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Non-invasive assessment of coronary artery bypass graft patency using 16-slice computed tomography angiography
https://doi.org/10.1186/1749-8090-2-27
© Houslay et al; licensee BioMed Central Ltd. 2007
Received: 11 January 2007
Accepted: 05 June 2007
Published: 05 June 2007
Abstract
Background
Invasive coronary angiography is the gold standard means of imaging bypass vessels and carries a small but potentially serious risk of local vascular complications, including myocardial infarction, stroke and death. We evaluated computed tomography as a non-invasive means of assessing graft patency.
Methods
Fifty patients with previous coronary artery bypass surgery who were listed for diagnostic coronary angiography underwent contrast enhanced computed tomography angiography using a 16-slice computed tomography scanner. Images were retrospectively gated to the electrocardiogram and two dimensional axial, multiplanar and three dimensional reconstructions acquired. Sensitivity, specificity, positive and negative predictive value, accuracy and level of agreement for detection of graft patency by multidetector computed tomography.
Results
A total of 116 grafts were suitable for analysis. The specificity of CT for the detection of graft patency was 100%, with a sensitivity of 92.8%, positive predictive value 100%, negative predictive value 85.8% and an accuracy of 94.8%. The kappa value of agreement between the two means of measuring graft patency was 0.9. Mean radiation dose was 9.0 ± 7.2 mSv for coronary angiography and 18.5 ± 4 mSv for computed tomography. Pooled analysis of eight studies, incorporating 932 grafts, confirmed a 97% accuracy for the detection of graft patency by multidetector computed tomography.
Conclusion
Computed tomography is an accurate, rapid and non-invasive method of assessing coronary artery bypass graft patency. However, this was achieved at the expense of an increase in radiation dose.
Keywords
Background
Coronary artery bypass grafting (CABG) was first performed in 1967 by Garrett et al[1], who successfully employed a saphenous vein graft (SVG) for the treatment of coronary artery disease. This procedure has now become a widespread treatment for intractable angina and, in high risk patients, improves survival[2]. However, the benefits of surgery may be lost with graft failure or occlusion. Vein graft patency has been found to be reduced to 81% at one year, 75% at 5 years and less than 50% at 15 years[3]. This has led to the increasing use of arterial conduits, such as left internal mammary grafts (LIMA), that are associated with improved long term (10–15 year) patency and survival[4, 5].
Vein graft occlusion may occur early or late and is due to three distinct, well described disease processes. Acute graft failure and thrombosis may occur in the first 30 days postoperatively, and affects up to 12% of vein grafts[3]. Neointimal hyperplasia occurs between one month and a year, and is the result of accumulation of smooth muscle cells and extracellular matrix in the intimal compartment. While this rarely causes clinically significant stenosis[6], it provides the foundation for the development of graft atheroma. Late graft failure results from an accelerated form of atherosclerosis called 'graft vasculopathy'. This process predominates beyond the first year after surgery and is present in 17% of grafts at 6 years and 46% of grafts at 11 years[7].
The gold standard method of assessing graft patency is coronary angiography. This invasive procedure carries the small risk (10 in 1000) of potentially serious local vascular complications, including myocardial infarction, stroke and death. Studies have shown that elective coronary angiography in clinically stable patients with saphenous vein grafts carries a 0.08% risk of myocardial infarction, while 0.7% of subjects experienced clinically important complications. The risk of myocardial infarction increased to 1.3% for urgent studies[8]. The assessment of graft patency in a non-invasive readily applicable manner would have major benefits for the management and treatment of patients with prior CABG. The large calibre and more static location of bypass grafts make them particularly suitable for investigation by potential non-invasive imaging modalities. Computed tomography angiography was first described as a means of determining bypass graft patency in 1980[9, 10]. With advances in spiral and multidetector computed tomography (MDCT) technology, there has emerged a growing body of evidence to support the use of computed tomography for non-invasive bypass graft assessment [11–20]. Using the reference gold-standard of invasive coronary angiography, we aimed to assess whether contrast enhanced MDCT can reliably predict graft patency in patients who have previously undergone CABG.
Methods
Patient population
Fifty consecutive patients who had undergone previous coronary artery bypass graft surgery and were listed for diagnostic coronary angiography between June 2004 and June 2005 were recruited into the study. Exclusion criteria were the presence of implanted metallic cardiac devices which may interfere with image quality (prosthetic heart valves, implantable pacemaker or cardiodefibrillator), renal impairment, atrial fibrillation or those patients unable to tolerate the supine position. The study was conducted with the approval of the local research ethics committee, in accordance with the Declaration of Helsinki and the written informed consent of each subject.
