Influence of Sedation Strategies on Hospital LOS and ICU LOS in Patients Cardiac Surgery

NCT ID: NCT05809518

Last Updated: 2023-04-12

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 194 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-01-01
• Study Completion Date: 2019-12-31

Brief Summary

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.

Detailed Description

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.

Conditions

Sedation Complication

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Propofol Group

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

Group Type: EXPERIMENTAL

Propofol injection

Intervention Type: DRUG

sedation after cardiac surgery

Dexmedetomidine group

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

Group Type: EXPERIMENTAL

Dexmedetomidine injection

Intervention Type: DRUG

sedation after cardiac surgery

Dexmedetomidine and propofol group

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

Group Type: EXPERIMENTAL

Dexmedetomidine and Propofol

Intervention Type: DRUG

sedation after cardiac surgery

Interventions

Propofol injection

sedation after cardiac surgery

Intervention Type: DRUG

Dexmedetomidine injection

sedation after cardiac surgery

Intervention Type: DRUG

Dexmedetomidine and Propofol

sedation after cardiac surgery

Intervention Type: DRUG

Other Intervention Names

Pr; Dx; DxPr

Eligibility Criteria

Inclusion Criteria

• 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;

Exclusion Criteria

• 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.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Anesthesia Research Group UA

OTHER

Sponsor Role: lead

Responsible Party

Plechysta Yelyzaveta

chief of the anesthesia department

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Yelyzaveta Plechysta

Role: PRINCIPAL_INVESTIGATOR

Chief of the anesthesia department

Locations

Medical Network Dobrobut

Kyiv, , Ukraine

Countries

Ukraine

Other Identifiers

5-08-039.35

Identifier Type: -

Identifier Source: org_study_id