(Circulation. 2005;112:2222-2225.)
© 2005 American Heart Association, Inc.
Editorial |
From the University of Vermont, Burlington.
Correspondence to Timothy F. Christian, MD, Prof of Medicine and Radiology, University of Vermont, Baird 191, 111 Colchester Ave, Burlington, VT 05401. E-mail timothy.christian{at}uvm.edu
Key Words: Editorials coronary disease diagnosis imaging imaging
| Introduction |
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He that will divide a minute into a thousand parts and break but a part of the thousandth part of a minute in the affairs of love, it may be said of him that Cupid hath clapped him o the shoulder, but Ill warrant him heart-whole. Shakespeare, As You Like It
The wheel is come full-circle. Shakespeare, King Lear
The study by Mollet et al on CT coronary angiography in this issue of Circulation is important for several reasons.1 The 64-multislice technology for acquiring tomographic x-rays of the coronary vessels during the arterial phase of a bolus of iodinated contrast introduces several technical advances: improved spatial resolution (thinner slices), improved temporal resolution (less time needed to acquire an image means less time for the vessel to move), and improved spatial coverage of the heart (reduction of registration errors). Unlike previous studies, the authors attempted to analyze the entire length of all of the major arteries, not just those in which image quality was optimal. All patients had the definitive end point comparison to invasive angiography, which was not prompted by the results of the CT examination. The authors report sensitivity for the detection of significant obstructive disease of 99% and a specificity of 95%, confirming a slight propensity of CT to generate false-positive lesions in the presence of vessel wall calcification. Although the results were excellent, it is clear that this study and others have struggled with the question as to how to best evaluate CT angiography.
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New tests face validation challenges that are both common to all emerging technologies and unique to the specific test. CT coronary angiography is a purely anatomical (at least at present) result of a structure that is variable between individuals. It is also noninvasive, therefore, it cannot be compared with a direct pathological analysis clinically. These conditions give rise to 4 issues that have a direct impact on the evaluation and use of this technology: division of a complex structure into inflexible units, evaluation of what cannot be seen, referral bias, and efficacy and the effectiveness of a test.
| Segmentation |
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The achievement of significance for conventional statistical tests is a function of the number of observations. As an example, consider a study for the detection of viability using 99mTc sestamibi perfusion imaging at rest in an animal model of myocardial infarction, in which the pathological infarct size is known in 6 animals. A linear correlation of 6 data points is unlikely to be significant in the absence of a close agreement between the studies. By segmenting the myocardium into the standard American College of Cardiology/American Heart Association myocardial model,2 the number of data points is expanded from 6 to 102 for the group. Now, even modest correlations are significant; however, the global amount of scar tissue (the truth) is unaltered, as is the difference between the measures.
Segmental paring does not impart independence. The segments from a coronary CT scan are linked. They were acquired with a certain degree of motion, with a given attenuation from body habitus, with the same contrast bolus timing and dosage, and with a specific coronary anatomy. It is conceivable that in a cohort of patients in whom the prevalence of disease is low, all of the abnormal (diseased) segments originated from a handful of patients, and all of the scans had excellent image quality. Conventional statistical tests ignore the interdependence of segments that originate from the same patient. More rigorous statistics are necessary to assess the impact of linked segments on the outcome of the comparison of the tests.3 Mollet et al performed a subanalysis of a random single segment from each patient to determine whether the accuracy was altered (single bootstrap), but they did not statistically adjust for interdependence.
Analysis of individual coronary segments can be misleading. For simplicity, consider 20 patients undergoing coronary CT in which the coronary vasculature is divided into a 17-segment model. A total of 10 segments are reported as abnormal. The number of patients with disease by noninvasive testing can then be anywhere from 1 to 10 (5% to 50% depending on the "nesting" distribution). Independent segmental analysis provides no information on the distribution of disease in the cohort. Segmentation separates the coronary tree from the heart as a whole.
| Impact of Missing Segments |
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Missing segments are not reported, but 3% of the extant segments were "poorly" visualized.1 Poor visualization, despite the multiplication of detectors, will be a reality with this technique in certain patients and may be hard to predict in advance (eg, motion during the acquisition, poor bolus of contrast, premature beats) and the impact harder to deal with. Stress echocardiography may have lung interference and nuclear perfusion imaging may have bowel interference precluding the visualization of certain segments of myocardium. They generate other variables such as exercise duration, ECG response, exercise-induced chest pain, LV function, transient LV dilatation, and lung tracer uptake, which can be factored into the final impression and are strong prognosticators. CT angiography receives no such help at present.
