Non-steroidal anti-inflammatory drugs have long been known to cause gastro-
duodenal damage. However all parts of the gastrointestinal tract may be aff
ected including the small intestine, colon and oesophagus. Non-steroidal an
ti-inflammatory drugs can cause dyspeptic symptoms, erosions, ulceration, w
hich may lead to haemorrhage or perforation, and a requirement for surgery.
The purpose of this report is to assess risk factors which may lead to gas
trointestinal damage and, thus to identify those patients at greatest risk
of non-steroidal anti-inflammatory drug damage. Possible risk factors inclu
de age, sex, previous ulcer history, the presence of Helicobacter pylori, t
he type and severity of arthritis, individual nonsteroidal anti-inflammator
y drugs (dose, duration of treatment, route of administration), other debil
itating diseases, smoking, alcohol, and the use of concomitant drugs. Risk
of non-steroidal anti-inflammatory drug damage is higher in older patients
(RR>60 5.52; <60 1.65), but there is no convincing sex difference. There is
increased risk in patients with a previous history of peptic ulceration (R
R first gastrointestinal event 2.39; subsequent gastrointestinal event 4.76
), and in the first three months of treatment. Debate continues about the r
elevance of Helicobacter pylori and this will be discussed in a later repor
t There is no strong evidence that patients with rheumatoid arthritis are m
ore likely to have more trouble than those with osteoarthritis, but the for
mer are more likely to require higher doses of non-steroidal anti-inflammat
ory drugs. Highest risk non-steroidal anti-inflammatory drugs include azapr
opazone, ketoprofen and piroxicam, and those with least risk include ibupro
fen, diclofenac and etodolac. There is an increased risk of gastrointestina
l complications with relatively small-dose prophylactic aspirin. Other fact
ors increasing the risk are smoking and the presence of chronic underlying
respiratory and cardiovascular disease. Risk of gastrointestinal problems i
s increased with concomitant drugs, especially corticosteroids (RR 14.6 if
given with non-steroidal anti-inflammatory drugs), but also with anticoagul
ants and some other drugs. The clinical importance of identifying possible
risk factors lies in being aware of likely problem patients and in the use
of safer non-steroidal anti-inflammatory drugs or combination therapy with
protective drugs in these patients.