Pulm part 2 Flashcards

1
Q

Step 1 asthma tx for 12 yrs or older

A

SABA PRN

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2
Q

Step 2 asthma tx for 12 yrs or older: preferred

A

Low-dose ICS

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3
Q

Step 2 asthma tx for 12 yrs or older: alternative

A

Cromolyn
LTRA
Nedocromil
or Theophylline

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4
Q

Step 3 asthma tx for 12 yrs or older: preferred

A

Low-dose ICS + LABA
OR
Medium-dose ICS

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5
Q

Step 3 asthma tx for 12 yrs or older: alternative

A

Low-dose ICS + either:
LTRA
Theophylline
or Zileuton

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6
Q

Step 4 asthma tx for 12 yrs or older: preferred

A

Medium-dose ICS +

LABA

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7
Q

Step 4 asthma tx for 12 yrs or older: alternative

A

Medium-dose ICS + either:
LTRA
Theophylline
or Zileuton

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8
Q

Step 5 asthma tx for 12 yrs or older

A

High-dose ICS +
LABA
AND consider omalizumab for pts who have allergies

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9
Q

Step 6 asthma tx for 12 yrs or older

A

High-dose ICS +
LABA +
oral corticosteroid
AND consider omalizumab for pts who have allergies

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10
Q

MC age for foreign body aspirations

A

Children younger than 3 yrs

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11
Q

Reasons children are more prone to foreign body aspirations

A

Lack of molar teeth that decreases their ability to sufficiently chew food
Propensity to talk, laugh, and run while chewing
Examination of even non-food substances in the mouth

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12
Q

Presentation of foreign body aspiration

A

Often, presents after sudden episode of coughing or choking while eating with subsequent wheezing, coughing, or stridor
When not witnessed, persistent or recurring cough, wheezing, persistent or recurrent PNA, lung abscess, focal bronchiectasis, or hemoptysis

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13
Q

PE of foreign body aspiration

A

New abnl airway sounds
Sounds are inspiratory if in the extrathoracic trachea.
Noises are more prominent in the central airways if in the intrathoracic trachea

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14
Q

Workup of foreign body aspiration

A

Radiography
Bronchoscopy
Heimlich maneuver only if child is unable to speak

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15
Q

Tx of foreign body aspiration

A

Endoscopic removal

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16
Q

Causes of hyaline membrane disease

A

Occurs after the onset of breathing and is associated with an insufficiency of pulmonary surfactant

17
Q

RFs of hyaline membrane disease

A
Prematurity is the greatest risk
Delivery of a previous preterm infant with hyaline membrane disease
Maternal diabetes
Hypothermia
Fetal distress
Asphyxia
Male sex
White race
Being the second-born of twins
Delivery by C-section without labor
18
Q

Presentation of hyaline membrane dz

A
Cyanosis
Tachypnea
Nasal flaring
Intercostal and sternal retractions
Grunting
19
Q

Tx of hyaline membrane disease

A

Antenatal administration of corticosteroids to the mother 48 hrs prior to labor
After birth, intratracheal administration of exogenous surfactant
Maintain pH above 7.25
Increased concentration of warm and humidified inspired oxygen
Nasal continuous positive airway pressure
Ventilator

20
Q

Cause of cystic fibrosis

A

Autosomal recessive disorder

Mutation of the cystic fibrosis transmembrane regulator (CFTR)

21
Q

Manifestations of cystic fibrosis initially in older children

A
Poorly controlled asthma and chronic respiratory infections
Persistent or recurrent cough that is often productive of sputum
Digital clubbing
Chronic sinusitis
Nasal polyposis
Pneumothoraces
Steatorrhea
Deficiencies of fat-soluble vitamins
Distal intestinal obstruction syndrome
Insulin deficiency
Hyponatremia and hypochloremic metabolic acidosis
Reproductive dysfunction
22
Q

Presentation of cystic fibrosis in infants

A
Meconium ileus
Failure to thrive
Cholestatic jaundice
Chronic respiratory sx
Electrolyte abnormalities
23
Q

Dx of cystic fibrosis

A

DNA testing

Sweat chloride test

24
Q

Tx of cystic fibrosis

A

Chest physiotherapy
Antibiotic therapy
Enteric-coated pancreatic enzyme capsules
High-calorie diets with the addition of nutritional supplements
Insulin for CF-related diabetes
Multifactorial