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43 Cards in this Set
- Front
- Back
what are some concentration dependent drugs |
aminoglycosides, quinolones, daptomycin, |
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what are some time dependent drugs |
carbapenems, PCN, cephalosporins |
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what are some other factors that influence probability of killing bugs, other than time & conc |
distribution of organism MICs for the drug, population distribution of pharmacokinetic parameters, drug protein binding |
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what are some ways to titrate abx so that it hits the right MIC and kill the bugs |
1. give the dose over a couple of hours rather than all at once 2. doubling the dose is not better - give agent over longer period of time instead 3. use a combo of drugs to manipulate half-lives and to be more effective against resistance |
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what are some ways bugs resist drugs |
they intrinsically or acquire ability to do: efflux, inactivation by microbial enzymes, or reduce uptake/affinity of drug by altering themselves |
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which PK factors affect your selecting the drug |
consider ADME, oral bioavailability, IV, serum conc, distribution in site of infection, route of elimination, half life, antibiogram, resistance patterns |
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which areas have compromised drug penetration? |
CSF, bone, prostate, eye, abscesses (meningitis inflammation makes drugs harder to get in. UTIs are actually easy to treat because drug concentrates in urine) |
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oral contraceptives with abx interaction? |
if you take drugs that disturb hormonal balance, use backup BC method. |
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warfarin and abx interaction? |
warfarin: disrupts synthesis of K, check INR |
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1st dosing for aminoglycosides in renal patients |
use a normal first dose |
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general rule with combination abx therapy |
avoid using 2 agents with same mechanism of action |
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how do you take cultures from people with endocarditis |
additional blood cultures bc yield is low. do at least 3 blood cultures for native valve endocarditis, 4-5 for prosthetic valve endocarditis |
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blood cultures from suspected bacteremia or candidemia |
single set not enough. do 3-4 cultures |
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pneumonia cultures: how do you do it |
sputum if non-intubated, BAL/ET aspirate if intubated |
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how do you send labs for: skin, meningitis, abscesses |
debrided tissue, CSF, and pus in that order |
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what do you do before giving antibiotics |
2 blood cultures done at least 10 mins apart, and a culture from infected site. use catheter tip +3 (4) for peripheral cultures. cultures for strict anaerobes should be sent via anaerobic transport media, duh |
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when do you do swab cultures |
only body fluids, tissue, pus and exudates, nothing else. |
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does time above MIC matter for conc dependent drugs |
NOOOOO |
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what do you consider when choosing the right drug |
site of infection, patient, allergies, antibiogram, spectrum of activity |
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which drugs target cell wall synthesis? |
cephalosporins d-cycloserine cephamycins vancomycin pcn bacitracin beta lactam antibiotics carbapenems |
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which drugs target DNA synthesis |
metronidazole |
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which drug targets DHA gyrase (nucleic acid metabolism) |
quinolone |
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which drug targets RNA polymerase (nucleic acid metabolism) |
rifamycins
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which drug targets phospholipid membranes |
polymyxins amphotericin ketoconazole |
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which drug targets protein synthesis |
chloramphenicol tetracyclines glycycline macrolides clindamycin streptogramins oxazolidinones aminoglycosides |
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which drug inhibits folate synthesis |
sulfonamides trimethoprim |
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what are some beta lactam drugs and what do they do |
pcn cephalosporins monobactam carbapenems
they work at the cell wall to inhibit it |
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what is a glycopeptide drug and what does it do |
vancomycin, it does cell wall inhibition |
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what are the three phases of cell wall synthesis |
monomer synthesis monomer polymerization cross linking of polymers |
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describe monomer synthesis |
1st phase of cell wall synthesis, takes place in cytoplasm where peptidoglycan monomers from amino acids and sugars synthesize. precursor formation. |
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describe monomer polymerization |
2nd sty of cell wall synth: links to form long polymer, lipid mediated and takes place at cytoplasmic membrane |
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describe cross linking of polymers |
mediated by transpeptidases. facts: pcn binding proteins (PBPs), extracellular, takes place in periplasmic space. |
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describe structure of b lactam drugs |
has thiazolidine ring and b lactam ring attached to side chain. nucleus is structural requirement for main bio activity side chain determines characteristics you get different PCNs by adding side chains |
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how do b lactams work |
interferes with last step of cell wall synthesis (transpeptidation or cross linkage) inactivates PBPs by binding to them, leads to autolysis/cell death time dependent kill bactericidal against actively dividing bacteria |
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how do bugs resist b lactams? |
b lactamase enzymes hydrolyzes b lactam rings decreased permeability thru cell membrane altered PBPs with lower affinity efflux (gram -) |
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what are some natural PCNs |
PCN G (parenteral): potassium or sodium salt, procaine IM (comparable levels to IV for 24 hrs), benzathine IM (maintains low levels for weeks) PCN VK (oral) |
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spectrum of activity for natural PCNs |
active against sensitive strains of gram + cocci, anaerobes (clostridium per fringes), and some gram - cocci (neisseria) spirochetes hydrolyzed by penicillinase (beta lactamase) works well for STIs but usually for wimpy bugs |
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penicillinase resistant PCNs? |
antistaphylococcal penicillins: methicillin (not available), nafcillin, oxacillin (both parenteral) and PO: cloxacillin, dicloxacillin |
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for which bugs do penicillinase resistant PCNs work |
penicillinase producing staphylococci (methicillin susceptible s. aureus (MSSA)) pcn susceptible streptococcus sp. PO for skin/soft tissue infections, IV for endocarditis, osteomyelitis, etc. well tolerated, good oral absorption NOT FOR MRSA, ENTEROCOCCI, LISTERIA |
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what are some aminopenicillins |
ampicillin (parenteral, PO) amoxicillin PO |
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spectrum of aminopenicillins? |
similar to PCN G, additional activity against enterococci, listeria, select gram - (e coli, proteus mirabilis, haemophilus influenza, salmonella that is not producing beta lactamase |
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does amino penicillin gets hydrolyzed by beta lactamase |
yes |
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clinical use of aminopenicillins |
strep infections enterococcus - endocarditis listeria - bacteremia, meningitis prophylaxis of neonatal group b strep disease and rheumatic fever (dental) |