Enhanced Recovery After Surgery (ERAS) in Coronary Artery Bypass Graft / Off Pump Coronary Artery Bypass (CABG/OPCAB)
NCT03956420 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 100
Last updated 2019-05-20
Summary
It has been assumed that some elements of the ERAS protocol may contribute to the reduction of complications and improve the satisfaction of patients undergoing coronary artery bypass surgery.
Elements of the ERAS strategy will be tested in this study. The elements that prove to be feasible and have a positive effect on the treatment process will be introduced into everyday clinical practice.
In the next stage of the research, we are planning to investigate whether the introduction of the ERAS strategy has had a long-term positive effect on the quality of life after treatment (a survey 1 month and 6 months after leaving the hospital).
Conditions
- Coronary Artery Disease
- Coronary Stenosis
Interventions
- BEHAVIORAL
-
Premedication visit
detailed information about surgery, anaesthesia and postoperative period
- DIETARY_SUPPLEMENT
-
Preoperative period
avoidance of prolonged fasting, intake of fluids with carbohydrates before surgery
- DRUG
-
Preoperative period
administration of melatonin 5 mg in the evening and pregabalin 75 mg one hour before entering the operating theatre
- OTHER
-
Postoperative period
Fluids 1 ml/kg/h; Discontinuation of propofol at the moment of drainage and cardiovascular system stabilization; Fluids administered orally 2 hours after extubation; Early mobilisation
- OTHER
-
Intraoperative period
deep temperature (necessity to maintain normothermia during the stay in the operating theatre 36 °C. Normothermia should be maintained rather than restored.
- DRUG
-
Intraoperative period
Pyralgin 1 g i.v. after induction of anaesthesia; in patients allergic to Pyralginum, Perfalgan 1 g i.v.
- DRUG
-
Intraoperative period
Ketamine 30 mg i.v. after induction of anaesthesia
- DRUG
-
Intraoperative period
Sevoflurane 1.5 MAC higher in patients \< 60 years old
- DRUG
-
Intraoperative period
Propofol infusion in patients at risk of postoperative vomiting (Apfel ≥ 2 points), sevoflurane administration at the moments of strong stimuli from the operating field
- DRUG
-
Intraoperative period
Continuous infusion of balanced multi-electrolyte fluids 1-3 ml/kg/h
Sponsors & Collaborators
-
Silesian University of Medicine
lead OTHER
Principal Investigators
-
Ewa Kucewicz-Czech · Upper-Silesian Medical Centre; DEPARTMENT OF ANAESTHESIOLOGY AND INTENSIVE CARE WITH CARDIAC MONITORING
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-05-03
- Primary Completion
- 2020-01-31
- Completion
- 2021-05-31
Countries
- Poland
Study Locations
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