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. 2016 Apr 27;3(1):e000388. doi: 10.1136/openhrt-2015-000388

Bias associated with left ventricular quantification by multimodality imaging: a systematic review and meta-analysis

Marzia Rigolli 1,2, Sulakchanan Anandabaskaran 1, Jonathan P Christiansen 1, Gillian A Whalley 1,3
PMCID: PMC4854151  PMID: 27158524

Abstract

Purpose

Cardiac MR (CMR) is the gold standard for left ventricular (LV) quantification. However, two-dimensional echocardiography (2DE) is the most common approach, and both three-dimensional echocardiography (3DE) and multidetector CT (MDCT) are increasingly available. The clinical significance and interchangeability of these modalities remains under-investigated. Therefore, we undertook a systemic review to evaluate the accuracy and absolute bias in LV quantification of all the commonly available non-invasive imaging modalities (2DE, CE-2DE, 3DE, MDCT) compared to cardiac MR (CMR).

Methods

Studies were included that reported LV echocardiographic (2DE, CE-2DE, 3DE) and/or MDCT measurements compared to CMR. Only modern CMR (SSFP sequences) was considered. Studies involving small sample size (<10 patients) and unusual cardiac geometry (ie, congenital heart diseases) were excluded. We evaluated LV end-diastolic volume (LVEDV), end-systolic volume (LVESV) and ejection fraction (LVEF).

Results

1604 articles were initially considered: 65 studies were included (total of 4032 scans (echo, CT, MRI) performed in 2888 patients). Compared to CMR, significant biased underestimation of LV volumes with 2DE was seen (LVEDV—33.30 mL, LVESV −16.20 mL, p<0.0001). This difference was reduced but remained significant with CE-2DE (LVEDV −18.05, p<0.0001) and 3DE (LVEDV −14.41, p<0.001), while MDCT values were similar to CMR (LVEDV −1.20, p=0.43; LVESV −0.13, p=0.91). However, excellent agreement for echocardiographic LVEF evaluation (2DE LVEF 0.78–1.01%, p=0.37) was observed, especially with 3DE (LVEF 0.14%, p=0.88).

Conclusions

Comparing imaging modalities to CMR as reference standard, 3DE had the highest accuracy in LVEF estimation: 2DE and 3DE-derived LV volumes were significantly underestimated. Newer generation CT showed excellent accuracy for LV volumes.

Keywords: CARDIAC FUNCTION, IMAGING AND DIAGNOSTICS


Key questions.

What is already known about this subject?

  • Anecdotally, clinicians understand that different imaging methods give different results. For example, echo is known to underestimate LV volumes compared with MRI and these differences are ameliorated with the addition of contrast or 3D echo.

What does this study add?

  • This study compares all imaging modalities to provide an overall picture of the differences that might be anticipated. Previous studies have evaluated and presented the bias (in percentage units) between echo and MRI, but not the actual values. A unique feature of this meta-analysis is that bias is presented in terms of millilitres (for volumes) and percentage points for ejection fraction; values that translate into clinical practice easily.

How might this impact on clinical practice?

  • Increasingly, multi-modality imaging is being used to determine left ventricular volumes and ejection fraction. Since these measurements are essential components of clinical management, understanding the anticipated differences that may arise due to different imaging techniques alone, and differentiating these from potential clinical changes, is a key component of clinical management.

Introduction

In the modern era of cardiovascular multimodality imaging, accurate assessment of left ventricular (LV) function is of paramount importance: LV volumes and ejection fraction (LVEF) are crucial parameters in clinical decision-making, diagnosis and outcome and are included in the main guidelines and trials.1–5 The absolute LV parameters, derived from imaging, and their variation over time, are used to guide surgical timing, device implantation and medical therapy introduction.1 2 Although several imaging methods are widely available for LV quantification, cardiac MR (CMR) is considered the most accurate modality and is recognised as the gold standard.6 Nevertheless, non-contrast two-dimensional echocardiography (2DE) is still the most widespread method used in clinical practice, mainly due to feasibility, wide distribution and rapid acquisition.7 However, 2DE has several intrinsic weaknesses, it is: user-dependent; affected by geometrical assumptions; often subject to foreshortening and limited by poor endocardial definition. By reducing these limitations, three-dimensional echocardiography (3DE) has been reported as a more reproducible and accurate modality for LV volume assessment.8–10 In addition, multidetector CT (MDCT) is increasingly available for its clinical applications and as a possible alternative in those patients for whom echocardiography may be unreliable or CMR contraindicated.11 In the past few years, the development of newer MDCT generation scanners has significantly lowered radiation exposure, which is gradually leading to increased adoption.12 13

