Renovascular Disease and Renal Artery Revascularization
Renovascular disease as a clinical syndrome rather than an angiographic finding: renal-artery obstruction, kidney function, blood-pressure behavior, and cardiac decompensation considered together before any revascularization decision. The chapter frames medical therapy, selective renal-artery revascularization, and the boundaries of intervention.
Planning conference: A practical planning-room conversation: anatomy, device or operative choices, surveillance, complications, and decision boundaries.
Choose the hostsTreat the syndrome, not the picture
Renovascular disease is not an angiographic diagnosis that obligates repair. It is a clinical syndrome in which renal arterial obstruction, kidney function, blood pressure behavior, cardiac decompensation, and systemic atherosclerotic risk intersect. In adults, atherosclerosis accounts for roughly 90% of renal-artery obstruction, so an older patient with ostial renal-artery stenosis, hypertension, chronic kidney disease, and other vascular disease should be approached as having atherosclerotic renovascular disease unless the phenotype argues otherwise . That presumption should not become diagnostic laziness. Fibromuscular dysplasia, vasculitis, neurofibromatosis, congenital bands, extrinsic compression, and radiation injury remain important alternative causes, particularly when the patient is younger, female, pediatric, lacks systemic atherosclerotic disease, or has mid- or distal-vessel involvement rather than typical ostial disease.
- In adults presenting with renal-artery stenosis, treat atherosclerosis as the prior diagnosis but explicitly consider FMD, vasculitis, and rare causes when the phenotype does not fit.
- Trigger
- Adults with renal-artery obstruction of any cause.
- Branch / Endpoint
- Distribution shifts toward FMD and inflammatory disease in younger women and in pediatric populations.
Citation - Plan imaging and intervention with the assumption that ostial/proximal aorto-renal disease dominates, and that intervention technique must address aortic plaque shoulder.
- Trigger
- Adults with atherosclerotic renal-artery stenosis.
- Branch / Endpoint
- Mid- and distal-vessel disease should prompt re-evaluation for FMD or inflammatory etiology.
Citation - Apply CORAL conclusions specifically to populations matching its inclusion criteria; extend cautiously to flash pulmonary edema or rapidly progressive renal failure not represented in the trial.
- Trigger
- Adults with severe ARAS and hypertension or CKD.
- Branch / Endpoint
- Inclusion required stable renal function and no nephrotic-range proteinuria.
Citation - Filter referrals through a structured indication checklist that documents resistant hypertension definition, rate of GFR decline, or episodes of flash pulmonary edema.
- Trigger
- Adults with atherosclerotic renovascular disease being considered for revascularization.
- Branch / Endpoint
- Narrative review; recommendations integrate evidence and expert opinion rather than de novo RCT data.
Citation
The first decision for the surgeon is not whether the artery looks narrow, but whether the stenosis plausibly explains a treatable clinical problem. Atherosclerotic renal-artery stenosis may present as renovascular hypertension, ischemic nephropathy, or both, with substantial overlap; the physiology is driven in part by renin-angiotensin-aldosterone activation and sodium retention . A practical consultation note should therefore state the clinical indication in one sentence: preservation of renal function, treatment of truly resistant hypertension, prevention of recurrent flash pulmonary edema, or no current indication for revascularization. This framing prevents the common error of escalating from “stenosis present” to “stent indicated” without proving that the patient has a syndrome likely to benefit.
Assessment should be directed at findings that will change management. The history should establish the trajectory of kidney function, the number and adequacy of antihypertensive agents, the presence of pulmonary edema episodes, and the competing likelihood of intrinsic renal disease. Documentation should identify whether renal function has been stable or rapidly declining, whether hypertension is resistant despite optimal medical therapy, and whether pulmonary edema has occurred in a pattern compatible with renovascular cardiac destabilization . When the patient resembles those enrolled in randomized trials of atherosclerotic renal-artery stenosis, the default treatment is optimized medical therapy; when the patient has flash pulmonary edema, rapidly declining renal function, or truly resistant hypertension with hemodynamically confirmed stenosis, selective revascularization becomes a reasonable multidisciplinary discussion.
Imaging should answer a management question, not merely decorate the chart. Duplex ultrasound is useful for surveillance and for following known disease over time, but cross-sectional imaging is often needed when anatomic planning will influence intervention. Renal-artery MRI can provide non-contrast and contrast-enhanced angiographic assessment without iodinated contrast, making it a practical alternative when iodinated CTA is undesirable and local renal-MRA expertise is reliable . The trainee should learn to read the report with the intended treatment in mind: ostial versus mid-vessel disease, bilateral involvement, solitary functioning kidney, renal size, adjacent aortic plaque, and whether the stenosis is being called severe enough to explain the syndrome .
