Binaural fusion and listening effort in children who use bilateral cochlear implants: a psychoacoustic and pupillometric study

Morrison M Steel, Blake C Papsin, Karen A Gordon, Morrison M Steel, Blake C Papsin, Karen A Gordon

Abstract

Bilateral cochlear implants aim to provide hearing to both ears for children who are deaf and promote binaural/spatial hearing. Benefits are limited by mismatched devices and unilaterally-driven development which could compromise the normal integration of left and right ear input. We thus asked whether children hear a fused image (ie. 1 vs 2 sounds) from their bilateral implants and if this "binaural fusion" reduces listening effort. Binaural fusion was assessed by asking 25 deaf children with cochlear implants and 24 peers with normal hearing whether they heard one or two sounds when listening to bilaterally presented acoustic click-trains/electric pulses (250 Hz trains of 36 ms presented at 1 Hz). Reaction times and pupillary changes were recorded simultaneously to measure listening effort. Bilaterally implanted children heard one image of bilateral input less frequently than normal hearing peers, particularly when intensity levels on each side were balanced. Binaural fusion declined as brainstem asymmetries increased and age at implantation decreased. Children implanted later had access to acoustic input prior to implantation due to progressive deterioration of hearing. Increases in both pupil diameter and reaction time occurred as perception of binaural fusion decreased. Results indicate that, without binaural level cues, children have difficulty fusing input from their bilateral implants to perceive one sound which costs them increased listening effort. Brainstem asymmetries exacerbate this issue. By contrast, later implantation, reflecting longer access to bilateral acoustic hearing, may have supported development of auditory pathways underlying binaural fusion. Improved integration of bilateral cochlear implant signals for children is required to improve their binaural hearing.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Fig 1. Age at CI-1 and pre-implant…
Fig 1. Age at CI-1 and pre-implant hearing.
Children who were implanted at later ages (n = 15) had better residual hearing (ie. lower aided thresholds) at 250 Hz when assessed with standard audiometric testing prior to implantation (R = -0.50, p = 0.026). This relationship is was also present at 500 Hz (R = -0.50, p = 0.013), but not 1000 Hz (R = -0.28, p = 0.23), 2000 Hz (R = -0.01, p = 0.97), or 4000 Hz (R = 0.15, p = 0.57).
Fig 2. Schematic diagrams of experimental conditions.
Fig 2. Schematic diagrams of experimental conditions.
a: Bilateral level cues were presented by either holding stimulus levels constant in the left normal ear/CI-2 and increasing level in the right normal ear/CI-1 or the reverse. Increases in stimulus level are represented by the size of the circle. The circles are fairly small as levels were presented at threshold levels (T) or slightly above (T+10 or 20 dB or CU). Unilateral control conditions were also presented (T+10 in either right ear/CI-1 or left ear/CI-2 with 0 in the opposite side). Mean (±1 SD) cochlear implant unilateral stimulation levels (T+10 in each ear) and presented ILDs are shown. b) Bilateral input containing interaural/implant timing differences are shown. These were presented from e20 on both implants at levels which were comfortably loud and behaviorally balanced as shown by the larger circles at the apical end of the schematic cochlear implant array. c) Bilateral input presented at different places along the electrode array (for CI users only). Levels were comfortably loud and behaviorally balanced. The presentations were simultaneous (ITD = 0).
Fig 3. Mean (± 1SE) proportions of…
Fig 3. Mean (± 1SE) proportions of 1 response across all conditions are shown by the black bars.
Overall CI listeners (n = 25 perceived 1 sound less frequency than NH peers (n = 24; p

Fig 4. Fusion with interaural level differences.

Fig 4. Fusion with interaural level differences.

a) Group performance for conditions containing ILDs (ITD…

Fig 4. Fusion with interaural level differences.
a) Group performance for conditions containing ILDs (ITD = 0 ms). Biphasic pulses were delivered from electrode 20 in the CI group (n = 25). CI listeners consistently perceived one image when there were level differences, albeit less frequently than NH peers (n = 24; p 0.05). For CI users, the majority of curves tend to decrease as a function of increasing ILD. Significant slopes (n = 3) are represented by dark grey solid lines.

Fig 5. Fusion with interaural timing differences.

