COMPARISON OF CLINICAL EXAMINATION, CURRENT AND VIBRATORY PERCEPTION THRESHOLD IN DIABETIC POLYNEUROPATHY

Citation
Cjj. Tack et al., COMPARISON OF CLINICAL EXAMINATION, CURRENT AND VIBRATORY PERCEPTION THRESHOLD IN DIABETIC POLYNEUROPATHY, Netherlands journal of medicine, 44(2), 1994, pp. 41-49
Citations number
32
Categorie Soggetti
Medicine, General & Internal
ISSN journal
03002977
Volume
44
Issue
2
Year of publication
1994
Pages
41 - 49
Database
ISI
SICI code
0300-2977(1994)44:2<41:COCECA>2.0.ZU;2-4
Abstract
The study of diabetic polyneuropathy is complicated by a lack of clear definitions and the absence of a simple reliable test procedure. Rece ntly, a new sensory perception testing device has been introduced for detection of thresholds for electrical stimuli (current perception: CP T) at different frequencies (Neurometer(R)). We compared standardized clinical examination scores with measurements of vibratory perception threshold (VPT) and CPT (foot) and obtained reproducibility figures. P articipants in the study were healthy controls (H, n = 33), diabetic p atients without clinical signs of neuropathy (DN - , n = 23), diabetic s with overt diabetic neuropathy (DN + , n = 22), and patients with a diabetes duration of over 20 years (D20, n = 38). As expected, there w ere highly significant differences (Wilcoxon) in CPT, VPT and neurolog ical scores between H/DN - and DN + (p < 0.001), but not between H and DN - . Correlation between CPT and total as well as partial (reflecti ng small and large fibre functions) neurological examination score wer e highest at 2000 Hz (r = 0.88); no advantage of lower frequency CPT c ould be identified. CPT seemed rather insensitive in detecting neuropa thy. Correlations between CPT and VPT were only moderate and maximal a t 2000 Hz (r = 0.61). Reproducibility of CPT was good at 2000 Hz (coef ficient of variation 13.3-20.2%), but moderate to poor at lower freque ncies (ranging to 62%). We conclude that CPT and VPT quantitative sens ory testing is only of limited value, mainly because of high variabili ty and poor reproducibility.