Author
Listed:
- Michele Fusaroli
(University of Bologna)
- Francesco Salvo
(Université de Bordeaux, INSERM, BPH, Team AHeaD, U1219
CHU de Bordeaux, INSERM, U1219)
- Bernard Begaud
(Université de Bordeaux, INSERM, BPH, Team AHeaD, U1219)
- Thamir M. AlShammari
(Almaarefa University)
- Andrew Bate
(Global Safety, GSK
London School of Hygiene and Tropical Medicine)
- Vera Battini
(ASST Fatebenefratelli-Sacco University Hospital, Università degli Studi di Milano)
- Andreas Brueckner
(Novartis)
- Gianmario Candore
(Bayer AG, Medical Affairs and Pharmacovigilance)
- Carla Carnovale
(ASST Fatebenefratelli-Sacco University Hospital, Università degli Studi di Milano)
- Salvatore Crisafulli
(University of Verona)
- Paola Maria Cutroneo
(Sicily Pharmacovigilance Regional Centre, University Hospital of Messina)
- Charles Dolladille
(UNICAEN, EA4650 SEILIRM, CHU de Caen Normandie, Normandie University
CHU de Caen Normandie)
- Milou-Daniel Drici
(Université Côte d’Azur Medical Center)
- Jean-Luc Faillie
(INSERM, Univ Montpellier, Regional Pharmacovigilance Centre, CHU Montpellier)
- Adam Goldman
(Sheba Medical Center
Sackler School of Medicine, Tel Aviv University)
- Manfred Hauben
(Pfizer Inc.
New York Medical College)
- Maria Teresa Herdeiro
(IBIMED-Institute of Biomedicine, University of Aveiro)
- Olivia Mahaux
(Global Safety, GSK)
- Katrin Manlik
(Bayer AG, Medical Affairs and Pharmacovigilance)
- François Montastruc
(Toulouse University Hospital (CHU)
Toulouse University Hospital)
- Yoshihiro Noguchi
(Gifu Pharmaceutical University)
- G. Niklas Norén
(Uppsala Monitoring Centre)
- Roberta Noseda
(Ente Ospedaliero Cantonale)
- Igho J. Onakpoya
(University of Oxford)
- Antoine Pariente
(Université de Bordeaux, INSERM, BPH, Team AHeaD, U1219
CHU de Bordeaux, INSERM, U1219)
- Elisabetta Poluzzi
(University of Bologna)
- Myriam Salem
(Health Canada)
- Daniele Sartori
(Uppsala Monitoring Centre
University of Oxford)
- Nhung T. H. Trinh
(University of Oslo)
- Marco Tuccori
(University Hospital of Pisa)
- Florence Hunsel
(Netherlands Pharmacovigilance Centre Lareb
University of Groningen, Groningen Research Institute of Pharmacy, PharmacoTherapy, Epidemiology and Economics)
- Eugène Puijenbroek
(Netherlands Pharmacovigilance Centre Lareb
University of Groningen, Groningen Research Institute of Pharmacy, PharmacoTherapy, Epidemiology and Economics)
- Emanuel Raschi
(University of Bologna)
- Charles Khouri
(Univ. Grenoble Alpes, Grenoble Alpes University Hospital
Univ. Grenoble Alpes, INSERM, Grenoble Alpes University)
Abstract
Background and aim Disproportionality analyses using reports of suspected adverse drug reactions are the most commonly used quantitative methods for detecting safety signals in pharmacovigilance. However, their methods and results are generally poorly reported in published articles and existing guidelines do not capture the specific features of disproportionality analyses. We here describe the development of a guideline (REporting of A Disproportionality analysis for drUg Safety signal detection using individual case safety reports in PharmacoVigilance [READUS-PV]) for reporting the results of disproportionality analyses in articles and abstracts. Methods We established a group of 34 international experts from universities, the pharmaceutical industry, and regulatory agencies, with expertise in pharmacovigilance, disproportionality analyses, and assessment of safety signals. We followed a three-step process to develop the checklist: (1) an open-text survey to generate a first list of items; (2) an online Delphi method to select and rephrase the most important items; (3) a final online consensus meeting. Results Among the panel members, 33 experts responded to round 1 and 30 to round 2 of the Delphi and 25 participated to the consensus meeting. Overall, 60 recommendations for the main body of the manuscript and 13 recommendations for the abstracts were retained by participants after the Delphi method. After merging of some items together and the online consensus meeting, the READUS-PV guidelines comprise a checklist of 32 recommendations, in 14 items, for the reporting of disproportionality analyses in the main body text and four items, comprising 12 recommendations, for abstracts. Conclusions The READUS-PV guidelines will support authors, editors, peer-reviewers, and users of disproportionality analyses using individual case safety report databases. Adopting these guidelines will lead to more transparent, comprehensive, and accurate reporting and interpretation of disproportionality analyses, facilitating the integration with other sources of evidence.
Suggested Citation
Michele Fusaroli & Francesco Salvo & Bernard Begaud & Thamir M. AlShammari & Andrew Bate & Vera Battini & Andreas Brueckner & Gianmario Candore & Carla Carnovale & Salvatore Crisafulli & Paola Maria C, 2024.
"The Reporting of a Disproportionality Analysis for Drug Safety Signal Detection Using Individual Case Safety Reports in PharmacoVigilance (READUS-PV): Development and Statement,"
Drug Safety, Springer, vol. 47(6), pages 575-584, June.
Handle:
RePEc:spr:drugsa:v:47:y:2024:i:6:d:10.1007_s40264-024-01421-9
DOI: 10.1007/s40264-024-01421-9
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