Skip to main content

Audiology Masterclass Series 2022

This series of lectures will be expanded as new episodes are scheduled.
A teacher with her reading material

Selecting an option will move you to a different section of the page.

Key Details

Categories
Masterclass Series
Course Code
CPE22MC-AUD
Start Date
31 May 2022
Time
9:00 am – 10:00 am

Course Information

Audiology Masterclass Series 2022

Session 1: Why music is a powerful (re)habilitation tool for children who are deaf and hard-of-hearing

Presented by: Chi Lo

Recorded and available for viewing

This presentation explores the benefits of music for children who are deaf and hard-of-hearing (DHH). Music is often viewed as a higher-order auditory activity which may serve as a barrier to participation. However, this workshop will explore how music is a rich and powerful multi-modal activity, and participation has broad benefits for the brain, and specific benefits for DHH children.


Session 2 (2 parts) Genetic testing for hearing loss - clinical utility and latest developments

Presented by: Mona Saleh and Radhika Rajkumar

Recorded and available for viewing

Did you know that 50% of hearing loss has a genetic basis1? Genetic causes include over 100 genes associated with non-syndromic hearing loss and over 400 syndromic conditions that can include hearing loss as well as other malformations and medical problems. Syndromic and non-syndromic deafness are genetically heterogeneous disorders characterized by mild to profound deafness in early adulthood, childhood, or infancy. The genetic heterogeneity associated with these conditions can make it difficult to use phenotype as the sole criterion to select a definitive cause.

Understanding the cause of hearing loss can be empowering and beneficial to both a child and their family by confirming a diagnosis, helping guide treatment and management decisions and enabling early interventions to maximise speech and learning potential. Identification of a disease-causing variant can also inform recurrence-risk assessment and genetic counselling.

With technical advances and incorporation of genomics into routine healthcare gaining momentum, Invitae is endeavouring to provide high quality genetic testing that is affordable and accessible to all patients and their families. In addition, our commitment to professional development aims to ensure that health professionals are aware of and empowered by this opportunity to integrate genetic testing into their practice.

Invitae’s team will provide a tailored educational session, to update researchers and clinicians on the genetics of hearing loss and the utility of genetic testing. Topics will include the impact of genetics on hearing loss, why and when to test a patient, benefits and limitations of next generation sequencing, clinical utility, costs and accessibility. We will also cover the latest genetic developments and industry partnerships that allow clinicians to use genetics to better diagnose, manage and treat their patients.

In part 1 participants will get an overview of genetics and how it impacts on all stages of life including reproduction, birth, growth and development. An introduction to the utility and process of taking a family health history will also be covered. The inheritance patterns for the main causes of genetic hearing loss will be discussed as well as some case studies to illustrate the way in which genetics can impact on families with an inherited form of hearing loss.

Part 2 delves deeper into the application of genetic testing for individuals and families with hearing loss. An overview of the techniques used for genetic testing with some case examples will illustrate its utility, ethical implications and how to access Invitae’s sponsored testing program.


Session 4 Structural Abnormalities of the cochlea and auditory nerve: considerations in paediatric cochlear implantation

Presented by: Dr Kirsty Gardner-Berry

9-10am AEST 31 May 2022

Structural abnormalities of the cochlea and auditory nerve hold a number of implications that need to be taken into consideration when counselling families about expected outcomes with cochlear implantation, and for surgical planning. This presentation reports on the 20% of children identified with structural abnormalities within a population of 346 pediatric cochlear implant recipients at NextSense. Topics will include key time points during embryological development that can impact on the severity of the anatomical abnormality, implications for choice of cochlear implant array, surgical considerations, and the potential impact on signal transmission.

Session 5: Single Sided Deafness

Presented by: Dr Dayse Tavora

12-1pm AEST 27 July 2022

Single sided deafness (SSD) is defined as a severe to profound hearing loss (>70dB HL) in one ear and hearing thresholds within normal limits in the contralateral ear (<30dB HL). People with SSD are deprived of binaural cues – squelch and summation – and have difficult hearing sound that is projected directly at their non-hearing ear because of the head shadow effect. Furthermore, SSD reduces social and psychological QoL and imposes a remarkable level of handicap as per general and specific self-assessments tool.

For the last decade, several research groups have demonstrated that CI provides a significant improvement in function including speech understanding in noise and localisation ability, as well as improving QoL and reducing tinnitus significantly in both the early and long-term.

This event has been endorsed for 2 CEUs by the AG Bell Academy of Listening and Spoken Language.

Sessions 2 and 3 have been endorsed by Audiology Australia with endorsement number CPE2122 056 and Category and CPD points: Category 1.2- 2 CPD Points.

Session 4 has been been endorsed by Audiology Australia with endorsement number is CPD2122 075 and the category and CPD points: Category 1.2 – 1 CPD point

Tickets

Also in this section

Learn more about NextSense

Back to Professional education