9-1 Intro to Abx Flashcards

1
Q

What are the 3 Factors that determine appropriate Abx therapy?

A
  1. Host Characteristics
  2. Abx abilities
  3. Infection SITE and Pathogen involved
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2
Q

List the 7 Sterile Body Sites and their associated fluids

A

Pts Should Produce Sterile Blood Upon Probing”

ºPericardium = Pericardial Fluid

ºSubArachnoid Space = CSF

ºPleural Space = Pleural Fluid

ºSynovium = Synovial Fluid

ºBloodstream = Blood

ºUrinary Tract = DIRECT URINE FROM BLADDER

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3
Q

A: Define Contamination

B: example

A

A: Organism is inadvertently introduced to the pt during collection or processing smh

B: Coag-neg staph in blood of pt

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4
Q

A: Define Colonization

B: example

A

A: Organism is present at body site BUT IS NOT INVADING OR CAUSING HARM

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5
Q

Empiric Therapy

A

Giving Abx that will treat what’s LIKELY thought to be the pathogen (pre-lab)

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6
Q

A: Antimicrobial Susceptibility Testing includes ____ and _____ and is performed on individual _____ isolates once grown up and identified in _______

B: Define the 2 components

C: Which one should be Larger in #?

A

A: Antimicrobial Susceptibility Testing includes [Minimum Inhibitory Concentration-MIC] and [Minimum BacterioCIDAL Concentration-MBC] and is performed on individual BACTERIAL isolates once grown up and identified in CULTURE

B:
1. MIC= Minimum INHIBITORY Concentration of Abx needed to STOP Visible Bacterial Growth. (Can be further described in [3 Susceptibility Breakpoints] )

MBC= Minimum Abx Concentration needed to KILL BACTERIA and REDUCE INOCULUM BY 99.9%

C: MBC ≥ MIC

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7
Q

A: Susceptibility Breakpoints (3)

B: What do they describe?

A

A:
1) Susceptible= Organism’s MIC is within normal range and can be eradicated w/normal abx dose

2) Intermediate= Organisms’s MIC is at MAX DOSE OF ABX and so tx MAY be successful
3) Resistant= Organisms’s MIC EXCEEDS [Toxic MAX DOSE OF ABX] –> likely subOptimal outcome

B: [S.I.R.] further describe [MIC - Susceptibility Testing]

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8
Q

There are 4 test used to determine MIC. [MACROdilution vs. microdilution vs. [Disk Diffusion Kirby Bauer] vs. [E-test]

A: Describe MACROdilution

B: Why isn’t this performed routinely?

C: What type of MIC does this give you? [Exact vs. Range]

A

A: MACROdilution: [TWO fold serial dilutions of abx] are incubated with [bacterial inoculum] in several test tubes. 1st test tube to show NO VISIBLE GROWTH= [EXACT MIC]

B: (x) Labor and Resource intensive (x)

C: [EXACT MIC]

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9
Q

There are 4 test used to determine MIC. [MACROdilution vs. microdilution vs. [Disk Diffusion Kirby Bauer] vs. [E-test]

A: Describe microdilution

B: Why is this the preferred method?

C: Con of microdilution

D: List two companies that perform microdilution

E:What type of MIC does this give you? [Exact vs. Range}

A

A: microdilution: [serial dilutions of abx] are incubated with [bacterial inoculum] in several [microtiter plates/cassettes] and ELECTRONICALLY tested simultaneously

B: Automated Process

C: Small cassettes impede ability to test all abx concentrations –> Results are reported as [MIC Range]

D: Vitek and Microscan

E: [MIC Range]

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10
Q

There are 4 test used to determine MIC. [MACROdilution vs. microdilution vs. [Disk Diffusion Kirby Bauer] vs. [E-test]

A: Does [Disk Diffusion Kirby Bauer] Determine MIC?

B: What do the Zone Diameters tell you?

C: Quantitative or Qualitative Test?

A

[Disk diffusion Kirby Bauer] - DdKB

A: DOES NOT TELL YOU MIC !

B: Zone Diameters (measured in mm) correlates with [S.I.R. - Susceptibility Testing]

C: QuaLitative

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11
Q

There are 4 test used to determine MIC. [MACROdilution vs. microdilution vs. [Disk Diffusion Kirby Bauer] vs. [E-test]

A: Describe [E-Test]

B: Does [E-Test] Determine the MIC?

A

A: [E-test] Combines [Quantitative Serial Dilution] with [QuaLitative DdKB]. Plastic Strip with different concentrations of abx is placed on agar plate covered in bacteria.

B: YES. Area Where Ellipse crosses the strip = MIC

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12
Q

4 Criteria that’ll affect [Susceptibility Breakpoints: S.I.R.] for an Abx

A

“The PIG Criteria is Susceptabile

  1. Pharmacokinetics of the Abx Drug
  2. General Activity of the Abx
  3. Infection SITE
  4. Clinical Data
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13
Q

Empiric therapy is based on ________ and _______. It is given _____(after/before) [culture and susceptibility reports] have returned

A

Empiric therapy is based on [DOC for most likely organism] and [regional susceptibility]. It is given BEFORE [culture and susceptibility reports] have returned

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14
Q

Describe the 3 Outcomes of Combination Therapy B: Combination therapy allows coverage of the entire ______ and prevents _____

A

ºAdditive: [[A and B]] = (A alone) + (B alone)
——————————————————————————-
ºAntagonistic: [[A and B]]

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15
Q

Name 4 Dz that BacteriCidals are specifically needed to treat

A

“You can only kill FOME with BacteriCidals

  1. [Febrile neutropenia]
  2. Osteomyelitis
  3. Meningitis
  4. Endocarditis
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16
Q

[β-Lactams] Abx

A: bacteriostatic or BacteriCidal?

B: [Post Abx Effect] Time

A

BacteriCidal

B: PAE = 2 Hours

17
Q

Lipopeptide Abx

A: bacteriostatic or BacteriCidal?

B: ex

A

BacteriCidal

ex: Daptomycin

18
Q

A: Name the Only 7 [Abx Classes] that are bacteriostatic

B: These all are _______ Inhibitors

A

Macrolides: Some Of Them Can Limit Growth “

  1. Macrolides
  2. Streptogramins
  3. Oxazolidinones
  4. Tetracyclines
  5. Chloramphenicol
  6. Lincosamides
  7. ## GlycylcyclinesB: These ALL are PROTEIN SYNTHESIS Inhibitors
19
Q

[Post Abx Effect] - PAE

A

Time it takes for a bacteria to “recover” and REgrow after an abx has fallen BELOW [Minimal Inhibitory Concentration]

(Depends on the [Abx Drug] and [specific Bacteria] )

20
Q

A: [Gram ✚ Bacteria] ALL have some amount of {PAE}. What is [Gram ✚ Bacteria] {PAE} with [β-Lactams Abx]?

B: [Gram negative Bacteria] have ______ {PAE} when treated with _____ and______ inhibitors

A

A:What is [Gram ✚ Bacteria] {PAE} with [β-Lactams Abx]? = 2 HOURS

B: [Gram negative Bacteria] have prolonged {PAE} when treated with Aminoglycoside and Fluoroquinolones inhibitors = it’ll take them a long time to recover

21
Q

5 Steps for Antimicrobial Selection

A

CEiSM

1st: Confirm presence of actual infection
2nd: Empiric Therapy
3rd: Identify Pathogen
4th: STREAMLINE Abx therapy

5th: Monitor Therapeutic Response
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