(Vestibular Evoked Myogenic Potential (VEMP) Testing -- Cervical (SCM)
We will use the terminology "cVEMP" to denote vestibular evoked myogenic potentials elicited from the sternocleidomastoid muscle. When we use the terms "oVEMP" or tVEMP or whatever, the small letter indicates that a muscle other than the SCM is being monitored - - such as ocular or triceps. When we use the unqualified "VEMP", we mean any vestibular evoked myogenic potential (i.e. cVEMP, oVEMP, tVEMP, etc).
The purpose of the cVEMP test is to determine if the saccule, one portion of the otoliths, as well the inferior vestibular nerve and central connections, are intact and working normally. Both of the otolith orgais have a slight sound sensitivity and this can be measured. This sensitivity is thought to be a remnant from the otolith organs use as an organ of hearing in lower animals.
?How are cVEMP's generated
In general, one needs to consider the input, central processing, and output for physiological responses.
The pathway supposed to account for the cVEMP response is shown in figure 2 above. Sound stimulates the saccule, traverses the vestibular nerve (mainly inferior, but a bit also in the superior) and ganglion to reach the vestibular nucleus in the brainstem. From there, impulses are sent to the neck muscles via the medial vestibulospinal tract (MVST), then the spinal accessory nucleus, and the accessory nerve. For most muscles, the net effect of saccule stimulation is inhibition, but excitation from electrical stimulation of the saccule has also been reported in some muscles in animals (Uchino et al., 1997;Kushiro et al., 1999).
This wiring diagram may be appropriate for normal people, but due to considerations above, may be incorrect for disorders where the semicircular canals become sensitive to sound, such as in SCD or canal fistulae.
While the clinical literature concerning cVEMPs suggest that they are almost entirely saccular in origin, the animal literature does not support this claim. Many studies of monkeys show that all 5 vestibular endorgans phase lock to loud clicks (Xu et al, 2009). It is also currently thought that the utricle responds to sound (see ovemp page).
It would also seem very possible that in certain disorders of the ear, such as SCD, or cholesteatoma, the semicircular canals might also be a source of cVEMPs. In these disorders, the canals become sensitive to sound, and sound can make the eyes move through activation of the semicircular canal. It seems very likely that it might also activate the neck as well as the vertical eye muscles (i.e. inferior rectus and inferior oblique, such as are measured with the oVEMP test).
According to Naranjo, VEMP amplitudes are increased by threat and fear (Naranjo et al, 2016) showing that there are also other inputs to consider. The implication is that cVEMPs are not simple saccule reflexes, but have multiple inputs.
So overall, things are messy. It is fairly reasonable to assume that the main source of the cVEMPs in normal people is the saccule. It is probably not correct to assume this is the case for patients with ear disease, and due to this, it is also not safe to assume that VEMP wiring is as simple as shown in figure 2 above in all cases.
According to Oh et al (2016), the cVEMPs are mediated by the vestibular nuclei and uncrossed medial vestibulospinal tract descending in the lower brainstem and spinal cord. Therefore, lesions involving the vestibular nuclei can present abnormalities of cVEMPs and medullary lesions involving the descending MLF or the spinal accessory nucleus impair cVEMPs.
Sound evoked cVEMPs recorded from the neck are claimed to be almost completely unilateral. (Colebach et al, 1994; Uchino et al, 1997; Kushiro et al, 2000; Murofushi et al, 1996; Wilson et al, 1995), but in clinical practice this can't be counted upon (see example below). It also is likely wrong when the semicircular canals are activated by sound as discussed above.
The output for cVEMP responses is by definition the sternocleidomastoid (SCM) muscle, which is innervated by the accessory (11th) cranial nerve. If either one of these structures were disturbed, one would expect alterations in the cVEMP as well. One would expect there might be many other muscles that activate the neck and are relevant to posture that are also activated by sound.
Additionally, when the semicircular canals are sensitive to sound, such as in SCD or some canal fistulae, it would also seem very likely that vertical eye muscles on both sides of the head might be activated by the VEMP protocol. Thus the ipsilateral wiring assumptions may be incorrect in certain ear diseases.
