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Erschienen in: European Radiology 8/2022

Open Access 10.03.2022 | Cardiac

Computed tomography angiography versus Agatston score for diagnosis of coronary artery disease in patients with stable chest pain: individual patient data meta-analysis of the international COME-CCT Consortium

Erschienen in: European Radiology | Ausgabe 8/2022

Abstract

Objectives

There is conflicting evidence about the comparative diagnostic accuracy of the Agatston score versus computed tomography angiography (CTA) in patients with suspected obstructive coronary artery disease (CAD).

Purpose

To determine whether CTA is superior to the Agatston score in the diagnosis of CAD.

Methods

In total 2452 patients with stable chest pain and a clinical indication for invasive coronary angiography (ICA) for suspected CAD were included by the Collaborative Meta-analysis of Cardiac CT (COME-CCT) Consortium. An Agatston score of > 400 was considered positive, and obstructive CAD defined as at least 50% coronary diameter stenosis on ICA was used as the reference standard.

Results

Obstructive CAD was diagnosed in 44.9% of patients (1100/2452). The median Agatston score was 74. Diagnostic accuracy of CTA for the detection of obstructive CAD (81.1%, 95% confidence interval [CI]: 77.5 to 84.1%) was significantly higher than that of the Agatston score (68.8%, 95% CI: 64.2 to 73.1%, p < 0.001). Among patients with an Agatston score of zero, 17% (101/600) had obstructive CAD. Diagnostic accuracy of CTA was not significantly different in patients with low to intermediate (1 to < 100, 100–400) versus moderate to high Agatston scores (401–1000, > 1000).

Conclusions

Results in our international cohort show CTA to have significantly higher diagnostic accuracy than the Agatston score in patients with stable chest pain, suspected CAD, and a clinical indication for ICA. Diagnostic performance of CTA is not affected by a higher Agatston score while an Agatston score of zero does not reliably exclude obstructive CAD.

Key Points

• CTA showed significantly higher diagnostic accuracy (81.1%, 95% confidence interval [CI]: 77.5 to 84.1%) for diagnosis of coronary artery disease when compared to the Agatston score (68.8%, 95% CI: 64.2 to 73.1%, p < 0.001).
• Diagnostic performance of CTA was not affected by increased amount of calcium and was not significantly different in patients with low to intermediate (1 to <100, 100–400) versus moderate to high Agatston scores (401–1000, > 1000).
• Seventeen percent of patients with an Agatston score of zero showed obstructive coronary artery disease by invasive angiography showing absence of coronary artery calcium cannot reliably exclude coronary artery disease.
Begleitmaterial
Hinweise

Supplementary Information

The online version contains supplementary material available at https://​doi.​org/​10.​1007/​s00330-022-08619-4.
The original online version of this article was revised due to a retrospective Open Access order.
The original online version of this article was revised: the author name Bjarne L. Nørgaard was incorrectly given as Bjarne L. Nørgard.
A correction to this article is available online at https://​doi.​org/​10.​1007/​s00330-022-08760-0.

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
CAC
Coronary artery calcium
CAD
Coronary artery disease
CI
Confidence interval
COME-CCT
Collaborative Meta-Analysis of Cardiac CT
CTA
Computed tomography angiography
ICA
Invasive coronary angiography
IPD
Individual patient data
IQR
Interquartile range
PTP
Pre-test probability
SD
Standard deviation

