and Mario Di Napoli1
(1)
Neurological Service, S. Camillo de’ Lellis General Hospital, Rieti, Italy
Original Settings
Sensitivity was 500 μV/division, low-frequency filter was 3 Hz, high-frequency filter was 10 kHz, sweep speed was 2 ms/division, and the machine used was a 2-channel Medelec Synergy EMG machine. Duration of pulse was not specified.
Position
This study was performed in the supine position.
Recording
Using the technique [1] by Preston and Logigian [2], the authors placed the active electrode (A) slightly lateral to the midpoint of the third metacarpal space, over the belly (motor point) of both the second lumbrical (2L) and interossei (INT) muscles (Fig. 1). The reference (R) was placed over a bony prominence of the proximal interphalangeal joint of digit II. The motor point to the 2L was identified by an initial negative deflection with the fastest rise time. Surface recording was made with monopolar recording electrodes. The ground (G) electrode position was not mentioned in the text; it could be placed on the palm or on the dorsum of the hand. The figure shows the ground positioned on the palm.


Fig. 1
Sensory nerve action potential (SNAP) recorded at the hand from the second lumbrical (2L) muscle, stimulation of the wrist
Stimulation
The stimulation was at the wrist on the median nerve at a 10 cm fixed distance, and a bipolar handheld surface stimulator was used to obtain the sensory nerve action potentials (SNAPs).
Measurements
Peak latency (ms) of the premotor potential from the 2L muscle (PMP–2L) was measured from the stimulus onset to the peak of the negative deflection of the SNAP. Amplitude (μV) of the PMP–2L potential was measured, but the authors did not specify if onset to peak or peak-to-peak amplitude was reported. Since test sensitivity is highest [3] when a parameter most likely to be affected by the carpal tunnel syndrome (CTS) – as the sensory median nerve conduction in the digit III–wrist segment – is compared to one least likely to be affected, as the motor ulnar conduction to the abductor digiti minimi (ADM) muscle, the authors measured the latency difference between the sensory PMP–2L potential and the motor INT potential. The authors also measured the median–ulnar 2L–INT latency difference (ms). All tests were performed in a quiet air-conditioned room (22–24 °C), and palmar skin temperature was measured and maintained above 32 °C. The authors studied 50 control hands (Table 1) of 27 healthy subjects (16 women, 59 %; age range 30–54 years, mean 41 years) and 52 hands (Table 2) from 33 patients with a clinical diagnosis of CTS (21 women, 64 %; age range 34–65 years, mean 49 years).
Amplitude | Mean ± SD |
---|---|
Wrist–2L (μV) | 88.1 ± 36.4 |
INT–PMP–2L latency difference | Mean ± SD | Limit of normal |
---|---|---|
Wrist–2L (ms) | 0.91 ± 0.27 | ≥0.5 |
Amplitude | Mean ± SD |
---|---|
Wrist–2L (μV) | 57.4 ± 43.3 |
Peak latency | Mean ± SD | Limit of normal |
---|---|---|
Wrist–2L (ms) | 2.99 ± 0.55 | ≤2.7 |
INT–PMP–2L latency difference | Mean ± SD | Limit of normal |
---|---|---|
Wrist–2L (ms) | 0.14 ± 0.67 | ≥0.5 |
2L–INT latency difference | Mean ± SD | Limit of normal |
---|---|---|
Wrist–2L (ms) | 1.4 ± 1.3 | >0.6 |
Comment
Therimadasamy et al. [1] investigated the premotor potential from the median–motor conduction studies, especially from the thenar muscles like others [4–6]. In normal subjects using the Preston and Logigian’s [2] method (Fig. 2), they observed a small negative potential (usually in the range of 10–80 µV) to precede the median 2L CMAP.


Fig. 2
Compound muscle action potentials (CMAPs) recorded at the hand from the second lumbrical (2L) and interossei (INT) muscles, 2L recording – a little deflection can be observed just before the motor potential (upper trace) and INT recording (lower trace), stimulation at the wrist
Hasegawa et al. [7] suggested that the premotor potential from the 2L muscle (PMP–2L) might represent potentials arising from the antidromically activated digital sensory branches. As a result of this, Therimadasamy et al. [1] investigated the further advantage to the 2L–INT recording technique, which can simultaneously provide information concerning both motor–and sensory–median nerve fibers that have crossed the carpal tunnel, as well as from the ulnar–motor fibers. They compared the PMP-2L potential (which they called “2-LUMP”) with other standard nerve conduction techniques, such as sensory orthodromic nerve conduction to the wrist stimulating digit III (middle finger) and conventional motor conduction technique to the abductor pollicis brevis (APB) muscle. They concluded that in the CTS, the use of PMP–2L and other 2L–INT-associated parameters could replace the recording of a conventional median–sensory conduction to the digits and motor studies of the median and ulnar nerves. The authors found some limitations of PMP–2L in CTS complicated by additional ulnar neuropathy or polyneuropathy because the study was designed to test the practicability of the PMP–2L in healthy subjects and those with uncomplicated carpal tunnel.
Patients affected by CTS were electrodiagnostically graded with the standard scale of Bland [8]: normal (grade 0), very mild (grade 1: abnormal 2L–INT DIFF test only, i.e., >0.6 ms), mild (grade 2: abnormal sensory orthodromic median nerve conduction, i.e., <40 m/s), moderate (grade 3: abnormal sensory orthodromic potential but preserved and prolonged distal CMAP latency to the abductor pollicis brevis muscle, i.e., >3.9 ms and <6.5 ms), severe (grade 4: sensory orthodromic potential absent and prolonged distal CMAP latency to the abductor pollicis brevis muscle, i.e., >3.9 ms and <6.5 ms), very severe (grade 5: sensory orthodromic potential absent and prolonged distal CMAP latency to the abductor pollicis brevis muscle, i.e., >6.5 ms), and extremely severe (grade 6: sensory and motor potentials both absent and unrecordable). The authors developed a scale for the PMP–2L potential, similar to that of Bland [9] as follows: normal (grade 0), very mild (grade 1: abnormal ulnar interossei motor to the PMP–2L sensory latency comparison only, i.e., ≥0.5 ms), mild (grade 2: abnormal premotor potential latency, i.e., >2.7 ms, or motor 2L–INT latency difference >0.8 ms), moderate (grade 3: abnormal PMP–2L latency >3.2 ms or 2L–INT latency difference >2.5 ms), severe (grade 4: absent sensory PMP–2L potential or 2L–INT latency difference >2.5 ms), very severe (grade 5: absent sensory PMP–2L potential or 2L–INT latency difference >4.0 ms), and extremely severe (grade 6: sensory and motor potentials both absent and unrecordable). They examined whether motor and sensory data obtained with a 2L–INT recording could reduce the number of tests used to support a diagnosis of CTS by comparing data derived from the 2L–INT recording with data from the recording techniques commonly used for the electrodiagnosis of CTS. Sensitivity was calculated as the proportion of people with CTS having a positive test result, and specificity was the proportion of healthy people having a negative test result. The authors found the ulnar interossei motor to the PMP–2L sensory latency comparison to have the highest sensitivity (79 %) and specificity (94 %), the PMP–2L sensory peak latency to have high sensitivity (77 %) and specificity (94 %), and the 2L–INT LAT difference to have high sensitivity (75 %) and specificity (94 %).

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