VEMPs are recorded using an evoked response computer, a sound generator, and surface electrodes to pick up neck muscle activation or other muscles if this is of interest. Figure 3 above illustrates the basic rather minimal equipment needed. In the author's laboratory, a Bio-Logic Navigator Pro does nearly all of the work, and sends the results to a desktop computer.
VEMP testing is not hard, but there are a lot of technical pitfalls. The basics can be learned by a technician in about 30 minutes. It is a very big response, and as long as the person doing the test is attentive to details (getting the sound in both ears with proper placement of inserts or headphones, having the person lift their head through the entire trial, electrodes in the right place with proper impedance), it is very straightforward. The details (see below) take much longer to learn.
The figure below illustrates a cVEMP test printout. The cVEMP response consists of an initial positivity (p1 or p13) followed by a negativity (n1 or n23), see figure 4 below. It is an evoked potential. Although P1 is positive, it is shown negative on many cVEMPs, because of electrode placement (basically putting them on backwards). The most reliable measure of the cVEMP response is the amplitude (Isaradisaikul et al, 2008).
Later cVEMP components have a lower stimulus threshold and are thought to be nonvestibular. This is not well understood and we are frankly dubious about this idea - -they might simply be part of the same spike train. As VEMP's are easily elicited without the need for EMG rectification, and EMG spikes occur at roughly the same latency as the waves in a cVEMP, coherent spike trains are a reasonable alternative explanation. In other words, later waves may all be part of the same response. In our opinion, a VEMP system that does rectification is not necessary. To be fair though, there are some that differ from this opinion (Lee et al, 2008). Rectification can correct in part for technical errors involving head positioning, at the price of adding more "noise" to the entire system.
Higher than normal thresholds or low amplitudes may be found in persons with saccule disorders as well as conductive hearing loss. Reduced amplitudes are commonly found in vestibular nerve disturbances. Lower than normal thresholds as well as asymmetrical amplitudes are found in persons with Tullio's phenomenon, which is dizziness induced by sound. Prolonged latencies of P13 may be found in central disturbances (Murofushi et al, 2001), but practically these are very rarely encountered, and technical error is the source of most prolonged latencies.
The general rule of thumb with hearing and cVEMP's is that conductive hearing loss obliterates air conducted VEMP's, and that sensorineural hearing loss does little or nothing to VEMP's. The two plots below illustrate this.
A potential pitfall in a person with a complete sensorineural hearing loss, is that one has no way of determining whether they also have also have a conductive component to their hearing loss. For example, someone might have far advanced otosclerosis. Thus, one could falsely conclude that there was no vestibular function on one side based on an absent VEMP. Bone VEMP's are one way to get around this problem.
Basic head positioning and electrode layout
Best practice, as shown below, is to apply EMG electrodes to the middle third of anterior neck muscles (sternocleidomastoids) and the supine patient holds their head up unsupported, using the anterior neck muscles. Subjects are instructed to tense the muscle during runs of acoustic stimulation, and relax between runs. If the neck muscles are not activated, no cVEMP is produced. The reflex scales to tonic EMG -- once again -- if you don't activate the neck muscle, you don't get a response. A corollary, is that if you get a response without neck muscle activation, it isn't a VEMP (maybe a PAM ? see below).
The EMG electrodes should not be the kind that use alligator clips to attach to foil, because the head moves around during the cVEMP. These types of electrodes generate massive amounts of noise with movement. Instead, electrodes should be used that are "hard wired" to the cable.
People with fat necks have lower responses, as the signal from the muscle is underneath the fat and has to go a longer distance. Similarly, people with long necks have later responses, as the signal again has to go a longer distance (Chang et al, 2007)
Some patients are unable to hold their heads up at the angle shown. In this case, some experts recommend simply tilting the entire body up by about 30 degrees, so that there is less torque needed by the patient to hold their head up (Colebatch, personal communication). We think this is an excellent idea, but at present there are no amplitude norms for this procedure.
