Ménière's Disease Registry

Ménière's disease is an inner ear disorder characterised by recurrent episodes of spontaneous vertigo, fluctuating hearing loss and tinnitus, often with a feeling of fullness in the ear. The exact aetiology remains unknown. Ménière's disease is estimated to have a prevalence of 0.25% in the UK (around 162,000 individuals) (Tyrrell 2016) and is associated with significant physical, psychological and socioeconomic morbidity (Anderson 2001, Tyrrell 2014).

There is a substantial lack of knowledge regarding many aspects of Ménière's disease, including a fuller understanding of epidemiological aspects of the disease, aetiological factors, pathogenesis, clinical course and treatment outcomes. The James Lind Alliance cites Ménière's disease as the theme for four of their top ten priorities for addressing uncertainties in the field of balance disorders (JLA 2018).

There is mounting unease regarding the definition of Ménière's disease as a single clinical entity. Many consider it to represent the final pathway of a number of individual disease processes. This is reflected by the progressive and varied development of diagnostic criteria over the last few decades (Gurkov 2016). It is in the context of these observations that Ménière's disease is likely to represent a heterogeneous clinical condition defined only by small groups of common, but not always mandatory, symptoms. Understanding how Ménière's disease may exist as a cluster of clinical sub-types is key to allowing further research into its underlying pathophysiological mechanisms, and the targeting of specific treatment strategies; as well as allowing a better understanding of the physiology of the inner ear micro-environment (Phillips 2018).

This project will provide the initial steps necessary to set-up a UK Ménière's disease registry by primarily investigating a single clinical subtype of Ménière's disease: bilateral disease. The development of bilateral Ménière's disease has significant implications for short and long-term opportunities for treatment and rehabilitation; this in turn has significant implications for communication and employment. Previous literature on bilateral disease has offered widely ranging estimates of the likelihood that it will occur in cases where unilateral disease is confirmed, and no clear predictors have been identified (Huppert 2010). However, it is a sub-type which is relatively well-defined with standard internationally agreed criteria for diagnosis.

In areas of research such as this, the implementation of bespoke data collection platforms and national registries have been demonstrated to be both effective and efficient (Mandavia 2017). The use of national registries has many advantages over conventional data collection methods. When implemented correctly, national registries can allow the appraisal of a more representative sample of the target population. Furthermore, a national approach broadens the opportunities both for participation among the patient population to be served by such a venture, and for public engagement and dissemination activities.

A national registry would allow the identification of features at presentation that predict disease course and long-term outcome, improving the understanding of disease progression, treatment response, and underlying aetiology. A UK Ménière's disease registry would also provide a resource for broad and far reaching research into Ménière's disease beyond that of defining clinical sub-types. Registries offer other benefits to patients, carers (including partners and family), researchers, clinicians and other individuals that are involved with the provision of services for those affected by the condition being studied. Individual hospitals and the NHS as a whole can use registry data to improve the services they offer. Individual patients and carers can use registries to learn more about their condition and this can lead to a better understanding of how people's lives are affected. It is anticipated that this work will lead to further registry development and expansion with a broad remit of aims via further awards from major research funders.

To develop the methods and infrastructure for a national registry by recruiting participants from three distinct urban and rural regions within the UK (Norfolk, Leicestershire and London). This will include an appraisal of a number of practical processes of recruitment, such as data acquisition, data processing and data management. This will inform future stages to expand the infrastructure to support a registry for widespread national use.

This project will require the retrospective collection of data from existing Ménière's patients.

Potential participants with a diagnosis of probable or definite unilateral or bilateral Ménière's Disease as defined by the 2015 edition of the American Academy of Otolaryngology-Head and Neck Surgery (AAO-HNS) criteria (Goebel 2016) in their hospital records will be identified at ENT secondary care and private clinics. Potential participants must have received a diagnosis of Ménière's Disease within the previous 10 years or have received a new diagnosis during the recruitment window of the study. Unilateral and bilateral Ménière's disease will be defined as follows:

Unilateral Ménière's Disease

At least two episodes of vertigo each lasting at least 20 minutes, where each episode is associated with aural symptoms in a single ear.

Bilateral Ménière's Disease

At least two episodes of vertigo each lasting at least 20 minutes, where each episode is associated with aural symptoms in both ears.

Data will include contemporaneous and historical information regarding medical and relevant social/occupational history, audiometric data, vestibular testing data, radiological data and symptom specific and health related quality of life questionnaires. Clinical data will be requested, collected and extracted locally and entered directly into the Study Dataset managed by Norwich Clinical Trials Unit at the University of East Anglia.

Participants will be offered the option of completing the study questionnaires online or on paper (for entry by a member of the research team). No additional outpatient appointments outside normal care pathways will be required.

The full dataset will be composed of three components:

1. Medical history. This will be completed by the participant onto a predefined data collection form - see additional document: MDR_NVPQ
2. Symptom questionnaires. These will be completed by the participant
3. Audiometric, Vestibular and Radiological test results. This will be completed by the local investigator team.

The investigators anticipate that participants will spend no longer than 60 minutes to complete the necessary forms and questionnaires.

Participants will be asked to complete a non-validated Ménière's disease questionnaire about their Ménière's disease including demographics, history, symptoms including triggers of Ménière's disease related vertigo attacks, comorbidities, current treatment and past treatments tried for Ménière's disease.