University of Pennsylvania Medical Center Guidelines for Antibiotic Use
|
Clinical Setting |
Empiric Treatment |
Likely Pathogens |
Definitive Treatment |
Dosage Regimen |
Duration |
|
Cellulitis | |||||
|
Extremities Normal Host |
cefazolin1 |
S. aureus group A streptococcus |
same as empiric |
500mg IV q 8 hour |
7-10 days2 |
|
Diabetic Host (including diabetic foot) |
TMP/SMX + metronidazole3,4 |
polymicrobial |
same as empiric |
TMP/SMX 8-10mg/kg/day TMP IV/PO in 3-4 divided doses metronidazole 500mg IV/PO q 12 h |
14 days2 |
|
Decubitus Ulcer5 |
cefazolin1 |
polymicrobial |
same as empiric |
cefazolin 500mg IV q 8 hour |
7-10 days2 |
|
Wound Infection6 Trauma (soft tissue wound, no bowel or bone
involvement) |
cefazolin1 + metronidazole3 |
polymicrobial (consider Pseudomonas spp., Aeromonas spp. if trauma associated with water) |
base therapy upon culture & sensitivity results |
cefazolin 500mg IV q 8 hour metronidazole 500mg IV/PO q 12 h |
7 days |
1If beta-lactam allergy use clindamycin or trimethoprim sulfamethoxazole; if MRSA-use vancomycin
2Can switch to oral therapy once clinical improvement occurs
3Not for aggressive anaerobic cellulitis
4Metronidazole: use if foul odor present
5Adequate wound debridement required; antibiotics only necessary for surrounding cellulitis
6Adequate wound debridement required
|
Clinical Setting |
Empiric Treatment |
Likely Pathogens |
Definitive Treatment |
Dosage Regimen |
Duration |
|
|
Wound1 Post-operative- GI/GU |
ampicillin/ sulbactam2 |
S. aureus |
nafcillin3 or cefazolin3 |
2gm IV q 4-6 hour 500mg IV q 8 hour |
10 days1 |
|
|
|
Streptococcus spp. |
ampicillin |
1gm IV q 6 hour |
| ||
|
Enterococcus spp.4 |
ampicillin + gentamicin |
2gm IV q 6 hour peak conc. of 3-4 mcg/ml |
| |||
|
Enterobacteriaceae |
TMP/SMX |
8-10mg/kg/day TMP IV in 3-4 divided doses |
| |||
|
P. aeruginosa |
piperacillin + gentamicin |
4gm IV q 6 hour |
| |||
|
anaerobes |
metronidazole (may need to add to above regimen) |
500mg IV q 12 hour |
| |||
|
Post-operative- sternal5 |
vancomycin + gentamicin |
S. aureus |
nafcillin3 or cefazolin3 |
2gm IV q 4-6 hour 500mg IV q 8 hour |
1-6 weeks depending upon clinical setting |
|
|
|
coagulase negative staphylococcus |
vancomycin |
| |||
|
Streptococcus spp. |
ampicillin |
1gm IV q 6 hour |
| |||
|
Enterobacteriaceae |
TMP/SMX |
TMP/SMX 8-10mg/kg/day TMP IV/PO in 3-4 divided doses |
| |||
|
Bites |
| |||||
|
Animal/Human1,6 no bone or joint involvement |
amoxicillin/clavulanic acid7 |
depends on the animal |
same as empiric |
500mg PO q 8 hour |
7-10 days |
|
|
bone and joint involvement |
ampicillin/sulbactam7 |
depends on the animal |
change empiric therapy to amoxicillin/clavulanic acid after adequate debridement and microorganism identification |
ampicillin/sulbactam: 1.5 gm IV q 6 hour |
Depends on the extent of disease |
|
1Adequate wound debridement required
2Ampicillin/sulbactam dosage Regimen: 1.5 gm IV q 6 hour
3If beta-lactam allergy-use clindamycin or trimethoprim/sulfamethoxazole; if MRSA-vancomycin
4Review susceptibilities-30% of isolates multidrug resistant
5Rule-out osteomyelitis
6Patient should receive tetanus booster if series not up to date
7Penicillin allergy: human bite-erythromycin 500mg IV/PO q 6hr; animal bite-doxycycline 100mg IV/PO q 12hr
updated 9/28/04 by Lori LaRosa