Introduction

Coronary artery calcium (CAC) has become an independent diagnostic marker besides traditional risk factors of atherosclerosis for the detection of coronary artery disease (CAD) [1] and is most commonly quantified using the Agatston score method [2]. CAC quantification is frequently used in asymptomatic patients for risk stratification. While there is evidence that traditional risk factors are associated with an increase in arterial calcification [3], others report on a discrepancy between traditional risk factors and coronary artery calcification when countries are downgraded as low-risk countries. Diederichsen et al showed through the example of Germany and Denmark using low-risk models, that individuals with severe coronary atherosclerosis are more commonly assigned to low to intermediate pre-test probability of CAD [4]. The absence of CAC is associated with low rates of cardiovascular events such as myocardial infarction, cardiovascular death, or unstable angina pectoris in asymptomatic individuals [5]. Evaluation of CAC as an independent parameter for the detection of obstructive CAD has yielded inconsistent results. In contrast, the absence of coronary artery calcium does not reliably exclude CAD based on non-calcified plaque lesions [6, 7].
The CORE-64 international multicentre study showed computed tomography angiography (CTA) to have significantly lower diagnostic accuracy in patients with CAC elevated above 600 [8]. As commonly known, CTA shows good diagnostic accuracy in detecting obstructive CAD in patients with stable chest pain [9, 10].
Overall, there is conflicting evidence about the comparative diagnostic accuracy of the Agatston score versus CTA, and thus, the diagnostic role of the Agatston score in detecting obstructive CAD is still unclear. Therefore, different international guidelines call for more scientific evidence from large cohorts to reliably decide how to use the Agatston score in patients with stable chest pain [6, 11, 12].
We sought to collaboratively determine and compare the diagnostic accuracy of CTA and the Agatston score in detecting obstructive CAD in stable chest pain patients with a clinical indication for invasive coronary angiography (ICA) by using individual patient data (IPD) from the worldwide Collaborative Meta-Analysis of Cardiac CT (COME-CCT) Consortium. Furthermore, we investigated if the diagnostic accuracy of CTA was affected by higher Agatston scores.

Methods

Patients

Patients with a clinical indication for ICA, who were also prospectively enrolled to undergo cardiac CT, from the COME-CCT provided the basis for our comparison of the diagnostic accuracy of the Agatston score versus that of CTA with ICA as the reference standard using individual patient data [13]. Patients with unstable presentation, such as known CAD, coronary stents, or bypass grafts, were excluded (Fig. 1).
The international COME-CCT Consortium consists of 76 worldwide studies with a total of 7813 individual patient datasets. Eligible studies were identified by the meta-analysis of Schuetz et al [9], and additional unpublished search updates were performed to ensure inclusion of the most recent studies. Participating partners were asked to provide detailed information on a per-patient basis as follows: patient characteristics, technical information, procedure and results of CTA and ICA, risk factors, and additional tests. All included patients prospectively underwent both tests, ICA and CTA, on CT scanners with at least 12 rows, and obstructive CAD was defined as ≥ 50% diameter stenosis by ICA. Details of enrolment and methods are available described elsewhere [13], and the study was registered in the PROSPERO Database for Systematic Reviews (CRD42012002780). The current analysis included all patients from the main collaborative analysis cohort with information on the Agatston score [10] and was a prospectively defined outcome measure of the COME-CCT Consortium [13].

CTA and Agatston scores

In this analysis, we used the Agatston score for CAC quantification [2] using unenhanced images obtained before the CTA scan. CTA was read by experienced investigators as part of prospective study protocols on workstations enabling two- and three-dimensional postprocessing of CTA datasets, and at least 50% coronary diameter stenosis was considered to represent obstructive CAD. Agatston scores of > 400 were considered positive for obstructive CAD [11, 14, 15]. Following Agatston et al, any value below 1.0 was classified as an Agatston score of zero. The ranges for scores of 1 to < 100, 100 to 400, 401 to 1000, and above 1000 were defined as follows: between 1.0 and below 100.0, exactly 100.0 to less than or equal to 400.0, larger than 400.0 to less than or equal to 1000.0, and larger than 1000.0. Pre-test probability (PTP) was calculated as previously described [10] using information on sex, age, and angina pectoris type on the patient level, and categorized into low (< 15%), intermediate (15 – 65%), and high (> 65%). PTP was not a pre-defined inclusion criterion of the COME-CCT Consortium, but was assessed as a mandatory item for analysis on the per patient level in all included patients in this sub-analysis of the COME-CCT Consortium.

ICA

Obstructive CAD was defined as a diameter reduction of at least 50% of the coronary artery by ICA as the reference standard and was analyzed on the patient level. ICA was performed according to local standards and was available in all included patients.

