Topic 1-General considerations of antimicrobial therapy. Disinfectants and antiseptics Flashcards

1
Q

Examples of bactericidal agents

A

-beta lactams -glycopeptides -aminoglycosides -fluoroquinolones

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2
Q

Examples of bacteriostatic abx

A

-choramphenical -macrolides -tetracyclines

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3
Q

Three types of abx therapy

A

-empiric-no time to identify microorganism responsible for the infection -sensitivity-make antibiogram to know which abx they are sensitive to -prophylactic

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4
Q

Effective therapy depends on which characteristics of the drug

A

1.)pathogen has to be sensitive to abx 2.)antimicrobial has to be in effective concentration at site of infection -pharmacokinetics of the drugs -route of administration -dose -adverse effects

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5
Q

What is post antibiotic effect

A

The period of time when the bacteria doesn’t continue it’s growth after levels of abx has fallen below MIC (This means that abx with long PAE like fluoroquinolones only require one dose per day)

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6
Q

What is MIC and MBC

A

The lowest antimicrobial concentration that prevents visible growth of an organism after 24 hours. MBC is minimum of bactericidal concentration

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7
Q

3 types of MBC ABX types

A

1.) Concentration dependent abx activity -aminoglycosides and daptomycin -once a day infusion achieves high peak levels, favoring rapid killing of the infecting pathogens (not always done) 2.)Time-dependent antibacterial activity -beta lactams -multiple dosing or continuous infusion to prolong MIC 3.)AUC/MIC -Fluoroquinolones -concentration dependent ABX, but resistant mutants are formed, high concentration maintained maintained for long time to be effective

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8
Q

Time-dependent antibacterial activity? (Example)

A

How long will effective ABX present at site of infection

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9
Q

3 reasons to have combination therapy?

A

1.) Synergistic effect 2.)To extend the antibacterial spectrum 3.)To prevent the development of resistance

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10
Q

Indications of prophylactic treatment (2 reasons and explanation)

A

1.) Surgical prophylaxis-Decreases incidence of potential infection after procedure (dental or heart valve procedure) 2.) Non-surgical prophylaxis- Individuals with high risk (immunocomprised) Recurrent infections Close contact (meningococcal) Risk of infection (malaria, anthrax)

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11
Q

3 antibacterial spectrum types and a example

A

1.) Narrow spectrum -Gram +/aerobic/anaerobic (vancomycin) 2.) Extended spectrum? 3.) Broad spectrum -Gram +/-/aerobic/anaerobic (carbapenems)

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12
Q

What do you have to take in account for dosing?

A

1.) Newborns vs Elderly have different means of elimination 2.) Weight (aminoglycosides don’t enter fat so it’s not a proportional increase with weight 3.) Increased extracellular space (ascites, newborns, pregnant) so a higher does is needed

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13
Q

During of treatment typically? UTI? Pneumonia? Chronic treatment/difficult to reach site (chronic prostitis)? Osteomyelitis? Tuberculosis?

A

Typically 5 days UTI is 5 day treatment pneumonia is 7-10 days chronic treatment is 3-6 weeks osteomyelitis is 4-6 months tuberculosis is half a year

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14
Q

Main compications of ABX therapy ( 4 answers)

A

1.) hypersensitivity 2.) direct toxicity (aminoglycosides cause ototoxicity and nephrotoxicity) 3.)super-infections 4.) High concentration of penicillin cause seizures

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15
Q

3 Antibiotics that are safe in pregnancy?

A

beta lactams, macrolides, and cephalosporins

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16
Q

Which antibiotics can go intracellularly? How?

A

Macrolides, fluroquinolones, or tetracyclines can be uptaken by active transport

17
Q

Types of antibiotic mechanism

A

1.) cell wall synthesis inhibitors 2.)protein inhibitors 3.) DNA damagers

18
Q

How do bacteria form resistance (4 methods)

A

1.) Bacteria creates enzyme to break down abx Such as beta lactamases, sensitivity varies Most sensitivity=penicillin Moderate sensitivity=cephalosporin Least sensitive=carbapenems 2.)Changing of PBP binding site MRSA This is not the case in 5th generation cephalosporins 3.)Decreased permeability Gram - change number of pores or absence of pores 4.)Efflux pump