ID I Flashcards

1
Q

Gram positive

A

thick cell wall, dark purple or bluish from crystal violet stain

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2
Q

Staphylococci (gram-positive organisms occurring in cluster) can be differentiated with a coagulase (enzyme) test. Which is coagulase positive?

A

Staphylococcus aureus

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3
Q

Gram negative

A

thin cell wall, pick or reddish from the safranin counterstain

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4
Q

What is minimum inhibitory concentration (MIC)?

A

minimum concentration of each antibiotic that inhibits bacterial growth

REMEMBER: MICs are specific to each antibiotic & organism -> cannot be compared among different antibiotics

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5
Q

example of synergism

A

Aminoglycosides & beta-lactams can be used together synergistically to treat certain invasive gram-positive infections (e.g., infective endocarditis

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6
Q

COMMON RESISTANT PATHOGENS

A

Remember: Kill Each And Every Strong Pathogen

Klebsiella pneumoniae (ESBL, CRE)
Escherichia coli (ESBL, CRE)
Acinetobacter baumannii
Enterococcus faecalis, Enterococcus faecium (VRE)
Staphylococcus aureus (MRSA)
Pseudomonas aeruginosa

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7
Q

Risk of C. diff is highest with…

A

broad-spectrum penicillins and cephalosporins, quinolones, carbapenems, & clindamycin (which has a BBW)

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8
Q

Generally, cell wall & cell membrane inhibitors, DNA/RNA inhibitors, and aminoglycosides are __________ (kill bacteria or inhibit bacterial growth?).

A

bactericidal (kill bacteria)

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9
Q

Generally, most protein & folic acid synthesis inhibitors are __________.

A

bacteriostatic (inhibit growth)

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10
Q

Folic acid synthesis inhibitors

A
  • Sulfonamides
  • Trimethoprim*
  • Dapsone

*often combined with sulfamethoxazole to overcome resistance

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11
Q

Protein synthesis inhibitors

A
  • Aminoglycosides
  • Macrolides
  • Tetracyclines
  • Clindamycin
  • Linezolid, tedizolid
  • Quinupristin/dalfopristin
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12
Q

DNA/RNA inhibitors

A
  • Quinolones (DNA gyrase, topoisomerase IV)
  • Metronidazole, tinidazole
  • Rifampin
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13
Q

Cell membrane inhibitors

A
  • Polymyxins
  • Daptomycin
  • Telavancin
  • Oritavancin
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14
Q

Protein synthesis inhibitors

A
  • Aminoglycosides
  • Macrolides
  • Tetracyclines
  • Clindamycin
  • Linezolid, tedizolid
  • Quinupristin/dalfopristin
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15
Q

Cell wall inhibitors

A
  • Beta-lactams (penicillins, cephalosporins, carbapenems)
  • Monobactams (aztreonam)
  • Vancomycin, dalbavancin, telavancin, oritavancin
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16
Q

Hydrophilic agents

A
  • Beta-lactams
  • Aminoglycosides
  • Vancomycin
  • Daptomycin
  • Polymyxins
17
Q

Features of hydrophilic agents

A

1) Small volume of distribution -> less tissue penetration
2) Mostly renally eliminated -> drug accumulation & side effects (e.g., nephrotoxicity) can occur if not dose adjusted
3) Low intracellular concentrations -> not active against atypical (intracellular pathogens)
4) Poor-moderate bioavailability -> IV:PO ratio not 1:1

18
Q

Lipophilic agents

A
  • Quinolones
  • Macrolides
  • Rifampin
  • Linezolid
  • Tetracyclines
19
Q

Features of lipophilic agents

A

1) Large Vd -> better tissue penetration
2) Mostly hepatically metabolized -> potential for hepatotoxicity & DDIs
3) Achieve intracellular concentrations -> active against atypical (intracellular) pathogens
4) Excellent bioavailability -> IV:PO ratio often 1:1

20
Q

Drugs with concentration-dependent killing can be dosed ______ frequently and in _______ doses. These antibiotics include…

A

Drugs with concentration-dependent killing can be dosed less frequently and in higher doses. These antibiotics include:
- aminoglycosides
- quinolones
- daptomycin

21
Q

Drugs with time-dependent killing can be dosed ______ frequently. These antibiotics include…

A

Drugs with time-dependent killing can be dosed more frequently or each dose can be administered for a longer duration to maximize the time above MIC.
- Examples include extending the infusion time of beta-lactams or administering drug as continuous infusion

These antibiotics include…
- beta-lactams (penicillins, cephalosporins, carbapenem)

22
Q

AUC:MIC (exposure-dependent) drugs

A

Vancomycin, macrolides, tetracyclines, polymyxins

23
Q

MOA of penicillins

A

inhibit bacterial cell wall synthesis by binding to PBPs -> prevent final step of peptidoglycan synthesis in bacterial cell walls

24
Q

BOXED WARNING of penicillin G benzathine (Bicillin L-A)

A

NOT for IV use -> can cause cardiorespiratory arrest & death

25
Q

Severe renal impairment (CrCl <30) -> do not use…

A

extended-release forms of amoxicillin & amoxicillin/clavulanate (Augmentin XR), or the 875 mg strength of Augmentin

26
Q

side effects of penicillins

A
  • Seizures (with accumulation) when not correctly dose adjusted in renal dysfunction
  • GI upset, diarrhea
  • Rash (including SJS/TEN/allergic rxns/anaphylaxis
  • Hemolytic anemia (identified with positive Coombs test)
  • Renal failure
  • Myelosuppression with prolonged use
  • increased LFTs
27
Q

Which penicillins do NOT require renal dose adjustments?

A

Antistaphylococcal penicillins (dicloxacillin, naficillin, oxacillin)

28
Q

What is special to know about naficillin specifically?

A

Naficillin is a vesicant -> administration through central line preferred. If extravasation occurs, use cold packs & hyaluronidase injections

29
Q

What medication can increase the levels of beta-lactams by interfering with renal excretion? (but combination sometimes used intentionally in severe infections to increase antibiotic levels)

A

Probenecid

30
Q
A