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Scientific Articles   |    
4.5-Gram Monofilament Sensation Beneath Both First Metatarsal Heads Indicates Protective Foot Sensation in Diabetic Patients
Charles L. Saltzman, MD1; Rola Rashid, MD1; Andrea Hayes1; Chris Fellner, BA1; Denise Fitzpatrick, RN1; Aimee Klapach, MD1; Rita Frantz, PhD1; Stephen L. Hillis, PhD1
1 Department of Orthopaedic Surgery, University of Iowa, UIHC, 200 Hawkins Drive, Iowa City, IA 52246. E-mail address for C.L. Saltzman: charles-saltzman@uiowa.edu
The Journal of Bone & Joint Surgery.  2004; 86:717-723 
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Abstract

Background: Loss of protective plantar foot sensation is the major cause of diabetic foot ulcerations and ultimate limb loss. Identification of patients without protective sensation can reduce the risk of unrecognized foot injury. The current recommended screening protocol requires 10-g monofilament testing of ten foot sites with use of a forced-choice paradigm. The objective of the present study was to determine whether testing of fewer than ten sites could provide accuracy comparable with that obtained by testing all ten sites.

Methods: A cross-sectional comparative study of plantar sensory levels in diabetic subjects with and without plantar ulceration was conducted in a tertiary-care teaching hospital setting. We examined forty-seven diabetic subjects with a history of foot ulceration and forty-five diabetic subjects with no history of foot ulceration. Plantar sensory threshold values at five sites on the sole of each foot were measured with a quasi-continuous range of applied forces, and receiver operating characteristic analysis techniques were applied.

Results: Screening on the basis of only the maximum force threshold for the left and right first metatarsal head sites provided comparable or better performance at high levels of sensitivity than did either the mean or the maximum force threshold across all ten sites. A sensory threshold of 4.5 g for both the left and right first metatarsal head sites predicted the risk of ulceration with a sensitivity of 100% and a specificity of 67%.

Conclusions: Testing of diabetic patients for protective sensation may be simplified to testing under both first metatarsal heads with a 4.5-g monofilament. If a patient cannot sense the application of a 4.5-g monofilament under either first metatarsal head, he or she probably has lost protective sensation and should be considered to be at risk for undetected injury.

Level of Evidence: Diagnostic study, Level II-1 (development of diagnostic criteria on the basis of consecutive patients [with universally applied reference "gold" standard]). See Instructions to Authors for a complete description of levels of evidence.

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    These activities have been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint sponsorship of the American Academy of Orthopaedic Surgeons and The Journal of Bone and Joint Surgery, Inc. The American Academy of Orthopaedic Surgeons is accredited by the ACCME to provide continuing medical education for physicians.
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    Govind N. Malaviya, MS, FICS, DHRM
    Posted on July 14, 2004
    Threshold of Protective Sensation in Diabetic Patients
    Head, Reconstructive Surgery Unit, Central Jalma Institute for Leprosy, Tajganj Agra-282001, INDIA

    To the Editor,

    The article by Saltzman et.al.(1),argues for a redefinition of the cut off levels of monofilament nylon sensory thresholds in the diabetic foot. We have reported similar observations in patients with leprosy wherein we defined the levels of protective sensation as double the normal sensory thresholds ( 4.7 gms compared to a normal threshold of 2.35 gms. as revealed by 20 filament set supplied by North coast medical and Inc. California USA). (2)

    We tested 3 sites in each foot of 57 normal controls: first metatarsal head: fifth metatarsal head: and center of heel. These areas are innervated by three branches of the posterior tibial nerve which can be affected in different combinations in leprosy. We also examined 40 patients with leprosy who had sensory impairments of varying degrees with and without ulcers. We concluded that all patients who did not have normal sensation were at risk to develop ulcers. Also, if their thresholds were double the normal value, the risk increased many fold. (3)

    I agree with the authors that there can be "over detection" and the un-necessary inclusion of some patients in the ulcer risk group. However, this may prove beneficial to these patients because health education and proper self-care practices will be imparted to them.

    The authors have correctly observed that Birke and Sims made their observations (4) with only 3 nylons and 4.5 gms. Ten grams makes a big difference. Hammond and Klenerman (5) using a 20 nylon set noted these levels to be 11.8 gms., but several of their patients had foot ulcers.

    The first metatarsal area of the sole has been found to have lower thresholds than other areas of foot. In diabetic neuropathy, presumed to be uniformly diffuse, sensory testing at one site might be "adequate" but we prefer testing at three sites until it is established with certainty that selective involvement of branches of posterior tibial nerve does not occur.

    References:

    1. Saltzman CL, Rashid R, Hayes A, Fellner C, Fitzpatrick D, Klapach A, Frantz R and Hillis SL. 4.5 Gram monofilament sensation beneath both first metatarsal heads indicates protective foot sensation in diabetic patients. J Bone Joint Surg. 86-A: 717-723,2004

    2.Malaviya GN, Husain S, Girdhar A, Girdhar BK. Sensory functions in limbs of normal persons and leprosy patients with peripheral trunk damage. Indian J Leprosy 66: 157-164,1994.

    3. Malaviya GN, Husain S, Mishra B, Girdhar A, Girdhar BK. Protective Sensibility - Its monofilament threshold equivalents in leprosy patients. Indian J Leprosy 69: 149-158,1997.

    4. Birke JA and Sims DS. Plantar sensory threshold in the ulcerative foot. Lepr. Rev. 57:261-267,1986.

    5. Hammond CJ and Klenerman P. Protective sensation in the foot in leprosy. Lepr. Rev. 59:347-354,1988.

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