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Validated 60-Second General Foot Screen

A Pilot Trial and Guide to Diagnoses and Treatment

Sibbald, R. Gary MD, DSc (Hons), MEd, FRCPC (Med Derm), ABIM, FAAD, MAPWCA; Maliyar, Khalad BA; Persaud-Jaimangal, Reneeka MD, MScCH; Elliott, James A. MSc; Brandon, Alisa BSc; Kotru, Bharat PhD, MSc, BSc, PT Podiatry; Armstrong, David G. DPM, MD, PhD

doi: 10.1097/01.ASW.0000582624.75772.52

GENERAL PURPOSE To provide information on a 60-second General Foot Screen to assist in the prevention and/or identification and management of common foot problems.

TARGET AUDIENCE This continuing education activity is intended for physicians, physician assistants, nurse practitioners, and nurses with an interest in skin and wound care.

LEARNING OBJECTIVES/OUTCOMES After participating in this educational activity, the participant should be better able to:

1. Use the 60-second General Foot Screen to assist healthcare professionals in the recognition of common foot problems.

2. Identify risk factors, causes, and treatment of selected foot problems.

ABSTRACT Foot health is important to overall patient health. Early diagnosis and treatment of diabetes, neuropathy, fungal foot infections, foot deformity, and vascular disease/lower leg edema can improve patient quality of life. One way to achieve this is effective screening. To this end, researchers piloted a validated 10-item screening tool to assess foot health on 120 patients; 74.17% had at least one positive abnormality, demonstrating the critical importance of these early findings. Only 25.83% of individuals had completely low-risk feet. This easy-to-use tool can assist healthcare professionals in the recognition and treatment of common foot problems. The article also outlines the early signs of disease by screening item and provides a guide to treatment to enable effective prevention and quality care.

R. Gary Sibbald, MD, DSc (Hons), MEd, FRCPC (Med Derm), ABIM, FAAD, MAPWCA • Professor • Medicine and Public Health • Director • International Interprofessional Wound Care Course and Masters of Science in Community Health (Prevention and Wound Care) • Dalla Lana Faculty of Public Health • University of Toronto • Lead Project ECHO Ontario Wound & Skin Care • Toronto, Ontario, Canada • Investigator, Institute for Better Health, Trillium Health Partners • co-Editor-in-Chief • Advances in Skin and Wound Care • Philadelphia, Pennsylvania

Khalad Maliyar, BA • Medical Student • Faculty of Medicine • University of Toronto • Toronto, Ontario, Canada

Reneeka Persaud-Jaimangal, MD, MScCH • Clinical Coordinator • Project ECHO Skin and Wound • Research Coordinator and Special Projects • Toronto Regional Wound Healing Clinic • Adjunct Faculty • International Interprofessional Wound Care Course • Toronto, Ontario, Canada

James A. Elliott, MSc • Faculty • International Interprofessional Wound Care Course • Member • Wounds Canada Research Committee • Toronto, Ontario, Canada

Alisa Brandon, BSc • Medical Student • Faculty of Medicine • University of Toronto • Toronto, Ontario, Canada

Bharat Kotru, PhD, MSc, BSc, PT Podiatry • Clinical Integrity & Wound Management • Faculty Member of the International Interprofessional Wound Care Course (IIWCC) • Max Super Speciality Hospital • Punjab, India

David G. Armstrong, DPM, MD, PhD • Director • Southwestern Academic Limb Salvage Alliance • Professor of Surgery • Keck School of Medicine • University of Southern California • Los Angeles, California

Acknowledgments: This work was made possible by an unrestricted educational grant from Bausch Health (previously Valeant Pharmaceutical). The author, faculty, staff, and planners, including spouses/partners (if any), in any position to control the content of this CME/CNE activity have disclosed that they have no financial relationships with, or financial interests in, any commercial companies relevant to this educational activity.

To earn CME credit, you must read the CME article and complete the quiz online, answering at least 13 of the 18 questions correctly.

This continuing educational activity will expire for physicians on October 31, 2021, and for nurses September 3, 2021.

All tests are now online only; take the test at for physicians and for nurses. Complete CE/CME information is on the last page of this article.

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Foot health is a key component of overall health and well-being. The foot is a complex structure with 26 bones, 133 joints, 107 ligaments, and 19 muscles. The average lifetime wear and tear on a foot are equivalent to an estimated 100,000 miles.1 Unhealthy feet can have a negative impact on walking, curtail physical activity, and decrease quality of life. Unhealthy feet can also be a source of pain as well as contribute to body image problems.2–4 An ability to walk and participate in activities of daily living depends on foot health. More than 75% of older adults (individuals 65 years or older) will complain of foot pain associated with arthritic changes that may be seen with radiographic examination.5,6 Moreover, 90% of older adults will have some type of foot problem including corns/calluses, bunions, hammer toes, or fungal infection.6

Both health providers and patients often overlook foot health, delaying early diagnosis and treatment of common foot problems.7,8 This is true in both primary care and in specialized clinics.7 Many healthcare providers find foot history and examination challenging and complicated to perform. This problem is exacerbated when patients afflicted by foot diseases do not inform their healthcare professionals.9

Foot abnormalities can be detected by a screening examination or by reviewing the common problems including fungal infection. Recently, a simple foot screen by Miller et al9 called the “3-minute diabetic foot exam” was developed to help physicians and other healthcare professionals screen for lower extremity complications in patients with a suspected or confirmed diagnosis of diabetes. This exam is efficient, comprehensive, and requires no equipment.

