abx: actions against intracellular activity Flashcards
moa
inhibit or alter protein synthesis: transcription and translation
aminoglycosides
gentamicin, amikacin, tobramycin
gram -, also gram + but need other abx for synergistic effect (vancomycin, beta lactam - give these first so aminoglycosides can get into cell)
peak/trough levels
transitioned from 3/day to 1/day
aminoglycosides SE
nephrotoxicity (reversible, monitor creatinine levels)
ototoxicity (permanent)
peak trough levels
aminoglycosides I
complicated infections
UTI/pyelonephritis, gynecoid infections, peritonitis, endocarditis, pna, osteomyelitis (DM related)
aminoglycosides moa
inhibit bacterial ribosomes
gentamycin
if given with NM blockade (paralytic) -> be careful, can cause profound resp distress (myasthenia gravis)
CNS SE: confusion, depression, disorientation, numbness, tingling
cochlear damage: ototoxicity, high freq hearing loss, high pitched tinnitus
lincosamides: clindamycin
bactericidal or bacteriostatic - depending on drug []
same moa
I: chronic bone infections, GU tract infections, intraabd infections, anaerobic pna, septicemia, serious skin infections, prophylaxis for endocarditis
PO and IV
monitor use with NM blockade meds
very toxic - monitor levels (resp distress)
can cause deadly pseudomembranous colitis (disabiling d -> c. Diff -> colitis)
VRE and CRE and other enterobacter bacteria are resistant to this drug
macrolides
erythromycin and ezithromycin
bacteriostatic in general, bactericidal in high enough concentrations
YUCK drugs: GI SE profil intense (esp erythromycin)
moa: inhibit protein synthesis by binding to ribosomes
I: various infections of upper and lower respiratory infections, skin infections, soft tissue infections, STI; legionnaires, listeria, mycoplasma pna can all be treated with macrolides
erythromycin
hypomotility benefits for diabetic gastroparesis and increase gastric motility and emptying (given to people with DM which sometimes affect gastric mobility)
doesn’t cross BBB
PO (abs not great, dont take on empty stomach) and IV (painful), topical and ophthalmic also available
lots of drug interactions
azithromycin
Z pack!
differ structurally from other macrocodes, has some advantage in coverage compared to erythromycin
less GI upset, still some
Longer DOA (2/day -> 1/day)
very good tissue penetration and long durations of action
taking with food decreases absorption, so dont take with food
tetracyclines
tetracycline, doxycycline, minocycline
bacteriostatic, inhibit protein synthesis by binding to ribosomes
broad spectrum, major resistance has developed
tetracyclines: I
Rickettsia (Rocky Mountain spotted fever), chlamydia and trichomonas, Lyme, cholera, pelvic inflammatory disease, mycoplasma pneumonia, acne
tetracyclines: CI
pregnant and nursing, <8yo
tetracyclines: SE
discoloration of permanent teeth and tooth enamel hypoplasia in fetuses and children, photosensitivity (sunscreen!), many others - d, yeast infection, thrombocytopenia
tetracycline
bacteriostatic
not available parenterally (PO only): fasting = 75-77% absorbed, gibing more decreases % abs
concentrates in bone, liver, tumor, spleen, teeth! (damage <8yr)
SE: nod, HA, photosensitivity, dizzy; rare = anaphylaxis and angioedema