Diabetic foot ulcers are one of several serious complications of diabetes progression. Major contributing causes to diabetic foot ulcers are peripheral neuropathy, peripheral arterial disease, and immunosuppression.1-3 Up to 15% of patients with diabetes have diabetic foot ulcers, and these ulcers lead to more than 80,000 amputations per year in the United States.4,5 The lifetime risk of diabetic foot ulcers for patients with diabetes may reach up to 68 per 1,000 persons as reported by some studies.6 As a diabetic foot ulcer progresses, the patient's risk for amputation increases; in nearly 84% of patients who have a lower limb amputation secondary to diabetes, the amputation is preceded by a diabetic foot ulcer.7 Peripheral neuropathy secondary to diabetes is an etiologic factor of diabetic foot ulcers and is estimated to affect 5.5 million people in the United States.8 The estimated annual cost of treating peripheral neuropathy in patients with diabetes is $10.91 billion.8 These collective findings indicate that diabetic foot ulcers lead to serious disability, serious reduction in patient quality of life, and high financial costs for society.9 With increased vigilance on risk assessment, diagnosis, and management of diabetic foot ulcers, clinicians can improve patient outcomes and reduce healthcare costs.
Risk factors for foot ulcers in patients with diabetes include:
- previous lower extremity amputation
- history of a foot ulcer
- anatomic foot deformity
- peripheral vascular disease
- diabetic nephropathy in those on dialysis
- poor glycemic control
The pathophysiology of diabetic foot ulcers has neuropathic, vascular, and immune system components, which all show a base relationship with the hyperglycemic state of diabetes.11,12 Hyperglycemia produces oxidative stress on nerve cells and leads to neuropathy.11 Additional nerve dysfunction follows from glycosylation of nerve cell proteins, leading to further ischemia. These cellular changes manifest in motor, autonomic, and sensory components of neuropathic foot ulcers. Damage to motor neurons of the foot musculature may lead to an imbalance of flexors and extensors, anatomic deformities, and eventual skin ulcerations. Damage to autonomic nerves impairs sweat gland function, and the foot may develop decreased ability to moisturize skin, leading to epidermal cracks and skin breakdown. Lastly, patients may not notice foot wounds because of decreased peripheral sensation. Because the blood supply required to heal a diabetic foot ulcer is greater than that needed to maintain intact skin, chronic ulceration can develop.9
Vascular changes that lead to diabetic foot ulcers correlate with hyperglycemia-induced changes in the peripheral arteries of the foot and begin on the cellular level.11 Endothelial cell dysfunction leads to a decrease in vasodilators; also, plasma thromboxane A2 levels become elevated.13 The result is vasoconstriction and plasma hypercoagulation in peripheral arteries leading to ischemia and increased risk of ulceration.
Immune changes include reduced healing response in diabetic foot ulcers. Increased T lymphocyte apoptosis, which inhibits healing, has been observed in patients with diabetic foot ulcers.14
ASSESSMENT AND DIAGNOSIS
Patients with diabetes should be assessed for arterial insufficiency and neuropathic disease on a structured schedule based on defined risk factors.9 Assess the patient's temperature, respirations, heart rate, and BP in both extremities and document any abnormalities.9 Fever, tachycardia, or tachypnea may indicate an infected ulcer. Evaluate the patient's vascular status by palpating all peripheral pulses and assessing the appearance and temperature of the patient's extremities. Measure the arterial-brachial index (ABI); a result of 1 to 1.2 is normal, and a result below 0.6 indicates claudication. For patients with medial sclerosis, a toe-brachial index (TBI) may be preferred; a result of 0.6 or less indicates a need for vascular intervention.
Arterial insufficiency is characterized by intermittent claudication or limb ischemia; dry, shiny, hairless skin on the affected limb; brittle nails; and skin that is cool to the touch. A patient with arterial insufficiency also may have a history of erectile dysfunction or cardiovascular disease. Assess arterial flow by elevating the limb above the level of the heart, letting pooled blood drain. A normal limb will remain pink; one with arterial insufficiency becomes pallid.
