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Volume 88, Issue 4, Pages 477-480 (April 2007)


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Comparing Saphenous Nerve Conduction Study Techniques at the Knee and at the Ankle and Their Relationship to Body Mass Index

Anthony Chiodo, MDabCorresponding Author Informationemail address, Teresa Spiegelberg, BSc, Henry C. Tong, MD, MSab

Abstract 

Chiodo A, Spiegelberg T, Tong HC. Comparing saphenous nerve conduction study techniques at the knee and at the ankle and their relationship to body mass index.

Objective

To evaluate the saphenous sensory response by 2 methods and the correlation of obtaining responses bilaterally with body mass index (BMI).

Design

Twenty patients evaluated by 1 electromyographer and 10 patients evaluated by 2 blinded electromyographers.

Setting

University electromyography laboratory.

Participants

Thirty healthy adult volunteers.

Interventions

Saphenous sensory response with the recording electrode at the level of the medial malleolus, saphenous sensory response with the recording electrode at the level of the proximal tibia, and sural sensory response with the recording electrode posterior to the lateral malleolus.

Main Outcome Measures

Sensory-evoked amplitude and distal latency.

Results

The saphenous sensory response was obtained bilaterally at the knee in 77% of subjects, whereas it was obtained bilaterally at the ankle in only 50% of subjects (P<.05). BMI of greater than 25kg/m2 resulted in more difficulty in obtaining the saphenous sensory response at the ankle compared with the response at the knee (P<.05).

Conclusions

The saphenous sensory response at the knee is more consistently obtained than the saphenous sensory response at the ankle, and it is not affected by BMI.

Article Outline

Abstract

Methods

Statistical Analyses

Results

Discussion

Conclusions

References

Copyright

THE SAPHENOUS NERVE IS A terminal sensory nerve of the lumbar plexus. It provides sensory information through the posterior division of the third and fourth lumbar nerve root. It is the first of 6 terminal branches of the femoral nerve, arising medially after the nerve exits the femoral triangle. It descends beneath the sartorius muscle and then becomes superficial between it and the gracilis muscle. It passes down the medial side of the leg ending at the distal medial tibia, except for a branch that innervates the medial aspect of the foot.1 The saphenous sensory response is important in the evaluation of a saphenous mononeuropathy, which can occur iatrogenically after varicose vein surgery,2 knee surgery,3 knee arthroscopy,4 and vascular surgery.5 Saphenous mononeuropathy is also seen in association with pes anserine bursitis6 and vascular impingement.7 Examining this nerve also helps distinguish between L3-4 radiculopathies and lumbar plexus or femoral nerve injuries.8

Two methods have been described to evaluate the saphenous nerve. A study2 of 230 subjects performed by using a bar electrode at the medial ankle and stimulation 14cm proximally showed a mean distal latency of 3.8ms, peak latency of 4.4ms, and duration of 1.9ms. The peak-to-peak amplitude was 1μV, whereas the onset to peak amplitude was 2μV. The temperature was controlled at 32° to 37°C. The saphenous response was absent on the nondominant side (7%), on the dominant side (11%), and bilaterally (25%). Older, taller, and heavier subjects were more apt to have absent responses.2

Wainapel et al3 evaluated 40 subjects with a bar electrode placed lateral to the medial malleolus and medial to the anterior tibialis tendon with stimulation 14cm proximally. The responses were averaged with room temperature controlled at 22.8°C and without skin temperature controlled. The peak latency was 3.6±0.4ms and the amplitude was 9±.4μV, with 34% of responses less than 5μV. In general, the response showed an amplitude about one half that of the sural response.3

Izzo et al4 evaluated 80 patients with 1-cm disk electrodes placed 3cm apart lateral to the medial malleolus. Skin temperature was controlled to greater than 28°C. The average onset latency was 2.9±0.4ms, average peak latency was 3.5±0.4ms, and mean amplitude 5.4±2.5μV, with 13% absent responses.4

