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The large number of treatment modalities for patients diagnosed with Menière's disease (MD) complicates the selection of the best available treatment as the comparative efficacy of these interventions is not clear. We aim to identify the treatment or treatments with the highest efficacy of current pharmacological and non-pharmacological treatments for MD.
We will identify all available systematic reviews on the treatment of MD. An online database search will be conducted in association with the UK Cochrane Centre, particularly the Ear, Nose and Throat Group. We will screen the systematic reviews for eligible randomised controlled trials (RCTs) to execute a network meta-analysis. In addition, online databases will be checked for eligible RCTs on treatments that were published after the latest systematic search was conducted. The characteristics of each RCT will be summarised, including the general design, the participants, the interventions, the outcome measurements, the duration of therapy and adverse events. The risk of bias will be assessed by means of the Cochrane Collaboration's risk of bias tool. The included studies will be assessed for methodological and statistical heterogeneity; the latter will be quantified by means of the I2 statistic. The primary outcome will be the efficacy of treatment in terms of control of vertigo attacks. Secondary outcome measures will be the loss or improvement of hearing, severity of vertigo attacks and tinnitus, perception of aural fullness, quality of life, and the incidence of adverse events and complications.
Formal ethical approval is not required as primary data will not be collected. The review will be disseminated in peer-reviewed publications and conference presentations.
Menière's disease (MD) is an inner ear disorder characterised by incapacitating attacks of vertigo accompanied by nausea and vomiting, fluctuating sensorineural hearing loss as well as tinnitus and/or aural fullness. Even though the disease was first described in 1861 by Menière,1 there are still many unanswered questions regarding the pathophysiology of the disease. Furthermore, a definite and effective evidence-based treatment has not been established yet.
The main aim of the treatment in MD is to reduce the frequency and intensity of the vertigo attacks and, at the same time, to preserve hearing and vestibular function.2 Psychological suffering and reduced quality of life are linked to MD, as disabling vertigo attacks can occur without warning.3 4 Therefore, an effective prophylactic treatment is necessary to improve the quality of life of patients with MD. Current pharmacological treatment options include betahistine, diuretics, oral steroids or intratympanic application of gentamicin or corticosteroids.5 However, evidence in terms of reducing vertigo symptoms has never been conclusive,6–8 except for intratympanic gentamicin treatment.9 Non-pharmacological treatment options include positive pressure therapy (the Meniett device), ablative surgery such as vestibular nerve section, labyrinthectomy and endolymphatic sac surgery.2 5 10 As for the pharmacological treatment modalities, high-quality evidence is also lacking for non-pharmacological therapies.10 11 Since so many treatments exist without conclusive results, it may be hard for patients and their physicians to select the best available treatment. Until now, no umbrella systematic review (SR) exists that summarises the body of evidence and states implications for clinical practice.
The present study aims to systematically summarise the interventions for MD, aiming to identify the treatment or treatments with the highest efficacy and to identify areas for future valuable research.
A large number of pharmacological and non-pharmacological trials for the treatment of MD exist. We will conduct an umbrella SR of published randomised controlled trials (RCTs) of those interventions that have been systematically reviewed. From here we seek to evaluate the efficacy of therapy for MD. The current review has been registered at PROSPERO CRD42015024243. The steps throughout the conduct of the umbrella SR are shown in figure 1. This protocol is reported in line with PRISMA-P.12
The following study designs will be eligible for inclusion:
We will screen interventional SRs for eligible RCTs and data from these RCTs will be extracted to execute a network MA. In addition, online databases will be checked for eligible RCTs on treatments that were systematically reviewed yet published subsequent to the date the latest systematic search was conducted.
Owing to the great variability in the clinical presentation of MD, the disorder is not always easy to diagnose. The American Academy of Otolaryngology—Head and Neck Surgery (AAO-HNS) has produced diagnostic guidelines in order to facilitate the diagnosis of MD and to improve comparability of outcome measures when performing trials on patients with MD.13 In 2015, a new set of diagnostic criteria were jointly formulated by the Classification Committee of the Bárány Society, the Japan Society of Equilibrium Research, the European Academy of Otology and Neurotology, the AAO-HNS and the Korean Balance Society in order to develop an international consensus on diagnostic criteria for MD in order to facilitate future collaborative studies.14 However, since these international diagnostic criteria were only published recently and previous research widely used the AAO-HNS 1995 diagnostic guidelines, the latter set of criteria will be used to identify patients with ‘definite’ MD in the current review.