Another (but bad) method of obtaining activation is to have patients sit upright with their chin turned over the contralateral shoulder to tense the SCM muscle.
We think this is a bad idea because you have no way of knowing how much tension the patient is producing, it is tiring, and patients can do something different on the right than on the left, without you knowing. It is also well known that head position on body can change cVEMP responses. This adds another variable.
Because the response is generally ipsilateral (carefully note the qualification), one theoretically can use bilateral stimuli and bilateral recording to reduce the number of trials (Huang et al, 2006; Young, 2006). We tried this method in our clinical practice, but discarded it for reasons explained below. It has the advantage of using the same stimulus when recording each side, which reduces some of the considerable variability. The limits of normal for the amplitude with the head-raising technique are roughly 70 to 700. Regarding the upper limit, there is no disease that we know of that can be diagnosed by larger than normal cVEMPs on both sides, but in our clinical experience, we have seen this primarily in persons with hyperacusis.
We think that binaural stimulation is generally a bad idea. The figure above illustrates why we have discarded this technique. While cVEMP's are "generally ipsilateral", this doesn't mean that they are always, 100% ipsilateral. Artifacts can also go across the midline, which reduces much of the value of using a binaural stimulus. Because the sternum is rather close to the sternocleidomastoid muscles, there can also be artifact due to "volume conduction" -- meaning electrical activity from one side getting confused with the other (Li et al, 1999). There is also the problem that in SCD, the canals may be activated by sound, and then all bets are off regarding laterality.
If you really care that what you are measuring reflects the side you think you are measuring, don't use a bilateral cVEMP. In our opinion, this pretty much eliminates the technique. The bottom line is don't use a bilateral VEMP.
Loud clicks or tone bursts (typically 95-100 DB nHL or louder) are repetitively presented to each ear in turn at 200 msec intervals (5/second). The optimum frequency lies between 500 and 1000 Hz. The sternum is generally used as a reference and the forehead as a ground. There is some evidence that linked wrists might be a better choice for a reference though (Li et al, 1999).
We generally use a Bio-logic Nav-Pro set up with the parameters documented here.
Note that binaural presentations of sound is not recommended (by us anyway). It is faster but it reduces ones ability to localize the side of lesion because of crossover. Our recommendation, based on some unfortunate clinical experiences where binaural stimulation lead us astray, differs from others in the literature (e.g. Young, 2006).
Myogenic potentials are amplified, bandpass filtered (30-3K Hz), and averaged for 200 presentations. The response evoked in the neck EMG is averaged and presented as a cVEMP (see figure 2). The latency, amplitude, and threshold for the p13-n23 wave is measured. The amplitude is the most reliable measure (Isaradisaikul et al, 2008). Latencies are less reliable but are useful in deciding whether a particular waveform is a "cVEMP" or just noise.
Because of the high intensity of the sound used to evoke these responses, carefully checked inserts should be used. Headphones are less reliable than inserts, because small errors in headphone placement can result in substantial changes in sound intensity, and loss of a cVEMP. When the head is being held upright, headphones can shift easily.
The cVEMP is generally quick and easy to obtain because it is a strong potential and only requires about a minute of stimulation to get 100 presentations. We usually use 200 presentations ourselves. This means that you can easily repeat the cVEMP test. In our opinion, a minimum of two repetitions should be obtained on each side, to be sure that the VEMP is reproducible or absent, as the case may be. Three is generally aimed for. An exception to this can be made if the first two repetitions are of large amplitude and nearly identical (e.g. see figure 2). We generally use monaural recordings.
We recommend tone bursts rather than clicks -- here is the reasoning. A similar response is produced using tone bursts instead of clicks (Murofushi, Matsuzaki et al. 1999; Welgampola and Colebach, 2001; Cheng, Huang et al. 2003). Either 500 or 1000 hz tones are presented at a 5/second rate. They suggested using an intensity of 120 db SPL. A stimulus duration of 7 msec was found optimal. The advantage of the tone burst stimulus compared to a click is that it requires lower absolute stimulus intensities. This is important if you are using equipment that doesn't produce optimally loud stimuli (see below). We suspect that it produces longer and more variable latencies. At the present writing however, the clinical value of measuring latency (other than being sure you have a VEMP), remains somewhat elusive. Amplitudes are much more reliable.
