The Third Central Clinical College of Tianjin Medical University, Tianjin, 300170, China.
The Third Central Hospital of Tianjin, 83 Jintang Road, Hedong District, Tianjin, 300170, China.
BMC Anesthesiol. 2023 Feb 10;23(1):51. doi: 10.1186/s12871-023-01983-8.
Esmolol as one treatment of sepsis induced cardiomyopathy (SIC) is still controversial. The objective of this study is to evaluate cardiac function after reducing heart rate by Esmolol in patients with SIC using speck-tracking echocardiography.
This study was a single-center, prospective, and randomized controlled study. A total of 100 SIC patients with a heart rate more than 100/min, admitted to the Intensive Care Department of Tianjin Third Central Hospital from March 1, 2020 to September 30, 2021, were selected as the research subjects. They were randomly divided into the Esmolol group (Group E) and the conventional treatment group (Group C), each with 50 cases. The target heart rate of patients in Group E was controlled between 80/min and 100/min. Speck-tracking echocardiography (STE) and pulse indicating continuous cardiac output monitoring (PICCO) were performed in both groups at 1 h, 24 h, 48 h, 72 h, 96 h and 7 d after admission, with data concerning left ventricular global longitudinal strain (GLS), left ventricular ejection fraction (LVEF) and global ejection fraction (GEF), left ventricular systolic force index (dP/dtmx) were obtained, respectively. Hemodynamics and other safety indicators were monitored throughout the whole process. These subjects were followed up to 90 d, with their mortality recorded at Day 28 and Day 90, respectively. Statistical analyses were performed using SPSS version 21.
With 24 h of Esmolol, all patients in Group E achieved the target heart rate, and there was no deterioration of GLS, or adverse events. However, compared with those in Group C, their GLS, GEF and dP/dtmx were increased, and the difference was statistically significant (P > 0.05). Compared with patients in Group C, those in Group E had lower short-term mortality, and logistic regression analysis also suggested that Esmolol improved patient outcomes.
In SIC patients, the application of Esmolol to lower heart rate decreased their short-term mortality while not making any impairment on the myocardial contractility.
Chinese Clinical Trial Registry, ChiCTR2100047513. Registered June 20, 2021- Retrospectively registered, http://www.chictr.org.cn/index.aspx . The study protocol followed the CONSORT guidelines. The study protocol was performed in the relevant guidelines.
艾司洛尔作为治疗脓毒症性心肌病(SIC)的一种方法仍存在争议。本研究旨在使用斑点追踪超声心动图评估 SIC 患者通过艾司洛尔降低心率后的心功能。
本研究为单中心、前瞻性、随机对照研究。选取 2020 年 3 月 1 日至 2021 年 9 月 30 日期间因心率>100/min 入住天津市第三中心医院重症监护病房的 100 例 SIC 患者为研究对象,随机分为艾司洛尔组(E 组)和常规治疗组(C 组),每组 50 例。E 组患者的目标心率控制在 80/min 至 100/min 之间。两组患者入院后 1 h、24 h、48 h、72 h、96 h 和 7 d 分别行斑点追踪超声心动图(STE)和脉搏指示连续心输出量监测(PICCO),获取左心室整体纵向应变(GLS)、左心室射血分数(LVEF)和整体射血分数(GEF)、左心室收缩力指数(dP/dtmx)等数据。整个过程中监测血流动力学等安全指标。所有患者随访 90 d,分别记录第 28 天和第 90 天的死亡率。采用 SPSS 21.0 进行统计学分析。
E 组患者在应用艾司洛尔 24 h 内均达到目标心率,GLS 无恶化,无不良事件发生。但与 C 组比较,E 组患者 GLS、GEF 和 dP/dtmx 增加,差异有统计学意义(P>0.05)。E 组患者短期死亡率较 C 组低,Logistic 回归分析提示艾司洛尔改善患者预后。
在 SIC 患者中,应用艾司洛尔降低心率可降低短期死亡率,且不会损害心肌收缩力。
中国临床试验注册中心,ChiCTR2100047513。于 2021 年 6 月 20 日注册-回顾性注册,http://www.chictr.org.cn/index.aspx。研究方案遵循 CONSORT 指南。研究方案符合相关指南。