Pulmonology additional (Seth's Additional info) (12%) Flashcards

1
Q

Leading cause of infant hospitalization

A

Bronchiolitis

2 months - 2 years

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2
Q

MCC of acute bronchilolitis

A

RSV

Respiratory Syncytial Virus

in the winter, spring, and sorta fall

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3
Q

what is acute bronchilitis inflammation of?

A

Bronchioles

smallest air passages

Defined as a clinical syndrome of respiratory distress in children under 2 years of age

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4
Q

MC age of acute bronchilits

A

2 months - 2 years

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5
Q

desribed the symptom evolution of bronchiolitis

A

upper respiratory symptoms, followed by the acute onset of wheezing, crackles, hyperinflation, and tachypnea

Resulting in acute inflammation of airways

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6
Q

PE of bronchiloitis
RR ()
Prolonged ()
Cough
() wheeze
otitis media

A

RR increased
Prolonged expiration
Cough
expiratory wheeze
otitis media

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7
Q

t/f first line dx of bronchilitis is imaging showing inflammed airways

A

FALSE

clinically typically, xray only sometimes

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8
Q

Treatment of acute bronchilitis

A

Supportive and hydration

f/u patient in 2 days if outpatient

if hypoxia/apnea/ect consider hospitalization

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9
Q

which (rarely used) antiviral has a good treatment response for bronchilitis

A

Ribavirin

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10
Q

what pulm medications should be AVOIDED with bronchilitis?

A

Bronchodilators (albuterol)
Systemic glucocorticoids

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11
Q

MC lethal genetic disease in the US

A

Cystic fibrosis :(

Median survival 47 years

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12
Q

inheritance pattern of CF

A

Autosomal recessive

Spells CAR

Seen in caucasians mostly

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13
Q

Overview of CF
(obstructive/restrictive) disease that leads to progressive respiratory failure and death

A

Obstructive

secrections get in the way

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14
Q

Chromsome # that contains CF gene and is defected in CF

A

Chromosome 7

Cystic Fibrosis averages 7 letters each

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15
Q

What does the CF gene on chromosome 7 typically code for

A

epithelial chloride channel (CF transmembrane conductance regulator protein)—(CFTR)

found on MANY organs

This in turn leads to problems in salt and water movement across cell membranes resulting in abnormally thick secretions in various organs

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16
Q

Early symptoms that key you into CF shortly after birth

A

Meconium ileus
Respirtory symptoms
FTT

if meconium ileus assume CF until confirmed with sweat tests and genotyping

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17
Q

Meconium ileus is obstruction of bowel by meconium in newborn infant that occurs at this anatomic site ().

virtually diagnostic of CF

A

terminal ileum

in the name!

think crohn’s I guess

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18
Q

What age do kiddos typically get diagnosed with CF?

A

Upon heel prick while in hospital

early diagnoses

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19
Q

what is the overview of upper respiratory, lower respiratory, GI, and pancreas symptoms

for CF

A

GI: volvulus, poor hydration, rectal prolapse
UR: Chronic sinusitis, nasal polyps, persistent cough
LR: infections, pneomothrax, right-sided heart failure (from pulm congestion)
Pancreas = abnormal electrolyte secretions, destruction of acini cells (leading to decreased pancreatic enzymes and pancreatic insuffiency in 85%+ of CF patients), DM, pancreatitis, malabsorbtion of fat soluble vit (DAKE), FTT

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20
Q

Electrolyte abn sometimes seen in CF and why

A

metabolic alkalosis

d/t losing electrolytes

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21
Q

Although typically initially dx with a heel stick, what is the gs dx of CF?

A

Sweat chloride test

Collection of sweat with pilocarpine iontophoresis

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22
Q

what is a borderline sweat-chloride test for CF?

above = dx
below = normal

A

40-60 mmol/L

50 +/- 10
think of sweat being 5 letters (so 50)

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23
Q

What do you do after you get 60+ sweat chloride test?

