ISSN : 1301-5680
e-ISSN : 2149-8156
Turkish Journal of Thoracic and Cardiovascular Surgery     
Diagnosis of renal arterial stenosis and quantification of the degree of stenosis: multidetector computed tomography angiography versus digital subtraction angiography
Sinan Şahin, Cemile Banu Küçükkırım
Department of Radiology, Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital, İstanbul
DOI : 10.5606/tgkdc.dergisi.2011.044

Abstract

Background: We determined the diagnostic value of multidetector computed tomography angiography (MDCTA) for detection and gradation of renal arterial stenosis (RAS).

Methods: Seventy-eight patients (53 males, 25 females; mean age 60.8±14.9 years; range 18 to 86 years) who suffered from hypertension and were found to have RAS on MDCTA or who were found suitable for endovascular treatment of an abdominal aortic aneurysm during the evaluation with MDCTA underwent digital subtraction angiographic (DSA) examinations. The MDCTA findings were compared with the DSA findings. Statistical analysis of data was performed to detect renal arterial stenosis and the degree of stenosis based on diameter measurement. The study was carried out prospectively and approved by the hospital institutional review board. Informed consent was obtained from all patients.

Results: Seventy-nine of 156 renal arteries were found to have stenosis and six were found to have occlusion while 71 were normal on MDCTA. Seventy of 156 renal arteries were found to have stenosis and six to have occlusion while 80 were normal on DSA. Overall sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy rate were found to be 97.4%, 86.3%, 87.1%, 97.2% and 91.7%, respectively. For determination of the degree of stenosis, the sensitivity was in the range of 74.1-100%, the specificity was in the range of 93.7-100%, the PPV was in the range of 55-100%, the NPV was in the range of 94.5-100%, and the accuracy rate was in the range of 90.4-100%.

Conclusion: Multidetector computed tomography angiography can be accepted as a noninvasive and reliable modality for the evaluation of RAS with high sensitivity, specificity, and diagnostic accuracy rates.

Renal artery stenosis (RAS) is one of the the underlying cause of renovascular hypertension (RVH).[1] Renal artery stenosis is one of the most frequent causes of progressive ischemic nephropathy and secondary hypertension with an estimated prevalence of 3-5% in the general population of hypertensive patients.[2-4] Despite this low proportion, the detection of RAS is important because it is a potentially curable cause of hypertension. Renovascular hypertension is mostly caused by either atherosclerotic RAS or fibromuscular dysplasia (FMD).[5] Atherosclerosis accounts for 70-90% of cases of RAS, and FMD is responsible for 10-30% of cases of RAS.[5-11] Renovascular hypertension becomes symptomatic when the stenosis of the renal artery exceeds 60%. This should be investigated in the following instances: in patients younger than 30 or older than 50 years of age with newly-developed hypertension; in patients older than 60 years of age with previously well-controlled hypertension that is now uncontrolled; in patients with the need for more than three antihypertensive drugs for controlling blood pressure; in patients with the presence of a murmur in the abdomen: and in patients with asymmetric kidney sizes that have been detected at ultrasonographic examination. The differentiation between RVH, in which the frequency varies between 0.5-5%, and primary hypertension is of high importance as treatment is possible with interventional radiological or surgical procedures. The sensitivity and specificity of clinical surveys for the determination of the disease is low. Digital subtraction angiography (DSA) is regarded as the gold standard modality to diagnose RAS. However, the invasive nature of DSA and the difficulty in assessing the pathophysiological significance of stenotic lesions with DSA have encouraged the search for more widely available, non-invasive or minimally invasive diagnostic tests, such as contrast-enhanced magnetic resonance angiography, multidetector computed tomography angiography (MDCTA), and color Doppler ultrasonography.[5,12-15]

The purpose of this study was to determine the accuracy of MDCTA as a non-invasive modality for detection and graduation of RAS by comparing it with DSA as a gold standard modality.

Methods

The prospective study was approved by the hospital institutional review board, and informed consent was obtained from all patients.

