1/34
(antibacterial)
Name | Mastery | Learn | Test | Matching | Spaced |
---|
No study sessions yet.
antimicrobial stewardship
a coordinated program that promotes the appropriate use of antibiotics, which improves patient outcomes and reduces microbial resistance
sulfonamides
penicillin
cephalosporins
macrolides
quinolones
aminoglycosides
tetracyclines
common categories of antimicrobial
sulfonamides
were one of the first groups of drugs used as antibiotics
do not actually destroy bacteria but rather inhibit their growth - considered bacteriostatic antibiotics
inhibit the growth of susceptible bacteria by preventing bacterial synthesis of folic acid
for: UTI, Enterobacter species, Escherichia coli, Klebsiella spp., proteus mirabilis, proteus vulgaris, respiratory tract infection, prophylaxis, Stenotrophomonas maltophilia
contraindicated: pregnant women at term and in infants younger than 2 months of age
beta-lactam antibiotics
are so named because of the beta-lactam ring that is part of their chemical structure
Penicillins
are a very large group of chemically related antibiotics that were first derived from a mold (fungus) often seen on bread or fruit
indication: prevention and treatment of infections caused by gram-positive bacteria, gram-negative and anaerobic coverage, pneumonia, intraabdominal infections, sepsis
contraindications: drug allergy
natural penicillins
penicillinase-resistance penicillins
aminopenicillins
extended-spectrum penicillins
4 subgroups of penicillins
lethargy, anxiety, depression, seizures
adverse effects of penicillin (LADS)
cephalosporins
are semisynthetic antibiotics widely used in clinical practice
are structurally and pharamacologically related to penicillin which works by interfering bacterial cell wall synthesis
carbapenems
have the broadest antibacterial action of any antibiotic to date; are bactericidal and inhibit cell wall synthesis
often reserved for complicated body cavity and connective tissue infections in acutely ill hospitalized patients
adverse effect: drug-induced seizure activity
contraindication: anaphylactic-type reactions to penicillin
aztreonam
is most commonly used when gram-negative coverage is needed in patients with a penicillin allergy
the only one monobactam in clinical use
macrolides
are a large group of antibiotics that first became available in the early 1950s with the introduction of erythromycin
are considered bacteriostatic; however, in high enough concentrations they may be bactericidal to some susceptible bacteria
MOA: inhibit protein synthesis by binding reversely to the 50S ribosomal subunits of susceptible microorganisms
indications: streptococcus pyogenes, Haemophilus influenzae, spirochetal infections, gonorrhea and chlamydia and mycoplasma infections
palpitations, chest pain, QT prolongatio
adverse effects of macrolides (PCQ)
tetracyclines
are bacteriostatic drugs that inhibit bacterial protein synthesis by binding to the 30S bacterial ribosome
tigecycline
is structurally related to minocycline, but is the first in a new class called glycylcyclines
MOA: inhibiting protein synthesis in susceptible bacteria; inhibit the growth of and kill
indications: mycoplasma, chlamydia, rickettsia, balantidiasis
contraindications: drug allergy, avoided in pregnant women and nursing women and in children younger than 8 years of age
coccus
bacillus
coccobacillus
fusiform bacillus
vibrio
spirillum
spirochete
bacterial morphology shapes (CBCFVSS)
(1) gram-positive organisms
(2) gram-negative organisms
(1) bacteria that stain purple
(2) bacteria that stain red
fevers, chills, sweats, redness, pain and swelling, fatigue, weight loss, increased rbc count, formation of pus
signs and symptoms of infection (FCSRPFWIF)
antibiotics
are most effective when their actions are combined with functioning bodily defense mechanisms
community-associated infection
an infection that is acquired by a person who has not recently (within the past year) been hospitalized or had a medical procedure (e.g., dialysis, surgery, catheterization)
health care-associated infection/ nosocomial infection
an infection that a patient acquires during the course of receiving the treatment for another condition in a health care institution.
the infection was not present or incubating at the time of admission but occurs greater than 48 hours after admission
methicillin-resistant staphylococcus aureus (MRSA)
enterococcus, klebsiella, acinetobacter
1 being one of the most common (MRSA)
2 other serious pathogens (EKA)
handwashing
is the single most important health care professionals can do to not prevent the spread of these potentially deadly infections
empiric therapy
the antibiotic selected is one that can best kill the microorganisms known to be the most common causes of infection
definitive therapy
once the results of culture and sensitivity testing are available (usually in 48-72 hrs), the antibiotic therapy is then tailored to treat the identified organisms by using the most narrow-spectrum, least toxic drug based on sensitivity results
prophylactic antibiotic therapy
this is often the case patients are scheduled to undergo a procedure in which the likelihood of dangerous microbial contamination is high during or after the procedure, that is antibiotics are given for prophylaxis
broad-spectrum antibiotics
narrow-spectrum antibiotics
are those that are active against numerous organisms (gram- postive, negative, anaerobic)
are effective against only a few organisms
age, allergy history, kidney or live function, pregnancy status, genetic characteristics, site of infection, host defenses
host factors (AAKPGSH)
teratogens
drugs that cause developmental abnormalities in the fetus
slow acetylation
a common genetic host factor in which the rate of metabolism of certain drugs is reduced
glucose-6-phosphate dehydrogenase deficiency
an inherent disorder in which the RBC are partially or completely deficient of this, a critical enzyme in metabolism of glucose
penicillin
cephalosporins
carbapenems
monobactams
beta-lactam antibiotics 4 major subclasses
they share a common structure and mechanism of action; they inhibit the synthesis of the bacterial peptidoglycan cell wall
natural penicillin
penicillin G
penicillin V
although many modifications of the original natural structure have been made, these are the only 2 in clinical use
for IV or IM
for PO dosage
penicillinase resistant drugs (cloxacillin, dicloxacillin, nafcillin, oxacillin)
stable against hydrolysis by most staphylococcal penicillinases
aminopenicillins (amoxicillin, ampicillin)
have an amino group attached to the basic penicillin structure that enhances their activity against gram-negative bacteria compared with natural penicillins
extended spectrum drugs (piperacillin, ticarcillin, carbenicillin)
have wider spectra of activity than do all other penicillins