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Guidelines: Specific guidelines on diagnosing and treating the infected diabetic foot

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Based upon: The International Consensus on Diagnosing and Treating the Infected Diabetic Foot

Introduction
Pathophysiology
Diagnosis
Classification
Microbiology
Non-antimicrobial treatment
Antimicrobial therapy
Appendix


Introduction

Based upon the International Consensus on Diagnosing and Treating the Infected Diabetic Foot and prepared by the IWGDF working group on diagnosing and treating the infected diabetic foot in 2003

The Working Group recognizes that the availability of diagnostic procedures and antimicrobial agents will vary greatly in different clinical sites and in different countries. While the basic principles of treating diabetic foot infections are the same in all situations, they have provided guidance that must be adapted to local circumstances.

Pathophysiology

  1. Foot infections in persons with diabetes usually begin with a break in the skin, especially a neuropathic ulceration.
  2. This allows colonizing skin flora to invade the skin and subcutaneous tissues.
Diagnosis

  1. Diagnose wound infections clinically (recognizing that the inflammatory response may be mitigated by diabetic complications), by the presence of purulent secretions or local evidence of inflammation, or occasionally systemic toxicity.
  2. Laboratory tests, including cultures, may suggest but do not establish the presence of infection, with the exception of reliably obtained deep bone cultures in suspected osteomyelitis.
Classification

  1. Assess the severity of the infection by examining the wound, limb, and the overall status of the patient, to determine the appropriate approach to treatment.
  2. Classifying infections by their severity helps determine the site, type and urgency of treatment.
Microbiology


1. Cultures
  1. Obtaining proper specimens for culture is usually advisable, to help select an appropriate antibiotic regimen. Cultures may not be necessary in previously untreated, mild infections.
  2. Take wound cultures by obtaining tissue (by curettage or biopsy) of the debrided wound base or by aspirating pus, rather than by swabbing. If swabs are the only option, take them from the ulcer base after debridement, and process quickly.
  3. Consider obtaining blood cultures from systemically toxic patients and consider bone cultures from patients with osteomyelitis



2. Etiologic agents

  1. Aerobic gram-positive cocci (especially staphylococci) are usually the initial, often the only, and almost always the most frequently isolated pathogens in soft tissue and bone infections.
  2. Gram-negative and anaerobic bacteria are commonly isolated, but usually as part of a polymicrobial, chronic or necrotic infection.


Non-antimicrobial treatment

  1. Consult a diabetic foot care team or specialist, where available.
  2. Correct any metabolic derangements, optimize wound care, and assess vascular status.
  3. Hospitalize patients: with a severe infection, needing multiple or complex diagnostic or surgical procedures; having critical foot ischemia; needing intravenous therapy; or unlikely to comply with therapy.
  4. In case of severe infection, consult appropriate specialists promptly for any necessary invasive diagnostic or surgical procedures.
Antimicrobial therapy


1. General principles

  1. Prescribe for all clinically infected wounds immediately, but not for uninfected wounds.
  2. Select the narrowest spectrum therapy possible for mild or moderate infections.
  3. Choose initial therapy based on the commonest pathogens and known local antibiotic sensitivity data.
  4. Adjust (broaden or constrain) empiric therapy based on the culture results and clinical response to the initial regimen.



2. Specific choices (see below)

  1. Cover staphylococci and streptococci in almost all cases.
  2. Broaden the spectrum if necessary based on the clinical picture, or previous culture or current Gram-stained smear results.
  3. Topical therapy for mild superficial infections has not been adequately studied; oral therapy is effective for most mild to moderate infections; parenteral therapy (at least initially) is advisable for severe infections.
  4. Choose agents that have demonstrated efficacy in treating complicated skin and soft tissue infections. These include semi-synthetic-penicillins, cephalosporins, penicillin-?-lactamase inhibitors, clindamycin, fluoroquinolones, carbapenems, and oxazolidinones.
  5. Treat soft tissue infections for 1-2 weeks if mild infections, and about 2-4 weeks for most that are moderate and severe. When the clinical evidence of infection has resolved antibiotic therapy can be stopped.


Appendix

Suggested systemic antibiotic regimens for treating diabetic foot infections

Severity of Infection Usual Pathogen(s) Potential Regimens
Non-severe (oral for entire course)
No complicating features GPC S-S pen; 1 G Ceph
Recent antibiotic therapy GPC +/- GNR FQ, ß-L-ase
Drug allergies   Clindamycin; FQ; T/S
Severe (intravenous until stable, then switch to oral equivalent)
No complicating features GPC2 +/- GNR ß-L-ase; 2/3 G Ceph
Recent antibiotic/necrosis GPC + GNR/anaerobes 3/4 G Ceph; FQ + Clindamycin
Life-threatening (prolonged intravenous)
MRSA unlikely GPC + GNR + anaerobes Carbapenem; Clindamycin Aminoglycoside
MRSA likely   Glycopeptide or linezolid + 3/4 G Ceph or FQ + metronidazole


1Given at usual recommended doses for serious infections; modify for azotemia, etc.; based upon theoretical considerations and available clinical trials

2 A high local prevalence of methicillin-resistance among staphylococci may require using vancomycin or other appropriate anti-staphylococcal agents active against these organisms

GPC = gram-positive cocci
GNR = gram-negative rod
S-S pen = semi-synthetic (anti-staphylococcal) penicillin (e.g., flucloxacillin, oxacillin)
1 G Ceph = first generation cephalosporins (e.g., cephalexin, cefazolin)
FQ = fluoroquinolones (e.g., ciprofloxacin, levofloxacin)
ß-L-ase = lactam- ß lactamase- ß inhibitor (e.g., amoxicillin/clavulanate, piperacillin/tazobactam)
T/S = trimethoprim/sulfamethoxazole
2/3/4 G Ceph = 2nd/3rd/4th generation cephalosporins (e.g., cefoxitin, ceftazidime, cefepime)
Carbapenem: e.g., imipenem/cilastatin, meropenem, ertapenem
Aminoglycoside: e.g., gentamicin, tobramycin, amikacin
Glycopeptide: e.g., vancomycin, teicoplanin

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