TO THE EDITOR: We were interested in the conclusions of Schepis et al. (1), who stated that there is good agreement between left ventricular (LV) ejection fraction (LVEF) and LV functional parameters estimated using CT and gated SPECT across a wide range of clinically relevant values. They appear to base this statement on the good correlation between parameters estimated using the 2 techniques. However, good correlation does not, in itself, indicate good clinical agreement (2).
The authors presented Bland–Altman plots and reported limits of agreement. These are a good indicator of the level of clinical agreement, but the results shown were not adequately discussed. We would argue that limits of agreement of ±15.1% on LVEF, where the threshold of normality is 50% and mean values in the study were 59% (SPECT) and 60% (CT), do not indicate good agreement, because the potential level of difference in individual cases is large. Similarly, the limits of agreement for end-diastolic volume and end-systolic volume of ±51.7 mL and ±32 mL, respectively, do not indicate good agreement.
The authors' conclusions are somewhat inconsistent. They suggest that although the techniques agree for LVEF, they should not be used interchangeably for LV volumes; LVEF is calculated from LV volumes.
Intraobserver reproducibility was reported as excellent for SPECT. The SD of 4.6% is again high relative to the normal threshold; a potential error of greater than 4.6% in 1 in 3 patients is significant. Interobserver error was not reported for SPECT but is likely to be higher than intraobserver error. The 6.4% SD of interobserver differences for CT is high. The authors should investigate the sources of these differences; in our experience, intra- and interobserver differences of this magnitude are unusual.
A further point of interest is the systematic difference between the 2 techniques in the estimation of muscle mass. In determining likely explanations, it would be useful to know the extent of myocardium included and whether analysis of the SPECT images included nonperfused muscle.
We would also like to point out an error in the presentation of data. The percentage mean differences shown in Table 2 are given in the text as SD on the absolute mean difference; the actual SDs are considerably larger. This may lead to an incorrect conclusion regarding intraobserver reproducibility.
In conclusion, we believe that the data show poor intraobserver reproducibility in the estimation of LVEF and very poor clinical agreement between SPECT and CT for the estimation of LVEF and LV functional parameters. LVEF and LV functional parameters as determined by 64-slice CT do not agree with gated SPECT and should not be used interchangeably. Furthermore, the large random differences between the techniques suggest that neither provides a clinically reliable measure of LVEF in this study.
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