Symptoms of neuropathic disease include numbness, paresthesia, and burning sensations. All patients with diabetes should be assessed regularly for loss of protective sensation; any of the following five tests may be used.15
- The 10-g monofilament test determines a patient's sensitivity to touch. With the patient's eyes closed, touch the monofilament to one or more anatomic sites, including reference sites to verify sensation detection; inability to detect this touch at the test site indicates loss of large nerve fiber function. Test the first, third, and fifth metatarsal heads and the plantar surface of the distal hallux.
- A 128-Hz tuning fork used to detect vibratory sensation. This test uses a tuning fork held bilaterally over the toes to elicit vibratory sensation. Have the patient close his or her eyes. To conduct the test, touch the base of a vibrating 128-Hz tuning fork to a bony surface of each bare toe in succession, and ask the patient to acknowledge when the vibration is felt and when it is removed.
- A pinprick test is administered just proximal to the toenail of the dorsal aspect of the hallux. Inability to detect the pinprick is an abnormal result and indicates neuropathy.
- The ankle reflexes test of the Achilles tendon is done with the patient sitting in a chair or on an examination table. Place the foot in a neutral position, slightly stretching the Achilles tendon. Strike the tendon with a tendon hammer. If no tendon response occurs, ask the patient to lock his or her fingers together and pull; then retest the tendon reflex. Absence of an ankle reflex is an abnormal result that may indicate peripheral neuropathy.
- The vibration perception threshold test uses a biothesiometer to make a semiquantitative assessment of the patient's vibration perception threshold (VPT). With the patient lying supine, a VPT is measured at a proximal control site by placing the instrument stylet on the skin and increasing the amplitude until vibration is detected. VPT measurement is then conducted at each hallux using the mean of three measurements for each. A VPT greater than 25 V has been correlated with later development of diabetic foot ulcers.15
If the patient has soft-tissue wounds on the feet, inspect, palpate, and probe them on initial presentation and in follow-up to evaluate and track the extent of soft-tissue damage and to assess for bone involvement (osteomyelitis).16
Diabetic foot ulcers can be classified by wound depth and by level of infection (Tables 1, 2, and 3).11,16
Suspect osteomyelitis if the patient's ulcer is over a bony prominence and fails to heal with adequate pressure-reduction. Diagnostic tests for osteomyelitis include probe to bone and erythrocyte sedimentation rate (ESR). In the probe-to-bone test, a blunt sterile probe is inserted into the wound; a hard, gritty feel is a positive finding (Figure 1). An ESR of greater than 70 mm/hour suggests osteomyelitis in a patient with a diabetic foot ulcer (normal range is 0 to 22 mm/hour for men and 0 to 29 mm/hour for women).16
Plain radiographs also can support a diagnosis of osteomyelitis. Depending on when radiographs are taken, they are 28% to 75% sensitive and 64% specific for osteomyelitis.16 Patients with longer term diabetic foot ulcers are more likely to show bone abnormality changes in plain radiographs.16 Serial radiographs have a higher predictive value.16 MRI has been shown to have a sensitivity of 77% to 100% and specificity of 40% to 100% for detecting osteomyelitis.17 MRI also provides significant soft-tissue detail on edema, fluid accumulation, and bone changes associated with osteomyelitis. Limited studies suggest that CT, in combination with positron emission tomography (PET), is highly sensitive (81%), specific (93%), and accurate (90%) for diagnosing osteomyelitis.16 Although CT/PET is an attractive option for diagnosing osteomyelitis, this test may not be practical or economical. If the clinician suspects osteomyelitis, front-line tests such as radiographs and MRI should be used first before considering tests that may have limited availability. A leukocyte or antigranulocyte scan, in conjunction with a bone scan, is a recommended alternative diagnostic imaging approach for osteomyelitis in a diabetic foot ulcer if MRI is unavailable or contraindicated.10
If imaging results strongly suggest osteomyelitis, the diagnosis may be confirmed by bone biopsy. Microbiology and histology cultures of the bone can identify pathogens and their antibiotic susceptibility.10,17 However, false-positives may result if bone biopsies are obtained through the ulcer; samples should instead be taken through clinically uninvolved skin or after careful wound debridement. Similarly, soft-tissue cultures should be taken at the deep base of a diabetic foot ulcer via curettage and aspiration and after debridement; this provides the most reliable results for guiding treatment.16
Primary care providers are likely to identify diabetic foot ulcers in patients under their care, and can manage these patients with appropriate interdisciplinary support such as wound care specialists. Based on the patient's history, physical examination, and diagnosis, determine the patient's risk category and initiate an appropriate treatment plan (Table 4). Refer high-risk patients with open ulcers to orthopedic practices for appropriate surgical management.
