Impact of Intraoperative Perfusion Variability on Postoperative Troponin Elevation in Geriatric Patients Undergoing Major Oncologic Surgery

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age65+
SponsorDr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital

About this trial

This prospective observational study aims to evaluate the association between intraoperative perfusion variability and postoperative troponin elevation in geriatric patients undergoing major oncologic surgery. Intraoperative hemodynamic and perfusion-related parameters will be recorded, and postoperative troponin levels will be assessed to investigate whether intraoperative perfusion changes are associated with myocardial injury. Troponin measurements will be obtained preoperatively and at 24 hours after surgery

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 65 years or older

Undergoing major abdominal oncologic surgery

Availability of preoperative and 24-hour postoperative troponin measurements

Complete intraoperative and postoperative patient monitoring records

Disqualifiers

Age younger than 65 years

Absence of preoperative or 24-hour postoperative troponin measurements

Incomplete intraoperative or postoperative patient monitoring records

Undergoing emergency surgery

Trial population

Geriatric patients aged 65 years or older undergoing major abdominal oncologic surgery who meet the predefined eligibility criteria and have preoperative and 24-hour postoperative troponin measurements. Intraoperative hemodynamic and perfusion parameters, including PI, PVI, and cerebral oxygen saturation measured by NIRS, will be monitored throughout surgery and recorded at 15-minute intervals.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

70 Participants
are grouped into 1 trial group
Group A: Geriatric Patients Undergoing Major Oncologic Surgery

Trial outcomes

Primary outcomes

1

Change in Serum Troponin Concentration From Preoperative Baseline to 24 Hours After Surgery

Postoperative troponin elevation will be assessed by comparing serum troponin levels measured preoperatively and 24 hours after surgery. Its association with intraoperative perfusion variability will be evaluated.

Time frame
Preoperatively and 24 hours after surgery

Secondary outcomes

1

Association Between Intraoperative Perfusion Index and Postoperative Troponin Elevation

Perfusion Index (PI) will be continuously monitored intraoperatively and recorded at 15-minute intervals. The association between intraoperative PI values and postoperative troponin elevation at 24 hours after surgery will be evaluated.

Time frame
Intraoperative monitoring from the start to the end of surgery; troponin measured preoperatively and at 24 hours postoperatively
2

Association Between Intraoperative Pleth Variability Index and Postoperative Troponin Elevation

Pleth Variability Index (PVI) will be continuously monitored intraoperatively and recorded at 15-minute intervals. The association between intraoperative PVI values and postoperative troponin elevation at 24 hours after surgery will be evaluated.

Time frame
Intraoperative monitoring from the start to the end of surgery; troponin measured preoperatively and at 24 hours postoperatively.
3

Association Between Intraoperative Cerebral Oxygen Saturation and Postoperative Troponin Elevation

Cerebral oxygen saturation measured by near-infrared spectroscopy (NIRS) will be continuously monitored intraoperatively and recorded at 15-minute intervals. The association between intraoperative cerebral oxygen saturation values and postoperative troponin elevation at 24 hours after surgery will be evaluated.

Time frame
Intraoperative monitoring from the start to the end of surgery; troponin measured preoperatively and at 24 hours postoperatively.

Other outcomes

Sponsors and contacts

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