pharmacology 3 Flashcards

1
Q

minimum inhibitory concentrations (MIC)

A

lowest concentration of drug that inhibits visible bacterial growth
MIC90 concentration for inhibiting 90% of the bacteria

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2
Q

Minimum bactericidal concentration (MBC)

A

the lowest concentration of a drug that kills 99.9% of bacteria

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3
Q

mutant prevention concentration (MPC)

A

the concentration of the least susceptible single-step mutant
in theory, kills them all so mutant so they cant form

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4
Q

bacteriostatic

A

stop bacteria from multiplying: don’t kill them
MBC much larger than MIC
elimination of infection requires host immune response
requires an immunocompetent patient

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5
Q

bactericidal

A

kill bacteria if concentrations reach MBC for a certain period of time
MBC at or near the MIC
preferred for immunosuppressed animals
preferred for severely ill patients

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6
Q

bactericidal antimicrobials are not always bactericidal

A

static at concentration below MBC
dose dependent
bacteria dependent
bacterial must be multiplying for cidial to work

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7
Q

postantibiotic effect (PAE)

A

persistent drug effect
after plasma concentration decline below the MIC/MBC

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8
Q

mechanisms of PAE

A

decreased virulence of bacteria
development of abnormal cell wall or septum
increased susceptibility to host defenses
persistence at site of infection
only occurs with some drugs and is bacteria-dependent

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9
Q

pharmacokinetic-pharmacodynamic interaction

A

predict the success of antimicrobial therapies
relate concentration of drug to MIC of the pathogens
vary by class of drug
vary with each pathogen
drug-bug interaction

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10
Q

time-dependent antibiotics

A

T>MIC
duration plasma concentration if above the MIC over 24 hours

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11
Q

concentration dependent antibiotics

A

Cmax:MIC
ratio of the maximum plasma concentration to the MIC

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12
Q

Concentration/time dependent antibiotics

A

AUC:MIC
ratio of the AUC.24 to the MIC

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13
Q

narrow spectrum

A

implies activity against a limited subset of bacteria

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14
Q

broad spectrum

A

implies activity against a wide range of bacteria
may include mycoplasma, rickettsia, and chlamydia

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15
Q

spectrum of activity

A

tells you that the bacteria can be affected by antimicrobial

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16
Q

aerobic bacteria

A

gram +
streptococci
staphylococci
gram -
respiratory pathogens
enteric pathogens

17
Q

anaerobic bacteria

A

gram +
gram -

18
Q

penicillins

A

active against streptococci, but NOT staphylococci
NOT active against gm - (Cell wall blocks)
active against most gm + and gm - anaerobes

19
Q

aminoglycosides

A

active against staphylococci but NOT streptococci
active against respiratory and enteric gm -
NO activity against anaerobes

20
Q

macrolides

A

active against gm + aerobes
active against respiratory gm - but NOT enteric
active against most gm + anaerobes

21
Q

facultative anaerobes

A

are aerobes
can grow in anaerobic conditions
culture as aerobes
test susceptibility in aerobic conditions
in vitro susceptibility may not equal in vivo susceptibility

22
Q

additive/indifferent

A

2+2=4
used to extend spectrum
does not enhance activity of either

23
Q

synergism

A

what we hope for
combination enhances activity
static alone, cidial together
2+2=6

24
Q

antagonism

A

what we worry about
2-+2=2
activity of the combination is less than sum

25
Q

first questions for antibacterial use

A

is an antibacterial necessary

26
Q

use an antimicrobial when

A

bacterial infection systemic

27
Q

do not use an antimicrobial when

A

viral infection
fungal infection
parasitic infection

28
Q

maybe use an antimicrobial when

A

protozoal infection
bacterial infection-local

29
Q

intravenous judicious use

A

highest concentrations
highest risk of adverse effects
severe systemic illness
owner comfort level/animal temperament

30
Q

IM/SC judicious use

A

bioavailability is often complete
risk of drug toxicity less than IV
injection site reactions
owner comfort level/animal temperatment

31
Q

oral judicious use

A

ileus-gi too slow
colitis-gi too fast
malabsorption
drug interaction

32
Q

transdermal judicious use

A

not recommended no no no

33
Q

others routes of administration for judicious use

A

topical-eye,skin, wound
inhaled
intraarticular/regional limb perfusion

34
Q

site of infection

A

for most pathogens, the site of infection is the interstitial fluid
protein binding is a major determinant of drug distribution of ISF
low protein bound drugs have good destruction
highly protein bound drugs have limited distribution>80%

35
Q

site of infection-exception to the rule

A

CNS, eye, prostate, bronchus, testes
protective barriers that consist of tight junction between the endothelial
limited drug movement into these areas
lipids solubility or active transport

36
Q

site of infection-intracellular infection

A

lipophilic drugs have better penetration into cell than do hydrophilic drugs

37
Q

site of infection-abscesses and granulomas

A

drug diffusion slow
lower cmax
slower equilibrium
lower blood supply to the area
treatment unsuccessful without draining
if you can drain and lavage the abcsess, antibacterial may not be necessary
if can not drain-choose a more lipophilic drug. treat for al long time

38
Q

local tissue factors

A

affect the efficacy of some drugs
purulent debris
acidic environment
hemoglobin/hemorrhages
anaerobic conditions/necrotic tissue-decreased blood supply

39
Q

choosing an antibiotic

A

empiric treatment
know which bacteria are commonly involved in which infections
choose a drug likely to treat that bacteria