However, the use of resource-consuming modalities requires evidence of additive impact on clinical management. It is still not clear if the quantitative advantages of these newer modalities have clinical significance. The physician should be aware of the difference between modalities when applying the common cut-off for evaluation and follow-up of patients who frequently undergo different types of tests. Moreover, the advances in multi-imaging may have recently been granted higher accuracy due to technical improvements and greater experience. These are the reasons why we sought to assess the difference in absolute values of bias in volumetric and functional LV quantification that may help clinical evaluation. Thus, the aim of our systematic review was to investigate the accuracy of LV assessment by different non-invasive imaging modalities, with a focus on the measurements adopted for patient management.

Materials and methods

The meta-analysis conforms to the Meta-analysis Of Observational Studies in Epidemiology (MOOSE) guidelines.

Search strategy

The authors developed these strategies for database searching: the MEDLINE/PubMed database was searched from January 1995 in consideration of the fact that the steady state free precession (SSFP) MRI technique that is currently used for CMR cine images acquisition was only available in the late 1990s. The literature search was limited to human adults in order to exclude studies involving children with congenital heart disease and consequent abnormal cardiac geometry. Abstracts and articles published in languages other than English were not excluded. A total of 1604 articles published over a period of 19 years were identified for initial review: 1020 and 584 in the echocardiography and CT groups, respectively.

Echocardiographic modalities versus CMR search

The search strategy was determined (by GW and JC) and the first initial literature search carried out (by SA), and an updated version (by MR) was then performed, using the following search terms: heart OR heart ventricles OR ventric*.mp AND left.mp AND cardiac volume OR heart volume OR cardiac output OR ventricular function OR ventricular dysfunction AND echocardiography OR echo.mp OR echocardiogram*.mp AND MRI OR magnetic resonance spectroscopy OR MRI.mp OR MR scan.mp OR magnetic resonance scan*.mp. The titles and abstracts of all studies identified were initially screened (by SA and MR) and reviewed (by MR and GW).

CT versus CMR search

The initial search for volumetric comparison between CT and CMR was conducted using the following search terms: heart OR cardiac OR ventricular OR ventricle OR cardiovascular AND volume OR volumes OR volumetric OR function OR dysfunction OR cardiac output AND magnetic resonance OR MRI OR MR OR MRI AND CT OR CT OR dual-source OR multi-detector OR MDCT. The titles and abstracts of all studies identified were initially screened (by SA) and reviewed (by MR and GW).

All modalities

A cross-reference process was undertaken (by SA) to search and the studies initially identified in the separate searches and the final papers were reviewed by the other authors (MR and GW). The reference lists were manually searched for potential other studies, and duplicate studies were identified and excluded.

Criteria for study selection

We excluded individual case reports, studies involving a sample size of <10 patients and those that included patients with unusual geometry (eg, congenital heart disease, Takotsubo and hypertrophic cardiomyopathy). Only newer generation CT scanners were included: at least MDCT 64 slice or dual source CT (DSCT) 2×32 slice for their improved temporal resolution and Z-axis coverage. Following these exclusions, 351 echocardiography and 93 MDCT articles were available for full review.

Data extraction

Data were extracted and recorded in an electronic database including: number of patients who received echocardiography, CT and MRI; and group mean values and SDs for LV end-diastolic volume (LVEDV), LV end-systolic volume (LVESV) and LVEF. Where the article content was insufficient, the corresponding or senior authors of the studies were contacted for further information. In the case of potential duplicate publications, clarification was sought from the authors and the largest single published data set was used for the systematic review. At the same time, additional references to either published or unpublished studies were sought.

