Hap Flashcards

1
Q

Risk factors for increased mortality:

A

S

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2
Q

Risk factor for MDR Pseudomonas, other gram-negative bacilli, and MRSA:

A

L

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3
Q

Risk factors for MDR Pseudomonas and other gram-negative bacilli:

A

L

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4
Q

Risk factor for MRSA

A

D

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5
Q

Ventilatory support for HAP

A

F

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6
Q

Septic shock

A

E

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7
Q

IV antibiotics within the past 90 days

A

R

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8
Q

Structural lung disease (bronchiectasis or cystic fibrosis)

A

D

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9
Q

A respiratory specimen Gram stain with numerous and predominant gram-
negative bacilli

A

R

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10
Q

Colonization with OR prior isolation of MDR Pseudomonas or other gram-negative

A

D

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11
Q

Risk factors for MRSA:

A

R

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12
Q

Treatment in a unit in which >20 percent of S. aureus isolates associated with HAP
are methicillin resistant

A

R

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13
Q

Treatment in a unit in which the prevalence of MRSA is not known

A

R

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14
Q

Colonization with OR prior isolation of MRSA

A

G

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15
Q

No MDR risk factors or increased risk of mortality—

A

D

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16
Q

Risk factors for MDR gram-negative bacilli and MRSA or for increased mortality

A

D

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17
Q

should receive one agent that has activity against Pseudomonas and MSSA.

A

D

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18
Q

Piperacillin-tazobactam

A

R

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19
Q

Cefepime

A

R

20
Q

Levofloxacin

A

R

21
Q

imipenem and meropenem as options,

A

R

22
Q

two agents with activity against P. aeruginosa and other gram-negative bacilli and one agent with activity against MRSA.

A

E

23
Q

Amikacin

A

D

24
Q

Gentamicin

A

D

25
Q

Tobramycin

A

R

26
Q

have poor lung penetration, increased risk of nephrotoxicity and ototoxicity, and poorer clinical response rates compared with other antibiotic classes,

A

R

27
Q

are not recommended as monotherapy for gram-negative infections

A

D

28
Q

Linezolid

A

D

29
Q

Vancomycin

A

D

30
Q

Tedizolid

A

R

31
Q

Telavancin

A

F

32
Q

receive two agents with activity against P. aeruginosa; the regimen should also have activity against MSSA.

A

D

33
Q

receive one agent with activity against P. aeruginosa and other gram-negative bacilli and one agent with activity against MRSA.

A

K

34
Q

because they are more likely to have activity against gram-negative bacilli
than the fluoroquinolones or aztreonam.

A

O

35
Q

DURATION

A

K

36
Q

for seven days,

A

K

37
Q

Other potential toxicities of antibiotics used for HAP and VAP include the following:

A

K

38
Q

cannot be used to treat pneumonia because it is inactivated by surfactant and does not achieve adequate concentrations in the respiratory tract.

A

D

39
Q

It has been approved by the FDA for community-acquired pneumonia (CAP) but not for CAP caused by MRSA, nor for HAP or VAP.

A

D

40
Q

Ceftaroline

A

D

41
Q

has been approved by the FDA for skin and skin structure infections and intra-abdominal infections caused by MRSA.

A

D

42
Q

has also been approved for CAP but not for CAP caused by MRSA or for HAP or VAP.

A

D

43
Q

Tigecycline

A

D

44
Q

Ceftobiprole

A

E

45
Q

It has not been approved by the FDA, but it has been approved in Europe and Canada for treatment of HAP and CAP but not VAP.

A

D