Statistical analysis

All results are reported as mean ± standard deviation (SD) for quantitative data with normal distribution, median with interquartile range (IQR) for ordinal or not normally distributed data, and proportion of 95% confidence interval (CI) for categorical data. Nondiagnostic CTA results were implemented in a worst-case scenario using an intention-to-diagnose approach by counting CTA results as positive when ICA was negative and as negative when ICA was positive (treating nondiagnostic CTA cases as if they were false positive or false negative by ICA result, respectively). Diagnostic performance (in terms of diagnostic accuracy defined as the proportion of correct test results, sensitivity, specificity, and predictive values) was calculated and compared between both tests versus the reference standard ICA.
For statistical comparison of diagnostic performance of CTA with Agatston score results, we applied a logistic regression model with random effects [16] to account for dependencies of the two diagnostic tests within patients and for study-specific clustering [1719].
Overall diagnostic accuracies (percentage and 95% CI) of CTA in patients with different Agatston score groups, zero Agatston score, low (1 to < 100), intermediate (100 to 400), moderately (401 to 1000), and highly increased (above 1000) Agatston score, were calculated on the per-patient level. Calculations were done using exact binomial distribution. Statistical significance was assumed for p ≤ 0.05. Statistical analyses were performed using SAS (version 9.4).

Results

A total of 2452 stable chest pain patients with suspected CAD and an indication for ICA were included (Fig. 1) in this collaborative meta-analysis of the COME-CCT Consortium comparing CTA findings with Agatston scores for CAD diagnosis based on both published and unpublished results of 28 studies (from 29 original datasets as two studies were combined due to small sample size of each subset) conducted in 14 countries [2046]. The median Agatston score in the total of 2452 patients was 74.1 with an IQR of 1 to 389. Obstructive CAD by ICA was diagnosed in 45% of patients (1100 of 2452, Table 1, Fig. 2). About two-thirds of the patients were male (1603 of 2452); mean age of included patients was 62 ± 10 years; and half of the patients had arterial hypertension (56%) and hyperlipidemia (52%; Table 1, detailed characteristics by Agatston score subgroup are provided in Appendix Table 4 and Appendix Table 5). PTP calculation identified twelve patients (0.49%) with low PTP, 1884 patients (76.77%) with intermediate PTP, and 558 with high PTP (22.74%). In the 2452 patients suitable for intraindividual patient-based analysis of CTA findings and Agatston scores, CT was performed in 334, 660, 1202, 227, and 29 patients on CT scanners with 16 rows, 32 rows, 64 rows, 128 rows, and 320 rows, respectively.
Table 1
Characteristics of the 2452 patients with stable chest pain*
Characteristics
n = 2452
  Age, y
62 ± 10
  Male sex, n (%)
1603 (65.4)
Agatston score
    Median
74.1
    Range (minimum to maximum)
0 to 6209.6
    IQR
1 to 389
  Arterial hypertension, n (%)§
1332/2381 (55.9)
  Diabetes mellitus, n (%)§
442/2395 (18.5)
  Hyperlipidaemia, n (%)§
1172/2273 (51.6)
  Current smoker, n (%)§
708/2396 (29.5)
  Body mass index
26.8 ± 4.1
  Prevalence of obstructive CAD on ICA
1100 (44.9)
Angina pectoris classification, n (%)
    Typical angina
1078 (44.0)
    Atypical angina
746 (30.4)
    Nonanginal chest pain
467 (19.0)
    Other chest discomfort
161 (6.6)
  Pre-test probability, %
49 ± 17
*Plus-minus values are means ± SD unless otherwise stated. Percentages are based on analysis of all 2452 patients unless otherwise stated. §Missing information as follows per category, n (%): hypertension 71 (2.9%), diabetes mellitus 57 (2.3%), hyperlipidaemia 179 (7.3%), current smoker 56 (2.3%). Calculated as the weight in kilogrammes divided by the square of the height in metres; body mass index calculation based on 2425 patients (1.1% missing information on BMI). CAD coronary artery disease, ICA invasive coronary angiography

