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Disclosure of Potential Conflicts of Interest. Has received honoraria, travel expenses and hospitality for serving on speakers bureaux and advisory boards for RPR (Synercid), Pfizer (Linezolid) MSD (Ertapenem) and MacroChem (Pexiganin)Vice-Chair of IDSA Clinical Practice Guidelines Committee for D
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1. Diabetic Foot Infection: A challenge for primary and secondary care? Dr Tony Berendt
Consultant Physician
Bone Infection Unit
NOC NHS Trust, Oxford
2. Disclosure of Potential Conflicts of Interest Has received honoraria, travel expenses and hospitality for serving on speakers bureaux and advisory boards for RPR (Synercid), Pfizer (Linezolid) MSD (Ertapenem) and MacroChem (Pexiganin)
Vice-Chair of IDSA Clinical Practice Guidelines Committee for Diabetic Foot Infections; Chair of IWGDF Osteomyelitis Sub-group
Member of Oxfordshire Priorities Forum and ORH-NOC Medicines Advisory Committee
DIPC at NOC, Chair of TV (South Central) CHAIN and Steering Group for pan-Oxfordshire C. difficile intervention project
3. Infection and Healing
4. Learning objectives Be able to discuss the epidemiological importance of DFI
Know how to assess risk of diabetic foot ulceration and infection
Be able to assess a patient with a diabetic foot infection, in the context of published guidelines, and make rational antibiotic choices
5. General epidemiology 252 million diabetics worldwide
7. General epidemiology 252 million diabetics worldwide
Foot problems account for largest number of hospital bed days used for diabetic patients
1-4% of diabetics develop foot ulcer annually, 25% in lifetime
45-75% of all lower extremity amputations are in diabetics
85% of these preceded by foot ulcer
Two-thirds of elderly patients undergoing amputation do not return to independent life
Studies have shown less costs for saving a limb cf. amputation
8. Pathophysiology: diabetic foot ulceration Neuropathy
10. Pathophysiology: diabetic foot ulceration Neuropathy
11. 30-second foot examination Any previous diabetes related foot problems?
Are both foot pulses palpable?
Is protective sensation intact?
Is there evidence of significant foot deformity?
13. Two-minute foot examination Examine feet for ulcers, callus, blisters, maceration, skin breaks, infection
Examine the toenails
Identify nature of any foot deformity
Examine the shoes
Observe patient’s ability to perform foot care and examination (by observing them replace socks and shoes)
Establish need for patient education
14. Standard ulcer care Evaluate for infection
Debride ulcer, remove callosities
Check for sensation (monofilament)
Check for circulation (pulses, Dopplers)
Probe to bone?
Adequate offloading
Antibiotics if infected
Secondary prevention of ulcer and of major diabetes related events
15. Overview of Diabetic Foot Infections
16. Independent Risk Factors* for Foot Infection:Diabetex Prospective Trial Variable Risk Ratio (95%CI) p Value
Wound depth to bone 6.7 (2.3–19.9) 0.001
Wound duration >30 days 4.7 (1.6–13.4) 0.004
Recurrent foot wound 2.4 (1.3–4.5) 0.006
Traumatic wound etiology 2.4 (1.1–5.0) 0.02
Peripheral vascular disease 1.9 (1.0–3.6) 0.04
17. Microbiology Popular mythology = all infections are polymicrobial
19. Treatment: myths Treat uninfected ulcers to promote healing
Treat infected ulcers until the ulcer is healed
Treat all the organisms isolated from the microbiological specimens
Hospitalise all infections
Give lots of intravenous therapy
20. Timeline of Staphylococcal antibiotic resistance
22.
24. Evaluating the Patient with a DFI Patient
Systemic response
Fever, chills, sweats, cardiovascular status
Metabolic status
Hyperglycaemia, electrolyte imbalance, hyperosmolality, renal impairment
Cognitive function
Delirium, depression, dementia, psychosis
Social situation
Support, self-neglect
· Limb/Foot
· Wound
25. Evaluating the Patient with a DFI Patient
Limb or Foot
Biomechanics
Vascular
Ischaemia
Venous insufficiency
Neuropathy
Infection
Wound
Size, depth
Necrosis, gangrene
Infection
27. Clinical Classification of Diabetic Foot Infection Wound without purulence or other evidence of inflammation
?More than 2 of purulence, erythema, pain, tenderness, warmth or induration. Any cellulitis/erythema extends =2 cm around ulcer and infection is limited to skin/superficial subcut tissues. No local complications or systemic illness
Infection in patient who is systemically well & metabolically stable but has any of: cellulitis extending >2 cm; lymphangitis; spread beneath fascia; deep tissue abscess; gangrene; muscle, tendon, joint or bone involved
Infection in a patient with systemic toxicity or metabolic instability
28. Outcomes By IDSA DFI Severity Classification
32. Table 8: Suggested Antibiotic Regimens: DFI
35. The diabetic foot: Charcot foot with “rocker bottom” deformity
36. Charcot foot
grossly disordered architecture and biomechanics
midfoot ulceration
instability of midfoot
note previous minor amputations
still well-vascularised
37. Bone resorption and destruction
38. Bone regeneration on antibiotic therapy
39. Conclusions Ulceration is a common consequence of diabetic neuropathy
To understand and treat ulceration, understand the pathophysiology and biomechanics
Infection (DFI) is a common and frequently serious consequence of diabetic foot ulceration (DFU)
A structured approach to assessment and treatment, using international or local guidelines, provides a means to rationalise care and improve outcomes
Care must be multidisciplinary to achieve this; agreed pathways, health service management and audit are required