Low-risk patients without anatomic foot deformities should receive patient education on foot care, appropriate footwear recommendations to reduce pressure points, and a careful assessment of glycemic control. Monitor and optimize blood glucose levels, aiming for a hemoglobin A1C level of 7% or less to reduce the patient's risk of microvascular disease.9
For patients in higher risk classifications, who may have anatomic foot deformities or active ulcers, surgical intervention may be necessary.
• Ulcer debridement (Figure 2) removes necrotic tissue, foreign material such as bacteria, and hyperkeratosis that may surround the wound.10 Sharp debridement using a scalpel cleans the wounds, excises the margins, and exposes a healthy tissue granulation base for epithelial layer regeneration; specimens also may be taken at this time for culture.9,15,16 Selective sharp debridement followed by saline-moistened gauze has been used widely in managing diabetic foot ulcers.18 Superficial ulcer debridement can usually be carried out in the clinic or at the bedside using local anesthesia, where necessary. Local anesthesia may not be required with more advanced manifestations of peripheral neuropathy. Advanced ulcers requiring deep tissue debridement require surgery in the OR so that appropriate specimens for culture can be obtained.10
Chemical debridement is an alternative to sharp or mechanical debridement. Clostridial collagenase ointment debridement has been shown to provide improved healing of diabetic foot ulcers.18 A study by Tallis and colleagues found that clostridial collagenase ointment debridement reduced mean wound area significantly compared with selective sharp debridement followed by saline-moistened gauze.18 In addition, economic analysis indicated that clostridial collagenase ointment is cost-effective in multiple care settings.
Other debridement methods include hydrocolloid and hydrogel dressings, which facilitate autolysis of necrotic wound tissue but cannot be used on infected wounds. Alginate and silver-impregnated dressings and maggot debridement therapy also may be appropriate.19 However, there is no substitute for adequate wound debridement, appropriate systemic antibiotic therapy, and daily dressing changes and wound inspection.20
Patients with infected diabetic foot ulcers should be prescribed a targeted antibiotic regimen based on the wound culture results.9 Inspect the wound regularly to assess the patient's response to antibiotic therapy. Mild infections call for 2 weeks of antibiotic treatment; deep infections may require up to 2 months of therapy.9 A prospective study by Manisha and colleagues found that the major microorganisms were Pseudomonas aeruginosa (30.57%), Klebsiella (22.29%), Escherischia coli (16.56%), and Staphylococcus aureus (12.74%).21 Methicillin resistance was detected in 55% of the S. aureus cultures. Gram-negative isolates were found to be susceptible to ampicillin plus sulfobactam, cefepime plus tazobactam, and ceftriaxone plus tazobactam. Gram-positive isolates were found to be sensitive to teicoplanin, minocycline, and amoxicillin plus clavulanic acid. Appropriate antibiotic empirical treatment was identified as cefepime plus tazobactam, imipenem, and amikacin. The study also confirmed that infected diabetic foot ulcers are polymicrobial in nature and that these mixed infections show multidrug resistance, which creates a serious risk factor in infection management.21
Sotto and colleagues found marked differences between infected and uninfected ulcers.22 The presence of two methicillin-sensitive S. aureus clonal complexes was associated with a favorable outcome in uninfected wounds; 86% of the uninfected wound isolates contained these two clonal complexes. In addition, a virulence marker gene was identified with 96.5% sensitivity as a differentiation tool for uninfected and infected diabetic foot ulcers. The identified clonal complexes and virulence marker present potent prognostic tools for managing diabetic foot ulcers, and may lead to more judicious use of antibiotics.