Fig 5. Fusion with interaural timing differences.

a) Mean responses in children with normal hearing…

Fig 5. Fusion with interaural timing differences.
a) Mean responses in children with normal hearing (n = 24) and cochlear implants (n = 25) for conditions with varying ITDs (interaural/implant timing differences). Balanced stimuli presented for ITD-varying trials in the CI group contained a small mean ILD of-0.34 ± 0.90 dB. Children with normal hearing were more likely to hear two separate sounds as the ITD increased to ±2 ms (p 0.05). Negative values denote R/CI-1 leading ITDs. b) Individual regression functions are plotted across ITDs ranging from-2 to 2 ms. As shown in the bottom plot, ITDs did not affect fusion in 24/25 CI users (p > 0.05).

Fig 6. Fusion with interaural place of…

Fig 6. Fusion with interaural place of stimulation differences.

a) Mean responses in the CI…

Fig 6. Fusion with interaural place of stimulation differences.
a) Mean responses in the CI group (n = 25) are displayed as a function of increasing difference in the place of stimulation (IPlD) between sides. Place of stimulation was held constant at electrode 20 on one side while pulses were delivered from more basal electrodes on the contralateral side (electrode 16 for IPlD = 4 and electrode 9 for IPlD = 11). b) IPlDs did not affect fusion in 16/25 children with CIs (p > 0.05).

Fig 7. Predicting binaural fusion.

Multiple regression…

Fig 7. Predicting binaural fusion.

Multiple regression analysis revealed that mean proportion of 1 response…

Fig 7. Predicting binaural fusion.
Multiple regression analysis revealed that mean proportion of 1 response for individual CI users (n = 24) when level and place differences were absent can be predicted (p 0.05).

Fig 8. Fusion and reaction time.

a)…

Fig 8. Fusion and reaction time.

a) Mean overall RTs (reaction times) and RTs for…

Fig 8. Fusion and reaction time.
a) Mean overall RTs (reaction times) and RTs for each subset of conditions (ILDs = interaural/implant level differences; ITDs = interaural/implant timing differences; IPlDs = interaural/implant place of stimulation differences) are displayed for both groups. CI users (n = 24) had longer RTs than their peers with NH (n = 24; p 0.05).

Fig 9. Fusion and pupil diameter.

a)…

Fig 9. Fusion and pupil diameter.

a) Mean PCPD (percent of change in pupillary diameter)…

Fig 9. Fusion and pupil diameter.
a) Mean PCPD (percent of change in pupillary diameter) is shown for each group. Children with bilateral CIs (n = 21) had greater changes in pupillary diameter than their NH peers (n = 19; p 0.05).

Fig 10. Reaction time and pupil diameter.

Fig 10. Reaction time and pupil diameter.

