Stimulus Repetition Rate Research Articles

Newborns’ head orientation toward trains of brief sounds

Four experiments assessed the importance of stimulus number, repetition rate, and duration for newborns' head orientation toward brief sounds and related those parameters to the critical ones found for adults. Infants' responses to various trains of repeated 14-ms rattle sounds were compared with those to a 10-s rattle sound, known to elicit head orientation. Directional responses did not differ from the standard when rattle bursts were repeated at a rate of 20 per second for 1 s (experiment 1). Responding did differ from the standard and deteriorated to chance levels when either the number of moderately paced (6/s) stimulus bursts was decreased to six or fewer (experiments 2 and 3) or the duration of rapidly repeated (24/s) bursts was shortened to 500 ms (experiments 4A and 4B). These results suggest that newborns' head orientation depends, in part, upon the number of stimulus bursts and stimulus duration.

The effect of stimulus repetition rate on the diagnostic efficacy of the auditory nerve-brain-stem evoked response

This study investigates the hypothesis that an increase in the click presentation rate during diagnostic testing with the auditory nerve-brain-stem response (ABR) will increase the efficiency with which lesions may be detected in the nervous system. Cats were exposed to conditions of hypoxia, hypercapnia and acidemia, and hypoglycemia was induced in rats. ABR was recorded using the standard 10/sec click rate and also a higher (55/sec) rate during both the control state and the experimental state. Various parameters of the ABR were compared at the two click rates in the control and experimental states to see if the higher click rate was more effective in detecting pathology in the nervous system. It was found that in only a very few cases was the higher stimulus presentation rate more effective, and that in general ABR recordings at one stimulus rate only is quite sufficient for work in a clinical setting.

The effects of rate and forward masking on human adult and newborn auditory evoked brainstem response thresholds

Several investigators have reported that human newborn auditory brainstem evoked response (ABR) thresholds to clicks are about 10-20 dB higher than human adult thresholds to the same stimuli (Galambos & Hecox, 1978; Shulman-Galambos & Galambos, 1979; Lasky, Rupert, & Waller, 1987). The present study replicated these results, but, in addition, addressed developmental differences in ABR thresholds due to forward masking and changes in stimulus repetition rate. Eight human newborns and seven human adults served as subjects. Newborn ABR thresholds to a 100 microseconds click which followed a 82 db(A) SPL 50 ms broadband forward masker by 10 ms were significantly more elevated relative to their unmasked ABR thresholds than were those of the adults. Relatively loud sounds seem to have a greater effect on the newborn's ability to process subsequently presented soft sounds than they do on adult processing. In contrast, changes in repetition rate of 100 microseconds clicks from 10/s to 50/s had no greater effect on newborn than adult ABR thresholds. At near threshold stimulus levels, rate effects on the ABR are not apparent in newborns nor adults.

A Timesaving BERA Technique for Frequency-specific Assessment of the Auditory Threshold through tone-pulse Series Stimulation (TOPSTIM) with Simultaneous Gliding High-pass Noise Masking (GHINOMA)

A new stimulation paradigm is described for eliciting frequency-specific auditory brainstem responses (ABR) by stimulation with a series of seven Gaussian-shaped tone pulses with carrier frequencies descending, in half-octave steps, from 4,000 to 500 Hz, and an interstimulus interval between consecutive pulses of 18 ms. The pause between two consecutive series is 54 ms so that the interval between two tone pulses of the same frequency is 162 ms (stimulus repetition rate approximately 6/s). Simultaneously a high-pass noise masker is presented whose lower cut-off frequency is continuously diminished in such a way that, when a tone pulse is presented, the cut-off frequency of the masker is exactly one octave above the carrier frequency of the pulse. Forward masking effects of preceding tone pulses as well as forward and simultaneous masking effects of the high-pass noise suppress activity originating from those regions of the cochlea which are located basalwards to the region to be stimulated by the respective pulse, thus enhancing the frequency specificity, especially for low-frequency stimuli of higher intensity. The new stimulation paradigm was tested in 12 normal hearing subjects and turned out to be suitable to elicit frequency-specific ABR with frequencies as low as 500 Hz and intensities as low as 10 dB nHL. The main advantage of the described technique is that the time required for a complete assessment of the auditory threshold at seven test frequencies (covering the relevant speech frequency range) is substantially shorter as compared to conventional techniques so that it can routinely be employed in pedaudiology, where infants usually have to be investigated in sedation.

