In March 2020, we will set up the Guideline Working Group, divided into the Guideline Development Group, the Guideline Steering Group and the Guideline Secretary Group. The guideline working group will compose of multidisciplinary experts, including not only clinicians and methodologists, but also the values and wishes of potentially conflicting interests and patients.
Guideline Secretary Group
The Guideline Secretary Group will comprise the following experts: 3 evidence-based medicine experts, acupuncturists and statistician. The Guideline Secretary Group will be allotted the following works: (1) to collect clinical problems; (2) to search the literature and accomplish the systematic reviews; (3) to investigate the patients’ values and preferences; and(4) to coordinate the formulation of guidelines.
Members of the Guideline Working Group will fill in a declaration of interest form to determine whether they have a conflict of interest.
Guideline target users and population
Acupuncturists, physical therapists, nurses, editors and AR-related researchers become the guideline’s target users. Patients with AR treated with moxibustion constitute the target population.
Identifying questions and evaluating the importance of outcomes
After the Secretary Group has collected the clinical questions according to the scope of the guide, we will complete the PICOs. The Development Group will evaluate the importance of the outcomes. It will be assessed according to the approach recommended by the GRADE working group: a score of 7–9 indicates that the outcome is critical to the recommendation, 4–6 indicates important, 1–3 is not important.
We will employ a broad electronic searching, including PubMed, Embase, Cochrane Library, China National Knowledge Infrastructure (CNKI), WangFang Database(WF), Chinese Scientific Journal Database (VIP), Chinese Biomedical Literature Database (CBM), from establishment to March 31, 2020, and conduct normal searches according to the rules of each database. Evidence-based experts will help develop retrieval strategies. MeSH terms and free words to be searched will include: allergic rhinitis, anaphylactic rhinitis, AR, hay fever, pollinosis, nasal allergy, moxibustion, thunder fire needle, taiyi miraculous moxa roll. There will be no restrictions on publication language.
To ensure that the selection criteria of the literature are consistent, the members will conduct predictive tests. We will summarize the screening results and discuss the inconsistencies. After this test, each member will explicitly include and exclude criteria.
After the pre-test, we will formally select the literature. The major ranges will include systematic review, meta-analysis, and original studies. Members will exclude irrelevant literature by reading the title and abstract, and read the rest of the full text to select.
Through the assessment of literature quality, high-quality systematic reviews will be used directly, if it is published more than two years will be updated. If the relevant system reviews are of low quality or absent, the Guideline Secretary Group will prepare a new system reviews.
The GRADE approach will be used to evaluate the quality of evidence. The level of evidence is classified as high, medium, low and very low. Five downgrading factors: risk of bias, inconsistency, accuracy, publication bias and indirection; Three escalation factors: large effect size, confounding factor bias and dose effect. The Guidelines Development group will be responsible for the assessment of evidence and the drafting of evidence summaries.
We will conduct an investigation on the willingness of AR patients to treat AR with moxibustion. The researchers will ask relevant questions and record the results after letting the interviewees know the relevant medical vocabulary, background knowledge and analysis of advantages and disadvantages. Questions will include the effectiveness of moxibustion therapy for AR, adverse reactions, burdens, costs, potential benefits, etc. The findings will be summarized and analyzed for the reference of the experts in the guideline working group.
Developing recommendations
The Guideline Development Group will draft recommendations through 2–3 rounds of the Delphi process based on the quality of evidence, patient willingness, economic analysis, and balance of advantages and disadvantages. The process will use the GRADE grid. There are five recommendation levels( strong recommendation, weak recommendation, unclear, weak no recommendation, strong no recommendation), and the results will be obtained by voting. The drafted recommendation will be approved by the Guideline Steering Group.
The guideline will be reviewed by external peer experts, we will discuss feedback and recommendations from peer experts, and some recommendations may be revised.
Publishing and updating of the guideline
The reporting and publication of the guidelines will be conducted in a normative, systematic and transparent manner by the requirements of RIGHT. The guidelines will be published in one or two years. We plan to update it every 3–5 years.
Publicity and evaluation of the guideline
After the publication of the guideline, Affiliated Hospital of Jiangxi University of TCM and Jiangxi University of TCM will conduct the dissemination and promotion of the guideline: (1) The guideline will be presented and disseminated at relevant academic conferences; (2) A nationwide study program will be organized for relevant personnel, such as acupuncturists, physiotherapists and nurses; and(3) Members of the guidelines will write papers related to the guidelines and publish them in the journal.
The application and dissemination of the guidelines will be investigated, and the impact of the guidelines on clinical decision making will be assessed.