Mean overall pupillary responses were positively correlated with…

Fig 10. Reaction time and pupil diameter.
Mean overall pupillary responses were positively correlated with RTs (R = 0.69, p
All figures (10)
Similar articles
Cited by
References
    1. Gordon KA, Valero J, Papsin BC (2007) Binaural processing in children using bilateral cochlear implants. Neuroreport 18: 613–617. - PubMed
    1. Gordon KA, Valero J, van Hoesel R, Papsin BC (2008) Abnormal timing delays in auditory brainstem responses evoked by bilateral cochlear implant use in children. Otol Neurotol 29: 193–198. 10.1097/mao.0b013e318162514c - DOI - PubMed
    1. Gordon KA, Jiwani S, Papsin BC (2011) What is the optimal timing for bilateral cochlear implantation in children? Cochlear Implants Int 12: S8–S14. 10.1179/146701011X13074645127199 - DOI - PubMed
    1. Gordon KA, Salloum C, Toor GS, van Hoesel R, Papsin BC (2012) Binaural interactions develop in the auditory brainstem of children who are deaf: effects of place and level of bilateral electrical stimulation. J Neurosci 32: 4212–4223. 10.1523/JNEUROSCI.5741-11.2012 - DOI - PMC - PubMed
    1. Gordon KA, Wong DD, Papsin BC (2010) Cortical function in children receiving bilateral cochlear implants simultaneously or after a period of interimplant delay. Otol Neurotol 31: 1293–1299. 10.1097/MAO.0b013e3181e8f965 - DOI - PubMed
Show all 120 references
Publication types
MeSH terms
Related information
[x]
Cite
Copy Download .nbib
Format: AMA APA MLA NLM
Fig 4. Fusion with interaural level differences.
Fig 4. Fusion with interaural level differences.
a) Group performance for conditions containing ILDs (ITD = 0 ms). Biphasic pulses were delivered from electrode 20 in the CI group (n = 25). CI listeners consistently perceived one image when there were level differences, albeit less frequently than NH peers (n = 24; p 0.05). For CI users, the majority of curves tend to decrease as a function of increasing ILD. Significant slopes (n = 3) are represented by dark grey solid lines.
Fig 5. Fusion with interaural timing differences.
Fig 5. Fusion with interaural timing differences.
a) Mean responses in children with normal hearing (n = 24) and cochlear implants (n = 25) for conditions with varying ITDs (interaural/implant timing differences). Balanced stimuli presented for ITD-varying trials in the CI group contained a small mean ILD of-0.34 ± 0.90 dB. Children with normal hearing were more likely to hear two separate sounds as the ITD increased to ±2 ms (p 0.05). Negative values denote R/CI-1 leading ITDs. b) Individual regression functions are plotted across ITDs ranging from-2 to 2 ms. As shown in the bottom plot, ITDs did not affect fusion in 24/25 CI users (p > 0.05).
Fig 6. Fusion with interaural place of…
Fig 6. Fusion with interaural place of stimulation differences.
a) Mean responses in the CI group (n = 25) are displayed as a function of increasing difference in the place of stimulation (IPlD) between sides. Place of stimulation was held constant at electrode 20 on one side while pulses were delivered from more basal electrodes on the contralateral side (electrode 16 for IPlD = 4 and electrode 9 for IPlD = 11). b) IPlDs did not affect fusion in 16/25 children with CIs (p > 0.05).
Fig 7. Predicting binaural fusion.
Fig 7. Predicting binaural fusion.
Multiple regression analysis revealed that mean proportion of 1 response for individual CI users (n = 24) when level and place differences were absent can be predicted (p 0.05).
Fig 8. Fusion and reaction time.
Fig 8. Fusion and reaction time.
a) Mean overall RTs (reaction times) and RTs for each subset of conditions (ILDs = interaural/implant level differences; ITDs = interaural/implant timing differences; IPlDs = interaural/implant place of stimulation differences) are displayed for both groups. CI users (n = 24) had longer RTs than their peers with NH (n = 24; p 0.05).
Fig 9. Fusion and pupil diameter.
Fig 9. Fusion and pupil diameter.
a) Mean PCPD (percent of change in pupillary diameter) is shown for each group. Children with bilateral CIs (n = 21) had greater changes in pupillary diameter than their NH peers (n = 19; p 0.05).
Fig 10. Reaction time and pupil diameter.
Fig 10. Reaction time and pupil diameter.
Mean overall pupillary responses were positively correlated with RTs (R = 0.69, p
All figures (10)

