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The role of the critical event committee in a major cardiovascular outcome study
Anthony Heagerty1, Anne Deverly, Christopher Palmer
1Department of Medicine, University of Manchester, UK. tony.heagerty@man.ac.uk
Insights
A Critical Event Committee (CEC) significantly improved cardiovascular outcome study data quality. The CEC reclassified many events, enhancing database accuracy and impacting study conclusions.
Area of Science:
- Cardiology
- Clinical Trials
- Epidemiology
Background:
- Cardiovascular outcome studies, including hypertension trials, often involve multiple international centers.
- This multi-center approach can complicate the accurate evaluation and classification of study endpoints.
Purpose of the Study:
- To evaluate the role and effectiveness of a Critical Event Committee (CEC) in a large cardiovascular outcome study.
- To assess the impact of CEC reclassification on endpoint evaluation and database integrity.
Main Methods:
- The INSIGHT study established a CEC to review all events in 6321 patients.
- Events were classified according to pre-determined criteria by both investigators and the CEC.
Main Results:
- The CEC reclassified over 28% of primary and 41% of secondary investigator-coded events.
- Difficult diagnoses like myocardial infarction, angina, and heart failure saw substantial reclassification.
- Post hoc analysis showed a potential 18.8% reduction in primary events after CEC review.
Conclusions:
- A CEC is essential for large-scale cardiovascular outcome studies.
- CEC scrutiny significantly enhances the quality and reliability of study databases.
Abstract:
Outcome studies in cardiovascular diseases such as hypertension are often based in a number of countries recruiting from multiple centres. This can lead to difficulties in end-point evaluation and classification. The INSIGHT study provided the unique opportunity to examine the role and usefulness of a Critical Event Committee (CEC) established to examine all events occurring in a cohort of 6321 patients and classifying them according to pre-determined criteria. More than 28% of investigator-coded primary events and more than 41% of secondary events were re-classified by the CEC. Particularly difficult diagnoses included myocardial infarction, angina and heart failure, and the database finally analysed was substantially altered after CEC Committee evaluation. Post hoc analysis of the INSIGHT database demonstrated that the primary events compared would have been reduced from 6.3% vs 5.8% of those randomized on nifedipine vs co-amilozide to 5.1% vs 4.7%--an overall reduction of 72 events of 382, a fall of 18.8%. We conclude that a CEC should be a crucial component of any large outcome study and that if all events are subjected to scrutiny, the quality of the database is greatly enhanced.
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