The number of individuals with disabling hearing loss continues to increase globally.
1,2 Management and treatment options for hearing loss are expanding. Despite these trends, access to hearing health care remains disproportionately low.
1 Cochlear implants (CIs) are a widely accepted treatment option for patients with bilateral deafness. Advancements in surgical technique and electrode design have contributed to improved outcomes in patients with CIs, leading to a rapid push to expand indications set by the US Food and Drug Administration (FDA)
3 to allow increased access to CI technology. Along these lines, FDA criteria for CIs recently were expanded to include individuals with lesser degrees of hearing loss.
3 Evidence now exists to support the success of CIs in those with residual hearing who cannot benefit from traditional amplification.
4-8 In accordance with the expanded FDA criteria, testing measures have evolved to more appropriately assess candidacy and avoid potential ceiling effects.
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