However, there is a clear need for healthcare providers to implement routine foot screening protocols for the general population or those participating in specialized activities such as sports or athletic programs. Routine screening for patients with abnormal or high-risk feet can facilitate timely referral and appropriate healthcare resource utilization. Common foot abnormalities can be divided into four categories: skin changes, nail problems, bony abnormalities, and abnormal findings related to the vascular system.10

This article introduces an easy and quick, validated General Foot Screen with an enabler for interprofessional and primary care practice (Figure 1).

Figure 1

Figure 1

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Development of the General Foot Screen

Persaud et al10 developed this validated tool (previously published as the Healthy Foot Screen) to facilitate timely treatment of common foot problems and assessed it for interrater reliability and validity. This process involved 18 patients from a community dermatology clinic. Each individual was assessed independently by 11 interprofessional healthcare providers using the tool. The interrater reliability was calculated using Cronbach α with a minimum acceptable reliability value of 0.60. Subsequently, the assessors completed a short questionnaire to provide feedback on the screen (strengths, weaknesses, and areas of potential improvement).

Parameters that passed the threshold for acceptable reliability in both feet included diabetes, smoking, neuropathy, palpable foot pulse, abnormal fourth to fifth toe web space, previous ulcer/amputation, pitting edema, bony abnormality, and dry bottom of foot. Items on the screen that were removed because of low reliability included subsets of toenail infection (distal streaks, discoloration, subungual debris), subsets of abnormal toe webs (wet, other web spaces involved), and secondary skin lesions (other spots/lesions, and red areas/blisters/pustules). After identifying the items with low reliability and assessing the feedback and recommendations, a consensus among the authors and assessors was reached to develop a revised version of the screen. The final published version only contained valid and reliable items, for a total of 10 items with 18 responses: items 1 and 2 have one response, and items 3 through 10 have two responses (one for each foot).

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Pilot Study to Test Application to Practice

Researchers conducted a prospective cohort pilot study using this new screening tool. This study received ethics approval (#Pro00022415) from Institutional Review Board Services (Aurora, Ontario). Participants recruited were adult patients (18 years or older) attending a community dermatology clinic. Patients were excluded from the study if they had a known foot abnormality (eg, current foot ulcer, foot amputations) or if they were younger than 18 years. Convenience sampling was used, and verbal consent to participate was obtained by one of two assessors. Each patient was examined by one assessor for demographics (age and gender) and items of the screening tool (Figure 1). Data from the screening process were exported from paper to Microsoft Excel by a trained researcher, and results were then reviewed by the study authors.

A total of 120 patients (53 male and 67 female; mean age, 61.07 years) were analyzed. The parameters on the screen present in patients are outlined in Table 1. The screen was positive for one or more items in 74.17% of individuals, with only 25.83% having completely low-risk feet (no diabetes, no tobacco use, and no screened foot abnormalities). Several screened individuals had more than one positive item: 37.49% had two to four, 23.31% had five to eight, and 5.82% had nine or more positive items. Investigators also documented potential fungal foot infections: dry plantar skin was present in both feet in 36% of participants, potential onychomycosis was present in 31% (left foot) and 35% (right foot), and macerated toe webs in 11% (left) and 12% (right) of feet.

Table 1

Table 1

Diabetes was present in 15% of participants, 10% smoked, and 14% (left feet) and 15% (right feet) had potential neuropathy. Five percent had a previous foot ulcer or localized amputation. Bony abnormalities were noted in 29% (left feet) and 26% (right feet) of the study population. Nonpalpable pulses were recorded in 8% (left) and 9% (right), and pitting edema of the ankle in 13% (left) and 14% (right). These data are illustrated in Figure 2.

Figure 2

Figure 2

The results of this pilot study demonstrate that a significant majority (74%) of self-reported “healthy” adult patients had one or more extant foot pathologies. The following sections review the possible positive abnormal clinical findings and treatment for individual items.

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1. Does the patient have diabetes?

It is estimated that 9 million Canadians and 100 million Americans11 are currently living with diabetes, undiagnosed diabetes, or prediabetes.12 Patients with chronic and uncontrolled high blood glucose levels are at higher risk of developing microvascular complications including neuropathy, nephropathy, retinopathy, and macrovascular complications (coronary artery disease, peripheral arterial disease, and stroke).13

Persons with diabetes have 85% of the nontraumatic lower limb amputations in the developed world. The etiology of foot ulcers involves neuropathy, peripheral artery disease, or a combination of both (neuroischemic foot).14,15 Building on this information, the authors have developed16 and validated17 a simplified 60-second diabetic foot screen that should be administered for all persons with diabetes.

