Depending upon the definition used, restenosis occurs in 10-60% of pat
ients who undergo percutaneous transluminal coronary angioplasty. Rest
enosis appears to be the result of a combination of pathophysiological
processes, including elastic recoil of arterial walls, platelet depos
ition and thrombus formation and resultant fibro-cellular neointimal h
yperplasia. A range of pharmacological interventions has been used in
an attempt to reduce the rate of restenosis following angioplasty, wit
h little success. Furthermore, many patients who undergo angioplasty s
till suffer from ischaemia after the procedure. Calcium antagonists, s
uch as the long-acting dihydropyridine amlodipine, have been demonstra
ted to be effective in the control of both symptomatic and asymptomati
c ischaemia and are, therefore, likely to be of utility for this purpo
se in angioplasty patients. Calcium antagonists also exhibit character
istics that may lead to a reduction in restenosis, in that they inhibi
t platelet aggregation, reduce vasopasm and inhibit the action of mito
gens which stimulate proliferation and migration of smooth muscle cell
s. The results of five trials of calcium antagonists in angioplasty pa
tients have been individually unconvincing in terms of prevention of r
estenosis, only one trial demonstrated a significant effect. However,
a meta-analysis of these results has demonstrated an approximately 30%
reduction in the chance of restenosis in those patients treated with
calcium antagonists. The Coronary Angioplasty Amlodipine in Restenosis
(CAPARES) trial has been initiated to assess the impact of amlodipine
upon the rare of restenosis and angina/ischaemia after the procedure.