Coronary angiogram
Invasive coronary angiography was performed by an experienced cardiologist via standard percutaneous approach, using 6 French Judkins catheters. Images were obtained on a Innova digital flat plate system (Advantx, GE Medical Systems) following i.v. bolus injection of iopamidol contrast agent (Niopam, Bracco, Bucks, UK). Selective catheterisation of grafts or graft stumps was performed.
MDCT angiogram
MDCT angiography was performed using a 16-slice MDCT scanner (Aquilon; Toshiba, Tustin, CA). The scan volume was defined based on expected location of the coronary arteries and grafts, following a scout view. In patients with known internal mammary artery grafts, this area was extended to the origin of the IMA at the proximal subclavian arteries. Scanning parameter included a gantry rotation time of 0.5 seconds, 16 × 1 mm detector collimation, 0.35 to 0.5 × 0.35 to 1 mm voxel size resulting in 0.35 to 0.5 × 0.35 to 0.5 mm display voxel size on MPR workstation, 135 kV, 250 to 300 mA, 0.25 pitch, and inspiratory breath hold time 20–30 seconds. Iomeprol, 100 mL (400-strength, Bracco, Bucks, UK) contrast agent was administered intravenously at a flow rate of 3.5 mL/s. The SURECardio acquisition feature was utilised, which monitors the patient's heart rate for five consecutive beats, calculates an average and automatically selects optimal scan parameters. The contrast bolus was monitored using the SUREStart feature to initiate imaging when contrast density in the ascending aorta is 160–180 HU. The images were obtained during inspiratory breath hold and retrospectively cardiac gated.
Three dimensional reconstruction with volume rendering techniques demonstrating saphenous vein grafts to the first diagonal branch of the left anterior descending artery, obtuse marginal artery and right coronary artery and a left internal mammary graft to the left anterior descending artery.
Data analysis
Two-dimensional axial, multiplanar reconstruction and three-dimensional reconstructions with volume rendering techniques were constructed (Voxar 3D, Voxar) and analysed by a radiologist who was familiar with the cardiac anatomy but blinded to the result of the invasive coronary angiogram. Image quality was graded in terms of eligible or insufficient (motion artefact, artefact caused by surgical clip) and eligible grafts were assessed in terms of patency. The results of MDCT were compared with invasive coronary angiography, the gold standard reference. Sensitivity, specificity, positive and negative predictive value (PPV and NPV respectively) was calculated for the detection of graft patency by MDCT. Sensitivity was calculated as true patent/(true patent + false occluded) grafts. Specificity was calculated as the number of true occluded/(true occluded + false patent) grafts. The positive predictive value was a result of true patent/(true patent + false patent), and the negative predictive value as true occluded/(true occluded + false occluded). The accuracy was determined by (true patent + true occluded)/total number of grafts. In addition, accuracy for detection of graft patency was calculated on a per patient basis.
Radiation dose for invasive coronary angiography and MDCT angiography was calculated from the documented dose area product (cGycm2) and dose length product (mGycm) respectively.
Results
Baseline Characteristics
No. of patients | 50 |
|---|---|
Sex (% male) | 86 |
Mean age (SD) | 66 (9) years |
Heart Rate (Mean, Median Range) | 67, 68, 52–89 |
No. of bypass grafts | 116 |
No. of IMA grafts | 35 |
• IMA → LAD | 30 |
• IMA → OM | 2 |
• IMA → Diagonal | 2 |
• IMA → Circumflex | 1 |
No. of SVGs | 77 |
• SVG → OM | 26 |
• SVG → RCA | 25 |
• SVG → LAD | 13 |
• SVG → Diagonal | 7 |
• SVG → posterior descending | 6 |
Radial artery grafts | 4 |
• → OM | 3 |
• → posterior descending | 1 |
Mean graft age (SD) | 7 (5) years |
Graft characteristics
Angiography | MDCT | |||||
|---|---|---|---|---|---|---|
Patent | Occluded | True patent | False patent | True occluded | False occluded | |
Overall n = 116 | 83 | 33 | 77 | 0 | 33 | 6 |
IMA n = 35 | 30 | 5 | 25 | 0 | 5 | 5 |
SVG n = 77 | 52 | 25 | 51 | 0 | 25 | 1 |
Other n = 4 | 1 | 3 | 1 | 0 | 3 | 0 |
Diagnostic accuracy of MDCT for detection of graft patency
Sensitivity (%) | Specificity (%) | PPV (%) | NPV (%) | Accuracy (%) | |
|---|---|---|---|---|---|
Overall n = 116 | 92.8 | 100 | 100 | 84.6 | 94.8 |
IMA grafts n = 35 | 82.8 | 100 | 100 | 50 | 85.3 |
SVG n = 77 | 98.1 | 100 | 100 | 96.3 | 98.7 |
Other n = 4 | 100 | 100 | 100 | 100 | 100 |
Occluded saphenous vein graft; only graft stump visible (arrow).