What are the options for dealing with missed segments of anatomy? (1) Assume the missing segments are normal. (2) The test is invalidated because another test is now necessary to rule out disease (assume missing segments are positive). (3) The probability of disease in missing segments should be extrapolated from the prevalence in the other segments. (4) The probability of disease should be extrapolated from the condition of the other vessels. (5) The probability of disease should be estimated from the clinical risk factors and other available data.
None of these alternatives are entirely satisfactory. One may be tempted to make one of the above choices based on the location of the missing segment, but the prediction of the amount of myocardium supplied distal to a lesion is not overly accurate.4 Ultimately, clinicians will need to incorporate several of the above strategies into their decision algorithm.
| Verification Bias |
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What are the implications for referral bias on CT coronary angiography? The present study by Mollett et al has made a solid effort to avoid referral bias by including only patients already referred to angiography on the basis of other tests and historical variables. Selection bias is present as evidenced by the high prevalence of coronary disease in the cohort (75% of the group), and a large proportion of these with multivessel disease. It is unlikely that such a prevalence of disease will be present in the population that CT coronary angiography will be applied to clinically. By Bayes theorem, the performance of a test is a function of both its inherent accuracy and the prevalence of disease in the population to which it is applied. It is unlikely that CT angiography will perform near the levels reported here in a screening population, where disease prevalence is low and true positives hard to find.
Another sequela of verification bias will be the difficulty in comparing CT angiography to clinical variables or other noninvasive imaging tests for coronary artery disease detection when the invasive angiogram is the end point. Papers on this subject will almost certainly appear in the literature, which creates a problem: Assume all patients had a stress echocardiogram study in this cohort of 51 patients and the decision to perform angiography was based on that test result. Because only positive tests were likely to be referred and the test performs fairly well (75% sensitivity in this hypothetical situation), and nothing of the negative tests is known, only true positives and false positives are measured, with a high resultant disease prevalence. Consequently, the sensitivity of stress echocardiography will be somewhat inflated and the specificity low (0% in this case). The CT angiogram was not used to decide to do angiography and will be more accurate because the specificity will not be artifactually lowered (ie, all of the 4 possible outcomes will be known). The same issue applies to clinical risk variables, which were used to select the study group end point. When comparing 2 methods in which the established test was used to select which patients went to the definitive end point, the new test will almost always appear to be more accurate.
| Efficacy and Effectiveness |
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Accuracy measures should be adjusted for technical failures. Both contrast and radiation were received and no vessels visualized in the case of one patient in this study. Given the high prevalence of disease in the cohort, this could be viewed as a false-negative examination because no lesions were seen. The issue must be decided by a second test or invasive angiography. In the present study, this has little impact, bringing the sensitivity down to 97% on a "per patient" basis (38 true-positive tests/38 true positive+1 false negative). It can be a much bigger factor for technically demanding methods in less-experienced hands.
There are 3 questions to be asked of all noninvasive studies from an effective reference point: How does the prevalence of disease in this study translate to clinical practice? What proportion of patients in clinical practice can the test be applied to? How are accuracy measures adjusted for technical failures and other missing data?
| Conclusions |
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There are issues for using CT angiography as a diagnostic tool. Other noninvasive myocardial imaging tests (SPECT, stress echo) have consistently shown that the overall extent of abnormality is the single most important predictor of cardiac-related death, and that such test results correlate with more extensive anatomical disease. These tests were incorporated into clinical practice, not only to detect atherosclerosis indirectly but also to provide important physiological information about its impact. This has held up over time for both techniques in the form of powerful prognostic studies. Both nuclear stress imaging and stress echocardiography have shown incremental prognostic value in patients when the coronary anatomy is known.1115 These methods now form a strong symbiotic relationship with coronary anatomy, which can guide therapy. This is lost when CT is used in isolation.
Is a noninvasive anatomic picture what we want? For a time, invasive anatomy was the only imaging tool we had. Our concept of atherosclerotic disease has changed a lot since then. We know that a majority of myocardial infarctions occur because of plaque composition and structure rather than luminal obstruction.16 There is a difference in the atherosclerotic disease of diabetic patients that we are struggling to define.17 At times the angiogram can be misleading when judging the impact that a lesion imparts on the coronary circulation.18 It can be hard to estimate the amount of myocardium at risk for a specific vessel lesion4 and critical to know the viability of that zone. Finally, we know the impact of inflammation and other molecular mechanisms in the development of ischemic syndromes.19 To turn away from all that and go back to simple anatomy as our guide would be a step backward. This technology is remarkable and we should demand more from it. The noninvasive angiogram is an important step for CT, but it should not be the last stop. The wheel may come full circle, but it can also move forward.
| Acknowledgments |
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Dr Christian is the recipient of an American Heart Association Grant-in-Aid for high-field imaging of quantitative MRI perfusion.
| Footnotes |
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| References |
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