Hearing loss is one of the leading causes of disability worldwide, affecting more than 430 million people, a figure projected to exceed 700 million by 2050 with population aging [1]. Severe-to-profound hearing loss is associated with substantial reductions in communication, educational and employment opportunities, social participation, and quality of life, while also increasing the risks of depression, social isolation, and cognitive decline [1,2]. In the United Kingdom, approximately 1.2 million individuals are affected by severe-to-profound hearing loss, a condition projected to become a top 10 health burden by 2030, with an estimated annual cost of £38.6 billion (US $51.1 billion [£1=US $1.32] as of October 6, 2026) to the UK economy [3,4].

Cochlear implants (CIs) are transformative medical devices that provide electronic hearing to individuals with severe-to-profound hearing loss and have been shown to significantly improve quality of life [5]. They have been demonstrated to be a cost-effective intervention across multiple different health care systems [6,7]. According to recent estimates, around 25,000 children and adults in the United Kingdom are CI users [8]. Despite the well-documented benefits of CI, it is estimated that only 5% to 10% of potentially eligible patients currently receive a CI [9,10]. Numerous studies have demonstrated that only a minority of adults who fulfill referral or candidacy criteria are ultimately assessed for implantation internationally [9-12]. Barriers exist at multiple levels of the health care pathway, including limited awareness among health care professionals and patients, variation in referral practices, geographical inequity, socioeconomic disadvantage, cultural perceptions of hearing loss, and inconsistent access to specialist implant centers [12]. Consequently, improving equitable access to CI has become an important international priority in hearing health care.

A comprehensive national assessment of referral patterns was undertaken for the first time in 2022: the Cochlear Implant Referral Criteria Audit (CIRCA-1) study, which included 36 UK secondary care centers. In this study, 6171 adults who met audiometric criteria were identified, with only 35.7% being informed of their eligibility and just 9.7% being referred for CI assessment [13]. The CIRCA study also highlighted inequities in access, with lower referral rates among individuals from socioeconomically deprived areas, ethnic minority groups—particularly Asian and Black individuals, older adults, males, and those residing in London and the North [13]. Since its publication, the results of CIRCA-1 have been disseminated through national bodies, including the British Cochlear Implant Group (BCIG) and the British Association of Audiology (BAA). Nationwide awareness initiatives and educational content alongside expansion of the BAA “CI Champion” scheme, a job role where an audiologist has dedicated time to audit local referrals and work to improve referral pathways with a “mentor” at an implant center. However, there has not been an interval assessment on whether these interventions have influenced referral patterns or increased awareness of the National Institute for Health and Care Excellence (NICE) 2019 guideline changes [14]. Although national adult CI activity has begun to recover after the COVID-19–related dip in 2020 to 2021, recent figures (2024‐2025) show only a modest increase of around 6% compared with pre-TA566 levels, which is substantially lower than the 70% rise predicted by NICE when moving from TA166 to TA566. This discrepancy further highlights the need for a repeat national audit to evaluate progress, measure adherence to current standards, and identify persistent barriers.

In addition to individuals who meet current NICE criteria [14], there remains interest in the role of CI for those who fall outside current thresholds. The ongoing COACH (Comparing Cochlear Implants With Hearing Aids in Adults) trial is an ongoing randomized trial comparing hearing aids to CI for patients with hearing at 70 decibels or worse in 2 frequencies between 500 and 4000 Hz in both ears alongside speech perception <60% on Arthur Boothroyd Word Test [15]. The COACH trial criteria are more relaxed than current NICE guidelines, and adoption of these would make more patients eligible for CI and have corresponding implications on workforce planning and service design. The extent of this effect is uncertain, and a report on the proportions of additional patients meeting COACH entry criteria would be informative and will be performed alongside the primary reanalysis using existing NICE guidance. This will provide real-world context on the potential increased demand and capacity implications of potentially lowering the threshold of audiometric criteria for CI candidacy. As such, this study will help re-explore existing barriers that patients face accessing CIs and assess whether current interventions have been impactful. This will help direct future improvements to enable equitable access to CIs and the benefits they provide.

Understanding where potentially eligible patients are lost within referral pathways is fundamental to improving access to CI. National clinical audits provide an opportunity to benchmark practice against established standards, identify unwarranted variation between health care providers, evaluate the impact of quality improvement initiatives, and support evidence-informed service planning. Although referral criteria differ between health care systems, the underlying challenges of delayed identification and inconsistent referral are common internationally, making reproducible audit methodologies valuable beyond individual countries. This protocol provides a framework for such an assessment that can be implemented in other health care systems beyond the United Kingdom.