Statistical analysis

Analyses of the collected data were performed using the Cochrane Collaboration Program Review Manager V.5.2 software. Data were collected from individual studies and weighted according to number of patients in the sample. Mean LVEDV, LVESV, LVEF and correspondent SD were used to calculate a pool estimate of the three parameters. The χ2 test was adopted to determine heterogeneity. Study variation due to heterogeneity was evaluated with inconsistency (I2). I2 values >30% were considered as significant variation. Funnel plots were used to evaluate study-level and publication bias. Absolute pooled mean values and CIs (95%) were tested with the fixed effect model of Mantel-Hanszel in case of homogeneity, and with the random effect model of DerSimonian-Laird if heterogeneity was reported. A p value <0.05 was considered significant.

Results

We identified 1020 echocardiography and 584 CT publications. Of these, 351 and 93 were considered potentially eligible. Two additional studies were found from a cross-reference check of relevant studies. After screening the full-text articles for relevance and eligibility, 50 articles comparing echocardiography to MRI and 20 studies comparing CT to MRI remained (figure 1). Owing to the overlap of five studies that analysed both echocardiography and CT versus MRI, the total number of studies included was 65 (table 1, reference list is available as online supplementary data). All the articles or abstracts were published in peer-review journals.

Figure 1.

Figure 1

Study selection for inclusion.

Table 1.

