Status:
RECRUITING
Care Bundle's Impact on Delirium Prevention in CABG Patients
Lead Sponsor:
İslam Elagöz
Conditions:
Delirium
Bypass Complication
Eligibility:
All Genders
18+ years
Phase:
NA
Brief 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...
Detailed Description
Open-heart surgery is an effective treatment method used in the treatment of heart diseases today. However, after this operation, patients are at risk of postoperative delirium, which negatively affec...
Eligibility Criteria
Inclusion
- 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
- 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.
Key Trial Info
Start Date :
January 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 30 2024
Estimated Enrollment :
128 Patients enrolled
Trial Details
Trial ID
NCT06036017
Start Date
January 1 2024
End Date
August 30 2024
Last Update
January 17 2024
Active Locations (1)
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1
Islam
Kilis, Turkey (Türkiye), 79100