References

    1. Gordon KA, Valero J, Papsin BC (2007) Binaural processing in children using bilateral cochlear implants. Neuroreport 18: 613–617.
    1. Gordon KA, Valero J, van Hoesel R, Papsin BC (2008) Abnormal timing delays in auditory brainstem responses evoked by bilateral cochlear implant use in children. Otol Neurotol 29: 193–198. 10.1097/mao.0b013e318162514c
    1. Gordon KA, Jiwani S, Papsin BC (2011) What is the optimal timing for bilateral cochlear implantation in children? Cochlear Implants Int 12: S8–S14. 10.1179/146701011X13074645127199
    1. Gordon KA, Salloum C, Toor GS, van Hoesel R, Papsin BC (2012) Binaural interactions develop in the auditory brainstem of children who are deaf: effects of place and level of bilateral electrical stimulation. J Neurosci 32: 4212–4223. 10.1523/JNEUROSCI.5741-11.2012
    1. Gordon KA, Wong DD, Papsin BC (2010) Cortical function in children receiving bilateral cochlear implants simultaneously or after a period of interimplant delay. Otol Neurotol 31: 1293–1299. 10.1097/MAO.0b013e3181e8f965
    1. Gordon KA, Wong DD, Papsin BC (2013) Bilateral input protects the cortex from unilaterally-driven reorganization in children who are deaf. Brain 136: 1609–1625. 10.1093/brain/awt052
    1. Jiwani S, Papsin BC, Gordon KA (2013) Central auditory development after long-term cochlear implant use. Clin Neurophysiol 124: 1868–1880. 10.1016/j.clinph.2013.03.023
    1. Litovsky RY, Parkinson A, Arcaroli J, Peters R, Lake J, et al. (2004) Bilateral cochlear implants in adults and children. Arch Otolaryngol Head Neck Surg 130: 648–655.
    1. Litovsky RY, Johnstone PM, Godar S, Agrawal S, Parkinson A, et al. (2006) Bilateral cochlear implants in children: localization acuity measured with minimum audible angle. Ear Hear 27: 43–59.
    1. Litovsky RY, Goupell MJ, Godar S, Grieco-Calub T, Jones GL, et al. (2012) Studies on bilateral cochlear implants at the University of Wisconsin’s Binaural Hearing and Speech Laboratory. J Am Acad Audiol 23: 476–494. 10.3766/jaaa.23.6.9
    1. Van Deun L, van Wieringen A, Francart T, Scherf F, Dhooge IJ, et al. (2009) Bilateral cochlear implants in children: binaural unmasking. Audiol Neurootol 14: 240–247. 10.1159/000190402
    1. Van Deun L, van Wieringen A, Scherf F, Deggouj N, Desloovere C, et al. (2010) Earlier intervention leads to better sound localization in children with bilateral cochlear implants. Audiol Neurootol 15: 7–17. 10.1159/000218358
    1. Van Deun L, van Wieringen A, Wouters J (2010) Spatial speech perception benefits in young children with normal hearing and cochlear implants. Ear Hear 31: 702–713. 10.1097/AUD.0b013e3181e40dfe
    1. Grieco-Calub TM, Litovsky RY (2010) Sound localization skills in children who use bilateral cochlear implants and in children with normal acoustic hearing. Ear Hear 31: 645–656. 10.1097/AUD.0b013e3181e50a1d
    1. Salloum CA, Valero J, Wong DD, Papsin BC, van Hoesel R, et al. (2010) Lateralization of interimplant timing and level differences in children who use bilateral cochlear implants. Ear Hear 31: 441–456. 10.1097/AUD.0b013e3181d4f228
    1. Chadha NK, Papsin BC, Jiwani S, Gordon KA (2011) Speech detection in noise and spatial unmasking in children with simultaneous versus sequential bilateral cochlear implants. Otol Neurotol 32: 1057–1064. 10.1097/MAO.0b013e3182267de7
    1. Burkholder RA, Pisoni DB (2003) Speech timing and working memory in profoundly deaf children after cochlear implantation. J Exp Child Psychol 85: 63–88.
    1. Hughes KC, Galvin KL (2013) Measuring listening effort expended by adolescents and young adults with unilateral or bilateral cochlear implants or normal hearing. Cochlear Implants Int, 14: 121–129. 10.1179/1754762812Y.0000000009
    1. Nadol JB Jr (1997) Patterns of neural degeneration in the human cochlea and auditory nerve: implications for cochlear implantation. Otolaryngol Head Neck Surg 117: 220–228.
    1. D’Elia A, Bartoli R, Giagnotti F, Quaranta N (2012) The role of hearing preservation on electrical thresholds and speech performances in cochlear implantation. Otol Neurotol, 33: 343–347. 10.1097/MAO.0b013e3182487dbb
    1. Rubinstein JT, Hong R (2003) Signal coding in cochlear implants: exploiting stochastic effects of electrical stimulation. Ann Otol Rhinol Laryngol Suppl 191: 14–19.
