The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention.
Near real-time vaccine safety surveillance with partially accrued data†
Article first published online: 29 APR 2011
Copyright © 2011 John Wiley & Sons, Ltd.
Pharmacoepidemiology and Drug Safety
Volume 20, Issue 6, pages 583–590, June 2011
How to Cite
Greene, S. K., Kulldorff, M., Yin, R., Yih, W. K., Lieu, T. A., Weintraub, E. S. and Lee, G. M. (2011), Near real-time vaccine safety surveillance with partially accrued data. Pharmacoepidem. Drug Safe., 20: 583–590. doi: 10.1002/pds.2133
- Issue published online: 29 APR 2011
- Article first published online: 29 APR 2011
- Manuscript Accepted: 10 FEB 2011
- Manuscript Revised: 2 FEB 2011
- Manuscript Received: 22 SEP 2010
- Centers for Disease Control and Prevention (CDC). Grant Number: 200-2002-00732
- influenza vaccine;
- near real-time surveillance;
- quality control;
- vaccine safety
The Vaccine Safety Datalink (VSD) Project conducts near real-time vaccine safety surveillance using sequential analytic methods. Timely surveillance is critical in identifying potential safety problems and preventing additional exposure before most vaccines are administered. For vaccines that are administered during a short period, such as influenza vaccines, timeliness can be improved by undertaking analyses while risk windows following vaccination are ongoing and by accommodating predictable and unpredictable data accrual delays. We describe practical solutions to these challenges, which were adopted by the VSD Project during pandemic and seasonal influenza vaccine safety surveillance in 2009/2010.
Adjustments were made to two sequential analytic approaches. The Poisson-based approach compared the number of pre-defined adverse events observed following vaccination with the number expected using historical data. The expected number was adjusted for the proportion of the risk window elapsed and the proportion of inpatient data estimated to have accrued. The binomial-based approach used a self-controlled design, comparing the observed numbers of events in risk versus comparison windows. Events were included in analysis only if they occurred during a week that had already passed for both windows.
Analyzing data before risk windows fully elapsed improved the timeliness of safety surveillance. Adjustments for data accrual lags were tailored to each data source and avoided biasing analyses away from detecting a potential safety problem, particularly early during surveillance.
The timeliness of vaccine and drug safety surveillance can be improved by properly accounting for partially elapsed windows and data accrual delays. Copyright © 2011 John Wiley & Sons, Ltd.