Elsevier

The Lancet

Volume 367, Issue 9521, 6–12 May 2006, Pages 1503-1512
The Lancet

Articles
Non-invasive imaging compared with intra-arterial angiography in the diagnosis of symptomatic carotid stenosis: a meta-analysis

https://doi.org/10.1016/S0140-6736(06)68650-9Get rights and content

Summary

Background

Accurate carotid imaging is important for effective secondary stroke prevention. Non-invasive imaging, now widely available, is replacing intra-arterial angiography for carotid stenosis, but the accuracy remains uncertain despite an extensive literature. We systematically reviewed the accuracy of non-invasive imaging compared with intra-arterial angiography for diagnosing carotid stenosis in patients with carotid territory ischaemic symptoms.

Methods

We searched for articles published between 1980 and April 2004; included studies comparing non-invasive imaging with intra-arterial angiography that met Standards for Reporting of Diagnostic Accuracy (STARD) criteria; extracted data to calculate sensitivity and specificity of non-invasive imaging, to test for heterogeneity and to perform sensitivity analyses; and categorised percent stenosis by the North American Symptomatic Carotid Endarterectomy Trial (NASCET) method.

Results

In 41 included studies (2541 patients, 4876 arteries), contrast-enhanced MR angiography was more sensitive (0·94, 95% CI 0·88–0·97) and specific (0·93, 95% CI 0·89–0·96) for 70–99% stenosis than Doppler ultrasound, MR angiography, and CT angiography (sensitivities 0·89, 0·88, 0·76; specificities 0·84, 0·84, 0·94, respectively). Data for 50–69% stenoses and combinations of non-invasive tests were sparse and unreliable. There was heterogeneity between studies and evidence of publication bias.

Interpretation

Non-invasive tests, used cautiously, could replace intra-arterial carotid angiography for 70–99% stenosis. However, more data are required to determine their accuracy, especially at 50–69% stenoses where the balance of risk and benefit for carotid endarterectomy is particularly narrow, and to explore and overcome heterogeneity. Methodology for evaluating imaging tests should be improved; blinded, prospective studies in clinically relevant patients are essential basic characteristics.

Introduction

The clinical burden of stroke and transient ischaemic attack now exceeds that of coronary heart disease.1 Effective stroke prevention is vital to reduce this burden. Carotid endarterectomy reduces the risk of ipsilateral ischaemic stroke in patients with 70–99% symptomatic carotid stenosis (North American Symptomatic Endarterectomy Trial [NASCET] criteria),2 and also in some patients with 50–69% stenosis, if the stenosis is removed quickly.3

Endarterectomy trials have measured the percentage of carotid stenosis from intra-arterial angiography (IAA), an invasive, risky,4 and expensive procedure that could require admission to hospital. The wait for a hospital bed and limited availability of IAA delays surgery, and the strokes that the endarterectomy should prevent may occur during the wait.5

The carotid endarterectomy trials were undertaken during the 1980s, up to the mid-1990s. Since then, non-invasive and much less risky, carotid imaging techniques have become widely available. Techniques of Doppler ultrasound (DUS), computed tomographic angiography (CTA), magnetic resonance angiography (MRA), and contrast-enhanced MRA (CEMRA), have gradually replaced intra-arterial angiography,6 but on what evidence is this based? Primary studies testing non-invasive carotid imaging accuracy, while numerous, are usually small. A systematic review allows an unbiased pooling of available evidence regarding the efficacy of any given intervention, but previous systematic reviews of carotid imaging were either done some years ago,7, 8, 9, 10 only included some non-invasive imaging modalities,7, 8, 9, 11, 12, 13, 14, 15 or included studies with possibly7, 9, 10, 11 or definitely8, 16 sub-optimal study design.17

For example, studies in which researchers interpreting non-invasive tests were not blinded to the reference standard could overestimate non-invasive test accuracy.8, 16 None examined heterogeneity or undertook sensitivity analyses. Thus, it remains unclear whether, and in what circumstances, these non-invasive tests (individually or in combination) could replace IAA as the definitive diagnostic test before carotid endarterectomy.

We therefore systematically reviewed published reports to determine the accuracy of DUS, CTA, MRA, or CEMRA, alone or in combination, compared with IAA for diagnosing clinically-relevant carotid stenosis by the NASCET method in patients with carotid territory ischaemic symptoms.

Section snippets

Design

We used the Standards for Reporting of Diagnostic Accuracy (STARD) criteria and Cochrane Database of Systematic Reviews (CDSR) methods.17 Key STARD criteria include factors such as whether: the study population was relevant to the clinical question being addressed; there was a careful description of the population from which the patients were drawn, as well as actual inclusions and exclusions; recruitment and the mode of sampling were carefully described; researchers interpreting the

Results

Our search yielded 672 primary studies, of which 625 (93%) were excluded (figure 1). The main reasons for exclusion were publication between 1980 and 1986 (n=161, the Doppler ultrasound technology was not relevant to current colour Doppler techniques), other reasons such as preliminary reports of new technologies, poor methodologies (n=131), and when it was impossible to tell what proportion of patients or arteries were symptomatic (n=108). Of the remaining 47 reports, six were secondary

Discussion

Our systematic review suggests that DUS, MRA, CTA, and CEMRA all have high sensitivities and specificities for diagnosing 70–99% carotid stenosis in patients with ipsilateral carotid territory ischaemic symptoms, but might be substantially less accurate for 50–69% stenosis. CEMRA seems marginally more accurate, but it is a relatively new technique—early publications concerning new techniques tend to be over-positive—and the published studies so far come from research environments and not

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