Pharmacology Flashcards

1
Q

Mechanisms of resistance

A

malabsorption, pumping out, inactivation, ineffective, increased production of target molecules, develop alter metabolic pathways

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2
Q

how does resistance arise

A

temporarily, chomosomally, extrachromosomally (addition of plasmid, multiple gene combination)

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3
Q

how to minimize emergence of resistence

A

only use when clearly indicated, use as narrow spectrum as possible, use effective dose, consider phenotype/genotype of patient, ensure adequate duration, use older drugs when possible and combination drugs

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4
Q

superinfections

A

alter the normal flora by removing some, others overgrow in its place

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5
Q

how to distinguish superinfections from side-effects

A

if they have symptoms immediately after drug infection, it’s a side effect. but if it takes a couple days to set in, it’s a superinfection

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6
Q

three major classes of GI superinfections

A

candidiasis, staph enterocolitis, and psudomembranous colitis

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7
Q

candidiasis superinfection

A

fungal overgrowth, most common, continue antibiotic but add antifungal

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8
Q

staphylococcal enterocolitis superinfection

A

life-threatening superinfection, altered bacterial populations allow the overgrowth of staph, discontinue antibacterial and administer anti-staph penicillin or vancomycin

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9
Q

pseudomembranous colitis superinfection

A

life-threatening C. diff overgrowth, discontinue antibacterial and administer metronidazole or vancomycin

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10
Q

toxicity

A

dose-related, tissues that experience higher concentrations are more susceptible

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11
Q

hypersensitivity

A

drug allergies, immune-mediated, not related to therapeutic dose range

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12
Q

idiosyncratic responses

A

linked to drugs, but low frequency and not really related to dose, more genetically determined

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13
Q

how to administer the appropriate chemotherapy

A

based on culture AND susceptibility testing, monitor for therapeutic and toxic effects

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14
Q

purpose of combination therapy

A

enhanced therapeutic effect (synergism), allow use of lower doses to minimize toxicity, can combine 2 statics and they’ll become cidal, delay resistance, treat mixed infections, and initiate therapy in life-threatening situations before pathogen is known

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15
Q

who is a candidate for chemoprophylaxis

A

healthy individuals following known exposure, individuals with known dormant pathogen to minimize episodes, post-surgical patients and patients susceptible to endocarditis

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16
Q

drug selection in 4 steps

A
  1. can the drug affect the pathogen, based on susceptibilities?
  2. are the pharmacokinetics appropriate (renal failure, drug-drug interactions, etc.)
  3. is the drug appropriate for the patient (age, reproductive status, allergies, etc.)
  4. is this the ideal drug? (oral, cytocidal, cost, stage of the drug development?)