Diagnostic performance of CTA and Agatston score

The cross-tabulation of CTA and Agatston score versus the reference standard ICA and the cross-tabulation of CTA versus Agatston score are shown in Tables 2 and 3, respectively. Nondiagnostic CT examinations occurred in 11.2% of patients and were implemented in an intention-to-diagnose approach as previously described; detailed results for diagnostic performance excluding nondiagnostic examinations are presented in the Supplement (Appendix Table 1-3). Diagnostic accuracy of CTA was significantly higher than that of the Agatston score for the detection of obstructive CAD (81.1%, 95% CI: 77.5 to 84.1% versus 68.8%, 95% CI: 64.2 to 73.1%, p < 0.0001, Table 4) with a positive likelihood ratio of 3.3 versus 3.5 and a negative likelihood ratio of 0.2 versus 0.7. The sensitivity of an Agatston score above 400 for identifying patients with CAD (40.9%, 95% CI: 36.6 to 45.3%) was significantly lower than that of CTA (86.4%, 95% CI: 83.7 to 88.7%, p < 0.0001). The specificity of the Agatston score above 400 was significantly higher compared with CTA (88.2%, 95% CI: 85.8 to 90.2% versus 73.2%, 95% CI: 69.5 to 76.6%, p < 0.0001, Table 4). The area under the receiver operating characteristics curve for CTA was larger (79.8%, 95% CI: 78.2 to 81.4%) compared to that for the Agatston score (75.0%, 95% CI: 73.1 to 77.0%, Fig. 3). Summary receiver operating characteristics curve (SROC) and study-specific forest plots are shown in Figs 4 and 5, respectively. Funnel plots for CTA and Agatston score can be found in the Supplement (Appendix Figure 1A, Appendix Figure 1B, respectively). The negative predictive value of CTA (85.2%, 95% CI: 81.3 to 88.3%) was significantly higher than that of the Agatston score (64.1%, 95% CI: 58.4 to 69.4%, p < 0.0001). Most importantly, among the 1100 patients with obstructive CAD on ICA, 657 showed a false negative Agatston score of up to 400 whereas only 157 were false negative on CTA (Table 2).
Table 2
Direct comparison of CTA and Agatston score versus the reference standard of invasive coronary angiography according to STARD (47)
 
Invasive coronary angiography
Positive
Negative
CTA
  Positive
943 (85.7%)
353 (26.1%)
  Negative
157 (14.3%)
999 (73.9%)
  Total
1100 (100.0%)
1352 (100.0%)
Agatston score*
  Positive
443 (40.3%)
156 (11.5%)
  Negative
657 (59.7%)
1196 (88.5%)
  Total
1100 (100.0%)
1352 (100.0%)
*An Agatston score above 400 was considered positive. STARD Standards for Reporting of Diagnostic Accuracy, CTA computed tomography angiography
Table 3
2-by-2 table of CTA and Agatston score according to STARD (47)*
 
CTA
Positive
Negative
Agatston score§
  Positive
447 (18.2%)
152 (6.2%)
  Negative
849 (34.6%)
1004 (41.0%)
*Percentages are based on 2452 patients. STARD Standards for Reporting of Diagnostic Accuracy, CTA computed tomography angiography. §An Agatston score above 400 was considered positive
Table 4
Diagnostic performance of CTA and Agatston score on the patient level*
 
CTA
n/total n (% [95% CI*])
Agatston score§
n/total n (% [95% CI*])
p-value*
Diagnostic accuracy
1942/2452 (81.1% [77.5 – 84.1])
1639/2452 (68.8% [64.2–73.1])
< 0.0001
Sensitivity
943/1100 (86.4% [83.7 – 88.7])
443/1100 (40.9% [36.6–45.3])
< 0.0001
Specificity
999/1352 (73.2% [69.5 – 76.6])
1196/1352 (88.2% [85.8–90.2])
< 0.0001
Negative predictive value
999/1156 (85.2% [81.3 – 88.3])
1196/1853 (64.1% [58.4–69.4])
< 0.0001
Positive predictive value
943/1296 (73.1% [67.9 – 77.8])
443/599 (75.8% [70.2–80.7])
0.2206
Positive likelihood ratio
3.54 [2.61–4.81]
3.10 [2.37–4.06]
 