Patient selection
Seventy-eight patients (53 males, 25 females; mean age 60.8±14.9 years; range 18 to 86 years) who were either referred for renal artery MDCTA for evaluation of RVH or for abdominal aorta MDCTA for evaluation of endovascular treatment suitability for an abdominal aortic aneurysm were included in the study. Exclusion criteria for participation in the study were a history of renal insufficiency and adverse reactions to iodinated contrast agents. During the study period, no patient was excluded from the study.

All patients first underwent a MDCTA examination followed by a DSA examination. The time interval between the two examination was at least one week but not more than 25 days. Multidetector computed tomography angiography and DSA findings were independently evaluated for main renal artery stenosis by two different radiologists, each with more than four years of experience. The results were compared and a statistical analysis of data was performed to detect the main renal arterial lesions and the degree of stenosis separately. Accessory renal arteries were excluded.

Multidetector computed tomography angiography procedure
Multidetector computed tomography angiography evaluation was carried out with a 16-detector CT system (Somatom Sensation 16, Siemens, Germany). After obtaining an initial scout image (120 kV, 50 mAs), the scanning range was planned to cover the aortoiliac vascular system from the proximal abdominal aorta to the level of the inguinal ligaments. For optimal intraluminal contrast enhancement, the delay time between the start of contrast material administration and the start of scanning was obtained for each patient individually by using a bolus tracking technique (CARE-Bolus, Siemens). For this purpose, a single non-enhanced low-dose scan at the level of the proximal abdominal aorta was obtained first. Based on this axial image, a region of interest with an area of 5-15 mm2 was set in the lumen of the proximal abdominal aorta. This region of interest served as a reference for the dynamic measurements of contrast enhancement. Subsequently, a nonionic iodinated contrast medium (370 mgI/100 ml iopromidum or 350- 370 mgI/100 ml iohexol) was administered with an injection rate of 4-5 ml/sec via a 18-20 gauge needle that was placed into a superficial vein located in the antecubital fossa. The volume of contrast medium (mean, 95 ml; range, 70-120 ml) was adjusted to 1.5-2 mgI/kg. The contrast medium was administered with an automated injector (Ulrich 200, Ulrich Medical, Germany). The contrast material bolus was followed by 25 ml of saline administered at the same flow rate. At 10 seconds after the start of contrast material administration, repetitive low-dose monitoring scans (120 kV, 20 mAs, 0.5-second scanning time, onesecond interscan delay) were obtained. After reaching the preset contrast enhancement level of 100 HU, the scan initiated automatically four seconds later. During these four seconds, a signal was given for the patient to hold their breath. Data acquisition was performed craniocaudally with a protocol 16x0.75 mm detector line configuration, 3 cm section thickness, 13.5 mm/s feed rotation, 420 msec rotation time. The X-ray tube voltage setting was 120 kV, and the current varied between 140 mAs and 200 mAs, depending on the size of the patient and the heat limitations of the tube. All scanning was performed with the patients holding their breath. (mean, 13 seconds; range, 10-17 seconds). Multidetector computed tomography angiography was performed on all patients without any complications, and none of the studies were repeated because of technical problems. The intravenous catheter was inserted while the patient was in the CT suite. The examination time, defined as the time from patient entry into the CT suite until the source data was available for three-dimensional reconstruction, was recorded for each patient.

Image post-processing
The axial source images were reconstructed retrospectively with a 1 mm slice thickness and a 0.7 mm interval. This was then post-processed on a workstation (Navigator, Siemens Medical Systems, Germany) to obtain multiplanar reformation (MPR) images and maximum intensity projection (MIP) images. Curved planar reformat (CPR) images were generated in axial and coronal planes. Curved planar reformat images were obtained by manually paralleling the center of the renal artery.

The degree of stenosis was determined by a combined evaluation of axial images with coronal MIP along with axial and coronal CPR images. Image post-processing was performed by a technician with three years of experience in angiographic image post-processing in MDCTA. If there was any hesitation, the post-processing was repeated and re-evaluated by one of the radiologists. The degree of stenosis was determined by the ratio of the diameter of the most stenotic segment of the renal artery in compared to the diameter of the normal part of the renal artery just distal part of the stenotic segment. If post-stenotic dilatation was present, the normal part was accepted after that segment.

