- Pictorial Review
- Open Access
Endovascular intervention in renovascular disease: a pictorial review
© The Author(s) 2014
- Received: 13 February 2014
- Accepted: 23 September 2014
- Published: 12 October 2014
Interventional radiologic procedures offer a significant and expanding role in the management of various renovascular diseases including renal artery stenosis, renal artery aneurysm and pseudoaneurysm, renal vascular malformations, renal tumours, trauma, and resistant hypertension. In this article, we discuss these entities in the context of currently accepted definitions, incidence, modes of diagnosis, and management as they pertain to the practice of interventional radiology. Particular emphasis is placed on current interventional procedures for managing and treating these diseases as well as emerging procedures and technologies.
• Highlights the literature on renovascular diseases
• Reviewing the role of various interventional procedures in the management of renovascular disease
• Review of imaging techniques in the identification and characterisation of renovascular disease
- Endovascular procedures
- Renal artery obstruction
- Arteriovenous malformations
The role of interventional radiology in disease management is rapidly advancing. With ongoing innovation, interventional procedures are playing a growing role in the treatment of various renovascular diseases. This article highlights the literature on renovascular diseases with an emphasis on the current endovascular procedures for managing and treating these diseases as well as emerging procedures and technologies.
Renal artery stenosis (RAS) is a narrowing of the renal arteries, often associated with renovascular hypertension and an increased risk of renal insufficiency. Atherosclerotic RAS constitutes 90 % of RAS cases, increasing in prevalence in patients with diabetes, hypertension, aortoiliac occlusive disease, and coronary artery disease, as well as with age . Fibromuscular dysplasia (FMD) accounts for fewer than 10 % of RAS cases. FMD occurs nine times more frequently in females than in males , tending to affect women aged 15 to 50 .
Numerous physiologic and imaging-based modalities exist for the evaluation of patients with clinical suspicion of RAS . Generally, noninvasive evaluations by duplex ultrasonography, magnetic resonance angiography (MRA), or computed tomographic angiography (CTA) serve as initial diagnostic tools . Subsequent catheter-based angiography permits confirmation of the RAS, aetiology, extent of intrarenal vascular disease, as well as intervention planning [1, 2]. Contrast medium must be used cautiously in patients with renal failure given the risk of contrast-induced nephropathy. Digital subtraction techniques may decrease the required contrast volume, thereby minimising impact on renal function .
The role of percutaneous transluminal renal angioplasty (PTRA) in the treatment of renovascular hypertension caused by RAS is debatable. While improvement or cure of hypertension is consistently shown in 70–98 % of FMD-induced hypertension cases , the success of atherosclerotic RAS angioplasty remains unclear. Retrospective and registry analyses have demonstrated enhanced blood pressure control and improved or stabilised renal function following RAS angioplasty [4–6]. Despite these findings, several randomised trials have consistently failed to reflect similar clinical benefit—both with and without stenting—when compared to medical therapy alone [4, 7–9]. Furthermore, while demonstrating no clear clinical benefit with regards to renal function, blood pressure, renal or cardiovascular events, or mortality, angioplasty carried substantial risk, including pulmonary oedema, myocardial infarction, renal embolisation, and renal artery perforation .
Nonetheless, many experts continue to advocate for PTRA in specific cases of RAS, such as resistant hypertension, haemodynamically significant atherosclerotic RAS (Fig. 1b), FMD-associated RAS (Fig. 2b), deteriorating renal function, bilateral atherosclerotic RAS, tight atherosclerotic RAS in a single kidney, unexplained CHF, and recurrent episodes of flash pulmonary oedema [4, 10].
True aneurysms are saccular or fusiform in morphology, encompassing all layers of the vascular wall. Generally, these lesions are secondary to underlying inherited disorders such as FMD and Ehlers-Danlos syndrome .
