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Ann Thorac Surg 2006;81:820-827
© 2006 The Society of Thoracic Surgeons
a Department of Cardiovascular Surgery, Tokyo Women's Medical University, Daini Hospital, Tokyo, Japan
b Department of Radiology, Tokyo Women's Medical University, Daini Hospital, Tokyo, Japan
Accepted for publication August 18, 2005.
* Address correspondence to Dr Yamamoto, Department of Cardiovascular Surgery, Tokyo Women's Medical University Daini Hospital, 2-1-10 Nishiogu, Arakawa-ku, Tokyo 116-8567, Japan (Email: rhgcp476{at}ybb.ne.jp).
| Abstract |
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METHODS: The study, conducted from April 2003 to March 2004, involved 42 patients who underwent off-pump coronary artery bypass graft surgery. Samples yielded a total of 96 arterial grafts, 5 vein grafts. Sixteen-channel MDCT (LightSpeed Ultra 16; GE Healthcare, Milwaukee, Wisconsin) was performed on each patient using 500-ms or 600-ms rotation time, 0.625-mm slice thickness, and mean scanning time of approximately 24 seconds.
RESULTS: If several sequential anastomoses in one graft existed, each was calculated as a separate graft. Selective bypass graft angiography yielded a patency rate of 97% (155 of 160). Multidetector-row computed tomography enabled detection of 143 of 155 patent grafts and all 5 occluded grafts visualized by selective bypass graft angiography (100% sensitivity and 93% specificity for graft occlusion after exclusion of grafts not evaluated by MDCT). In 149 graft anastomoses of 143 patent grafts viewed by MDCT, 2 significant stenoses were detected by both selective bypass graft angiography and MDCT. Twelve distal anastomoses were not evaluated by MDCT because of metallic clip artifacts. Evaluation possible graft anastomoses were 92%. Sensitivity and specificity for significant stenosis after exclusion of graft anastomoses not evaluated by MDCT were 100% and 99%, respectively.
CONCLUSIONS: High-quality 16-channel MDCT images allowed detection of graft occlusion and significant stenosis of graft anastomosis after off-pump coronary artery bypass graft surgery, demonstrating an alternative tool less invasive than selective bypass graft angiography to assess grafts after surgery.
| Introduction |
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Both noninvasive electron-beam computed tomography and magnetic resonance imaging used for coronary assessments have been evaluated, but significant limitations remain in their production of reliable images [612]. Four-channel multidetector-row computed tomography (MDCT) was considered a valuable and reliable diagnostic tool in assessing bypass graft patency and stenosis [1317], but the long breath-holding time required and poor Z-axis spatial resolution for thick slices preclude quality images of bypass graft stenosis. Sixteen-channel MDCT requires less breath-holding time with less motion artifact and has improved Z-axis spatial resolution because of increased detector number, thinner detector width, and faster rotation speed [1823]. The modified version allows detection of coronary lesions and coronary bypass grafts with high sensitivity and specificity.
We prospectively investigated the diagnostic accuracy of the 16-channel MDCT by comparing it with SGA in detecting early OPCABG graft occlusion and significant stenosis of graft anastomosis.
| Patients and Methods |
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Two were repeat cases, and 6 patients had chronic renal failure on hemodialysis (Table 1). The patients had neither atrial fibrillation nor any contraindication for the administration of a contrast material. The study protocol was approved by our hospital Ethics Committee, and informed consent was obtained from each patient.
Selective bypass graft angiography and MDCT were performed an average of 16.1 ± 20.5 and 20.3 ± 20.7 days, respectively, after OPCABG. The mean time between SGA and MDCT was 4.4 ± 5.7 days.
The mean scanning time for MDCT was 24.4 ± 3.0 seconds. Patients received 20 mg to 60 mg oral metoprolol tartrate in accordance with their weight and blood pressure 1.5 hours before the MDCT scan when their heart rates were more than 70 beats per minute, and they received 0.3 mg nitroglycerin immediately before the MDCT scan when their systolic blood pressures were more than 100 mm Hg. Consequently, the average heart rate of patients during the MDCT scan was 67 ± 10.1 beats per minute (range, 46 to 90). Among the 30 patients who received metoprolol tartrate, 28 patients were given nitroglycerin (Table 1).