Digital subtraction angiography procedure
Angiographic examination were performed with a DSA equipped system (Axiom Artis FC, Siemens, Germany) with either a femoral or high brachial (axillary) approach. Renal arteries were evaluated by an abdominal aortogram followed by selective catheterization in patients referred for evaluation of renal artery stenosis. They were then evaluated with abdominal aortograms with a 14 cm or 20 cm field of view at various projections in patients referred for evaluation of abdominal aortic aneurysm for endovascular therapy. In the first group, a non-calibrated pigtail catheter (Boston Scientific, USA) was used while a calibrated pigtail catheter (Pbn, Netherlands) was used in the second group. The pigtail catheter tip was positioned between the 12th thoracic and first lumbar vertebrae, and 18-25 ml of a nonionic iodinated contrast material (370 mgI/100 ml of iopromidum) was injected. Then each renal artery was catheterized selectively with either a cobra catheter (Boston Scientific, USA) or a Simmons 1 catheter (Boston Scientific, USA), and 8-15 ml of nonionic contrast material was administered in each run for the first group. In the second group, the catheter tip was subsequently positioned above the aortic bifurcation for DSA of the pelvic arteries, and 20 ml of contrast material was injected in each run. In all patients, additional oblique projections were obtained for evaluation of the aortoiliac arteries. In particular, the arterial segments of both renal arteries were examined by using additional 15°-25° left and right anterior oblique projections. Lateral projections were performed in the second group of patients and performed only if necessary in the first group of patients. No prior conscious sedation was performed in any patient. Digital subtraction angiography was performed in all patients without any complications. All patients who had more than 70% stenosis on MDCTA images were premedicated (starting four days before the procedure with clopidogrel 75 mg/day, aspirin 100 mg/day) before the DSA examination. If renal arterial stenosis was confirmed at DSA, stent implantation or percutaneous transluminal angioplasty was performed during the same session. The calculation of the degree of stenosis was performed on the projection where the renal arterial stenosis and pre-stenotic and post- stenotic renal arterial segments were best visualized full of contrast. The degree of stenosis was determined via an automated calculation program on the angiographic equipment or manually calculated by dividing the diameter of the most stenotic segment by the diameter of the normal part of the renal artery just distal part of the stenotic segment. If post-stenotic dilatation was present, the normal part was accepted after that segment. Manual calculation was performed if renal arterial tracing was not optimal in the automated calculation.

Statistical analysis
Renal artery lesions were grouped as normal (<10%), mild (11-49%), moderate (50-70%), severe (70%<), and occluded. Both MDCTA and DSA findings were compared for detection of renal arterial lesions (stenosis and occlusion) and for determining the degree of stenosis. Digital subtraction angiography was accepted as the gold standard modality and sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy rate (AR) were calculated.

Results

Fifty-one (65.4%) patients were referred for RVH evaluation, and 27 (34.6%) patients were referred for abdominal aortic aneurysm evaluation. Demographic data of the patients is given in table 1.

Table 1: Demographic data of the patients for MDCTA angiography and DSA

In 78 patients a total of 156 renal arteries (78 left, 78 right) were evaluated with both MDCTA and DSA. Multidetector computed tomography angiography showed 85 renal arterial lesions, and DSA showed 76 (Table 2). Multidetector computed tomography angiography revealed 71 (45.5%) normal, 79 (50.7%) stenotic, and six (3.8%) occluded arteries. Digital subtraction angiography revealed 80 (51.3%) normal, 70 (44.9%) stenotic, and six (3.8%) occluded arteries. Sixtynine arteries were normal; 20 were mildly stenotic, 11 were moderately stenotic, 29 were severely stenotic, and six were occluded on both modalities (Figure 1-3). Eleven arteries that had mild (n=8), moderate (n=2), and severe (n=1) stenosis on MDCTA were found to be normal in DSA (Figure 1, 4). Two arteries were normal in MDCTA while one was mildly stenotic, and one was moderately stenotic in DSA. Six arteries were moderately stenotic at MDCTA while all were mildly stenotic in DSA. One artery was severely stenotic in MDCTA while it was moderately stenotic in DSA (Table 3).

