Pulm 6/17 Quiz Review Flashcards

1
Q

Lung CA:

define pulmonary nodule

A

Lung CA

= small opacities,
less than 3 cm in size

Notes:
usually asymptomatic
usually detected incidentally
or at time of screening

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2
Q

Lung CA:

define lung mass

A

Lung CA

= any opacity larger than 3 cm in size

Notes:
malignant until proven otherwise

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3
Q

Lung CA:

two primary categories of Lung CA are:

A

Lung CA

  • non small cell lung cancer (NSCLC)
  • small cell lung cancer (SCLC)
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4
Q

Lung CA:

growth rate of small cell lung cancer (SCLC) =

A

Lung CA

grow very very fast

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5
Q

Lung CA:

who predominantly gets SCLC?

A

Lung CA

```
smokers do
“occur predominantly in smokers”
~~~

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6
Q

Lung CA:

what are the two stages of SCLC? How are they defined?

A

Lung CA

Limited Stage & Extensive Stage

Limited Stage = all disease w/in single radiation field (i.e. single hemithorax, possibly with some supraclavicular lymph nodes thrown in)
Extensive Stage = disease OUTSIDE a single hemithorax

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7
Q

Lung CA:

what is the most common non-small cell lung cancer (NSCLC)?

A

Lung CA

adenocarcinoma

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8
Q

Lung CA:

what is the TNM system of staging? What does TNM stand for?

A

Lung CA

T = tumor
N = node
M = metastasis

I = solitary tumor, tumor <= 4 cm, no lymph node involvement

II = tumor > 4 cm, regional lymph nodes involved, invasion into local structures

III = medistinal lymph nodes positive

IV = distant metastatic disease (includes pleural effusion)

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9
Q

Lung CA:

how to treat lung cancers at different stages –>

A

Lung CA

FIRST = biopsy, determine if NSCLC or SCLC!

I - surgical resection
II - surgical resection + chemo
III = chemoradiation
IV = palliative care (incurable)

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10
Q

Lung CA:

name some NSCLC presentations

A

Lung CA

hyperalcemia
hypertrophic pulm osteoarthropathy (NOT finger clubbing)
inflammatory myopathies

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11
Q

Lung CA:

what is most common subtype of lung cancer?

A

Lung CA

NON-small cell lung cancer (NSCLC)

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12
Q

Lung CA:

common symptoms for lung cancer = ?

A

Lung CA

typical: cough, increased sputum, shortness of breath
common: fatigue, wt loss, anorexia, low-grade fever

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13
Q

Lung CA:

name some SCLC presentations

A

Lung CA

paraneoplastic syndromes:
hyponatremia (SIADH)
hypertrophic pulm osteoathropathy (NOT finger clubbing, same as NSCLC)
inflammatory myopathies (same as NSCLC)
Cushing Syndrome
Lambert-Eaton syndrome
cerebellar degeneration
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14
Q

CF Dx/Trtmt: Epi

What ethnicity carries highest rates of cystic fibrosis?

A

CF Dx/Trtmt: Epi

Caucasian

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15
Q

CF Dx/Trtmt: Dx approach, newborn screening:

To dx CF, pt must have at least one of these three symptoms:

A

CF Dx/Trtmt: Dx approach, newborn screening

  >1 typical phenotypic features of CF
  sibling with CF
  positive newborn screening test
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16
Q

CF Dx/Trtmt: Dx approach, newborn screening:

To dx CF, pt must ALSO have one of these three symptoms (in addition to the three required):

A

CF Dx/Trtmt: Dx approach, newborn screening

- elevated sweat chloride on 2 occasions
 - TWO disease-causing CFTR mutations
 = abnormal nasal potential difference
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17
Q

CF Dx/Trtmt: Dx approach, newborn screening:

Why is newborn screening helpful/important?