Radiation exposure
The mean radiation exposure for invasive coronary angiography was 9.0 ± 7.2 mSv with mean screening time of 11 ± 7.3 minutes. The mean radiation exposure for MDCT angiography was 18.5 ± 4 mSv with a mean scan time of 24 s (range 18–26).
Discussion
Invasive coronary angiography of coronary artery bypass grafts, in particular selective catheterisation of arterial conduits, is technically demanding, time consuming and involves day case admission. MDCT provides a highly specific means of detecting coronary artery bypass graft patency in a clinical setting. It is safe and abolishes the need for invasive coronary angiography which is associated with the small but significant risk of major complications. In contrast to invasive coronary angiography, it can be performed on a scheduled out-patient basis rather than requiring admission to a day case unit.
Computed tomography was first investigated as a possible method of determining patency of coronary artery bypass grafts in the early 1980s. Gunthaner et al[10] found that they were able to determine patency in 77.5% of left anterior descending (LAD) and right coronary artery (RCA) grafts and 40% of obtuse marginal (OM) grafts. Brundage et al[9] also found 95% correlation between single slice CT and conventional angiographic detection of graft patency. With the advent of spiral and MDCT scanners, image quality has improved and, in line with this, interest in minimally invasive imaging techniques has grown. Since these first studies, further larger scale studies have been undertaken to assess the ability of CT to assess graft patency. Recently, Song and colleagues reported that MDCT imaging resulted in 99.4% specificity and 100% sensitivity, with 100% PPV and 80% NPV for detection of bypass graft patency[20]. This study, however, looked at patients (n=50) immediately post-coronary artery bypass operation, who may be expected to have a high patency rate and no graft vasculopathy, thereby minimising any ambiguity caused by poor flow in chronically diseased grafts. Recent studies (n = 25–65) looking specifically at graft patency in study populations similar to the present, have reported sensitivities of 90–98% and specificities of 88–100% for detection of graft patency[11, 15, 21]. Consistent with our findings, detection of patency in vein grafts is more reliable than for internal mammary grafts[12, 22].
We performed a pooled analysis of all available data from studies investigating CT as a non-invasive means of assessing coronary artery bypass grafts (Table 4)[11, 12, 14, 15, 18, 23–27]. The paper by Nieman et al was not included in the analysis due to incomplete data on detection of graft occlusion by MDCT[28]. The pooled data gave an overall sensitivity of 96% and specificity of 99% (n=1498) for the detection of graft patency. As we have observed, studies with a preponderance of vein grafts displayed more reliable patency rates than those with a large proportion of arterial grafts. Pooled analysis focussing on the breakdown of available data for IMAs (n = 268) gave a sensitivity of 93%, specificity 97%, PPV 99.5%, NPV 67% and an accuracy of 94%[11, 12, 14, 15, 18]. Pooled analysis of vein grafts in the same studies (n = 399) gave a sensitivity of 97%, specificity 97%, PPV 99%, NPV 92% and an accuracy of 97%.
Characteristics of studies assessing non-invasive imaging of coronary artery bypass grafts.
