Care Bundle's Impact on Delirium Prevention in CABG Patients (CareBundle)
Delirium, Bypass Complication, Coronary Artery Bypass
About this trial
This is an interventional prevention trial for Delirium focused on measuring Coronary Artery Bypass Graft Surgery, Care bundle Application, Delirium Prevention, Postoperative Care, Cardiac Surgery, Intensive Care, Quality of Care, music
Eligibility Criteria
Inclusion Criteria: Participants and Sample Criteria Inclusion criteria for the study: Over 18 years of age, Considered as a low-risk group according to American Society of Anesthesiologists (ASA) I-II and EUROSCORE scores Undergoing open-heart surgery for the first time Having an operation with on-pump and median sternotomy technique, Mild and moderate hypothermia applied, One to three coronary artery bypass grafts performed, Left internal mammary artery and saphenous vein graft applied, Surgery initiated between 08:00-12:00 hours, Having no psychiatric diagnosis and therefore no drug therapy, Not using corticosteroid derivative drugs, No complications observed that may affect the surgery and ICU process, Having a family member who can support the patient in the postoperative wake-up process, Patients who voluntarily agree to participate in the research will be included. Exclusion Criteria: Extended surgery due to complications, Completion of the intraoperative process falls into the evening hours (after 16:00), Consciousness level after extubation prevents participation in the study (Glasgow Coma Score <15), Corticosteroid derivative drugs applied at any stage of the perioperative process, Surgery is canceled, No family member is available to stay in the intensive care unit, Wishing to withdraw from the research at any stage after voluntarily agreeing to participate in the study, At any stage of the research, patients who do not wish to use earplugs or listen to music and wish to withdraw from the research, their data will be excluded from the study.
Sites / Locations
- Islam
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Control groups
Study groups
T1: TBF, GCS, GKS, RCUOS, RASS, CAM-ICU forms will be filled out from the patients and blood samples will be taken. T2: GCS, GKS, RCUOS, RASS, CAM-ICU forms will be filled out from the patients and blood samples will be taken. Additionally, durations of anesthesia, intubation and sedation as well as the amount of medication used for sedation will be recorded. The care package prepared will be applied to this group by the nurses working at the ward. T3: GCS, GKS, RCUOS, RASS, CAM-ICU forms will be filled out from the patients and blood samples will be taken. Their length of stay in the intensive care unit will be noted.
T1: TBF, GCS, GKS, RCUOS, RASS, CAM-ICU forms will be filled out from the patients and blood samples will be taken. T2: GCS, GKS, RCUOS, RASS, CAM-ICU forms will be filled out from the patients and blood samples will be taken. Additionally, durations of anesthesia, intubation and sedation as well as the amount of medication used for sedation will be recorded. T3: GCS, GKS, RCUOS, RASS, CAM-ICU forms will be filled out from the patients and blood samples will be taken. Their length of stay in the intensive care unit will be noted.