carbapenems/monobactams Flashcards

1
Q
  • synthetic monocyclic beta lactams
  • single ring as the core structure
  • binds to PBPs and disrupts cell wall synthesis
  • bacteriocidal
  • resistance to many beta lactamases
  • ONLY active against gram neg aerobes
  • NO activity against gram pos\anaerobes\bacteriodes fragilis
  • minimal effect on GI flora
A

monobactams

- Aztreonam

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2
Q

monobactams/aztreonam have activity against

A
  • Neisseria
  • Haemophilus
  • Psuedomonas
  • Enterobacter
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3
Q
  • administered IV/IM only NOT orally
  • t1/2 is 1.7 hrs
  • shows allergic cross reactivity w other beta lactam antibiotics
  • relatively nontoxic and is renal sparing
  • alternative to aminoglycosides or 3rd gen cephs for pataients w gram neg infections and beta lactam allergy
A

Aztreonam

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4
Q

aztreonam indications

A
  • intra abdominal
  • joint and bone
  • skind and soft tissue
  • lower respiratory
  • gyenocologic and obestitrics
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5
Q

aztreonam antibiotic map coverage

A
  • all gram negs!
  • Proteus mirabilis
  • e. coli
  • Klebsiella pneumonia
  • Serratia
  • H. Influenzae
  • N. meningitis
  • Enterobacter spp
  • Pseudomonas
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6
Q
  • inhibitors of beta lactamases
  • pyrrolidine ring increases stability and spectrum
  • Last line antibiotics
  • trans configuration increases potency
A
  • carbepenems
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7
Q
  • must be administered w DHP-1 inhibitor cilastatin
A

imipenem

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8
Q
  • mechanism of action and resistance of carbapenems
A
  • PBP inhibitors
  • inhibiting certain beta lactamases
  • stable in presence of AmpC beta lactamases and extended spectrum beta lactamases
  • resistance includes sstructural changes to PBP
  • metallo beta lactamases
  • changes in membrane permeability
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9
Q
  • broadest spectrum activity
  • active against gram pos and neg including anaerobes except c. diff
  • lack activity against MRSA, enterococcus faecium and stenotrophomonas amltophilia or atypical bacteria
A

ertapenem carbapenems

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10
Q
  • imipenem
  • meropenem
  • doripenem
    are typically fairly active against most…
A
  • Psuedomonas
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11
Q
  • ertapenem is less active against gram pos and not active against
A
  • P. aueruginosa or enerococci
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12
Q
  • given IV/IM
  • R1 is H, no R group
  • given w Cilastatin blocking degragation by renal enzymes
A

Imipenem

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13
Q
  • IV
  • does not require cilistatin booster
  • R1 is CH3
A
  • Meropenem
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14
Q
  • IV
  • very broad spectrum
  • needs more clinical data
  • t 1/2 is 1 hr
  • not used much and availability varies
A
  • Doripenem
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15
Q
  • iV/IM

- given once daily injectable carbapenem which has 4 fold longer plasma halflife

A
  • ertapenem
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16
Q

goracillins over…think APE

A
  • Acinetobacter
  • Psuedomonas
  • Enterococcus
17
Q

only carbapenem active against atypical bacteria

A
  • Imipenem
18
Q

carbapenems lack activity against

A
  • MRSA
  • Enterococcus
  • Stenotrophomonas
19
Q
  • combo of beta lactamase inhibitor (cyclic boronic complex)
  • approved for complicated UTI
  • extended coverage against resistant gram neg organisms except resistant APEs
  • side effects include headache, nauseam diarrhea, seizure, anaphylaxis
  • have to use in 4 hours after mixing
  • very expensive
A
  • Meropenem/vaborbactam
20
Q

clinical uses for carbapenems

A
  • lower respiratory
  • intrabdominal
  • UTIs
  • skin/soft infections
  • CSF/CNS infetions
21
Q
  • indicated for moderate to sever nosocomial infections and polymicrobial infections
A
  • Imipenem\cilastatin

- meropenem

22
Q
  • indicated for community acquired infections, outpatient IV antimicrobial therap
A
  • entrapenem
23
Q
  • similar to meropenem but more active against p aeruginosa
A
  • doripenem
24
Q
  • antibiotic map covergame for imipenem/meropenem/doripenem
A
  • covers everything but MRS and VRE
25
Q
  • ertapenem antibiotic map coverage
A
  • covers all but enterococcus’s, MRSA and pseudomonas