| style="font-size: 90%; padding: 0 5px; background: #DCDCDC;" align=left | ▸ '''''[[Cefotaxime]] 1-2 g IV/IM q8-12 (up to 2 g q4-6h)''''' <br> OR <br> ▸ '''''[[Ciprofloxacin]] 400 mg IV q8-12h x 7-14 days'''''<br> OR <br> ▸ '''''[[Ciprofloxacin]] 500-750 mg PO q8-12h x 7-14 days'''''
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC;" align=left | ▸ '''''[[Meropenem]] 0.5-1 g IV q8h (infuse over 15-30 min or in bolus over 3-5 min)''''' <br> OR <br> ▸ '''''[[Imipenem]]-cilastatin 250-1000 mg IV (max: 50mg/kg/day)'''''
| style="font-size: 90%; padding: 0 5px; background: #DCDCDC;" align=left |▸ '''''[[Cefotaxime]] 1-2 g IV/IM q8-12 (up to 2 g q4-6h)''''' <br> OR <br> ▸ '''''[[Ciprofloxacin]] 400 mg IV q8-12h x 7-14 days'''''<br> OR <br> ▸ '''''[[Ciprofloxacin]] 500-750 mg PO q8-12h x 7-14 days''''' <br> OR <br> ▸ '''''[[Imipenem]]-cilastatin 250-1000 mg IV (max: 50mg/kg/day)'''''
|}
|}
|}
|}
|}
|}
====Orbital Cellulitis====
* Treatment regimens are usually empiric and designed to address the usual pathogens like [[Streptococcus pneumoniae]], [[Hemophilus influenzae]], [[Moraxella catarrhalis]], [[Staphylococcus aureus]], [[anaerobes]] (when intracranial extension is suspected), group A streptococci, and sometimes gram negative bacilli because, in the absence of surgical intervention, reliable culture results are difficult to obtain.
<SMALL><font color="#FF4C4C">'''▸ Click on the following categories to expand treatment regimens.'''</font></SMALL><div style="-webkit-user-select: none;"><ref name="pmid21217178">{{cite journal| author=Liu C, Bayer A, Cosgrove SE, Daum RS, Fridkin SK, Gorwitz RJ et al.| title=Clinical practice guidelines by the infectious diseases society of america for the treatment of methicillin-resistant Staphylococcus aureus infections in adults and children: executive summary. | journal=Clin Infect Dis | year= 2011 | volume= 52 | issue= 3 | pages= 285-92 | pmid=21217178 | doi=10.1093/cid/cir034 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21217178 }} </ref>
** Bite wounds suffered from a mammal often contain polymicrobial sources that are anaerobic in nature.<ref name="pmid21482724">{{cite journal |author=Abrahamian FM, Goldstein EJ |title=Microbiology of animal bite wound infections |journal=Clin. Microbiol. Rev. |volume=24 |issue=2 |pages=231–46 |year=2011 |month=April |pmid=21482724 |pmc=3122494 |doi=10.1128/CMR.00041-10 |url=}}</ref>
** Mild cases can be treated with [[amoxicillin]] and clavulanate, and in cases of [[penicillin allergy]] cotrimoxazole along with [[metronidazole]] is used.
** In severe cases, [[piperacillin]] and tazobactum are used.
*'''Acquatic punctures and lacerations.'''<ref name="pmid16112981">{{cite journal |author=Noonburg GE |title=Management of extremity trauma and related infections occurring in the aquatic environment |journal=J Am Acad Orthop Surg |volume=13 |issue=4 |pages=243–53 |year=2005 |pmid=16112981 |doi= |url=}}</ref>
** This is seen mainly in professional swimmers and divers both in freshwater and in brackish water.
** Failure to recognize these wounds and delay treatment may cause a larger morbidity.
** Wounds in fresh water are treated with [[doxycycline]] and [[ceftazidime]] (or fluroquinolones).
** Wounds in brackish water are treated with [[ceftazidime]] and [[levofloxacin]].
Beta-lactam antibiotics against Streptococcus and penicillinase-producing Staphylococcus aureus are the usual drugs of choice. Ancillary measures include elevation of the affected area to reduce fluid accumulation and cool sterile saline dressings to remove purulent debris from open wounds.
Empiric TherapyAdapted from Clinical Practice Guidelines CID 2011[1] and Guidelines for Skin and Soft-Tissue Infections CID 2005[2]
Empiric therapy would depend on the clinical presentation of the cellulitis.
Non-purulent cellulitis refers to the infection without purulent drainage or exudate and not associated with an abscess.
