C14 Flashcards

1
Q

what about Quinolones?

A
  • Broad-spectrum bacterioCIDals
  • Nearly all quinolones in use are fluoroquinolones (contain a fluorine)
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2
Q

name Fluoroquinolones

A

1st generation (narrow spectrum ) : Nor-floxacin

2nd gen (wide spectrum ) - ciprofloxacin, Ofloxacin

3rd gen (wide spectrum) - Levo-floxacin, Moxifloxacin

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3
Q

1stG Fluoroquinolone

A

Norfloxacin

*does NOT achieve adequate plasma levels for use in most systemic infections*

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4
Q

Norfloxacin spectrum?

A

1st gen narrow spectrum !
the common pathogens causing UTIs

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5
Q

2ndG Fluoroquinolone?

A

Ciprofloxacin and ofloxacin

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6
Q

Ciprofloxacin and ofloxacin spectrum?

A
  • aerobic gram negatives
  • Pseudomonas
  • Atypical pneumonia ( H.influenza, M.catarrhalis)
  • G-‘s cocci
  • Mycoplasma pneumoniae
  • Chlamydophila pneumoniae

*effective in GUT, GIT, some respiratory infections
*Rapidly declining activity against gonoccocus

ofloxacin- UTI

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7
Q

3rdG fluoroquinolones?

A

Respiratory fluoroquinolones

  • levo.floxacin
  • moxi.floxacin
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8
Q

Levofloxacin & Moxifloxacin spectrum?

A
  • Respiratory tract infections
  • enhanced activity against gram + cocci :
    (1. S.pneumoniae
    2. Enterococci
    3. MRSA)
  • activity against Atypicals (chlamydia, mycoplasma)
  • less active against G-‘s (than 2nd gen)
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9
Q

broadest spectrum fluoroquinolones?

A

moxifloxacin

  • enhanced activity against anaerobes
  • NOT recommended for UTIs
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10
Q

fluoroquinolones pharmacoKinetix?

A

oral, IV
- oral bioavailability: good

  • distribution: penetrate most body tissues
  • Elimination: kidneys (active tubular secretion) (elimination blocked by probenecid.)

***moxifloxacin: eliminated partly by hepatic and biliary excretion***

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11
Q

fluoroquinolones MOA?

A
  • bactericidal
  • Inhibits DNA replication via:
  • in G-‘s: binding to DNA gyrase (topo 2) >inhibit bacterial DNA synthesis
  • in G+’s: binding to topoisomerase IV –> inhibit with bacterial DNA synthesis
  • exhibit postantibiotic effects
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12
Q

what is PostAntibiotic effect?

A

bacterial growth continues to be inhibited even after the plasma concentration of the drug has fallen below the min inhibitory concentration of the bacterium

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13
Q

Resistance against fluoroquinolones?

A
  • Efflux pumps or changing porin structure –> decreased intracellular accumulation of the drug
  • Point mutations in the ABx binding regions –> Changes in the sensitivity of the target enzymes (eg. dna gyrase)
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14
Q

Fluoroquinolones Clinical use?

A
  • mainly in urogenital and GITIs by G-‘s:
    (gonococci, E coli, P aeruginosa, Salmonella, shigella)
  • meningococcal carrier state
  • tuberculosis
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15
Q

Ofloxacin clinical use?

A

UTI

  • eradicates Chlamydia trachomatis
  • 7d of treatment is required
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16
Q

Levofloxacin clinical use?

A

RTI
enhanced activity against gram + cocci

  • community-acquired pneumonia
  • against atypicals :
    1. Chlamydiae
    2. Mycoplasma
    3. Legionella
17
Q

fluoroquinolones Toxicity?

A
  • GI distress
  • Neurotoxicity
  • dizziness, headache
  • prolong the QT interval (levofloxacin, moxifloxacin)
  • CONTRAINDICATED: children or pregnant women (damage growing cartilage & cause arthropathy)