Table 4

Specific TNFI and risk of non-viral opportunistic infections in RA patients

ExposuresEventsPerson-yearsCrude rate
(per 1000 person-years), 95% CI
Adjusted HR*
Comparison of specific TNFI to non-biological DMARD
 Non-biological DMARD1374431.7 (1.0 to 3.0)1.00 (Reference)
 Etanercept1386411.5 (0.9 to 2.6)0.8 (0.4, 1.8)
 Any baseline glucocorticoid use1.7 (0.7, 4.1)
Non-biological DMARD1374431.7 (1.0 to 3.0)1.00 (Reference)
Adalimumab1542823.5 (2.1 to 5.8)1.8 (0.6, 5.3)
Any baseline glucocorticoid use2.8 (0.8, 9.9)
Non-biological DMARD1374431.7 (1.0 to 3.0)1.00 (Reference)
Infliximab5513 5194.1 (3.1 to 5.3)2.6 (1.2, 5.6)
Any baseline glucocorticoid use1.7 (0.9, 3.4)
Comparison of specific TNFI to etanercept
Etanercept1386411.5 (0.9 to 2.6)Reference
Adalimumab1542823.5 (2.1 to 5.8)1.8 (0.8, 4.0)
Any baseline glucocorticoid use2.5 (0.9, 7.3)
Etanercept1386411.5 (0.9 to 2.6)Reference
Infliximab4092634.3 (3.2 to 5.9)2.9 (1.5, 5.4)
Any baseline glucocorticoid use1.6 (0.8, 3.1)
  • *Adjusted by propensity score quintile and baseline glucocorticoid use 1 year before time zero (reference=no use).

  • Estimates were stratified by site and all 95% CI were based on robust SE.

  • DMARD, disease-modifying anti rheumatic drug; RA, rheumatoid arthritis; TNFI, tumour necrosis factor α inhibitor.