When resistant hypertension is the dominant syndrome, patient selection must be particularly disciplined. A covered-stent registry in adults with severe atherosclerotic renal-artery stenosis of at least 80% and resistant hypertension on at least three antihypertensive agents reported 94.3% primary patency at 9 months and a mean systolic blood pressure reduction of 15.7 mm Hg . The same cohort reported a 36-month clinically driven target-lesion revascularization rate of 7.3% and major adverse events in 8.8% of treated subjects. These data support a careful conversation in a selected resistant-hypertension phenotype, but they should not be generalized into routine stenting for every severe stenosis because the evidence is registry-based, small, and device-focused rather than a broad event-reduction trial.
Medical therapy and trial boundary
Optimized medical therapy is the default treatment for unselected atherosclerotic renal-artery stenosis. The reason is not therapeutic nihilism; it is that the randomized evidence has repeatedly failed to show that routine revascularization improves the outcomes patients care about most. In CORAL, adults with atherosclerotic renal-artery stenosis and hypertension or chronic kidney disease were randomized to stenting plus multifactorial medical therapy versus medical therapy alone. At a median follow-up of 43 months, the primary composite of cardiovascular and renal events occurred in 35.1% of the stent group and 35.8% of the medical-therapy group, with a hazard ratio of 0.94 and a 95% confidence interval from 0.76 to 1.17 . For a patient who fits the CORAL population, renal-artery stenting should not be offered as a procedure to prevent that composite endpoint.
The blood pressure signal in unselected trial populations is real but small. In CORAL, stenting produced a statistically consistent mean systolic blood pressure difference of approximately -2.3 mm Hg compared with medical therapy alone, but that modest improvement did not translate into fewer cardiovascular or renal events . Longitudinal quality-of-life analysis from the CORAL cohort similarly did not show a sustained quality-of-life advantage from adding stenting to medical therapy . The clinical implication is straightforward: do not promise the patient a meaningful symptomatic or prognostic gain from stenting when the patient has stable kidney function, no pulmonary edema syndrome, and hypertension that can be managed medically.
Systematic reviews reinforce this boundary. A Cochrane review of eight trials including 2222 hypertensive patients with atherosclerotic renal-artery stenosis concluded that balloon angioplasty, with or without stenting, was not clearly superior to medical therapy for blood pressure or renal outcomes, although it produced a small reduction in diastolic blood pressure and antihypertensive drug requirement . A later systematic review of nine randomized trials including 2309 patients found lower odds of refractory hypertension with percutaneous transluminal renal angioplasty plus best medical therapy, but no significant differences in stroke, cardiac, renal, or all-cause mortality endpoints . A 2015 pooled evidence update likewise concluded that adding revascularization to optimal medical therapy did not reduce clinical events or mortality in unselected atherosclerotic renovascular disease .
The trial boundary matters at the bedside. CORAL required stable renal function and absence of nephrotic-range proteinuria, so it should be applied to comparable patients and extended cautiously to those with syndromes under-represented in the randomized cohorts . RADAR was also designed as a multicentre prospective randomized comparison of best medical treatment alone versus best medical treatment plus renal-artery stenting, with renal-function change at one-year follow-up as the primary endpoint; its published results did not demonstrate a renal-function or hard-event advantage of stenting, but the trial enrolled fewer patients than planned and is best read as directionally supportive of the CORAL and ASTRAL experience rather than as a standalone mandate . For the resident, the practical lesson is to know exactly which patient is being compared with the randomized evidence and which patient is not.
- Do not offer renal-artery stenting for the purpose of preventing the CORAL composite endpoint in patients meeting CORAL inclusion criteria.
- Trigger
- Adults with atherosclerotic renal-artery stenosis and hypertension or chronic kidney disease.
- Branch / Endpoint
- Trial inclusion required nephrotic-range proteinuria absent and creatinine stability; results do not apply to flash pulmonary edema or rapidly declining renal function.
- Counsel patients that the magnitude of any BP benefit from stenting in unselected ARAS is small and unlikely to change global cardiovascular risk.
- Trigger
- Adults with atherosclerotic renal-artery stenosis and hypertension or CKD.
- Branch / Endpoint
- Modest BP reduction did not translate into clinical event reduction.
