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临床试验/TCTR20210706003
TCTR20210706003尚未招募不适用

Comparison of 28-days mortality rate in patients with cardiogenic shock receiving between norepinephrine and dopamine.

Faculty of Pharmaceutical Sciences, Chulalongkorn University0 个研究点目标入组 476 人开始时间: 2021年7月6日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
476

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 N/A (No limit)(—)
性别
All

入选标准

  • Patients with cardiogenic shock who admitted to the CCU and ICCU at King Chulalongkorn Memorial Hospital between 1 January 2014 to 31 December 2021.
  • All adults patients age greater than 18 who receieved norepinephrine or dopamine. Patients diagnosed with cardiogenic shock were identified by the presence of International Classification of Disease, tenth revision, ICD 10th code R570 in the list of diagnosed generated during the course of their hospital stay or identified by clinical criteria (SBP< 90 mmHg despite adequate amount of fluids had been administration and if there were signs of tissue hypoperfusion (e.g. altered mental state, cold extremities, urine output of < 0.5 ml/kg/h or < 30 ml/h, arterial blood pH < 7.35, arterial blood lactate > 2 mmol/L or serum creatinine rising at least 0.3 mg/dL or increasing more than 1.5 to 1.9 times of baseline serum creatinine) or hemodynamic criteria (e.g. cardiac index less than 2.2 L/min/m2 and pulmonary capillary wedge pressure more than 15 mmHg) in 24 to 48 hours before received norepinephrine or dopamine.

排除标准

  • 1. Shock from other cause such as hypovolemic shock, sepsis shock or anaphalaxis shock in 24 to 48 hours before received norepinephrine or dopamine.
  • 2. Patients with cardiogenic shock who recieved both norepinephrine and dopamine.

研究者

发起方
Faculty of Pharmaceutical Sciences, Chulalongkorn University

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