Chapter 8: Antimicrobial Therapy Flashcards
In patients being treated with parenteral antibiotic, when is switching to oral indicated
Patient is responding to therapy, patient can take oral medications and absorb them, an oral equivalent is available
Endocarditis most likely organism/s
Staph aureus
Intrabdominal tissue most likely organism/s
E Coli, enterococcus, anaerobes, negative aerobic bacilli
Meningitis <2 months most likely organism/s
E coli, Group B strep, listeria
Meningitis 2 month-12 years most likely organism/s
Strep pneumoniae, N. meningitidis, H. Influenzae
Meningitis adult most likely organism/s
Strep pneumoniae, N. meningitidis
Upper respiratory tract most likely organism/s
S. Pneumoniae, H. Influenzae, moreaxella catarrhalis, Group A strep
Lower respiratory tract most likely organism/s
S. Pneumoniae, H. Influenzae, M. Catarrhalis, Klebsiella pneumoniae, mycoplasma pneumoniae, c. pneumoniae, viruses
Aspiration pneumonia most likely organism/s
Mouth flora
Lower tract hospital acquired most likely organism/s
S. Aureus, pseudomonas, other G- aerobic bacilli
Respiratory tract HIV coinfected most likely organism/s
Pneumocystis, S. Pneumoniae
Diabetic ulcer most likely organism/s
Staph, Strep, G- aerobic bacilli, anaerobes
UTI community most likely organism/s
E coli, enterococcus, staph saprophyticus
UTI hospital
E coli, enterococcus
Penicilin MOA
Bactericidal
Interferes with cell wall synthesis
Inactivates protein binding proteins
Penicilin active against
Staph, strep, most enterococcus
No activity against MRSA
DOC G+ infections such as endocarditis
Beta lactamase inhibitors
Clavulanic acid, avibactam, sulbactam, tazobactam
Use of beta lactam/beta lactamase inhibitors
intraabdominal and gynecological and skin/soft tissue infections, aspiration pneumonia, sinusitis, lung abscesses
Beta lactam/lactamase inhibitors are incompatible with
Aminoglycosides
Cephalosporins MOA
Bactericidal
Cell wall synthesis inhibition
Progression from 1st to 4th generation cephalosporins
Reflects an increase in G- coverage and loss of G+ activity
3rd and 4th cephalosporins can penetrate
CSF
Can treat meningitis
1st generation cephalosporins can treat
G+ skin infections, pneumoccoal respiratory, UTI, surgical prophylaxis
2nd generation cephalosporins treat
Community acquired pneumonia, other respiratory and skin infections
Monobactam agent
Aztreonam
Inhibits cell wall synthesis
Bactericidal
Aztreonam is active against
G-, including pseudomonas
Aztreonam to treat
Complicated and uncomplicated UTI and respiratory tract infections (pneumonia and bronchitis)
Carbapenems
Bactericidal Most broad spectrum agents available Not absorbed orally widely distributed with some CSF penetration Inhibit cell wall synthesis
Most broad spectrum carbapenems
Imipenem, meropenem, doripenem
Carbapenems useful in treating
Polymicrobial infections; skin and soft tissue, bone and joint, intrabdominal and lower respiratory tract
What can decrease clearance of meropenem and doripenem
Probenecid
Fluoroquinolones
-Floxacin
Bactericidal
Inhibits DNA gyrase and topoisomerase IV
Fluoroquinolones have activity against
G- aerobic bacteria and some G+
Only oral flouroquinolones active against pseudomonas
Ciproflaxacin and levofloxacin
Fluoroquinolones are drug of choice
UTI
Other uses for fluoroquinolones
UTI, pneumonia, STD, skin and soft tissue infections, GI infections, travelers diarrhea, osteomyelitis
DOC fluoroquinolone for nosocomial pneumonia
Cipro and levofloxacin
Cipro metabolism
Inhibitor of CYP450 enzyme
What can decrease absorption of fluoroquinolones
Antacids, sucralfate, magnesium, Ca, Fe
If fluoroquinolones are combined with steroids…
Risk of tendonitis
Prototypical macrolide
Erythromycin
Bacteriostatic
Inhibits bacterial protein synthesis by binding to 50S
Macrolide that has long half life–can use once daily dosing
Azithromycin
Macrolides are active against
G+ and G- aerobes and atypical organisms–broad spectrum
Macrolides used to treat
Respiratory tract infections, skin and soft tissue infections, STD, other atypical infections
Erythromycin and clarithromycin metabolism
Inhibitor of CYP450
Aminoglycosides
gentomicin, streptomycin
Bacteriostatic
Use and length of therapy is restricted due to drug related toxicities–nephrotoxicity and ototoxicity
