CONSUMPTION OF NONSTEROIDAL ANTIINFLAMMATORY DRUGS AND THE DEVELOPMENT OF FUNCTIONAL RENAL IMPAIRMENT IN ELDERLY SUBJECTS - RESULTS OF A CASE-CONTROL STUDY
D. Henry et al., CONSUMPTION OF NONSTEROIDAL ANTIINFLAMMATORY DRUGS AND THE DEVELOPMENT OF FUNCTIONAL RENAL IMPAIRMENT IN ELDERLY SUBJECTS - RESULTS OF A CASE-CONTROL STUDY, British journal of clinical pharmacology, 44(1), 1997, pp. 85-90
Aims The aim of the present study was to explore the level of risk ass
ociated with community use of non-steroidal anti-inflammatory drugs (N
SAIDs). Methods We carried out a matched case-control study of the rel
ationship between recent use of NSAIDs and the presence of functional
renal impairment present at the time of hospitalisation with a range o
f clinical problems. Cases (n = 110) were consecutive patients admitte
d acutely to hospital who had serum creatinine levels greater than or
equal to 0.15 mmol l(-1), which improved by 20% or more within the nex
t 14 days, or prior to discharge from hospital. Controls (n = 189) wer
e subjects of the same sex and age (to within 5 years) as the cases, w
ho were admitted to the same hospital, who had normal serum creatinine
levels (< 0.12 mmol l(-1)) throughout their hospital stay. Informatio
n on a number of study factors, including recent use of aspirin and ot
her NSAIDs, was obtained by structured interview. Results Overall, the
re was a weak association between consumption of NSAIDs (including non
-prophylactic aspirin) and the development of functional renal impairm
ent-adjusted odds ratios (OR) with use of NSAIDs in the previous week
or in the previous month: OR 1.5 (95% CI 0.80, 2.9) and 1.8 (95% CI 0.
97, 3.4) respectively. In subjects with a previous history of renal di
sease the adjusted OR was 6.6 (0.75, 57.8) and in those with a history
of gout or hyperuricaemia the OR was 7.2 (1.3, 40.2). There was a wea
k positive relationship between the dose of drug consumed in the previ
ous week and the odds of functional renal impairment. The relationship
between risk and published figures for drug half-lives (t(1/2)) was s
tronger. The odds ratio increased from 1.2 (95% CI 0.61, 2.4) with a t
(1/2) less than or equal to 4 h, to 4.8 (1.5, 15.8) with a t(1/2) of l
ess than or equal to 12 h (P = 0.012, test for trend). This relationsh
ip remained statistically significant after adjustment for a number of
clinical variables and the dose of drug ingested. Conclusions NSAIDs
are an important cause of functional renal impairment in subjects with
renal disease or a history of gout or hyperuricemia. The half-Life of
the drug is more important than the ingested dose in determining the
risk of this outcome. Long half-life drugs should be avoided in indivi
duals who are at risk of developing renal impairment.