Journal List > J Korean Rheum Assoc > v.17(3) > 1003734

Kim, Kang, Ju, Kim, and Park: The Incidence of Serious Infection among Rheumatoid Arthritis Patients Exposed to Tumor Necrosis Factor Antagonists

Abstract

Objective

We wanted to investigate the incidence of serious infections among the rheumatoid arthritis (RA) patients who were treated with tumor necrosis factor α (TNF-α) antagonists.

Methods

We enrolled the 175 RA patients who were treated with TNF-α antagonists for at least 3 months during February 2003 to July 2008, and these patients were in the SMART-b cohort of Kangnam St. Mary's hospital. Patients were prescribed infliximab, etanercept or adalimumab. The data was retrospectively collected.

Results

The incidence of serious infections among the RA patients treated with TNF-α was significantly increased according to the survival analysis, as compared with that of those patient treated with conventional DMARDs (p < 0.01). The most common serious infection was pneumonia. There was no significant difference in the incidence of serious infections among the three TNF-α antagonists used in this study (p=0.96). But the serious infections occurred more often in the patients who received more than 10 mg methotrexate (MTX) per week (p=0.02).

Conclusion

RA patients treated with TNF-α antagonists had a higher incidence of serious infection. Therefore, close monitoring for serious infection is needed for RA patients who are receiving TNF-α antagonists.

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Fig. 1.
Incidence of serious infection in rheumatoid arthritis patients according to TNF- antagonists exposure (p.01). ∗TNF- antagonists group, conventional DMARDs group.
jkra-17-246f1.tif
Fig. 2.
Incidence of serious infection among TNF- antagonists (p=0.96). ∗Inflixim ab, Etanercept, Adalimumab
jkra-17-246f2.tif
Table 1.
Baseline characteristics of enrolled RA patients
Characteristics TNF-α antagonists group (%) Conventional DMARDs group (%) p-value
Number of patients 175 375
Age (years) 51.7±12.4 53.9±12.8 p=0.05
Male:Female (%) 26 (14.9):149 (85.1) 49 (13.1):326 (86.9) p=0.57
Duration of disease (years) 11.0±7.7 9.5±5.5 p<0.01
Dose of MTX (mg) 11.0±4.3 10.6±3.8 p=0.09
Dose of prednisolone (%) p<0.01
0 mg 44 (25.1) 15 (4.0)
<5 mg 115 (65.7) 321 (85.6)
5~10 mg 15 (8.6) 39 (10.4)
> 10 mg 1 (0.6)
Comorbid conditions (%)
Hypertension 25 (14.3) 80 (21.3) p=0.05
Diabetes mellitus 16 (9.1) 25 (6.7) p=0.30
Cardiac disease 7 (4.0) 11 (2.9) p=0.51
Renal disease 2 (1.1) 10 (2.7) p=0.26
Pulmonary disease 6 (3.4) 27 (7.2) p=0.08
Table 2.
Incidence of serious infection in RA patients
Serious infection TNF α antagonists group (%) Conventional DMARDs group (%)
Pneumonia 4 (2.3) 4 (1.1)
Herpes zoster 3 (1.7) 4 (1.1)
Tuberculosis 2 (1.1) 2 (0.5)
Abscess 2 (1.1) 1 (0.3)
Cellulitis 2 (1.1) 3 (0.8)
Sinusitis 1 (0.6) 1 (0.3)
Pyelonephritis 3 (0.8)
Upper respiratory infection 1 (0.3)
Total 14 (8.0) 19 (5.1)
Table 3.
Characteristics in RA patients exposed to TNF α antagonists according to serious infection
Characteristics Serious infection Non-serious infection p-value
Number of patients 14 161
Age of patients (years) 48.4±9.3 52.0±12.6 p=0.3
Age of RA diagnosis (years) 35.6±12.0 41.3±12.9 p=0.13
Male:Female (%) 3 (21.4):11 (78.6) 23 (14.3):138 (85.7) p=0.47
Prednisolone p=0.98
0 mg 4 40
≤ 5 mg 9 106
5~10 mg 1 14
> 10 mg 1
Comorbid conditions (%)
Hypertension 1 24 p=0.43
Diabetes mellitus 1 15 p=0.79
Cardiac disease 7 p=0.43
Renal disease 2 p=0.68
Pulmonary dis 1 5 p=0.43
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