Introduction to Antimicrobials Flashcards

1
Q

Mordant for Gram staining

A

Iodine

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2
Q

Class of antimicrobials that has no effect on anaerobes since it needs to enter the cell wall via an oxygen dependent process

A

Aminoglycoside

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3
Q

Space between the outer envelope and peptidoglycan

A

periplasmic space

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4
Q

Which of the following is the target of aminoglycosides?
A. Bacterial cell wall synthesizing enzymes
B. Bacterial ribosomes
C. Enzymes for nucleotide synthesis and DNA replication
D. Viral replication machinery

A

B. Aminoglycosides and tetracycline targets the 30s subunit

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5
Q

Which of the following targets enzymes required for nucleotide synthesis and DNA replication?
A. Streptomycin
B. Lincosamides
C. Streptogramin
D. Quinolones

A

D. Quinolones and Sulfa drugs target enzymes for nucleotide synthesis and DNA replication

Streptomycin, Macrolides, Lincosamides, Streptogramin all target the 50s subunit ribosome

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6
Q

Which of the following is the target of Beta-lactams?
A. Bacterial cell wall synthesizing enzymes
B. Bacterial ribosomes
C. Enzymes for nucleotide synthesis and DNA replication
D. Viral replication machinery

A

A. Beta-lactams penetrate peptidoglycan layer of gram-positive organisms

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7
Q

Better choice of antimicrobial for life-threatening infections in immunocompromised patients
(Bactericidal or bacteriostatic)

A

bactericidal

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8
Q

Which antimicrobial has more chances of developing ADRs?
(Absorbable or non-absorbable)

A

absorbable

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9
Q

Concentration of drug required to kill the organism

A

Minimal bactericidal concentration

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10
Q

Increasing the concentration drug increases the extent and rate of microbial killing

A

Concentration-dependent antibiotics

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11
Q

Concentration of drug required to inhibit growth of the organism

A

Minimal inhibitory concentration

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12
Q

Bactericidal activity continues as long as serum concentrations are greater than the MBC

A

Time-dependent antibiotics

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13
Q

Persistent suppression of bacterial growth after limited exposure to an antimicrobial agent

A

Postantibiotic effect

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14
Q

Macrolides were found to have increased the susceptibility of bacteria to activity of leukocytes. This is known as:

A

Postantibiotic leukocyte enhancing effect (PALE)

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15
Q

T>MIC is expressed in what unit?

A

percentage

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16
Q

Which of the following is T>MIC at least 40-50% of dosing interval but with minimal or no PAE effects?
A. Beta-lactams
B. Macrolides
C. Clindamycin
D. AOTA

A

D. AOTA

17
Q

T/F: IV drugs usually have 100% bioavailability

A

true

18
Q

This reflects the actual body exposure to drug after administration of a dose of the drug and is expressed in mg*h/L.

A

Area under the curve (AUC)

19
Q

AUC is dependent on (2):

A

Rate of elimination and Dose administered

20
Q

This pertains to medical treatment based on possible etiology of infection without direct evidence of what type of bacteria is present

A

Empiric therapy

21
Q

T/F:
Azalides and Oxazolidenons follows a time-dependent killing with a moderate to persistent PAE

A

True
Azalides (azithromycin)
Oxazolidinons (linezolid)

22
Q

Which of the two has activity against anaerobes as it needs a reduced, devoid of oxygen, environment to gain access to bacterial cell?
(Metronidazole or Aminoglycoside)

A

Metronidazole

23
Q

T/F:
Nafcillin, a pencillinase-resistant penicillin, is frequently used for treatment of staphylococcal infections in hemodialysis patients.

A

T: Unlike other penicillins, nafcillin exhibits primarily hepatic clearance rather than renal clearance.

24
Q

Which among the third generation cephalosporins has a dual route of elimination?
A. Ceftriaxone
B. Ceftazidime
C. Cefotaxime

A

A. Ceftriaxone

25
Q

T/F: Monotherapy is preferred in patients with Pulmonary TB

A

False

26
Q

T/F: Vancomycin level are expected to be decreased in hemodialysis patients

A

T

27
Q

Conversion of IV medication to a PO equivalent within the same class and has the same level of potency, but of a different compound
A. Oral switch
B. Step-down
C. Sequential therapy

A

A. Oral switch

28
Q

Conversion from an injectable medication to an oral agent in another class
A. Oral switch
B. Step-down
C. Sequential therapy

A

B. Step-down

29
Q

Act of replacing a parenteral version of a medication with its oral counterpart of the same compound
A. Oral switch
B. Step-down
C. Sequential therapy

A

C. Sequential therapy

30
Q

T/F:
If procalcitonin starts to go up, antibiotics can be stopped

A

F:
procalcitonin should decrease to warrant discontinuation of antibiotics

31
Q

T/F:
Antifungals target ergosterol or ergosterol synthesis

A

T

32
Q

Pattern of antimicrobial activity of Carbapenems
A. Type I
B. Type II
C. Type III

A

B. Type II: T>MIC (Time-dependent killing with minimal PAE)
CCELP (Carbapenem, Cephalosporin, Erythromycin, Penicillin)

33
Q

Pattern of antimicrobial activity of Ketolides
A. Type I
B. Type II
C. Type III

A

A. Type I: Concentration-dependent killing
ADFK (aminoglycoside, daptomycin, fluoroquinolones, ketoldies)

34
Q

Pattern of antimicrobial activity of Carbapenems
A. Type I
B. Type II
C. Type III

A

C. Type III: 24h-AUC/MIC (Time-dependent killing with moderate to prolonged PAE)
OCTAV (Oxazolidinone, Clindamycin, Tetracycline, Azithromycin, Vancomycin)

35
Q

The goal of therapy for 24h-AUC/MIC is to maximize the:

A

amount of drug