Included studies

First author* Publication year Number of patients Population Modalities compared to MRI
Hundley 1998 35 Patients referred for evaluation of LV function 2D-echo (non-contrast), 2D-echo (contrast)
Schmidt 1999 25 4 normal volunteers; 21 cardiac patients 3D-echo (non-contrast)
Chuang 2000 35 10 healthy adult volunteers; 25 patients with dilated cardiomyopathy 2D-echo (non-contrast), 3D-echo (non-contrast)
Qin 2000 16 Patients with normal LV 2D-echo (non-contrast), 3D-echo (non-contrast)
Chuang 2001 24 12 obese/overweight patients and 12 lean patients 2D-echo (non-contrast), 3D-echo (non-contrast)
Schalla 2001 34 Cardiac patients 2D-echo (non-contrast)
Mannaerts 2003 17 7 healthy volunteers and 20 patients with: hypertrophic cardiomyopathy, aortic or mitral regurgitation, or AMI 3D-echo (non-contrast)
Zeidan 2003 15 Healthy volunteers 3D-echo (non-contrast)
Jenkins 2004 50 Patients referred to the echo laboratory 2D-echo (non-contrast), 3D-echo (non-contrast)
Malm 2004 87 Patients referred to the cardiology department 2D-echo (non-contrast), 2D-echo (contrast)
Caiani 2005 46 Patients with normal LV function 2D-echo (non-contrast), 3D-echo (non-contrast)
Corsi 2005 16 Normal volunteers and patients with CAD, dilated cardiomyopathy, valvular disease 3D-echo (non-contrast)
Lim 2005 36 Stable patients with post-AMI 2D-echo (non-contrast), 2D-echo (contrast)
Wang 2005 11 Patients with chronic CAD 2D-echo (non-contrast)
Chan 2006 30 Patients with previous AMI with altered shape and wall-motion abnormalities 3D-echo (non-contrast)
Dewey 2006 30 Patients with suspected CAD 2D-echo (non-contrast)
Jenkins 2006 110 Patients referred to the echo laboratory for measurement of LV volumes and EF 2D-echo (non-contrast), 3D-echo (non-contrast)
Krenning 2006 15 Male patients with a history of AMI and various degrees of wall-motion abnormalities 3D-echo (non-contrast)
Liew 2006 32 Outpatient cardiac clinic patients with known CAD 2D-echo (non-contrast), MDCT 64-slice
Malm 2006 50 Patients submitted to echocardiography were enrolled 2D-echo (non-contrast), 2D-echo (nontrast)
Nigri 2006 70 35 patients with aortic stenosis and 35 with aortic regurgitation with surgical indication 2D-echo (non-contrast)
Nikitin 2006 64 40 cardiac patients with LVEF <45%, 14 with EF >45% and 10 normal volunteers 3D-echo (non-contrast)
Sugeng 2006 31 Patients referred for clinically indicated CT angiography 3D-echo (non-contrast)
Brodoefel 2007 20 Patients with chronic CAD Dual source CT 2×32
Demir 2007 21 Patients with known or suspected CAD 2D-echo (non-contrast)
Giakoumis 2007 135 Patients with thalassaemia major attending an outpatient clinic 2D-echo (non-contrast)
Jenkins 2007 50 Patients with LV dysfunction due to previous AMI 2D-echo (non-contrast), 3D-echo (non-contrast)
Jenkins 2007 30 Patients referred to the echo laboratory for measurement of LV volumes and EF 2D-echo (non-contrast), 3D-echo (non-contrast)
Krenning 2007 39 Patients referred for routine evaluation of cardiac function after AMI 3D-echo (non-contrast)
Qi 2007 58 44 patients with various cardiac disorders referred for clinical MRI studies and 14 normal patients 3D-echo (non-contrast)
Schlosser 2007 21 Patients referred for CTCA MDCT 64-slice
Soliman 2007 53 Patients with a cardiomyopathy and adequate 2D image quality 3D-echo (non-contrast)
