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* Peak sensory latency, sensory nerve action potential amplitude (SNAP).
Median nerve peak sensory latency > 3.5 ms (stimulated at wrist at distance from active electrode = 13 cm).
Objectives: To establish the average distal sensory latency and amplitude of the dorsal ulnar cutaneous nerve under controlled temperature and settings.
Results: Significant decreases in MPQ score, median nerve sensory latency, and Phalen and Tinel signs after the real treatment series but not after the sham treatment series.
The following parameters were measured: * Distal latency (DL), compound motor action potential (CMAP) amplitude, and conduction velocity (CV) of motor and sensory nerves * Peak sensory latency, sensory nerve action potential amplitude (SNAP) * F-wave (latency and persistence).
Measurements were performed before and after treatment and at follow up four weeks later, and included pain assessment by visual analogue scale; electroneurographic measurement (motor and sensory latency, motor and sensory action potential amplitude); and pinch and grip strength.
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Results: Results showed that distal sensory latencies were normally distributed.
Moderate CTS is abnormal median sensory latencies as noted for mild CTS plus prolongation of median motor distal latency (> 4.4 ms), with no evidence of axon loss.
Also, an inverse correlation was seen between vitamin D levels and peak sensory latencies but it did not reach a significant level (p = 0.24) (Table 4).
The average distal sensory latencies at 8cm and 10cm were 1.84 ±.20msec and 2.09 ±.21msec, respectively, with average amplitudes of 26.5 ± 9.7μV and 23.5 ± 8.8μV.
Main Outcome Measures: H-reflex latencies of the tibial nerve and nerve conduction studies (median motor and sensory, peroneal motor, sural sensory latencies) of the upper and lower extremity of each patient.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com