Department of Critical Care, The Second Affiliated Hospital of Guangzhou Medical University, No. 250 Changgang East Road, Haizhu District, Guangzhou, 510260, China.
Trials. 2024 Oct 23;25(1):710. doi: 10.1186/s13063-024-08560-5.
Sepsis, a life-threatening syndrome, is often accompanied by tachycardia in spite of hypovolemia and hypotension have been corrected. Recently, relevant studies have shown that sustained tachycardia in sepsis was related to high mortality, and appropriate control of heart rate (HR) could improve prognosis. Ivabradine reduces HR directly without a negative inotropic effect through inhibition of the I ionic current, which is different from the traditional rate control drug (beta-blockers).
This is a prospective, multicenter, randomized, open label study designed to investigate the effect of heart rate control with ivabradine on hemodynamic in patients with sepsis. Our study will enroll 172 patients with sepsis as defined by The Third International Consensus Definitions for Sepsis and Septic Shock criteria with sinus rate of 95 bpm or higher despite a hemodynamic optimization. Patients will be randomly assigned to standard treatment group (GS) or ivabradine group (GI, standard treatment for sepsis plus enteral ivabradine). Patients in GI will receive ivabradine to maintain HR between 70 and 94 bpm. The primary outcome is the difference of a reduction in HR below 95 bpm and the effect of ivabradine on hemodynamics between GI and GS group within the first 96 h after randomization. The secondary outcomes include organ function measures, the difference in SOFA score, incidence of adverse events, need for organ support, length of ICU stay, and 28-day overall mortality.
There are limited studies on ivabradine to control heart rate in patients with sepsis. Our study aims to evaluate whether direct sinus node inhibition can improve hemodynamics, as well as its impact on organ function and prognosis in patients with sepsis, so as to provide evidence for the safe usage in clinical practice.
ClinicalTrials.gov NCT05882708. Registered on May 11, 2023, https://clinicaltrials.gov/ct2/show/NCT05882708 .
败血症是一种危及生命的综合征,尽管已经纠正了低血容量和低血压,但常伴有心动过速。最近的相关研究表明,败血症持续心动过速与高死亡率有关,适当控制心率(HR)可以改善预后。伊伐布雷定通过抑制 I 离子电流直接降低 HR,而不产生负性肌力作用,这与传统的心率控制药物(β受体阻滞剂)不同。
这是一项前瞻性、多中心、随机、开放标签研究,旨在研究伊伐布雷定控制心率对败血症患者血流动力学的影响。我们的研究将纳入 172 名符合第三次国际脓毒症和脓毒性休克共识定义的败血症患者,这些患者窦性心率为 95 bpm 或更高,尽管进行了血流动力学优化。患者将被随机分配到标准治疗组(GS)或伊伐布雷定组(GI,败血症的标准治疗加肠内伊伐布雷定)。GI 组患者将接受伊伐布雷定治疗,以维持 HR 在 70 至 94 bpm 之间。主要结局是在随机分组后 96 小时内,GI 组与 GS 组之间 HR 降低至 95 bpm 以下的差异以及伊伐布雷定对血流动力学的影响。次要结局包括器官功能测量、SOFA 评分差异、不良事件发生率、器官支持需求、ICU 住院时间和 28 天总死亡率。
关于伊伐布雷定控制败血症患者心率的研究有限。我们的研究旨在评估直接窦房结抑制是否可以改善败血症患者的血流动力学,以及对器官功能和预后的影响,从而为临床实践中的安全使用提供证据。
ClinicalTrials.gov NCT05882708。于 2023 年 5 月 11 日注册,https://clinicaltrials.gov/ct2/show/NCT05882708。