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Reviews/Commentaries/ADA Statements

T A S K F O R C E R E P O R T

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
ANDREW J.M. BOULTON, MD, FRCP1,2 LAWRENCE A. LAVERY, DPM, MPH9 foot problems is the first step in prevent-
DAVID G. ARMSTRONG, DPM, PHD3 JOSEPH W. LEMASTER, MD, MPH10 ing such complications, this report will
STEPHEN F. ALBERT, DPM, CPED4 JOSEPH L. MILLS, SR., MD11 focus on key components of the foot
ROBERT G. FRYKBERG, DPM, MPH5 MICHAEL J. MUELLER, PT, PHD12 exam.
RICHARD HELLMAN, MD, FACP6,7 PETER SHEEHAN, MD13
M. SUE KIRKMAN, MD8 DANE K. WUKICH, MD14
COMPONENTS OF THE
FOOT EXAM

I
t is now 10 years since the last technical surgery, and the American Association of
review on preventative foot care was Clinical Endocrinologists. History
published (1), which was followed by While history is a pivotal component of
an American Diabetes Association (ADA) THE PATHWAY TO FOOT risk assessment, a patient cannot be fully
position statement on preventive foot care ULCERATION assessed for risk factors for foot ulceration
in diabetes (2). Many studies have been The lifetime risk of a person with diabetes based on history alone; a careful foot
published proposing a range of tests that developing a foot ulcer may be as high as exam remains the key component of this
might usefully identify patients at risk of 25%, whereas the annual incidence of process. Key components of the history
foot ulceration, creating confusion among foot ulcers is 2% (37). Up to 50% of include previous foot ulceration or ampu-
practitioners as to which screening tests older patients with type 2 diabetes have tation. Other important assessments in
should be adopted in clinical practice. A one or more risk factors for foot ulceration the history (Table 2) include neuropathic
task force was therefore assembled by the (3,6). A number of component causes, or peripheral vascular symptoms (7,8),
ADA to address and concisely summarize most importantly peripheral neuropathy, impaired vision, or renal replacement
recent literature in this area and then rec- interact to complete the causal pathway to therapy. Lastly, tobacco use should be re-
ommend what should be included in the foot ulceration (1,35). A list of the prin- corded, since cigarette smoking is a risk
comprehensive foot exam for adult pa- cipal contributory factors that might re- factor not only for vascular disease but
tients with diabetes. The committee was sult in foot ulcer development is provided also for neuropathy.
cochaired by the immediate past and cur- in Table 1.
rent chairs of the ADA Foot Care Interest The most common triad of causes
Group (A.J.M.B. and D.G.A.), with other that interact and ultimately result in ul- General inspection
panel members representing primary ceration has been identified as neuropa- A careful inspection of the feet in a well-lit
care, orthopedic and vascular surgery, thy, deformity, and trauma (5). As room should always be carried out after
physical therapy, podiatric medicine and identification of those patients at risk of the patient has removed shoes and socks.
Because inappropriate footwear and foot
deformities are common contributory
From the 1Manchester Diabetes Centre, Manchester, U.K.; the 2Division of Endocrinology, Diabetes & factors in the development of foot ulcer-
Metabolism, University of Miami School of Medicine, Miami, Florida; the 3Dr. William M. Scholl College ation (1,5), the shoes should be inspected
of Podiatric Medicine at Rosalind Franklin University of Medicine and Science, North Chicago, Illinois; and the question Are these shoes appro-
the 4Denver Department of Veterans Affairs Medical Center, Denver, Colorado; the 5Carl T. Hayden VA priate for these feet? should be asked.
Medical Center, Phoenix, Arizona; the 6American Association of Clinical Endocrinologists, Jacksonville,
Florida; the 7Department of Medicine, University of MissouriKansas City School of Medicine, Kansas
City, Missouri; the 8American Diabetes Association, Alexandria, Virginia; the 9Department of Surgery,
Texas A&M Health Science Center, Temple, Texas; the 10Department of Family & Community Medicine, Table 1Risk factors for foot ulcers
University of MissouriColumbia School of Medicine, Columbia, Missouri; the 11Department of Surgery,
University of Arizona Health Sciences Center, Tucson, Arizona; the 12Program in Physical Therapy and Previous amputation
Department of Radiology, Washington University School of Medicine, St. Louis, Missouri; the 13Depart- Past foot ulcer history
ment of Medicine, Mount Sinai School of Medicine, New York, New York; and the 14Department of Peripheral neuropathy
Orthopedic Surgery, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania. Foot deformity
Corresponding author: Andrew J.M. Boulton, aboulton@med.miami.edu.
Peripheral vascular disease
This report was peer reviewed and approved by the Professional Practice Committee of the American
Diabetes Association, the Endocrine Practice Editorial Board, and the Board of Directors of the American Visual impairment
Association of Clinical Endocrinologists. Diabetic nephropathy (especially patients
DOI: 10.2337/dc08-9021 on dialysis)
2008 by the American Diabetes Association. Readers may use this article as long as the work is properly Poor glycemic control
cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.
org/licenses/by-nc-nd/3.0/ for details. Cigarette smoking

