Rixe Johannes, Achenbach Stephan, Ropers Dieter, Baum Ulrich, Kuettner Axel, Ropers Ulrike, Bautz Werner, Daniel Werner G, Anders Katharina
Department of Internal Medicine 2 (Cardiology), University of Erlangen, Ulmenweg 18, 91054 Erlangen, Germany.
Eur Heart J. 2006 Nov;27(21):2567-72. doi: 10.1093/eurheartj/ehl303. Epub 2006 Oct 11.
We investigated the feasibility of assessing coronary artery stent restenosis using a new generation 64-slice multi-detector computed tomography-scanner (MDCT) in comparison to conventional quantitative angiography.
MDCT was performed in 64 consecutive patients (mean age 58+/-10 years) with previously implanted coronary artery stents (102 stented lesions: mean stent diameter 3.17+/-0.38 mm). Each stent was classified as 'evaluable' or 'unevaluable', and in evaluable stents, the presence of in-stent restenosis (diameter reduction >50%) was determined visually. Results were verified against invasive, quantitative coronary angiography. Fifty-nine stented lesions (58%) were classified as evaluable in MDCT. The mean diameter of evaluable stents was 3.28+/-0.40 mm, whereas the mean diameter of non-evaluable stents was 3.03+/-0.31 mm (P=0.0002). Overall, six of 12 in-stent restenoses were correctly detected by MDCT [50% sensitivity (confidence interval 22-77%)] and in 51 of 90 lesions, in-stent restenosis was correctly ruled out [57% specificity (46-67%)]. In evaluable stents, six of seven in-stent restenoses were correctly detected, and the absence of in-stent stenosis was correctly identified in 51 of 52 cases [sensitivity 86% (42-99%) and specificity 98% (88-100%)].
Stent type and diameter influence evaluability concerning in-stent restenosis by MDCT. The rate of assessable stents is low, but in evaluable stents, accuracy for detection of in-stent restenosis can be high.
我们研究了使用新一代64层多探测器计算机断层扫描扫描仪(MDCT)评估冠状动脉支架再狭窄的可行性,并与传统定量血管造影术进行比较。
对64例连续患者(平均年龄58±10岁)进行了MDCT检查,这些患者先前已植入冠状动脉支架(102个支架病变:平均支架直径3.17±0.38mm)。每个支架被分类为“可评估”或“不可评估”,对于可评估的支架,通过视觉确定支架内再狭窄(直径减少>50%)的存在。结果与有创定量冠状动脉造影进行了验证。MDCT将59个支架病变(58%)分类为可评估。可评估支架的平均直径为3.28±0.40mm,而不可评估支架的平均直径为3.03±0.31mm(P=0.0002)。总体而言,MDCT正确检测出12例支架内再狭窄中的6例[敏感性50%(置信区间22-77%)],在90个病变中的51个病变中,正确排除了支架内再狭窄[特异性57%(46-67%)]。在可评估的支架中,7例支架内再狭窄中的6例被正确检测出,52例中的51例正确识别出无支架内狭窄[敏感性86%(42-99%)和特异性98%(88-100%)]。
支架类型和直径影响MDCT对支架内再狭窄的可评估性。可评估支架的比例较低,但在可评估的支架中,检测支架内再狭窄的准确性可能较高。