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The effects of methylene blue on hemodynamic parameters and cytokine levels in refractory septic shock

机译:亚甲蓝对难治性脓毒性休克血流动力学参数和细胞因子水平的影响

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Background: Endogenous nitric oxide (NO) induces the peripheral vasodilation via the activation of guanylate cyclase in patients with septic shock. The purpose of this study was to assess the acute effects of methylene blue (MB), which is an inhibitor of guanylate cyclase, on the hemodynamics and on the production of pro-inflammatory cytokines and nitric oxide (NO) in patients with refractory septic shock. Methods: Twenty consecutive patients with refractory septic shock, which was defined as shock refractory to a dopamine infusion of more than 20 μg/kg/min with the appropriate use of antibiotics and adequate volume eplacement, received MB infusion of 1 mg/kg intravenously. The hemodynamic and respiratory variables were measured at baseline, 30, 60 and 120 min after an infusion of MB (1 mg/kg). The blood levels of NO, IL-1, IL-10 and TNF-α were measured at baseline, 30 and 120 min after MB infusion. Results: The administration of MB induced an increase in the systemic vascular resistance (SVR) that resulted in an increase of the mean arterial pressure (MAP) in patients with refractory septic shock, and this was without a decrease in cardiac output. The administered MB induced an increase in pulmonary vascular resistance (PVR) that resulted in an increase of pulmonary arterial pressure (PAP), without any deterioration of gas exchange. However, the increases in SVR and PVR were not associated with the alteration of endogenous production of NO, IL-1, IL-10 and TNF- α. Conclusion: MB transiently elevated the MAP by increasing the SVR without altering the endogenous productions of NO, IL-1, IL-10 and TNF-α during the study period in patients with refractory septic shock.
机译:背景:内源性一氧化氮 (NO) 通过激活脓毒性休克患者的鸟苷酸环化酶诱导外周血管舒张。本研究的目的是评估亚甲蓝 (MB) (鸟苷酸环化酶抑制剂)对难治性感染性休克患者血流动力学以及促炎细胞因子和一氧化氮 (NO) 产生的急性影响。方法:连续 20 例难治性脓毒性休克患者,定义为多巴胺输注超过 20 μg/kg/min 难治性休克,适当使用抗生素和足够的容量放置,接受 MB 静脉输注 1 mg/kg。在输注 MB (1 mg/kg) 后基线、30、60 和 120 分钟测量血流动力学和呼吸变量。在基线、MB 输注后 30 和 120 分钟测量血液中 NO、IL-1、IL-10 和 TNF-α 的水平。结果:MB 给药引起全身血管阻力 (SVR) 增加,导致难治性脓毒性休克患者的平均动脉压 (MAP) 升高,而这并没有减少心输出量。给药的 MB 诱导肺血管阻力 (PVR) 增加,导致肺动脉压 (PAP) 升高,而气体交换没有任何恶化。然而,SVR 和 PVR 的增加与 NO、IL-1、IL-10 和 TNF-α 的内源性产生的改变无关。结论:在难治性脓毒性休克患者的研究期间,MB通过增加SVR在不改变NO、IL-1、IL-10和TNF-α的内源性产生的情况下瞬时升高了MAP。

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