BUGS & DRUGS
Tips & Tricks
-
Beta-hemolytic streptococci are universally susceptible to penicillin (and amoxicillin), which is the drug of choice
-
Penicillin (or amoxicillin) is the drug of choice for S. pneumoniae infections when susceptible
-
High dose amoxicillin (90 mg/kg/day) is sufficient to treat most S. pneumoniae with higher MICs
-
-
Ampicillin is the drug of choice for E. faecalis
-
Vancomycin is inferior to oxacillin for the treatment of methicillin-susceptible S. aureus (MSSA)
-
Inducible AmpC beta-lactamase production can cause resistance to 3rd generation cephalosporins even if initially reported as susceptible
-
AmpC beta-lactamases are most commonly found in Enterobacter spp
-
Cefepime is the drug of choice for invasive Enterobacter infections if susceptible
-
-
Some bacteria cultured from blood may represent contamination
-
Common examples: coagulase-negative staphylococci, Bacillus spp,
Corynebacterium spp, Micrococcus spp, viridans group streptococci -
Consider culture from peripheral vs. central line, careful examination of patient, number of positive cultures compared to number of cultures taken (e.g., only 1 bottle positive out of 2), time to culture positivity
-
-
Consider using in MRSA Nasal swab when starting vancomycin to assess risk of MRSA. In an adult ICU populations, negative MRSA nasal swab found to have >99% negative predictive value for any invasive MRSA infections. Further evaluation for utility in pediatric patients is ongoing.¹⁴
Antimicrobial Dosing & Drug Monitoring
-
Amoxicillin-clavulanate
-
Formulations are not interchangeable. You must prescribe the correct formulation and dosing combination of amoxicillin-clavulanate to assure efficacy and to prevent side effects such as severe diarrhea.
-
Amoxicillin-Clavulanate Formulation-Based Dosing (amoxicillin:clavulanate) (NOTE: max dosing based on amoxicillin component)
-
14:1 Formulation: 90 mg/kg/day divided in 2 doses, max 4000 mg per day
-
Available 14:1 formulation:
-
amoxicillin 600 mg/clavulanate 42.9 mg
-
-
-
7:1 Formulation: 25–45 mg/kg/day divided in 2 doses, max 1750 mg per day
-
Available 7:1 formulations:
-
amoxicillin 200 mg/clavulanate 28.5 mg
-
amoxicillin 400 mg/clavulanate 57 mg
-
amoxicillin 875 mg/clavulanate 125 mg
-
-
-
4:1 Formulation: 20–40 mg/kg/day divided in 3 doses, max 1500 mg per day
-
Available 4:1 formulations:
-
amoxicillin 125 mg/clavulanate 31.25 mg
-
amoxicillin 250 mg/clavulanate 62.5 mg
-
amoxicillin 500 mg/clavulanate 125 mg
-
-
-
16:1 Formulation: Extended-Release, ONLY for those >40 kg: 2000 mg every 12 hours
-
Available 16:1 formulations:
-
amoxicillin 1000 mg/clavulanate 62.5 mg
-
-
-
-
-
-
Vancomycin
-
Troughs should be obtained immediately (0 to 30 minutes) prior to the 4th dose (i.e., after the 3rd dose, at steady state)
-
Troughs should be repeated weekly or with any change in dose (prior to the 4th dose on a new dosing regimen) or change in renal function
-
-
Goal trough is 10-15 mcg/mL for most indications unless otherwise specified by infectious diseases
-
-
*For patients with a CrCl <75mL/min/1.73m²or acute renal impairment, administer one time dose of vancomycin and check level following this dose
-
Approach to a Patient with a History of Penicillin Allergy
-
Incidence of penicillin reactions
-
Risk of acute penicillin allergy occurs in ~1% of the general population
-
Incidence of anaphylactic reactions: ≤0.015%
-
-
~90% of patients who report an allergy to penicillin have negative skin test results and are NOT at an increased risk of an acute allergic reaction
-
A careful history is required to assess true allergy
-
-
-
Rate of cross-reactivity between penicillins (e.g., penicillin, amoxicillin, oxacillin, piperacillin/tazobactam) and cephalosporins varies based on similarity of side chains
-
Risk of cross-reactivity is greater with 1st generation cephalosporins than 3rd or 4th generation cephalosporins
-
1st and 2nd generation: <5%
-
3rd generation: <2%
-
Carbapenems: <1%
-
-
-
Any patient who has a history consistent with anaphylaxis (immediate or accelerated) should NOT receive ANY beta-lactams (penicillins, cephalosporins, or carbapenems) without undergoing skin testing first
-
Beta-lactams should be avoided in patients with documented severe delayed adverse reactions such as Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), drug rash with eosinophilia and systemic symptoms syndrome (DRESS)
-
Questions to Ask Family
-
How long after beginning penicillin did the reaction occur?
-
Was there any wheezing, throat/mouth swelling, hives, or generalized itching?
-
If a rash occurred, what was the nature of the rash? Where was it and what did it look like?
-
Was the patient on other medications at the time of the reaction?
-
Since then, has the patient ever received another penicillin or cephalosporin (ask about brand names such as Augmentin, Keflex, Ceftin, Trimox, Vantin)?