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66 Cards in this Set

  • Front
  • Back
Block cell wall synthesis by inhibition of peptidoglycan cross-linking
Penicillin, ampicillin, ticarcillin, piperacillin, imipenem, aztreonam, cephalosporins
Block peptidoglycan synthesis
Bacitracin and vancomycin
Disrupt bacterial cell membranes
Polymyxins and daptomycin
Block nucleotide synthesis
Sulfonamides and trimethoprim
Block DNA topoisomerases
Fluoroquinolones
Block mRNA synthesis
Rifampin
Block protein sythesis at 50S ribosomal subunit
Chloramphenicol, macrolides, clindamycin, streptogramins (quinupristin, dalfopristin), linezolid, daptomycin
Macrolides
Erythromycin, clarithromycin, azithromycin
Block protein synthesis at 30S ribosomal subunit
Aminoglycosides, tetracyclines
Aminoglycosides (5)
Streptomycin, Gentamicin, Tobramycin, Amikacin, Neomycin
Tetracyclines (4)
Tetracycline, doxycycline, minocycline, tigecycline
Aminoglycosides good against
Gram negative aerobic infections
Aminoglycosides a DOC for these 3
Pseudomonas, Invasive enterococcal infections, Francisella tularensis
2 things that block the transport of Aminoglycosides
Anaerobic environment and low extracellular pH
Most common Aminoglycosides resistance mechanism
Aminoglycoside modifying enzymes (AME)
Aminoglycosides: IV or parenterally
Usually given parenterally unless local GI effect desired
How are aminoglycosides eliminated?
Largely eliminated by the kidneys; must adjust dose relative to creatinine clearance
Primary toxicities of Aminoglycosides
Nephrotoxicity, Ototoxicity, and Neuromuscular blockade
Absolute contraindication for aminoglycosides
Myasthenia gravis - high risk of neuromuscular blockade causing respiratory depression
How to reverse the neuromuscular blockade caused by aminoglycosides
Calcium gluconate or neostigmine
Can be used alone to treat tularemia and plague
Streptomycin
Drugs to treat brucellosis
Streptomycin and doxycycline
Used in combination with a cillin for Pseudomonas or Enterococcal; most frequently used AG
Gentamicin
Used when other Aminoglycosides fail; has the broadest spectrum
Amikacin
Primarily used orally to sterilize the gut; when taken systemically is the most toxic of the Aminoglycosides
Neomycin
The 4 tetracyclines
Tetracycline, doxycycline, minocycline, tigecycline
Preferred tetracycline for patients with poor renal function
Doxycycline
Preferred tetracycline for meningococcal carrier state (enters CSF in therapeutic amounts)
Minocycline
Drug of choice for Bacillus anthracis
Tetracyclines
Drug of choice for Mycoplasma p., chlamydia, Rickettsiae, Lyme disease
Tetracyclines
Tetracyclines: bacteriocidal or -static
Bacteriostatic
Primary resistance to tetracyclines via:
Efflux pumps and ribosome protection
Form stable 'chelates' with cations
Tetracyclines
Tetracycline given IV, with biliary excretion, and effective against resistant organisms (MRSA, etc)
Tigecycline
6 adverse reactions to tetracyclines
Gastrointestinal, Bony structures and teeth, liver toxicity, local tissue toxicity, photosensitization, vestibular reactions
Outdated and degraded tetracyclines can cause this if taken
Fanconi syndrome
50S inhibitor that can cause bone marrow suppression and serious and fatal blood dyscrasias
Chloramphenicol
Gray syndrome
Adverse effect of Chloramphenicol caused by a lack of glucuronyl transferase activity
Drug of choice for Campylocbacter jejuni, H. pylori, Shiggella spp
Macrolides
Drug of choice for children and pregnant females or allergic to penicillin
Macrolides
Macrolides: bacteriocidal or bacteriostatic
Bacteriostatic
Resistance to Macrolides via:
Active efflux pump and Ribosome modification
Less frequent dosing than erythromycin
Clarithromycin
Differs from erythromycin and clarithromycin in its long half-life (around 70 hours)
Azithromycin
Of the macrolides, which doesn't inhibit CYP3A4
Azithromycin
Inhibits CYP3A4
Macrolides
Macrolides adverse effects
CYP3A4 inhibitor, GI effects, Cholestatic hepatitis
Primary reason for stopping erythromycin
GI effects - epigastric distress
Fever, jaudice, impaired liver function primarily seen with erythromycin estolate dose form
Cholestatic hepatitis
Aerobic Gram negative bacilli are intrinsically resistant to
Clindamycin
Treatment of anaerobic and streptococcal and staphylococcal infections
Clindamycin
Drug of choice for C. perfringens
Clindamycin
Don't use this with erythromycin and chloramphenicol as it binds close to their binding sites
Clindamycin
Resistance to this drug primarily by methylation (like the macrolides)
Clindamycin
Adverse effects of Clindamycin
Severe diarrhea and Pseudomembranous colitis
Drug of choice for Vancomycin resistant Enterococcus faecium (VRE)
Quinupristin and dalfopristin; also linezolid/daptomycin
Quinupristin binds here:
At the same site as macrolides (50S)
Dalfopristin works via:
Directly interfers with polypeptide chain formation; synergistically enhances binding of quinupristin
Quinupristin and dalfopristin bacteriocidal or -static
Bacteriocidal
Adverse effects of Quinupristin and Dalfopristin
Infusion related events, severe arthralgias and myalgias, cost
Drug of choice for vancomycin resistant Enterococcus faecium and faecalis
Linezolid
Linezolid should be reserved for
Multi-Drug resistant Gram positives
Potent CYP3A4 inhibitor
Quinupristin and dalfopristin; also Macrolides
Adverse effects of Linezolid
Thrombocytopenia (most common), Anemia, leukopenia, cost
Mechanism of action via binding to bacterial membranes; causing rapid depolarization; loss of membrane potential; cell death
Daptomycin
Adverse effects of Daptomycin
Skeletal muscle damage, superinfection (pseudomembranous colitis), cost