Determining the Effect of Care Package Implementation in Preventing Delirium in Patients Undergoing Coronary Artery Bypass Graft Surgery

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This research investigates the effectiveness of a care package used in the care of patients undergoing coronary artery bypass graft (CABG) surgery in preventing postoperative delirium. CABG surgery is a common procedure used to increase blood flow to the heart and is typically applied in patients with severe cardiac diseases. However, this procedure can increase the risk of postoperative delirium, especially among elderly and critically ill patients. In this study, the goal is to reduce this risk by implementing a care package. The care package includes optimal pain management, sleep regulation, mobilization, ensuring patient orientation, and appropriate medication management. The results of the research will be used to determine whether the use of this care package is effective in reducing the risk of delirium after CABG surgery. This could potentially improve patient outcomes and allow for more efficient use of hospital resources.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

⁃ 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.

Locations
Other Locations
Turkey
Islam
RECRUITING
Kilis
Contact Information
Primary
İslam Elagoz, Ress. ass.
islam.elagoz@kilis.edu.tr
05072836124
Backup
aynur koyuncu, Dr.
aynurkoyuncu@hku.edu.tr
05072836124
Time Frame
Start Date: 2024-01-01
Estimated Completion Date: 2024-08-30
Participants
Target number of participants: 128
Treatments
No_intervention: Control 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.
Experimental: 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.~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.
Sponsors
Leads: İslam Elagöz

This content was sourced from clinicaltrials.gov