Exam 3 - LRTI Flashcards

1
Q

when does CAP occur

A

outside the hospital or within the first 48 hours of admission

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2
Q

what are the three main ways CAP can occur

A

aspiration
aerosolization
blood born

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3
Q

what are the main bacterial pathogens for CAP

A

strep pneumo
h. influenzae
Mycoplasma pneumo
legionella pneumo
chlamydia pneumo
staph aureus

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4
Q

what tests should be completed to assess risk for staph aureus in CAP patients

A

MRSA nasal pcr

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5
Q

what are additional risk factors for CAP patients

A

alcoholism
COPD/smoker
lung disease
ABX recently

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6
Q

what is more common for CAP bacteria or virus

A

virus

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7
Q

what is the classic presentation for CAP

A

sudden fever, chills, dyspnea, productive cough, chest pain

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8
Q

how do the elderly present with CAP

A

may not have classic signs of fever and leukocytosis
more likely to have altered mental status, weakness, functionality

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9
Q

what are the typical presenting vitals for a CAP patient

A

febrile (>38 degrees celsius)
tachycardia
hypotensive
tachypnea

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10
Q

what tests should be done for CAP diagnosis

A

chest x-ray for all suspicious cases
WBC w/ differential
SCr, BUN, electrolytes
PCR swabs
pulse ox
cultures (save for more severe)

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11
Q

how many minor criteria do you need to meet in order to have severe CAP

A

need at least 3

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12
Q

what are the minor criteria for severe CAP

A

Resp rate greater than 30
multilobar infiltrates
confusion/disorientation
uremia BUN > 30
leukopenia WBC <4000
thrombocytopenia
hypothermia
hypotension requiring aggressive fluids

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13
Q

how many major criteria are needed to classify as severe CAP and what are they

A

at least 1
septic shock requiring vasopressors
respiratory failure requiring mechanical ventilation

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14
Q

what is supportive care for CAP

A

humidified air
bronchodilators
fluids

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15
Q

CAP empiric therapy for:
outpatient
healthy w/o comorbidities

A

Amox 1gm PO Q8H
Doxy 100mg PO BID
Azith zpack (high resistance)

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16
Q

CAP empiric therapy for:
outpatient
w/ comorbidities

A
  • Levo 750mg PO QD
  • Moxi 400mg PO QD
  • b-lactam + macrolide or doxy (preferred option)
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17
Q

CAP what b-lactams should be used when treating outpatient CAP w/ comorbidities

A
  • Augmentin
  • Cefpodoxime
  • Cefuroxime
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18
Q

CAP empiric therapy for:
inpatient
non severe
no MRSA/pseudomonas

A
  • Levo 750 or Moxi 400
  • B-lactam + macrolide
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19
Q

CAP empiric therapy for:
inpatient
severe
no MRSA/pseudomonas

A
  • Levo or Moxi + B-lactam
  • B-lactam + macrolide
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20
Q

what b-lactams should be used inpatient w/ CAP

A
  • Amp/sulbactam
  • ceftriaxone
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21
Q

what can be used in place of a macrolide in inpatient CAP

A

doxycycline

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22
Q

what are risks for MRSA in CAP

A

2-14 days post influenza
previous MRSA
previous hospitalization and use of IV antibiotics within 90 days

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23
Q

what are risks for pseudomonas in CAP

A

previous pseudomonas
previous hospitalization and IV antibiotics in 90 days

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24
Q

CAP empiric therapy for:
inpatient
MRSA risks

A

Vanc or Linezolid

25
Q

CAP empiric therapy for:
inpatient
pseudomonas risk

A

-Pip/tazo
-cefopime
-meropenem

26
Q

when to use corticosteroids in CAP

A

only when there is septic shock

27
Q

duration of therapy for CAP

A

minimum of 5 days

28
Q

CAP pen-susc streptococcus pneumoniae 1st line treatment

A

pen G or amox

29
Q

CAP pen-resist strep pneumo 1st line treatment

A

ceftriaxone or respiratory FQ

30
Q

CAP h. influenzae first line treatment

A

2nd/3rd gen cephalosporin
unasyn
augmentin

31
Q

CAP mycoplasma pneumoniae 1st line treatment

A

macrolide or doxy

32
Q

CAP chlamydia pneumoniae first line treatment

A

macrolide or doxy

33
Q

CAP legionella first line treatment

A

FQ or azithromycin

34
Q

CAP MSSA first line treatment

A

cefazolin or nafcillin

35
Q

CAP MRSA first line treatment

A

vanc or linezolid

36
Q

CAP anaerobes first line treatment

A

b-lactam/bL inhibitor and add metronidazole if utilizing cephalosporin

37
Q

CAP enterbacterales first line treatment

A

3rd/4th gen cephalosporin
carbapenem

38
Q

what is hospital acquired pneumonia

A

greater than 48 hours after hospital admission

39
Q

what is VAP

A

greater than 48 hours after endotracheal intubation

40
Q

how to diagnose HAP/VAP

A

no standard diagnosis mostly based on timing and presentation

41
Q

what are the risks for HAP/VAP

A

advanced age
severe comorbidities
duration of hospitalization
multidrug resistance (prior ABX use)

42
Q

HAP common pathogens

A

Pseudomonas aeruginosa
Enterobacterales
Acinetobacter
Staph Aureus greatest concern!

43
Q

what is the duration of therapy for HAP

A

7 days if clinically stable

44
Q

what are MRSA risks in HAP

A

previous MRSA or ABX in 90 days
>10-20 MRSA rates
unknown MRSA prevalence

45
Q

what are pseudomonas risks in HAP

A

> 10% incidence
resistance rates unknown

46
Q

HAP empiric therapy for:
MRSA coverage

A

vanc or linezolid

47
Q

HAP empiric therapy for pseudomonas

A

pip/tazo
cefepime
imipenem
meropenem
levofloxacin

48
Q

HAP empiric therapy for:
not high risk

A

Pip/tazo
cefepime
imipenem
meropenem
levo

49
Q

what are you trying to cover in HAP w/ no high risk

A

goal is to cover MSSA and pseudomonas

50
Q

HAP empiric therapy for:
not high risk
w/ MRSA

A

pip/tazo, cefepime, imipenem, meropenem, levo PLUS vanc or linezolid

51
Q

what is the goal when treating HAP w/ no high risk but MRSA

A

goal is to cover MRSA and pseudomonas

52
Q

HAP empiric therapy for:
high risk
w/ MRSA

A

pick 2 different classes from pip/tazo, cefepime, imipenem, meropenem, levo, tobra/amikacin
PLUS vanc or linezolid

53
Q

what is the goal when treating HAP w/ high risk and MRSA

A

goal is to cover MRSA and multidrug resistant pseudomonas

54
Q

VAP empiric therapy

A

pick two from pip/tazo, cefepime, imipenem, meropenem, levo, tobra/amikacin PLUS vanc or linezolid

55
Q

what is the goal when treating VAP

A

goal is to cover MRSA and pseudomonas

56
Q

when should daptomycin be used in LRTI

A

NEVER! inactivated by pulmonary surfactant

57
Q

when should aminoglycosides be used in LRTI

A

never as monotherapy and avoid empiric unless necessary (lots of AEs)

58
Q

when to use polymyxins in LRTI

A

avoid empiric, reserve for high MDR patients

59
Q

when to use tigecycline

A

good if also intra-abdominal infections.