Atheromatous ischaemic renal vascular disease (AIRVD) comprises ischaemic r
enal disease, atheromatous disease of the large arteries and intra-renal at
heromatosis. Cholesterol emboli and lesions of nephroangiosclerosis are oft
en associated, affecting the two kidneys. It is an increasingly common caus
e of chronic renal failure in an aging population, affecting 12 to 14% of n
ew patients requiring dialysis in the United States.
Atheromatous stenoses are very progressive with a risk of renal atrophy; th
ey are a marker of polyvascular disease, often detected during other angiog
raphic investigation. Hypertension secondary to the stenosis, still incorre
ctly called renovascular hypertension, is, however rare, affecting less tha
n 0.5% of hypertensives. For economic reasons, it is important to select pa
tients who need complementary investigation. In view of the absence of spec
ific signs of the pathology, the "presumptive" diagnosis is based on a rang
e of clinical and biological results, especially in a high risk context. Th
e method of investigation varies from team to team, depending on the availa
bility of equipment, the experience of the operators and the patient himsel
f. Duplex Doppler, spiral angioscan and magnetic resonance angiography are
the most pertinent investigations for the management of AIRVD.
When the diagnosis of renal artery stenosis has been made, the problem of r
evascularisation, the objective of which is to preserve or restore the func
tional nephronic mass, has to be treated to prevent progression to end stag
e renal failure. Although epidemiological and physiopathological evidence i
s in favour of revascularisation, only renal salvage procedures are imperat
ive. Apart from these indications, the clinical benefits of revascularisati
on have not yet been demonstrated. In all cases, the control of associated
risk factors is essential to maintain the success of revascularisation and
slow down the progression of atheromatous disease.