Pressure-reducing strategies and negative-pressure wound therapy can help improve wound healing; negative-pressure wound therapy stimulates angiogenesis and increases granulation tissue.23,24 Driver and colleagues compared the outcomes of wound treatment with transdermal continuous oxygen therapy (treatment group) to standard debridement, offloading, and moisture therapy (control group).25 Weekly wound measurements were taken and wound fluid collected over 14 to 20 months. Biomarker levels of proinflammatory cytokines, proteases, and macrophages were analyzed in the fluid samples. Patients in the treatment group had significantly higher levels of interleukin-8 and interleukin-6, and significantly lower levels of macrophages, indicating that transdermal continuous oxygen therapy resolves inflammation and helps restore tissue turnover and healing.
• Vascular grafts or bypasses may be indicated in patients with peripheral arterial disease. Adequate peripheral circulation is key to fighting infection and promoting wound healing. To determine the patient's need for revascularization, evaluate the patient's vascular status, looking for flow-limiting vascular leg lesions. Vascular assessment methods include Doppler ultrasound, ABI, TBI, duplex ultrasound, MRI angiography, CT angiography, and contrast angiography.9,26 Because patients may have adverse reactions to contrast media, consider baseline tests such as ABI, TBI, plain radiography, and Doppler ultrasound before ordering studies such as MRI and CT angiography and contrast arteriography.
Proceeding with revascularization depends on many factors, mainly operative risk, arteriographic results, and available graft material. Candidates for revascularization surgery include patients with acceptable surgical risk, suitable life expectancy, and lesions technically unsuitable to endovascular repair or that have failed endovascular repair. Contraindications to revascularization include foot sepsis, extensive foot gangrene, and a nonambulatory status.9 The operative risk of revascularization depends on the method used, which can include surgical arterial bypass, endovascular angioplasty stenting, endovascular subintimal angioplasty, and endovascular artherectomy.9
Endovascular repair techniques have shown high success in patients with claudication.27 Comprehensive arteriographic studies help clinicians identify flow-limiting lesions and determine the repair procedure.28 Revascularization using a saphenous vein bypass graft is the gold standard in lower extremity revascularization.9 However, in patients without a suitable saphenous vein for grafting, polytetrafluoroethylene conduit material is a viable substitute. Revascularization surgery should be undertaken as soon as possible to avoid losing healthy limb tissue and reduce the risk of foot amputation.
Patients in higher risk categories, and those with infections including osteomyelitis, may need surgical resection or amputation. If debridement, antibiotic therapy, or resection fails and life-threatening infection develops, the patient will need foot amputation and, if appropriate, should be considered for a prosthesis.16
WHAT PATIENTS NEED TO KNOW
Patients must understand and adhere to optimal wound care for good outcomes in diabetic foot ulcers. The first step is to reduce repetitive pressure on the foot that caused the ulcer. Various pressure-reducing devices and shoe modifications may be used.9 Explain to patients that addressing causes of limb ischemia will require many office visits. Where appropriate, encourage patients to stop smoking and to gain control of hyperglycemia.11 Patients also must adhere to antibiotic therapy (which may be adjusted periodically) to control wound infection.16 Patients also must change wound dressings daily to encourage formation of healthy granulation tissue and wound healing.16,18
Patients with poorly controlled diabetes are at high risk for diabetic foot ulcers, and need appropriate medical care to reduce the risk of foot amputation. Patients who present with advanced diabetic foot ulcers may also have infected ulcers, greater tissue necrosis, and osteomyelitis (Figure 3). These high-risk patients should be referred to an appropriate orthopedic office for immediate evaluation and management.
A full vascular evaluation of the affected limb and treatment of ischemia should be performed before debridement, to ensure sufficient peripheral circulation for resolving the infection and healing the ulcer. Early, consistent patient education about managing blood glucose may help patients avoid peripheral arterial disease, peripheral neuropathy, and diabetic foot ulcers.
1. Armstrong DG, Lavery LA. Diabetic foot ulcers
: prevention, diagnosis and classification. Am Fam Physician
. 1998;57(6):1352–1332, 1337–1338.
2. Bowering CK. Diabetic foot ulcers
. Pathophysiology, assessment, and therapy. Can Fam Physician
3. Dinh T, Tecilazich F, Kafanas A, et al. Mechanisms involved in the development and healing of diabetic foot ulceration. Diabetes
4. Reiber GE. The epidemiology of diabetic foot problems. Diabet Med
. 1996;13(suppl 1):S6–S11.