Nonlinear system identification by m-pulse sequences: application to brainstem auditory evoked responses

The purpose of this paper is to introduce a method for characterizing the nonlinear behavior of the auditory system. The method uses an m-pulse sequence as the stimulus and employs a general nonlinear framework for the auditory system. Like Sutter's binary m-sequence approach, the m-pulse sequence approach is computationally efficient since calculation of the first-order input-output cross-correlation function is all that is necessary for obtaining the nonlinear characteristics of the system. The nonlinear system characteristics are reflected in pulse kernels in contrast to binary kernels associated with the binary m-sequence approach. By assuming the system under study is a third-order nonlinear system, binary and pulse kernels are shown to be related to Volterra kernels. The results suggest that the m-pulse sequence can be used to study the system nonlinear effects of varying the stimulus repetition rate more effectively than conventional methods. Preliminary physiological data obtained by applying m-pulse sequences to the brainstem auditory evoked response (BAER) clearly illustrates the feasibility of obtaining replicable evoked responses using this method.

Effects of stimulus repetition rate on ABR threshold, amplitude and latency in neonatal and adult Mongolian gerbils

The ABR wave forms of 16-day-old and adult Mongolian gerbils were evoked by click stimuli presented at rates ranging from 1 to 80/sec. Wave I and wave IV thresholds were determined for each of 5 click rates. Amplitudes and latencies of waves I and IV were measured at each of 7 click rates and 3 intensity levels (15, 40 and 65 dB above threshold). Thresholds for waves I and IV in the adult gerbil and wave I in the 16 day gerbil were unaffected by changes in stimulus repetition rate. Neonatal wave IV thresholds were unaffected by click rate for rates below 25/sec but increased approximately 7 dB/decade increase in click rate when rate exceeded 25/sec. Increasing click rate produced greater reductions in ABR amplitude among neonates than adults for both waves I and IV. Decreases in amplitude due to increasing rate were independent of intensity level in both neonatal and adult subjects. Increasing rate produced similar increases in wave I latency among 16 day and adult subjects, but produced much greater increases in wave IV latency among neonates. Stimulus intensity level and click rate acted independently on wave I and wave IV latency in adult subjects and wave I latency in neonates. However, an interaction between rate and intensity was observed with respect to neonatal wave IV latency.

Brain-stem auditory evoked potentials in squirrel monkey ( Saimiri sciureus)

To more fully characterize brain-stem auditory evoked potentials (BAEPs) in non-human primates, BAEPs were recorded from chronically implanted epidural electrodes in 10 squirrel monkeys ( Saimiri sciureus). The effects of stimulus intensity, repetition rate, and anesthesia (ketamine 20 mg/kg i.m.) on peak latencies and inter-peak intervals were evaluated. Monkey wave forms consisted of approximately 7 peaks (I–VII), each exhibiting similar latencies across sessions, with later peaks exhibiting greater variability. In some subjects, additional peaks (IIa, IIIa) and slow potentials were recorded. The slow potentials provided a substratum for peaks IV through VII. As with human, monkey peaks exhibited systematic changes in latency with changes in stimulus intensity or repetition rate. These shifts included significant decreases in latency with increasing intensity for peaks I–IV and increases in latency with increases in repetition rate for peaks III, V, and VI. Inter-peak intervals were similar to those observed in human. Furthermore, ketamine anesthesia significantly delayed the latencies of most peaks (except I, V, and VII). Some differences between monkey and human BAEPs were evident in the relative amplitude of specific peaks. For example, peak V is typically most prominent in human, while this was true for peak III in monkey. The similarities between unanesthetized monkey and human inter-peak intervals suggest that the times required for impulses to reach particular brain-stem areas are conserved across primate species that vary in brain size. This supports the hypothesis that comparably numbered BAEP peaks in monkey and human index homologous processes. The data also suggest that the differences between animal and human BAEPs commonly reported may result from the use of anesthetics. In summary, unanesthetized monkey BAEPs resemble human BAEPs in morphology, number of peaks, polarity, latency variability, inter-peak intervals, slow potentials superimposed on the high-frequency peaks, and variations in morphology, amplitude, and resolution of peaks as a function of recording site. Thus, unanesthetized monkey BAEPs may be an excellent model for investigating the neural substrates of human BAEP or for determining species differences in acoustic processing among primates.

