowly
  • maybe difficult to ventilate
  • ECMO
18
Q

What is ARDS

A
  • Acute lung injury characterized by pulmonary edema die to disruption of AC membrane, hypoxemia, bilateral infiltrates, P/F ratio <200mmHg
    *
19
Q

What are the stages of ARDS?

A

•Exudative Stage

−Diffuse injury to AC membrane by inflammatory mediators

−Alveoli fill with fluid

−Surfactant inactivation

−Widespread atelectasis

−Lung compliance decreases

  • Proliferative stage

−1-3 weeks after the initial injury

−Proliferation of Type 2 pneumocytes to replace the destroyed type 1 cells

Fibrotic Stage

−Severe ARDS cases

−Lung tissue is replaced by collagenous tissues

−Vascular remodeling

−Results in decreased surface area for gas exchange

−May need tracheostomy and home ventilation