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Med Decis Making. 2009 Mar-Apr;29(2):247-56. doi: 10.1177/0272989X08327110. Epub 2008 Nov 17.

Validation of an automated safety surveillance system with prospective, randomized trial data.

Author information

  • 1Department of Radiology, Division of General Medicine, Brigham & Women's Hospital, Boston, MA, USA. michael.matheny@vanderbilt.edu

Abstract

OBJECTIVE:

We sought to validate 3 methods for automated safety monitoring by evaluating clinical trials with elevated adverse events.

METHODS:

An automated outcomes surveillance system was used to retrospectively analyze data from 2 randomized, TIMI multicenter trials. Trial A was stopped early due to elevated 30-day mortality rates in the intervention arm. Trial B was not stopped early, but there was transient concern regarding 30-day intracranial hemorrhage rates. We compared statistical process control (SPC), logistic regression risk adjusted SPC (LR-SPC), and Bayesian updating statistic (BUS) methods with a standard prospective 2-arm event rate analysis. Each method compares observed event rates to alerting boundaries established with previously collected data. In this evaluation, the control arms approximated prior data, and the intervention arms approximated the observed data.

RESULTS:

Trial A experienced elevated 30-day mortality rates beginning 7 months after the start of the trial and continuing until termination at month 14. Trial B did not experience elevated major bleeding rates. Combining the alerting performance of each method across both trials resulted in sensitivities and specificities of 100% and 85% for SPC, 0% and 100% for BUS, and 100% and 93% for both LR-SPC models, respectively.

CONCLUSION:

Both SPC and LR-SPC methods correctly identified the majority of months during which the cumulative event rates were elevated in trial A but were susceptible to false positive alerts in trial B. The BUS method did not result in any alerts in either trial and requires revision.

PMID:
19015285
[PubMed - indexed for MEDLINE]
PMCID:
PMC2743924
Free PMC Article

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