Negative likelihood ratio
0.14 [0.09–0.23]
0.67 [0.60–0.75]
 
DOR
31.42 [13.68–72.14]
5.40 [3.60–8.09]
 
*CI, confidence interval. Estimates, 95% CI, and p-values are based on a model with study-specific random intercept taking test correlation within patients into account. §An Agatston score above 400 was considered positive
Positive likelihood ratio, negative likelihood ratio, and diagnostic odds ratio (DOR) based on random effect models for each test

Zero Agatston score

A total of 600 patients had a zero Agatston score. Diagnostic accuracy of CTA in this subgroup was 80.7% (95% CI: 77.5 to 83.8%) with a negative predictive value of 95.5% (95% CI: 93.5 to 97.5%) and positive predictive value of 45.8% (95% CI: 38.5 to 53.1%). Pre-test probability in this subgroup was 42% (± 16%).
16.8% of patients with a zero Agatston score had obstructive CAD by ICA (101 of 600), whereas only 3.2% of those were false negative by CTA (19 of 600).

CTA accuracy in patients with higher Agatston scores

Frequency of patients per Agatston score subgroup of 1–100, 101–400, 401–1000, and > 1000 (Appendix Table 5) was as follows: 702, 551, 338, and 261 patients, respectively. The diagnostic accuracy of CTA was not significantly different between subgroups with Agatston scores of 1–100, 101–400, 401–1000, and > 1000 (Fig. 6) with overall diagnostic accuracies of 79.6% (95% CI: 76.7 to 82.6%), 79.9% (95% CI: 76.5 to 83.2%), 77.8 (95% CI: 73.4 to 82.2%), and 75.1% (95% CI: 69.9 to 80.3%), respectively.

Discussion

The easy applicability, short examination time, low radiation exposure, and the fact that no contrast medium is required make the Agatston score a promising prognostic test for the evaluation of suspected CAD and prediction of cardiovascular events in clinical routine. However, the diagnostic performance of the Agatston score for detecting CAD has not been examined as intensively as that of CTA [9]. We therefore compared the diagnostic performance of the Agatston score with CTA in symptomatic patients with stable chest pain.

Clinical implications

CTA performed better than the Agatston score in general, and diagnostic accuracy of CTA was accurate in all subanalyses, independent of the total calcium burden. Hence, CTA is superior to the Agatston score for CAD diagnosis. Moreover, we found that a zero Agatston score does not confidentially rule out obstructive CAD in symptomatic stable chest pain patients. Further, performance of CTA provides more additional information and may result in further therapeutic steps. CTA is able to show anatomy of coronary artery including diagnosis of myocardial bridging if present for example [48], but also characterization of plaques and plaque features is one of the major advantages of CTA including indication of and adherence to lipid lowering agents in patients with plaques [49]. As a result, we suggest that current international guidelines should include a consistent recommendation to always use CTA in patients with suspected CAD for ruling out obstructive CAD.

Comparison with previous studies

Published studies provide conflicting evidence on the benefit of coronary artery calcium scoring for diagnosing CAD in clinical routine [5057]. Controversial prevalence rates of CAD in the subgroup of zero CAC score in patients with stable chest pain can be found in the literature ranging from reported prevalence rates of 0 [52] to 20% [53]. For a better comparison of the results of our IPD meta-analysis cohort with previous studies, we performed a systematic literature search in Medline via PubMed for reported prevalence rates of CAD in patients with zero coronary artery calcium; detailed comparison of prevalence rates can be found in the Supplement (Appendix Table 6). Several studies report the CAC score to be an appropriate diagnostic test to rule out CAD in stable chest pain patients or generally symptomatic patients [50, 54] while others conclude that the Agatston score does not allow confident exclusion of obstructive CAD [55, 56]. As in our analysis, Gottlieb et al [51] found that a zero Agatston score did not reliably exclude obstructive CAD. Raff et al found lower specificity and negative predictive value in patients with severe CAC scores (> 400) in a cohort of 70 patients with suspected CAD [57]. Our comparison of diagnostic accuracy of CTA in subgroups with moderate (≤ 400) versus high (> 400) Agatston score revealed no significant difference (p = 0.0746, Figure 6), confirming our overall observation that CTA is superior to the Agatston score regardless of a patient’s total CAC.
To the best of our knowledge, we here for the first time investigate the diagnostic accuracy of CTA in comparison to the Agatston score and systematically analyse its performance in subgroups with increasing Agatston scores using data from an IPD meta-analysis cohort. Our approach clearly shows that the Agatston score should not be used in any case to exclude CAD. Instead, CTA should be used routinely in all symptomatic patients with suspected CAD for diagnosis of obstructive CAD independent of the amount of CAC.

