Respiratory Diseases Flashcards

1
Q

List some early signs of respiratory distress/respiratory failure.

A
  • Tachypnea
  • Tachycardia
  • Irritability, restlessness
  • Nasal Flaring
  • Retractions
  • Expiratory grunting
  • Hypertension
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2
Q

List some late/severe signs of respiratory distress/respiratory failure.

A
  • Depressed respirations
  • Bradycardia
  • Lethargy, drowsy
  • Cyanosis
  • Hypotension
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3
Q

What is the etiology of Croup (acute laryngotracheobronchitis).

A

Viral

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4
Q

What is a defining characteristic of Croup?

A

Barking cough

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5
Q

Croup treatment?

A
  • Racemic epinephrine nebulizer
  • Oxygen if O2 sat < 92% : Blow-by oxygen most effective.
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6
Q

What is the etiology of Epiglottitis?

A
  • Life threatening condition
  • Inflammation of the epiglottis
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7
Q

Epiglottitis clinical manifestations?

A
  • irritability and restlessness
  • drooling
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8
Q

How do you prevent Epiglottitis?

A

Haemophilus influenzae type B vaccine

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9
Q

Epiglottitis emergency treatment?

A
  • Primary (A-B-C)
    ~ Airway management (intubation) – if possible in the operating room
  • Secondary
    ~ IV antibiotics
    ~ IV corticosteroids
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10
Q

Why is Epiglottitis life threatening?

A

Respiratory distress can lead to respiratory failure

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11
Q

What is the etiology of Respiratory Syncytial Virus (RSV).

A

Viral

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12
Q

Respiratory Syncytial Virus (RSV) manifestations?

A
  • excessive clear nasal secretions
  • poor appetite
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13
Q

Respiratory Syncytial Virus (RSV) treatment?

A
  • Palivizumab (Synagis) prophylaxis
  • Nasopharnyx suction
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14
Q

Describe sequelae of Acute Streptococcal Pharyngitis (Strep Throat).

A

Risk for serious sequelae if strep throat infection untreated:

  • Acute rheumatic fever-Rheumatic Heart Disease
  • Acute glomerulonephritis
  • Scarlet fever
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15
Q

How is Acute Streptococcal Pharyngitis (Strep Throat) diagnosed?

A

Diagnostic evaluation-throat culture

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16
Q

Acute Streptococcal Pharyngitis (Strep Throat) treatment?

A

Antibiotics

17
Q

Tonsillitis manifestations?

A

Inflammation

18
Q

Tonsillitis treatment?

A
  • Surgical
    ~ May be indicated with massive hypertrophy
19
Q

What are some post-op considerations for tonsillectomy?

A
  • Observation—frequent swallowing may indicate bleeding
  • NO suctioning
20
Q

Describe the pathophysiology of asthma.

A
  • Reversible airflow obstruction
    ~ Bronchoconstriction
    ~ Inflammation
    ~ Secretions
21
Q

What are some risk factors of asthma?

A
  • Family History-genetic susceptibility
  • Allergies (environmental, food)
  • Exposure to smoke
  • Frequent respiratory infections (RSV, influenza)
  • Obesity
22
Q

Asthma clinical manifestations?

A
  • Wheezing
  • Shortness of breath
  • Chest tightness
  • Cough (often worse at night)
23
Q

What is a Peak Flow Meter and how do you use it?

A
  • Measures how fast air is expelled from the lungs during forceful expiration.
  • Blow out as hard and quick as you can.
  • Repeat 2x (30 seconds between)
24
Q

What is a spacer?

A

A spacer is an attachment that fits onto the end of your inhaler. If you use your inhaler without a spacer, then most of the medicine ends up inside your mouth or stomach, instead of your lungs, where it works best.

25
Asthma rescue drug therapy?
- Rescue (Quick Relief) medications ~ Short-acting β2-agonists (SABA) - Corticosteroids-Inflammation
26
How do you manage status asthmaticus?
- IV Epinephrine - Corticosteroid (Solu Medrol) first line of treatment.
27
Asthma long-term treatment?
Long-term control meds (Maintenance) ~ LABAs
28
Describe SDOH considerations on asthma.
- SDOH factors associated with increased asthma morbidity: ~ Environmental ~ Social
29
Describe environmental impact on asthma?
- Allergen exposure - Environmental pollution
30
Describe social impact on asthma?
- Racial or ethnic prejudice or discrimination - Poverty - Exposure to high levels of stress or violence - Food or housing insecurity
31
What is the etiology of Cystic Fibrosis?
- Cystic fibrosis is an autosomal recessive disease due to mutations in cystic fibrosis transmembrane regulator (CFTR) gene.
32
Describe the physiology of Cystic Fibrosis.
Both parents are **carriers**, there is a 1 in 4 (25%) chance of each child having CF.
33
Cystic Fibrosis manifestations?
- Abnormal thick mucus - Crackles
34
Cystic Fibrosis diagnostic evaluation?
Repeated Bronchitis and Pneumonia
35
Cystic Fibrosis life-threatening complication?
Spontaneous pneumothorax
36
Cystic Fibrosis treatment?
Antibiotics (Tobramycin) aerosolized is the main treatment for Pseudomonas aeruginosa
37
Describe the prognosis of Cystic Fibrosis.
Chronic and Progressive
38
What do you do in the case of accidental decannulation (accidentally remove tracheostomy)?
**Always have two extra tracheostomy tubes at the bedside: one same size and one smaller**
39
How do you change trachea ties during care of tracheostomy?
Change trachea ties with 2 people