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Comprehensive foot examination and risk assessment

Table 2Essential features of history Dermatological assessment. The der- screening examnormally the 10-g
Past history
matological assessment should initially monofilament and one other test. One or
ulceration include a global inspection, including in- more abnormal tests would suggest
amputation terdigitally, for the presence of ulceration LOPS, while at least two normal tests (and
Charcot joint or areas of abnormal erythema. The pres- no abnormal test) would rule out LOPS.
vascular surgery ence of callus (particularly with hemor- The last test listed, vibration assessment
angioplasty rhage), nail dystrophy, or paronychia using a biothesiometer or similar instru-
cigarette smoking should be recorded (9), with any of these ment, is widely used in the U.S.; however,
Neuropathic symptoms findings prompting referral to a specialist identification of the patient with LOPS
positive (e.g., burning or shooting or specialty clinic. Focal or global skin can easily be carried out without this or
pain, electrical or sharp sensations, temperature differences between one foot other expensive equipment.
etc.) and the other may be predictive of either 10-g monofilaments. Monofilaments,
negative (e.g., numbness, feet feel vascular disease or ulceration and could sometimes known as Semmes-Weinstein
dead) also prompt referral for specialty foot care monofilaments, were originally used to
Vascular symptoms (10 13). diagnose sensory loss in leprosy (21).
claudication Musculoskeletal assessment. The mus- Many prospective studies have confirmed
rest pain culoskeletal assessment should include that loss of pressure sensation using the
nonhealing ulcer evaluation for any gross deformity (14). 10-g monofilament is highly predictive of
Other diabetes complications Rigid deformities are defined as any con- subsequent ulceration (3,21,22). Screen-
renal (dialysis, transplant) tractures that cannot easily be manually ing for sensory loss with the 10-g mono-
retinal (visual impairment) reduced and are most frequently found in filament is in widespread use across the
the digits. Common forefoot deformities world, and its efficacy in this regard has
that are known to increase plantar pres- been confirmed in a number of trials, in-
sures and are associated with skin break- cluding the recent Seattle Diabetic Foot
down include metatarsal phalangeal joint Study (4,21,23,24).
Examples of inappropriate shoes include hyperextension with interphalangeal flex- Nylon monofilaments are con-
those that are excessively worn or are too ion (claw toe) or distal phalangeal exten- structed to buckle when a 10-g force is
small for the persons feet (too narrow, too sion (hammer toe) (1517). (Examples of applied; loss of the ability to detect this
short, toe box too low), resulting in rub- these deformities are shown in Fig. 1.) pressure at one or more anatomic sites on
bing, erythema, blister, or callus. Features An important and often overlooked the plantar surface of the foot has been
that should be assessed during foot in- or misdiagnosed condition is Charcot ar- associated with loss of large-fiber nerve
spection are outlined in Table 3 and are thropathy. This occurs in the neuropathic function. It is recommended that four
discussed below. foot and most often affects the midfoot. sites (1st, 3rd, and 5th metatarsal heads
This may present as a unilateral red, hot, and plantar surface of distal hallux) be
swollen, flat foot with profound defor- tested on each foot.
Table 3Key components of the diabetic foot mity (18 20). A patient with suspected The technique for testing pressure
exam Charcot arthropathy should be immedi- perception with the 10-g monofilament is
ately referred to a specialist for further illustrated in Fig. 2; patients should close
Inspection assessment and care. their eyes while being tested. Caution is
Dermatologic necessary when selecting the brand of
skin status: color, thickness, dryness, monofilament to use, as many commer-
cracking Neurological assessment cially available monofilaments have been
sweating Peripheral neuropathy is the most com- shown to be inaccurate. Single-use dis-
infection: check between toes for mon component cause in the pathway to posable monofilaments or those shown to
fungal infection diabetic foot ulceration (1,4,5,7). The be accurate by the Booth and Young (23)
ulceration clinical exam recommended, however, is study are recommended. The sensation of
calluses/blistering: hemorrhage into designed to identify loss of protective sen- pressure using the buckling 10-g mono-
callus? sation (LOPS) rather than early neuropa- filament should first be demonstrated to
Musculoskeletal thy. The diagnosis and management of the patient on a proximal site (e.g., upper
deformity, e.g., claw toes, prominent the latter were covered in a 2004 ADA arm). The sites of the foot may then be
metatarsal heads, Charcot joint (Fig. 1) technical review (7). The clinical exami- examined by asking the patient to re-
muscle wasting (guttering between nation to identify LOPS is simple and re- spond yes or no when asked whether
metatarsals) quires no expensive equipment. the monofilament is being applied to the
Neurological assessment Five simple clinical tests (Table 3), particular site; the patient should recog-
10-g monofilament 1 of the following 4 each with evidence from well-conducted nize the perception of pressure as well as
vibration using 128-Hz tuning fork prospective clinical cohort studies, are identify the correct site. Areas of callus
pinprick sensation considered useful in the diagnosis of should always be avoided when testing
ankle reflexes LOPS in the diabetic foot (17). The task for pressure perception.
VPT force agrees that any of the five tests listed 128-Hz tuning forks. The tuning fork is
Vascular assessment could be used by clinicians to identify widely used in clinical practice and pro-
foot pulses LOPS, although ideally two of these vides an easy and inexpensive test of vi-
ABI, if indicated should be regularly performed during the bratory sensation. Vibratory sensation

