Mjs. Langman et al., RISKS OF BLEEDING PEPTIC-ULCER ASSOCIATED WITH INDIVIDUAL NONSTEROIDAL ANTIINFLAMMATORY DRUGS, Lancet, 343(8905), 1994, pp. 1075-1078
Treatment with non-steroidal anti-inflammatory drugs (NSAIDs) is assoc
iated with an increased risk of peptic ulcer complications, but it is
not clear whether some drugs are more likely than others to cause such
complications. We compared previous use of NSAIDs in 1144 patients ag
ed 60 and older admitted to hospitals in five large cities with peptic
ulcer bleeding and in 1126 hospital controls and 989 community contro
ls matched for age and sex. Peptic ulcer bleeding was strongly associa
ted with use of non-aspirin NSAIDs of any type during the 3 months bef
ore admission (411 cases, 351 controls; odds ratio 4.5 [95% Cl 3.6 to
5.6]). The odds ratios for peptic ulcer bleeding were lowest for ibupr
ofen (2.0 [1.4-2.8]) and diclofenac (4.2 [2.6-6.8]), and intermediate
for indomethacin, naproxen, and piroxicam (11.3 [6.3-20.3], 9.1 [5.5-1
5.1], and 13.7 [7.1-26.3]). Azapropazone and ketoprofen carried the hi
ghest risks (31.5 [10.3-96.9] and 23.7 [7.6-74.2]). Risks also increas
ed with drug dose (low dose 2.5 [1.7-3.8], intermediate 4.5 [3.3-6.0],
and high 8.6 [5.8-12.6]) for all drugs combined. Appropriate clinical
strategies could prevent many episodes of peptic ulcer bleeding: NSAI
Ds should be used only in patients who do not respond to other analges
ics; the lowest possible doses should be used; and the least toxic NSA
IDs should be selected.