Bastarrika 2008 12 Patients heart transplant recipients Dual source CT 32×2
Busch 2008 15 Mixed population of patients Dual source CT 32×2
Chukwu 2008 69 35 with normal LV systolic function and 34 with AMI and depressed LV function 2D-echo (non-contrast), 3D-echo (non-contrast)
Leonardi 2008 24 Patients with thalassaemia 2D-echo (non-contrast)
Mor-Avi 2008 92 Patients referred for CMR evaluation of LV size and function 3D-echo (non-contrast)
Pouleur 2008 83 20 volunteers and 63 patients with heart disease including aortic valve disease, severe mitral regurgitation and previous AMI 3D-echo (non-contrast)
Puesken 2008 28 Patients with known/suspected CAD MDCT 64-slice
Rutten 2008 78 Mild to moderate patients with COPD with and without heart failure 2D-echo (non-contrast)
Soliman 2008 24 17 patients with impaired LV systolic function due to CAD or idiopathic dilated cardiomyopathy 3D-echo (non-contrast)
Wu 2008 41 Mixed population of patients MDCT 64-slice
Akram 2009 20 Patients with suspected CAD MDCT 64-slice
Garcia-Alvarez 2009 65 Patients with first STEMI admitted to a tertiary care hospital and reperfused within 12 h of symptom onset 2D-echo (non-contrast)
Gardner 2009 47 Patients with AMI greater than 6 weeks previously and scheduled for imaging evaluation 2D-echo (non-contrast)
Gjesdal 2009 61 Healthy controls and patients with acute STEMI and treated with PCI 2D-echo (non-contrast)
Guo 2009 51 Patients with mitral regurgitation confirmed by 2D-echo and colour Doppler 2D-echo (non-contrast), MDCT 64-slice
Jenkins 2009 50 Patients with past AMI who underwent echocardiographic assessment of LV volume and function 2D-echo (non-contrast), 2D-echo (contrast), 3D-echo (non-contrast)
Nowosielski 2009 52 Patients with first AMI and PCI 2D-echo (non-contrast)
Sarwar 2009 21 Patients with STEMI MDCT 64-slice
Abbate 2010 10 Patients with ST-segment elevation AMI 2D-echo (non-contrast)
Claver 2010 43 Unselected patients who underwent CMR; mixed cardiac pathologies 3D-echo (non-contrast)
Palumbo 2010 181 Patients with suspected CAD, indexed volumes MDCT 64-slice
Whalley 2010 25 Patients with at least moderate MR due to MV prolapse 2D-echo (non-contrast)
De Jonge 2011 26 Patients referred for CTCA Dual source CT 2×32
Arraiza 2012 25 Patients heart transplant recipients 2D-echo (contrast), dual source CT 2×32
Bak 2012 111 Patients referred for CTCA before valve surgery 2D-echo (non-contrast), dual source 2×32
Brodoefel 2012 20 Patients with known or suspected CAD Dual source CT 2×32
Coon 2012 18 Patients with CAD, dilated cardiomyopathy, post-AMI, aortic abnormalities and mitral valve disease 3D-echo (non-contrast), 3D-echo (contrast)
Fuchs 2012 53 Patients with previous AMI MDCT 64-slice
Greupner 2012 36 Patients referred for CTCA 2D-echo (non-contrast), 3D-echo (non-contrast), MDCT 64-slice
Lee 2012 30 Patients who had undergone clinically indicated, routine CCTA studies MDCT 64-slice
Li 2012 72 Mixed population of cardiac patients 2D-echo (non-contrast)
Maffei 2012 79 Patients referred for CTCA, indexed volumes MDCT 64-slice
Takx 2012 20 Patients with known or suspected CAD Dual source CT 2×32
Total 1998-2013 2888 2D Echo (NC): 32 studies/1663 examinations
2D Echo (C): 6 studies/283 examinations
3D Echo (NC): 27 studies/1137 examinations
3D Echo (C): 3 studies/107 examinations
MDCT: 20 studies/842 examinations
50 Echo and 20 CT (5 of these included echo and CT)

