Table 3.
Unadjusted stabilised IPTW* Cox model† | Adjusted stabilised IPTW* Cox model†‡ | |||||
cHR | 95% CI | P value | wHR | 95% CI | P value | |
Treatments (reference: adalimumab) | ||||||
Etanercept | 0.72 | 0.54 to 0.96 | 0.0261 | 0.72 | 0.53 to 0.97 | 0.0305 |
Golimumab | 0.79 | 0.39 to 1.60 | 0.5148 | 0.79 | 0.40 to 1.58 | 0.506 |
Certolizumab | 0.86 | 0.48 to 1.54 | 0.6156 | 0.84 | 0.47 to 1.50 | 0.5488 |
Infliximab | 2.01 | 0.67 to 6.02 | 0.2127 | 1.75 | 0.54 to 5.63 | 0.3486 |
Secukinumab | 1.09 | 0.79 to 1.51 | 0.6015 | 1.07 | 0.77 to 1.50 | 0.6821 |
Ixekizumab | 0.81 | 0.41 to 1.60 | 0.5383 | 0.77 | 0.38 to 1.57 | 0.4767 |
Ustekinumab | 0.58 | 0.35 to 0.94 | 0.0258 | 0.57 | 0.35 to 0.93 | 0.0256 |
Tofacitinib | 1.16 | 0.37 to 3.66 | 0.801 | 1.07 | 0.33 to 3.44 | 0.9089 |
Time-dependent covariates | ||||||
csDMARDs | NA | NA | NA | 0.9 | 0.71 to 1.15 | 0.4035 |
NSAIDs | NA | NA | NA | 1.04 | 0.80 to 1.35 | 0.7668 |
Prednisone | NA | NA | NA | 1.9 | 1.47 to 2.46 | <0.0001 |
Values in bold correspond to significant results.
*Estimated with a multinomial logistic regression including age, sex, complementary universal health coverage, active skin psoriasis, diabetes, chronic heart failure, coronary heart disease, chronic respiratory disease, chronic liver disease, sequelae of stroke, obesity (proxy), tobacco use (proxy), alcohol intake, (proxy) consumption of csDMARDS, NSAIDs, or prednisone in the 2 years before inclusion and at inclusion, and weak and strong opioids analgesics use in the 2 years before inclusion.
†Using the Sandwich estimator, with adalimumab as the comparator.
‡Adjusted for time-dependent covariates (csDMARDs, NSAIDs, and prednisone) and calendar year.
cHR, crude HR; csDMARDs, conventional synthetic disease-modifying antirheumatic drugs; IPTW, inverse probability of treatment weighting; NA, not applicable; NSAIDs, non-steroidal anti-inflammatory drugs; wHR, weighted HR.