Kimura et al9 conducted a study that looked at 40 subjects with recording electrode lateral to the medial malleolus. Distal latency was 2.0±0.3ms at a distance of 10cm, with an amplitude of 10.7±4.3μV.9

A saphenous sensory response at the knee has also been described. In 28 subjects aged 20 to 56 years, a saphenous sensory response across the knee at a distance of 14cm was obtained with a mean amplitude 10.2μV, distal latency of 2.5ms, and a conduction velocity of 59m/s.10

Two methods of obtaining the saphenous nerve conduction study have been described. However, no study has compared these methods. The first purpose of this study was to compare the ability to obtain the saphenous nerve conduction response by using 2 previously reported techniques: recording an antidromic response at the knee and recording an antidromic response at the ankle. The second purpose was to determine if body mass index (BMI) affects the ability to obtain the saphenous sensory response.

Methods 

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Thirty healthy adult volunteers were recruited after institutional review board approval. Subjects were excluded if they had a history of peripheral neuropathy or diabetes mellitus. After informed consent was obtained, the lower limbs were warmed with hot packs. By using a surface thermometer on the electromyography machine, leg temperatures were confirmed to be 32° to 36°C at the lateral calf. The nerves were tested in the following order in 1 leg and then the other: antidromic sural response at the calf, antidromic saphenous response at the ankle, and antidromic saphenous response at the knee.

The antidromic sural sensory response (fig 1) was obtained by using a 3-cm bar electrode with the active recording electrode posterior to the lateral malleolus. The stimulus cathode was placed 14cm proximally at the posterolateral aspect of the calf.


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Fig 1. Sural sensory response.


The saphenous sensory response was obtained by using 2 techniques. The antidromic saphenous response at the ankle (fig 2) was obtained using a 3-cm bar electrode with the active electrode placed anterior to the medial malleolus just medial to the anterior tibialis tendon. The stimulus cathode was placed 14cm proximally along the medial tibia. The antidromic saphenous response at the knee (fig 3) was obtained with a 3-cm bar with the active electrode medial to the tibia about 14cm distal to the medial popliteal fossa. The stimulus cathode was placed 14cm proximally between the sartorius and gracilis muscles, where the saphenous nerve is superficial.


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Fig 2. Saphenous sensory response at the ankle.



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Fig 3. Saphenous sensory response at the knee.


Statistical Analyses 

Amplitude, onset latency, peak latency, and conduction velocity were recorded for each response. Responses that were unobtainable were listed as no response. The response was not listed as unobtainable until the subject could feel paresthesias in the distribution of the nerve to ensure correct stimulus placement. In addition, the recording electrode was moved 2 additional times to be sure that no signal could be obtained. Mean, standard deviations (SDs), and outer limits of normal were calculated for each response. For amplitude, which was not normally distributed because of the absent responses and the spread of amplitudes obtained as evidenced by the large SDs, we used a protocol similar to the one used by Buschbacher2 and used the actual 3% cutoff value. For onset latency, peak latency, and conduction velocity, which were more normally distributed, we used the mean and SD with a z score of 1.96 to determine the 97%, 97%, and 3% cutoff, respectively.

For side-to-side differences, the upper limit of normal was taken as the 97th percentile of percentage drop from 1 side to the other for amplitude. For duration and latency, the upper limit of normal was taken as the 97th percentile difference from the dominant to nondominant side. The lower limit of normal for amplitude and area was taken as the third percentile of observed values.

To determine if the percentage of subjects who had bilateral obtainable saphenous responses at the knee was different than the percentage of subjects who had bilateral obtainable saphenous responses at the ankle, we used a chi-square test. Knowing how often a response was present bilaterally was believed to be important because if a response is not commonly obtainable bilaterally in healthy subjects, then it would be hard to clinically interpret unilateral obtainable responses in symptomatic subjects.

Height and weight were patient reported. BMI was calculated by dividing body mass in kilograms by the square of the height in meters. To determine if BMI affected response rates, we first divided the subjects into the following 3 categories: obese (BMI ≥30kg/m2), overweight (BMI range, 25–30kg/m2), and normal or underweight (BMI <25kg/m2). We then used a chi-square test to determine if this was statistically significant.