A

CF Dx/Trtmt: Dx approach, newborn screening

“With widespread adoption of newborn screening in recent years, we have seen a….an increasing number of infants diagnosed before a month of age”

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18
Q

CF Dx/Trtmt: Dx approach, newborn screening:

Three most common phenotypical symptoms seen in CF diagnoses

A

CF Dx/Trtmt: Dx approach, newborn screening

acute/persistent respiratory symptoms (37.3%)
steatorrhea (22.4%)
meconium ileus/intestinal obstruction (17.6%)

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19
Q

CF Dx/Trtmt: Dx approach, newborn screening:

What is the GOLD STANDARD For CF dx?

A

CF Dx/Trtmt: Dx approach, newborn screening

SWEAT CHLORIDE TESTING (done at an accredited CF Care Center)

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20
Q

CF Dx/Trtmt: Dx approach, newborn screening:

What is required for a positive genetic test for CF?

A

CF Dx/Trtmt: Dx approach, newborn screening

“TWO defective genes in trans configuration”

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21
Q

CF Dx/Trtmt: Dx approach, newborn screening:

What is the most common mutation for CF?

A

CF Dx/Trtmt: Dx approach, newborn screening

F508del (70% of mutations)

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22
Q

CF Dx/Trtmt: Dx approach, newborn screening:

How do we test newborns for CF?

A

CF Dx/Trtmt: Dx approach, newborn screening

We check for immunoreactive trypsinogen

(this is an exocrine pancreatic protein, which is elevated in newborns with CF (3-5 x higher))

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23
Q

CF Dx/Trtmt: CF pathophys:

Describe CFTR

A

CF Dx/Trtmt: CF pathophys

what is it? gene
location: long arm of chromosome 7
function: codes for protein in cell membrane of many organs
action: acts as chloride channel
(also controls other channels)

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24
Q

CF Dx/Trtmt: CF pathophys:

name three basic symptoms of CFTR mutation

A

CF Dx/Trtmt: CF pathophys

GI
Upper Respiratory System
Lower Respiratory System

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25
Q

CF Dx/Trtmt: CF pathophys:

Name three common GI symptoms of CF

A

CF Dx/Trtmt: CF pathophys

pancreatic insufficiency (85%)
hepatobiliary disease (70%)
GERD (25-100%)
26
Q

CF Dx/Trtmt: CF pathophys:

Name two common upper respiratory symptoms of CF

A

CF Dx/Trtmt: CF pathophys

recurrent or chronic sinus disease (100% of CF pts)
nasal polyps (up to 25% of CF pts)
27
Q

CF Dx/Trtmt: CF pathophys

four manifestations of lower respiratory symptoms of CF

A

CF Dx/Trtmt: CF pathophys

inflammation (occurs early after birth)
CF-specific pathogens
bronchiectasis
pulmonary exacerbations (lead to loss of lung fxn)

28
Q

CF Dx/Trtmt: Epi:

Why do we see increased numbers of adult patients?
two reasons

A

CF Dx/Trtmt: Epi

mild phenotype diagnosis discovered in adulthood

increased life expectancy

29
Q

CF Dx/Trtmt: Dx approach, newborn screening:

What are three requirements for sweat chloride testing?

A

CF Dx/Trtmt: Dx approach, newborn screening

newborn > 36 weeks (gestational age)

two weeks old (post-partum)

minimum body wt = 2 kg

30
Q

CF Dx/Treatment:

quality care is dependent upon these two factors

A

CF Dx/Trtmt

CF Foundation’s evidence-based or consensus standards

Healthcare Team of PCP and CF Care Center personnel
they have to coordinate & communicate

31
Q

CF Dx/Treatment

Functional Mutation Classes
Should we know this slide???

A

Class I – altered biosynthesis
No CFTR produced
Class II – altered maturation
Minimal and dysfunctional CFTR at cell surface
Class III – altered regulation
Adequate CFTR at cell surface, reduced or no function
Class IV – altered conductance
Adequate CFTR at cell surface, reduced function
Class V – reduced synthesis
Decreased but functional CFTR
Class VI – increased turnover

32
Q

CF Dx/Treatment: CF clinical practice guidelines:

What three pharmacological interventions are used as anti-inflammatory treatments for CF?