Figure 1: Selective (a) substracted and (b) native angiography images show severe stenosis (arrow) at the proximal part of the right main renal artery and normal left main renal artery (not shown), (c) volume rendering technique image shows the moderate degree of stenosis (arrow) and hypodense millimetric area (arrowhead, also seen on axial images, but not shown, confirmed as cyst on ultrasound exam), (d, e) Maximum intensity projection images show severe degree of stenosis (arrow), (f, g) Coronal and axial curved planer reformat images show the severe degree of stenosis (arrow) and mild stenosis on the left main renal artery. Coronal curved planer reformat image also shows the extension of the plaque from the aorta to both main renal arteries (arrowheads).

Figure 2: Abdominal aortogram (a, b) shows severe osteal stenosis (arrows) at the left main renal artery and mild osteal stenosis on the right, (c) volume rendering technique image shows the severe degree of stenosis (arrows), but normal right renal artery, (d) Maximum intensity projection image shows the severe degree of stenosis (arrows) and renal artery wall calcification on the right (arrowhead), (e, f) Coronal and axial curved planer reformat images show the severe degree of stenosis (arrow) on the left and show mild osteal stenosis (arrowheads) on the right.

Figure 3: (a) Selective right renal angiogram shows severe stenosis (arrow) in the mid portion of the right main renal artery and poststenotic dilatation (arrowheads), (b, c) volume rendering technique images show the severe degree of stenosis (arrow), post-stenotic dilatation, and normal left main renal artery, (d, e) Maximum intensity projection images show the severe degree of stenosis (arrow), post-stenotic dilatation, and normal left main renal artery, (f, g) Coronal and axial curved planer reformat images show the severe degree of stenosis (arrow), post-stenotic dilatation, and normal left main renal artery, On all reformatted computed tomography images, there is a cortical defect at the right kidney that may be the result of a sequel (asterix).

Figure 4: Abdominal aortogram (a) shows moderate-severe stenosis at the proximal part of the right main renal artery and normal left main renal artery, (b) selective right main renal artery angiogram shows severe stenosis (arrow), (c, d) volume rendering technique image shows the severe degree of stenosis (arrow) and mild osteal stenosis at the left main renal artery (arrowhead), (e, f) Maximum intensity projection images show the severe degree of stenosis on the right and moderate degree of stenosis on the left, (g, h) Coronal and axial curved planer reformat images show the severe degree of stenosis (arrow) on the right and moderate stenosis on the left.

Table 2: Comparison of the MDCTA findings with DSA findings

Table 3: Correlation of the degree of stenosis between the multidetector computed tomography angiography and digital subtraction angiography findings

These findings revealed 97.4% sensitivity, 86.3% specificity, 87.1% PPV, 97.2% NPV, and 91.7% AR for the MDCTA in detecting renal arterial lesions, including stenosis and occlusions. For determining the degree of stenosis, the sensitivity, specificity, PPV, NPV, and AR values were found to be in the range of 74.1-100%, 93.7- 100%, 55-100%, 94.5-100%, 90.4-100%, respectively (Table 4).

Table 4: Statistical parameters in the degree of stenois

Discussion

The early diagnosis and treatment of renovascular hypertension, a relatively rare cause of hypertension, has significantly reduced the development of cardiovascular diseases, renal failure, and cerebrovascular events in critical patients. Since DSA is still accepted as the gold standard method, screening of hypertensive patients with an invasive method would not be appropriate. However, considering the presence of a treatable serious complication, the determination or elimination of stenosis is very important.[16]