5. Boulton AJ, Vileikyte L, Ragnarson-Tennvall G, Apelqvist J. The global burden of diabetic foot disease. Lancet
6. Lavery LA, Armstrong DG, Wunderlich RP, et al. Diabetic foot syndrome: evaluating the prevalence and incidence of foot pathology in Mexican Americans and non-hispanic whites from a diabetes
disease management cohort. Diabetes Care
7. Pecoraro RE, Reiber GE, Burgess EM. Pathways to diabetic limb amputation
. Basis for prevention. Diabetes Care
8. Gordois A, Scuffham P, Shearer A, et al. The health care costs of diabetic peripheral neuropathy
in the US. Diabetes Care
9. Sumpio BE. Contemporary evaluation and management of the diabetic foot. Scientifica
10. Lipsky BA, Berendt AR, Cornia PB, et al. 2012 Infectious Diseases Society of America clinical practice guideline for the diagnosis and treatment of diabetic foot infections. Clin Infect Dis
11. Clayton W Jr, Elasy TA. A review of the pathophysiology, classification and treatment of foot ulcers
in diabetic patients. Clinical Diabetes
12. Wolf G. New insights into the pathophysiology of diabetic nephropathy: from haemodynamics to molecular pathology. Eur J Clin Invest
13. Paraskevas KI, Baker DM, Pompella A, Mikhailidis DP. Does diabetes
mellitus play a role in restenosis and patency rates following lower extremity peripheral arterial revascularization? A critical overview. Ann Vasc Surg
14. Arya AK, Garg S, Kumar S, et al. Estimation of lymphocyte apoptosis in patients with chronic non-healing diabetic foot ulcer. Int J Med Sci Pub Health
15. Boulton AJ, Armstrong DG, Albert SF, et al. Comprehensive foot examination and risk assessment: a report of the task force of the foot care interest group of the American Diabetes
Association, with endorsement by the American Association of Clinical Endocrinologists. Diabetes Care
16. Lipsky BA, Peters EJ, Senneville E, et al. Expert opinion on the management of infections in the diabetic foot. Diabetes Metab Res Rev
. 2012;28(suppl 1):163–178.
17. Kapoor A, Page S, Lavalley M, et al. Magnetic resonance imaging for diagnosing foot osteomyelitis: a meta-analysis. Arch Intern Med
18. Tallis A, Motley TA, Wunderlich RP, et al. Clinical and economic assessment of diabetic foot ulcer debridement with collagenase: results of a randomized controlled study. Clin Ther
19. Marineau ML, Herrington MT, Swenor KM, Eron LJ. Maggot debridement therapy in the treatment of complex diabetic wounds. Hawaii Med J
20. Hilton JR, Williams DT, Beuker B, et al. Wound dressings in diabetic foot disease. Clin Infect Dis
. 2004;39(suppl 2):S100–S103.
21. Manisha J, Patel MH, Sood NK, et al. Spectrum of microbial flora in diabetic foot ulcer and its antibiotic sensitivity pattern in tertiary care hospital in Ahmedabad, Gujarat. Nat J Med Res
22. Sotto A, Richard JL, Messad N, et al. Distinguishing colonization from infection with Staphylococcus aureus
in diabetic foot ulcers
with miniaturized oligonucleotide arrays: a French multicenter study. Diabetes Care
23. Wagner FW Jr. The diabetic foot. Orthopedics
24. Bus SA. Offloading the diabetic foot: evidence and clinical decision making. EWMA J
25. Driver VR, Yao M, Kantarci A, et al. A prospective, randomized clinical study evaluating the effect of transdermal continuous oxygen therapy on biological processes and foot ulcer healing in persons with diabetes
mellitus. Ostomy Wound Manage
26. Park SC, Choi CY, Ha YI, Yang HE. Utility of toe-brachial index for diagnosis of peripheral artery disease. Arch Plast Surg
27. Slovut DP, Lipsitz EC. Surgical technique and peripheral artery disease. Circulation
28. Serrano Hernando FJ, Martín Conejero A. Peripheral artery disease: pathophysiology, diagnosis and treatment. Rev Esp Cardiol
Keywords:Copyright © 2015 American Academy of Physician Assistants
diabetes; foot ulcers; amputation; peripheral neuropathy; glycemic control; peripheral arterial disease