Need parenteral administration due to poorly absorbed orally
Inhibit bacterial protein synthesis by binding to 30S
Aminoglycosides active against
Primarily G- aerobic (E Coli, klebsiella, proteus mirablis, enterobacter, pseudomonas)
Can be active against G+ but must be in combo with cell wall active agent (ampicillin, vanco, nafcillin)
Aminoglycosides uses
G- infections; neutropenic fever and nosocomial infections
Used in combo to treat pneumonia, bacteremia, intraabdominal and skin/soft tissues
Monotherapy not recommended
Streptomycin
Aminoglycoside used for TB treatment
Other examples of aminoglycosides
Gentamicin, tobramycin, amikacin
Aminoglycosides may cause
Neuromuscular blockade
Ca gluconate will reverse this
Tetracyclines
Bacteriostatic
Broad spectrum
Have short, intermediate, long acting agents
Best taken on empty stomach
Inhibit protein synthesis by binding to 30S
Used as alternatives if beta lactams not available
Tetracyclines examples
Doxycycline, demeclocycline, minocycline
Uses of tetracyclines
Rickettsial, chlamydial, acne, vulgaris, PID
DOC for lyme disease
Doxycycline
Tetracyclines that can treat MRSA
Doxycycline and minocycline
Dental side effect of tetracyclines
brown-gray discoloration of teeth that can be permanent
Drug interactions of tetracyclines
Divalent/trivalent cations decrease absorption, milk and dairy decrease absorption, can decrease levels of oral contraceptives, increases effect of warfarin
Sulfonamides
Absorbed in all body fluids and enters CSF, pleural fluid and synovial fluid
Inhibits synthesis of folic acid in bacteria
Usually used in combo with other antibiotics
Examples of sulfonamides
Suldafiazine, sulfisozazole, trimethoprim
Coverage of sulfonamides
G+ and G- except pseudomonas and group A strep
Bactrim
Trimethoprim-Sulfamethoxazole
DOC for treating UTI, PCP, toxoplasmosis
Drug interactions of sulfonamides
increase effects of warfarin, phenytoin, hypoglycemic agents, methotrexate
Glycopeptides
Vancomycin
Bactericidal
Narrow spectrum of activity against G+ organisms (MRSA)
Inhibits binding of d-ala-D-ala portion of cell wall precursor
DOC for MRSA
Vancomycin
Other uses of vancomycin
Neutropenic fever, endocarditis, meningitis
Most common SE vanco
fever, chills, phlebitis, red man syndrome (pruritus, flushing, hypotension)
Oxazolidinones
Linezolid and tedizolid only agents
Binds to 50S
Bacteriostatic
Antagonist of clindamycin
Activity of oxazolidinones
Active against G+ aerobic, MRSA, VRE, Penicillin resistant strep
Clindamycin
Bacteriostatic or bactericidal depending on dose
G+ and anaerobic infections
Binds to 50S–similar to macrolides
Uses of clindamycin
Mixed infections; toxoplasmosis, PCP, PID, toxic shock
Main SE of clindamycin
Diarrhea and C. Diff colitis
Metroniadzole
Flagyl
Bactericidal
Inhibits bacterial DNA
DOC for bacterial vaginosis, trich, and C.diff diarrhea
What will increase metabolism of metronidazole and cause treatment failure
Phenobarb, phenytoin, rifampin
Chloramphenicol
Bactericidal or bacteriostatic
G+, G-, anaerobic
Binds to 50S subunit
Use limited due to toxic profile–gray baby syndrome, optic neuritis, fatal aplastic anemia
Rifampin
Decreased RNA synthesis
Bactericidal or bacteriostatic
Active against G+ and some against G-: Neisseria meningitidis, N. gonorrhoeae, and H. Influenzae most sensitive
First line agent for TB
Rifampin
DOC for postexposure meningitis prophylaxis
Rifampin
SE of rifampin
Changes body fluids to red/orange
Rifampin metabolism
Inducer of CYP
Nitrofurantoin
Only used for UTI
Bacterial cell wall synthesis interruption through inhibition of several bacterial enzymes
Bacteriostatic or bactericidal depending on dose
Ineffective in patients with renal failure
Should not be used for complicated UTI–pyelonephritis
Linezolid SE
can cause thrombocytopenia in some patients
Also a mild MAO inhibitor
Erythromycin SE
Can cause rhabdomyolysis in combination with statins
Sulfamethoxazole- Trimethoprim
Bactrim
Bacteriostatic
Inhibits dihydrofolate reductase, which inhibits folic acid production in bacteria
Active against staph, strep, and MRSA
Streptogramins
quinupristin + dalfopristin combo
Bactericidal
Binds to 50S subunit inhibiting protein synthesis
Must be administered IV
Active against staph, strep, enterococcus and MRSA