    1. Rubinstein JT (2004) How cochlear implants encode speech. Curr Opin Otolaryngol Head Neck Surg 12: 444–448.
    1. Poon BB, Eddington DK, Noel V, Colburn HS (2009) Sensitivity to interaural time difference with bilateral cochlear implants: Development over time and effect of interaural electrode spacing. J Acoust Soc Am 126: 806–815. 10.1121/1.3158821
    1. Kan A, Stoelb C, Litovsky RY, Goupell MJ (2013) Effect of mismatched place-of-stimulation on binaural fusion and lateralization in bilateral cochlear-implant users. J Acoust Soc Am 134: 2923–2936. 10.1121/1.4820889
    1. Furst M, Levine RA, McGaffigan PM (1985) Click lateralization is related to the beta component of the dichotic brainstem auditory evoked potentials of human subjects. J Acoust Soc Am 78: 1644–1651.
    1. Wightman FL, Kistler DJ (1992) The dominant role of low-frequency interaural time differences in sound localization. J Acoust Soc Am 91: 1648–1661.
    1. Seeber BU, Fastl H (2008) Localization cues with bilateral cochlear implants. J Acoust Soc Am 123: 1030–1042. 10.1121/1.2821965
    1. Van Deun L, van Wieringen A, Van den Bogaert T, Scherf F, Offeciers FE, et al. (2009) Sound localization, sound lateralization, and binaural masking level differences in young children with normal hearing. Ear Hear 30: 178–190. 10.1097/AUD.0b013e318194256b
    1. Babkoff H, Sutton S (1966) End point of lateralization for dichotic clicks. J Acoust Soc Am 39: 87–102.
    1. Colburn HS (1977) Theory of binaural interaction based on auditory-nerve data. II. Detection of tones in noise. J Acoust Soc Am 61: 525–533.
    1. Sayers BM, Cherry EC (1957) Mechanism of binaural fusion in the hearing of speech. J Acoust Soc Am 29: 973–987.
    1. Carr CE, Konishi M (1990) A circuit for detection of interaural time differences in the brain stem of the barn owl. J Neurosci 10: 3227–3246.
    1. Jeffress LA (1948) A place theory of sound localization. J Comp Physiol Psychol 41: 35–39.
    1. Colburn HS (2006) The perceptual consequences of binaural hearing. Int J Audiol 45: S34–S44.
    1. Breebaart J, van de Par S, Kohlrausch A (2001) Binaural processing model based on contralateral inhibition. I. Model structure. J Acoust Soc Am 110: 1074–1088.
    1. McAlpine D, Jiang D, Palmer AR (2001) A neural code for low-frequency sound localization in mammals. Nat Neurosci 4: 396–401.
    1. Goupell MJ, Stoelb C, Kan A, Litovsky RY (2013) Effect of mismatched place-of-stimulation on the salience of binaural cues in conditions that simulate bilateral cochlear-implant listening. J Acoust Soc Am 133: 2272–2287. 10.1121/1.4792936
    1. Zhou J, Durrant JD (2003) Effects of interaural frequency difference on binaural fusion evidenced by electrophysiological versus psychoacoustical measures. J Acoust Soc Am 114: 1508–1515.
    1. McPherson DL, Starr A (1995) Auditory time-intensity cues in the binaural interaction component of the auditory evoked potentials. Hear Res 89: 162–171.
    1. Smith ZM, Delgutte B (2007) Using evoked potentials to match interaural electrode pairs with bilateral cochlear implants. J Assoc Res Otolaryngol 8: 134–151.
    1. Riedel H, Kollmeier B (2006) Interaural delay-dependent changes in the binaural difference potential of the human auditory brain stem response. Hear Res 218: 5–19.
    1. Dobie RA, Norton SJ (1980) Binaural interaction in human auditory evoked potentials. Electroencephalogr Clin Neurophysiol 49: 303–313.
    1. Wada S, Starr A (1989) Anatomical bases of binaural interaction in auditory brain-stem responses from guinea pig. Electroencephalogr Clin Neurophysiol 72: 535–544.
    1. Krumbholz K, Schonwiesner M, Rubsamen R, Zilles K, Fink GR, et al. (2005) Hierarchical processing of sound location and motion in the human brainstem and planum temporale. Eur J Neurosci 21: 230–238.
    1. Chermak GD, Lee J (2005) Comparison of children’s performance on four tests of temporal resolution. J Am Acad Audiol 16: 554–563.
    1. Fiedler A, Schroter H, Seibold VC, Ulrich R (2011) The influence of dichotical fusion on the redundant signals effect, localization performance, and the mismatch negativity. Cogn Affect Behav Neurosci 11: 68–84. 10.3758/s13415-010-0013-y
