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首页> 外文期刊>European radiology >Contrast enhanced ultrasound in the detection of liver metastases: a prospective multi-centre dose testing study using a perfluorobutane microbubble contrast agent (NC100100).
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Contrast enhanced ultrasound in the detection of liver metastases: a prospective multi-centre dose testing study using a perfluorobutane microbubble contrast agent (NC100100).

机译:在肝转移的检测中对比增强超声:一项使用全氟丁烷微泡造影剂(NC100100)的前瞻性多中心剂量测试研究。

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摘要

OBJECTIVE: To conduct a dose testing analysis of perfluorobutane microbubble (NC100100) contrast-enhanced ultrasound (CEUS) to determine the optimal dose for detection of liver metastases in patients with extra-hepatic primary malignancy. METHODS: 157 patients were investigated with conventional US and CEUS. CEUS was performed following intravenous administration of perfluorobutane microbubbles (using one dose of either 0.008, 0.08, 0.12 or 0.36 muL/kg body weight). Three blinded off-site readers recorded the number and locations of metastatic lesions detected by US and CEUS. Contrast enhanced CT and MRI were used as the "Standard Of Reference" (SOR). Sensitivity, specificity and accuracy of liver metastasis detection with US versus CEUS, for each dose group were obtained. Dose group analysis was performed using the Chi-square test. RESULTS: 165 metastases were present in 92 patients who each had 1-7 lesions present on the SOR. Sensitivity of US versus CEUS (for all doses combined) was 38% and 67% (p = 0.0001). The 0.12 dose group with CEUS (78%) had significantly higher sensitivity and accuracy (70%) compared to other dose groups (p < 0.05). CONCLUSION: The diagnostic performance of CEUS is dose dependent with the 0.12 muL/kg NC100100 dose group showing the greatest sensitivity and accuracy in detection of liver metastases.
机译:目的:对全氟丁烷微泡(NC100100)对比增强超声(CEUS)进行剂量测试分析,以确定用于检测肝外原发恶性肿瘤患者肝转移的最佳剂量。方法:对157例患者进行了常规US和CEUS检查。静脉内注射全氟丁烷微泡后(使用一剂0.008、0.08、0.12或0.36μL/ kg体重)进行CEUS。三个盲人的异地读者记录了US和CEUS检测到的转移性病变的数量和位置。对比增强的CT和MRI用作“参考标准”(SOR)。获得了每个剂量组的US vs CEUS肝转移检测的敏感性,特异性和准确性。使用卡方检验进行剂量组分析。结果:92例患者中有165例转移,每例SOR上有1-7处病变。 US对CEUS的敏感性(所有剂量组合)分别为38%和67%(p = 0.0001)。与其他剂量组相比,CEUS的0.12剂量组(78%)的敏感性和准确性显着更高(70%)(p <0.05)。结论:CEUS的诊断性能与剂量有关,0.12μL/ kg NC100100剂量组显示出最大的灵敏度和准确性。

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