Rauch et al (2004) also advocate using tone bursts, and suggest a 500 hz frequency is optimal. They suggest monitoring ongoing EMG activity to ensure that the SCM muscles are activated as without muscle activation, a cVEMP does not occur. In their study, a cVEMP was judged absent when no replicable response was observed and enough responses were averaged for residual noise to be less than 3 uv. They suggest that thresholds are more useful than amplitudes. We do not agree -- we feel that amplitudes are more useful than thresholds, given a well standardized protocol. The literature suggests that amplitudes are more reliable than thresholds too (Isaradisaikul et al, 2008).
Practically, one cannot do both -- 3 repetitions as well as thresholds, because of fatigue. We have also found many patients with low thresholds, but no dehiscence. See more discussion of the problems inherent in doing thresholds below under technical pitfalls.
Technical pitfalls in doing VEMPs
Nearly all VEMP problems are caused by operator error. The VEMP is a relatively new test, and so far, manufacturers have not built into the protocols methods of quality assurance. In fact, after an FDA review in the US, manufacturers had to PULL some protocols they had put in to be helpful. Our government restricting innovation.
When cVEMP's make no sense in the overall clinical context, we think it is a good idea to just repeat them on a later visit, and inservice the technician if there is a big discrepancy
Assuring neck muscle activation is the biggest problem. While one can run a cVEMP very successfully with the patient's head being held up vs. gravity, this is tiring. A common quality control problem in the cVEMP is an overly nice technician who allows the patient to put their head down during the test. cVEMPs can be run with the head being actively turned to one side, thus fatiguing only one side rather than both, but this procedure also has it's pitfalls, as it is less reliable and produces smaller potentials (Wang and Young, 2006). A suggestion for any manufacturer who might be reading this is to add a method of determining if the head is off the table (a simple pressure switch would work). A few more comments about VEMP biomechanics are here.
In persons who can't cooperate, assuring neck muscle activation is a gigantic problem. Consider, for example, attempting to do a cVEMP in an infant. How do you ensure that the neck muscle is activated ? This is an intrinsic problem with doing cVEMP's in very young children, and perhaps it should just not be attempted at all. There are some reports of doing oVEMPS in children however. At a minimum, cVEMP's done in persons who are (perhaps) not cooperative should be done with equipment that can monitor the EMG.
Another technical "gotcha" in the cVEMP is a sound not getting to the ears. This is very very important ! Common things that go wrong here are asymmetrical placement of inserts, wax occluding one side, or a defective sound generator (the Bio-logic ones seem to go bad very often, when used for VEMPs -- it has happened to us 3 times in just 2 years !). Because cVEMP's are not far above the threshold provided by most evoked potential equipment, little things like not putting the insert in as far in one ear as the other can make a big difference. Just 10 dB can be important. Regarding checking of the inserts, we suggest a sound-check with every single VEMP. The easiest way to do this is to run an initial cVEMP without lifting the head -- this both assess for PAM artifact (see below), as well as can provide a good time to do a sound check. It would make sense for the cVEMP protocol to include a threshold check at 500 hz, using the inserts and transducer of the evoked potential machine, but so far, this is not available.
Thresholds can also be problematic. There are several major problems. The first is that there is a subjective element to picking a threshold. One person's response might be another person's noise. The second is that if you do thresholds, you can't do a lot of repetition (because people get tired). The third is that they don't always work -- low thresholds are NOT always accompanied by radiographic evidence of superior canal dehiscence. We have encountered several patients with thresholds of 60, but normal temporal bone CT's. Our present position is that thresholds should not be done routinely, as they prevent one from doing a reliable amplitude.
