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首页> 外文期刊>Journal of critical care >Effects of propofol and dexmedetomidine on indocyanine green elimination assessed with LIMON to patients with early septic shock: a pilot study.
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Effects of propofol and dexmedetomidine on indocyanine green elimination assessed with LIMON to patients with early septic shock: a pilot study.

机译:用LIMON评估早期脓毒性休克患者的异丙酚和右美托咪定对吲哚菁绿消除的影响:一项初步研究。

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BACKGROUND: We aimed to select the sedative drug with the least impact on hepatic blood flow in sedation-administered patients. In our study, we aimed to establish whether dexmedetomidine and propofol affect liver function during early septic shock. The hepatic blood flow is evaluated by the transcutaneous assessment of indocyanine green plasma disappearance rate (ICG-PDR) in critically ill patients. METHODS: Forty early septic shock patients were included in the study and administered either the loading dose infusion of propofol (n = 20, group P) of 1 mg/kg over 15 minutes followed by a maintenance dose of 1 to 3 mg/kg per hour (n = 20, group P), or a loading dose of dexmedetomidine 1 microg/kg over 10 minutes followed by a maintenance of 0.2 to 2.5 microgg/kg per hour (n = 20, group D) (24-hour infusion). Indocyanine green (ICG) elimination tests were conducted concurrently using the noninvasive liver function monitoring system (LiMON; Pulsion Medical Systems, Munich, Germany). A dose of 0.3 mg/kg of ICG was given through a cubital fossa vein as a bolus and immediately flushed with 10 mL of normal saline. We calculated ICG-PDR. Indocyanine green plasma disappearance rate measurements were obtained at baseline (before start of the propofol or dexmedetomidine infusion) and were repeated at the 24th hour. Biochemical and hemodynamic parameters and ICG-PDR were recorded before start of the study and at 24th hour. RESULTS: Biochemical and hemodynamic parameters did not differ significantly between the groups (P < .05). Baseline ICG-PDR levels of group P compared to group D were 24.7 +/- 14.4 vs 22.2 +/- 10.7, respectively, and after the study, ICG-PDR levels (26.5 +/- 13.7 vs 23.7 +/- 12.4) did not differ in groups (P > .05). When we examined ICG-PDR changes between groups before and after administration, there was no significant difference (P > .05). CONCLUSION: In our study, we found that neither propofol nor dexmedetomidine infusion affected hepatic blood flow.
机译:背景:我们的目的是选择对镇静药物患者的肝血流影响最小的镇静药物。在我们的研究中,我们旨在确定右美托咪定和丙泊酚是否在早期败血症性休克期间影响肝功能。通过对重症患者进行吲哚菁绿血浆消失率(ICG-PDR)透皮评估来评估肝血流量。方法:40名早期败血症性休克患者被纳入研究,并在15分钟内给予丙泊酚(n = 20,P组)负荷剂量输注1 mg / kg,随后维持剂量为每剂1至3 mg / kg小时(n = 20,P组),或右美托咪定的负荷剂量在10分钟内为1 microg / kg,然后维持每小时0.2至2.5 microgg / kg(n = 20,D组)(24小时输注) 。同时使用无创肝功能监测系统(LiMON; Pulsion Medical Systems,慕尼黑,德国)同时进行了吲哚菁绿(ICG)消除测试。通过肘窝静脉推注ICG剂量为0.3 mg / kg,并立即用10 mL生理盐水冲洗。我们计算了ICG-PDR。在基线时(开始输注异丙酚或右美托咪定之前)获得吲哚菁绿血浆消失率测量值,并在第24小时重复进行。在研究开始之前和第24小时记录生化和血液动力学参数以及ICG-PDR。结果:两组之间的生化和血液动力学参数无显着差异(P <.05)。与D组相比,P组的基线ICG-PDR水平分别为24.7 +/- 14.4和22.2 +/- 10.7,在研究之后,ICG-PDR水平(26.5 +/- 13.7与23.7 +/- 12.4)各组之间没有差异(P> .05)。当我们检查给药前后各组之间的ICG-PDR变化时,没有显着差异(P> 0.05)。结论:在我们的研究中,我们发现丙泊酚和右美托咪定输注均不会影响肝血流。

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