This study is a national, multicenter, retrospective observational audit of practice. The overall study workflow is demonstrated in Figure 1. This study will be reported in accordance with the STROBE (Strengthening the Reporting of Observational Studies in Epidemiology) guidelines.

A multicenter study will be conducted in units providing ear, nose, and throat (ENT) and audiology services within the NHS across the United Kingdom. Any unit with ENT and audiology services will be eligible to recruit patients if they use Auditbase or Practice Navigator software. Auditbase is the most common database in UK audiology departments. The second most common, Practice Navigator, has been progressively phased out since 2022 and will be used in fewer sites than when the original study was conducted. The increased use of Auditbase by sites across the United Kingdom will facilitate engagement from an increased number of sites compared with CIRCA-1 and will likely facilitate a larger sample size and more representative results. Since the original audit, there is now a method to perform searches in Practice Navigator, enabling inclusion of centers that use the 2 largest audiology databases in the United Kingdom.

The study will be delivered by INTEGRATE, the UK ENT Trainee Research Collaboration [16], supported by INDICIA and the CI Champion Scheme. This collaborative structure consists of a central Project Management Team (PMT), with invitations to all eligible sites for audiologists, ENT clinicians, or audiovestibular medicine physicians to join as collaborators on this project. This collaborative framework mirrors the CIRCA-1 audit, which is outlined in detail below.

INTEGRATE will identify regional leads for each UK region who will, in turn, help recruit local leads for each hospital. Each hospital will have a local audiology and/or ENT resident doctor lead and/or audiovestibular medicine clinician lead. The local lead will collaborate with the local audiology team and then register the study with the audit department locally before data collection begins. For units with more than 100 eligible patients, the local lead may choose another collaborator to divide the data capture work with, with a further collaborator granted for each additional 100 patients. An effort will be made to rerecruit all original CIRCA sites.

Patients will be included if they meet the following criteria:

Patients will be excluded if they meet the following criterion:

Project registration and governance processes will follow the same structure as the CIRCA-1 audit, which is outlined below.

The primary outcome is to determine the factors associated with referral after completing audiometric evaluation for implant assessment. The secondary outcome is to identify the factors impacting whether health care professionals have discussed the option of referral after completing audiometric evaluation with the patient.

Based on patient hospital records, site leads will determine whether a CI referral was discussed with the patient. This will form the basis of the primary (whether a patient was referred) and secondary (whether a patient was informed that they were eligible for referral) outcomes. The different types of discussions will be coded as follows:

Local leads will extract data from clinical and audiological records to identify potential predictors of referral for CI assessment for eligible patients and to determine which factors may be positive or negative predictive factors. These can be subdivided into patient and center predictors.

Patient predictors will include the following: age, sex, ethnicity, indices of multiple deprivation: rank and decile (measured by postcode), languages spoken (including whether English is the primary language), audiometric data (including severity of hearing loss), medical comorbidities, physical disability (defined according to International Classification of Diseases codes “reduced mobility,” dependence on a wheelchair, dependence on other enabling machines or devices, or paralysis, excluding those with temporary changes), and cognitive disability (record of “dementia/cognitive decline/AMTS<8/MMSE<24”).

Center predictors will include the following: colocation (or not) with a CI center; distance to the closest CI center; socioeconomic status of the center’s region; CI Champion presence (or not); CI Champion duration in role (months); CI Champion proportion of nonclinical time allocated to this role within their work schedule; in the calendar year of 2025, did the CI Champion consistently undertake the 1 hour of protected time each week? (5-point Likert scale: Never-Always); presence of speech testing availability at the local center; frequency of running of the Crystal Report or audit of local referral practice; changes in practice since CIRCA-1 if the site took part; and which version of Auditbase or Practice Navigator the site uses (this is relevant as newer versions have built-in features and prompts that could infer an increased likelihood of discussion and/or referral).

Descriptive statistics will be used to summarize patient, audiometric, and site characteristics. Categorical variables will be presented as frequencies, percentages, and 95% confidence intervals, with the number of patients contributing to each analysis clearly stated. Continuous variables will be presented as means with SDs or medians with IQRs, according to their distribution. The number and proportion of patients classified within each CI outcome category will be reported, together with the relevant denominator.

The prespecified primary outcomes are: (1) documented discussion of CI and (2) referral for CI assessment. These will be analyzed as binary outcomes using multilevel logistic regression with a random intercept for hospital to account for clustering of patients within sites. Results will be presented as adjusted odds ratios with 95% confidence intervals. Candidate predictors will be selected a priori on the basis of the CIRCA-1 analytical framework and clinical plausibility. When CIRCA-1 and CIRCA-2 data are analyzed together, audit cycle will be included as an indicator variable, and interaction terms will be used to examine whether selected associations differ between audit cycles.