Results 

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There were 30 subjects with a mean age of 35±8.4 years (range, 25–59y), of which 7 (23%) were women. Mean height was 1.8±1.5m, mean weight was 79.5±15.5kg, and mean BMI was 25.4±4.8kg/m2. No potential subjects met the exclusion criteria of a history of diabetes or peripheral neuropathy. Sural response was obtained bilaterally in all subjects tested.

The results of both saphenous nerve conduction techniques are shown in table 1. The saphenous response at the knee, in general, had a larger amplitude, shorter onset and peak latency, and faster conduction velocity. This is consistent with the fact that the more proximal nerve segments have more nerve axon fibers and have faster conduction velocities. As shown in table 2, the saphenous ankle response rate of 50% was significantly lower than the saphenous knee response rate of 77% (χ2 test=6.9, P=.03). As shown in table 3, the saphenous ankle response was affected by BMI, in which the response was less likely to be obtainable bilaterally in subjects who were overweight or obese (χ2 test=6.7, P=.03). In contrast, the saphenous knee response was not affected by BMI (χ2 test=1.2; BMI, .54kg/m2).

Table 1.

Saphenous Nerve Conduction Results

Study ParametersMean ± SDAbsolute CutoffSide-to-Side Difference (mean ± SD)Relative Cutoff
RightLeft
Saphenous ankle
Amplitude (μV)4.7±3.14.1±1.81.31.1±2.257%
Onset latency (ms)2.8±0.42.8±0.33.60.0±0.40.7
Peak latency (ms)3.5±0.43.5±0.44.30.1±0.40.8
Conduction velocity (m/s)51.3±9.250.1±5.833.20.7±9.018.3
Saphenous knee
Amplitude right (μV)5.9±3.06.1±2.52.40.1±2.574%
Onset latency right (ms)2.5±0.32.4±0.23.10.1±0.20.6
Peak latency right (ms)3.1±0.33.0±0.23.70.1±0.30.6
Conduction velocity right (m/s)57.8±7.558.4±5.742.00.9±6.713.9

Three percent lower limit of normal for amplitude and conduction velocity. Ninety-seven percent upper limit of normal cutoff for onset latency and peak latency.

Table 2.

Bilateral Obtainable Saphenous Ankle Response Versus Saphenous Knee Response

Nerve Conduction ResultSaphenous Ankle, n (%)Saphenous Knee, n (%)χ2 Test
Responses bilaterally15(50)23(77)6.9(P=.03)
Responses not present bilaterally15(50)7(23)
Table 3.

Bilateral Obtainable Saphenous Responses at Ankle and Knee by BMI

Nerve Conduction ResultSaphenous Ankle Response by BMI (kg/m2)Saphenous Knee Response by BMI (kg/m2)
BMI ≥30BMI 25–30BMI <25BMI ≥30BMI 25–30BMI <25
Response not present bilaterally465133
Responses bilaterally1(20%)2(25%)12(71%)4(80%)5(63%)14(82%)
χ2 test6.7(P=.03) 1.2(P=.54)

Discussion 

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The first purpose of this study was to compare the ability to obtain the saphenous nerve conduction response by using 2 previously reported techniques: recording an antidromic response at the knee and recording an antidromic response at the ankle. The results show that recording from the knee obtains bilateral responses more frequently than recording from the ankle. Thus, recording from the knee can be used instead of recording from the ankle to help detect the presence of a femoral mononeuropathy or lumbar plexopathy. The saphenous knee response, because it tests nerve fibers more proximal than the saphenous ankle response, is less likely to be affected by peripheral neuropathies that tend to affect more distal fibers first. Thus, an absent knee response is more likely to be caused by a lumbar plexopathy and less likely to be caused by a peripheral neuropathy than an absent saphenous ankle response. Because the saphenous ankle response is commonly not present bilaterally, if the clinical goal is to look for a peripheral neuropathy, other distal sensory nerves (eg, sural, superficial peroneal sensory) should probably be examined instead of the saphenous ankle response. This finding cannot be compared with previous studies because we were unable to find a previous study comparing the saphenous knee response to the saphenous ankle response. Buschbacher’s study2 only used the dominant-side saphenous nerve responses to determine their prevalence of 25% nonresponse rate and did not present the prevalence of obtaining bilateral saphenous responses. The saphenous response at the knee has the disadvantage in that it is not possible to detect an injury to the saphenous nerve distal to the knee unless the response is obtained at the ankle. In addition, the response at the ankle may be more convenient to perform in conjunction with other sensory responses at the ankle.