The MDCTA has become one of the most preferred, non-invasive methods for evaluating many arterial systems in the body. Rapid developments in CT technology, like MDCT usage, is eliminating the need for the conventional spiral CT to evaluate arterial systems. With MDCT, a larger volume can be scanned in less time with higher spatial resolution using less contrast agents. This may facilitate multiplanar reconstructed and reformatted images.[14,17]

Evaluation of axial images with reformatted images, such as MIP, volume rendering technique (VRT) and CRP, facilitates clearer evaluation and helps to determine details not previously seen.[14,18] However, arteries evaluated with only VRT or MIP images can lead to exaggerated results with inner lumen stenosis and calcifications.[18] Only using the axial images to evaluate tortuous vessels may lead to false positive results.[19] Johnson et al.[20] compared the MIP and VRT protocols with DSA for renal arterial stenosis of over 50% in 25 patients and reported the sensitivity and specificity as 94% and 87% versus 89% and 99%, respectively. They also reported that combining both protocols increases the sensitivity and specificity. Rubin et al.[21] also reported the sensitivity and specificity for MIP protocol in determining the renal arterial stenosis of over 70% in 31 patients as 92% and 83%, respectively. Although Saba et al.[22] suggested that the best performance for the study of the renal arteries was given by MIP and VRT, they did not correlate the results with DSA.

Prokop[23] suggested a bolus triggering technique for optimal imaging of the renal arteries and for the evaluation of axial images with MIP and VRT reformatted images. He reported sensitivity, specificity, and NPV as 90%, 98% and 95%, respectively. Hahn et al.[24] e valuated 63 renal arteries with MDCTA and DSA, and they reported sensitivity, specificity, PPV, and NPV as 90%, 98%, 90% and 98%, respectively. Fraioli et al.[25] compared the diagnostic value of MDCT with DSA for the detection and quantification of both main and accessory renal artery stenosis in patients with secondary hypertension, and they reported 100% sensitivity, 97.3% specificity, 97.8% AR, 98.2% PPV, and 97.8% NPV for 50%-100% luminal narrowing. They concluded that MDCTA is very accurate and robust, even for the assessment of renal artery stenosis and that it has the potential to become a viable substitute, in most cases, for diagnostic, catheter-based DSA.

There are many reports in the literature that confirm the sensitivity and specificity of the MDCTA / CTA being as high as 97-100% compared to DSA.[9,20,26-31] Vasbinder et al.[26] in one of the largest reported series, studied the accuracy of the MDCTA and MRA by comparing the findings with DSA for the diagnosis of renal artery stenosis in 356 patients. They reported 20% of the patients had 50% or more stenotic segments in all three methods and reported the sensitivity and specificity for MDCTA is 64% and 92% while for MRA it is 62% and 84% respectively. They pointed out that technical insufficiencies, lack of experience in grading the stenosis, and poor patient selection might be reasons for the low sensitivity results.

In our study, we used a bolus triggering technique, and all renal arterial branches were clearly visualized and evaluated. We compared MDCTA findings with DSA findings in the evaluation of RAS and the determination the degree of stenosis. For detection of renal arterial lesions, the overall sensitivity was 97.4%, specificity was 86.3%, PPV was 87.1%, NPV was 97.2%, and AR was 91.7%. In three patients, renal arteries were moderately and severely stenotic in MDCTA while normal in DSA (Figure 3). In two patients, false positive results were attributed to obesity in one patient and tortuosity of the vessel in the other. We believe that in the case of obesity, modifying the examination parameters (kV and mA) may prevent such false positive results. In the latter case, the reason may be a lack of experience. We established that CPR images are more helpful than VRT images in determining stenosis, especially in tortuous anatomy, if processed both in axial and in coronal planes. Also, evaluating axial images with CPR and MIP images facilitates the diagnosis of stenosis and determines the degree of stenosis more accurately than evaluation with axial images or MIP images alone. Nevertheless, it should be kept in mind that experience in image post-processing is very important, especially in CPR images; the degree of stenosis may be upgraded or downgraded if image post-processing is done only in one plane.

