This scoping review will be conducted in accordance with the scoping review methodological frameworks described by Arskey and O’Malley (11); Levac et al (12); Colquhoon et al (13); and the Joanna Briggs Institute reviewer’s manual (14).
The protocol will be reported in accordance with the reporting guidance provided by the Preferred Reporting Items for Systematic Reviews and Meta-Analysis Protocol – Extension for Scoping Reviews (PRISMA-ScR) checklist (15) (additional file 1) and has been registered within the Open Science Framework platform (osf.io/e47sa).
The methodological frameworks for performing a scoping review will involve the following stages:
- Define the research question.
- Identify relevant published literature.
- Selection of relevant literature.
- Extract and chart the data collected from the literature.
- Collate, summarise and report the results.
- Consultation exercise.
Stage 1: Define the research question
Inhaler technique assessment is a crucial part of all asthma review appointments (7, 8). We want to explore if there are standardised and validated methods of assessing inhaler technique to ensure accuracy and consistency of assessment.
Following a preliminary search of the literature and discussion amongst the research team (which includes experienced academics in the field of paediatric asthma), the following specific research question was decided upon:
‘In children and young people with wheeze and/or asthma, what methods are used to assess inhaler technique in clinical practice and are these methods valid and reliable?’
Allowing for the iterative nature of a scoping review, following the initial piloting process we will review and consider refining the research question including the terms within it.
Stage 2: Identify relevant published literature.
Under the guidance of the Queen’s University Belfast (QUB) medical librarian the search will include a range of terms and keywords related to the research question.
The following search terms will be used:
Asthma OR wheeze OR viral induced wheeze.
AND
Child OR young people OR adolescent OR paediatrics OR pediatrics.
AND
Inhaler technique OR inhaler management OR inhaler method.
AND
pMDI OR MDI OR DPI OR Spacer
AND
Checklists OR score OR assess OR assessment OR criteria
An initial pilot exercise will be undertaken using the online database MEDLINE before proceeding to a complete search of all available databases. The lead researcher (KF) will review 10 publications from this initial piloting exercise to ensure that we have chosen the most suitable search terms by considering the different concepts that each of these articles could be mapped to. For the MEDLINE search appropriate MeSH terms will be included.
The lead researcher may consider modifying the search strategy and/or research question at this stage once we have a greater knowledge of the literature. A draft search strategy for MEDLINE is included (additional file 2).
Once the pilot is complete and consideration of new search terms made, a full search of MEDLINE will be completed followed by a full search of the subsequent chosen online databases (Embase, Cinahl and the Cochrane library). These databases provide a comprehensive list of relevant literature across a range of disciplines. A search of the grey literature (using google scholar) and discussion with a group of paediatric asthma specialists will also be undertaken to identify any additional relevant literature. We will make a record of the total number of citations yielded by these search terms from each of the databases. Duplications will then be removed before screening.
Stage 3: Selection of relevant literature.
Eligibility criteria:
We will include studies published since the year 1956 when the pressurised metered-dose inhaler (pMDI) was first brought into clinical practice (16). We will include randomised control trials, case control studies, cohort studies and retrospective studies which investigate methods used to assess inhaler technique in children and young people.
Studies involving both adults and children together will be included as these will still be relevant to our research question if these methods have been employed in children and young people. We do not wish to be ‘device specific’ and so we will include studies of metered-dose inhalers and dry powder inhalers (DPI), with and without the use of spacer devices.
We will include studies which have taken place in the emergency department, the out-patient department, the hospital ward and/or the community including general practice as these are all areas where inhaler technique assessment occurs. We will include studies conducted by healthcare professionals who usually undertake inhaler assessments in practice, this will include trained doctors and those in training, trained nurses and those in training, pharmacists, and physician associates.
To include a breadth of knowledge in this area we will include conference abstracts, presentations and scholarly information that may not have been peer reviewed.
Exclusion criteria:
We will exclude studies which explore the use of nebulised therapies as this involves a different technique. We will exclude studies which involve adult participants only.
Publications not in English will be excluded due to time and resource constraints as we will not be able to accurately translate the data and translated articles can have an inaccurate interpretation from the original article.
Screening
Initial screening will be based on the title with further screening based on the abstract, to ensure they fulfil the eligibility criteria. This will be conducted by lead researcher KF. Documents not meeting eligibility criteria will be excluded from further analysis.
The remaining publications will undergo full text analysis by three reviewers, from the research team (KF, PMcC and DOD). These three reviewers will independently analyse the full text articles. In the case of uncertainty, the text will be re-evaluated by a fourth independent reviewer (JP or MDS). The final search results will be exported into EndnoteTM at which point all duplicates will be identified and removed.
A flow diagram in keeping with PRISMA will be used to report the searches and inclusion/exclusion pathway.Data will be stored and charted using a Microsoft Excel spreadsheet.
Stage 4: Extract and chart the data collected from the literature.
Two reviewers (KF and PMcC) will complete all screening and data abstraction independently. Data will be extracted onto a data-charting table (see Table 1) to create a descriptive summary of the results.
The charting table will record the characteristics of the included studies and the key information relevant to the research question. Given the iterative nature of a scoping review this table will be subject to further development following a review of this process with the first 2 or 3 studies.
Authors will be contacted directly for data clarification as necessary.
Information to be included in the charting table:
- Study characteristics: Design, year of publication, journal, year study was conducted (or period of time), sample size, country, setting, profession(s) of those conducting the study and study aims.
- Participant characteristics: age (e.g., mean with standard deviation, range) and gender.
- Inhaler characteristics: device type, use of inhaler adjunct devices such as spacers.
- Outcome measures.
- Key findings.
- Methods used in the study to provide an assessment of inhaler technique. In what context these methods have been used and if there has there been an assessment of inter/intra observer variability.
- Whether the assessment method was validated or not. If it has been validated, how has this been done.
- Whether objective methods of assessing inhaler technique were used (e.g flow meter attached to inhaler). If yes- which.
- Study concept- as defined by research group following discussion.
At intervals during the data extraction and charting process, charted data will be compared and discussed to ensure consistency between reviewers and to enable iterative reflection on emerging themes and categories.
During the review process, any amendments to the protocol deemed necessary by the team will be recorded in the master protocol document with the reason for amendment noted.
Stage 5: Collate, summarise and report the results.
We will aim to create a visual map categorising inhaler type and the assessment tools used for each.
We will present the qualitative results as a ‘map’ of the data in a descriptive format and diagrammatic format by classifying them under main conceptual categories. Numerical data will be analysed using Microsoft excel and presented in table format.
Stage 6: Consultation exercise
The consultation exercise will be used to add value to and validate our findings. The consultation exercise will consist of a focus group with our research group PPI team and volunteers through Asthma UK Centre for applied Research (AUKCAR) advertisement; these key stakeholders will be children and young people and/or their parents and carers who will have experience of being taught how to use an inhaler.
The focus groups will be held on Microsoft teams. The authors will compile a selection of inhaler assessment tools for discussion during the consultation exercise and some pre-set questions will be used to initiate and guide the discussion. Discussions will be recorded and transcribed on Microsoft teams and transcriptions checked verbatim. Written consent will be obtained. Focus group findings will be presented and shared along with the scoping review findings.