首页> 外文期刊>The Journal of Nuclear Medicine >Acute thromboscintigraphy with (99m)Tc-apcitide: results of the phase 3 multicenter clinical trial comparing 99mTc-apcitide scintigraphy with contrast venography for imaging acute DVT. Multicenter Trial Investigators (see comments)
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Acute thromboscintigraphy with (99m)Tc-apcitide: results of the phase 3 multicenter clinical trial comparing 99mTc-apcitide scintigraphy with contrast venography for imaging acute DVT. Multicenter Trial Investigators (see comments)

机译:(99m)Tc-apcitide的急性血栓造影:比较99mTc-apcitide闪烁显像和对比静脉造影对急性DVT成像的3期多中心临床试验结果。多中心试验研究者(请参阅评论)

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摘要

(99m)Tc-apcitide (formerly known as (99m)Tc-P280) is a radiolabeled peptide that binds with high affinity and specificity to the glycoprotein IIb/IIIa receptors expressed on the activated platelets that are involved in acute thrombosis. The purpose of the phase 3 multicenter clinical trials was to compare (99m)Tc-apcitide scintigraphy with contrast venography for imaging acute deep venous thrombosis (DVT). METHODS: A total of 280 patients were enrolled in 2 clinical trials conducted in North America and Europe. Patients were to be within 10 d of onset of signs and symptoms of acute DVT or within 10 d of surgery associated with a high risk of DVT. (99m)Tc-apcitide scintigraphy and contrast venography were to be performed within 36 h. Planar scintigraphic images were obtained at 10, 60, and 120-180 min after injection. (99m)Tc-apcitide scintigrams and contrast venograms were read with masking and also by the institutional investigators. RESULTS: Of a total of 243 patients who were evaluable, 61.7% were receiving heparin at the time of imaging. Masked reading of (99m)Tc-apcitide scintigraphy, compared with masked reading of contrast venography, had a sensitivity, specificity, and agreement of 73.4%, 67.5%, and 69.1%, respectively, which met the prospectively defined target efficacy endpoint in both trials. Institutional reading of (99m)Tc-apcitide scintigraphy, compared with institutional reading of contrast venography, had a sensitivity, specificity, and agreement of 75.5%, 72.8%, and 74.0%, respectively. However, the entire trial population included patients with a history of DVT who may have had old, nonacute venous thrombi that could confound the venography results. Therefore, data from patients having no history of DVT or pulmonary embolism and who presented within 3 d of onset of signs and symptoms (n = 63), i.e., patients for whom a venogram would be expected to be positive only if acute DVT were present, also were analyzed as a subset. In these patients, institutional reading of (99m)Tc-apcitide scintigraphy, compared with institutional reading of contrast venography, had a sensitivity, specificity, and agreement of 90.6%, 83.9%, and 87.3%, respectively. CONCLUSION: (99m)Tc-apcitide scintigraphy is a new diagnostic modality that is highly sensitive for imaging acute DVT.
机译:(99m)Tc-apcitide(以前称为(99m)Tc-P280)是一种放射性标记的肽,与参与急性血栓形成的活化血小板上表达的糖蛋白IIb / IIIa受体具有高亲和力和特异性结合。 3期多中心临床试验的目的是比较(99m)Tc-apcitide闪烁显像和对比静脉造影对急性深静脉血栓形成(DVT)的成像。方法:总共280名患者参加了在北美和欧洲进行的2项临床试验。患者应在急性DVT的体征和症状发作后10天内,或与DVT高风险相关的手术后10天内。 (99m)Tc-阿普西肽闪烁显像和对比静脉造影应在36 h内进行。注射后10、60和120-180分钟获得平面闪烁图像。 (99m)Tc-apcitide闪烁图和对比静脉图在掩蔽下以及由机构研究人员阅读。结果:在总共243例可评估的患者中,有61.7%的患者在影像学检查时接受了肝素治疗。 (99m)Tc-apcitide闪烁显像的掩盖读数与对比静脉造影的掩盖读数相比,分别具有73.4%,67.5%和69.1%的敏感性,特异性和一致性,在这两个方面均达到了预期的目标疗效终点审判。与造影剂静脉造影的机构读数相比,(99m)Tc-磷酰胺闪烁体显像的机构读数分别具有75.5%,72.8%和74.0%的敏感性,特异性和一致性。但是,整个试验人群均包括具有DVT历史的患者,这些患者可能患有陈旧的非急性静脉血栓,可能使静脉造影结果混淆。因此,来自无DVT或肺栓塞病史且在症状和体征发作后3 d内出现的患者(n = 63)的数据,即,只有存在急性DVT时,静脉造影预期为阳性的患者的数据,也作为子集进行了分析。在这些患者中,与造影剂静脉造影的机构读数相比,(99m)Tc-apcitide闪烁显像的机构读数分别具有90.6%,83.9%和87.3%的敏感性,特异性和一致性。结论:(99m)Tc-磷酰胺闪烁体显像是一种新的诊断手段,对急性DVT的成像高度敏感。

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