Diabetes necessitates a very complex and demanding treatment protocol that depends on patients to self-manage their blood glucose levels at acceptable levels.18 If a patient is diagnosed with diabetes, clinicians should refer him/her to interprofessional diabetes education teams including physicians (endocrinologist or other specialists, family medicine), nurses (with diabetes expertise), foot specialists (podiatry, orthopedics, other), allied health practitioners (dietician, social worker, a psychologist), and rehabilitation specialists (physiotherapist, occupational therapist). These teams can carefully educate patients on how to manage their diabetes. Primary care providers should also take time to educate patients on the ABCDES of diabetic care:

  • A1 target of 7.0% or less with exceptions for hypoglycemia
  • BP targets of less than 130/80 mm Hg
  • Cholesterol targets of a low-density lipoprotein cholesterol less than 2.0 mmol/L
  • Drugs for cardiovascular disease risk reduction
  • Exercise and healthy eating
  • Smoking
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2. Is the patient currently a smoker?

Smoking has profound deleterious effects on wound healing and compromised blood flow to tissues. The toxic compounds in cigarette smoke (including nicotine, tar, and carbon monoxide) have been shown to inhibit wound healing through the actions of anoxia, vasoconstriction, and hypoxia.19,20 Moreover, smoking contributes to the development of peripheral arterial disease and angina by dysregulating normal endothelial function and being an important factor in the process of atherosclerosis.21 Jensen et al22 calculated that every cigarette decreases the circulation in the leg or foot up to 30% for an hour.

Unfortunately, the average smoker may need 30 or more attempts to stop smoking.23 The most successful strategies include a combination of behavioral modification techniques (counseling, support groups) and medications. Coexisting psychosocial issues including other substance dependencies, depression, or anxiety need to be addressed if smoking cessation is to be successful. Medications that may be useful include nicotine replacement patches or gum, varenicline, and bupropion.

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3. Does the patient have neuropathy?

Detectable peripheral neuropathy is common in persons with diabetes, with approximately 30% to 50% of patients affected.24 Patients with neuropathy (particularly the sensory component of peripheral neuropathy) may lose the protective sensation in their feet, causing the experience of neuropathic pain (burning, stinging, shooting, or stabbing sensations). Neuropathic pain is a debilitating complication of diabetes; patients report poorer quality of life, decreased sleep, and higher anxiety and depression scores compared with individuals without neuropathic pain.25

If there is no diagnosis of diabetes, providers should check hemoglobin A1c levels. Other conditions associated with neuropathy include:26

  • systemic disease: thyroid disease, advanced liver or kidney disease
  • vitamin deficiencies: low levels of B12, vitamin E, thiamine
  • toxins: excessive alcohol consumption, chemotherapy drugs, immunosuppressive drugs, heavy metals
  • trauma: bone fractures, nerve compression
  • infection: Lyme disease, HIV, syphilis
  • connective tissue disease: rheumatoid arthritis, systemic lupus erythematosus, scleroderma, dermatomyositis

Treatment should include the correction of the spontaneous nerve pain. For daytime relief, antiepileptic drugs including gabapentin or pregabalin are often useful first-line drugs. For night pain, low doses of tricyclic antidepressants can facilitate sleep and control pain. Nortriptyline or desipramine are second-generation agents with more antinoradrenaline levels than amitriptyline at equal dosage levels. Other antiepileptic drugs may also be useful and include carbamazepine or lamotrigine. Resistant cases may respond to serotonin norepinephrine reuptake inhibitors that include duloxetine and venlafaxine. Patients with vitamin deficiencies need appropriate replacement therapy, and treatment is often required for other neuropathy associations.

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4. Has the patient had a previous foot ulcer or amputation on either foot?

History of a foot ulceration and/or amputation is associated with an increased risk of future ulceration. Prior foot ulcers are indicative of an underlying foot abnormality, and previous amputations can induce changes in gait and foot shape and thus impact the risk of subsequent ulcer formation.27

Not all persons with a previous foot ulcer or amputation have diabetes. More than one-third of individuals who have had any two of the following: previous foot ulcer, previous lower limb amputation, neuropathy, or peripheral vascular disease, are likely to develop a foot ulcer in the next year.28 This means that they need careful follow-up on a regular basis with a foot care specialist.

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5. Are there signs of toenail fungal infection?

Approximately half of abnormal toenail findings are attributable to fungal infection.29 Fungal infection of the nails has recently been added as a new criterion for a high-risk diabetic foot by the International Diabetic Federation.30

Tinea pedis is a cutaneous fungal infection that usually starts on the plantar skin and toe webs. The fungus then spreads to the nails (a state known as onychomycosis or tinea unguium) through the distal nail fold to the nail plate, creating a streak that is wider on the distal nail and narrow as it precedes proximally through the nail plate. This is distal subungual onychomycosis, the most common type of tinea pedis (Figure 3A). White superficial onychomycosis (Figure 3B) is less common than distal subungual onychomycosis and is characterized by the invasion of fungi into the superficial layers of the nail plate. It is identified by the presence of well-demarcated opaque “white islands” on the external nail plate that usually coalesce and spread as the disease progresses.31 Treatment of white superficial onychomycosis consists of topical antifungal medication (Table 2).

