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临床试验/NCT05809518
NCT05809518已完成不适用

Influence of Sedation Strategies on Hospital LOS and ICU LOS in Patients After Cardiac Surgery With Cardiac Pulmonary Bypass. Comparison of Propofol-based, Dexmedetomidine-based Sedation or Their Combination.

Anesthesia Research Group UA1 个研究点 分布在 1 个国家目标入组 194 人开始时间: 2017年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
194
试验地点
1
主要终点
ICU LOS

研究概览

简要总结

Preoperative, intraoperative and postoperative management of the patient are some of the main stages that can affect the hospital LOS and ICU LOS. Experience on the evidence-based approach and the progressive guidelines implementation of recommendations, the issue of the choice of drugs for sedation in the family and their impact on the length of stay in the intensive care unit and the length of hospitalization remain unsolved.

详细描述

Optimization of sedation regimes can become one of the factors that will help to reduce the length of hospital and ICU stay. The purpose of the study is to track is there a relationship between the drug for sedation and the length of stay of patients in the intensive care unit and in hospital treatment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Multi vascular lesions of the coronary arteries according to coronary angiography;
  • Heart valve damage was confirmed by heart ultrasound, which is subject to surgical correction (aortic stenosis of III degree with a gradient on the aortic valve of more than 42 mmHg, aortic insufficiency III, mitral valve stenosis II-III, mitral regurgitation II-III)
  • Patient consent to participate in the study;
  • Women who have a negative pregnancy test and use effective contraception throughout the study and for 3 weeks after its completion, or women who are unable to have children (women who have undergone a hysterectomy (removal of the uterus) or tubal ligation, women with a clinical diagnosis of infertility) or are menopausal for more than 1 year (absence of menstruation for at least 12 months). Adequate methods of contraception include: surgical sterilization, double barrier method of contraception, local contraception;

排除标准

  • Refusal to participate;
  • Hypersensitivity to propofol, dexmedetomidine;
  • Prolonged mechanical ventilation in case of surgical complications (bleeding, inadequate perfusion of the myocardium);
  • Occurred ischemic stroke;
  • History of the ischemic stroke;
  • History of the neurodegenerative diseases;
  • History of the mental disorders;
  • Use of neuroleptics, antidepressants for the last 5 years;
  • History of the cardiac surgery in the past;
  • Patients with chronic pulmonary disease (GOLD 3-4)
  • Patients with asthma (moderate or severe),
  • Participation in any other clinical trial;
  • Gastric or duodenal ulcer with risk of bleeding;
  • Chronic renal failure (ClCr less than 50 ml / h)
  • Acute renal failure that occurred during surgery (ClCr less than 50 ml / h, or a decrease in the rate of diuresis to 0.1 ml / h in the first 4 hours after surgery and does not respond to diuretic therapy)
  • Chronic hepatic insufficiency if there are laboratory signs of hypo coagulation without the use of anticoagulant therapy (INR> 1.5)
  • If the patient has not stopped taking anticoagulants or antiplatelet agents in the preoperative period: warfarin 5 days before surgery, clopidogrel 5-7 days before surgery, xarelto / pradaxa 3 days before surgery),
  • History of the hematological disease;
  • Alcohol abuse in the anamnesis (3-4 times a week).
  • Condition after chemotherapy; Pregnancy, lactation.

研究组 & 干预措施

Propofol Group

Experimental

Patient sedation after cardiac surgery at the intensive care unit.

Sedation group (Pr):

continuous infusion of propofol using a syringe pump at the dose of 1-1.5 mg / kg / h

干预措施: Propofol injection (Drug)

Dexmedetomidine group

Experimental

Patient sedation after cardiac surgery at the intensive care unit.

Sedation group Dexmedetomidine (Dx):

continuous infusion of Dexmedetomidine using a syringe pump at the dose of 0.5-1.0 mcg/ kg / h

干预措施: Dexmedetomidine injection (Drug)

Dexmedetomidine and propofol group

Experimental

Patient sedation after cardiac surgery at the intensive care unit.

Sedation group DxPr:

continuous infusion of propofol using a syringe pump at the dose of 0.5-1.5 mg / kg / h and dexmedetomidine 0.2-0.7 mcg\kg\h

干预措施: Dexmedetomidine and Propofol (Drug)

结局指标

主要结局

ICU LOS

时间窗: before discharging from ICU to the ward ( up to 7 days)

measure at days

hospital LOS

时间窗: from admission to discharge ( up to 20 days)

measure at days

次要结局

  • difference in ICU LOS in patients with vasopressors and without vasopressors(before discharging from ICU to the ward ( up to 7 days)

研究者

发起方
Anesthesia Research Group UA
申办方类型
Other
责任方
Principal Investigator
主要研究者

Plechysta Yelyzaveta

chief of the anesthesia department

Anesthesia Research Group UA

研究点 (1)

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