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Postoperative Stroke and Epiaortic Ultrasound in CABG (EAU and POCD)

A

Ataturk University

Status

Completed

Conditions

Postoperative Stroke
Postoperative Delirium

Treatments

Procedure: Intraoperative Epiaortic Ultrasound (EAU)

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

This study aims to investigate the incidence of postoperative stroke and neurocognitive impairment in patients undergoing coronary artery bypass grafting (CABG), with or without the use of epi-aortic ultrasound (EAU). Atherosclerosis in the ascending aorta is a known risk factor for perioperative stroke and systemic embolization. The identification of atherosclerotic plaques before manipulation of the ascending aorta is important in minimizing embolic complications. Neurocognitive function will be assessed using the standardized Mini-Mental State Examination (SMMSE) before surgery and within 7 days postoperatively or at discharge. This prospective, observational, case-control study will evaluate the relationship between the presence of atherosclerotic plaques detected by EAU and neurocognitive and neurologic outcomes following CABG surgery.

Full description

This is a prospective, observational case-control study designed to evaluate the association between the use of epi-aortic ultrasound (EAU) and the incidence of postoperative stroke and neurocognitive impairment following coronary artery bypass grafting (CABG) surgery. Patients undergoing elective CABG between December 2023 and December 2024 will be enrolled. Patients will be assigned to one of two groups based on the intraoperative use of EAU: the EAU group and the non-EAU group. EAU will be used to detect the presence, location, and characteristics of atherosclerotic plaques in the ascending aorta. Plaques will be categorized according to location and thickness (Stage 1-2: <3 mm, Stage 3-4-5: ≥3 mm). Neurocognitive function will be assessed preoperatively and postoperatively using the standardized Mini-Mental State Examination (SMMSE). Demographic variables and perioperative factors such as aortic cross-clamp time, cardiopulmonary bypass duration, and length of ICU stay will also be collected for analysis. The study aims to clarify the relationship between ascending aortic atherosclerosis detected by EAU and adverse neurological and cognitive outcomes, and to determine whether intraoperative EAU alters surgical decision-making.

Enrollment

150 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients scheduled for isolated, elective coronary artery bypass grafting (CABG)
  • Age 18 years or older

Exclusion criteria

  • Illiteracy (inability to read or write)
  • Visual and/or hearing impairment
  • Non-citizens/foreign nationals
  • Refusal to participate in the study
  • Presence of neuropsychiatric disorders that may affect postoperative cognitive evaluation (e.g., psychosis, dementia, mental retardation)
  • History of cerebrovascular accident (CVA/stroke)
  • Preoperative rhythm disturbances associated with stroke risk (e.g., atrial fibrillation, atrial flutter)
  • Presence of intracardiac thrombus (ventricular or atrial) on preoperative echocardiography
  • Patients undergoing concomitant cardiac procedures (e.g., valve or aortic surgery)
  • Emergency CABG surgery
  • Recent myocardial infarction
  • Use of intra-aortic balloon pump (IABP)
  • Redo CABG surgery
  • Significant carotid stenosis or plaque detected on preoperative carotid Doppler ultrasonography
  • Chronic renal failure and/or liver failure

Trial design

150 participants in 1 patient group

EAU Use in CABG
Description:
This cohort includes patients who underwent isolated coronary artery bypass grafting (CABG) surgery between December 2023 and December 2024. The intervention group (EAU group) consisted of patients in whom epiaortic ultrasound (EAU) was used intraoperatively to assess atherosclerotic burden in the ascending and arch aorta. Findings from EAU guided intraoperative decision-making, including cannulation site and cross-clamp strategy. The control group comprised patients who underwent CABG without EAU. The primary outcomes evaluated were postoperative stroke incidence and neurocognitive impairment.
Treatment:
Procedure: Intraoperative Epiaortic Ultrasound (EAU)

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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