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
CF Dx/Trtmt: CF pathophys: Name three common GI symptoms of CF
CF Dx/Trtmt: CF pathophys ``` pancreatic insufficiency (85%) hepatobiliary disease (70%) GERD (25-100%) ```
26
CF Dx/Trtmt: CF pathophys: Name two common upper respiratory symptoms of CF
CF Dx/Trtmt: CF pathophys ``` recurrent or chronic sinus disease (100% of CF pts) nasal polyps (up to 25% of CF pts) ```
27
CF Dx/Trtmt: CF pathophys four manifestations of lower respiratory symptoms of CF
CF Dx/Trtmt: CF pathophys inflammation (occurs early after birth) CF-specific pathogens bronchiectasis pulmonary exacerbations (lead to loss of lung fxn)
28
CF Dx/Trtmt: Epi: | Why do we see increased numbers of adult patients? two reasons
CF Dx/Trtmt: Epi mild phenotype diagnosis discovered in adulthood increased life expectancy
29
CF Dx/Trtmt: Dx approach, newborn screening: What are three requirements for sweat chloride testing?
CF Dx/Trtmt: Dx approach, newborn screening newborn > 36 weeks (gestational age) two weeks old (post-partum) minimum body wt = 2 kg
30
CF Dx/Treatment: quality care is dependent upon these two factors
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
CF Dx/Treatment Functional Mutation Classes Should we know this slide???
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
CF Dx/Treatment: CF clinical practice guidelines: What three pharmacological interventions are used as anti-inflammatory treatments for CF?
CF Dx/Treatment: CF clinical practice guidelines corticosteroids, oral ibuprofen (high dose) azithromycin (macrolide anitbiotics)
33
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).
CF Dx/Treatment: CF clinical practice guidelines H. influenza Strep pneumo MSSA (methicillin-susceptible Staphylococcus aureus)
34
CF Dx/Treatment: CF clinical practice guidelines: As CF pts get older, two bacteria are the most common infection threat. They are _________ .
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
CF Dx/Treatment: CF clinical practice guidelines: What is done to monitor for bacterial infection in CF patients?
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
CF Dx/Treatment: CF clinical practice guidelines: What are the four basic components of lower respiratory tract therapy pulmonary toilette?
CF Dx/Treatment: CF clinical practice guidelines Bronchodilators Mucolytics Hypertonic Saline Airway Clearance
37
Pulm HTN: definition Define pulmonary hypertension
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
Pulm HTN: WHO definition What is Group 1 Pulmonary Hypertension?
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
Pulm HTN: WHO definition What is Group 2 Pulmonary Hypertension?
Pulm HTN: WHO definition Group 2 = PH due to L heart disease (most common)
40
Pulm HTN: WHO definition What is Group 3 Pulmonary Hypertension?
Pulm HTN: WHO definition Group 3 = PH due to lung disease and/or hypoxemia
41
Pulm HTN: WHO definition What is Group 4 Pulmonary Hypertension?
Pulm HTN: WHO definition Group 4 = PH due to chronic thromboembolism
42
Pulm HTN: WHO definition What is Group 5 Pulmonary Hypertension?
Pulm HTN: WHO definition Group 5 = PH with unclear multifactorial mechanisms
43
Pulm HTN: where would you expect back flow in the heart in a case of Pulmonary Hypertension?
Pulm HTN backflow of blood from pulmonary artery into R ventricle and even further back into R tricuspid and R atrium
44
Pulm HTN: Name some signs of PH
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
Pulm HTN: What does a split in the S2 heart sounds indicate?
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
Pulm HTN: How do we assess PH?
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
Pulm HTN: What is the basic pathogenesis of PH?
Pulm HTN increased vasoconstrictors decreased vasodilators
48
Pulm HTN: What three therapy pathways do we use to treat Pulmonary Hypertension via Vascular Biology?
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
Foxworth Pharm: Pneumonia Trtmt, adults, first line:
Foxworth Pharm Amoxicillin Doxycycline
50
Foxworth Pharm: Pneumonia Trtmt, adults, if comorbidity exits
Foxworth Pharm amox/CA + AZ
51
Foxworth Pharm: Pneumonia Trtmt, adults, if pneumonia is respiratory
Foxworth Pharm quinolone or amox/CA
52
Foxworth Pharm: If pneumonia treatment resistance to macrolides is <25%, what treatment should be chosen?
Foxworth Pharm AZ
53
Foxworth Pharm: How long do we usually treat pneumonia?
Foxworth Pharm 5-7 days (pt should be afebrile >48 hrs, clinically stable, not vomiting, able to eat (these are all po treatments!))
54
Foxworth Pharm: How do we treat pneumonia with alcoholism, COPD, or post-influenza comorbidity?
Foxworth Pharm ``` respiratory flouroquinolones (FQ) or AZ + high dose amox or high dose amox/CA ```
55
Foxworth Pharm: List some side effects for flouroquinolones (FQ)
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
Foxworth Pharm: Explain admission criteria CURB-65 and CRB-65
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
Foxworth Pharm: When would you admit w/ a CURB-65 of 0?
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
Foxworth Pharm: After culture confirms bacterial agent, how would one treat CAP with a hospitalized (not ICU) pt?
Foxworth Pharm ceftriaxone (CFTX) IV + AZ
59
Foxworth Pharm: After culture confirms bacterial agent, how would one treat CAP with AN ICU pt?
Foxworth Pharm ``` ceftriaxone (CFTX) IV + levofloxacin + AZ IV + van or linezolid ```
60
Foxworth Pharm: After culture confirms bacterial agent, how would one treat nosocomial pneumonia?
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
Foxworth Pharm: resistance Which antibiotic has shown some Strep pneumo resistance?
Foxworth Pharm AZ Note: use FQ as an alternative
62
Foxworth Pharm: What is recommended treatment for bronchitis?
Foxworth Pharm NO ANTIBIOTICS Note: treatment is controversial! maaayyybeeee consider AZ for persistent cough bronchitis.