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Bias, Precision and Timeliness of Historical (Background) Rate Comparison Methods for Vaccine Safety Monitoring: An Empirical Multi-Database Analysis.
Li, Xintong; Lai, Lana Yh; Ostropolets, Anna; Arshad, Faaizah; Tan, Eng Hooi; Casajust, Paula; Alshammari, Thamir M; Duarte-Salles, Talita; Minty, Evan P; Areia, Carlos; Pratt, Nicole; Ryan, Patrick B; Hripcsak, George; Suchard, Marc A; Schuemie, Martijn J; Prieto-Alhambra, Daniel.
Afiliação
  • Li X; Centre for Statistics in Medicine, NDORMS, University of Oxford, Oxford, United Kingdom.
  • Lai LY; School of Medical Sciences, University of Manchester, Manchester, United Kingdom.
  • Ostropolets A; Department of Biomedical Informatics, Columbia University, New York, NY, United States.
  • Arshad F; Department of Biostatistics, University of California, Los Angeles, California, United States.
  • Tan EH; Centre for Statistics in Medicine, NDORMS, University of Oxford, Oxford, United Kingdom.
  • Casajust P; Real-World Evidence, Trial Form Support, Barcelona, Spain.
  • Alshammari TM; College of Pharmacy, Riyadh Elm University, Riyadh, Saudi Arabia.
  • Duarte-Salles T; Institut Universitari D'Investigació en Atenció Primària Jordi Gol (IDIAPJGol), Barcelona, Spain.
  • Minty EP; O'Brien Institute for Public Health, Faculty of Medicine, University of Calgary, Calgary, AB, Canada.
  • Areia C; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
  • Pratt N; Quality Use of Medicines and Pharmacy Research Centre, Clinical and Health Sciences, University of South Australia, SA, Australia.
  • Ryan PB; Observational Health Data Sciences and Informatics, New York, NY, United States.
  • Hripcsak G; Observational Health Data Analytics, Janssen R&D, Titusville, NJ, United States.
  • Suchard MA; Department of Biomedical Informatics, Columbia University, New York, NY, United States.
  • Schuemie MJ; Medical Informatics Services, NewYork-Presbyterian Hospital, NewYork, NY, United States.
  • Prieto-Alhambra D; Department of Biostatistics, University of California, Los Angeles, California, United States.
Front Pharmacol ; 12: 773875, 2021.
Article em En | MEDLINE | ID: mdl-34899334
Using real-world data and past vaccination data, we conducted a large-scale experiment to quantify bias, precision and timeliness of different study designs to estimate historical background (expected) compared to post-vaccination (observed) rates of safety events for several vaccines. We used negative (not causally related) and positive control outcomes. The latter were synthetically generated true safety signals with incident rate ratios ranging from 1.5 to 4. Observed vs. expected analysis using within-database historical background rates is a sensitive but unspecific method for the identification of potential vaccine safety signals. Despite good discrimination, most analyses showed a tendency to overestimate risks, with 20%-100% type 1 error, but low (0% to 20%) type 2 error in the large databases included in our study. Efforts to improve the comparability of background and post-vaccine rates, including age-sex adjustment and anchoring background rates around a visit, reduced type 1 error and improved precision but residual systematic error persisted. Additionally, empirical calibration dramatically reduced type 1 to nominal but came at the cost of increasing type 2 error.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article