Exam 1 - Cushman (Lecture 2) Flashcards

1
Q

cephamycins are ____ _____ cephalosporins

A

2nd gen

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

Explain the difference between bacteriostatic and bactericidal

A

baceriostatic prevent bacteria from growing and bactericidal actively kill bacteria (and prevent new growth of it)

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

Cefotetan has (broad/narrow) spectrum of activity

A

broad

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

Cefotetan has a similar reaction to ____ as ____

A

ethanol, disulfuram

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

polar molecules are (more/less) likely to pass through porins

A

more

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

Which are more reactive and why: carbapenems or penicillins?

A

carbapenems because sulfur in penicillin is replaced by methylene, which is smaller and produces more ring strain

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

imipenem administered with _____ has (broad/narrow) antibioitic activity

A

cilastatin, broad
-active against gram (-) and (+)
-called “magic bullet” and should be avoided unless last option or serious infection

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

Aztreonam inspired by ____

A

monobactams

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Aztreonam only works on gram (-/+)?

A

gram (-)

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

aztreonam place in therapy

A

used in serious gram (-) infections, particularly those that are penicillin resistant organism acquired in hospitals

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

only cephalosporin reported to have cross allergenicity with penicillins

A

ceftazidime
-oxime ether group makes it resistant to hydrolysis by B-Lacatamases

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

Cephamycin example

A

cefotetan

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

carbapenem example

A

imipenem (can be used with cilastatin)

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

monobactam example

A

aztreonam

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

glycopeptide example (only two in clinical use)

A

vancomycin
teicoplanin

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

vancomycin works on gram (-/+)? Why?

A

gram (+), vanco is too big to fit through porins in gram (-) cell wall

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

mechanism of vancomyin

A

D-Ala-D-Ala binds to peptidoglycan precursor before cross-linking. Vanco has high affinity for this substrate, which inhibits the transpeptidase reaction required for cross-linking

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

vanco is (bactericidal/bacteriostatic) and active against gram (-/+)

A

bactericidal, gram (+)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

susceptible strains (to vanco) usually have MIC _ micrograms/mL

A

4

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Why did VREs become more common in europe?

A

Avoparcin, a glycopeptide antibiotic, was used in livestock. Once banned, VRE became less common. The mechanism of resistance appeared to be because of a mutation of the peptidoglycan cell wall precursor from D-Ala-D-Ala to D-Ala-D-Lactate and vancomycin has 1000x less affinity for the D-Ala-D-Lactate precursor, leading to linkage between the D-Ala-D-Lactate precursor and the peptidoglycan precursor, which allowed the transpeptidase reaction to occur.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

vanco is used IV except in the case of: _____

22
Q

vanco is used to treat what common resistance infection?

A

MRSA (methicillin resistant staphylococcus aureus

23
Q

describe vanco toxicity and SE

A

hypersensitivity rxn: red rash on skin and potential anaphylaxis
nephrotox. (rare)
ototox. (rare)

24
Q

lipoglycopeptide antibiotics examples

A

oritavancin
telavancin
dalbavancin

25
oritavancin is active against gram (-/+) bacteria and is (broad/narrow) spectrum
gram (+), active against a broad spectrum, including MRSA
26
telavancin is active against gram (-/+) infections, including ____
gram (+), MRSA
27
dalbavancin is active against gram (-/+) infections, including ____ and ____
gram (+), MRSA, MRSE
28
half lives of vanco tela dalba orita
4-6h 7-9h 204h 245h
29
streptogramin examples
quinupristin dalfopristin
30
Synercid is comprised of 30% _____ and 70% _____
quinupristin, dalfopristin
31
quinupristin and dalfopristin are (bacteriostatic/bactericidal/both)
bacteriostatic (together as synercid or alone)
32
Synercid is bactericidal against strains of _______ -_____ and ______-_______ staphylococci
methicillin-susceptible and methicillin-resistant
33
Synercid is bacteriostatic against _______
Enterococcus faecium
34
Synercid clinical uses
IV for tx of: 1. Vancomycin resistant Enterococcus faecium bacteremia (but not Enterococcus faecalis). Certain Enterococcus faecium bacteremia are resistant to all other antibiotics 2. skin infections caused by MRSA 3. vancomycin resistant Enterococcus faecium urinary tract infections
35
quinupristin resistance mechanism (1)
adenine methylation of A2058 in the 23S rRNA -causes Synercid to be bacteriostatic instead of bactericidal at normal dose
36
quinupristin resistance mechanism (2)
efflux pumps and bacterial metabolism
37
List Synercid tox.
none known
38
Synercid SE
pain and inflammation at injection site N/D rash muscle weakness
39
list the one major drug interaction of streptogramins
inhibit CYP3A4, which metabolizes a long list of drugs
40
oxazolidinone examples
Linezolid Tedizolid (2nd gen)
41
Linezolid MOA
Inhibit protein synthesis at the 50S ribosomal subunit. Normally, 50S subunit associates with fMet-tRNA and a complex comprised of the 30S ribosomal subunit and mRNA to form the functional 70S initiation complex. Linezolid blocks 50S from becoming 70S.
42
Linezolid used to treat:
1.vancomycin resistant Enterococcus faecium 2. nosocomial pneumonia caused by methicillin-resistant strains of Staph. aureus 3. skin infections caused by methicillin-resistant strains of Staph. aureus
43
Linezolid is available as (oral/IV/both/neither)
both
44
when should linezolid be used?
only to treat or prevent infections that are proven or strongly suspected to be caused by multiple drug resistant Gram(+) bacteria or when pts are allergic to alternative therapies
45
resistance to linezolid associated with
G to U substitution in the peptidyl transferase center of 23S rRNA at position 2576
46
SE of linezolid
NVD HA tongue discoloration oral candidiasis (thrush) reversible myelosuppresion
47
weekly monitoring during linezolid
CBC
48
major linezolid drug interaction
moderately potent, reversible, nonselective inhibitor of monoamine oxidase -caution in adrenergic and serotonergic agents -caution in high tyramine containing foods
49
Tedizolid uses
treats acute bacterial skin and skin structure infections
50
(tedizolid/linezolid) is more potent against MRSA
tedizolid