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Influence of noninvasive central blood pressure devices for afterload monitoring with aortic velocity-pressure Loop in anesthetized patients

机译:麻醉患者主动脉速度压力回路的非侵入性中枢血压装置的影响

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Background Global afterload angle (GALA) is a parameter derived from velocity-pressure loop (VP Loop), for continuous assessment of cardiac afterload in the operating room. It has been validated with invasive measure of central pressure. The aim of this study was to evaluate the feasibility of noninvasive VP Loop obtained with central pressure measured with two different noninvasive tonometers. Methods A prospective, observational, monocentric study was conducted in 51 patients under general anesthesia. Invasive central pressure (cP(INV)) was measured with a fulfilled intravascular catheter, and noninvasive central pressure signals were obtained with two applanation tonometry devices: radial artery tonometry (cP(SHYG): Sphygmocor tonometer) and carotid tonometry (cP(COMP): Complior tonometer). Three VP Loops were built: VP Loop(INV), VP Loop(SPHYG)and VP Loop(COMP). Patients were separated according to cardiovascular risk factors. Results In the 51 patients under general anesthesia, cP(SHYG)was adequately obtained in 48 patients (89%) but, compared to cP(INV), SBP was underestimated (-4 +/- 6 mmHg,P< 0.0001), augmentation index (AIX(SPHYG)) and a GALA(SPHYG)were overestimated (+13 +/- 19%,P= 0.0077 and +4 +/- 8 degrees,P= 0.0024, respectively) with large limit of agreement (LOA) (-21 to 47% and -13 to 21 degrees for AIX(SPHYG)and GALA(SPHYG), respectively). With the Complior, the failure rate of measurement for cP(COMP)was 41%. SBP was similar (3 +/- 17 mmHg,P= 0.32), AIX(COMP)was underestimated (-11 +/- 19%,P= 0.0046) and GALA(COMP)was similar but with large LOA (-50 to 26% and -20 to 18 degrees for AIX(COMP)and GALA(COMP), respectively). Conclusion In anesthetized patient, the reliability of noninvasive central pressure monitoring by tonometry seems too limited to monitor cardiac afterload with VP Loop.
机译:背景技术全局后载角(Gala)是从速度 - 压力环(VP环路)导出的参数,用于连续评估手术室的心脏后载。它已被侵入措施的中央压力验证。本研究的目的是评估使用两种不同的非侵入性眼压计测量的中央压力的非侵入性VP环路的可行性。方法在全身麻醉下的51例患者中进行了前瞻性观察,单眼的研究。用满足的血管内导管测量侵入中央压力(CP(INV)),并使用两种施孔型器件获得非侵入性中央压力信号:桡动脉矫形器(CP(SHYG):脊髓囊眼压计)和颈动脉曲线(CP(COMP) :复制眼压计)。构建了三个VP环:VP环路(INV),VP环路(SPHYG)和VP环路(COMP)。患者根据心血管危险因素分离。结果在全身麻醉下51例患者,CP(SHYG)在48名患者(89%)中得到充分获得(89%),但与CP(INV)相比,SBP低估(-4 +/- 6 mmHg,P <0.0001),增强指数(AIX(SPHYG))和GALA(SPHYG)高估(+13 +/- 19%,p = 0.0077和+ 4 + / + 4 +/- 8度,分别是一致的一致性限制(LOA) (分别为AIX(SPHYG)和GALA(SPHYG)的-21至47%和-13至21度)。随着CP(CP)的测量失败率为41%。 SBP是相似的(3 +/- 17 mmHg,P = 0.32),低估(COMP)被低估(-11 +/- 19%,P = 0.0046)和GALA(COMP)是相似的,但大约(-50到AIX(COMP)和GALA(COMP)分别为26%和-20至18度)。结论在麻醉的患者中,Tononetry非侵入性中央压力监测的可靠性似乎过于有限,以监测VP环路的心脏后载。

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