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. 2022 Nov 13;10(1):201–223. doi: 10.1007/s40744-022-00505-1

Table 1.

Contribution of patients and person-time to VTE analyses, by data source

Data source Country Eligible (unmatched) patients Patients included in analysesa
Baricitinib
(n)
TNFi
(n)
Baricitinib
(n)
Baricitinib exposure
(PY)
TNFi
(n)
TNFi exposure
(PY)
US data
 Aetna/Healthagen US 69 289 37 13 37 22
 Anthem (HIRD) US 255 1304 123 69 123 99
 CorEvitas US US 118 1897 112 76 112 85
 HealthVerity PS20 US 933 3953 748 236 748 3785
 Humana US 89 154 49 20 49 21
 Marketscan US 257 1599 185 84 185 78
 MDR US 188 1686 114 61 114 70
 Optum® Clinformatics® US 348 1441 284 118 284 163
 PharMetrics Plus US 473 6576 261 141 261 159
Europe and Japan data
 ARTIS Sweden 1737 6230 1685 2314 1685 2608
 BKK Germany 851 3332 765 539 765 544
 CorEvitas JP Japan 210 354 171 200 171 248
 JMDC Japan 243 1721 213 154 213 115
 SNDS France 3242 10,202 2859 1855 2859 1923
Total 9013 40,738 7606 5879 7606 6512

ARTIS anti-rheumatic therapy in Sweden, BKK Betriebskrankenkasse, HIRD HealthCore Integrated Research Database, JMDC JMDC, Inc.’s claims database, JP Japan, MACE major adverse cardiovascular event, MDR military health system data repository, n number of patients, Optum® Clinformatics® Optum’s de-identified Clinformatics® Data Mart Database, PS20 Private Source 20, PY person-years, SNDS Système National des Données de Santé, TNFi tumor necrosis factor inhibitor, US United States, VTE venous thromboembolism

aAvailable information on sample size (n) and baricitinib exposure (PY) among eligible propensity score-matched patients analyzed to assess risk of VTE