Figure 3

Figure 3

Table 2

Table 2

Severe infections that are harder to treat involve the entire nail plate (whole-plate onychomycosis; Figure 3C) including the matrix, and the nail may be thickened with powdery subungual debris often accompanied with thickened scale along the nail fold.38,39 These are prognostic signs with a lower treatment success. The lunula (white moon of the proximal nail) is the distal end of the nail matrix that extends proximally under the skin surface ending halfway to the distal interphalangeal joint.40 Primary involvement of the lunula (proximal subungual onychomycosis; Figure 3D) is most likely because of immune deficiency including HIV hyponychial infection.41

Onychomycosis diagnosis requires laboratory confirmation for systemic therapy. A variety of topical and oral antifungal medications are available for the treatment of onychomycosis.42 Hygiene measures43 are also important for preventing onychomycoses and recurrence. Nail infections are often acquired from health clubs, bathroom floors, around swimming pools, and from pedicures. Protective footwear on wet common area surfaces, avoiding foot soaks (especially for persons with diabetes), and ensuring hygienic conditions in foot spas also prevent fungal foot infections. Footwear and socks should breathe; tightly woven nonbreathable socks should be avoided because they may hold moisture. Instead, socks with moisture-wicking technology and breathable hybrid combination materials are encouraged. Aluminum chloride hexahydrate preparations from 6.25% to 20% at night can often inhibit sweating and prevent moist feet during the day for individuals prone to hyperhidrosis.44 Treating tinea pedis before onychomycosis develops, smoking cessation, and control of chronic disease will also help prevent fungal foot infections.

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6. Are the toe webs abnormal?

Fungal infections usually spread from the plantar surface of the skin to the toe webs and the toenails. Web involvement usually starts with dry scale that can become macerated with sweat from warm shoes or boots.45,46 The macerated skin is a prime target for secondary bacterial growth including Gram-positive or Gram-negative organisms.47,48 The Gram-positive organisms can invade the adjacent skin and cause bacterial lymphangitis and cellulitis of the lower leg. The fourth/fifth toe web space is the tightest and least ventilated interdigital web space, typically rendering it the first involved web space; this is followed by spread proximally to the other web spaces. Topical antiseptics in a water or lotion base are often useful to decrease microbial organisms in the web spaces. Povidone-iodine or chlorhexidine have a broad spectrum of action covering bacteria, yeast, and dermatophytes.

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7. Is the bottom of the foot dry?

Dry skin on the plantar aspect of the foot can be seen with neuropathy or fungal infections. Neuropathy is associated with sensory (identified with monofilament test), autonomic (dryness is usually limited to the plantar skin), and/or motor components (loss of reflexes).49 Autonomic neuropathy can cause dry skin on the plantar aspect of the skin, but this needs to be distinguished from fungal infections. Fungal involvement of the plantar skin also may manifest as dry feet, but the infection often involves the sides of the feet in a “moccasin” distribution (a fine red line at the distal end of the involvement).50 There may be coexisting fourth/fifth toe web involvement as well as onychomycosis. Less commonly, three other clinical variants can be present: a hyperkeratotic thick change on the plantar aspect of the foot, an inflammatory presentation with small papulovesicules or pustules clustered around the plantar surface, and an even less common tiny erosive or ulcerative variant caused by a bacterial infection called erythrasma.51

Accurate diagnosis of tinea pedis is essential for proper treatment (Table 3), because tinea pedis can mimic other dermatologic conditions. To diagnose the presence of dermatophytes, lesion scrapings are performed with either the use of a blade (no. 15) or banana-shaped knife, and blister/pustule tops can be ruptured to remove culture samples. The sample is then analyzed with direct microscopy and fungal culture.29

Table 3

Table 3

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8. Is there a significant bony abnormality or associated change?

A foot deformity is a disorder of the foot that can be congenital or acquired; they involve structural abnormalities or muscular imbalances that affect the function of the foot. The deformities are classified according to clinical appearance. The most common structural deformities of the foot are hammer toe, claw toe, mallet toe, hallux valgus, and flat foot. Bony/structural deformities are important to identify as a risk factor for foot ulceration.53 Any significant bony change should trigger a foot specialist referral.

The most recognizable congenital foot deformity is clubfoot. It is characterized by dorsiflexion/plantar flexion of the ankle, inversion of the foot, and adduction of the forefoot. Manipulative treatment of congenital foot deformities, which requires manual repositioning and serial casting, should be initiated immediately after birth. The outcome depends primarily on whether the deformity responds well to manual repositioning with casting and splinting (flexible deformities). Resistant deformities often require surgical correction to reposition structures or relieve muscle contractures.

Hammer toe (Figure 4A) involves a flexion (downward) contracture of the middle toe joint or the proximal interphalangeal joint.54 This deformity may be associated with a hereditary etiology or motor neuropathy.55 Acquired causes include tight shoe boxes or pointed shoes that force the toe to bend forward. The compressive forces leading to hammer toe can be treated by ensuring shoes have enough space for toes to stretch.54

Figure 4

Figure 4

Claw toe (Figure 4B) is a deformity involving the most toe joints, resulting in hyperextension of the metatarsophalangeal joint and flexion at the proximal interphalangeal joint, and flexion of the distal interphalangeal joint.54 It results from neurologic disorders (eg, rheumatoid arthritis, diabetes, cerebral palsy, stroke, etc) that cause muscle imbalances, leading to altered structural anatomy.56 Treatment of claw toe includes conservative options such as roomy, well-fitting shoes, with a deep and wide toe box. If the deformity is fixed, surgical intervention is required to resect the bone and release the contraction of the tendons.