We will include RCTs analysing the efficacy of any treatment modality in MD. Treatment modalities that have not been assessed systematically will not be included in the umbrella SR. Since the natural course of MD has a waning pattern, time should be regarded as a therapeutic factor when analysing the efficacy of a therapeutic intervention. Therefore, a study design including a placebo arm is essential to account for the illusion of therapeutic efficacy. Pharmacological trials with a placebo group will be included; trials comparing different pharmacological treatments without a placebo will be excluded. We will include trials that investigated non-pharmacological interventions and compared the efficacy of the intervention with a sham intervention group, a placebo pill group or a placebo control group.
Outcomes as defined by the AAO-HNS guidelines of 199513 will be included in this umbrella SR. The following outcomes are listed as primary and secondary outcomes:
Secondary outcome measures will be:
In association with the UK Cochrane Centre, particularly the Ear, Nose and Throat Review Group, we will conduct a systematic search for all SRs for pharmacological and non-pharmacological interventions for MD. We will search the Database of Abstracts of Reviews of Effect (DARE), MEDLINE and EMBASE for SRs, and eligible RCTs will be extracted that examine the efficacy of pharmacological and non-pharmacological therapies in MD. In case several SRs investigate exactly the same treatment modality in the same population, we will extract the RCTs from the most recent published review. Since no current worldwide-recommended guidelines exist for the treatment of MD, we intend to include all systematically reviewed interventions. We will use Medical Subject Headings (MeSH) and key words in the search strategy containing ‘Menière’s disease’, ‘systematic review’, 'randomised controlled trial’ and ‘placebo controlled trial’. Details of the search strategy are shown in tables 1 and and22.
Two independent reviewers (BFvE and HJvdZ-L) will screen the title and abstract for potentially eligible SRs. These will be downloaded for full-text screening and further evaluation. Authors and journal names will be blinded. No restriction on language will be used. After identifying all interventions that were systematically reviewed, we will screen the title and abstract for potentially eligible RCTs that were published since the publications of these SRs. Similar to the selection of SRs, these RCTs will be screened on full text and evaluated. We will remove all duplicate RCTs after full-text screening and reference checking. The reviewers will examine and extract all data from the included RCTs into a data set.
After we selected eligible RCTs, the two reviewers (BFvE and HJvdZ-L) will independently extract information from the RCTs on predesigned data extraction forms. To begin with, we will extract the general information from each RCT covering the country, number of centres, number of participants, study design, the number of treatment arms, allocation ratio, and conflict of interest and funding. Then the study characteristics of the patients with MD will be extracted including sex, age, age at onset of disease, subclassification of MD types (diagnostic criteria defined by the AAO-HNS of 1995) and duration and frequency of vertigo attacks before start of treatment. Furthermore, details of the interventions will be extracted for the experimental and control groups. For the pharmacological interventions, we will record the drug category (eg, anticholamines, diuretics), generic name of the drug, dose per day, way of administration (eg, oral, intratympanic), additional treatments and period of treatment. In addition, for the non-pharmacological interventions, we will extract the type of intervention (eg, Meniett device, endolymphatic sac surgery) and any additional treatments (prestudy or during trial participation). Lastly, we will extract information of the effect on the primary and secondary outcome measures and record the incidence of adverse events and complications. We will extract the information from the intervention arm in pharmacological and non-pharmacological RCTs using a standard form (tables 3 and and4).4). In addition, tables 5 and and66 display the standard form that will be used to extract information from the placebo arm in pharmacological RCTs and the sham arm in non-pharmacological RCTs, respectively.
We aim to investigate the efficacy of treatment for MD in controlling vertigo attacks (primary outcome). As defined in the AAO-HNS guideline of 1995,13 the control of vertigo will be calculated and classified (class A, 100% control of vertigo, class B, 40% control of vertigo). Ideally, the primary outcome is again evaluated after 18 and 24 months following randomisation. However, it is unlikely that a placebo-controlled trial will last this long. Therefore, we will include papers that have assessed the efficacy of the therapy reflected by the primary outcome at 3–6 months of follow-up. We will ensure accurate assessment of the outcome measures as independent reviewers (BFvE and HJvdZ-L) extract the information from the selected RCTs and a third reviewer (TDB and/or PPGvB) will check the completeness and correctness of the extracted data.
