Objective: To evaluate the mixed nerve action potential of the medial and lateral plantar nerve conduction studies in diabetic patients with the various factors.
Method: 69 healthy adults without foot trauma as control group and 78 diabetic patients without foot trauma as subject group were studied. The study was performed by using the orthodromic surface stimulation and recording method of evaluating of the mixed nerve action potential of the medial and lateral plantar nerve conduction studies.
Results: The differences in the distal latency (p<0.05), amplitude (p<0.05) and nerve conduction velocity (p<0.05) of the mixed nerve action potential of the medial and lateral plantar nerve conduction studies were statistically significant between the diabetic group and the normal control group. Same results also could be obtained in diabetic patients relating to longer duration of diabetes, presence of diabetic retinopathy, higher blood glucose level, longer duration of oral hypoglycemic agent and insulin treatment (p<0.05).
Conclusion: The mixed nerve action potential of the medial and lateral plantar nerve conduction studies are useful for the detection of diabetic neuropathic foot.
Objective: Tarsal tunnel syndrome (TTS) is relatively rare and can be difficult to diagnose with conventional electrodiagnostic techniques. To increase the diagnostic sensitivity, we measured transtarsal conduction velocities of medial and lateral plantar nerves recorded by orthodromic near-nerve recording.
Method: Twenty normal subjects (aged 24∼59) were studied. For below flexor retinaculum (BFR) recordings, near-nerve needle recording electrodes were positioned posteriorly to the flexor digitorum longus tendon in medial plantar nerve and anteriorly to the calcaneus in lateral plantar nerve at the level of lower border of medial malleolus. For above flexor retinaculum (AFR) recordings, near-nerve needle recording electrodes were positioned anteriorly to the Achilles tendon 4 cm proximal to the BFR recording electrodes in medial and lateral plantar nerves. Stimulating ring electrodes were placed to the digit I and V.
Results: Transtarsal latencies and conduction velocities for medial plantar nerve were 0.7⁑0.1 msec, 56⁑6 m/sec, respectively. Transtarsal latencies and conduction velocities for lateral plantar nerve were 0.8⁑0.1 msec, 54⁑6 m/sec, respectively.
Conclusion: This approach may improve the diagnostic sensitivity in TTS.
Objective: To determine the reference values for the diagnosis of isolated entrapment neuropathies of medial and lateral plantar nerve and inferior calcaneal nerve distal to the tarsal tunnel.
Method: The subjects were neurologically healthy 30 adults (15 males, 15 females). Distal motor nerve conduction study of medial and lateral plantar nerves and inferior calcaneal nerve was performed. The recording muscles for medial and lateral plantar nerves and inferior calcaneal nerve were flexor hallucis brevis, flexor digiti minimi brevis, and abductor digiti minimi pedis, respectively. The stimulation was done at distal and proximal to the tarsal tunnel to differentiate the tarsal tunnel syndrome and the entrapment neuropathy of distal to the tarsal tunnel. The distance of recording and distal stimulation site was fixed to 10 cm for medial and lateral plantar nerves. The skin temperature was maintained 33oC or above. The proximal latency, distal latency, peak to peak amplitude, conduction velocity and residual latency were measured. The reference values were obtained by 95 percentile values.
Results: The reference values for the diagnosis of isolated entrapment neuropathies of medial plantar nerve, lateral plantar nerve and inferior calcaneal nerve distal to tarsal tunnel are as follows.
1) Medial plantar nerve: distal latency, > 4.3 msec; side to side difference, > 0.7 msec
2) Lateral plantar nerve: distal latency, > 4.1 msec; side to side difference, > 0.6 msec
3) Latency difference of medial and lateral plantar nerve: > 0.7 msec
4) Inferior calcaneal nerve: distal latency, > 4.3 msec; distal peak latency, > 7.2 msec; side to side difference of distal onset latency, > 1.5 msec; side to side difference of distal peak latency, > 0.8 msec; residual latency, > 3.0 msec
Conclusion: The distal motor nerve conduction method used in this study and the reference values could be used to differentiate entrapment neuropathies of medial and lateral plantar nerve and inferior calcaneal nerve distal to the tarsal tunnel from tarsal tunnel syndrome.