Sixteen-channel MDCT (LightSpeed Ultra 16; GE Healthcare, Milwaukee, Wisconsin) was performed using 100 mL of nonionic contrast material (Iopamidol; 370 mg iodine/mL) in total. Scan parameters were 500-ms or 600-ms rotation time, 0.625-mm slice thickness, and 0.275 helical pitch (table feed per rotation divided by X-ray beam width). For best temporal resolution using multisector reconstruction, we employed a 600-ms rotation time in the 5 patients whose heart rates ranged from 75 to 85 beats per minute and 500-ms rotation time in the remaining 37 patients in our study.
We performed a test scan before the actual scan using a bolus injection of 10 mL of contrast agent followed by 15 to 20 mL of saline to estimate circulation time. During the study, 90 mL of contrast agent followed by 40 to 50 mL of saline were administered at an injection rate of 4 mL/s through a 20G needle into the antecubital vein. The scan started from 1 cm above the proximal anastomosis to the ascending aorta in cases using free grafts, or from just above the area of the right pulmonary artery in cases using in-situ arterial graft only, and ended at the area just below the diaphragm. Collected data were reconstructed using the retrospective electrocardiography-gated method and absolute antegrade reconstruction, 0.625-mm slice thickness and slice interval, standard reconstruction kernel, and 20-cm displayed field of view. With our machine, the selected percentage of the reconstructed phase implied the center of the acquisition window. For example, the center of the acquisition window for a cardiac phase of 75% was located at 75% of the RR interval from the first R wave. Because we set the machine to use a multisector reconstruction algorithm as often as possible; half reconstruction was used only when multisector reconstruction was not available, namely, at approximately 60 beats per minute at a 500-ms rotation time. Multiple cardiac phases were reconstructed around end-systolic (30% to 45% of the RR interval) and end-diastolic (70% to 80%) phases. The reconstructed multiphase images were transferred to a workstation (Advantage Workstation 4.1; GE Healthcare), and the best cardiac phase was selected. When one cardiac phase was not satisfactory for all grafts and anastomoses, we selected the best cardiac phase for each graft and for each anastomosis.
An independent radiologist without knowledge of the SGA results assessed the graft images taken by MDCT. The number and sites of anastomoses of the bypass grafts were known to the radiologist. Axial, three-dimensional volume-rendering, and multiplanar reformatted images were analyzed for graft occlusion and significant stenosis of graft anastomosis. Although whole courses of free grafts (RA and SV) were evaluated, in-situ arterial grafts were evaluated within limits from the area above the right pulmonary artery to the area just below the diaphragm. Because of the limited scan coverage range, the entire courses of the in-situ arterial grafts (LIMA, RIMA, RGEA) were not evaluated.
Graft occlusion was defined as absence of contrast material along the course of the graft, through the graft anastomosis to the native distal artery or to the next graft and the native distal artery in sequential anastomosis. In sequential anastomosis, each of several distal anastomoses of one graft was counted as several grafts. For example, sequential grafting of LIMA to LAD to diagonal branch was counted as two grafts. Significant stenosis of graft anastomosis in a patent graft was defined as reduction of luminal diameter by 50% or more.
The SGA was performed using the transfemoral or transbrachial approach in all cases. Nonionic contrast material (Iopamidol; 370 mg iodine/mL) was used in almost 100 mL to 150 mL. Graft occlusion was defined as absence of contrast material along the course of the graft, through the graft anastomosis to the native distal artery or to the next graft and the native artery in sequential anastomosis. In-situ arterial grafts were evaluated the entire course of proximal LIMA, RIMA and RGEA grafts. In sequential anastomosis, each of several distal anastomoses of one graft were counted as several bypass grafts. Selective bypass graft angiography was evaluated by quantitative coronary angiography with automated counter detection of vessels after catheter-based image calibration. Significant stenosis of graft anastomosis in patent graft was determined if reduction in mean diameter was 50% or more.
