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Case Report |
Department of Radiology, Duke University Medical Center, Box 3808, Durham, NC 27710.
Received May 11, 2004;
accepted after revision July 19, 2004.
Address correspondence to J. Thomas
(thoma120{at}mc.duke.edu).
Introduction
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The scans were obtained on a 16-MDCT scanner (LightSpeed, GE Healthcare) using the following protocol: An initial unenhanced CT scan and then a contrast-enhanced CT scan were obtained with a 16 x 1.25 mm detector configuration, pitch of 1.375:1, table speed of 27.5 mm per rotation, and rotation time of 0.5 sec. The images were then reconstructed at 0.625-mm thickness and reformatted in the coronal plane. Eighty milliliters (40 mmol) of gadopentetate dimeglumine (Magnevist [0.5 mmol/mL], Berlex Laboratories) was injected at 3 mL/sec after a 40-sec scanning delay interval, which was chosen by manual bolus tracking.
The CT scans showed an aortic endovascular stent-graft originating 2 cm below the ostia of the renal arteries (Figs. 1C and 1D). The graft was patent. Contrast material was noted to extravasate into the proximal aspect of the native aortic aneurysmal sac, consistent with a type I endovascular leak. Compared with the preoperative CT scan obtained 6 months earlier, the aneurysmal sac diameter was stable. Because the patient was asymptomatic, the surgical team opted for conservative management with follow-up imaging in 6 months. The follow-up CT examination, which was also performed with IV gadolinium, showed no change in the type I endoleak.
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The AneuRx Stent-Graft System was used in our patient. This is a modular stent with an external skeleton composed of nitinol and an internal graft composed of polyethylene terephthalate fiber (Dacron, DuPont). In a review of the MR appearance of stent-grafts by Merkle et al. [2], this system is partly MR-compatible. However, visualization of the aortic sac was obscured by blooming artifact. Consequently, in our patient, we decided to use gadolinium CT angiography instead of MR angiography.
One of the important complications related to endovascular stent-grafts is endoleak. Endoleak refers to persistent blood flow outside the stent lumen but within the native aneurysmal sac or adjacent vascular segment. A type I leak is a perigraft leak where aortic flow escapes around the cuff of the stent into the aneurysmal sac. A type II leak refers to retrograde flow through collateral arteries into the aneurysmal sac. A type III leak occurs from flow through the graft due to tears, disconnection, or disintegration of stent fabric. A type IV endoleak refers to increased graft porosity. The presence of an endoleak suggests that the procedure has failed to completely exclude the aneurysm from the aortic circulation. Such failure, especially if systemic arterial pressures are maintained within the aortic sac, may lead to continued expansion of the aneurysmal sac and risk of rupture.
The postoperative assessment of stent-grafts is based primarily on the results of CT using IV iodinated contrast material [5]. We presume the diagnosis of endoleak would have been established using either 4-, 8-, or 16-MDCT. An alternative method of assessment of these grafts is color Doppler sonography or MR angiography using IV gadolinium [2]. The significant limitation of color Doppler sonography is acoustic shadowing from the stent-graft itself or overlying bowel gas that may obscure visualization of the aortic sac and stent. Furthermore, the absence of color flow does not exclude endoleak, because slow flow may not be detected on sonography. MR angiography is also limited in some grafts because of metal artifact that may obscure the flow lumen and aortic sac. Nevertheless, a large leak, like the one seen in our patient, may be seen on MR angiography. In addition, MRI is contraindicated in patients with pacemakers, claustrophobia, or recently placed metallic stents or surgical clips.
The IV administration of gadolinium chelated with diethylenetriamine pentaacetic acid (DTPA) has been found to be safe and well tolerated [7]. The physiologic half-life in patients with normal renal function is approximately 1.5 hr. The manufacturer's recommended dose is 0.1 mmol/kg. Prince et al. [7] reviewed patients who had higher doses of gadolinium. The range of gadolinium chelate used in their series was 0.2-0.4 mmol/kg. They concluded that such high doses are significantly less nephrotoxic than IV iodinated contrast medium.
Quinn et al. [8] have shown that for cranial CT, diagnostic vascular enhancement with gadopentetate dimeglumine may be achieved with doses as high as 0.5 mmol/kg. Similarly, enhancement of 100 H has been achieved in the thoracic aorta and its branches using gadolinium doses of 0.5 mmol/kg [9]. For our patient, a dose of 80 mL of gadolinium (0.4 mmol/kg) resulted in aortic enhancement of 61 H, which was sufficient to show the type I endoleak. The decision to use 80 mL of gadolinium was based in part on such work indicating that a dose of approximately 0.5 mmol/kg is suitable for aortic opacification [8, 9]. A higher dose of gadolinium was not considered for fear of toxicity. The approximate charge for 80 mL of gadolinium was $350-400. Similar enhancement was reproduced on the follow-up scan 6 months later.
In the appropriate setting, patients with renal insufficiency (serum creatinine level, > 2.0 mg/dL) will be considered for gadolinium-enhanced CT. Although our report shows that CT using gadolinium as the contrast agent is able to show the presence of an endoleak, there have been no studies comparing the efficacy of gadolinium-enhanced CT with that of iodinated contrast-enhanced CT for endoleak detection. Hence, the technique of choice in the clinical setting of renal failure will depend on local imaging practice patterns.
In conclusion, we report a patient with renal insufficiency in whom enhanced CT using gadolinium successfully diagnosed a type I endoleak. Although the enhancement after gadolinium administration was less vivid than that expected with iodine, diagnostic images were obtained. Gadolinium-enhanced CT angiography is an acceptable alternative to iodinated contrast-enhanced CT angiography in selected scenarios in which imaging is required to rule out endoleak.
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