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Figure 1Foot deformities. These sites are frequent locations for diabetic foot ulceration. A: Claw toe deformity. Note the buckling phenomenon that
causes increased pressure on the dorsal hammer digit deformity, as well as on the plantar metatarsal head. B: Bunion and overlapping toes. This
deformity can lead to pressure ulceration between the digits, on the dorsal or plantar surfaces of displaced digits, and over the medial first
metatarsophalangeal joint. C: A rocker-bottom deformity secondary to Charcot arthropathy can cause excessive pressure at the plantar midfoot,
increasing risk for ulceration at that site.

should be tested over the tip of the great form the skin. Inability to perceive pin- pull, with the ankle reflexes then retested
toe bilaterally. An abnormal response can prick over either hallux would be with reinforcement. Total absence of an-
be defined as when the patient loses vi- regarded as an abnormal test result. kle reflex either at rest or upon reinforce-
bratory sensation and the examiner still Ankle reflexes. Absence of ankle re- ment is regarded as an abnormal result.
perceives it while holding the fork on the flexes has also been associated with in- Vibration perception threshold testing.
tip of the toe (3,4). creased risk of foot ulceration (4). Ankle The biothesiometer (or neurothesiom-
Pinprick sensation. Similarly, the in- reflexes can be tested with the patient ei- eter) is a simple handheld device that
ability of a subject to perceive pinprick ther kneeling or resting on a couch/table. gives semiquantitative assessment of vi-
sensation has been associated with an in- The Achilles tendon should be stretched bration perception threshold (VPT). As
creased risk of ulceration (4). A dispos- until the ankle is in a neutral position be- for vibration using the 128-Hz tuning
able pin should be applied just proximal fore striking it with the tendon hammer. If fork, vibration perception using the
to the toenail on the dorsal surface of the a response is initially absent, the patient biothesiometer is also tested over the pulp
hallux, with just enough pressure to de- can be asked to hook fingers together and of the hallux. With the patient lying su-

