E2 Erdman Carbapenems Flashcards

1
Q

4 carbapenems to know

A

imipenem
meropenem
ertapenem
doripenem

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

carbapenem moa, primary target

A

they bind to PBPs but primary one is PBP-2***

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

T or F:
carbapenems penetrate very well into bacterial cell walls

A

true

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Carbapenems are (bactericidal/bacteriostatic) in a (time/conc) dependent manner

A

cidal
time

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

T or F:
carbapenems have greater stability against most b-lactamase enzymes compared to cephs

A

true

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

T or F:
cephs are the most broad spectrum agents avaiable

A

false, carbapenems are

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

T or F:
carbapenems have activity against GP and GN aerobes but no activity against anaerobes

A

false, they do all listed

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

3 mechs of resistance for carbapenems

A
  • alterations to outer membrane porin proteins
  • b-lactamase OR carbapenemase (KPC, OXA, etc) enzymes
  • alterations in PBPs
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

which 2 exhibit the best activity against GP aerobes
imipenem
meropenem
ertapenem
doripenem

A

imipenem and doripenem *

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

target organism for imip and dori

A

meth-susc S. aureus**

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

imipenem is special because it covers one specific bacteria that others dont, what is it?

A

enterococcus FAECALIS (bacteriostatic too)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

which 2 exhibit the best activity against GN aerobes?
imipenem
meropenem
ertapenem
doripenem

A

mero and dori

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

carbapenems are the DRUG OF CHOICE for _____ and _______ producing bacteria

A

ESBL
AmpC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

does not cover pseudomonas aeruginosa
imipenem
meropenem
ertapenem
doripenem

A

ertapenem

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

does not have activity against acinetobacter spp
imipenem
meropenem
ertapenem
doripenem

A

ertapenem (again)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

carbapenems SoA:
GP anaerobes (4)

A
  • Peptococcus spp
  • Peptostreptococcus spp
  • Veillonella
  • Clostridium spp (NOT C. DIFF tho)
17
Q

carbapenems SoA:
GN anaerobes (3)

A
  • bacteroides spp (ALL)*
  • Fusobacterium
  • Prevotella spp
18
Q

T or F:
most carbapenems are active against MRSA and PRSP

A

false, none are i think

19
Q

do carbapenems have activity against atypical bacteria?

20
Q

T or F:
Carbapenems are highly stable against many β-lactamase enzymes and are considered the drugs of choice for serious infections due to ESBL- and AmpC-producing bacteria.

21
Q

T or F:
Meropenem-vaborbactam and imipenem-relebactam were developed to provide activity against KPC-producing Enterobacterales.

22
Q

clinically useful synergy, carbapenems:
GN aerobes

A

any carbapenem + gent/tobra/amik

23
Q

T or F:
carbapenems are bactericidal against enterococcus

A

false, static

24
Q

all carbapenems penetrate the CSF, but which one is the best at it?

A

meropenem**

25
undergoes hydrolysis by dehydropeptidase enzyme in the renal brush border to a nephrotoxic metabolite A. Meropenem B. Imipenem C. Carbapenem D. Ertapenem
B, administer with cilastatin
26
has a half life of 4 hours A. Meropenem B. Imipenem C. Carbapenem D. Ertapenem
D
27
T or F: all carbapenems require dose adjustment in pts with renal dysfunction
true
28
clinical uses: carbapenems are "typically" used for?
polymicrobial infections
29
T or F: Imipenem does not have activity against pseudomonas aeruginosa
false, ertapenem is the one that doesnt
30
carbapenems can be used as empiric therapy for _______ infections
nosocomial (hospital acquired)
31
clinical uses: carbapenems infections due to ?
b-lactamase producing organisms (SPICE, SPACE, ESBLs, etc)
32
clinical uses: febrile neutropenia
imipenem and meropenem
33
clinical uses: meningitis
meropenem (penetrates best)
34
clinical uses: complicated UTIs caused by KPC-producing enterobacterales
the combo ones
35
if pseudomonas is known or suspected do NOT use _____
ertapenem
36
direct toxic AE of carbapenems
CNS: seizures main thing here
37
3 risk factors for CNS effects from carbapenems
- preexisting CNS disorder - high doses - renal insufficiency
38
2 super random AEs affiliated with carbepenems
LFT increases yeast infections