Laryngeal Brain-Stem-Evoked Response

At the annual meeting of the American Laryngological Association in San Francisco, Calif, Drs Cynthia Anonsen and Lauren Lalakea, Stanford (Calif) University, and Dr Maureen Hannley, Washington, DC, presented their work in evaluating far-field brain-stem recordings in response to electrical stimulation of the superior laryngeal nerve in cats. In the first part of the study, nasopharyngeal and posterior cervical electrodes were used for recording, and animals were anesthetized and paralyzed. Six positive and five negative reproducible waves were observed, which corresponded closely to those previously reported by investigators in Japan. Anonsen and coworkers also looked at the effects of stimulus intensity and repetition rate on this response. In contrast to the auditory brain-stem response, the laryngeal brain-stem response does not appear to change as a function of these parameters. This study also explored the possibility of obtaining brain-stem recordings without paralysis. By

Auditory brainstem responses in the normal beagle.

The latencies of the peaks in brainstem responses and the threshold response were determined in 18 healthy beagles. In the first series of measurements the dogs were sedated and the stimulus was delivered via an in-the-ear transducer. The latencies, the threshold levels, and the influence of the stimulus repetition rate on the latencies were measured. Using a miniature electric microphone in the outer ear canal near the tympanic membrane, it was found that at a level setting corresponding to 0 dB human level (HL) the major peak in damped oscillation during condensation reached a sound pressure level (SPL) of about 27 dB and the secondary rarefaction peak reached 24 dB SPL. In the second series of measurements the dogs were not sedated and the stimulus was delivered via a headphone. The wave forms, the mean latencies for peaks I to V as a function of the stimulus level, and the threshold of each wave are presented from both series. In the first series the latency values at 80 dB HL (107 dB SPL) were 1.21, 1.97, 2.67, 3.12 and 3.61 ms for peaks I, II, III, IV and V, respectively. The thresholds for peaks I to V were 47.5 +/- 9.5, 47.5 +/- 11.5, 41.3 +/- 13.0, 63.3 +/- 17.4 and 28.0 +/- 9.7 dB HL, respectively. The difference in peak latency between the first and the second series was 0.065 ms. This difference corresponded to the difference in length of the acoustic pathways.(ABSTRACT TRUNCATED AT 250 WORDS)

Early deflections of cerebral magnetic responses to median nerve stimulation

We have recorded early components of somatosensory evoked magnetic fields with a sensitive 7-channel first-order gradiometer using a wide recording passband (0.05–2000 Hz) and high sampling frequency (8000 Hz). The left median nerve was stimulated at the wrist and responses were recorded over the right hemisphere. The responses typically consisted of a N20m peaking at 18–20 msec, a small P22m peaking at 21–23 msec and a P27m peaking at 29–31 msec. The topography of N20m could be explained by a tangential current dipole in the posterior wall of the central sulcus (probably in area 3b). The equivalent dipoles of P27m were located on average 10 mm antero-medially to the sources of N20m. This suggests that P27m may get a contribution from the anterior wall of the central sulcus. An increase of stimulus repetition rate from 2 to 5 Hz decreased the amplitude of P27m more than that of N20m, which implies that these two deflactions are generated by different neural netwoks.

Physiology of lateral line mechanoreceptive regions in the elasmobranch brain

The physiology of mechanoreceptive lateral line areas was investigated in the thornback guitarfish, Platyrhinoidis triseriata, from medulla to telecephalon, using averaged evoked potentials (AEPs) and unit responses as windows to brain functions. Responses were analysed with respect to frequency sensitivity, intensity functions, influence of stimulus repetition rate, response latency, receptive field (RF) organization and multimodal interaction. 1. Following a quasi-natural vibrating sphere stimulus, neural responses were recorded in the medullary medial octavolateralis nucleus (MON), the dorsal (DMN) and anterior (AN) nucleus of the mesencephalic nuclear complex, the diencephalic lateral tuberal nucleus (LTN), and a telencephalic area which may correspond to the medial pallium (Figs. 2, 3, 13, 14, 15, 16). 2. Within the test range of 6.5-200 Hz all lateral line areas investigated responded to minute water vibrations. Best frequencies (in terms of displacement) were between 75 and 200 Hz with threshold values for AEPs as low as 0.005 microns peak-to-peak (p-p) water displacement calculated at the skin surface (Fig. 6). 3. AEP-responses to a vibrating sphere stimulus recorded in the MON are tonic or phasic-tonic, i.e., responses are strongest at stimulus onset but last for the whole stimulus duration in form of a frequency following response (Fig. 3). DMN and AN responses are phasic or phasic-tonic. Units recorded in the MON are phase coupled to the stimulus, those recorded in the DMN, AN or LTN are usually not (Figs. 5, 8, 9). Diencephalic LTN and telencephalic lateral line responses (AEPs) often are purely phasic. However, in the diencephalic LTN tonic and/or off-responses can be recorded (Fig. 11). 4. For the frequencies 25, 50, and 100 Hz, the dynamic intensity range of lateral line areas varies from 12.8 to at least 91.6 dB (AEP) respectively 8.9 and 92 dB (few unit and single unit recordings) (Fig. 7). 5. Mesencephalic, diencephalic, and telecephalic RFs, based on the evaluation of AEPs or multiunit activity (MUA), are usually contralateral (AN and LTN) or ipsi- and contralateral (telencephalon) and often complex (Figs. 10, 12, 16). 6. In many cases no obvious interactions between different modalities (vibrating sphere, electric field stimulus, and/or a light flash) were seen. However, some recording sites in the mesencephalic AN and the diencephalic LTN showed bimodal interactions in that an electric field stimulus decreased or increased the amplitude of a lateral line response and vice versa (Fig. 13 B).