Electrical artifact. cVEMP's are huge (compared to ABR or ECochG) and there should not be much random electrical artifact. If you see stimulus artifact, or sinusoidal undulations to the trace, it is very likely that the electrodes are bad, someone put the sound generator box too close to the electrodes, the impedance was too high, or the evoked potential machine needs service. In our experience with the latter, the thing that routinely goes bad with the evoked potential machine are the connectors and the insert driver.
In the cVEMP trace above, there is stimulus artifact. After it went away when the sound generator was moved, we realized that the sound generator cannot be very close to the EMG leads. The sound generator produces a magnetic field which induces a strong artifact, if one places it close to one of the electrical leads.
Other artifact. Occasional patients have "VEMP like potentials" (? VLP), that are not VEMP's.
In some instances, this is caused by the "posterior auricular muscle (PAM)", a sound evoked twitch of the ear. The PAM is a small muscle behind the ear that can "wiggle" the ear. Actually, there are three of these muscles -- posterior, superior and anterior auricular muscles - -all vestigial. PAM is innervated by the facial nerve. The latency of the response is about 11 msec, making it overlap with the VEMP. (Funahashi et al, 1992). The literature about PAM is confused -- some authors may have mistaken the much larger cVEMP's for PAM responses, and vice versa. See Gibson (1978) for a review of the older literature.
To rule out PAM potentials, you can run your cVEMP initially or perhaps in between other runs, without contracting the SCM.
In other instances, this is due to "volume conduction" -- electrical activity from one side showing up on the other side. Volume conduction problems can be best solved by monaural stimulation. For reasons developed above, we think that a run or two of monaural stimulation is a very good idea.
Logical inference. While cVEMP's are "generally ipsilateral", this doesn't mean that they are always, 100% unilateral. If you are trying to "rule out" any vestige of remaining vestibular function -- don't use a binaural stimulation cVEMP. As nearly always one is trying to localize the side of lesion, we think that binaural cVEMP's are best avoided. An exception is when one is trying to diagnose bilateral vestibular loss, when it is OK.
One can also broadly criticize all studies of VEMPs in that the core dogma driving the enthusiasm in doing VEMP tests is implausible. The core dogma is that things are very simple, allowing one to make diagnostic inferences. While not emphasized much in the literature, VEMP tests likely involve input from many senses, and are not confined to saccule or utricle inputs as has been suggested. It is also implausible that the wiring is "unilateral". Thus we have a large clinical database that has not produced very impressive results, perhaps based on an oversimplified idea about how the ear is wired up to the nervous system.
Clinical utility of VEMPs
What does it test ?
Figure 2 illustrates the pathway for the acoustic VEMP response, which includes the saccule, the inferior vestibular nerve, the vestibular nucleus, the medial vestibulospinal tract, the accessory nucleus, the 11th nerve, and finally the sternocleidomastoid muscle. Abnormal VEMPs might be caused by abnormalities in any of these structures. The sound induced VEMP also requires conduction of sound to the inner ear, which means that an intact middle ear is needed.
While VEMPs are presently attributed to the saccule, the data presented so far suggests that hearing is not necessary for VEMPs. This does not exclude the possibility that hearing is sufficient for a low-level VEMP, as it is unusual to encounter a human subject with a well documented vestibular lesion that is confined to the saccule. There are some data however suggesting that vestibular nerve section abolishes VEMPs, which would be against this idea (Watson and Colebatch, 1998). It is also possible that hearing is synergistic with vestibular input -- i.e. you get more of a response with multisensory convergence. We are presently of this opinion, but these are issues that need to be worked out.
Normal Values for cVEMPs
In our clinic setting in Chicago, we consider VEMPS to be abnormal when they are very asymmetrical (one is 2 times or more as large as the other -- an RVR of 33% or greater), low in amplitude (less than 70 for a young population), or absent (no reproducible wave, or P1 latency outside of our norms). We use tone-burst VEMPs, which produce modestly larger responses than clicks. We do this because our equipment (Bio-Logic Nav-Pro), peculiarly enough, does not produce as loud a stimulus as we would prefer (only 95 dB). As mentioned above, we tried bilateral binaural recording and stimulation, but we switched back to monaural stimuli because of some bad diagnostic experiences where it appeared that there was a VEMP with binaural stimulation, but there was clearly no VEMP with monaural stimulation.
