Steady state vascular imaging with extracellular gadobutrol: evaluation of the additional diagnostic benefit in patients who have undergone a peripheral magnetic resonance angiography protocol
© Ong et al.; licensee BioMed Central Ltd. 2013
Received: 6 April 2013
Accepted: 18 September 2013
Published: 25 October 2013
To evaluate the feasibility and additional diagnostic benefit of a high-resolution steady state 3D-volume interpolated breath-hold exam (VIBE) sequence between a continuous table movement (CTM) MR angiography of the entire runoff vasculature and a time-resolved (TWIST) MRA of the calves.
In this retrospective IRB approved study 224 patients (72 women, 152 men, mean age 67.29 ± 13.9) were included who had undergone a low-dose MR angiographic protocol at 3T (Siemens TimTrio) after injection of 0.1 mmol/kg gadobutrol including a CTM MRA, a time-resolved MRA of the calf station and a steady state 3D VIBE sequence prior to the time-resolved MRA. One board-certified radiologist rated the image quality of the steady state VIBE sequences on an ordinal three point scale (excellent, good, poor) and analyzed the images for additional diagnostic findings of and beyond the vascular system in comparison to the CTM MRA and the time-resolved MRA. Descriptive statistics and demographic patient data were used for further evaluation.
The image quality of the steady state imaging of the pelvis, upper and lower leg was excellent in up to 88%, 84% and 47%, respectively, while poor image quality was only detected in the upper (2%) and lower leg (6%). An additional diagnostic benefit was found in 44% of the patients overall. The most common relevant pathologies included inflammatory processes of the soft tissues (26%), thrombi (14%), abscesses (13%) and tumors (11%). In subgroups of patients above the age of 60, 65, 70, 75 and 80 years an additional pathology was found in 50% 33%, 44%, 65% and 58%, respectively. There was no significant difference in terms of additional findings between men and women (46% and 39%, p > 0.05) and inpatients and outpatients (42% and 45%, p > 0.05).
Steady state imaging is also feasible with extracellular contrast agents with good image quality yielding additional diagnostic findings in up to 44% and above in patients older than 60 years of age irrespective of gender or patient status. Given the short acquisition time of 4 minutes this sequence could be added to all peripheral MRA exams.
KeywordsSteady state Magnetic resonance angiography Vascular imaging Venous imaging Gadobutrol 3T
Several imaging modalities allow for the depiction of the vascular anatomy of patients with peripheral arterial occlusive disease (PAOD). Digital subtraction angiography (DSA) has been the gold standard method , but it involves iodinated and potentially nephrotoxic contrast agents as well as ionizing radiation and the accompanied risks. In addition, DSA is expensive and invasive compared to other imaging methods. Significant complications such as hemorrhage or emboli following peripheral DSA occur in approximately 2% .
In contrast, computed tomography angiography (CTA) is a minimally invasive imaging method with a shorter examination time while maintaining a high diagnostic accuracy . As in DSA, CTA is also limited by potentially nephrotoxic contrast agents, decreased diagnostic accuracy in heavily calcified vessels, use of ionizing radiation and its limited soft tissue contrast .
Peripheral contrast enhanced (CE)-MRA has been proven as the method of choice for non-invasive imaging of the vasculature without radiation exposure or nephrotoxic contrast agents while maintaining high diagnostic accuracy . The basic technique employed for peripheral CE-MRA is the bolus-chase method which involves intravenous injection of a paramagnetic MR contrast agent and acquisition of T1-weighted images in the subsequent arterial first-pass phase . In order to achieve high quality MR angiograms without interfering venous contamination or artifacts optimization of peripheral CE-MRA by implementing hybrid scan protocols have been proposed and proven to be feasible [7–9]. This involves a separate injection of contrast media to image the calf region for a time-resolved MRA to safely depict this critical vascular territory and to increase the diagnostic accuracy .
