Hardness of Plantar Skin in Diabetic Neuropathic Feet

To evaluate if skin hardness in diabetic neuropathic feet was increased and if its eventual modifications could be correlated to the severity of neuropathy, we studied a group of diabetic outpatients with and without neuropathy. Patients, selected among those who were attending their routine screeni...

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Veröffentlicht in:Journal of diabetes and its complications 1999-05, Vol.13 (3), p.129-134
Hauptverfasser: Piaggesi, Alberto, Romanelli, Marco, Schipani, Elena, Campi, Fabrizio, Magliaro, Antonio, Baccetti, Fabio, Navalesi, Renzo
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container_end_page 134
container_issue 3
container_start_page 129
container_title Journal of diabetes and its complications
container_volume 13
creator Piaggesi, Alberto
Romanelli, Marco
Schipani, Elena
Campi, Fabrizio
Magliaro, Antonio
Baccetti, Fabio
Navalesi, Renzo
description To evaluate if skin hardness in diabetic neuropathic feet was increased and if its eventual modifications could be correlated to the severity of neuropathy, we studied a group of diabetic outpatients with and without neuropathy. Patients, selected among those who were attending their routine screening for diabetic neuropathy at our diabetologic clinic, were divided into two groups according to the presence (ND+) or absence (ND−) of diabetic neuropathy with the criteria of the S. Antonio Consensus Conference on Diabetic Neuropathy. Patients then underwent an evaluation of vibration perception threshold (VPT) by means of a biotesiometer, measurement of skin hardness (DMT) by means of a durometer, and transcutaneous oxygen tension (TcPO2) determination. VPT was determined at allux (VPT-A) and external malleolus (VPT-M), DMT was measured at heel (DMT-H), at medial (DMT-M) and lateral (DMT-L) midfoot, and at posterior midcalf (DTM-C) as a control site; TcPO2 was evaluated at dorsum (TcPO2-D) and at medial midfoot (TcPO2-M), respectively. All measurements were performed on the nondominant side with the patients supine. Patients were compared with age and gender-matched healthy volunteers (Controls), who underwent the same evaluations in the same order. ND+ patients showed higher values of VPT than ND− and Controls, both at first toe and at malleolus analysis of variance (ANOVA) p < 0.01), as well of DMT in all the three sites explored (ANOVA, p < 0.01). Moreover, ND+ showed no difference in DMT among the sites, while both in ND− and in controls DMT-M was significantly (p < 0.05) lower than DMT-H and DMT-L. No difference among the three groups were observed in TcPO2 measurements, and no difference in DMT-C was observed either. A significant correlation was observed between DMT-H and VPT-M (r2 = 0.516) and between DMT-M and VPT-A (r2 = 0.624) in ND+ patients. Skin hardness was diffusely increased in ND+ patients, and this increase strongly correlates with the severity of neuropathy. Simple, noninvasive determination of skin hardness could identify patient at potential risk to develop neuropathic foot ulcers.
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Patients, selected among those who were attending their routine screening for diabetic neuropathy at our diabetologic clinic, were divided into two groups according to the presence (ND+) or absence (ND−) of diabetic neuropathy with the criteria of the S. Antonio Consensus Conference on Diabetic Neuropathy. Patients then underwent an evaluation of vibration perception threshold (VPT) by means of a biotesiometer, measurement of skin hardness (DMT) by means of a durometer, and transcutaneous oxygen tension (TcPO2) determination. VPT was determined at allux (VPT-A) and external malleolus (VPT-M), DMT was measured at heel (DMT-H), at medial (DMT-M) and lateral (DMT-L) midfoot, and at posterior midcalf (DTM-C) as a control site; TcPO2 was evaluated at dorsum (TcPO2-D) and at medial midfoot (TcPO2-M), respectively. All measurements were performed on the nondominant side with the patients supine. Patients were compared with age and gender-matched healthy volunteers (Controls), who underwent the same evaluations in the same order. ND+ patients showed higher values of VPT than ND− and Controls, both at first toe and at malleolus analysis of variance (ANOVA) p &lt; 0.01), as well of DMT in all the three sites explored (ANOVA, p &lt; 0.01). Moreover, ND+ showed no difference in DMT among the sites, while both in ND− and in controls DMT-M was significantly (p &lt; 0.05) lower than DMT-H and DMT-L. No difference among the three groups were observed in TcPO2 measurements, and no difference in DMT-C was observed either. A significant correlation was observed between DMT-H and VPT-M (r2 = 0.516) and between DMT-M and VPT-A (r2 = 0.624) in ND+ patients. Skin hardness was diffusely increased in ND+ patients, and this increase strongly correlates with the severity of neuropathy. Simple, noninvasive determination of skin hardness could identify patient at potential risk to develop neuropathic foot ulcers.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>10509872</pmid><doi>10.1016/S1056-8727(98)00022-1</doi><tpages>6</tpages></addata></record>
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subjects Adult
Associated diseases and complications
Biological and medical sciences
Blood Gas Monitoring, Transcutaneous
Diabetes. Impaired glucose tolerance
Diabetic Foot - diagnosis
Diabetic Foot - physiopathology
Diabetic Neuropathies - physiopathology
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Female
Humans
Male
Medical sciences
Middle Aged
Perception
Skin - physiopathology
Vibration
title Hardness of Plantar Skin in Diabetic Neuropathic Feet
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