Concerning effects of age, 3 studies have been done -- using 3 different techniques. For clicks, compared to young persons, decreased amplitudes (roughly a factor of two) are seen on persons 70 and older (Su et al, 2004). Similarly, also using clicks but not using commercial equipment, Ochi reported amplitudes of approximately 250 for 20 year olds vs. 90 for 80 year olds.
Basta et al reported similar results for 500 hz tone bursts (2007) but with lower overall amplitudes using a Viking system. These systems seem to produce lower amplitude results, perhaps due to differences in calibration. It has been our general experience that the device that we use (Bio-Logic NavPro) produces larger potentials than most competing devices.
At the present writing (2011), it appears to us that in normal persons, and using the Bio-logic Nav-Pro, average VEMP amplitude decline from approximately 150 at the age of 20 to approximately 75 at the age of 70.
What data is there concerning particular disorders in the literature ?
The VEMP literature is rapidly increasing and it seems that there are considerable valuable diagnostic information to be obtained.
See the following sections for brief discussions of VEMPs, illustrated with traces from our practice, in
- Superior canal dehiscence
- Vestibular nerve disorders
- Vestibular Neuritis
- Acoustic Neuroma
- Bilateral vestibular loss (such as due to gentamicin)
- Benign paroxysmal positional vertigo (BPPV)
- Central vestibular disorders
- Meniere's disease
- Hearing disorders
For some of the more popular disorders where VEMPs are used, we have separate pages, and have combined data from other VEMP protocols as well.
VEMPs in Superior Canal Dehiscence Syndrome -- See this page for detail.
Vemps as a test of vestibular nerve disease -- sometimes works
Suggesting that cVEMPs are sensitive to saccule pathway disease, Ochi and associates (2003) reported use of cVEMPs to diagnose vestibular neuritis involving the inferior division of the vestibular nerve. Because the saccule is supplied by the inferior division, cVEMPs should be absent in this situation. cVEMP does not distinguish between the saccule and inferior vestibular nerve, and available techniques seem unlikely to be able to resolve between these two.
As most types of vestibular neuritis spare the inferior vestibular nerve, cVEMPs would be expected to generally be normal in vestibular neuritis. In fact, in our clinical practice in Chicago, we sometimes use the pattern of very abnormal VENG, accompanied by very normal cVEMP to strongly suggest Vestibular neuritis -- i.e. we use it to exclude total vestibular nerve disease rather than to detect vestibular nerve disease. We also use similar logic to diagnose bilateral vestibular neuritis. When cVEMP's are abnormal in vestibular neuritis, they recover more rapidly than canal related tests (Kim et al, 2008)
Galvanic VEMP stimulation stimulates the entire vestibular nerve and accordingly would be expected to be normal even if the inferior vestibular nerve were damaged. Thus an absent sound-VEMP and present galvanic-VEMP would not differentiate between a saccule lesion and an inferior vestibular nerve lesion.
Prolonged latency of cVEMPs has recently been suggested to be a sign of a retrocochlear (vestibular nerve) lesion, such as is found in vestibular neuritis. We are somewhat dubious about this and think that in this case the first wave of the cVEMP may simply be missing, but later waves related to cochlear function are preserved, causing the appearance of a prolonged latency. Abnormal cVEMPs (asymmetrical or long latency) are reported in about 25% of persons diagnosed with vestibular neuritis (Murofuschi et al, 1996). Prolonged latency also occurs in persons with long necks (of course).
In Vestibular neuritis, cVEMP's reportedly normalize more rapidly than canal related tests (Kim et al, 2008). However, this conclusion is suspect as the VEMP technique used in this study (head-turning) is intrinsically flawed (see discussion above).
VEMPS are generally absent or reduced in persons with acoustic neuroma (see figure above).
Failed vestibular nerve section: Not very likely to work
cVEMPs should be and nearly always are absent in persons with vestibular nerve section.