Purulent cellulitis is associated with purulent drainage or exudate in the absence of a drainable abscess, and it is associated to Staphylococcus aureus.
Complicated cellulitis refers to a deeper soft-tissue infection and/or the association with necrotizing fasciitis, septic arthritis, or osteomyelitis.
For patients with purulent cellulitis, cultures are recommended and empirical therapy for Community Associated-MRSA (CA-MRSA) should be started.
For patients with non-purulent cellulitis, empirical therapy for β-hemolytic streptococci should be started; if the patient does not respond to B-lactam antibiotics, empirical coverage for CA-MRSA should be initiated.
The duration of the therapy should be individualized for the clinical response of each patient; 5-10 days is usually recommended.
The treatment of cellulitis in neonates usually requires hospitalization and parenteral therapy. Oral therapy is given for completion of the treatment when the pathogen is unknown.
The optimal dose should be based on determination of serum concentrations and patients with renal insufficiency may require dose adjustment in case of cephalosporins.
▸ Cephalexin 25 mg/kg/day PO divided q6h x 5-10 days OR ▸ Dicloxacillin 25 mg/kg/day PO divided q6h x 5-10 days OR ▸ Clindamycin 10-13 mg/kg IV q6-8h (max:40 mg/kg/day) OR ▸ TMP-SMX 4-6 mg/kg PO q12h (TMP component) OR ▸Doxycycline¶ 2 mg/kg PO q12h† OR ▸ Linezolid 10 mg/kg PO q8h (max: 600mg/dose)
¶ Not recommended for children < 8 years of age † For children ≤45 kg. Children >45 kg receive adult dosing.
▸ Linezolid 10 mg/kg PO q8h (max: 600mg/dose) OR ▸ Clindamycin 10-13 mg/kg IV q6-8h (max:40 mg/kg/day) OR ▸ Minocycline 4 mg/kg PO 1 dose, then2 mg/kg/dose PO q12h OR ▸ Doxycycline¶ 2 mg/kg PO q12h† OR ▸ TMP-SMX 4-6 mg/kg PO q12h (TMP component)
¶ Not recommended for children < 8 years of age † For children ≤45 kg. Children >45 kg receive adult dosing.
For the following conditions, an additional antibiotic therapy should be added to the usual regimen in order to cover specific pathogens associated to those circumstances.
▸ Click on the following categories to expand treatment regimens.
Special Considerations
▸ Diabetic Foot Ulcer
▸ Neutropenic Patients
▸ Sal Water Wound Exposure
▸ Fresh Water Wound Exposure
▸ Butcher, Fisherman, Veterinarian
Diabetic Foot Ulcer
▸ Empirical therapy should be started depending on the suspicion of a MRSA infection and the severity of the infection.
▸ Definitive therapy would be directed based on the results of culture and susceptibility tests from wound specimens, as well as the clinical response to the empiric regimen.
Neutropenic Patients
▸ Initial therapy consist of empirical broad-spectrum antibiotics.
▸ Definite therapy would depend on the severity of the cellulitis and the isolated pathogen
Salt Water Wound Exposure (Vibrio vulnificus)
Preferred Regimen
▸ Doxycycline 200 mg IV initial dose, then 50-100 mg IV q12h
Alternative Regimen
▸ Cefotaxime 1-2 g IV/IM q8-12 (up to 2 g q4-6h) OR ▸ Ciprofloxacin 400 mg IV q8-12h x 7-14 days OR ▸ Ciprofloxacin 500-750 mg PO q8-12h x 7-14 days
▸ Cefotaxime 1-2 g IV/IM q8-12 (up to 2 g q4-6h) OR ▸ Ciprofloxacin 400 mg IV q8-12h x 7-14 days OR ▸ Ciprofloxacin 500-750 mg PO q8-12h x 7-14 days OR ▸ Imipenem-cilastatin 250-1000 mg IV (max: 50mg/kg/day)
Non-Antibiotic Therapy
Elevation of the affected area facilitates gravity drainage of edema and inflammatory substances. Compressive stockings and diuretic therapy may help patients with edema.
The skin should be sufficiently hydrated to avoid dryness and cracking without maceration.
References
↑Mathews, CJ.; Weston, VC.; Jones, A.; Field, M.; Coakley, G. (2010). "Bacterial septic arthritis in adults". Lancet. 375 (9717): 846–55. doi:10.1016/S0140-6736(09)61595-6. PMID20206778. Unknown parameter |month= ignored (help)