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Table 6 Adjusted HRs and 95% CIs for time to serious infection (n = 21,832)

From: Effectiveness and safety of tofacitinib in rheumatoid arthritis: a cohort study

Parameter

Adjusted HR

95% CI

Drug therapy

 Non-TNF biologic ± DMARDs

Reference

 DMARDs

0.80

0.62–1.03

 TNFi ± DMARDs

1.14

0.95–1.37

 Tofacitinib ± DMARDs

1.54

0.93–2.56

Current use of methotrexatea

1.19

1.04–1.37

Previous use of biologicsa

1.32

1.12–1.57

Previous use of other DMARDsa

1.04

0.86–1.27

Sex (female)

1.02

0.87–1.18

Age

1.04

1.03–1.04

Year of cohort entry

 2011

Reference

 2012

1.10

0.92–1.31

 2013

0.85

0.66–1.08

 2014

0.97

0.70–1.35

Oral glucocorticoid use one year prior to cohort entry

 No use

Reference

 Use of ≤ 7.5 mg/day of prednisone equivalent dose

1.23

1.05–1.44

 Use of > 7.5 mg/day of prednisone equivalent dose

1.36

1.00–1.84

Current use of oral glucocorticoida

 No use

Reference

 Use of ≤ 7.5 mg/day of prednisone equivalent dose

1.90

1.64–2.20

 Use of > 7.5 mg/day of prednisone equivalent dose

2.83

1.37–5.83

Nonsteroidal anti-inflammatory drugs use 1 year prior to cohort entry

0.93

0.81–1.06

Selective COX-2 inhibitors use 1 year prior to cohort entry

1.13

0.95–1.35

Charlson comorbidity index 1 year prior to cohort entry

1.72

1.49–1.99

Infection related hospitalization 1 year prior to cohort entry

2.19

1.68–2.86

Number of emergency department visits 1 year prior to cohort entry

1.04

1.01–1.06

Number of physician visits 1 year prior to cohort entry

1.01

1.00–1.01

Number of rheumatology visits 1 year prior to cohort entry

1.00

0.99–1.02

Number of hospitalizations 1 year prior to cohort entry

1.33

1.24–1.43

  1. DMARDs Disease-modifying antirheumatic drug, TNFi Tumor necrosis factor inhibitors
  2. aTime-varying covariates