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首页> 外文期刊>The Journal of extra-corporeal technology >Should Air Bubble Detectors Be Used to Quantify Microbubble Activity during Cardiopulmonary Bypass?
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Should Air Bubble Detectors Be Used to Quantify Microbubble Activity during Cardiopulmonary Bypass?

机译:是否应该使用气泡检测器来量化心肺旁路过程中的微气泡活动?

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摘要

Air bubble detectors (ABDs) are utilized during cardiopulmonary bypass (CPB) to protect against massive air embolism. Stockert (Munich, Germany) ABD quantify microbubbles >300 μm; however, their reliability has not been reported. The aim of this study was to assess the reliability of the microbubble data from the ABD with the SIII and S5 heart-lung machines. Microbubble counts from the ABD with the SIII (SIII ABD) and S5 (S5 ABD) were measured simultaneously with the emboli detection and classification (EDAC) quantifier in 12 CPB procedures using two EDAC detectors and two ABDs in series in the arterial line. Reliability was assessed by the Spearman correlation co-efficient (r) between measurements for each detector type, and between each ABD and EDAC detector for counts >300 μm. No correlation was found between the SIII ABD (r = .008, p = .793). A weak negative correlation was found with the S5 ABD (r = -.16, p < .001). A strong correlation was found between the EDAC detectors (SIII; r = .958, p < .001), (S5; r = .908, p < .001). With counts >300 μm, the SIII ABDs showed a correlation of small-medium effect size between EDAC detectors and ABD1 (r = .286, p < .001 [EDAC1], r = .347, p < .001 [EDAC2]). There was no correlation found between ABD2 and either EDAC detector (r = .003, p = .925 (EDAC1), r = .003, p = .929 [EDAC2]). A correlation between EDAC and the S5 ABD, was not able to be determined due to the low bubble count detected by the EDAC >300 μm. Both SIII ABD and S5 ABD were found to be unreliable for quantification of microbubble activity during CPB in comparison with the EDAC. These results highlight the importance of ensuring that data included in the CPB report is accurate and clinically relevant, and suggests that microbubble counts from devices such as the SIII ABD and S5 ABD should not be reported.
机译:在体外循环(CPB)期间使用气泡检测器(ABD)来防止大量的空气栓塞。 Stockert(德国慕尼黑)ABD可以量化> 300μm的微气泡;但是,尚未报告其可靠性。这项研究的目的是评估使用SIII和S5心肺机从ABD获得的微气泡数据的可靠性。在两个CPB程序中,使用两个EDAC检测器和两个串联在动脉管线中的ABD,在12个CPB过程中同时测量了带有SIII(SIII ABD)和S5(S5 ABD)的ABD的微气泡计数。可靠性通过Spearman相关系数(r)进行评估,每种计数类型之间的测量值之间,以及每个ABD和EDAC探测器之间的计数> 300μm。在SIII ABD之间未发现相关性(r = .008,p = .793)。发现与S5 ABD的负相关性较弱(r = -.16,p <.001)。发现EDAC检测器之间存在很强的相关性(SIII; r = .958,p <.001),(S5; r = .908,p <.001)。当计数> 300μm时,SIII ABD显示出EDAC检测器和ABD1之间的中小效应大小的相关性(r = .286,p <.001 [EDAC1],r = .347,p <.001 [EDAC2]) 。在ABD2和任一EDAC检测器之间均未发现相关性(r = .003,p = .925(EDAC1),r = .003,p = .929 [EDAC2])。由于EDAC检测到的气泡数> 300μm,因此无法确定EDAC与S5 ABD之间的相关性。与EDAC相比,发现CPIII期间SIII ABD和S5 ABD对定量微气泡活性均不可靠。这些结果凸显了确保CPB报告中包含的数据准确且具有临床相关性的重要性,并建议不应报告来自SIII ABD和S5 ABD等设备的微气泡计数。

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