For statistical analysis, all data were expressed as mean ± SD. The reliability of MDCT was evaluated by calculating sensitivity, specificity, positive and negative predictive values, and diagnostic accuracy using 2 x 2 contingency tables. The results of SGA served as a standard of reference. Sensitivity was calculated as true positive / (true positive + false negative). Specificity was calculated as true negative / (true negative + false positive). Positive predictive value resulted from true positive / (true positive + false positive), and negative predictive value resulted from true negative / (true negative + false negative). Diagnostic accuracy was determined by (true positive + true negative) / total number. The percentage and 95% confidence interval was calculated for each value.
| Results |
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When electrocardiography-gated contrast-enhanced MDCT was performed using scan mode 0.625-mm x 16, rotation time 500-ms, pitch 0.275, tube current 350mA, and scan length 15cm, dose length product was calculated as 1096.1 mGy · cm. Because the average ratio of effective dose to dose length product for CT of the trunk is 1.90 x 10-2 mSV (mGy cm)-1, the effective dose estimated by dose length product was calculated as 20.8 mSV [24].
If several sequential anastomoses in 1 graft existed, we calculated as several grafts. Of 160 bypass grafts, including 3 I-composite graft, SGA showed 155 to be patent and 5 (2 RA distal anastomoses to native coronary artery, 2 RA distal anastomoses to next grafts in sequential anastomosis, and 1 RGEA distal anastomosis to native coronary artery) to be occluded (97% patency rate). Compared with SGA, MDCT correctly showed 143 of 155 patent (Fig 1) and 5 of 5 occluded grafts (Fig 2). Of the 12 grafts for which MDCT failed to show correct diagnosis, 2 were not evaluated because of the metallic clip artifacts of the RGEA anastomosis in 1 and motion artifacts of RGEA in the other. Therefore, evaluation possible grafts were 99% (158 of 160). Among the remaining 10 grafts, 2 (LIMA) were of competing counterflow arteries (Fig 3). Six (3 LIMA, 2 RA, and 1 RGEA) resulted from sequential anastomoses to very small native coronary arteries (diameter < 1.5 mm) undetectable by the MDCT. Two (1 LIMA and 1 RGEA) poor-quality images were caused by insufficient contrast material. When 2 grafts not evaluated by MDCT were not included in the analysis, the sensitivity, specificity, positive predictive value, negative predictive value, and diagnostic accuracy were 100% (5 of 5), 93% (143 of 153), 33% (5 of 15), 100% (143 of 143), and 94% (148 of 158), respectively. The sensitivities of graft occlusion for LIMA, RIMA, RGEA, RA, and SV were (0 of 0), (0 of 0), 100% (1 of 1), 100% (4 of 4), and (0 of 0), respectively; and the specificities for LIMA, RIMA, RGEA, RA, and SV were 91% (64 of 70), 100% (31 of 31), 94% (31 of 33), 78% (7 of 9) and 100% (10 of 10), respectively (Table 2).
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| Comment |
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Selective bypass graft angiography is one method used to confirm surgical results. However, invasive SGA after CABG has a higher risk than standard coronary angiography to produce life-threatening arrhythmia and damage of graft vessels [35]. In addition, cost of SGA (about $1,400 US) is almost four times more expensive than cost of MDCT (about $340 US) in Japan. At our facility, most in-situ arterial grafts are performed on patients with triple-vessel disease. Tortuosity or spasm of the arteries proximal to the grafts sometimes precludes their visualization by postoperative SGA, particularly in RGEA. Because SGA was used as a standard of reference in this study, grafts not evaluated by SGA were not included.
Electron-beam computed tomography and magnetic resonance imaging are useful in noninvasively assessing graft patency, but both imaging techniques have major limitations in assessing bypass stenosis. Electron-beam computed tomography yields poor image quality for three-dimensional visualization of the coronary arteries as a result of limited spatial resolution because only a 3-mm slice can be obtained with sequential electrocardiography triggering [7, 8]. Magnetic resonance imaging provides information about graft morphology and function, but morphologic delineation of bypass grafts could be improved by contrast-enhanced three-dimensional magnetic resonance angiography. However, contrast-enhanced magnetic resonance angiography is strongly affected by metallic clip artifacts and requires improved spatial resolution to enable depiction of distal anastomosis [912].