2D, two-dimensional echo; AMI, acute myocardial infarction; C, contrast; CAD, coronary artery disease; CMR, cardiac MR; COPD, chronic obstructive pulmonary disease; CTCA, CT coronary angiography; EF, ejection fraction; LV, left ventricular; LVEF, left ventricular ejection fraction; MDCT, multidetector CT; MV, mitral valve; NC, non-contrast; PCI, percutaneous coronary intervention; STEMI, ST segment elevation myocardial infarction.

*See online supplementary file for citations.

Supplementary data

openhrt-2015-000388supp.pdf (55.3KB, pdf)

2D Echocardiography and CMR comparison

Overall, 2888 patients (4032 scans) were included. Compared to CMR, there were significant differences in LVEDV and LVESV, with observed high levels of heterogeneity (87%) and bias from funnel plots (table 2, figures 2 and 3). Although a significant bias was not detected for LVEF (mean difference: −0.78% (95% CI −2.24% to −0.68)), similar high levels of heterogeneity (72%) and bias were observed (table 2 and figure 4). This heterogeneity renders the calculated mean difference unreliable, but it does highlight a clinically relevant underestimation of the volumes and supports the overall findings that these methods are not interchangeable.

Table 2.

Summary of meta-regression of differences observed by each method

Mean difference compared to cardiac MR
Imaging modality Year published LVEDV (mL) (95% CI) Overall p value I2
p value
LVESV (mL) (95% CI) Overall p value I2
p value
LVEF (%) (95% CI) Overall p value I2
p value
2D-echocardiography
Volumes N=1579, LVEF N=1683
Overall −33.26 (−43.42 to −20.65) <0.0001 87% p<0.0001 −16.20 (−21.36 to −11.04) <0.0001 73% <0.0001 −0.66 (−2.14 to 0.82) 0.38 72% <0.0001
<2005 −23.23 (−43.86 to −2.59) 0.03 77% p<0.0001 −12.15 (−18.55 to --5.75) 0.0002 0% 0.05 −2.11 (−4.48 to 0.26) 0.08 3% 0.40
2005–2009 −33.49 (−46.88 to −20.09) <0.0001 90% p<0.0001 −17.73 (−25.11 to −10.36) <0.0001 81% <0.0001 −0.26 (−2.32 to 1.81) 0.81 81% <0.0001
>2009 −46.46 (−72.27 to −20.65) 0.0004 83% p<0.0001 −18.73 (−29.46 to −8.01) 0.0006 58% 0.05 −1.14 (−3.03 to 0.21) 0.09 0% 0.67
2D-echocardiography with contrast
Volumes and LVEF N=283
Overall* −18.05 (−6.39 to −9.7) <0.0001 0% p=0.45 −7.84 (−14.46 to −1.22) 0.02 0% p=0.99 −1.03 (−3.38 to 1.35) 0.39 0% p=0.61
3D-echocardiography
Volumes N=1159, LVEF N=1104
Overall −14.16 (−18.66 to −9.66) <0.0001 23% p=0.12 −6.49 (−9.91 to −3.07) 0.0002 0% p=0.96 0.13 (−0.91 to 1.16) 0.81 0% p=1.00
<2005 −15.14 (−25.17 to −5.12) 0.003 0% p=0.49 −6.38 (−13.36 to 0.60) 0.07 0% p=0.91 0.25 (−2.09 to 2.59) 0.83 0% p=1.00
2005–2009 −13.32 (−18.64 to −8.01) <0.0001 43% p=0.01 −6.27 (−10.41 to −2.13) 0.003 0% p=0.72 0.02 (−1.20 to 1.23) 0.98 0% p=0.99
>2009 −18.95 (−34.54 to −3.36) 0.02 0% p=0.86 −8.77 (−21.00 to 3.47) 0.16 0% p=0.84 0.89 (−2.93 to 4.70) 0.65 9% p=0.33
Multidetector CT
Volumes N=790, LVEF N=780
Overall −1.16 (−4.14 to 1.83) 0.45 0% p=0.90 −0.11 (−2.40 to 2.18) 0.93 0% p=0.96 0.86 (−0.21 to 1.94) 0.12 0% p=0.55
2007–2009 5.21 (−2.13 to 12.54) 0.16 0% p=0.74 2.59 (−1.19 to 6.36) 0.18 0% p=0.93 0.45 (−1.27 to 2.17) 0.51 0% p=0.94
>2009 −2.41 (−5.68 to 0.85) 0.15 0% p=0.99 −1.68 (−4.56 to 1.21) 0.25 0% p=0.97 1.13 (−0.25 to 2.50) 0.11 4% p=0.40

Values are mean (95% CI).

*Insufficient number of studies for subgroup analysis.

LVEDV, Left ventricular end-diastolic volume; LVEF, left ventricular ejection fraction; LVESV, left ventricular end-systolic volume.

Figure 2.

Figure 2

Left ventricular end-diastolic volume: 2D echo versus CMR. CMR, cardiac MR; 2D, two-dimensional.

Figure 3.

Figure 3

Left ventricular end-systolic volume: 2D echo versus CMR. CMR, cardiac MR; 2D, two-dimensional

Figure 4.

Figure 4

Left ventricular ejection fraction: 2D echo versus CMR. CMR, cardiac MR; 2D, two-dimensional

2D echocardiography with contrast and CMR comparison

When contrast was added to 2DE, significant differences in LVEDV and LVESV remained: CE-2DE underestimated both volume measurements (table 2, figures 5 and 6) but LVEF was similar compared to CMR and neither heterogeneity nor bias was seen (table 2 and figure 7).

Figure 5.

Figure 5

Left ventricular end-diastolic volume: 2D echo with contrast versus CMR. CMR, cardiac MR; 2D, two-dimensional.

Figure 6.

Figure 6

Left ventricular end-systolic volume: 2D echo with contrast versus CMR. CMR, cardiac MR; 2D, two-dimensional.

Figure 7.

Figure 7

Left ventricular ejection fraction: 2D echo with contrast versus CMR. CMR, cardiac MR; 2D, two-dimensional.

3D echocardiography and CMR comparison

Using 3DE further reduced the absolute size of the bias, but significant underestimation remained for LVEDV and LVESV (table 2, figures 8 and 9). However LVEF was similar and neither heterogeneity nor bias was seen (table 2 and figure 10).

Figure 8.

Figure 8

Left ventricular end-diastolic volume: 3D echo versus CMR. CMR, cardiac MR; 3D, three-dimensional.

Figure 9.

Figure 9

Left ventricular end-systolic volume: 3D echo versus CMR. CMR, cardiac MR; 3D, three-dimensional.

Figure 10.

Figure 10

Left ventricular ejection fraction: 3D echo versus CMR. CMR, cardiac MR; 3D, three-dimensional.

CT and CMR comparison

Of the 20 CT studies that were included, 12 adopted a 64-slice MDCT, while the remaining eight employed a dual source technology (2×32 slices). No differences were observed between CT and CMR for any volume or LVEF measure, and heterogeneity was uniformly absent; also, the funnel plots revealed no bias (table 2 and figures 11–13).