    1. Mickey BJ, Middlebrooks JC (2001) Responses of auditory cortical neurons to pairs of sounds: correlates of fusion and localization. J Neurophysiol 86: 1333–1350.
    1. Terayama Y, Kaneko Y, Kawamoto K, Sakai N (1977) Ultrastructural changes of the nerve elements following disruption of the organ of Corti. I. Nerve elements in the organ of Corti. Acta Otolaryngol 83: 291–302.
    1. Schwartz IR, Higa JF (1982) Correlated studies of the ear and brainstem in the deaf white cat: changes in the spiral ganglion and the medial superior olivary nucleus. Acta Otolaryngol 93: 9–18.
    1. Tirko NN, Ryugo DK (2012) Synaptic plasticity in the medial superior olive of hearing, deaf, and cochlear-implanted cats. J Comp Neurol 520: 2202–2217. 10.1002/cne.23038
    1. Gordon KA, Papsin BC, Harrison RV (2006) An evoked potential study of the developmental time course of the auditory nerve and brainstem in children using cochlear implants. Audiol Neurotol 11: 7–23.
    1. Hancock KE, Noel V, Ryugo DK, Delgutte B (2010) Neural coding of interaural time differences with bilateral cochlear implants: effects of congenital deafness. J Neurosci, 30: 14068–14079. 10.1523/JNEUROSCI.3213-10.2010
    1. Tillein J, Hubka P, Syed E, Hartmann R, Engel AK, et al. (2010) Cortical representation of interaural time difference in congenital deafness. Cereb Cortex 20: 492–506. 10.1093/cercor/bhp222
    1. Rauschecker JP (1999) Auditory cortical plasticity: a comparison with other sensory systems. Trends Neurosci 22: 74–80.
    1. Eisenberg LS (2007) Current state of knowledge: speech recognition and production in children with hearing impairment. Ear Hear 28: 766–772.
    1. Kral A (2007) Unimodal and cross-modal plasticity in the ‘deaf’ auditory cortex. Int J Audiol 46: 479–493.
    1. Lomber SG, Meredith MA, Kral A (2010) Cross-modal plasticity in specific auditory cortices underlies visual compensations in the deaf. Nat Neurosci 13: 1421–1427. 10.1038/nn.2653
    1. Lee DS, Lee JS, Oh SH, Kim SK, Kim JW, et al. (2001) Cross-modal plasticity and cochlear implants. Nature 409: 149–150.
    1. Meredith MA, Lomber SG (2011) Somatosensory and visual crossmodal plasticity in the anterior auditory field of early-deaf cats. Hear Res 280: 38–47. 10.1016/j.heares.2011.02.004
    1. Cheng AK, Grant GD, Niparko JK (1999) Meta-analysis of pediatric cochlear implant literature. Ann Otol Rhinol Laryngol Suppl 177: 124–128.
    1. Kirk KI, Hill-Brown C (1985) Speech and language results in children with a cochlear implant. Ear Hear 6: 36S–47S.
    1. Miyamoto RT, Kirk KI, Robbins AM, Todd S, Riley A (1996) Speech perception and speech production skills of children with multichannel cochlear implants. Acta Otolaryngol 116: 240–243.
    1. Hopyan T, Gordon KA, Papsin BC (2011) Identifying emotions in music through electrical hearing in deaf children using cochlear implants. Cochlear Implants Int 12: 21–26. 10.1179/146701010X12677899497399
    1. Steel MM, Abbasalipour P, Salloum CAM, Hasek D, Papsin BC, et al. (In press) Unilateral cochlear implant use promotes normal-like loudness perception in adolescents with childhood deafness. Ear Hear.
    1. Papsin BC, Gordon KA (2008) Bilateral cochlear implants should be the standard for children with bilateral sensorineural deafness. Curr Opin Otolaryngol Head Neck Surg, 16: 69–74. 10.1097/MOO.0b013e3282f5e97c
    1. Lieu JE (2004) Speech-language and educational consequences of unilateral hearing loss in children. Arch Otolaryngol Head Neck Surg 130: 524–530.
    1. Giolas TG, Wark DJ (1967) Communication problems associated with unilateral hearing loss. J Speech Hear Disord 32: 336–343.
    1. van Hoesel RJ, Tyler RS (2003) Speech perception, localization, and lateralization with bilateral cochlear implants. J Acoust Soc Am 113: 1617–1630.
    1. van Hoesel RJ (2004) Exploring the benefits of bilateral cochlear implants. Audiol Neurootol 9: 234–246.
    1. van Hoesel RJ (2007) Sensitivity to binaural timing in bilateral cochlear implant users. J Acoust Soc Am 121: 2192–2206.
    1. Litovsky RY, Jones GL, Agrawal S, van Hoesel R (2010) Effect of age at onset of deafness on binaural sensitivity in electric hearing in humans. J Acoust Soc Am 127: 400–414. 10.1121/1.3257546