Positive test for CF

A

Genetic testing + therapy

can also get fecal elastase, pancreatic elastase-1 absent in 80% with CF

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24
Q

Tx of CF respiratory

A
  1. Follow with CF foundation
  2. Every 3 months
  3. Pulmozyme (mucolytic to decrease viscosity of purulent CF sputum)
  4. Hypertonic saline
  5. Bronchodilators
  6. Chest phsyio
  7. ABX for infections
  8. CFTR modulators
  9. Vaccines
25
Tx of CF GI
1. Pancreatic enzyme supplementation combined with high calorie, high protein, high fat diet 2. Daily vitamins 3. Caloric supplements 4. G-tube placement and supplemental feedings in FTT
26
Tx of acute exacerbation of CF ## Footnote increased sputum, increased cough, DOE, fatigue, decreased apetite, fever, increased nasal congestion
1. systemic ABX 2. Sputum cultures 3. **1 abx to target microbe grown** on culture and **2 for pseodomonas**
27
What is hyaline membrane disease AKA?
Infant respiratory distress syndrome
28
#1 RF associated with hyaline membrane disease
Preterm | DM moms with term babies sometimes as well, but not nearly as common ## Footnote Approximately 50% of infants born between 26 and 28 weeks gestation develop RDS, drops to 20 - 30% at 30 - 32 weeks
29
Pathophys of hyaline membrane disease
1. Deficiency in **pulmonary surfactant** d/t prematurity 2. Leads to noncompliant, stiff lungs 3. Amount of pressure needed to open alveoli is increased, leading to atelectasis at end expiration 4. Leads to a ventilation/perfusion mismatch, hypoxemia, hypercarbia, and persistent HTN
30
When do the manifestations of hyaline membrane disease (IRDS) typically present by?
min-hours after birth
31
s/s of hyaline membrane disease (IRDS)
1. Premature infant 2. Tachypnea 3. Intercostal retractions 4. Expiratory grunting 5. Diminished breath sounds 6. Cyanosis 7. *Progressively worsening*
32
Dx and classic CXR finding of hyaline membrane disease (IRDS)
Clinically + cxr, pulse ox, ABG **diffuse ground-glass appearance**
33
Treatment of hyaline membrane disease (what O2 delivery is used?)
**Multidisciplanary** + **Nasal CPAP** (initial preferred intervention) and **surfactant replacement**
34
What might you give to prevent hyaline membrane disease (IRDS) and when?
Prenatal administration of a **single course of steroids** **to women in preterm labor or at risk of delivery** within the next 7 days between **24 - 34 weeks gestation**
35
Asthma is a reversible (obstructive/restrictive) disease
obstructive
36
The pathogenesis of asthma involves Inflammatory cell infiltration with ___ ____ hyperplasia Plugging of ___ airways with thick mucus Hypertrophy of ____ muscle Airway _____ ___ cell activation
Inflammatory cell infiltration with **eosonophils** **Goblet cell hyperplasia** **Plugging of small airways** with thick mucus **Hypertrophy of smooth muscle** **Airway edema** **Mast cell activation**
37
strongest RF for asthma
atopy ## Footnote but lots of others as well
38
MC age range that marks the beginning of asthma
< 5 yo ## Footnote 77% of asthma begins in children <5 years old
39
What is the difference between extrinsic and intrinsic asthma and which is most common?
**Extrinisic = allergic** (MC) Intrinsic = anything other than allergies
40
Overall common s/s of asthma
1. Cough 2. Chest tightness 3. SOB/dyspnea 4. difficulty breathing 5. **Episodic wheezing** with expiration, hyperexpansion of thorax, use of accessory muscles. 6. Decreased tactile fremitus (sometimes) 7. Increased nasal secretions 8. Atopy 9. Hunched shoulders to breathe 10. Percusion is normal to hyperresonant
41
Other than clinical suspicion, what is the main diagnostic tool for asthma and what does it show (in general).
Spirometry | Shows reversibility with bronchodilator + obstruction ## Footnote Reduced FEV1/FVC and increased FEV1 after bronchodilator therapy
42
Explain the steps to diagnosing asthma for patients 5-18 yo with a obstructive pattern