The effects of voluntary contraction on the H reflex of human limb muscles.

The effects of a voluntary contraction on the H reflexes of various muscles were quantified to determine whether the reflex responses were sufficiently reproducible to be used in diagnostic studies. During a voluntary contraction, H reflexes could be recorded reliably from tibialis anterior and abductor pollicis brevis, but accurate identification of the onset of the H wave from the on-going background EMG required duplicate averages of multiple responses. During a contraction the H reflex could be obtained at lower stimulus intensities in the forearm flexor muscles than when relaxed, and a more clear separation of the H wave from the M wave was possible. The background contraction abolished the attenuation of reflex amplitude with increasing stimulus repetition rates, such that repetition rates of up to 4 Hz could be used without significant loss of reflex amplitude. There were only small and usually insignificant differences in the latency of the H reflex or its variability when elicited with the forearm muscles relaxed and when flexor carpi radialis was contracting steadily. The reflex latencies of abductor pollicis brevis, tibialis anterior and soleus were compared with F wave latencies for these muscles. The minimal F wave latencies were shorter than the H reflex latencies for abductor pollicis brevis (mean 2.2 ms) and tibialis anterior (mean 1.0 ms) but not for soleus. Comparison of the spread of F wave latencies (F max-F min) suggests that, for soleus, F waves are recorded only from the faster conducting motor units in the pool, presumably those less readily recruited in the H reflex. It was calculated that the distribution of motor conduction velocities responsible for the F waves of abductor pollicis brevis was 8.8 m.s-1. This value underestimates the likely distribution of motor conduction velocities for the thenar muscle by as much as 50%, consistent with the view that F waves rarely occur in slowly conducting motor units, the units of lowest threshold in reflex studies. It is concluded that, for many motoneuron pools, the H reflex and the F wave appear preferentially in different motoneurons, low and high threshold, respectively, and that reflex studies can provide information not available from somatosensory evoked potentials or F wave studies.

Effects of cocaine on the brain-stem auditory evoked potential in the Long-Evans rat

The present study examined the effects of an acute psychoactive dose of cocaine hydrochloride (HCl) in the rat, using the brain-stem auditory potential (BAEP) as an objective, quantitative measure of this substance's effects on brain and auditory electrophysiology. The animals were 8 adult Long-Evans rats (4 female, 4 male). BAEPs were recorded from skull screw electrodes during a baseline period as well as 30–90 min after cocaine HCl treatment (10 mg/kg, i.p.). Normothermia was maintained to control for possible temperature-related effects. Cocaine's effects on the BAEP were examined over a broad range of stimulus intensities (intensity profiles) and repetition rates (rate profiles). Cocaine prolonged latencies of several BAEP components at low stimulus intensities and shortened these latencies at high stimulus intensities. The average BAEP threshold was alos increased by cocaine treatment. These results were not strong, but were suggestive of a recruitment type change in auditory function. Cocaine treatment had no convincing effects on the BAEP as a function of stimulus repetition rate.