At our site a low-dose MR angiographic protocol that consists of a continuous table movement MRA (CTM-MRA) of the entire runoff vasculature with 0.07 mmol/kg Gd-chelate and a time-resolved MRA with stochastic interleaved trajectories (TWIST-MRA) of the calf station with 0.03 mmol/kg Gd-chelate as described in the literature is being followed . Additionally, a high-resolution steady state 3D-volume interpolated breath-hold exam sequence was introduced prior to the time-resolved MRA with two aims: make positive use of the time delay between the CTM-MRA and the TWIST-MRA and to be able to assess extra-vascular and venous structures more closely. Steady-state imaging is a concept in CE-MRA that offers depiction of both arteries and veins – yet so far, steady state imaging has only been performed after the application of intravascular contrast agents such as gadofosveset [11–13].
Up until now there has been no research pursued regarding the feasibility of steady state imaging with injection of gadobutrol – an extracellular contrast agent – and the additional vascular and non-vascular pathology found in this kind of imaging. Therefore, the aim of this study was to assess the feasibility of such imaging and to investigate if specific subgroups of patients show a greater benefit from steady state imaging.
This retrospective single-center study was pursued without any financial support from industry. The authors had complete control of the data submitted for publication. This study was approved by our local ethics committee (medical ethics committee II, University Medicine Mannheim, Ruprecht-Karls-University Heidelberg), reference number 2008-338N-MA and pursued in compliance with the Helsinki Declaration. Due to its retrospective nature of our study informed consent has been waived and all data has been analysed anonymously.
Characteristics of the study population
Mean age (years)
Age range (years)
15 - 95
Further analysis included extraction of the patients clinical information out of the clinical information system (ISH-Med, SAP, Walldorf, Germany) concerning the following risk factors: hypertension, hyperlipidemia, smoking and diabetes.
For this study gadobutrol (1.0 M Gadovist®; Bayer Healthcare, Berlin, Germany), a gadolinium-based, macrocyclic, paramagnetic contrast agent was administered in the abovementioned protocol. A cumulative dose of 0.1 mmol/kg (1.0 mol/L; 0.07 mmol/kg for CTM MRA, 0.03 mmol/kg for TWIST MRA) was used. For equalization of injection volumes gadobutrol was diluted with saline in a 1:1 ratio. Contrast agent was injected at a rate of 1.5 ml/sec via an 18-gauge needle in the left or right cubital vein by using an automated power injector (Spectris Solaris EP; Medrad, Indianola, PA). Subsequently, an injection of a 30-mL saline bolus was administered at the same injection rate.
Image analysis of MRA
One board-certified radiologist (blinded, >10 years of experience in vascular imaging) performed image analysis of the steady state MRA including pelvis, upper and lower leg regions offline with an OsiriX DICOM viewer 3.8.1 (OsiriX Foundation, Geneva, Switzerland). Overall image quality was analyzed on a three point scale (3: excellent image quality allowing assessment of arteries, vessels and soft tissue; 2: good image quality allowing impaired assessment of arteries, vessels and soft tissue; 1: poor image quality not allowing sufficient assessment of the vascular and/or soft tissue structures). The presence of additional diagnostic findings of the vascular system and beyond was noted. All findings which could not be seen on either the CTM-MRA or the TWIST-MRA were considered to represent additional findings.
Descriptive statistics (median, mean, 95% confidence interval and standard deviation (SD)) were used for all data including evaluation of overall image quality, additional diagnostic findings, as well as patient status and demographic patient data. A Wilcoxon rank sum test was used to analyze a relation between age and additional pathology. Relationship between specific risk factors and additional pathology was analyzed by chi-square test. The results were considered statistically significant if the p value was no greater than 0.05. SAS statistical software (SAS 9.2 TS Level 2M3, 2012, SAS Institute Inc., Cary, NC, USA) was used for statistical analysis.
Results of image analysis
Image quality score
Results of gender analysis
No additional pathology
Results of patient status analysis
No additional pathology
Over the past 5 years MRA has undergone substantial improvements including high image quality and high diagnostic accuracy at low amounts of Gd-chelate [14, 15]. For patients with peripheral arterial occlusive disease (PAOD) contrast-enhanced MRA has become the most appropriate noninvasive diagnostic method of choice . Systematic reviews have confirmed the high diagnostic accuracy of peripheral CE-MRA .