Vestibular nerve sections fail to control intractable vertigo due to Meniere's disease in about 5% of patients. When they fail, the question can arise whether the nerve section was incomplete. VEMPs might, in theory, be useful for detecting residual function in the inferior vestibular nerve, as this branch of the vestibular nerve is sometimes intermingled with cochlear fibers (Lehnen et al, 2004). However, as cVEMPs require a very strong stimulus, it seems unlikely that they would be very sensitive. Head impulse tests for the posterior canal reveal residual function more more frequently than do cVEMPs (Lehnen et al, 2004). More study of this question is needed.
A potential pitfall in doing cVEMP's in persons with VNS are contralateral responses and extraneous responses (mainly posterior auricular muscle responses). You should NOT do bilateral stim cVEMP's in persons with VNS. You should also check for the PAM (by doing a test with the head resting on the table) if there is something that appears to be a response on the sectioned side.
cVEMPs as a test for bilateral vestibular loss -- works !
VcEMPs would be expected to be reduced or absent in persons with bilateral vestibular loss, such as due to aminoglycoside ototoxicity.
Gentamicin obliterates cVEMPs in guinea pigs. (Cheng et al, 2010)
Only a few patients have been studied so far with gentamicin (Murofushi et al, 1998). In our practice, we have tested many patients with bilateral vestibular loss and normal hearing, and find that it is a good test (Hain et al, 2006). We have also tested two deaf patients with bilateral loss, one due to Cogan's syndrome and another due to a Mondini malformation, and found absent or nearly absent responses in both. This is as would be expected if one believes that the saccule is affected in these conditions. Nevertheless, this conclusion can be questioned as a problem intrinsic to testing persons with bilateral hearing loss is that one does not know if they might also have a conductive hearing disturbance superimposed on the sensorineural loss. Because conductive hearing loss obliterates sound-induced cVEMPs, one cannot clearly relate an absent cVEMP to absent saccule function in this situation.
cVEMP's also appear to be absent after unilateral gentamicin treatment used for Meniere's disease (Helling et al, 2007). They may be useful in deciding whether or not more drug is indicated. A possible confounding problem is that there may be middle ear disease after the injection due to the perforation required for transtympanic gentamicin.
cVEMPs in BPPV -- doesn't work.
One might think that as VEMP's assess the saccule (an otolith organ), and because BPPV is thought to be due to another otolithic disease (loose otoconia from the utricle), that there might be abnormal VEMP's in persons with BPPV. Yang et al (2008) asked this question, and reported that latency was slightly increased. As we are dubious that latency is a useful measure at all, we are also dubious about the use of cVEMP's in BPPV. On the other hand, there is a literature suggesting that oVEMPs are helpful in BPPV.
VEMP's in Otosclerosis - -should be absent.
In Otosclerosis, air conducted VEMPs should be absent. A person with a present air conducted VEMP and conductive hearing loss may have SCD.
VEMPS in Meniere's disease -- see this page.
VEMPs in central disorders -- rarely works.
We have not been impressed with sensitivity of cVEMPs to central disorders such as brainstem strokes. The difficulty seems to be that the latencies in cVEMPs (at least with tone bursts), are so variable that there is inadequate sensitivity to disease. This may be an artifact of our methodology (tone burst), which is temporally a longer stimulus than a click. We don't have any examples to show here, so we will just mention what is in the literature.
cVEMPs are often asymmetrical in spasmodic torticollis (Colebatch, Di Lazzaro et al. 1995).
cVEMP's are reduced in progressive supranuclear palsy (PSP), according to Liao et al (2008). PSP is a rare degenerative disorder of the CNS that generally results in death within 5 years of diagnosis. The average VEMP amplitude was reported to be 54, with a range of 16.8 to 214. This range overlapped substantially with age-matched controls, but may be another helpful method of identifying PSP. No data is presently available concerning progression of VEMP's in PSP patients over time. One would expect a decline. These patients are unusual however and a longitudinal study would not be easy to carry out.