Medical therapy must be active and longitudinal. Because renovascular hypertension reflects RAAS activation and sodium retention, ACE inhibitors or ARBs are often physiologically appropriate, but bilateral stenosis or a solitary functioning kidney requires special caution and creatinine monitoring after initiation or dose escalation . Risk-factor treatment should be handled as systemic vascular secondary prevention, not as kidney-only management: statin therapy, antiplatelet therapy when otherwise indicated, blood-pressure control, glycemic control, and smoking cessation belong in the same plan as renal duplex surveillance and nephrology follow-up . The surgeon should not let a “no stent” decision become a “no treatment” decision; atherosclerotic renal-artery stenosis is a marker of diffuse vascular risk .
There remains a narrow but important group in whom revascularization is clinically sensible despite the randomized trial boundary. Patients with flash pulmonary edema, rapidly declining renal function, or truly resistant hypertension despite optimal medical therapy and hemodynamically confirmed stenosis are the group in whom selective intervention may be appropriate . A prospective two-center cohort of consecutive high-risk patients undergoing renal-artery stenting reported clinical benefit signals in patients with rapidly declining renal function or flash pulmonary edema, supporting referral of these CORAL-excluded phenotypes for multidisciplinary review . Pharmacologic adjuncts to renal stenting, including mitochondrial-protection strategies such as elamipretide, remain investigational and should not be offered outside clinical-trial settings .
Technique follows indication
The operative plan follows the indication, not the other way around. In atherosclerotic renal-artery stenosis, disease usually involves the ostium and proximal third of the renal artery and often includes the adjacent aorta; advanced cases may also have segmental and diffuse intrarenal atherosclerosis . This anatomy explains why an apparently simple renal lesion can be technically unforgiving. The lesion is frequently an aorto-ostial plaque shoulder rather than an isolated tubular narrowing, and a procedure that fails to treat the ostium adequately risks leaving the hemodynamic problem behind. Conversely, mid- or distal-vessel disease should make the surgeon reconsider the diagnosis and look for fibromuscular dysplasia or inflammatory disease rather than forcing an atherosclerotic template onto the case.
- Kidney-transplant recipient with hypertension, graft dysfunction, bruit, or high-risk anastomotic configuration.
- Interval
- Early post-transplant assessment and symptom-triggered reassessment.
- Action
- Evaluate for transplant renal-artery stenosis when clinical graft dysfunction or resistant hypertension emerges.
- Modality
- Duplex ultrasound with CTA/MRA or angiography when findings would change treatment.
- Caveat
- Reported prevalence varies by definition, center, and screening strategy.
Citation - Transplant recipients with delayed graft function, cardiovascular comorbidity, donor-age risk, or complex anastomosis.
- Interval
- Risk-stratified post-transplant surveillance rather than native-ARAS progression follow-up.
- Action
- Intensify TRAS surveillance when risk markers cluster and graft function or blood pressure deteriorates.
- Modality
- Risk-stratified duplex follow-up, with cross-sectional confirmation before intervention.
- Caveat
- Risk-marker strength varies by transplant center and era.
Citation
The pre-procedural plan should explicitly connect the target lesion to the clinical objective. If the objective is blood pressure control, the patient should have truly resistant hypertension despite appropriate medical therapy and severe, hemodynamically meaningful atherosclerotic renal-artery stenosis . If the objective is preservation of kidney function, the record should show a trajectory of rapid decline rather than chronic stable renal impairment of uncertain cause. If the objective is prevention of pulmonary edema, the episodes should be clearly documented and clinically compatible with renovascular destabilization . A technically successful stent placed for a poorly defined indication is not a successful vascular operation; it is an anatomic intervention without a durable clinical endpoint .
Baseline risk stratification should include factors that make benefit less predictable. Atherosclerotic renal-artery stenosis is associated with progressive loss of renal mass and function, with renal atrophy reported in roughly 21% of patients with 60% obstruction in a renovascular hypertension subgroup . Advanced renal atrophy and diffuse intrarenal atherosclerosis reduce the plausibility that restoring main renal-artery caliber will restore renal function. Elevated serum uric acid was associated with worse renal and blood-pressure outcomes after renal-artery stenting in a renal revascularization registry, making it a reasonable baseline variable to document as a candidate prognostic marker, while recognizing that it is not a randomized selection criterion .