Conventional peripheral CE-MRA is based on a bolus-chase method which involves imaging over three stations from the aortic bifurcation to the periphery after single-injection of contrast media. This may result in venous contamination of the lower leg region particularly in patients with higher stages of PAOD and concomitant risk factors . To overcome venous contamination in order to maintain high diagnostic accuracy for every station, new techniques have been developed such as the hybrid scan protocol which can be performed by two different ways: a large field-of-view MRA after the first injection of contrast agent followed by a time-resolved (TWIST) MRA of the calf station after the second injection or by scanning the peripheral region first followed by the pelvic/thigh region after the second injection of contrast media [9, 18]. Both techniques have specific advantages but both have a time delay between the two contrast agent injections in common. This time delay was filled with the acquisition of a steady state MRA at our institution aiming at the detection of additional – particularly extra-vascular – pathology. Due to the time lag between the CTM and TWIST MRA there is almost no significant time loss by implementing the steady state VIBE sequence. Up until now, there has been no research pursued concerning the impact and occurrence of additional pathology in steady state imaging: initial steady state imaging with intravascular contrast agents was not suited for the detection of extra-vascular pathologies and steady state imaging with extracellular contrast agents has not been attempted or at least not been published. This led to initiating the present retrospective study.
This study has proven that by implementing a steady state VIBE sequence in a routine MRA, relevant additional pathology can be acquired with good image quality that allows identification of additional pathologic findings without added injection of contrast media and with almost no time loss. In contrast to our initial assumptions, the presence of additional pathology was found irrespective of gender or patient status. We evaluated the incidence of risk factors for PAOD such as hypertension, hyperlipidemia, smoking and diabetes [19, 20]. The results of our study could not show an increased number of additional pathologies in patients with the aforementioned risk factors for PAOD. There was no difference in the incidence of additional pathology between inpatients and outpatients either. This was unanticipated since a higher incidence of pathologies was expected in inpatients. The additional pathologies included a wide range of diseases: from less important findings such as bursitis (17%) to relevant pathologies that required medical attention and treatment such as deep venous thrombi (14%), soft tissue abscesses (13%) and malignant tumors (11%).
Our findings concur with a previous publication that has used the intravascular contrast agent gadofosveset which thus implicate a blood pool role for extracellular contrast agents such as Gadobutrol. Hadizadeh et. al have investigated the prevalence of incidental deep venous thrombosis (DVT) in patients with clinically suspected PAOD who had undergone CE-MRA on a 1.5T scanner. Similar to our sample size 245 patients were included. Incidental DVT was observed in 11%, comparable to our results with 14% of incidental thrombi . The image quality of the steady state VIBE images tended to be worse at the calf station in our study. This was due to the limited spatial resolution that did not always allow separating arteries and veins. A previous study using gadofosveset demonstrated that a spatial resolution of 0.5 mm isotropic was necessary to safely identify arterial and venous structures .
Since this study was conducted as a retrospective analysis of peripheral MRA at our institution not all of the clinical information for each patient could be retrieved. The influence of additionally found pathologies with regard to possible changes in patient care has not yet been analyzed. However, the main goal of our study was to quantify additional pathology found, as well as analysis regarding patient characteristics including risk factors. Therefore, further investigation concerning therapeutic management changes have not been part of this study. Future studies will be needed to assess the true clinical value of applying steady state VIBE sequences in patients who undergo a peripheral MRA. Given that all of the examinations were scanned on a 3T scanner where the contrast agent efficacy is higher than at 1.5T results may not be transferable to a 1.5T scanner . Theoretically, the protocol used for this study can be implemented on a 1.5T scanner.
Our study has shown that steady state 3D VIBE imaging with extracellular contrast agents is feasible with good image quality and additional diagnostic findings in 44% and above in patients older than 60 years irrespective of gender or patient status.
Without additional contrast media application or significant time loss, steady state imaging may further improve the diagnostic value of peripheral MRA.
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