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etioologies of DFI
peripheral arterial disease (PAD) and peripheral neuropathy - arise from an ulcer or from wound caused by trauma
how are chronic ulcers formed?
foot deformitiy —→ repetitive trauma —→ chronic ulcer
poor vascular supply —→ delayed wound healing —→ chronic ulcer
hyperglycemia —→ oxidative stress —→ chronic ulcer
classic clinical presentation of DFI
redness, warmth, swelling, tenderness, pain, purulent drainage (>= 2 are necessary to call a wound infected)
secondary findings for DFI
non-purulent secretions, discolored granualtion tissue, foul odor
assessment of wound:
depth and tissues involved, requires debridement of necrotic tissue, looking for abscesses, sinus tracts, foreign bodies, probe to bone
T/F: x-rays are recommended for all DF wounds and if bone involvement is suspected, an MRI is the study of choice
true
classify mild DFI
local infection involving only the skin and the subq tissue, if erythema is present, must be 0.5-2 cm aaround the ulcer, exclude other causes of inflammatory response of skin
Classify moderate DFI
Local infections as described in mild scenarios with erythema > 2 cm or involving structures deeper than skin and subway tissues, no SIRS
Classify severe DFI
Local infection as described in moderate scenarios with signs of SIRS as manifested by >= 2 of the following: temp 38-36 Celsius, HR >90, RR >20, WBC >12,000 or <4,000
Define wound
Penetrates to subcutaneous tissues (fascia, tendon, muscle, joint and bone)
Define cellulitis
Extensive (>2 cm) distance from ulceration or rapidly progressive
Define local signs
Severe inflammation or induration, crepitus, Bullard, discoloration, necrosis or gangrene, chemises or petechiae, and new anesthesia
Presentation of systemic DFI
Acute onset/worsening or rapidly progressive
Systemic signs of DFI
Fever, chills, hypotension, confusion, and volume depletion
Lab tests for systemic DFI
Leukocyte is, very high CRO/ESR, severe/worsening hyperglycemia, acidosis, AKI, and electrolytes abnormalities
Complicating features of systemic DFI
Presence of a foreign body (accidentally or surgically implanted), puncture wound, deep abscess, arterial or venous insufficiency, lymphedema, immunosuppressive illness or treatment
Treatment for systemic DFI
Progression on appropriate antibiotic and supportive therapy
T/F: you should not culture a clinically uninfected wound
True
In moderate and severe infections multiple organisms are likely and multi-resistant organisms may be possible therefore _______ are essential
Cultures
How should samples/cultures be obtained for DFIs?
Deeper tissue cultures or aspirates of prudent secretions - superficial swabs are much less helpful
Typical bacteria involved in DFIs:
staph and strep most common, sometimes pseudomonas, and anaerobes play more of a role in moderate-severe infections (may not need to cover if wound has been adequately debriefed)
Risk factors for MRSA DFIs
History of MRSA colonization, severe infections, extensive surgical procedures
Risk factors for pseudomonas DFIs:
Warm climate and frequent exposure to water
Risk factors for MRSA and pseudomonas DFIs:
Extensive antimicrobial use in the past 30-60 days, hx infections for each respectively, and high local prevalence
Empirical therapy for mild DFI
cephalexin (MSSA), Amox/clav, clindamycin, Bactrim (MRSA), and doxycycline (MRSA)
Empiric therapy for moderate-severe DFI for MSSA
Amp/sulb, dedication, ceftriaxon + metronidazole, cipro + blinds, moxifloxacin, and ertapenem
Empiric therapy for MRSA mod-severe DFI
Vanco, linezolid, and dapto
Empiric therapy for mod-severe DFI from pseudomonas
P/T and Cefepime
Empiric therapy for MRSA + pseudo + anaerobe DFIs
Vanco + P/T
Vanco + cefepime + metronidazole
Vanco + meropenem
Route of antibiotics for mild DFI
Oral
Duration of therapy for mild DFI
1-2 weeks - may require longer if slow to respond
Route of antibiotic in moderate DFI
Oral or IV transition to oral
Duration of therapy for moderate DFI
1-3 weeks
Route of antibiotics for severe DFI
IV transitioned to oral
Duration of therapy for severe DFI
2-4 weeks