cVEMPS, like other evoked potential tests, can also be abnormal in central diseases such as multiple sclerosis (MS). (Shimizu, Murofushi et al. 2000; Versino, Colnaghi et al. 2002; Murofuschi et al, 2001) and brainstem stroke (Chen et al. 2003). VEMPs test mainly measure lower brainstem function (medulla), while the ABR also tests upper brainstem function (medulla pons and midbrain). Here, latency measures would seem more logical than amplitude measures.
cVEMP's are reported abnormal in certain cerebellar degenerations (i.e. Machado Joseph disease), but normal in others (e.g. OPCA, cortical cerebellar degeneration). (Tagegoshi and Murofushi, 2000). As VEMP circuitry is not thought to involve the cerebellum, it would be surprising to find abnormal VEMP's in any purely cerebellar condition. In our own practice (see above), but we have only studied two patients and found abnormally reduced amplitude for age in one and an absent VEMP in the other. As Machado-Joseph affects the brainstem, the mechanism for the reduced VEMP may lie in damage to other locations than the cerebellum.
cVEMPs in hearing disorders -- needs more data.
Although VEMPs can be obtained in people with complete hearing loss, the hearing loss has to be of the sensorineural type. Just because cVEMP's can be "obtained" it doesn't mean that they are uncorrelated with hearing loss, and in our experience, both hearing and vestibular function correlate with cVEMP amplitude. However, this conclusion is not (so far) well documented in the literature.
Persons with conductive hearing loss, even just a small amount such as 10-15 dB, often do not have air conducted cVEMPs, presumably because the sound stimulus, conventionally delivered by earphones, does not get to the saccule. The saccule has a high threshold, and if you are stimulating the ear close to that threshold (i.e. 95 dB), it is easy to drop below it. This means that cVEMPs are less useful in older persons, who often have a component of conductive hearing loss due to otosclerosis and related disorders, and also should be interpreted with a recent audiogram, including bone and air conduction testing, in hand. A way around this may be to do bone-conduction cVEMPs when the air-conduction cVEMP is absent. While this substitutes for the bone conduction audiogram, it requires more testing and potentially may fatigue the patient. Also, bone-conduction stimuli are generally not very strong.
Several groups (Wang and Young, 2007; Akin et al, 2012) reported that cVEMP's are reduced in persons with noise induced hearing loss. They attributed this effect to saccule damage. While theoretically possible, we are dubious that a structure that requires 70db to elicit a minimal response would be very sensitive to noise. The saccule would more reasonably be damaged by excessive changes in linear acceleration as it is loaded by the otoconia.
Instead our opinion is that there simply is reduction of air conducted VEMP's from hearing reduction. Similarly, Zhou, Kenna, Stevens and Licameli (2008) reported cVEMP's are reduced in children with sensorineural hearing loss, and attributed this effect to saccule damage. We think that these authors made the same logical error as Wang and Young. cVEMP tests are generally normal in sudden hearing loss (Wu and Young, 2002).
Who does VEMP testing and who should interpret VEMP tests ?
VEMP tests are commonly performed by an audiologist or an electrophysiology technician. Oddly enough, cVEMP's are sometimes even done by physical therapy practices. Audiologists are often associated with otolaryngology practices (ENT doctors), while electrophysiology technicians are often associated with neurology practices. cVEMP's are easy to obtain, but there are many pitfalls involving hearing.
We strongly suggest having an audiologist or audiology technician do this test.
We do not think that this test should be done by people who are not familiar with hearing -- i.e. physical therapy practices or general neurology practices, because a good working understanding of how hearing interacts with VEMPs is essential. We shudder to think of what might go on in a practice where testing is being done universally without any knowledge of whether the patient has a conductive hearing deficit, or sound-checks being done on the equipment.
Regarding interpretation, it is simply not reasonable for general audiologists, who have no neurological background, to make inferences about brain function. Similarly, in our opinion, most physical therapists do not have appropriate audiology training to interpret cVEMP's. Because the interpretation process involves both peripheral and CNS pathways, we think that a team combining an experienced audiologist and otoneurologist is optimal