Device choice should be discussed in the context of the lesion and the strength of evidence. For the selected severe ostial atherosclerotic stenosis with resistant hypertension, covered-stent treatment has registry support: the ARTISAN experience reported high 9-month primary patency and meaningful mean systolic blood pressure reduction, with late clinically driven target-lesion revascularization that must be included in consent . That evidence is useful for counseling but limited by single-arm design and small cohort size. A good resident should be able to say both parts in the same sentence: the device may be reasonable for a carefully selected resistant-hypertension phenotype, and the data do not overturn the randomized trial conclusion against routine stenting in unselected atherosclerotic renal-artery stenosis .
Transplant renal-artery stenosis is a distinct technical and surveillance problem. Contemporary systematic reviews identify recipient cardiovascular comorbidity, delayed graft function, surgical anastomotic factors, and donor age among consistent risk markers, supporting intensified surveillance in higher-risk transplant recipients . A separate systematic review estimates transplant renal-artery stenosis prevalence at several percent globally, with substantial heterogeneity driven by geography and stenosis definitions . In practice, transplant cases should be evaluated with attention to anastomotic configuration, graft function, and center-specific imaging quality; the clinical question is preservation of graft function and blood pressure control, not treatment of a native ostial plaque phenotype.
Clinical integration, follow-up, and evidence boundaries
Follow-up after a diagnosis of atherosclerotic renal-artery stenosis should be planned even when no intervention is performed. In a duplex-surveillance cohort of 170 patients with atherosclerotic renal-artery stenosis, the cumulative 5-year incidence of stenosis progression reached approximately 51% . That figure justifies longitudinal surveillance rather than a one-time diagnostic declaration. A practical schedule should include at least annual renal duplex in patients with documented disease and ongoing risk factors, with earlier reassessment when blood pressure control deteriorates, renal function declines, or pulmonary edema occurs .
Surveillance findings should be interpreted with the clinical course. Progression on duplex is important, but it does not automatically create an indication for stenting; it becomes meaningful when paired with a management-changing syndrome such as rapidly declining kidney function, truly resistant hypertension, or flash pulmonary edema . Similarly, stable duplex findings do not end the surgeon’s responsibility if the patient’s systemic vascular risk is poorly controlled. Atherosclerotic renal-artery stenosis is associated with coronary event risk and progressive renal mass loss, so each follow-up visit should revisit cardiovascular prevention, blood pressure regimen, renal function trajectory, and whether the working diagnosis still fits the anatomy and clinical pattern .
After renal-artery intervention, surveillance has two purposes: detecting lesion failure and judging whether the clinical endpoint was achieved. The operative note and follow-up plan should state the preoperative indication, technical result, intended clinical endpoint, and the first surveillance interval. Blood pressure, medication burden, serum creatinine trajectory, and recurrent pulmonary edema are more important than patency alone because the operation was performed to treat a clinical syndrome . Late failure is not rare enough to ignore; in the covered-stent resistant-hypertension cohort, clinically driven target-lesion revascularization was 7.3% at three-year follow-up . A surveillance report that suggests restenosis should trigger a return to the indication checklist before any repeat intervention .
Complication counseling should be specific. In the Cochrane review of renal angioplasty with or without stenting, procedural complications included groin hematoma in roughly 6.5%, femoral pseudoaneurysm in less than 1%, renal-artery or kidney perforation/dissection in about 2.5%, and peri-procedural death in approximately 0.4% . These older aggregate rates may not match a contemporary high-volume practice exactly, but they are useful benchmarks for consent and for deciding whether an institution’s threshold for intervention is appropriately selective. The resident should learn to present these risks plainly, especially when the expected benefit is a small blood pressure change rather than prevention of a clear high-risk syndrome .
- Adults with established ARAS undergoing serial renal duplex.
- Action
- Schedule serial renal duplex follow-up at least annually in patients with documented ARAS and ongoing risk factors.
- Clinical point
- In a 170-patient duplex-surveillance cohort with atherosclerotic renal-artery stenosis, cumulative 5-year incidence of stenosis progression reached approximately 51 percent, supporting longitudinal monitoring rather than one-time evaluation.
- Caveat
- Single-center cohort; absolute progression rates may be lower with intensive contemporary risk-factor control.
Citation - Hypertensive ARAS patients undergoing renal angioplasty with or without stenting.
- Action
- Heterogeneity in trial design limits subgroup conclusions; high-risk phenotypes (flash pulmonary edema, rapidly declining renal function) are under-represented.