Current guidelines in light of our results

The recent European guideline for the diagnosis and management of chronic coronary syndromes by Knuuti et al [6] states that coronary artery calcium scoring may be used for cardiovascular risk assessment in asymptomatic patients (Class IIb, Level B recommendation) to improve pre-test probability calculation. In contrast, this guideline does not recommend coronary artery calcium scoring for diagnosing obstructive CAD (Level III, Class C), but recommends CTA as a first-line examination (Class I). Accordingly, a zero Agatston score has a low prevalence of obstructive CAD but is not able to exclude coronary artery stenosis caused by noncalcified stenosis. The latest version of the ACCF/AHA guideline for management of patients with stable ischemic heart disease by Finh et al [12] discusses the use of the CAC score controversially. While referencing promising evidence such as the CONFIRM registry showing 3.5% of patients with calcium score of zero having obstructive CAD [7], Finh et al very clearly conclude that more data from large study populations are needed to decide if and how CAC scoring can be used in ruling out CAD. The recent Appropriate Use Criteria introduced by Wolk et al [58] for cardiac CT propose rating the use of the Agatston score for further diagnostic decisions as rarely appropriate in symptomatic patients independent of the pre-test probability. In patients with repeated testing Agatston scores above 400, Taylor et al discourage its use for decision making. Conversely, our analysis found CTA performance not to be affected by the total amount of CAC.
Still, a consistent guideline recommendation for the use of the Agatston score in patients with a score unequal zero is missing.
In summary, the results of the COME-CCT Consortium support the current guideline of the American College of Cardiology and the European Society of Cardiology in the general message. Following, referring to the results of the COME-CCT Consortium, we call for a consistent statement and implementation for use of the CACS worldwide and cross-guidelines. With the results of our worldwide collaborative analysis, we show that it is possible to draw more specific conclusions for the use of the Agatston score and we can provide valuable scientific evidence with our IPD meta-analysis as called for by the abovementioned guidelines. Based on our results, we recommend to always perform CTA to reliably exclude CAD regardless of the total amount of coronary artery calcium measured by the Agatston score, especially in patients with a zero Agatston score. Also, in patients with an increased Agatston score, CTA might be considered. Alternatively, the Agatston score can be omitted entirely in diagnosing CAD in symptomatic patients, while keeping in mind that the Agatston score might be a useful predictor of cardiovascular events.

Limitations

Although Agatston score analysis was a prospectively defined outcome measure of the COME-CCT Consortium, only 45% of the sites contributed data for this subanalysis, which might compromise generalizability despite the use of a well-characterized multicentre dataset. Thus, the distribution of countries and sites in this subanalysis differs from the entire study population. There was a relatively high proportion of nondiagnostic CTA examinations of 11%, which were handled in an intention-to-diagnose approach using a worst-case scenario. This may have reduced overall diagnostic performance especially when taking into account that 41% of the CT examinations were performed on CT scanners with less than 64 detector rows. Thus, accuracy of clinical CTA performed on scanner with at least 64 rows is likely higher while the accuracy of the Agatston score remains unchanged. Further technical progress in equipment and wider distribution of CTA will result in even more precision in future years, and probably decreasing the number of nondiagnostic examinations. In contrast to the current ESC guidelines (6), the proportion of patients with high pre-test probability in this analysis was relatively high with 22.7%. Inclusion criteria for the international COME-CCT Consortium were predefined before current ESC guideline; this should be highlighted in regard to the present cohort and comparability to other study cohorts. Additionally, vessel-/coronary segment-specific data, high-risk plaque features and follow-up data including occurrence of cardiovascular events were not assessed in our worldwide multicentre cohort.

