Table 1.
Subsets of the OMOP reference standard used in the three experiments
Reference Set 1 FAERS and NYP/CUMC EHR |
Reference Set 2 FAERS and GE EHR |
Reference Set 3 FAERS and claims data |
||||
---|---|---|---|---|---|---|
P | N | P | N | P | N | |
Acute renal failure | 16 | 37 | 21 | 48 | 21 | 51 |
Acute liver injury | 52 | 16 | 75 | 30 | 77 | 32 |
Acute myocardial infarction | 10 | 28 | 33 | 51 | 33 | 58 |
Upper GI bleed | 17 | 38 | 24 | 57 | 24 | 63 |
Total | 95 | 119 | 153 | 186 | 155 | 204 |
EHR electronic health record, FAERS FDA Adverse Event Reporting System, GE EHR GE Healthcare MQIC (Medical Quality Improvement Consortium) database, N negative controls, NYP/CUMC New York Presbyterian Hospital at Columbia University Medical Center, OMOP Observational Medical Outcomes Partnership, P positive controls in the reference standard