- Clinical point
- In the Cochrane systematic review, procedural complications of renal angioplasty/stenting included groin hematoma in roughly 6.5 percent, femoral pseudoaneurysm in less than 1 percent, renal-artery or kidney perforation/dissection in about 2.5 percent, and peri-procedural death in approximately 0.4 percent.
- Caveat
- Rates aggregate older trials; modern devices and selection may yield different complication profiles.
Citation - Adults with documented ARAS, with or without renal atrophy.
- Action
- Pair renovascular evaluation with cardiovascular risk-factor escalation; do not treat ARAS as a kidney-only disease.
- Clinical point
- Atherosclerotic renal-artery stenosis is associated with progressive loss of renal mass and function (renal atrophy in roughly one in five with 60 percent obstruction) and with elevated coronary event rates, making it a vascular risk marker beyond local kidney disease.
- Caveat
- Atrophy rates depend on baseline stenosis severity and contralateral renal function.
Citation
Long-term care should not focus narrowly on the stent. In a large multicenter renal-stenting registry, long-term mortality in atherosclerotic renovascular disease was driven principally by cardiovascular causes rather than renal failure . That finding should shape survivorship care: the follow-up visit is an opportunity to intensify systemic vascular prevention, coordinate nephrology and hypertension management, and reassess whether new symptoms represent progression of diffuse atherosclerosis rather than isolated renal restenosis . For transplant renal-artery stenosis, follow-up should be risk-stratified because prevalence estimates vary and risk markers differ across centers; donor age, delayed graft function, anastomotic factors, and recipient cardiovascular comorbidity should influence how aggressively graft dysfunction or hypertension prompts imaging .
References
- 1.2024 ACC/AHA/AACVPR/APMA/ABC/SCAI/SVM/SVN/SVS/SIR/VESS Guideline for the Management of Lower Extremity Peripheral Artery Disease: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. 2024.PubMed-indexed articleClinical practice guideline2024
2024 ACC/AHA/AACVPR/APMA/ABC/SCAI/SVM/SVN/SVS/SIR/VESS Guideline for the Management of Lower Extremity Peripheral Artery Disease: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. 2024. doi:10.1016/j.jacc.2024.02.013.
- 2.
- 3.Atherosclerotic renal artery stenosis and renovascular hypertension: clinical diagnosis and indications for revascularization. Journal of clinical hypertension (Greenwich, Conn.). 2006.PubMed-indexed articleReview2006
Atherosclerotic renal artery stenosis and renovascular hypertension: clinical diagnosis and indications for revascularization. Journal of clinical hypertension (Greenwich, Conn.). 2006. doi:10.1111/j.1524-6175.2006.05442.x.
- 4.
- 5.Balloon angioplasty, with and without stenting, versus medical therapy for hypertensive patients with renal artery stenosis. The Cochrane database of systematic reviews. 2014.PubMed-indexed articleMeta-analysis / systematic review2014
Balloon angioplasty, with and without stenting, versus medical therapy for hypertensive patients with renal artery stenosis. The Cochrane database of systematic reviews. 2014. doi:10.1002/14651858.cd002944.pub2.
- 6.
- 7.Long-Term Outcomes and Causes of Death in Patients With Renovascular Disease Undergoing Renal Artery Stenting. Angiology. 2016.PubMed-indexed articleRegistry / cohort2016
Long-Term Outcomes and Causes of Death in Patients With Renovascular Disease Undergoing Renal Artery Stenting. Angiology. 2016. doi:10.1177/0003319715609013.
- 8.Impact of Serum Uric Acid Levels on Outcomes following Renal Artery Revascularization in Patients with Renovascular Disease. International journal of hypertension. 2019.PubMed-indexed articleRegistry / cohort2019
Impact of Serum Uric Acid Levels on Outcomes following Renal Artery Revascularization in Patients with Renovascular Disease. International journal of hypertension. 2019. doi:10.1155/2019/3872065.
- 9.Use of percutaneous transluminal renal angioplasty in atherosclerotic renal artery stenosis: a systematic review and meta-analysis. The Journal of international medical research. 2021.PubMed-indexed articleMeta-analysis / systematic review2021
Use of percutaneous transluminal renal angioplasty in atherosclerotic renal artery stenosis: a systematic review and meta-analysis. The Journal of international medical research. 2021. doi:10.1177/0300060520983585.
