Gram Positive Antibiotics Flashcards

1
Q

What are the glycopeptides?

A
•  Vancomycin 
•  Teicoplanin 
•  Dalbavancin 
•  Telavancin 
•  Oritavancin
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2
Q

What is the MOA of vancomycin?

A

Inhibits bacterial cell wall synthesis at a site different than β-lactams at the second stage of synthesis.

Binds firmly to D-alanyl-D-alanine portion of cell wall precursors to prevent cross-linking and further elongation of peptidoglycan; weakens cell wall.

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3
Q

What is the pharmokinetic activity of vancomycin?

A

Time-dependent bactericidal activity (kills bacteria slowly)

Bacteriostatic VS enterococcus

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4
Q

How are VRE and VRSA resistant to vancomycin?

A

Modification of D-alanyl-D-alanine binding site of peptidoglycan
! Terminal D-alanine replaced by D-lactate
! Loss of critical hydrogen bond
! Loss of antibacterial activity

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5
Q

How is VISA (Vancomycin Intermediate S. aureus) resistant to vancomycin?

A

Thickened cell wall

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6
Q

What is the spectrum of vancomycin activity?

A

Gram-positive bacteria
! MSSA/MRSA
! Coagulase-negative staphylococci*
! Streptococcus pneumoniae (including PRSP), viridans streptococcus, Group streptococcus
! Enterococcus spp.
! Corynebacterium, Bacillus. Listeria, Actinomyces
! Clostridium spp. (including C. difficile), Peptococcus, Peptostreptococcus

NO GRAM-NEGATIVE ACTIVITY

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7
Q

How is vancomycin administered?

A

Must be IV

Oral only for C. difficile

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8
Q

What is the elimination of vancomycin dependent upon?

A

Elimination half-life depends on renal function

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9
Q

Vancomycin SE

A

Red-Man Syndrome
! Flushing, pruritus, erythematous rash on face, neck, and upper torso within 5 to 15 minutes of starting infusion (His release)
! Related to RATE of intravenous infusion; doses should be infused over at least 60 minutes

Otoxicity

Nephrotoxicity

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10
Q

What is the MOA of dalbavancin?

A

D-ala D-ala binding, inhibiting cross-linkage similar to vancomycin. However, it has a lipid moiety that anchors to cell membrane.

More potent and cidal than vancomycin

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11
Q

What is the spectrum of dalbavancin activity?

A
MRSA
VISA
vanB and vanC VRE (NOT vanA though)
Bacillus, Listeria, Corynebacter
MRSE
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12
Q

How is dalbavancin administered?

A

IV only

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13
Q

What are the main uses for telavancin?

A

Complicated SSSI

Pneumonia (hospital acquired)

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14
Q

What are the main uses for oritavancin?

A

MSSA, MRSA, Enterococcus, Strep possible Bacillus anthracis

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15
Q

What is the MOA of oritavancin?

A

Same as vancomycin but it also disrupts the cell membrane

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16
Q

What are the Oxazolidinones drugs?

A

Linezolid

Tedizolid

17
Q

What is the MOA of linezolid?

A

Binds to the 50S ribosomal subunit near the surface interface of 30S subunit – causes inhibition of 70S initiation complex (unique binding site), which inhibits protein synthesis

18
Q

What are the pharmokinetics of linezolid?

A

Time dependent Bacteriostatic

19
Q

What is the spectrum of linezolid?

A
MSSA
MRSA
VRSA
E. faecium/E. faecalis and VRE
Some mycobacteria activity
20
Q

What is the CSF penetration of linezolid?

A

Decent (30%)

21
Q

Does linezolid dose have to be adjusted for renal failure?

A

No

22
Q

How is linezolid administered?

A

Oral or IV

23
Q

What is the oral bioavailability of linezolid?

A

100%

24
Q

What are the clinical uses of linezolid?

A

Use reserved for serious/complicated infections caused by resistant gram-positive bacteria:
! VRE bacteremia, NOT urinary tract infections
! Complicated skin and soft tissue infections due to
MSSA, MRSA or Streptococcus pyogenes
! Nosocomial pneumonia due to MRSA

25
Q

What is the major drug interaction of linezolid?

A

Serotonin syndrome with SSRIs/MAOIs

26
Q

Linezolid SE

A

Peripheral neuropathy

Thrombocytopenia or anemia

27
Q

What is an advantage of tedizolid over linezolid?

A

More potent and has no SSRI interaction like linezolid

28
Q

Daptomycin MOA

A

Binds to bacterial membranes → rapid depolarization of membrane potential → inhibition of protein, DNA, and RNA synthesis

29
Q

Daptomycin pharmokinetics

A

Concentration-dependent bactericidal activity

30
Q

Daptomycin Spectrum

A

! Methicillin-Susceptible, Methicillin-Resistant AND Vancomycin-Resistant Staph aureus* and coagulase-negative staphylococci
! Streptococcus pneumoniae (including PRSP), viridans streptococcus, Group streptococcus
! Enterococcus faecium AND faecalis (including VRE)

31
Q

Are dose adjustments required for daptomycin in renal failure patients?

A

Yes

32
Q

What is daptomycin ineffective in treating?

A

Pneumonia. It is inactivated by surfactant

33
Q

Daptomycin SE

A

Myopathy and CPK elevation

34
Q

What are the unique features of Quinupristin-Dalfopristin and its MOA?

A

They are both bacteriostatic protein synthesis inhibitors but together, they become bactericidal.

35
Q

What is the MOA of Quinupristin-Dalfopristin?

A

Dalfopristin enhances binding of quinupristin. Inhibits peptidyltransferase.
Quinupristin prevents elongation of polypeptide chain & causes incomplete chain release.

36
Q

What are the SE of Quinupristin-Dalfopristin?

A

Severe GI intolerance

37
Q

What is the spectrum of Quinupristin-Dalfopristin?

A

Gram Positive Organisms

38
Q

How is daptomycin resisted?

A

Alteration of membrane binding