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Intranasal antihistamines and corticosteroids in the treatment of allergic rhinitis: a systematic review and meta-analysis protocol

  • Bernardo Sousa-Pinto
  • , Rafael José Vieira
  • , Jan Brozek
  • , António Cardoso-Fernandes
  • , Nuno Lourenço-Silva
  • , Renato Ferreira-Da-Silva
  • , André Ferreira
  • , Sara Gil-Mata
  • , Anna Bedbrook
  • , Ludger Klimek
  • , Joao A. Fonseca
  • , Torsten Zuberbier
  • , Holger J. Schünemann
  • , Jean Bousquet
  • University of Porto
  • McMaster University
  • University Hospital Center of Santo António
  • MASK-air
  • Johannes Gutenberg University Mainz
  • Center for Rhinology and Allergology
  • Charité – Universitätsmedizin Berlin
  • Fraunhofer Institute for Translational Medicine and Pharmacology ITMP
  • ARIA

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Introduction Intranasal antihistamines and corticosteroids are some of the most frequently used drug classes in the treatment of allergic rhinitis. However, there is uncertainty as to whether effectiveness differences may exist among different intranasal specific medications. This systematic review aims to analyse and synthesise all evidence from randomised controlled trials (RCTs) on the effectiveness of intranasal antihistamines and corticosteroids in rhinitis nasal and ocular symptoms and in rhinoconjunctivitis-related quality-of-life. Methods and analysis We will search four electronic bibliographic databases and three clinical trials databases for RCTs (1) assessing patients ≥12 years old with seasonal or perennial allergic rhinitis and (2) comparing the use of intranasal antihistamines or corticosteroids versus placebo. Assessed outcomes will include the Total Nasal Symptom Score (TNSS), the Total Ocular Symptom Score (TOSS) and the Rhinoconjunctivitis Quality-of-Life Questionnaire (RQLQ). We will assess the methodological quality of included primary studies by using the Cochrane risk-of-bias tool. Certainty in the body of evidence for the analysed outcomes will be assessed using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach. We will perform a random-effects meta-analysis for each assessed medication and outcome, presenting results as pooled mean differences and standardised mean differences. Heterogeneity will be explored by sensitivity and subgroup analyses, considering (1) the risk of bias, (2) the follow-up period and (3) the drug dose. Ethics and dissemination Ethical considerations will not be required. Results will be disseminated in a peer-review journal.

Original languageEnglish
Article numbere076614
JournalBMJ Open
Volume13
Issue number11
DOIs
StatePublished - Nov 2 2023

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