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Comprehensive foot examination and risk assessment

Figure 2Upper panel: For performance of the 10-g monofilament test, the device is placed perpendicular to the skin, with pressure applied until
the monofilament buckles. It should be held in place for 1 s and then released. Lower panel: The monofilament test should be performed at the
highlighted sites while the patients eyes are closed.

pine, the stylus of the instrument is placed extremity risk status. Vascular examina- ankle systolic pressure by the higher of
over the dorsal hallux and the amplitude tion should include palpation of the the two brachial systolic pressures (8). An
is increased until the patient can detect posterior tibial and dorsalis pedis pulses ABI 0.9 is normal, 0.8 is associated
the vibration; the resulting number is (10,26), which should be characterized as with claudication, and 0.4 is commonly
known as the VPT. This process should either present or absent (26). associated with ischemic rest pain and
initially be demonstrated on a proximal Diabetic patients with signs or symp- tissue necrosis.
site, and then the mean of three readings toms of vascular disease (Table 2) or ab- The ADA Consensus Panel on PAD
is taken over each hallux. A VPT 25 V is sent pulses on screening foot examination recommended measurement of ABI in di-
regarded as abnormal and has been should undergo ankle brachial pressure abetic patients over 50 years of age and
shown to be strongly predictive of subse- index (ABI) pressure testing and be con- consideration of ABI measurement in
quent foot ulceration (15,22). sidered for a possible referral to a vascular younger patients with multiple PAD risk
specialist. The ABI is a simple and easily factors, repeating normal tests every 5
Vascular assessment reproducible method of diagnosing vas- years (8). ABI may therefore be part of the
Peripheral arterial disease (PAD) is a com- cular insufficiency in the lower limbs. annual comprehensive foot exam in these
ponent cause in approximately one-third Blood pressure at the ankle (dorsalis pedis patient subgroups. ABI measurements
of foot ulcers and is often a significant risk or posterior tibial arteries) is measured may be misleading in diabetes because the
factor associated with recurrent wounds using a standard Doppler ultrasonic presence of medial calcinosis renders the
(5,25). Therefore, the assessment of PAD probe. This technique is outlined in Fig. arteries incompressible and results in
is important in defining overall lower- 3. The ABI is obtained by dividing the falsely elevated or supra-systolic ankle

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Figure 3Lower-extremity circulation and the ABI test. A: Anterior view, right lower limb, normal arterial anatomy. B: ABI. Place blood pressure
cuff above pulse. Place Doppler probe over arterial pulse; a: posterior tibial artery, b: dorsalis pedis artery. ABI calculation: Divide ankle systolic
blood pressure by brachial artery systolic blood pressure. (ABI 0.9 is normal.) Adapted from Khan et al., JAMA 295:536 546, 2006.