There were also differences between MDCTA and DSA modalities in determining the degree of stenosis in the renal arteries (Table 3). For grading the stenosis with MDCTA, sensitivity was found to be in the range of 74.1-100%, specificity in the range of 93.7-100%, PPV in the range of 55-100%, NPV in the range of 94.5-100%, and AR values in the range of 90.4-100% (Table 4).

If the stenosis classification is rearranged according to the therapeutic approach criteria (medical therapy for ≤70% stenosis and surgical or interventional therapy for >70% stenosis), normal, mild, and moderate groups would be considered as one group (Table 5). After reclassification of the groups, sensitivity, specificity, PPV, NPV, and AR were found to be 98.3%, 97.2%, 99.2%, 94.5%, and 98.1%, respectively. These results show that sensitivity, specificity, PPV, NPV, and AR increased as the degree of stenosis increased. Reevaluation of the groups following reclassification according to the therapeutic approach criteria showed that the degree of stenosis was upgraded in three renal arteries and downgraded in one renal artery in MDCTA. Patients with upgraded results may undergo an angiographic procedure that will clearly delineate the degree of stenosis and may lead to a reliance on medical therapy instead of interventional therapy. The downgraded result may lead to a preference for medical therapy instead of interventional or surgical therapy which may increase the degree of ischemic nephropathy. It is obvious that misgraded results will cause a delay in the appropriate therapy to be scheduled, and we believe it may not only be related to technical reasons, but also to the experience of the reporters.

Table 5: Distribution of the lesions after unifying the normal, mild and moderate degree of stenosis groups in multidetector computed tomography angiography and digital subtraction angiography

As a result, we think MDCTA may be preferred as a noninvasive modality during the investigation or evaluation of RVH, RAS and also for the therapeutic planning of RAS. In addition, it will become an alternative to the DSA with high sensitivity, specificity, and accuracy as MDCT technology and image postprocessing software continue to develop.

Declaration of conflicting interests
The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.

Funding
The authors received no financial support for the research and/or authorship of this article.

References

1) Laragh J. Harry Goldblatt 1891-1977. Trans Assoc Am Physicians 1978;91:24-7.

2) Hillman BJ. Imaging advances in the diagnosis of renovascular hypertension. AJR Am J Roentgenol 1989;153:5-14.

3) Derkx FH, Schalekamp MA. Renal artery stenosis and hypertension. Lancet 1994;344:237-9.

4) Eardley KS, Lipkin GW. Atherosclerotic renal artery stenosis: is it worth diagnosing? J Hum Hypertens 1999;13:217-20.

5) Safian RD, Textor SC. Renal-artery stenosis. N Engl J Med 2001;344:431-42.

6) Detection, evaluation, and treatment of renovascular hypertension. Final report. Working Group on Renovascular Hypertension. Arch Intern Med 1987;147:820-9.

7) Slovut DP, Olin JW. Fibromuscular dysplasia. N Engl J Med 2004;350:1862-71.

8) Leiner T, de Haan MW, Nelemans PJ, van Engelshoven JM, Vasbinder GB. Contemporary imaging techniques for the diagnosis of renal artery stenosis. Eur Radiol 2005;15:2219-29.

9) Voiculescu A, Grabensee B, Jung G, Mödder U, Sandmann W. Renovascular disease: a review of diagnostic and therapeutic procedures. Minerva Urol Nefrol 2006;58:127-49.

10) Ram CV. Renovascular hypertension. Curr Opin Nephrol Hypertens 1997;6:575-9.

11) Spitalewitz S, Reiser IW. Atherosclerotic Renovascular Disease. Am J Ther 1996;3:321-328.

12) Schreij G, de Haan MW, Oei TK, Koster D, de Leeuw PW. Interpretation of renal angiography by radiologists. J Hypertens 1999;17:1737-41.

13) Taylor KJW, Burns PN, Wells PNT. Clinical applications of Doppler ultrasound. 2nd ed. Singapore: Raven Press; 1995.

14) Prokop M. Multislice CT angiography. Eur J Radiol 2000;36:86-96.