Figure 11.

Figure 11

Left ventricular end-diastolic volume: CT versus CMR. CMR, cardiac MR.

Figure 12.

Figure 12

Left ventricular end-systolic volume: CT versus CMR. CMR, cardiac MR.

Figure 13.

Figure 13

Left ventricular ejection fraction: CT versus CMR. CMR, cardiac MR.

When considered over time, no significant differences in the summary statistics were seen for any measure or modality with widely overlapping CIs, suggesting no obvious impact of improved technology over this time period.

Discussion

To the best of our knowledge, this is the first meta-analysis to evaluate all of the most commonly available non-invasive modalities for LV volume and LVEF quantification over nearly two decades of literature search. Our data show that 3DE provides the highest accuracy for LVEF quantification, while newer generation CT is the most precise method for assessment of LV volumes, when compared to CMR. Moreover, 2DE (non-contrast and contrast-enhanced) significantly underestimates LV volumes.

Despite the clinical importance of LV volumetric and functional quantification, no consensus remains on the best modality for assessment. Although it is acknowledged that bias may occur, the absolute differences in LV volumes and LVEF by various imaging methods are largely unquantifiable. It is important to determine, and quantify, if there is a significant absolute bias between modalities especially for follow-up that nowadays is increasingly performed with different types of tests. This may impact considerably on clinical management of various cardiac conditions, particularly in patients with borderline LV volumes and LVEF values. A better comprehension of their parameter variability between tests may enhance therapeutic decisions. Small studies evaluating echocardiography and CT in comparison to CMR demonstrated controversial results. Greupner et al14 reported the CT superiority in assessing all three global LV parameters compared to 2DE, 3DE and ventriculography when CMR values are used as reference standard. Interestingly, 3DE did not perform better than 2DE, in contrast with previous reports and prior meta-analyses.8 9 15 In our study, despite the underestimation of LV volume by 3DE, almost no difference was seen for LVEF when compared to CMR. The underestimation of volumes observed is concordant with the results of two previous meta-analyses8 9 that evaluated the sources of bias and limits of agreement affecting 3DE. When LV function was considered, there was no difference in bias between 2DE and 3DE, with only a modest difference in variance.8 In contrast to these previous studies, we decided to focus on the absolute difference between LV parameters and to exclude the cardiac conditions that markedly alter geometric shape. In fact, the inclusion of major anatomical ventricular alterations (eg, congenital and primary cardiomyopathies) may have influenced prior results, especially when 2DE geometrically based assessments were compared. These former systematic reviews included congenital heart abnormalities in which the global ventricular structure was markedly changed. This may have resulted in an unfair comparison for 2DE versus 3D modalities considering that congenital diseases represent a significantly reduced proportion of most common everyday clinical practice. Our data confirm that, even excluding limited cardiac diseases in which echocardiography has known limitations, 2DE and 3DE significantly underestimate LV volumes. Although 3DE relies on fewer geometrical assumptions than 2DE and approximately halves the absolute bias of underestimation, it still performs worse than CT, compared with CMR. This is probably due to the reduced spatial resolution and consequent lack of precision in distinguishing myocardial trabeculations and endocardial borders.9 16 17

The highest spatial resolution of CT and its similar 3D reconstruction method to CMR may explain the perfect agreement observed in quantification of volumes. Our results are complementary to two previous systemic reviews comparing CT and CMR, one on older and one on newer generation scanners.18 19 These have shown a good agreement for LVEF, but no analysis of LV volumes bias compared to CMR was performed. However, our data suggest that functional evaluation is not as good as echocardiography when compared to CMR. Although CT has the disadvantages of risk radiation and iodinated contrast exposure, it remains a useful method for second-level cardiac anatomical evaluation in those patients with contraindications to MRI (eg, implanted devices, claustrophobia) and its use has more than doubled over the past 10 years.12 Possible explanations of the reduced performance in functional assessment should consider the substantial differences in LV assessment between the various imaging modalities. First of all, with the exception of the newest whole-heart 320-slice scanner, CT acquires the cardiac volume in more heartbeats in contrast to echocardiography, by which LV evaluation is performed on a single heart beat acquisition. Furthermore, β-blockers commonly administered prior to cardiovascular and coronary CT scans to lower heart rate and limit cardiac motion-related artefacts, may directly affect the evaluation of LV function. Finally, most studies evaluating 2DE and 3DE have commonly excluded patients with poor echocardiographic views, leading to an overestimation of echocardiographic accuracy compared to routine practice. When good images are available, 3DE improves the accuracy and reproducibility of LV volume and EF measurements overall.20