A

CF Dx/Treatment: CF clinical practice guidelines

corticosteroids, oral
ibuprofen (high dose)
azithromycin (macrolide anitbiotics)

33
Q

CF Dx/Treatment: CF clinical practice guidelines:

When pts are diagnosed at a younger age, the community acquired bacteria that most commonly colonize the airways are _________ (name three).

A

CF Dx/Treatment: CF clinical practice guidelines

H. influenza
Strep pneumo
MSSA (methicillin-susceptible Staphylococcus aureus)

34
Q

CF Dx/Treatment: CF clinical practice guidelines:

As CF pts get older, two bacteria are the most common infection threat. They are _________ .

A

CF Dx/Treatment: CF clinical practice guidelines

Pseudomonas aeruginosa
MRSA (Methicillin-resistant Staphylococcus aureus)

Note: these two cause decreased life expectancy and worsening outcomes!

35
Q

CF Dx/Treatment: CF clinical practice guidelines:

What is done to monitor for bacterial infection in CF patients?

A

CF Dx/Treatment: CF clinical practice guidelines

throat cultures, 4x/year (have pt return to clinic 4x/year to culture and monitor for Pseudomonas and MRSA).

36
Q

CF Dx/Treatment: CF clinical practice guidelines:

What are the four basic components of lower respiratory tract therapy pulmonary toilette?

A

CF Dx/Treatment: CF clinical practice guidelines

Bronchodilators
Mucolytics
Hypertonic Saline
Airway Clearance

37
Q

Pulm HTN: definition

Define pulmonary hypertension

A

Pulm HTN: definition

condition of the lungs in which blood vessels of lungs become narrow

rare
pathological
narrowing progresses over time
results in increase of bp in these vessels

38
Q

Pulm HTN: WHO definition

What is Group 1 Pulmonary Hypertension?

A

Pulm HTN: WHO definition

Group 1 = pulmonary arterial hypertension (PAH)
Idiopathic, familial

(only group 1 is called pulmonary “arterial” hypertension, but all 5 grooups may be referred to as PH)

39
Q

Pulm HTN: WHO definition

What is Group 2 Pulmonary Hypertension?

A

Pulm HTN: WHO definition

Group 2 = PH due to L heart disease (most common)

40
Q

Pulm HTN: WHO definition

What is Group 3 Pulmonary Hypertension?

A

Pulm HTN: WHO definition

Group 3 = PH due to lung disease and/or hypoxemia

41
Q

Pulm HTN: WHO definition

What is Group 4 Pulmonary Hypertension?

A

Pulm HTN: WHO definition

Group 4 = PH due to chronic thromboembolism

42
Q

Pulm HTN: WHO definition

What is Group 5 Pulmonary Hypertension?

A

Pulm HTN: WHO definition

Group 5 = PH with unclear multifactorial mechanisms

43
Q

Pulm HTN:

where would you expect back flow in the heart in a case of Pulmonary Hypertension?

A

Pulm HTN

backflow of blood from pulmonary artery into R ventricle and even further back into R tricuspid and R atrium

44
Q

Pulm HTN:

Name some signs of PH

A

Pulm HTN

Cyanosis (bluish lips and skin)
Chest pain
Fluttering chest
Shortness of breath
Fatigue, weakness
Dizziness, lightheadedness
Dry cough
Abdominal bloating
Rapid weight gain
Swollen ankles, legs
45
Q

Pulm HTN:

What does a split in the S2 heart sounds indicate?

A

Pulm HTN

(this split is b/w aortic (A2) and pulmonic (P2) valve closures…Aortic valve may close earlier due to higher resistance from systemic circulation)

This means there is less resistance in the pulmonary arterial bed causing a later P2

46
Q

Pulm HTN:

How do we assess PH?

A

Pulm HTN

cardiac catheterization (“cath”) Gold Standard (just not always possible, esp for little kids)

echocardiogram –> R ventricle pressure estimated via flow through tricuspid valve

EKG

Chest Xray

47
Q

Pulm HTN:

What is the basic pathogenesis of PH?