- 10.Renal Artery Stenting in Consecutive High-Risk Patients With Atherosclerotic Renovascular Disease: A Prospective 2-Center Cohort Study. Journal of the American Heart Association. 2022.PubMed-indexed articleRegistry / cohort2022
Renal Artery Stenting in Consecutive High-Risk Patients With Atherosclerotic Renovascular Disease: A Prospective 2-Center Cohort Study. Journal of the American Heart Association. 2022. doi:10.1161/jaha.121.024421.
- 11.Magnetic Resonance Imaging in Atherosclerotic Renal Artery Stenosis: The Update and Future Directions from Interventional Perspective. Kidney diseases (Basel, Switzerland). 2024.PubMed-indexed articleReview2024
Magnetic Resonance Imaging in Atherosclerotic Renal Artery Stenosis: The Update and Future Directions from Interventional Perspective. Kidney diseases (Basel, Switzerland). 2024. doi:10.1159/000534499.
- 12.
- 13.De Novo Atherosclerotic Renal Artery Stenosis Covered Stent Treatment for Resistant Hypertension (ARTISAN) Results. Journal of the Society for Cardiovascular Angiography & Interventions. 2024.PubMed-indexed articleRegistry / cohort2024
De Novo Atherosclerotic Renal Artery Stenosis Covered Stent Treatment for Resistant Hypertension (ARTISAN) Results. Journal of the Society for Cardiovascular Angiography & Interventions. 2024. doi:10.1016/j.jscai.2024.102400.
- 14.Global prevalence and contributing factors of transplant renal artery stenosis in renal transplant recipients: A systematic review and meta-analysis. Narra J. 2024.PubMed-indexed articleMeta-analysis / systematic review2024
Global prevalence and contributing factors of transplant renal artery stenosis in renal transplant recipients: A systematic review and meta-analysis. Narra J. 2024. doi:10.52225/narra.v4i3.1782.
- 15.Predictors for transplant renal artery stenosis in kidney transplant recipients: a systematic-review and meta-analysis. International urology and nephrology. 2026.PubMed-indexed articleMeta-analysis / systematic review2026
Predictors for transplant renal artery stenosis in kidney transplant recipients: a systematic-review and meta-analysis. International urology and nephrology. 2026. doi:10.1007/s11255-025-04699-5.
- 16.RADAR - A randomised, multi-centre, prospective study comparing best medical treatment versus best medical treatment plus renal artery stenting in patients with haemodynamically relevant atherosclerotic renal artery stenosis. Trials. 2009.PubMed-indexed article2009
RADAR - A randomised, multi-centre, prospective study comparing best medical treatment versus best medical treatment plus renal artery stenting in patients with haemodynamically relevant atherosclerotic renal artery stenosis. Trials. 2009. doi:10.1186/1745-6215-10-60.
- 17.A randomized, multi-center, prospective study comparing best medical treatment versus best medical treatment plus renal artery stenting in patients with hemodynamically relevant atherosclerotic renal artery stenosis (RADAR) - one-year results of a pre-maturely terminated study. Trials. 2017.PubMed-indexed articleRandomized controlled trial2017
A randomized, multi-center, prospective study comparing best medical treatment versus best medical treatment plus renal artery stenting in patients with hemodynamically relevant atherosclerotic renal artery stenosis (RADAR) - one-year results of a pre-maturely terminated study. Trials. 2017. doi:10.1186/s13063-017-2126-x.
- 18.Phase 2a Clinical Trial of Mitochondrial Protection (Elamipretide) During Stent Revascularization in Patients With Atherosclerotic Renal Artery Stenosis. Circulation. Cardiovascular interventions. 2017.PubMed-indexed articleRandomized controlled trial2017
Phase 2a Clinical Trial of Mitochondrial Protection (Elamipretide) During Stent Revascularization in Patients With Atherosclerotic Renal Artery Stenosis. Circulation. Cardiovascular interventions. 2017. doi:10.1161/circinterventions.117.005487.
- 19.Quality of life effects of renal artery stenting versus medical therapy for atherosclerotic renal-artery stenosis: results from the randomized CORAL trial. European heart journal. Quality of care & clinical outcomes. 2025.PubMed-indexed articleRandomized controlled trial2025
Quality of life effects of renal artery stenting versus medical therapy for atherosclerotic renal-artery stenosis: results from the randomized CORAL trial. European heart journal. Quality of care & clinical outcomes. 2025. doi:10.1093/ehjqcco/qcae087.
Educational use only
AI assists this editorial workflow. Published updates are human-reviewed before publication.
Not intended to diagnose, monitor, predict, prognose, treat, or alleviate disease.
Verify clinically relevant information against primary sources and current guidelines.