Indications for therapeutic intervention of RAAs include rupture, diameter >2.0 cm, renovascular hypertension, dissection, rapid expansion on serial imaging, localised symptoms (haematuria), and distal embolisation impairing renal function . While uncommon (5.6 % incidence), mortality rates from RAA rupture may be as high as 80 % . Pregnancy carries a high risk of rupture—80 % in women with pre-existing RAA—and thus some studies suggest treatment of RAAs in all women of child-bearing age [14, 15, 17].
Renal artery aneurysm classification and management
Main renal artery or large segmental branches 
Neck opening <70%a 
Neck opening ≥70 % a 
Stent grafting 
Located at bifurcation 
Y-shaped stent grafting 
Covered stent grafting 
Intralobar, intraparenchymal 
Complications of the endovascular intervention in RAA include non-target embolisation (potentially resulting in renal failure or loss secondary to infarction), worsening hypertension, stent thrombus, infection, and radiation skin burns . Available short-term data have demonstrated promising findings with respect to safety, successful aneurysm exclusion, and improvement in hypertension and renal dysfunction . Unfortunately, studies analysing the long-term efficacy of endovascular RAA intervention are currently lacking.
Unlike true aneurysms, pseudoaneurysms are periarterial haematomas resulting from a tear of the arterial wall . Typically, pseudoaneurysms are acquired because of blunt or penetrating abdominal trauma, iatrogenic injury, or inflammation, and they possess subsequent potential for enlargement and/or rupture [20, 21]. These rare lesions are often saccular in appearance and may be either intraparenchymal or extraparenchymal.
Due to a propensity for severe haemorrhage, early detection and management, particularly in haemodynamically unstable patients, are essential. CT angiogram provides the mainstay in diagnosis . Subsequent angiography offers the benefit of guiding the intervention, allowing for target vessel localisation and assessment of inflow and outflow vessel size prior to management.
Renal arteriovenous malformations (RAVMs) and renal arteriovenous fistulas (RAVFs) represent arteriovenous communications of the renal vasculature. An RAVM is a congenital network of abnormal vessels characterised as cavernous (single arterial feeder) or cirsoid (multiple arterial feeders with corkscrew appearance) in nature . Large-scale autopsy studies have indicated the prevalence of RAVMs to be approximately 1 in 30,000, with cirsoid-type RAVMs occurring more frequently than cavernous types [16, 22].
An RAVF represents a direct communication between an artery and a vein [16, 23]. Greater than three-quarters of these lesions are acquired, often resulting from iatrogenic causes such as renal biopsy, percutaneous nephrostomy, or accidental trauma .
Pain, persistent haematuria, cardiac failure, and hypertension are all indications for potential interventional treatment of RAVMs . First-line management of RAVMs typically consists of malformation destruction and arterial occlusion with sclerosing agents such as absolute alcohol. These agents stimulate thrombus formation through toxic effects on the endothelium, arterial spasm, and perivascular necrosis . Autologous clot, polyvinyl alcohol, gelatin sponge, and n-butyl cyanoacrylate glue are also proven embolic agents in this setting . Selective coil embolisation of arterial feeders may be useful in the treatment of larger RAVMs (Fig. 5c) and RAVFs as well as to rapidly decrease blood flow in acute haemorrhage (Fig. 6b) [16, 23].
Transcatheter embolisation (TCE) as treatment for RAVMs and RAVFs is considered safe and effective with studies demonstrating excellent technical success (100 %) and resolution or improvement in clinical symptoms [25, 26]. Risks include non-target infarction, toxic effects from entry of absolute alcohol into the systemic vasculature, and coil migration to non-target/venous circulation [16, 27].
Renal artery transcatheter embolisation serves a variety of roles in RCC management (Fig. 7b, c). Preoperatively, TCE is useful in devascularisation to ease surgical resection and minimise blood loss. In the palliative setting, RCC TCE may provide symptom relief from haematuria and flank pain through reduction of tumour size [28, 30]. Technical success may be achieved with a variety of embolic agents. Ethanol, polyvinyl alcohol, and embospheres are often used for renal parenchyma capillary occlusion with subsequent coil embolisation of the main renal artery and any extrarenal feeding vessels . Controversy exists regarding the long-term benefit of pre-operative embolisation with one study reporting increased 5-year survival benefit over patients who undergo nephrectomy alone [31, 32], while others demonstrated no long-term survival benefit [31, 33].