pressures. In the presence of incompress- sociated with an increased risk for CONCLUSIONS It cannot be over-
ible calf or ankle arteries (ABI 1.3), ulceration, hospitalization, and amputa- stated that the complications of the dia-
measurements of digital arterial systolic tion (17). Patients in risk category 0 gen- betic foot are common, complex, and
pressure (toe pressure) or transcutaneous erally do not need referral and should costly, mandating aggressive and proac-
oxygen tension may be performed. receive general foot care education and tive preventative assessments by general-
undergo comprehensive foot examina- ists and specialists. All patients with
Risk classification and referral/ diabetes must have their feet evaluated at
follow-up tion annually. Patients in foot risk cate-
least at yearly intervals for the presence of
Once the patient has been thoroughly as- gory 1 may be managed by a generalist or
the predisposing factors for ulceration
sessed as described above, he or she specialist every 3 6 months. Consider- and amputation (neuropathy, vascular
should be assigned to a foot risk category ation should be given to an initial special- disease, and deformities). This report
(Table 4). These categories are designed ist referral to assess the need for summarizes a simple protocol for doing
to direct referral and subsequent therapy specialized treatment and follow-up. so. If abnormalities are present, more fre-
by the specialty clinician or team (17,20) Those in categories 2 and 3 should be re- quent evaluation of the diabetic foot is
and frequency of follow-up by the gener- ferred to a foot care specialist or specialty recommended depending on risk cate-
alist or specialist. Increased category is as- clinic and seen every 13 months. gory, as described above and in Table 4.

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Comprehensive foot examination and risk assessment

Table 4Risk classification based on the comprehensive foot examination

Risk category Definition Treatment recommendations Suggested follow-up


0 No LOPS, no PAD, no deformity Patient education including advice on Annually (by generalist and/or specialist)
appropriate footwear.
1 LOPS deformity Consider prescriptive or Every 36 months (by generalist or
accommodative footwear. specialist)
Consider prophylactic surgery if
deformity is not able to be safely
accommodated in shoes. Continue
patient education.
2 PAD LOPS Consider prescriptive or Every 23 months (by specialist)
accommodative footwear.
Consider vascular consultation for
combined follow-up.
3 History of ulcer or amputation Same as category 1. Every 12 months (by specialist)
Consider vascular consultation for
combined follow-up if PAD present.

It is through systematic examination tive foot care in people with diabetes. Di- monitoring as a self-assessment tool. Dia-
and risk assessment, patient education, abetes Care 26 (Suppl. 1):S78 S79, 2003 betes Care 30:14 20, 2007
and timely referral that we may further 3. Singh N, Armstrong DG, Lipsky BA: Pre- 12. Armstrong DG, Holtz-Neiderer K, Wen-
reduce the unnecessarily high preva- venting foot ulcers in patients with diabe- del CS, Mohler MJ, Kimbriel HR, Lavery
tes. JAMA 293:217228, 2005 LA: Skin temperature monitoring reduces
lence of lower-extremity morbidity in this
4. Abbott CA, Carrington AL, Ashe H, Bath the risk for diabetic foot ulceration in
population. S, Every LC, Griffiths J, Hann AW, Hus- high-risk patients. Am J Med 120:1042
sain A, Jackson N, Johnson KE, Ryder CH, 1046, 2007
Acknowledgments The meeting of the Torkington R, Van Ross ER, Whalley AM, 13. Lavery LA, Higgins KR, Lanctot DR, Con-
Task Force was supported by an unrestricted Widdows P, Williamson S, Boulton AJ: stantinides GP, Zamorano RG, Armstrong
educational grant from KCI, San Antonio, TX. The North-West Diabetes Foot Care DG, Athanasiou KA, Agrawal CM: Home
A.J.M.B. has received honoraria/consulting Study: incidence of, and risk factors for, monitoring of foot skin temperatures to
fees from Pfizer and Eli Lilly. R.G.F. has served new diabetic foot ulceration in a commu- prevent ulceration. Diabetes Care 27:
on the speakers bureaus of KCI, Oculus, nity-based patient cohort. Diabet Med 19: 26422647, 2004
Pfizer, and Organogenesis and has received re- 377384, 2002 14. Frykberg RG, Zgonis T, Armstrong DG,
search support from Regenesis Biomedical and 5. Reiber GE, Vileikyte L, Boyko EJ, del Driver VR, Giurini JM, Kravitz SR, Lands-
Derma Sciences. L.A.L. is a stockholder and on Aguila M, Smith DG, Lavery LA, Boulton man AS, Lavery LA, Moore JC, Schuberth
the board of directors of Diabetica Solutions AJ: Causal pathways for incident lower- JM, Wukich DK, Andersen C, Vanore JV:
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