Mallet toe (Figure 4C) is a downward bending of the distal interphalangeal joint. This deformity is commonly associated with friction and pressure from faulty footwear or other toe injuries, bone and muscle imbalance, or arthritis. The condition may also be congenital.54,57 It is most common in the second toe but can exist on other toes. Treatment may include a roomier shoe, cushioned padding, and avoiding high heels.55 This condition can be improved by strengthening and stretching the toe muscles or, in some cases, with successful surgery.

Hallux valgus (Figure 4D; also called a bunion) is usually a hereditary condition with medial deviation of the first metatarsal and lateral deviations of the great toe.58 This is commonly seen when patients have flexible joints and with the use of pointed shoes and high heels. People with flat feet are also susceptible to hallux valgus. They may occur in cultures in which shoes are not worn.59 Nonsurgical treatment can include a hallux valgus splint, wearing shoes with a flat and roomy toe box, and customized orthotic or bunion pads. If nonsurgical approaches fail to provide relief, surgery is an option.

Flat foot (Figure 4E; also known as pes planus) is characterized by a completely fallen midfoot arch.60 It may be best observed when the plantar foot comes in contact with ground during weight-bearing and standing. The condition may be congenital or acquired from a variety of conditions (stretched or torn tendons, broken or dislocated midfoot bones, rheumatoid arthritis, nerve degenerative problems, obesity, diabetes, pregnancy). Treatment often starts with arch supports, customized orthotics, or exercises; few individuals require surgery. Individuals with flat feet are more susceptible to plantar fasciitis or Achilles tendonitis. There may also be referred pain to the ankles, knees, hips, and back.

Pes cavus (Figure 4F) is a high arch that does not flatten with weight bearing; the foot stays locked.61 Because the foot is not flexible or hollow on standing, it pounds the ground as the person walks. This may be a hereditary condition or may be secondary to neurologic conditions including cerebral palsy and Charcot-Marie-Tooth disease.61 Many patients with a pes cavus can develop calluses and pain at the heel and ball of the foot. Treatment requires an accommodation to help absorb the increased pressures in these regions including different inserts to pad the foot (metatarsal pads and arch supports) that redistributes pressure to a larger portion of the plantar aspect of the foot rather than control its movement. Persons with pes cavus are very susceptible to plantar fasciitis.

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9. Can you feel a foot pulse?

A patient’s vascular status (ie, blood circulation) can provide important insight into common foot health issues. The presence of peripheral pulses (ie, dorsalis pedis and/or posterior tibial pulse) represents a minimum systolic BP of 80 mm Hg and suggests adequate vascular supply to support wound healing.62 A small percentage of individuals may have an absent or aberrant dorsalis pedis pulse, and the posterior tibial pulse should be palpated. Absent or diminished distal foot pulse(s) may be suggestive of peripheral vascular disease and should trigger a vascular laboratory assessment/referral.

Arterial disease can predispose individuals to “punched-out” arterial ulcers, critical limb ischemia, gangrene, and amputations.63 Risk factors for peripheral vascular disease include smoking (the most important risk factor), diabetes mellitus, hyperlipidemia, hypertension, and coronary artery disease.

If the pulse cannot be felt, an ankle-brachial pressure index (ABPI) should be recorded with a portable 8 MHz Doppler to determine if there is any impairment to the lower extremity arterial blood flow. An ABPI value greater than 1.3 means the arteries are often calcified, and the test is usually falsely high and inaccurate. An alternative to the ABPI is the audible handheld Doppler waveform signal.64 Monophasic audible waves or an ABPI of less than 0.6 identify poor circulation, and the need for the definitive noninvasive arterial vascular assessment is the segmental duplex Doppler in the vascular laboratory. Adequate circulation is confirmed when multiphasic waves elicit an audible signal indicating an ABPI greater than 0.9.

Patients can pursue conservative avenues to improve peripheral circulation. This includes smoking cessation, a graduated exercise program, foot care, atherosclerotic risk factor reduction (ie, control of hyperlipidemia, hypertension, weight, diabetes), and avoidance of extreme temperatures. Patients with advanced arterial disease (dependent rubor, elevation producing pallor) or claudication with walking or at rest may be candidates for dilation or bypass procedures.

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10. Any pitting edema of the foot/ankle?

Pitting edema of the lower limbs is a clinical sign of several disease states. If the pitting edema extends above the knee, systemic disease may be present, including anemia, congestive heart failure, or chronic liver/kidney disease.