Post-embolisation syndrome—consisting of flank pain, fever, nausea or vomiting, and leukocytosis 24–72 h post-procedure—is the most common complication following TCE, occurring in over 90 % of patients and generally resolving with conservative symptomatic management . Less frequently, coil migration, non-target embolisation, and impairment of renal function may occur following TCE.
Renovascular injury is relatively uncommon, the majority of cases resulting from blunt trauma or iatrogenic causes . Three-quarters of traumatic renal artery injuries are minor (contusions or superficial lacerations), requiring only conservative management .
Renovascular injury secondary to trauma may result in haemorrhage, devascularisation, or urinary tract laceration. Regardless of the suspected injury, CT with intravenous contrast enhancement is the test of choice in the evaluation and diagnosis of renovascular trauma . Occasionally, emergent angiography with embolisation in major renal vascular disruption may be both diagnostic and therapeutic.
Haemorrhage control by embolisation has been shown to be successful in 84–100 % of renal trauma cases [31, 38]. As outlined earlier, complications from embolisation include renal infarction, iatrogenic vascular injury, and post-embolisation syndrome .
Renal artery dissection, avulsion, or laceration secondary to trauma may result in devascularisation. Traumatic dissection develops secondary to intimal tearing and subsequent thrombus formation. Endovascular stenting can be used to restore arterial flow in these cases. Nephrectomy or early surgical vascular reconstruction is avulsion and laceration given propensity for significant haemorrhage .
Renal artery pseudoaneurysms, AVFs, arteriocalyceal fistulas, and urinomas are rare lesions that may also develop secondary to renal trauma. Arteriocalyceal fistulas often present as either gross or persistent haematuria following penetrating trauma or iatrogenic injury to vascular and collecting systems. These lesions are typically amenable to selective renal artery embolisation .
Resistant hypertension (RH) is defined as “blood pressure that remains above goal in spite of concurrent use of three antihypertensive agents of different classes” or hypertension requiring four or more medications for effective management . RH affects 9 % of all hypertensive patients and 13 % of those receiving antihypertensive therapy . These patients are at an increased risk for adverse cardiovascular events.
Various factors, including renal artery stenosis, have been implicated in the development of RH. Physiologically, RH has been associated with elevated activity in both the efferent and afferent renal sympathetic nerves. Fittingly, renal denervation is an emerging endovascular treatment modality in the management of this disease [41, 42].
The denervation procedure implements the delivery of catheter-based radiofrequency ablation through the main renal artery. Thermal energy generated in this process acts to effectively disrupt the sympathetic nerves in the adventitia, thus decreasing vascular tone. While studies are ongoing, suggested indications for renal denervation include patients with uncontrolled systolic BP (>160 mmHg; >150 mmHg in diabetics) despite optimised lifestyle factors and antihypertensive medications (>3 synergistic drugs) .
Studies comparing the effectiveness of renal sympathetic denervation to standard medical therapy have demonstrated contradictory results. Early nonrandomised studies and randomised, unblinded trials have shown significant blood pressure reduction in denervation patients (BP reduction of 33/11 mmHg at 6 months) with no evidence of decline in kidney function, renal artery stenosis, or aneurysmal dilatation [41, 42]. A more recent blinded, randomised trial that incorporated a sham control procedure and a significantly larger patient population did not demonstrate a significant reduction of systolic blood pressure at 6-month follow-up .
The role of endovascular intervention in the management of renovascular disease is vast and inevitably expanding. As outlined in this review, a variety of minimally invasive procedures have been employed to treat renal artery aneurysm and pseudoaneurysm, renal arteriovenous malformations and fistulas, renal tumours, and renovascular trauma in a safe and effective manner. Endovascular intervention in renal artery stenosis remains debatable, with indications in specific circumstances, and unclear in circumstances of resistant hypertension.
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