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对比增强型经支气管超声成像技术检测微泡。

Imaging Microbubbles With Contrast-Enhanced Endobronchial Ultrasound.

机构信息

Institute of Biomedical Engineering, University of Toronto, Toronto, ON, Canada.

Division of Thoracic Surgery, Toronto General Hospital, University Health Network, Toronto, ON, Canada.

出版信息

Ultrasound Med Biol. 2024 Jan;50(1):28-38. doi: 10.1016/j.ultrasmedbio.2023.08.020. Epub 2023 Oct 7.

Abstract

OBJECTIVE

Endobronchial ultrasound (EBUS) is commonly used to guide transbronchial needle biopsies for the staging of lymph nodes in non-small cell lung cancer patients. Although contrast-enhanced ultrasound (CEUS) and microbubbles (MBs) can improve the diagnostic accuracy in tumors, the ability of contrast-enhanced EBUS (CE-EBUS) to image MBs has not yet been comprehensively evaluated. In this study, we assessed the ability of a CE-EBUS system (Olympus EU-ME2 PREMIER and BF-UC180F bronchoscope) to detect laboratory-synthesized MBs in comparison to clinical (Toshiba Aplio SSA-790A) and pre-clinical (VisualSonics Vevo 2100) CEUS systems in vitro and in vivo, respectively.

METHODS

Agar flow phantoms and reference tissue were used to assess CE-EBUS MB imaging in vitro, and A549 tumor-bearing athymic nude and AE17-OVA tumor-bearing C57BL/6 mice were used to assess MB detectability and perfusion in vivo, respectively.

RESULTS

Results revealed that despite the lower sensitivity of CE-EBUS to MB concentration in comparison to clinical CEUS, CE-EBUS yielded a similar contrast-to-tissue ratio (CTR) in vitro of 28.9 ± 4.5 dB for CE-EBUS, compared with 29.7 ± 2.6 dB for clinical CEUS (p < 0.05). In vivo, CE-EBUS generated a perfusion curve highly correlated with that obtained with the pre-clinical CEUS system (Pearson correlation coefficient = 0.927, p < 0.05). Moreover, CE-EBUS yielded a CTR 2.7 times higher than that obtained with the pre-clinical ultrasound system.

CONCLUSION

These findings together suggest that CE-EBUS can perform contrast imaging comparable to that produced by commercial pre-clinical and clinical ultrasound systems, with potential for clinical characterization of mediastinal lymph nodes in lung cancer patients.

摘要

目的

支气管内超声(EBUS)常用于引导经支气管针吸活检术对非小细胞肺癌患者的淋巴结进行分期。尽管对比增强超声(CEUS)和微泡(MBs)可以提高肿瘤的诊断准确性,但对比增强 EBUS(CE-EBUS)成像 MBs 的能力尚未得到全面评估。在这项研究中,我们评估了 CE-EBUS 系统(Olympus EU-ME2 PREMIER 和 BF-UC180F 支气管镜)在体外与临床(东芝 Aplio SSA-790A)和临床前(VisualSonics Vevo 2100)CEUS 系统相比,检测实验室合成 MBs 的能力,分别在体内和体内进行了评估。

方法

琼脂流动体模和参考组织用于评估 CE-EBUS 中 MB 的体外成像,A549 荷瘤裸鼠和 AE17-OVA 荷瘤 C57BL/6 小鼠分别用于评估体内 MB 的检测能力和灌注。

结果

结果表明,尽管 CE-EBUS 对 MB 浓度的敏感性低于临床 CEUS,但 CE-EBUS 在体外产生的对比组织比(CTR)相似,CE-EBUS 为 28.9 ± 4.5dB,而临床 CEUS 为 29.7 ± 2.6dB(p<0.05)。在体内,CE-EBUS 产生的灌注曲线与临床前 CEUS 系统获得的灌注曲线高度相关(Pearson 相关系数=0.927,p<0.05)。此外,CE-EBUS 产生的 CTR 比临床前超声系统高 2.7 倍。

结论

这些发现表明,CE-EBUS 可以进行与商业临床前和临床超声系统相当的对比成像,有可能对肺癌患者的纵隔淋巴结进行临床特征描述。

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