Achenbach et al | Engleman et al | Engleman et al | Ropers et al | Ko et al | Marano et al | Schlosser et al | Martuscelli et al | Moore et al | Chiurlia et al | Houslay et al | Pooled data | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
Year of publication | 1997 | 1997 | 2000 | 2001 | 2003 | 2004 | 2004 | 2004 | 2005 | 2005 | 2005 | |
Method | Electron beam CT | Spiral CT | Spiral CT | Spiral CT | 4 slice CT | 4 slice CT | 16 slice CT | 16 slice CT | 4 slice CT | 16 slice CT | 16 slice CT | |
No. of patients | 25 | 49 | 24 | 65 | 39 | 57 | 51 | 96 | 50 | 52 | 50 | |
Mean age | 64 | 61 | 61 | 67 | 60 | 65 | 65 | 62 | 69 | 63 | 66 | |
Sex (% male) | 92 | 92 | 92 | 82 | 74 | 95 | 76 | 83% | 76 | 87 | 86 | |
No. grafts | 54 | 134 | 78 | 182 | 115 | 122 | 131 | 251 | 150 | 165 | 116 | 1498 |
IMA | 1 | 42 | 20 | 20 | 40 | 95 | 40 | 85 | 38 | 46 | 35 | 462 |
SVG | 53 | 92 | 58 | 162 | 54 | 27 | 91 | 166 | 112 | 117 | 77 | 1009 |
other | 21 | 2 | 4 | 27 | ||||||||
% vein grafts | 98% | 69% | 74% | 89% | 47% | 22% | 69% | 66% | 66% | 70% | 66% | |
Mean graft age (yrs) | 6.9 | 1.8 | 2.1 | 7.6 | 1.2 | 4.8 | 5.6 | 7 | 8 | 7.9 | 7.0 | |
Sensitivity | 100% | 92% | 90.1% | 97% | 93% | 93% | 96% | 100% | 91% | 100% | 93% | 96% |
Specificity | 100% | 97% | 100% | 98% | 99% | 98% | 95% | 100% | 100% | 100% | 100% | 99% |
PPV | 100% | 99% | 100% | 97% | 93% | 93% | 81% | 100% | 100% | 100% | 100% | 99% |
NPV | 100% | 78% | 74% | 98% | 99% | 98% | 99% | 100% | 96% | 100% | 85% | 95% |
Accuracy | 100% | 93% | 92% | 98% | 98% | 97% | 95% | 100% | 97% | 100% | 95% | 97% |
The main limitation of CT imaging is the high radiation doses that are incurred. This may be of limited relevance in the population under question as it has been shown that the elderly are less susceptible to the lifetime risk of radiation exposure for any given dose[29]. Nonetheless, the radiation dose is double that of invasive coronary angiography. Whilst there are no national dose limits, the doses such as are incurred with CT angiography equate to more than eight times the annual natural background radiation exposure.
Whilst CT angiography has shown promising results in the detection of bypass graft patency, a recent review article concluded that there is a lack of evidence-based data to support its use for evaluation of native vessels in patients presenting with chest pain[30]. CT angiography may be a helpful non-invasive imaging tool in evaluation of bypass grafts on a non-urgent outpatient basis, but clinical trials are needed before it can be used as a tool to evaluate native vessels in patients presenting acutely.
Study limitations
Image quality is highly dependent upon adequate heart rate control, with a great reduction in image quality in subjects with a heart rate of greater than 70 beats per minute, due to diastolic motion artefacts. While bypass grafts are less susceptible to cardiac motion artefacts than native vessels, this can still be an issue, in particular in posterior vessels, such as grafts to the circumflex artery. Not all of the patients who were recruited were on β-blockade therapy, which meant that image quality was in some cases suboptimal due to diastolic motion artefacts. In order to overcome this major limitation, it would have been helpful to have administered a short acting β-blocker prior to scanning. Additionally, in those patients who had IMA grafts, the increased scan volume necessitated a long breath hold. In some patients, this led to a degree of respiratory artefacts towards the end of the scan time, which tended to coincide with the base of the heart and therefore the distal graft anastamoses.
The use of 16 slice CT scanners has been superseded by newer 64 slice scanners, which have the advantage of narrow collimation and reduced scan times. Meyer et al report reliable assessment of graft patency and stenoses in unselected populations using 64 slice scanners[31]. Furthermore, Zhang et al highlight improved rated of evaluation of proximal anastamosis, graft, distal anastamosis and run off vessel for 64 slice scanners in comparison to 16 slice CT[32].
Conclusion
In line with recent studies, we can confirm that MDCT is highly specific for the detection of bypass graft patency. It provides a safe, fast and efficient means of imaging coronary artery bypass grafts but with the disadvantage of a high radiation dose. The introduction of new 64 slice MDCT scanners will result in shorter scan times and may further improve image quality that in turn may enable non-invasive imaging to become the mainstay of assessment of graft patency in the future.
Declarations
Acknowledgements
Grant Support: Chief Scientist Office of the Scottish Executive NHS Cardiovascular disease/Stroke program support grant (Ref. No. 906444).
Authors’ Affiliations
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