A recent study of four-channel MDCT angiography reported sensitivity of 97% and specificity of 98% for graft occlusion. However, requirements such as minimum heart rate and long breath-holding time to cover scan length and limited spatial resolution caused by thick collimation reduced ability to evaluate stenosis of patent grafts (evaluation-possible grafts: 62%) [13].
Sixteen-channel MDCT, which obtains 16 thin slices of 0.5 to 0.75 mm thickness per 375-ms to 500-ms gantry rotation, enables scanning of a large volume during a single breath hold with improved spatial and temporal resolutions. Therefore, recent reports on 16-channel MDCT have shown high-quality images and satisfactory accuracy in evaluating coronary artery stenosis and bypass graft patency [1823].
We analyzed several kinds of grafts (mainly in-situ arterial grafts), sequential grafting, and composite arterial grafts performed by OPCABG and achieved satisfactory MDCT images for diagnosis. Specificity in graft occlusion was 100% in both RIMA and SV grafts because most RIMA grafts were anastomosed to the LAD, which is easily revealed with MDCT because of the straight course and relatively large diameter of this artery and because SV grafts were large in diameter. Six sequential grafts (3 LIMA, 2RA, and 1 RGEA) undetectable by MDCT were connected to small native coronary arteries (3 branches of circumflex artery, 2 diagonal branches, and 1 posterior descending branch). In addition to their small diameter, the branches of circumflex artery and diagonal branch arteries are easily affected by cardiac motion artifact because they course along the atrioventricular groove or the left ventricle.
Multidetector-row CT demonstrated 2 LIMA grafts to be occluded, whereas SGA showed their patency with a competing counter blood flow from the native coronary artery (Fig 3). This false positive was caused by delayed LIMA blood flow resulting from a competing counter blood flow between the moderate stenosis of a native coronary artery and the smaller diameter of the LIMA graft [15].
In this study, 16-channel MDCT scanning was not extended to cover the entire course of proximal LIMA, RIMA and RGEA grafts, where obstructions are not frequently found by SGA. To view the entire course of grafts, beginning from their proximal sites (subclavian artery, celiac artery) to distal anastomoses, a long distance must be covered in the cranio-caudal direction while keeping good spatial resolution (namely, thin slice collimation and small pitch), which requires longer breath-holding time and increased radiation dose. We considered essential evaluation of graft patency and stenosis of graft anastomosis including distal and proximal aortic anastomosis and did not scan the entire course of the in-situ arterial grafts. However, the long distance of the entire in-situ grafts could be easily covered within a fairly short breath hold with newly developed 64-channel MDCT systems.
On MDCT, artifacts from metallic vascular clips, which may obscure the body and the anastomosis of grafts, prevent visualization. Because we performed side-to-side anastomosis even for distal anastomosis, metallic clips were always necessary to block blood flow from the distal grafts. To avoid metallic artifact on MDCT, for distal anastomosis in 18 grafts, we used Absolok Extra Ligating Clip (Ethicon Endo-Surgery, Cincinnati, Ohio), which is made of violet polydioxanone. However, these comparatively large clips in the anastomosis cause technical difficulty when suturing the edge near the clip. Therefore, we returned to using blocking metallic clips on distal grafts, placing them slightly away from the distal anastomosis to avoid metallic artifacts as much as possible. Although this method allows detection of anastomosis on MDCT, the metallic clips often obscured the native coronary arteries just distal to the graft anastomoses (Fig 4).
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Although we examined a large number of samples, surgery resulted in only 5 graft occlusions and 2 significant stenoses of graft anastomosis, which led to a low positive predictive value. A larger occlusion and stenosis sample is needed to confirm our results.
Despite a few unavoidable limitations, our study results showed that MDCT allows accurate assessment of graft occlusion and significant stenosis of graft anastomosis after OPCABG. The sensitivity and negative predictive value for graft occlusion and significant stenosis of graft anastomosis were all 100%. Because no false negative result was shown in graft occlusion or in significant stenosis of graft anastomosis, we consider MDCT the first choice for post-OPCABG graft assessment and the more physically invasive and expensive SGA as the next choice when MDCT shows graft occlusion or significant stenosis of graft anastomosis or cannot permit evaluation of the state of graft.
In conclusion, 16-channel MDCT is an effective noninvasive technique to assess post-OPCABG grafts.
| References |
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