Table 2

Clinical characteristics during follow-up of patients who developed LIP

ParametercsDMARDsTNFiTCZABARTX
N11131111
Age at LIP, years, mean (SD)66.8 (4.8)67.3 (8.3)69.2 (7.6)[73][61]
Female7 (63.6)7 (53.8)9 (81.8)[1 (100)][1 (100)]
Rheumatoid factor positive11 (100)12 (92.3)6 (54.5)[1 (100)][1 (100)]
No. of previous bDMARDs, mean (SD)0.7 (1.3)1.8 (0.8)3.3 (1.6)[4][4]
Cumulative NSAID treatment*, mean (SD)0.4 (0.4)0.4 (0.3)0.3 (0.4)[1][0.5]
Disease duration at LIP, years, mean (SD)13.2 (9.1)13.0 (7.5)15.7 (8.4)[13][12]
DAS28 prior to LIP
 ≤6 months, mean (SD)3.8 (0.7)4.0 (1.7)3.5 (2.1)[5.0][5.4]
 ≤12 months, mean (SD)3.8 (0.7)4.0 (1.6)3.7 (2.0)[5.0][5.5]
CRP (mg/L) prior to LIP
 ≤6 months, mean (SD)8.1 (7.9)25.8 (33.4)11.5 (17.6)[0.7][3.8]
 ≤12 months, mean (SD)10.6 (8.5)28.3 (33.0)16.0 (21.5)[0.7][4.2]
ESR (mm/hour) prior to LIP
 ≤6 months, mean (SD)19.4 (11.6)36.0 (27.6)14.8 (15.8)[12.0][12.0]
 ≤12 months, mean (SD)18.8 (11.3)36.0 (27.1)16.3 (13.9)[12.0][13.7]
Glucocorticoids prior to LIP
 Average over 6 months, mean (SD)5.6 (3.8)9.7 (9.3)7.5 (7.5)[5.0][10.0]
 Average over 12 months, mean (SD)5.6 (3.4)9.6 (9.0)8.1 (7.3)[5.0][10.0]
  • *Cumulative treatment with NSAID (range: 0 to 1) was calculated for each patient as: no. of follow-ups with concomitant NSAID use divided by the total no. of follow-ups.

  • ABA, abatacept; bDMARDs, biologic disease-modifying anti-rheumatic drugs; CRP, C reactive protein; csDMARDs, conventional synthetic disease-modifying anti-rheumatic drugs; DAS28, disease activity score based on 28 joints; ESR, erythrocyte sedimentation rate; LIP, lower intestinal perforation; NSAID, non-steroidal anti-inflammatory drug; RTX, rituximab; TCZ, tocilizumab; TNFi, tumour necrosis factor-α inhibitor.