Chronic venous insufficiency is the most common cause of lower leg pitting; this cause should be investigated further and managed. Venous disease can manifest with several progressive clinical signs.65 The disease often begins with a dilated saphenous vein, followed by superficial varicosities and varicose veins leading to a leakage of serum fluid resulting in pitting edema. This edema often starts around the medial malleolus where the long saphenous vein is most superficial and has its greatest curvature. When the veins become porous to red blood cells, hemosiderin and melanin deposits result in superficial dark brown pigment most commonly around the lower gaiter area.66 With chronic disease, fibrin also leaks out of the capillaries, causing lipodermatosclerosis such that the skin cannot be moved over the underlying structures. When the woody fibrosis spreads to the foot and toes, the changes are referred to as venolymphedema. Stemmer sign is the confirmatory test (when the skin on the dorsum of the second toe cannot be pinched between the thumb and index finger).67

Compression therapy with the use of elastic compression stockings is a well-known and established therapy used in the management of chronic venous insufficiency.68 Stockings work by applying greater pressures at the ankle, with gradually decreasing pressures up the garment toward the knee. This pressure gradient allows venous blood to flow upward to the heart rather than pooling in the foot and superficial veins.69 Many studies have shown that compression stockings reduce venous disease signs and symptoms, improve quality of life, and relieve lower limb aching, pain, and leg cramps.70–72 Patients should be encouraged to wear compression stockings, unless there is a contraindicated condition or advanced arterial disease.

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Foot health is a critical component of general well-being. The General Foot Screen is a validated, easy-to-use tool developed to identify common foot abnormalities for foot care clinicians, primary care providers, and any specialists regularly in contact with high-risk patients including those in endocrinology, dermatology, nephrology, and cardiology. The implementation of the General Foot Screen in everyday community clinical settings will improve the early identification of foot pathologies. The tool can improve patient outcomes with the basic diagnosis and treatment strategies outlined above and appropriate referral to other healthcare specialists (eg, chiropodists, podiatrists, endocrinologists, etc). Early detection of abnormal feet can improve general health!

