Internal Jugular Vein Ultrasound and Acute Kidney Injury After Abdominal Surgery

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorTîrgu Mureș Emergency Clinical County Hospital, Romania

About this trial

This observational study aims to learn whether changes in the internal jugular vein during anesthesia induction can help predict low blood pressure and kidney injury after surgery. The main questions it aims to answer are:

1. Can the internal jugular vein collapsibility index before anesthesia predict low blood pressure during induction? 2. Can the change in internal jugular vein collapsibility from before to just after anesthesia predict low blood pressure during surgery and acute kidney injury after surgery?

Participants will have routine ultrasound scans of the neck before anesthesia and again shortly after they fall asleep for surgery. Researchers will also record blood pressure during surgery and measure kidney function after surgery using routine blood tests. and again shortly after they fall asleep for surgery. Researchers will also record blood pressure during surgery and measure kidney function after surgery using routine blood tests.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Elective or Urgent (Non-emergent) major abdominal/ visceral surgery under general anesthesia

General anesthesia with propofol induction (TCI/ manual)

Expected surgical duration > 60 minutes

Continous BP monitoring (Invasive arterial line or non-invasive cuff at 2 minute recording intervals)

Disqualifiers

Emergency surgery (immediate life-saving, consent unobtainable)

End-stage renal disease (eGFR < 15 mL/min/1.73 m²) or dialysis-dependent

Concomitant cardiac surgery or carotid endarterectomy

Liver transplantation

Trial population

The study population consists of adults aged 18 years and older undergoing major abdominal or visceral surgery under general anesthesia with propofol induction at the Department of Anestesiology and Intensive Care Department in the Emergency County Hospital in Târgu Mureș. Patients will be enrolled prospectively in the preoperative period if they meet eligibility criteria, have routine perioperative blood pressure monitoring, and are able to undergo internal jugular vein ultrasound before and immediately after induction. The cohort will be followed through postoperative days 1 to 3 for creatinine-based assessment of acute kidney injury.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Internal Jugular Vein Ultrasound Assesment

    Procedure/Surgery

    Point-of-care Internal jugular vein ultrasound performed before induction and immediately after propofol induction to measure vein diameter and collapsibility index.

Treatment groups

150 Participants
are divided into 1 treatment group
Group A: Propofol Peri-induction IJV cohort1 intervention

Trial outcomes

Primary outcomes

1

Post-induction hypotension

Incidence of mean arterial pressure below 65 mmHg for atleast one consecutive minute during propofol induction

Time frame
Periprocedural
2

Change in Internal Jugular Vein Collapsibility Index

Difference between pre-induction and immediate post-induction internal jugular vein collapsibility index measured by point-of-care ultrasound

Time frame
From pre-induction to immediate post-induction

Secondary outcomes

1

Postoperative Acute Kidney Injury

Acute Kidney Injury defined according to KDIGO criteria based on postoperative serum creatinine measurements

Time frame
Postoperative days one to three
2

Cumulative Intra-operative Hypotension Burden

Total duration of mean arterial pressure threshold of 65 mmHg during the operative period

Time frame
Induction to End of Surgery

Other outcomes

1

Cummulative Intra-operative Hypotension burden

Area under the mean arterial pressure threshold of 65 mmHg during the operative period

Time frame
Induction to End of surgery

Sponsors and contacts

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