Pharmacology - Antimicrobials Flashcards
List the five factors that determine the risk of emergence of resistant bacterial strains.
- Size of the inoculum
- Ability of the bacteria to acquire mutations
- Ability of host defenses to eliminate resistant bacteria
- Drug concentrations at the site of infection
- Duration of exposure to AMDs
Define “antibiotic”
A natural chemical, produced by other organisms, that is designed to suppress the growth of other organisms (including bacteria, fungi, or protozoa).
Define “antimicrobial”
Any compound, natural or synthetic, that suppresses microbial growth.
Define “antibacterial”
Any compound that suppresses bacterial growth.
List major strategies that may reduce the selection for antimicrobial resistance.
- Documentation of the presence of infection
- Appropriate susceptibility testing
- Proper identification of the infecting organism
- The use of agents that are as specific for the pathogen as possible, at the proper dose and for the proper duration of time
First-line antibacterial drugs are those that could be used for empirical selection in the absence of or pending the results of culture and susceptibility testing. These include:
- Amoxicillin
- Amoxicillin-clavulanate
- Cephalexin
- Doxycycline
- Minocycline
- Trimethoprim-sulfonamides (TMS)
Second-line drugs are those to be used on the basis of culture and susceptibility testing and because of the lack of any appropriate first-line options. These include:
- Piperacillin-tazobactam
- Amikacin
- Third-generation cephalosporins
- Fluoroquinolones
The use of third-line drugs, including vancomycin, linezolid, rifampin, human-labeled third-generation cephalosporins (e.g., ceftazidime), and carbapenems such as imipenem and meropenem, is usually reserved for situations when certain criteria are met. What are those criteria?
- Infection must be documented based on clinical abnormalities and culture.
- The infection is serious and has the potential to be life threatening if left untreated.
- Resistance is documented to all other reasonable first- and second-line options.
- The infection is potentially treatable.
- The clinician may seek advice from an infectious disease clinician or a clinical microbiologist to discuss antimicrobial susceptibility test results, and to discuss the use of these agents if there is unfamiliarity with their use.
- The clinician should attempt for a duration of treatment that is as short as possible.
Which two antimicrobials exhibit concentration-dependent killing?
Fluoroquinolones and aminoglycosides. These drugs work optimally when the peak concentration in the plasma (Cmax) or the area under the curve (AUC) exceeds the MIC by a defined index factor.
Drugs that exhibit concentration-dependent killing also have postantibiotic effect (PAE). What is PAE?
A persistent antimicrobial effect after drug concentrations at the site of infection fall below the MIC.
Which antimicrobials exhibit time-dependent killing?
β-lactams (penicillins and cephalosporins), macrolides, clindamycin, vancomycin, and tetracyclines. The activity of these drugs is maximized by the time above the MIC rather than the magnitude of the concentration.
List three appropriate initial antimicrobial choices for bacterial skin infection
Cephalexin
Amoxicillin-clavulanate
Clindamycin
List four appropriate initial antimicrobial choices for bacterial urinary tract infection
Amoxicillin
Amoxicillin-clavulanate
Cephalosporins
Trimethoprim-sulfamethoxazole
List two appropriate initial antimicrobial choices for bacterial prostatic infection
Trimethoprim-sulfamethoxazole
Fluoroquinolones (enrofloxacin, marbofloxacin, orbifloxacin, levofloxacin)