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. 2017 Mar 31;26(10):1141–1148. doi: 10.1002/pds.4183

Table 1.

Baseline characteristics of cases with PUB and controls exposed to current use of conventional NSAIDs or selective COX‐2 inhibitors

Cases (n = 2634) Controls (n = 5074) p‐value
Age Mean (year ± SD) 68.75 ± 15.6 69.28 ± 14.6 0.135
Sex Women, n (%) 1576 (59.8) 3084 (60.8) 0.420
Concomitant drug(s) use at the index date Acid‐lowering drugs, n (%) 164 (6.2) 187 (3.7) 0.000*
Vitamin K antagonists, n (%) 399 (15.1) 244 (4.8) 0.000*
Platelet aggregation inhibitors, n (%)§ 707 (26.8) 999 (19.7) 0.000*
Glucocorticoids, n (%) 188 (7.1) 234 (4.6) 0.000*
Serotonin selective reuptake inhibitors, n (%) 132 (5.0) 205 (4.0) 0.048*
History of drug(s) use Conventional NSAIDs, n (%) 192 (7.3) 502 (9.9) 0.000*
Selective COX‐2 inhibitors, n (%) 409 (15.5) 619 (12.2) 0.000*
Conventional NSAIDs + selective COX‐2 inhibitors, n (%) 0 (0.0) 0 (0.0) NA
Acid‐lowering drugs, n (%) 1444 (54.8) 2432 (47.9) 0.000*

NSAIDs, nonsteroidal anti‐inflammatory drugs; COX‐2, cyclooxygenase‐2; PUB, perforation, ulcers, or bleeding; NA, not applicable; SD, standard deviation.

Acid‐lowering drugs (antacid and H2‐receptor antagonists).

Vitamin K antagonists (phenprocoumon and acenocoumarol).

§

Platelet aggregation inhibitors (clopidogrel, acetyl salicylic acid, dipyridamole, and prasugrel).

Acid‐lowering drugs (antacid, H2‐receptor antagonists, and proton pump inhibitors).

*

Statistically significant (p < 0.05).