Auditory brain-stem (ABP) and somatosensory evoked potentials (SEP) in an animal model of a synaptic lesion: elevated plasma barbiturate levels

Experiments were conducted to determine whether a consistent pattern of auditory nerve brain-stem evoked potential (ABP) abnormalities could be demonstrated in the presence of a synaptic lesion model in cats (elevated levels of the barbiturate thiopental). The ABP in response to low (10/sec) and high (80/sec) stimulus rates was recorded. In order to differentiate between the effects of the elevated drug levels on axonal propagation and on synaptic transmission, the early components of the somatosensory evoked potential (SEP) were also recorded, with particular attention to the first SEP wave, which is solely an axonal event without any intervening synapse. Calculations showed that the effect on synapses was 3.0–9.5 times greater than the effect of the drug on axonal propagation. As the level of barbiturates increased (representing a more severe synaptic lesion), the interpeak latencies of the ABP and the SEP became progressively prolonged, more so than the dependence of the first waves of both the ABP and the SEP on drug level. In general, amplitudes were not affected. At progressively elevated drug levels, higher stimulus repetition rates did not have an increasingly greater effect than lower rates on evoked response latencies and amplitudes so that this study also shows that the use of elevated stimulus rates does not hold much promise in the diagnosis of synaptic lesions.

Binaural interaction in brainstem auditory evoked potentials elicited by frequency-specific stimuli.

The frequency specificity of the binaural interaction in brainstem auditory evoked potentials (BAEP) was investigated in ten normal-hearing young adults. A novel stimulus paradigm was devised to reduce the influence of the acoustic reflex (middle ear muscle contraction) on the BAEP, and to minimize the effect of variations in noise level. Sequences of six stimuli (rarefaction clicks or Gaussian-shaped tone pulses with carrier frequencies of 1, 2, 4 and 6 kHz) were periodically presented in the following order: right monaural, left monaural, binaural, left monaural, right monaural, binaural, with an interstimulus interval of 22 ms. Since the sequence of monaural stimuli with binaural stimuli interposed produces a uniform loudness and since the acoustic reflex is a consensual reflex, the relative high stimulus repetition rate (approx. 45/s) causes a muscle contraction which is equal on both sides and rather constant in time. This paradigm turned out to be usable for stimulus intensities as high as 80 dB nHL. The binaural difference potential (BDP) was computed by subtracting the sum of the monaurally (ipsilateral and contralateral) evoked potentials from the binaurally evoked potential. The major binaural interaction occurred in the latency range of BAEP waves V and VI, and there was no evidence of interaction in the earlier portion of the BAEP. Both latency and amplitude of the BDP components were evaluated statistically. The latency of the BDP components - except of the lasted one - showed an almost linear dependence both on stimulus intensity and stimulus frequency. The amplitude grew larger with decreasing frequency, and the visual detection threshold elevated as the stimulus frequency increased. Click stimuli, however, produced the largest amplitudes with lowest visual detection threshold. This novel stimulus paradigm appears to be most suitable for routine clinical investigations since high stimulus intensities can be used.

Auditory spatial sensitivity of inferior collicular neurons of echolocating bats

The sensitivity of 94 inferior collicular (IC) neurons of Eptesicus fuscu and Myotis lucifugus to spatial location of the acoustic stimulus were studied under free-field stimulus conditions. The best frequency (BF) and minimum threshold (MT) of each neuron were determined with sound delivered in front of the bat. Then the variation in discharge rate of the neuron was measured with a BF sound broadcast from a moving loudspeaker at different angular positions along the horizontal, vertical or diagonal plane of the frontal auditory space. A wide range of stimulus intensities above the MT of the neuron was used. Neurons were classified into 3 classes on the basis of their spatial sensitivity: (1) omnisensitive neurons (15%) were broadly tuned to sound delivered in the frontal auditory space and their responses did not show any correlation with sound location; (2) stimulus intensity-dependent neurons (28%) varied their discharge rates with sound location and intensity so that the peak of their spatial response profiles also varied with stimulus intensity; and (3) stimulus intensity-independent neurons (57%) varied their discharge rates only with sound location over a wide range of stimulus intensities so that their peak discharge always appeared at the same or a small range of angle. In most cases, the medial limbs of spatial sensitivity curve for these neurons were extremely sharp and congruent. By moving the loudspeaker along the horizontal, vertical and diagonal planes, it was possible to approximate the boundary of the spatial response area of a neuron. Most IC neurons responded to sound delivered within 20° ipsilateral, 60° contralateral, 45° up and 40° down of the frontal auditory space, confirming previous similar studies. In general, an increasing stimulus repetition rate appeared to sharpen the spatial sensitivity curve of a neuron. Conversely, an increasing moving velocity of the stimulus decreased its response. The possible role of these 3 classes of neurons in echolocation and neural mechanisms underlying the spatial sensitivity of these neurons is discussed.