In addition to these considerations, although CMR is the gold standard for LV quantification, there still are significant limitations in LV quantification when comparing imaging techniques by setting CMR parameters as true values for bias estimation, such as basal slice selection and multiple breath-holds acquisition. Moreover, most clinical studies, and indeed clinical practice, are based on echocardiographic parameters, and 2DE cut-offs for EF are the most often reported and relied on.21–23 Although CMR parameters are compared to well-established normality databases,24 25 the data on patient management and outcome based on CMR are still limited. However, up to date CMR remains the highest reproducible LV quantification modality.26 Technical advances are allowing better semiautomatic acquisition and analysis for higher operator independency,27 28 and direct prognostic evidence with CMR is growing.29 30

Limitations

The majority of studies included a small number of patients with different baseline characteristics. Most of the studies analysed were single-centre retrospective trials, and, therefore, issues of potential referral bias and inconsistent data collection may be present. As in any meta-analysis, the validity of our results is dependent on the validity of the studies included but this variability reflects clinical practice. There are multiple risks of bias in systematic reviews; however, our funnel plot analyses mostly demonstrated no significant publication bias for the results without significant heterogeneity, except for 2DE. A few studies had to be excluded due to different numbers of patients undergoing different modalities. Technical issues in completing the scans mainly caused this inconsistency. We excluded these studies to keep the balance between the modality groups. Some studies did not report LVEF but only presented volumes. We chose to include these since the analyses for LV volumes and LVEF were performed separately and consequently we considered them as independent parameters. We did restrict inclusion of the CT studies to recent technology only, and did not do this for the echo studies. The advances in CT imaging over this time period have been substantial, and more so than echo. Nevertheless, in the analyses, we have subgrouped the studies by year of publication to partially account for this, and no chronological impact is apparent.

Conclusion

Comparing commonly available non-invasive imaging modalities to CMR as a reference standard, 3DE holds the highest accuracy in LVEF estimation, although 2DE and 3DE-derived LV volumes are significantly underestimated. Newer generation CT shows excellent accuracy for LV volumes quantification. These results may help clinicians to better understand the degree of absolute bias between different cardiac imaging modalities and may have potential implications for patient follow-up and management.

Acknowledgments

The authors thank the following people for providing additional data or confirming the data we had extracted from their studies: Dr Antonio Abbate, Dr Michael Chuang, Dr Ana Garcia-Alvarez, Dr Ola Gjessdal, Dr Sigrun Halvorsen, Dr Carly Jenkins, Dr Jens Kastrup, Dr Bernhard Metzler, Dr Masaaki Takeuchi, Dr Victor Mor-Avi, Dr Jürgan Scharhag, Dr Marta Sitges, Dr Osama Soliman, Dr Stefan Steorck and Dr Cezary Szmigielski.

Footnotes

Twitter: Follow Gillian Whalley at @GWhalleyPhD

Contributors: MR and SA conducted the searches. All four authors developed the search strategy. MR drafted the first manuscript, and SA, GAW and JPC offered feedback and edited the final version. All the authors contributed to the design and conduct of the study and have approved this final version.

Funding: This study was funded by Awhina Knowledge and Innovation Centre, Waitemata District Health Board (summer studentship).

Competing interests: None declared.

Provenance and peer review: Not commissioned; externally peer reviewed.

Data sharing statement: Our data are limited to the group level data for the individual studies we used. Some of these were easily, and some not so easily, accessible. We would be happy to share our data.

References

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Supplementary Materials

Supplementary data

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