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  • Foot health is an important component of general health and well-being that is commonly neglected by healthcare providers, leading to delayed diagnosis and treatment.
  • Common foot problems include fungal infection of the skin, toenails, and toe webs; signs of neuropathy; bony abnormalities; and comprised vascular status.
  • The validated 60-second General Foot Screen may promote the early identification and management of foot conditions.
  • Treatment of common foot problems can improve quality of life.
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1. American Podiatric Medical Association. Value of Podiatry. Last accessed August 20, 2019.
2. Mickle KJ, Munro BJ, Lord SR, Menz HB, Steele JR. Cross-sectional analysis of foot function, functional ability, and health-related quality of life in older people with disabling foot pain. Arthritis Care Res (Hoboken) 2011;63(11):1592–8.
3. Price P, Krasner DL. Health-related quality of life and chronic wounds: evidence and implications for practice. In: Chronic Wound Care: A Clinical Source Book for Healthcare Professionals. 5th ed. Malvern, PA: HMP Communications; 2012:1–8.
4. Katsambas A, Abeck D, Haneke E, et al. The effects of foot disease on quality of life: results of the Achilles Project. J Eur Acad Dermatol Venereol 2005;19(2):191–5.
5. Mitty E. Nursing care of the aging foot. Geriatr Nurs 2009;30(5):350–4.
6. Ebersole P, Hess P, Luggen AN. Toward Healthy Aging: Human Needs and Nursing Response. 6th ed. Milton, Ontario, Canada: Mosby/Elsevier; 2004.
7. Papaliodis DN, Vanushkina MA, Richardson NG, DiPreta JA. The foot and ankle examination. Med Clin North Am 2014;98(2):181–204.
8. Burzykowski T, Molenberghs G, Abeck D, et al. High prevalence of foot diseases in Europe: results of the Achilles Project. Mycoses 2003;46(11-12):496–505.
9. Miller JD, Carter E, Shih J, et al. How to do a 3-minute diabetic foot exam. J Fam Pract 2014;63(11):646–56.
10. Persaud R, Coutts PM, Brandon A, Verma L, Elliott JA, Sibbald RG. Validation of the Healthy Foot Screen: a novel assessment tool for common clinical abnormalities. Adv Skin Wound Care 2018;31(4):154–62.
11. Xu G, Liu B, Sun Y, et al. Prevalence of diagnosed type 1 and type 2 diabetes among US adults in 2016 and 2017: population based study. BMJ 2018; 362:k1497.
12. Recommendations by the Canadian Diabetes Association to the House of Commons Standing Committee on Health Study on Healthy Living. Working Together to Achieve Healthy Weights: Addressing the Tsunami of Diabetes. February 2011. Last accessed August 29, 2019.
13. Cade WT. Diabetes-related microvascular and macrovascular diseases in the physical therapy setting. Phys Ther 2008;88(11):1322–35.
14. Singh N, Armstrong DG, Lipsky BA. Preventing foot ulcers in patients with diabetes. JAMA 2005;293(2):217–28.
15. Armstrong DG, Boulton AJM, Bus SA. Diabetic foot ulcers and their recurrence. N Engl J Med 2017;376(24):2367–75.
16. Sibbald RG, Ayello EA, Alavi A, et al. Screening for the high-risk diabetic foot: a 60-second tool (2012). Adv Skin Wound Care 2012;25(10):465–76.
17. Woodbury MG, Sibbald RG, Ostrow B, Persaud R, Lowe JM. Tool for rapid & easy identification of high risk diabetic foot: validation & clinical pilot of the simplified 60 second diabetic foot screening tool. PLoS One 2015;10(6):e0125578.
18. Steed L, Cooke D, Newman S. A systematic review of psychosocial outcomes following education, self-management and psychological interventions in diabetes mellitus. Patient Educ Couns 2003;51(1):5–15.
19. McDaniel JC, Browning KK. Smoking, chronic wound healing, and implications for evidence-based practice. J Wound Ostomy Continence Nurs 2014;41(5):415–E2.
20. Wong LS, Green HM, Feugate JE, Yadav M, Nothnagel EA, Martins-Green M. Effects of “second-hand” smoke on structure and function of fibroblasts, cells that are critical for tissue repair and remodeling. BMC Cell Biol 2004;5:13.
21. Chalon S. Nicotine impairs endothelium-dependent dilatation in human veins in vivo. Clin Pharmacol Ther 2000;67(4):391–7.
22. Jensen JA, Goodson WH, Hopf HW, Hunt TK. Cigarette smoking decreases tissue oxygen. Arch Surg 1991;126(9):1131–4.
23. Chaiton M, Diemert L, Cohen JE, et al. Estimating the number of quit attempts it takes to quit smoking successfully in a longitudinal cohort of smokers. BMJ Open 2016;6(6):e011045.
24. Kumar S, Ashe HA, Parnell LN, et al. The prevalence of foot ulceration and its correlates in type 2 diabetic patients: a population-based study. Diabet Med 1994;11(5):480–4.
25. Attal N, Lanteri-Minet M, Laurent B, Fermanian J, Bouhassira D. The specific disease burden of neuropathic pain: results of a French nationwide survey. Pain 2011;152(12):2836–43.
26. Azhary H, Farooq MU, Bhanushali M, Majid A, Kassab MY. Peripheral neuropathy: differential diagnosis and management. Am Fam Physician 2010;81(7):887–92.
27. Assessment and Management of Foot Ulcers for People with Diabetes. 2nd ed. Toronto, Ontario, Canada: Registered Nurses’ Association of Ontario; 2013.
28. Lavery LA, Peters EJG, Williams JR, et al. Reevaluating the way we classify the diabetic foot: restructuring the diabetic foot risk classification system of the International Working Group on the Diabetic Foot. Diabetes Care 2008;31(1):154–6.
29. Faergemann J, Correia O, Nowicki R, Ro B-I. Genetic predisposition—understanding underlying mechanisms of onychomycosis. J Eur Acad Dermatol Venereol 2005;19 Suppl 1:17–19.
30. International Diabetic Federation. Clinical Practice Recommendations on the Diabetic Foot. 2017. Last accessed August 29, 2019.
31. Elewski BE. Onychomycosis: pathogenesis, diagnosis, and management. Clin Microbiol Rev 1998;11(3):415–29.
32. Evans EGV, Sigurgeirsson B. Double blind, randomised study of continuous terbinafine compared with intermittent itraconazole in treatment of toenail onychomycosis. BMJ 1999;318(7190):1031–5.