The 6-category CI1 to CI6 classification will provide a more detailed secondary description of the referral pathway. Frequencies and percentages will be presented for each category. Where category sizes permit, associations between patient- and hospital-level characteristics and the detailed pathway outcome will be explored using multinomial logistic regression, with CI1 or another clinically appropriate category specified as the reference group. Results will be presented as relative risk ratios with 95% confidence intervals. Patients already under CI assessment and patients already implanted will be reported separately and excluded from the primary binary outcome models.

For binary regression models, model performance and adequacy will be assessed using calibration plots, the area under the receiver operating characteristic curve, residual and influence diagnostics, and likelihood-based measures of fit. For multilevel models, between-hospital variance and the intraclass correlation coefficient will also be reported. Multinomial model fit will be examined using likelihood ratio tests and information criteria. Collinearity between predictors and the functional form of continuous variables will be assessed before final model specification.

As the purpose of the analyses is explanatory and comparative rather than the development of a clinical prediction model, the principal models will be fitted using the full available dataset. Where predictive performance is reported as a secondary analysis, internal validation will use bootstrapping or cross-validation rather than a single training/test split. The contribution of individual predictors will be assessed using adjusted effect estimates, confidence intervals, and likelihood ratio tests.

The PMT will run range, logic, and completeness checks on all submissions. Data queries will be sent to local leads to resolve discrepancies or complete missing critical fields (unique identifier, age, sex, audiometric thresholds used to define eligibility, and the primary outcome—outcome of CI eligibility discussion). Patients with untested frequencies on their audiograms will not be excluded, provided the index audiogram is sufficient to meet current NICE criteria. Records missing the primary outcome after query resolution will be excluded from the corresponding primary analysis but may contribute to secondary analyses where applicable.

Missingness will be described for each variable. Complete-case analysis will be used where missingness is limited; multiple imputation will be considered for predictors with more substantial missing data where its assumptions are considered reasonable. Sensitivity analyses will include exclusion of records with missing primary outcome data and exclusion of potentially duplicate records.

Individuals treated at more than one trust will have records linked through identification of a common unique code generated from the anonymized NHS number.

To assess progress since the original CIRCA audit, outcomes from the current reaudit (CIRCA-2) will be directly compared with those from CIRCA-1 (2021 data collection).

Primary comparisons include the proportion of patients meeting NICE criteria who were informed of their eligibility and the proportion referred for CI assessment.

Secondary comparisons include adherence to NICE TA566 standards [14] by region and unit; presence and role of CI Champions. This is predicted to be greatly expanded compared to CIRCA-1, and this further analysis will provide insight into the impact of this scheme on discussions and referrals; proportion of patients meeting COACH pure-tone audiometric thresholds [15]; and patient or center factors that are predictors of discussion about CI eligibility and/or referral to a CI center.

Statistical testing may include chi-square or Fisher exact tests for categorical variables (eg, proportion referred vs not referred); t tests or Mann-Whitney U tests for continuous variables, depending on distribution; and/or multivariable logistic regression models including an indicator variable for audit cycle (CIRCA-1 vs CIRCA-2) to explore whether predictors of referral and implantation have changed over time.

Data will be captured on the number of patients potentially within criteria (by center and region), the proportion with whom potential implantation was discussed, the proportion subsequently referred for assessment, and the proportion ultimately implanted. The proportion of potential candidates for each unit will be calculated by center and region.

As this is a reaudit, these figures will be compared directly with those from the original CIRCA audit to evaluate changes over time. Multiple regression analysis will again be used to identify predictors of discussion and referral. These predictors will include patient demographics (eg, age, gender, ethnicity, socioeconomic deprivation), geographical factors (region, presence of a colocated CI center, distance to the nearest CI center), and service factors (presence and role of a CI Champion, as recommended by BCIG and BAA). Where possible, shifts in the influence of these predictors will also be compared with those identified in the original audit.

The study launched January 1, 2026, to allow the collection of retrospective data for patients tested between July 1, 2025, and December 31, 2025. Final submission of data was at 3 months from the launch date, with a deadline of March 31, 2026. This was extended to May 31 to maximize the number of submitting sites. Data analysis is projected to be complete by October 2026. The publication of final results is projected in early 2027.

Eighty-three sites from all 4 devolved nations of the United Kingdom have submitted data relating to 15,060 patients with an audiogram meeting NICE criteria for a CI. Planned data analysis is underway and due to be complete by October 2026.