Evaluation of Fluid Responsiveness With Recruitment Maneuver After Sternotomy in Coronary Artery Bypass Surgery
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorAnkara City Hospital Bilkent
About this trial
Assuming that the basic reliability of dynamic indices will increase with the application of functional hemodynamic tests after sternotomy and protective lung ventilation in patients undergoing elective coronary artery bypass surgery, it is useful to predict fluid responsiveness after sternotomy in coronary artery bypass surgery patients ventilated with 6 ml/kg PBW (ideal body weight). We aimed to reveal the sensitivity and specificity of PPV and SVV changes by applying a lung opening maneuver.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
1-ASA2-3 patients between the ages of 18-80 who will undergo elective coronary bypass surgery under general anesthesia
Disqualifiers
1. Be younger than 18 years old, be over 80 years old
2. Patients with an ASA score greater than 3
3. EF<40%
4. Those with contraindications to anesthetic drugs
Trial population
ASA2-3 patients between the ages of 18-80 who will undergo elective coronary bypass surgery under general anesthesia
Trial design
Design model
Cohort
Time perspective
Cross-sectional
Treatments tested in this trial
Not listed
Trial groups
45 Participants
are grouped into 1 trial groupGroup A: patients who will have coroner arter bypass surgeon
Trial outcomes
Primary outcomes
1
Determination of fluid responsiveness in patients undergoing coronary arter bypass surgery.
: Demonstration of fluid responsiveness in patients who will undergo coronary artery bypass surgery will prevent unnecessary fluid administration in case of hemodynamic disturbance, and medical treatments and interventions can be performed in a timely and targeted manner. Researchers will perform a recruitment maneuver on the patients and record mean arterial pressure and stroke volume index. Researchers will perform a recruitment maneuver on the patients and record mean arterial pressure and stroke volume index. Afterwards, researchers will give 3ml/cc balanced fluid to the patient and record the change in mean arterial pressure and stroke volume index.
Time frame
from start to 4 monthsSponsors and contacts
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Source ClinicalTrials.gov