1. **FEV1/FVC is < 85% of predicted** 2. if **FVC < 80% predicted = obstructive** (A); if FVC > 80% predicted = mixed (B). 3. (A) For obstructive **administer brochodilater**, which **shows increase in FEV1 of > 12% = reversible condition = asthma** (if not increased by 12% consider alternative diagnosis) 4. (B) For mixed, adminster bronchodilator, which shows FVC > 80% = likely COPD ## Footnote obstrutive reversible is needed for dx
43
If spirometry is nondiagnostic, but you still are highly sus of asthma, what can you do? ## Footnote what is a positive result?
**Bronchoprovocation** testing with **inhaled** **methacholine**, histamine, or mannitol | worsens breathing d/t causing contraction/narrowing if hyperresponive ## Footnote Patients breathe in increasing amounts of methacholine and perform spirometry after each dose Increased airway hyperresponsiveness with a **≥ 20% decrease in FEV1 up to 16 mg/mL max dose** others include exercise challenge, peal flow meters, chest xray (especially with status asthmaticus to r/o other dx), skin testing, sputum for eosinophils
44
what testing can you use for exercise and cold-induced asthma?
Provocative testing ## Footnote In these tests, your doctor measures your airway obstruction before and after you perform vigorous physical activity or take several breaths of cold air
45
ABG findings of asthma commonly show (2)
1. Hypoxemia 2. Hypercarbia with decompensation
46
Sputum sample of asthma sometimes shows: () of small airways Thick, mucoid sputum and what other 2 classic findings?
**casts** of small airways Thick, mucoid sputum **Curschmann's spirals** (from shed epithelium) **Charcot-Leyden crystals** (crystalloids with galectin-10)
47
What is mild intermittent asthma? _ days a week _ night awakenings _ FEV1/FVC () exacerbations requiring glucocortidoids per year
**<= 2 days a week** **<= 2 night awakenings per month** **< 2 SABAs per week** No interfence with normal activites Normal FEV1/FVC 0-1 **exacerbations (< 2 basically)** | Rule of 2s
48
# [](http://) how often does some1 with moderate persistent asthma need a SABA?
Daily ## Footnote FEV1 between 60-80% of predicted and FEV1/FVC below normal
49
FEV1 of severe asthma
60% or less ## Footnote FEV1/FVC below normal
50
6 steps of asthma treatment
1. **SABA** + low dose ICS when symptomatic **OR low dose ICS daily** 2. SABA + **low dose ICS** 3. SABA + low dose ICS + **LABA ** **OR** **medium dose ICS alone** 4. SABA + **medium dose ICS AND LABA** 5. SABA + **high dose ICS** + LABA (or montelukast) 6. SABA + high dose ICS + **oral steroids** + LABA (or montelukast); consider monoclonal antibody
51
How often should patients with asthma f/u?
every 1-**6 months** depending on severity
52
when might you consider step down therapy for asthma?
if stable for 3 months
53
Your patient is dx with asthma - they can use this assessment tool at home to keep an "asthma diary" of how they are doing
Peak flow meter
54
t/f Peak flower meters consider height, weight, and age to measure normal values
FALSE ## Footnote NOT weight, but height and age are a factor
55
What are the 4 factors used to predict normal values of peak flow monitors?
1. Height 2. Age 3. Sex 4. Ethnicity sorta (AA and hispanic americans are approx 10% lower)
56
What are the different colors of a peak flow monitor and what is the "caution" zone color and range?
Green, **yellow**, red | yellow = caution (**50-80% predicted**) follow treatment plan ## Footnote below this = Bronchodilator therapy should be started immediately and clinician should be contacted
57
When to refer a pt with asthma to a pulmonologist or allergist
1. Experienced a life threatening attack 2. Hospitalized for attack 3. > 2 rounds of oral corticosteroids needed 4. Over 5 yo requiring step 4 care or higher 5. Under 5 yo and requiring step 3 care or higher 6. Unresponsive to treatment after 3-6 months 7. Candidate for allergen immunotherapy
58
When would you take a SABA for exercise induced asthma/bronchospasm?
15-30 min prior to exercise
59
Cough variant asthma is treated the same as other forms, but is characterized by: Cough lasting () Cough is (productive/nonproductive) Cough typically occurs at this hour ()
Cough lasting (**> 3 weeks**) Cough is (**nonproductive**) Cough typically occurs at this hour (**night**)