Table 2 |
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|
Baseline patient characteristics |
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|
Celecoxib (n = 28,614) |
nsNSAID (n = 15,278) |
Placebo (n = 5,827) |
Rofecoxib (n = 1,329) |
Total (n = 51,048) |
|
|
|
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|
Age, years |
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|
|
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|
Mean, SD |
60.1 (13) |
59.3 (13) |
57.2 (14) |
70.6 (9) |
59.8 (13) |
|
|
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|
≥ 65 years, n (%) |
11,404 (40) |
5,667 (37) |
1,901 (33) |
1,115 (84) |
20,087 (39) |
|
|
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|
≥ 75 years, n (%) |
3,421 (12) |
1,656 (11) |
513 (9) |
460 (35) |
6,050 (12) |
|
|
|||||
|
Female, n (%) |
18,819 (66) |
10,478 (69) |
3,251 (56) |
860 (65) |
33,408 (65) |
|
|
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|
Indication |
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|
|
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|
OA/RA, n (%) |
23,324 (82) |
13,911 (91) |
3,074 (53) |
1,329 (100) |
41,638 (82) |
|
|
|||||
|
Low-back pain, n (%) |
1,743 (6) |
850 (6) |
1,042 (18) |
0 (0) |
3,635 (7) |
|
|
|||||
|
Ankylosing spondylitis, n (%) |
895 (3) |
517 (3) |
232 (4) |
0 (0) |
1,644 (3) |
|
|
|||||
|
Alzheimer disease, n (%) |
329 (1) |
0 (0) |
158 (3) |
0 (0) |
487 (1) |
|
|
|||||
|
Oncology, n (%) |
2,323 (8) |
0 (0) |
1,321 (23) |
0 (0) |
3,644 (7) |
|
|
|||||
|
Duration, n (%) |
|||||
|
|
|||||
|
≤ 12 weeks |
15,597 (55) |
8,322 (55) |
3,871 (66) |
1,245 (94) |
29,035 (57) |
|
|
|||||
|
> 12 and ≤ 26 weeks |
7,878 (28) |
4,271 (28) |
675 (12) |
84 (6) |
12,908 (25) |
|
|
|||||
|
> 26 and ≤ 52 weeks |
2,307 (8) |
1,958 (13) |
90 (2) |
0 (0) |
4,355 (9) |
|
|
|||||
|
≥ 52 weeks |
2,832 (10) |
727 (5) |
1,191 (20) |
0 (0) |
4,750 (9) |
|
|
|||||
|
Total patient-years of exposure |
12,276.3 |
4,621.8 |
3,755.6 |
154.5 |
20,808.2 |
|
|
|||||
|
100 patient-years of exposure |
122.8 |
46.2 |
37.6 |
1.6 |
208.1 |
|
|
|||||
|
100 Patient-years of exposure = total patient-years of exposure divided by 100. nsNSAID, nonselective nonsteroidal antiinflammatory drug; OA, osteoarthritis; RA, rheumatoid arthritis. |
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|
Moore et al. Arthritis Research & Therapy 2013 15:R6 doi:10.1186/ar4134 |
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