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Updated: Jun 18, 2026

A Modified Two Kidney One Clip Mouse Model of Renin Regulation in Renal Artery Stenosis
Published on: October 26, 2020
Revascularization versus medical therapy for renal-artery stenosis
Insights
Percutaneous revascularization for atherosclerotic renovascular disease shows significant risks without clear clinical benefit. Medical therapy alone is a viable option, with similar outcomes for renal and cardiovascular events.
Area of Science:
- Cardiovascular Medicine
- Nephrology
- Interventional Cardiology
Background:
- Atherosclerotic renovascular disease (ARVD) affects renal artery patency through revascularization.
- Clinical benefit evidence for ARVD revascularization remains limited.
Purpose of the Study:
- To evaluate the clinical benefit of percutaneous revascularization in patients with ARVD.
- To compare renal function, blood pressure, and clinical events between revascularization and medical therapy alone.
Main Methods:
- A randomized, unblinded trial involving 806 patients with ARVD.
- Patients were assigned to either revascularization plus medical therapy or medical therapy alone.
- Primary outcome: renal function (reciprocal of serum creatinine); Secondary outcomes: blood pressure, renal/cardiovascular events, mortality. Median follow-up: 34 months.
Main Results:
- Revascularization showed a trend toward slower renal impairment progression (P=0.06) but no significant difference in mean serum creatinine levels.
- No significant differences were observed in systolic blood pressure, renal events, major cardiovascular events, or mortality between groups.
- Revascularization carried substantial risks, including 2 deaths and 3 amputations.
Conclusions:
- Percutaneous revascularization in ARVD patients presents significant risks.
- The study found no evidence of a worthwhile clinical benefit from revascularization compared to medical therapy alone.
Background:
Percutaneous revascularization of the renal arteries improves patency in atherosclerotic renovascular disease, yet evidence of a clinical benefit is limited.
Methods:
In a randomized, unblinded trial, we assigned 806 patients with atherosclerotic renovascular disease either to undergo revascularization in addition to receiving medical therapy or to receive medical therapy alone. The primary outcome was renal function, as measured by the reciprocal of the serum creatinine level (a measure that has a linear relationship with creatinine clearance). Secondary outcomes were blood pressure, the time to renal and major cardiovascular events, and mortality. The median follow-up was 34 months.
Results:
During a 5-year period, the rate of progression of renal impairment (as shown by the slope of the reciprocal of the serum creatinine level) was -0.07x10(-3) liters per micromole per year in the revascularization group, as compared with -0.13x10(-3) liters per micromole per year in the medical-therapy group, a difference favoring revascularization of 0.06x10(-3) liters per micromole per year (95% confidence interval [CI], -0.002 to 0.13; P=0.06). Over the same time, the mean serum creatinine level was 1.6 micromol per liter (95% CI, -8.4 to 5.2 [0.02 mg per deciliter; 95% CI, -0.10 to 0.06]) lower in the revascularization group than in the medical-therapy group. There was no significant between-group difference in systolic blood pressure; the decrease in diastolic blood pressure was smaller in the revascularization group than in the medical-therapy group. The two study groups had similar rates of renal events (hazard ratio in the revascularization group, 0.97; 95% CI, 0.67 to 1.40; P=0.88), major cardiovascular events (hazard ratio, 0.94; 95% CI, 0.75 to 1.19; P=0.61), and death (hazard ratio, 0.90; 95% CI, 0.69 to 1.18; P=0.46). Serious complications associated with revascularization occurred in 23 patients, including 2 deaths and 3 amputations of toes or limbs.
Conclusions:
We found substantial risks but no evidence of a worthwhile clinical benefit from revascularization in patients with atherosclerotic renovascular disease. (Current Controlled Trials number, ISRCTN59586944.)
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