15) Urban BA, Ratner LE, Fishman EK. Three-dimensional volume-rendered CT angiography of the renal arteries and veins: normal anatomy, variants, and clinical applications. Radiographics 2001;21:373-86.

16) Textor SC. Pitfalls in imaging for renal artery stenosis. Ann Intern Med 2004;141:730-1.

17) Akin O, Coşkun M. Multi-detector CT angiography: Technique and clinical applications. [Article in Turkish] Tani Girisim Radyol 2003;9:139-45.

18) Kalender WA, Prokop M. 3D CT angiography. Crit Rev Diagn Imaging 2001;42:1-28.

19) Kaatee R, Beek FJ, de Lange EE, van Leeuwen MS, Smits HF, van der Ven PJ, et al. Renal artery stenosis: detection and quantification with spiral CT angiography versus optimized digital subtraction angiography. Radiology 1997;205:121-7.

20) Johnson PT, Halpern EJ, Kuszyk BS, Heath DG, Wechsler RJ, Nazarian LN, et al. Renal artery stenosis: CT angiography-comparison of real-time volume-rendering and maximum intensity projection algorithms. Radiology 1999;211:337-43.

21) Rubin GD, Dake MD, Napel S, Jeffrey RB Jr, McDonnell CH, Sommer FG, et al. Spiral CT of renal artery stenosis: comparison of three-dimensional rendering techniques. Radiology 1994;190:181-9.

22) Saba L, Caddeo G, Sanfilippo R, Montisci R, Mallarini G. Multidetector-row CT angiography diagnostic sensitivity in evaluation of renal artery stenosis: comparison between multiple reconstruction techniques. J Comput Assist Tomogr 2007;31:712-6.

23) Prokop M. Protocols and future directions in imaging of renal artery stenosis: CT angiography. J Comput Assist Tomogr 1999;23 Suppl 1:S101-10.

24) Hahn U, König CW, Miller S, Brehm B, Heuschmid M, Kopp AF, Claussen CD. Multidetector CT Angiography - is it a valuable screening tool to detect significant renal artery stenosis?. Rofo 2001;173:1086-92. [Abstract]

25) Fraioli F, Catalano C, Bertoletti L, Danti M, Fanelli F, Napoli A, et al. Multidetector-row CT angiography of renal artery stenosis in 50 consecutive patients: prospective interobserver comparison with DSA. Radiol Med 2006;111:459-68.

26) Vasbinder GB, Nelemans PJ, Kessels AG, Kroon AA, Maki JH, Leiner T, et al. Accuracy of computed tomographic angiography and magnetic resonance angiography for diagnosing renal artery stenosis. Ann Intern Med 2004;141:674-82.

27) Bloch MJ, Basile J. Clinical insights into the diagnosis and management of renovascular disease. An evidence-based review. Minerva Med 2004;95:357-73.

28) Beregi JP, Elkohen M, Deklunder G, Artaud D, Coullet JM, Wattinne L. Helical CT angiography compared with arteriography in the detection of renal artery stenosis. AJR Am J Roentgenol 1996;167:495-501.

29) Olbricht CJ, Paul K, Prokop M, Chavan A, Schaefer-Prokop CM, Jandeleit K, et al. Minimally invasive diagnosis of renal artery stenosis by spiral computed tomography angiography. Kidney Int 1995;48:1332-7.

30) Farrés MT, Lammer J, Schima W, Wagner B, Wildling R, Winkelbauer F, et al. Spiral computed tomographic angiography of the renal arteries: a prospective comparison with intravenous and intraarterial digital subtraction angiography. Cardiovasc Intervent Radiol 1996;19:101-6.

31) Rountas C, Vlychou M, Vassiou K, Liakopoulos V, Kapsalaki E, Koukoulis G, et al. Imaging modalities for renal artery stenosis in suspected renovascular hypertension: prospective intraindividual comparison of color Doppler US, CT angiography, GD-enhanced MR angiography, and digital substraction angiography. Ren Fail 2007;29:295-302.

Keywords : Angiography; digital subtraction angiography; multidedector computed tomography; renal arterial stenosis
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