Department of Nuclear Medicine, Academic Medical Center, University of Amsterdam, P.O. Box 22700, 1100 DE, Amsterdam, The Netherlands.
Department of Cardiology, Zaans Medical Center, Zaandam, The Netherlands.
J Nucl Cardiol. 2018 Aug;25(4):1191-1197. doi: 10.1007/s12350-017-0782-6. Epub 2017 Jan 24.
Planar myocardial I-meta-iodobenzylguanidine (I-mIBG) scintigraphy is a highly reproducible technique. However, differences in collimator use are one of the most important factors that cause variation among institutions and studies in heart-to-mediastinum (H/M) ratio. Therefore, standardization among various gamma camera-collimator combinations is needed. Previously, a phantom has been developed to cross-calibrate different acquisition conditions in Japan. For further cross-calibration of European myocardial I-mIBG imaging, the aim of this study was to collect I-mIBG data for H/M ratios from common European gamma camera vendors.
210 experiments were performed in 27 European institutions. Based on these experiments, conversion coefficients for each gamma camera-collimator combination were calculated. An averaged conversion coefficient of 0.88 was used to calculate a standardized H/M ratio.
On average, LE-collimator-derived H/M ratios were significantly lower compared to ME-collimator-derived H/M ratios. The mean conversion coefficients ranged from 0.553 to 0.605 for the LE-collimator group and from 0.824 to 0.895 for the ME-collimator group.
Clinically established H/M ratios can be converted into standardized H/M ratios using cross-calibrated conversion coefficients. This standardization is important for identifying appropriate thresholds for adequate risk stratification. In addition, this cross-calibration enables comparison between different national and international data.
平面心肌 I-间位碘苄胍(I-mIBG)闪烁显像术是一种高度可重复的技术。然而,准直器的使用差异是导致不同机构和研究中心心脏与纵隔(H/M)比值差异的最重要因素之一。因此,需要对各种伽马相机-准直器组合进行标准化。以前,已经开发了一种体模来对日本的不同采集条件进行交叉校准。为了进一步对欧洲心肌 I-mIBG 成像进行交叉校准,本研究的目的是从常见的欧洲伽马相机供应商收集 I-mIBG 的 H/M 比值数据。
在 27 个欧洲机构进行了 210 次实验。根据这些实验,计算了每个伽马相机-准直器组合的转换系数。使用平均转换系数 0.88 来计算标准化的 H/M 比值。
平均而言,LE 准直器获得的 H/M 比值明显低于 ME 准直器获得的 H/M 比值。LE 准直器组的平均转换系数范围为 0.553 至 0.605,ME 准直器组的平均转换系数范围为 0.824 至 0.895。
可以使用经过交叉校准的转换系数将临床确定的 H/M 比值转换为标准化的 H/M 比值。这种标准化对于确定适当的风险分层阈值非常重要。此外,这种交叉校准使得不同国家和国际数据之间的比较成为可能。