We will assess the methodological quality of the RCTs by use of the Cochrane Collaboration's risk of bias tool14 within Review Manager V.5.3 software (Review Manager (Revman) V.5.3 Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2012). The tool is based on the following eight potential sources of bias: random sequence generation; allocation concealment; blinding of the participants; blinding of the outcome assessors; incomplete outcome data; missing data and selective outcome reporting, other bias (eg, improper statistical analysis). Two independent reviewers (BFvE and HJvdZ-L) will independently evaluate the quality of the RCTs. Each aspect will be graded with ‘yes’, ‘no’ or ‘unclear’, which will reflect a high risk of bias, low risk of bias and unclear risk of bias, respectively. For each study, all eight domains will be evaluated and displayed in a table (see table 7). If there is any disagreement on inclusion or exclusion, this will be settled by discussion, if necessary in the presence of a third reviewer (TDB and/or PPGvB). In addition, we will grade the diagnostic validity of studies on the basis of the robustness of the methods used to diagnose the disorder (homogeneity of the types of participants). This grading will form the basis to assess the risk of bias and perform sensitivity analyses. We will grade papers that used the AAO-HNS 1995 criteria for ‘definite’ and ‘certain’ MD as ‘I’. We will grade studies in which less clear but rigorous criteria were used as ‘II’. Studies in which no or less clear diagnostic criteria were used will be graded as ‘III’.
Data will be entered into Review Manager (V.5.3). For each treatment modality, we aim to perform a statistical analysis for the primary outcome comparing the interventional arm to the control group (placebo or sham). In addition, for studies that report the vertigo attack frequency as a continuous outcome, we intend to calculate the effect size using the mean difference (MD) or the standardised MD. The same applies for the loss of hearing. Where appropriate, data will be categorised or dichotomised for control of vertigo, severity of vertigo attacks, severity of tinnitus, perception of aural fullness, quality of life, complications and adverse events.
The included studies will be explored on methodological and statistical heterogeneity. The latter will be quantified by the I2 statistic. An I2 value >50% is considered to indicate substantial heterogeneity (Handbook 2011, The Cochrane Collaboration).15 If the data are sufficiently homogeneous, we will pool outcome data. It is expected that the data will carry a certain amount of heterogeneity and a random-effects model will be used. Forest plots will be shown for each intervention. If the data turn out to be too heterogeneous for pooling based on methodological heterogeneity and statistical heterogeneity, we will perform a descriptive review and summarise the available evidence for this intervention. The strength of the evidence will be evaluated by use of the GRADE method as generated by the Cochrane Collaboration. Table 8 shows the summary of findings per intervention based on the GRADE method.
We expect missing data in the selected trials for the SR. All corresponding authors will be contacted and asked for the original data. If only a per protocol analysis has been carried out, corresponding authors will be contacted for the original data on the intention-to-treat analysis.
We will perform subgroup analysis to investigate heterogeneity and inconsistency in the selected trials. Subgroup analysis will be performed with regard to subtype of MD (‘certain’, ‘definite’, ‘probable’ or ‘possible’ MD in accordance with the AAO-HNS 1995 criteria13), stage of disease (as defined by the AAO-HNS 1995 criteria13) and duration of treatment. Since the primary outcome is a patient-reported outcome, blinding can be of influence. Therefore, we will consider the method of blinding the most important subgroup analysis.
We will perform a sensitivity analysis to address whether the eight potential sources of bias played a relevant role in the robustness of our study findings. Studies with a high risk of bias will be analysed separately to evaluate if the efficacy of the intervention is not solely based on these trials and if trial results are robust.
Publication bias will be explored by performing funnel plots if sufficient data are available (10 or more studies).
Formal ethical approval is not required as primary data will not be collected. The findings will be disseminated in peer-reviewed journals and conference presentations.
We expect this umbrella SR to provide a systematic summary of evidence and aim to identify the treatment(s) with the highest efficacy for MD and areas for future valuable research.
The authors are grateful for the support of the members of the ENT Group of the UK Cochrane Centre, particularly Jenny Bellorini and Samantha Faulkner, for conducting the systematic searches for randomised controlled trials for interventions of Menière's disease.
Contributors: BFvE, HJvdZ-L, TDB and PPGvB contributed to the design and conception of the study protocol. The search strategy was developed and run by the ENT Group. BFvE and HJvdZ-L will screen studies on the title and abstract and full text. If disagreement over inclusion or exclusion arises, this will be settled by discussion with all authors (BFvE, HJvdZ-L, TDB and/or PPGvB). BFvE and HJvdZ-L will independently extract data from the articles and a third reviewer (TDB and/or PPGvB) will check the completeness and correctness of the extracted data of the outcome assessment. All authors drafted and revised this study protocol and approved it for publication.
Funding: This work was supported solely from institutional and/or departmental sources from the Apeldoorn Dizziness Centre, Gelre Hospital, Albert Schweitzerlaan 31, 7334 DZ Apeldoorn, The Netherlands.
Competing interests: None declared.
Provenance and peer review: Not commissioned; externally peer reviewed.