    1. Grantham DW, Ashmead DH, Ricketts TA, Labadie RF, Haynes DS (2007) Horizontal-plane localization of noise and speech signals by postlingually deafened adults fitted with bilateral cochlear implants. Ear Hear 28: 524–541.
    1. Aronoff JM, Yoon YS, Freed DJ, Vermiglio AJ, Pal I, et al. (2010) The use of interaural time and level difference cues by bilateral cochlear implant users J Acoust Soc Am, 127: 87–92.
    1. Mok M, Galvin KL, Dowell RC, McKay CM (2007) Spatial unmasking and binaural advantage for children with normal hearing, a cochlear implant and a hearing aid, and bilateral implants. Audiol Neurootol 12: 295–306.
    1. Galvin KL, Mok M, Dowell RC (2007) Perceptual benefit and functional outcomes for children using sequential bilateral cochlear implants. Ear Hear 28: 470–482.
    1. Grieco-Calub TM, Litovsky RY, Werner LA (2008) Using the observer-based psychophysical procedure to assess localization acuity in toddlers who use bilateral cochlear implants. Otol Neurotol 29: 235–239. 10.1097/mao.0b013e31816250fe
    1. Gordon KA, Papsin BC (2009) Benefits of short interimplant delays in children receiving bilateral cochlear implants. Otol Neurotol, 30: 319–331. 10.1097/MAO.0b013e31819a8f4c
    1. Finley CC, Holden TA, Holden LK, Whiting BR, Chole RA, et al. (2008). Role of electrode placement as a contributor to variability in cochlear implant outcomes. Otol Neurotol 29: 920–928. 10.1097/MAO.0b013e318184f492
    1. Long CJ, Eddington DK, Colburn HS, Rabinowitz WM (2003) Binaural sensitivity as a function of interaural electrode position with a bilateral cochlear implant user. J Acoust Soc Am 114: 1565–1574.
    1. Hartmann WM, Constan ZA (2002) Interaural level differences and the level-meter model. J Acoust Soc Am 112: 1037–1045.
    1. Gordon KA, Twitchell KA, Papsin BC, Harrison RV (2001) Effect of residual hearing prior to cochlear implantation on speech perception in children. J Otolaryngol 30: 216–223.
    1. Brand A, Behrend O, Marquardt T, McAlpine D, Grothe B (2002) Precise inhibition is essential for microsecond interaural time difference coding. Nature 41: 543–547.
    1. Gordon KA, Jiwani S, Papsin BC (2013) Benefits and detriments of unilateral cochlear implant use on bilateral auditory development in children who are deaf. Front Psychol, 4: 1–14. 10.3389/fpsyg.2013.00001
    1. Kahneman D (2003) A perspective on judgment and choice: mapping bounded rationality. Am Psychol 58: 697–720.
    1. Baddeley A (2012) Working memory: theories, models, and controversies. Annu Rev Psychol 63: 1–29. 10.1146/annurev-psych-120710-100422
    1. Kahneman DL, Beatty J (1967) Pupillary responses in a pitch-discrimination task. Percept Psychophys 2: 101–105.
    1. Baskent D (2012) Effect of speech degradation on top-down repair: phonemic restoration with simulations of cochlear implants and combined electric-acoustic stimulation. J Assoc Res Otolaryngol 13: 683–692. 10.1007/s10162-012-0334-3
    1. Hicks CB, Tharpe AM (2002) Listening effort and fatigue in school-age children with and without hearing loss. J Speech Lang Hear Res 45: 573–584.
    1. Pals C, Sarampalis A, Baskent D (2013) Listening effort with cochlear implant simulations. J Speech Lang Hear Res 56: 1075–1084. 10.1044/1092-4388(2012/12-0074)
    1. Shepherd RK, Hardie NA (2001) Deafness-induced changes in the auditory pathway: implications for cochlear implants. Audiol Neurootol 6: 305–318.
    1. Tremblay KL, Shahin AJ, Picton T, Ross B (2009) Auditory training alters the physiological detection of stimulus-specific cues in humans. Clin Neurophysiol 120: 128–135. 10.1016/j.clinph.2008.10.005
    1. Kraus N, Chandrasekaran B (2010) Music training for the development of auditory skills. Nat Rev Neurosci 11: 599–605. 10.1038/nrn2882
    1. Ponton CW, Eggermont JJ, Kwong B, Don M (2000) Maturation of human central auditory system activity: evidence from multi-channel evoked potentials. Clin Neurophysiol, 111: 220–236.
    1. Eggermont JJ, Ponton CW (2003) Auditory-evoked potential studies of cortical maturation in normal hearing and implanted children: correlations with changes in structure and speech perception. Acta Otolaryngol 123: 249–252.
    1. Naito Y, Tateya I, Fujiki N, Hirano S, Ishizu K, et al. (2000) Increased cortical activation during hearing of speech in cochlear implant users. Hear Res 143: 139–146.
