Bakker M Els, Stolk Jan, Putter Hein, Shaker Saher B, Parr David G, Piitulainen Eeva, Russi Erich W, Dirksen Asger, Stockley Robert A, Reiber Johan H C, Stoel Berend C
Division of Image Processing, Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands, and the Department of Respiratory Medicine, Gentofte Hospital, Hellerup, Denmark.
Invest Radiol. 2005 Dec;40(12):777-83. doi: 10.1097/01.rli.0000186418.31139.21.
The objectives of this study were to investigate whether computed tomography (CT) densitometry can be applied consistently in different centers; and to evaluate the reproducibility of densitometric quantification of emphysema by assessment of different sources of variation, ie, intersite, interscan and inter- and intraobserver variability, in comparison with intersubject variability.
In 5 different hospitals, 119 patients with emphysema were scanned using standardized protocols. In each site, an observer performed a quantitative densitometric analysis (including blood recalibration) on the corresponding patient group (n=23-25) and one observer analyzed the entire group of 119 patients. After several months, the latter observer analyzed all data for a second time. Subsequently, different sources of variation were assessed by variance component analysis with and without volume correction of the data.
Inter- and intraobserver variability marginally contributes to the total variability (<0.001%). The interscan variability was 0.02% of the total variation after application of volume correction. The intersite variability was 48% as a result of one deviating CT scanner. Air recalibration normalized deviating air densities in CT scanners. Within sites, the intersubject variability ranged between 93% and 99% based on the analysis of 2 subsequent CT scans of the patients.
Almost all variability in the density measurement of emphysema originates from differences between scanners and from differences in severity of emphysema between patients. Lung densitometry with multislice CT scanners is a highly reproducible measurement, especially if corrected for lung volume, because this reduces interscan variability.
本研究的目的是调查计算机断层扫描(CT)密度测定法能否在不同中心得到一致应用;并通过评估不同变异来源,即不同中心间、不同扫描间以及观察者间和观察者内的变异性,并与个体间变异性进行比较,来评估肺气肿密度定量的可重复性。
在5家不同医院,使用标准化方案对119例肺气肿患者进行扫描。在每个站点,一名观察者对相应患者组(n = 23 - 25)进行定量密度分析(包括血液重新校准),一名观察者分析全部119例患者。几个月后,后一名观察者再次分析所有数据。随后,通过方差成分分析评估不同变异来源,分析时对数据进行或不进行体积校正。
观察者间和观察者内变异性对总变异性的贡献微乎其微(<0.001%)。应用体积校正后,不同扫描间变异性占总变异的0.02%。由于一台CT扫描仪存在偏差,不同中心间变异性为48%。空气重新校准使CT扫描仪中偏差的空气密度标准化。在各站点内,根据对患者后续两次CT扫描的分析,个体间变异性在93%至99%之间。
肺气肿密度测量中几乎所有变异性都源于扫描仪之间的差异以及患者间肺气肿严重程度的差异。使用多层CT扫描仪进行肺密度测定是一种高度可重复的测量方法,尤其是在对肺体积进行校正后,因为这可降低不同扫描间的变异性。