Abstract
Background
Influenza antiviral drugs remain controversial and it is not clear if conclusions on their efficacy/effectiveness are based on high quality systematic reviews (SRs). We systematically identified, critically appraised, and summarized the characteristics and adherence to methodological standards in SRs with meta-analysis of efficacy/effectiveness of influenza antiviral drugs for prevention and/or treatment of influenza.
Methods
We searched MEDLINE, Embase, Scopus, CINAHL, Global Health, and CDSR for English-language SR publications up to July 2020. We summarized the characteristics, adherence to methodological standards and SR quality (AMSTAR 2).
Results
From a total 3,898 citations after removal of duplicates from all identified citations, we included 24 SRs. Seventy-five percent (n = 18) were of a critically low quality, 8% (n = 2) of a low quality, 17% (n = 4) of a moderate quality, and none were of a high quality. Seventeen percent (n = 4) were industry-funded, 4% (n = 1) coauthored by industry employee(s), and 33% (n = 8) commissioned by an organization or authority. Only 33% percent (n = 8) reported protocol registration, 4% (n = 1) reported collaboration with a knowledge synthesis librarian/information specialist, and 17% (n = 4) utilized a systematic review reporting checklist.
Conclusions
The evidence suggests that SRs of efficacy/effectiveness of influenza antiviral drugs are mostly of critically low quality and do not follow current best SR practices. These findings are significant in view of the important role of SRs in decision-making and the controversies that surround the use of the influenza antiviral drugs. However, the findings should not be interpreted to mean curtailment/cessation of use of antiviral drugs for influenza.
Transparency
Declaration of funding
This project received no funding.
Declaration of financial/other relationships
The authors (GNO, OLTL, VKR, YA, FR, NA) have no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.
A reviewer on this manuscript disclosed that they have received funding for consultation and clinical research from Genetech/Roche, Shionogi, Janssen, GSK, Gilead and Cidara. Peer reviewers on this manuscript have no other relevant financial relationships or otherwise to disclose.
Author contributions
Conceptualization and Methodology (GNO); Data acquisition (GNO, OLTL, VKR, YA, FR, NA); Formal analysis (GNO); Validation (GNO); Draft manuscript (GNO); Manuscript revisions (GNO, OLTL, VKR, YA, FR, NA); Final approval for submission (GNO, OLTL, VKR, YA, FR, NA)
Acknowledgements
Authors thank Mê-Linh Lê, MA, MLIS (Neil John Maclean Health Sciences Library, University of Manitoba, Winnipeg, MB, Canada) for retrieval of full-text articles.
Data availability statement
All the data for this study are reported in the text and supplementary information.
Protocol registration number: PROSPERO: CRD42020218008