The second purpose was to determine if BMI affects the ability to obtain a response. The results suggest that the saphenous ankle response may be difficult to obtain in subjects with BMI greater than 25kg/m2, whereas saphenous knee responses are commonly obtainable bilaterally in obese and overweight subjects.

We are also unable to directly compare this study to previous studies because Buschbacher’s study2 did not present their rate of obtaining bilateral responses at the ankle in different BMI groups. However, they did find that the BMI of subjects who had an obtainable saphenous ankle response on the dominant side differed from the BMI of subjects whose saphenous ankle response was unobtainable.

Conclusions 

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Saphenous nerve conduction study (NCS) at the knee is statistically more consistent than saphenous NCS at the ankle, especially in patients with a larger BMI. However, the number of absent responses in normal subjects highlights the limits of this NCS.

References 

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1. 1Warwick R, Williams PL. Gray’s anatomy. Philadelphia: WB Saunders; 1973;.

2. 2Buschbacher RM. Sural and saphenous 14-cm antidromic sensory nerve conduction studies. Am J Phys Med Rehabil. 2003;82:421–426. MEDLINE | CrossRef

3. 3Wainapel SF, Kim DJ, Ebel A. Conduction studies of the saphenous nerve in healthy subjects. Arch Phys Med Rehabil. 1978;59:316–319. MEDLINE

4. 4Izzo KL, Sridhara CR, Rosenholtz H, Lemont H. Sensory conduction studies of the branches of the superficial peroneal nerve. Arch Phys Med Rehabil. 1981;62:24–27. MEDLINE

5. 5Maeso J, Juan J, Escribano J. Comparison of clinical outcome of stripping and CHIVA for treatment of varicose veins in the lower extremities. Ann Vasc Surg. 2001;15:661–665. Abstract | Full-Text PDF (431 KB) | CrossRef

6. 6Nir-Paz R, Luder AS, Cozacov JC, Shahin R. Saphenous nerve entrapment in adolescence. Pediatrics. 1999;103:161–163.

7. 7Abram LJ, Froimson AI. Saphenous nerve injury (An unusual arthroscopic complication). Am J Sports Med. 1991;19:668–669. MEDLINE | CrossRef

8. 8Murayama K, Takeuchi T, Yuyama T. Entrapment of the saphenous nerve by branches of the femoral vessels (A report of two cases). J Bone Joint Surg Am. 1991;73:770–772. MEDLINE

9. 9Kimura I, Ayyar DR, McVeety JC. Saphenous nerve conduction in healthy subjects. Tohoku J Exp Med. 1983;140:67–71. MEDLINE | CrossRef

10. 10Liveson JA, Ma DM. Laboratory reference for clinical neurophysiology. Philadelphia: FA Davis; 1992;p 171-6.

a Department of Physical Medicine and Rehabilitation, University of Michigan, Ann Arbor, MI

b Spine Program, University of Michigan, Ann Arbor, MI

c Electromyography Laboratory, University of Michigan Hospital, Ann Arbor, MI.

Corresponding Author InformationReprint requests to Anthony Chiodo, MD, Dept of Physical Medicine and Rehabilitation, University of Michigan Health System, 325 E Eisenhower Pkwy, 1st Fl, Ann Arbor, MI 48108

 No commercial party having a direct financial interest in the results of the research supporting this article has or will confer a benefit upon the author(s) or upon any organization with which the author(s) is/are associated.

PII: S0003-9993(07)00006-8

doi:10.1016/j.apmr.2007.01.004


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