Graeme Clark Collection

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    Short-term auditory memory in children using cochlear implants and its relevance to receptive language
    Dawson, P. W. ; Busby, P. A. ; McKay, C. M. ; Clark, Graeme M. ( 2002)
    The aim of this study was to assess auditory sequential, short-term memory (SSTM) performance in young children using cochlear implants (CI group) and to examine the relationship of this performance to receptive language performance. Twenty-four children, 5 to 11 years old, using the Nucleus 22-electrode cochlear implant, were tested on a number of auditory and visual tasks of SSTM. The auditory memory tasks were designed to minimize the effect of auditory discrimination ability. Stimuli were chosen that children with cochlear implants could accurately identify with a reaction time similar to that of a control group of children with normal hearing (NH group). All children were also assessed on a receptive language test and on a nonverbal intelligence scale. As expected, children using cochlear implants demonstrated poorer auditory and visual SSTM skills than their hearing peers when the stimuli were verbal or were pictures that could be readily labelled. They did not differ from their peers with normal hearing on tasks where the stimuli were less likely to be verbally encoded. An important finding was that the CI group did not appear to have a sequential memory deficit specific to the auditory modality. The difference scores (auditory minus visual memory performance) for the CI group were not significantly different from those for the NH group. SSTM performance accounted for significant variance in the receptive language performance of the CI group. However, a forward stepwise regression analysis revealed that visual spatial memory (one of the subtests of the nonverbal IQ test) was the main predictor of variance in the language scores of the children using cochlear implants.
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    The development of speech perception in children using cochlear implants: effects of etiologic factors and delayed milestones
    PYMAN, BRIAN ; Blamey, Peter J. ; Lacy, Peter ; Clark, Graeme M. ; DOWELL, RICHARD ( 2000)
    Hypothesis: Speech perception outcomes for cochlear implantation of children vary over a wide range, and it is hypothesized that central pathologic states associated with certain causes of hearing impairment account for a substantial part of the variance. Study Design: A retrospective analysis was carried out to ascertain the relationships between speech perception, etiologic factors, and central pathologic states as indicated by preoperative delayed motor milestones and/or cognitive delays. Setting: Data were obtained from the pre-and postoperative records of patients attending a hospital cochlear implant clinic. Patients: Results for 75 consecutive patients up to age 5 years who underwent implantation were included in the study. Intervention: Patients received a 22-electrode cochlear prosthesis and were seen by the clinic for regular tune-up and assessments. Home-and school-based habilitation was recommended by the clinic. Main Outcome Measures: Speech perception measures were classified on a five-point scale to allow for different evaluation procedures at different ages and developmental stages. Results: The incidence of motor and cognitive delays were fairly evenly spread across etiologic factors, except for cytomegalovirus, which had a much higher than average incidence. Children with motor and/or cognitive delays were significantly slower than other children in the development of speech perception skills after implantation. Etiologic factors did not have a statistically significant effect on speech perception outcome. Conclusions: It is likely that central pathologic states account for a substantial part of the variance among children using cochlear implants. Specific indicators of central pathologic states should be used to assess a child's prognosis in preference to less specific information based on etiologic factors alone.
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    Building the bionic ear
    Clark, Graeme M. ( 2000)
    When I began my cochlear-implant research in 1967, one could do nothing to help profoundly deaf people hear. In normal hearing, hair cells in the cochlea, the snail-shaped inner ear, transduce sound vibrations into electrical signals. These signals produce patterns of electrical responses in the auditory pathways that convey the frequency and intensity of the sound to the brain. The profoundly deaf, however, have lost their hair cells, so even amplifying sound with a hearing aid fails to transmit information that the brain can interpret as sound.