    1. Limb CJ, Molloy AT, Jiradejvong P, Braun AR (2010) Auditory cortical activity during cochlear implant-mediated perception of spoken language, melody, and rhythm. J Assoc Res Otolaryngol 11: 133–143. 10.1007/s10162-009-0184-9
    1. Steinhauer SR, Siegle GJ, Condray R, Pless M (2004) Sympathetic and parasympathetic innervation of pupillary dilation during sustained processing. Int J Psychophysiol 52: 77–86.
    1. Kahneman D, Tursky B, Shapiro D, Crider A (1969) Pupillary, heart rate, and skin resistance changes during a mental task. J Exp Psychol 79: 164–167.
    1. Darwin C (1965) The expression of the emotions in man and animals. Chicago, IL: University of Chicago Press.
    1. Hess EH, Polt JM (1964) Pupil Size in Relation to Mental Activity during Simple Problem-Solving. Science 143: 1190–1192.
    1. Privitera CM, Renninger LW, Carney T, Klein S, Aguilar M (2010) Pupil dilation during visual target detection. J Vis 10: 1–14. 10.1167/10.13.1
    1. Takeuchi T, Puntous T, Tuladhar A, Yoshimoto S, Shirama A (2011) Estimation of mental effort in learning visual search by measuring pupil response. PLoS One 6: 1–5.
    1. Papesh MH, Goldinger SD, Hout MC (2012) Memory strength and specificity revealed by pupillometry. Int J Psychophysiol 83: 56–64. 10.1016/j.ijpsycho.2011.10.002
    1. Beatty J (1982) Task-evoked pupillary responses, processing load, and the structure of processing resources. Psychol Bull 91: 276–292.
    1. Beatty J (1982) Phasic not tonic pupillary responses vary with auditory vigilance performance. Psychophysiology 19: 167–172.
    1. Zekveld AA, Kramer SE, Festen JM (2010) Pupil response as an indication of effortful listening: the influence of sentence intelligibility. Ear Hear 31: 480–490. 10.1097/AUD.0b013e3181d4f251
    1. Yulek F, Konukseven OO, Cakmak HB, Orhan N, Simsek S, et al. (2008) Comparison of the pupillometry during videonystagmography in asymmetric pseudoexfoliation patients. Curr Eye Res 33: 263–267. 10.1080/02713680801915284
    1. Gordon KA, Papsin BC, Harrison RV (2004) Toward a battery of behavioral and objective measures to achieve optimal cochlear implant stimulation levels in children. Ear Hear 25: 447–463.
    1. Harrison RV, Gordon KA, Mount RJ (2005) Is there a critical period for cochlear implantation in congenitally deaf children? Analyses of hearing and speech perception performance after implantation. Dev Psychobiol 46: 252–261.
    1. Smith ZM, Delgutte B, Oxenham AJ (2002) Chimaeric sounds reveal dichotomies in auditory perception. Nature 416: 87–90.
    1. Hopyan T, Peretz I, Chan LP, Papsin BC, Gordon KA (2012) Children using cochlear implants capitalize on acoustical hearing for music perception. Front Psychol 3: 1–9. 10.3389/fpsyg.2012.00001
    1. Rubinstein JT, Parkinson WS, Tyler RS, Gantz BJ (1999) Residual speech recognition and cochlear implant performance: effects of implantation criteria. Am J Otol 20: 445–452
    1. Jung KH, Won JH, Drennan WR, Jameyson E, Miyasaki G, et al. (2012) Psychoacoustic performance and music and speech perception in prelingually deafened children with cochlear implants. Audiol Neurootol 17: 189–197. 10.1159/000336407
    1. Moore MJ, Caspary DM (1983) Strychnine blocks binaural inhibition in lateral superior olivary neurons. J Neurosci 3: 237–242.
    1. Gordon KA, Deighton M, Abbasalipour P, Papsin BC (In press) Perception of binaural cues develops in children who are deaf through bilateral cochlear implantation. PLOS ONE. 10.1371/journal.pone.0116463
    1. Litovsky RY, Colburn HS, Yost WA, Guzman SJ (1999) The precedence effect. J Acoust Soc Am 106: 1633–1654.
    1. Aharonson V, Furst M (2001) A model for sound lateralization. J Acoust Soc Am 109: 2840–2851.
    1. Casey BJ, Galvan A, Hare TA (2005) Changes in cerebral functional organization during cognitive development. Curr Opin Neurobiol 15: 239–244.
    1. Casey BJ, Tottenham N, Fossella J (2002) Clinical, imaging, lesion, and genetic approaches toward a model of cognitive control. Dev Psychobiol 40: 237–254.
    1. Gordon KA, Tanaka S, Papsin BC (2005) Atypical cortical responses underlie poor speech perception in children using cochlear implants. Neuroreport 16: 2041–2045.

Source: PubMed

3
購読する