A

Pulm HTN

increased vasoconstrictors
decreased vasodilators

48
Q

Pulm HTN:

What three therapy pathways do we use to treat Pulmonary Hypertension via Vascular Biology?

A

Pulm HTN

NO-cyclic guanosine monophosphate (cGMP)
(and phosphodiesterase inhibitors like Viagra)

ET-1 (Bosentan, Ambrisentan)

PGI2 (Epoprostenol, Flolan, as continuous IV….not the best option) Treprostinil is preferred now.

49
Q

Foxworth Pharm:

Pneumonia Trtmt, adults, first line:

A

Foxworth Pharm

Amoxicillin
Doxycycline

50
Q

Foxworth Pharm:

Pneumonia Trtmt, adults, if comorbidity exits

A

Foxworth Pharm

amox/CA + AZ

51
Q

Foxworth Pharm:

Pneumonia Trtmt, adults, if pneumonia is respiratory

A

Foxworth Pharm

quinolone or amox/CA

52
Q

Foxworth Pharm:

If pneumonia treatment resistance to macrolides is <25%, what treatment should be chosen?

A

Foxworth Pharm

AZ

53
Q

Foxworth Pharm:

How long do we usually treat pneumonia?

A

Foxworth Pharm

5-7 days

(pt should be afebrile >48 hrs, clinically stable, not vomiting, able to eat (these are all po treatments!))

54
Q

Foxworth Pharm:

How do we treat pneumonia with alcoholism, COPD, or post-influenza comorbidity?

A

Foxworth Pharm

respiratory flouroquinolones (FQ)
or
AZ + high dose amox
or
high dose amox/CA
55
Q

Foxworth Pharm:

List some side effects for flouroquinolones (FQ)

A

Foxworth Pharm

  • Wt bearing cartilage damage in children
  • Tendon rupture in adults
  • MS changes (agitation, delirium, nervousness, < memory)
  • Food and drug interactions
  • QTc
  • hypoglycemia & hyperglycemia (DM, > age, renal disease)
  • C diff
56
Q

Foxworth Pharm:

Explain admission criteria
CURB-65
and
CRB-65

A

Foxworth Pharm

give a point for each of the following ~
CURB-65 = 
   Confusion
   Uremia
   Resp rate
   Blood pressure
   >65 y/o
CRB-65 = 
   Confusion
   Resp rate
   Blood pressure
   >65 y/o
57
Q

Foxworth Pharm:

When would you admit w/ a CURB-65 of 0?

A

Foxworth Pharm

o	Immunocompromised
o	DM
o	Someone with pulse ox that’s low
o	Someone w/ complications
o	Someone who will not follow treatment plan after discharge
58
Q

Foxworth Pharm:

After culture confirms bacterial agent, how would one treat CAP with a hospitalized (not ICU) pt?

A

Foxworth Pharm

ceftriaxone (CFTX) IV
+
AZ

59
Q

Foxworth Pharm:

After culture confirms bacterial agent, how would one treat CAP with AN ICU pt?

A

Foxworth Pharm

ceftriaxone (CFTX) IV
\+
levofloxacin
\+
AZ IV
\+ 
van or linezolid
60
Q

Foxworth Pharm:

After culture confirms bacterial agent, how would one treat nosocomial pneumonia?

A

Foxworth Pharm

cefepime
or
“pip/tazo”

Note: add vanc if hospital acquired MRSA is >20% prevelant, or if antibiotics were used w/in 90 days, or in case of septic shock

61
Q

Foxworth Pharm: resistance

Which antibiotic has shown some Strep pneumo resistance?

A

Foxworth Pharm

AZ

Note: use FQ as an alternative

62
Q

Foxworth Pharm:

What is recommended treatment for bronchitis?

A

Foxworth Pharm

NO ANTIBIOTICS

Note: treatment is controversial! maaayyybeeee consider AZ for persistent cough bronchitis.