33. Gupta AK, Sibbald RG, Andriessen A, et al. Toenail onychomycosis-—a Canadian approach with a new transungual treatment: development of a clinical pathway. J Cutan Med Surg 2015;19(5):440–9.
34. Elewski BE, Rich P, Pollak R, et al. Efinaconazole 10% solution in the treatment of toenail onychomycosis: two phase III multicenter, randomized, double-blind studies. J Am Acad Dermatol 2013;68(4):600–8.
35. Elewski BE, Aly R, Baldwin SL, et al. Efficacy and safety of tavaborole topical solution, 5%, a novel boron-based antifungal agent, for the treatment of toenail onychomycosis: results from 2 randomized phase-III studies. J Am Acad Dermatol 2015;73(1):62–9.
36. Gupta AK, Fleckman P, Baran R. Ciclopirox nail lacquer topical solution 8% in the treatment of toenail onychomycosis. J Am Acad Dermatol 2000;43(4 Suppl):S70–80.
37. Figueiredo Souza LW, Souza SVT, Botelho ACC. Randomized controlled trial comparing photodynamic therapy based on methylene blue dye and fluconazole for toenail onychomycosis. Dermatol Ther 2014;27(1):43–7.
38. Scher RK, Tosti A, Joseph WS, et al. Onychomycosis diagnosis and management: perspectives from a joint dermatology-podiatry roundtable. J Drugs Dermatol 2015;14(9):1016–21.
39. Tasić S, Stojanović S, Poljacki M. Etiopathogenesis, clinical picture and diagnosis of onychomycoses [in Croatian]. Med Pregl 2001;54(1-2):45–51.
40. Cohen PR. The lunula. J Am Acad Dermatol 1996;34(6):943–53.
41. Gupta AK, Taborda P, Taborda V, et al. Epidemiology and prevalence of onychomycosis in HIV-positive individuals. Int J Dermatol 2000;39(10):746–53.
42. Asz-Sigall D, Tosti A, Arenas R. Tinea unguium: diagnosis and treatment in practice. Mycopathologia 2017;182(1-2):95–100.
43. Rodgers P, Bassler M. Treating onychomycosis. Am Fam Physician 2001;63(4):663–72, 677-8.
44. Woolery-Lloyd H, Valins W. Aluminum chloride hexahydrate in a salicylic acid gel. J Clin Aesthet Dermatol 2009;2(6):28–31.
45. Rosen J, Yosipovitch G. Skin manifestations of diabetes mellitus. In: Feingold KR, Anawalt B, Boyce A, et al, eds. Endotext. South Dartmouth, MA: Inc; 2000.
46. Sahoo AK, Mahajan R. Management of tinea corporis, tinea cruris, and tinea pedis: a comprehensive review. Indian Dermatol Online J 2016;7(2):77–86.
47. Driscoll JA, Brody SL, Kollef MH. The epidemiology, pathogenesis and treatment of Pseudomonas aeruginosa infections. Drugs 2007;67(3):351–68.
48. Casqueiro J, Casqueiro J, Alves C. Infections in patients with diabetes mellitus: a review of pathogenesis. Indian J Endocrinol Metab 2012;16 Suppl 1:S27–36.
49. Volmer-Thole M, Lobmann R. Neuropathy and diabetic foot syndrome. Int J Mol Sci 2016;17(6).
50. Ely JW, Rosenfeld S, Seabury Stone M. Diagnosis and management of tinea infections. Am Fam Physician 2014;90(10):702–10.
51. Canavan TN, Elewski BE. Identifying signs of tinea pedis: a key to understanding clinical variables. J Drugs Dermatol 2015;14(10 Suppl):s42–7.
52. Rotta I, Otuki MF, Sanches ACC, Correr CJ. Efficacy of topical antifungal drugs in different dermatomycoses: a systematic review with meta-analysis. Rev Assoc Med Bras (1992) 2012;58(3):308–18.
53. Frykberg RG. The team approach in diabetic foot management. Adv Wound Care 1998;11(2):71–7.
54. Malhotra K, Davda K, Singh D. The pathology and management of lesser toe deformities. EFORT Open Rev 2016;1(11):409–19.
55. Shirzad K, Kiesau CD, DeOrio JK, Parekh SG. Lesser toe deformities. J Am Acad Orthop Surg 2011;19(8):505–14.
56. Merashli M, Chowdhury TA, Jawad ASM. Musculoskeletal manifestations of diabetes mellitus. QJM 2015;108(11):853–7.
57. Coughlin MJ. Mallet toes, hammer toes, claw toes, and corns. Causes and treatment of lesser-toe deformities. Postgrad Med 1984;75(5):191–8.
58. Munir U, Morgan S. Hallux varus. Treasure Island, FL: StatPearls Publishing; 2019.
59. Bunions: Overview. Cologne, Germany: Institute for Quality and Efficiency in Health Care (IQWiG); 2018.
60. Raj MA, Kiel J. Pes Planus. Treasure Island, FL: StatPearls Publishing; 2019.
61. Maynou C, Szymanski C, Thiounn A. The adult cavus foot. EFORT Open Rev 2017;2(5):221–9.
62. Lavery L, Gazewood JD. Assessing the feet of patients with diabetes. J Fam Pract 2000;49(11 Suppl):S9–16.
63. Weir GR, Smart H, van Marle J, Cronje FJ. Arterial disease ulcers, part 1: clinical diagnosis and investigation. Adv Skin Wound Care 2014;27(9):421–8.
64. Alavi A, Sibbald RG, Nabavizadeh R, Valaei F, Coutts P, Mayer D. Audible handheld Doppler ultrasound determines reliable and inexpensive exclusion of significant peripheral arterial disease. Vascular 2015;23(6):622–9.
65. Santler B, Goerge T. Chronic venous insufficiency: a review of pathophysiology, diagnosis, and treatment. J Dtsch Dermatol Ges 2017;15(5):538–56.
66. Partsch H. Varicose veins and chronic venous insufficiency. VASA 2009;38(4):293–301.
67. Youn YJ, Lee J. Chronic venous insufficiency and varicose veins of the lower extremities. Korean J Intern Med 2019;34(2):269–83.
68. van Geest AJ, Franken CP, Neumann HA. Medical elastic compression stockings in the treatment of venous insufficiency. Curr Probl Dermatol 2003;31:98–107.
69. Lim CS, Davies AH. Graduated compression stockings. CMAJ 2014;186(10):E391–8.
70. Vayssairat M, Ziani E, Houot B. Placebo controlled efficacy of class 1 elastic stockings in chronic venous insufficiency of the lower limbs [in French]. J Mal Vasc 2000;25(4):256–62.
71. Couzan S, Leizorovicz A, Laporte S, et al. A randomized double-blind trial of upward progressive versus degressive compressive stockings in patients with moderate to severe chronic venous insufficiency. J Vasc Surg 2012;56(5):1344–50.
72. Schul MW, Eaton T, Erdman B. Compression versus sclerotherapy for patients with isolated refluxing reticular veins and telangiectasia: a randomized trial comparing quality-of-life outcomes. Phlebology 2011;26(4):148–56.

diabetes; foot screen; fungal infection; neuropathy; preventive care; vascular disease

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