Conclusion

CTA shows an overall superior diagnostic accuracy compared with the Agatston score for the detection of CAD in symptomatic patients with stable chest pain and a clinical indication for ICA. These findings hold across patients with different Agatston scores including those without coronary artery calcium. Furthermore, the diagnostic accuracy of CTA appears to be the same in patients with moderately and highly increased Agatston scores.

Acknowledgements

We thank all COME-CCT investigators for participation. We thank Bettina Herwig for her input in regard to copy editing the manuscript.

Declarations

Guarantor

The scientific guarantor of this publication is Prof. Dr. Marc Dewey.

Conflict of interest

VW reports grant support from the FP7 Program of the European Commission for the randomized multicentre DISCHARGE trial (603266-2, HEALTH-2012.2.4.-2). BLN reports grants from Siemens and HeartFlow. KN reports collaborations with and project funding from Siemens Healthineers, Bayer Healthcare, and GE Healthcare, and participation in Siemens Healthineers speakers bureau, Bayer Healthcare. RRB reports that the University Hospital Zurich holds a research agreement with GE Healthcare. PAK reports that the University Hospital Zurich holds a research agreement with GE Healthcare. PS and MD report support from the joint programme of the German Research Foundation and the German Federal Ministry of Education and Research for the submitted work. MJB reports grant support from General Electric and NIH. PS reports support from the German Research Foundation and grants from the European Union and grants from Bayer Pharma AG. MD has received grant support from the FP7 Program of the European Commission for the randomized multicentre DISCHARGE trial (603266-2, HEALTH-2012.2.4.-2). He also received grant support from German Research Foundation (DFG) in the Heisenberg Program (DE 1361/14-1), graduate program on quantitative biomedical imaging (BIOQIC, GRK 2260/1), for fractal analysis of myocardial perfusion (DE 1361/18-1), the Priority Programme Radiomics for the investigation of coronary plaque and coronary flow (DE 1361/19-1 [428222922] and 20-1 [428223139] in SPP 2177/1). He also received funding from the Berlin University Alliance (GC_SC_PC 27) and from the Digital Health Accelerator of the Berlin Institute of Health. Prof. Dewey has received lecture fees from Canon and Guerbet. Prof. Dewey is European Society of Radiology (ESR) Research Chair (2019–2022) and the opinions expressed in this article are the author’s own and do not represent the view of ESR. Per the guiding principles of ESR, the work as Research Chair is on a voluntary basis and only remuneration of travel expenses occurs. Prof. Dewey is also the editor of Cardiac CT, published by Springer Nature, and offers hands-on courses on CT imaging (www.​ct-kurs.​de). Institutional master research agreements exist with Siemens, General Electric, Philips, and Canon. The terms of these arrangements are managed by the legal department of Charité – Universitätsmedizin Berlin. Professor Dewey holds a joint patent with Florian Michallek on dynamic perfusion analysis using fractal analysis (PCT/EP2016/071551). MW, BD, HA, MFLM, AD, YLW, HM, AAS, BAH, EM, KS, BH, RM, SL, MG, KAO, JK, VMR, NB, SM, EZ, and JCT have nothing to disclose.

Statistics

At least two of the authors have significant statistical knowledge.
Written informed consent was obtained by all included sites of the COME-CCT Consortium individually during the conduct of the original studies.

Ethical approval

All original studies were approved by local ethics committees in the conduct of the original studies. The current analysis involves anonymized data only; hence, no separate ethical approval was required.

Methodology

  • Prospective
  • Diagnostic or prognostic study
  • Multicentre study
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Supplementary Information

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Metadaten
Titel
Computed tomography angiography versus Agatston score for diagnosis of coronary artery disease in patients with stable chest pain: individual patient data meta-analysis of the international COME-CCT Consortium
Publikationsdatum
10.03.2022
Erschienen in
European Radiology / Ausgabe 8/2022
Print ISSN: 0938-7994
Elektronische ISSN: 1432-1084
DOI
https://doi.org/10.1007/s00330-022-08619-4

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