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Current Approaches to Vaccine Safety Using Observational Data: A Rationale for the EUMAEUS (Evaluating Use of Methods for Adverse Events Under Surveillance-for Vaccines) Study Design.
Lai, Lana Yh; Arshad, Faaizah; Areia, Carlos; Alshammari, Thamir M; Alghoul, Heba; Casajust, Paula; Li, Xintong; Dawoud, Dalia; Nyberg, Fredrik; Pratt, Nicole; Hripcsak, George; Suchard, Marc A; Prieto-Alhambra, Dani; Ryan, Patrick; Schuemie, Martijn J.
Afiliação
  • Lai LY; Division of Informatics, Imaging and Data Sciences, University of Manchester, Manchester, United Kingdom.
  • Arshad F; Department of Biostatistics, University of California, Los Angeles, Los Angeles, CA, United States.
  • Areia C; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, United Kingdom.
  • Alshammari TM; Medication Safety Research Chair, King Saud University, Riyadh, Saudi Arabia.
  • Alghoul H; Faculty of Medicine, Islamic University of Gaza, Gaza, Palestine.
  • Casajust P; Real-World Evidence, Trial Form Support, Barcelona, Spain.
  • Li X; Centre for Statistics in Medicine, NDORMS, University of Oxford, Oxford, United Kingdom.
  • Dawoud D; Faculty of Pharmacy, Cairo University, Giza, Egypt.
  • Nyberg F; School of Public Health and Community Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Pratt N; Clinical and Health Sciences, University of South Australia, Adelaide, SA, Australia.
  • Hripcsak G; Department of Biomedical Informatics, Columbia University, New York, NY, United States.
  • Suchard MA; Department of Biostatistics, University of California, Los Angeles, Los Angeles, CA, United States.
  • Prieto-Alhambra D; Department of Human Genetics, University of California, Los Angeles, Los Angeles, CA, United States.
  • Ryan P; Centre for Statistics in Medicine, NDORMS, University of Oxford, Oxford, United Kingdom.
  • Schuemie MJ; Health Data Sciences, Medical Informatics, Erasmus Medical Center University, Rotterdam, Netherlands.
Front Pharmacol ; 13: 837632, 2022.
Article em En | MEDLINE | ID: mdl-35392566
ABSTRACT
Post-marketing vaccine safety surveillance aims to detect adverse events following immunization in a population. Whether certain methods of surveillance are more precise and unbiased in generating safety signals is unclear. Here, we synthesized information from existing literature to provide an overview of the strengths, weaknesses, and clinical applications of epidemiologic and analytical methods used in vaccine monitoring, focusing on cohort, case-control and self-controlled designs. These designs are proposed to be evaluated in the EUMAEUS (Evaluating Use of Methods for Adverse Event Under Surveillance-for vaccines) study because of their widespread use and potential utility. Over the past decades, there have been an increasing number of epidemiological study designs used for vaccine safety surveillance. While traditional cohort and case-control study designs remain widely used, newer, novel designs such as the self-controlled case series and self-controlled risk intervals have been developed. Each study design comes with its strengths and limitations, and the most appropriate study design will depend on availability of resources, access to records, number and distribution of cases, and availability of population coverage data. Several assumptions have to be made while using the various study designs, and while the goal is to mitigate any biases, violations of these assumptions are often still present to varying degrees. In our review, we discussed some of the potential biases (i.e., selection bias, misclassification bias and confounding bias), and ways to mitigate them. While the types of epidemiological study designs are well established, a comprehensive comparison of the analytical aspects (including method evaluation and performance metrics) of these study designs are relatively less well studied. We summarized the literature, reporting on two simulation studies, which compared the detection time, empirical power, error rate and risk estimate bias across the above-mentioned study designs. While these simulation studies provided insights on the analytic performance of each of the study designs, its applicability to real-world data remains unclear. To bridge that gap, we provided the rationale of the EUMAEUS study, with a brief description of the study design; and how the use of real-world multi-database networks can provide insights into better methods evaluation and vaccine safety surveillance.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies / Risk_factors_studies / Screening_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies / Risk_factors_studies / Screening_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article