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Stroke Volume Variation-guided Fluid Infusion in Major Liver Tumour Resection

Not Applicable
Completed
Conditions
Fluid Management
Interventions
Procedure: SVV-guided fluid management
Registration Number
NCT05361252
Lead Sponsor
Kaohsiung Veterans General Hospital.
Brief Summary

Studies have demonstrated that the rate of change in stroke volume variation (SVV) can be used to determine the volume of body fluids during major abdominal surgery. Anaesthesiologists can use SVV as a guide for the appropriate administration of intraoperative fluids to improve postoperative prognoses. Liver surgery is a major abdominal operation, and the amount of blood lost is typically higher than that during other general abdominal surgeries. Blood loss is positively correlated with the intraoperative fluid infusion volume, and greater blood loss is associated with more postoperative complications. Additionally, comorbid liver disease or cirrhosis can increase the complexity of liver tumour resection, causing difficulty in assessing intravascular volume and determining the appropriate intraoperative infusion volume.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
118
Inclusion Criteria
  • We initially selected 118 patients who required hepatectomy.
  • The physiological status of the patients was assessed in terms of American Society of Anesthesiologists scores I-III
Exclusion Criteria
  • Extreme body mass index (BMI)
  • Age under 20 or over 75 years
  • Emergency surgery
  • Preexisting cardiac, hepatic, renal, or coagulation disorder; hyperthyroidism; and sinus arrhythmia.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
the high-SVV groupSVV-guided fluid managementthe value of stroke volume variation will be higher than 10 this group
the low-SVV groupSVV-guided fluid managementthe value of stroke volume variation will be less than or equal to 10 this group
Primary Outcome Measures
NameTimeMethod
The incidence of postoperative complications in the two groups.From day 1 to day 30 after surgery.

calculate the incidence of postoperative complication within 30 days

Secondary Outcome Measures
NameTimeMethod
The differences of perioperative ALTExamination report on the 1st postoperative day.

Calculate the difference of the perioperative physiological variables

The differences of perioperative T.bilExamination report on the 1st postoperative day.

Calculate the difference of the perioperative physiological variables

The differences of perioperative arterial lactateExamination report on the 1st postoperative day.

Calculate the difference of the perioperative physiological variables

The differences of perioperative albuminExamination report on the 1st postoperative day.

Calculate the difference of the perioperative physiological variables

The differences of perioperative creatinineExamination report on the 1st postoperative day.

Calculate the difference of the perioperative physiological variables

The differences of perioperative HbExamination report on the 1st postoperative day.

Calculate the difference of the perioperative physiological variables

The pain scaleup to three days postoperatively

Assessment of postoperative pain scale

The differences of perioperative eGFRExamination report on the 1st postoperative day.

Calculate the difference of the perioperative physiological variables

Trial Locations

Locations (1)

Kaohsiung Veterans General Hospital

🇨🇳

Kaohsiung, Taiwan

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