The effect of stimulus repetition rate on interaural ABR latency differences in normal and hearing-impaired subjects

Twenty-five subjects with normal hearing and 15 with bilateral high-frequency sensorineural hearing impairment were presented click stimuli at four repetition rates (11, 33, 67, and 89 clicks/s) to access interaural symmetry of wave V latency and amplitude. Predictably, amplitude was significantly decreased and latency increased across all subjects at the higher repetition rates. In both groups, however, interaural latency differences (ILDs) remained with the 0.3-ms normal criterion previously established for slow repetition rates. Thus, both abnormal repetition rate effects and interaural latency differences can serve as reliable indicants of retrocochlear auditory dysfunction, even when peripheral hearing impairment exists.

Influence of anesthesia on spontaneous activity and receptive field size of single units in rat Sm1 neocortex

Spontaneous and cutaneously driven unit activity was recorded in the hindfoot region of rat Sm1 neocortex under controlled intravenous infusion, at three selected rates, of the steroid anesthetic agent Althesin. Increasing depth of anesthesia decreased average spontaneous firing rates of 67 single units from 2.5 to 11 Hz during light anesthesia to 0 to 2.5 Hz in deep anesthesia. Thresholds to cutaneous stimulation for 58 units were innocuous (from 15 to 190 μm) using a 5-ms ramp displacement of the skin in the center receptive field. Responses from 13 sites on the hindfoot were classified according to response probability for each of the 58 units in reply to stimuli at 1.5 times center receptive field threshold. Small receptive fields were seen only under conditions of deep anesthesia, considerable expansion of both center and excitatory surrounds occurring with lighter anesthesia. Mean values for total receptive field size (center plus surround excitatory receptive field) were 10.8, 7.8, and 3.4 sites, respectively, for light, moderate, and deep anesthesia. The size of the receptive field was also influenced by stimulus repetition rate; moderate increases of this and anesthetic depth could eliminate substantial receptive fields. Surround inhibition of evoked activity was more effective in deeper anesthesia with little effect in light anesthesia. We suggest that receptive field expansion in light anesthesia arises from a relative increase in excitability of afferent pathways and an accompanying increase in the preponderance of surround excitation vis à vis surround inhibition.

The effect of stimulus repetition rate on the auditory brainstem response in tumor and nontumor patients.

Auditory brainstem responses were recorded in two groups of adult subjects with asymmetric sensorineural hearing loss. Clicks were presented at repetition rates of 9.7, 39.7, 49.7, and 59.7/s. One group was composed of 20 patients with no known otoneurologic lesion (cochlear group), and one group was composed of 8 patients with a surgically confirmed acoustic neuroma in the ear with poorer hearing sensitivity (retrocochlear group). Detection of wave V at different repetition rates was not significantly different between the two groups. Average wave-V latency shift was not significantly different between the two groups as repetition rate increased from 9.7/s to 39.7/s but was significantly greater for the retrocochlear group as repetition rate increased from 9.7/s to 49.7/s and 59.7/s. However, the wave-V latency shift showed no improvement over the slow-rate interaural wave-V latency difference in discriminating between the two groups of patients. No significant correlation between the amount of wave-V latency shift and hearing loss at 2000 Hz or 4000 Hz was found for the ears with poorer hearing sensitivity.

Effect of high stimulation rates and paired stimuli on the electrically evoked brain‐stem response

Temporal cues are a primary source of information for the single‐channel cochlear implant subject. Two temporal features of the electrical auditory brain‐stem response (EABR) in patients implanted with single‐channel devices are being investigated. In the first of these studies the stimulus rate is varied from 10 to 150/s and changes in wave V amplitude and latency are recorded. Increasing the stimulus repetition rate causes a prolongation of wave V latency and a decrease in amplitude. These changes are particularly prominent for stimulation rates exceeding 70/s. In the second experiment the EABR response to the second stimulus of a stimulus pair is computed as the time interval between the two stimuli is varied from 0.5 to 10 ms. Initial data indicate a significant interaction only for interstimulus intervals less than 4 ms. In these two studies, variations across patients have been found and an attempt is being made to correlate these variations with other measures of the subjects' implant performance. Findings and clinical implications will be reported.