Peroperative Fluid Management in Major Gynecological Cancer Surgeries

Bakirkoy Dr. Sadi Konuk Training and Research Hospital

Status: Completed

Conditions: Acute Kidney Injury; Perioperative/Postoperative Complications; Fluid Loss; Fluid Overload

Treatments: Diagnostic Test: Akut kidnet injury(AKI)

Study type: Interventional

Funder types: Other

Identifiers

NCT06101498

2023.478

Details and patient eligibility

About

The aim of this study is to evaluate the effect of perioperative fluid management on postoperative kidney damage in gynecological cancer surgeries.

The main question[s] it aims to answer are:

Does fluid management applied with different hemodynamic monitoring methods affect the risk of postoperative AKI? In our clinic, three different fluid management strategies are applied depending on the anesthetist experience. Acute kidney injury will be evaluated according to the postoperative AKIN classification of conventional fluid therapy and targeted fluid therapy with noninvasive or minimally invasive monitoring.

Full description

Our study was designed as a retrospective study. The files of patients over the age of 18 who underwent open abdominal surgery due to ASAII and III gynecological malignancy will be examined retrospectively. Patients who cannot be monitored peroperatively and who undergo HIPEC will be excluded from the study. Patients will be divided into 3 groups according to the fluid management strategy and the hemodynamic monitoring used: Group 1: patients receiving conventional fluid therapy; Group 2: patients receiving targeted fluid therapy with noninvasive monitoring; Group 3: patients receiving targeted fluid therapy with minimally invasive monitoring.

Enrollment: 180 patients

Sex: Female

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• >18 years
• ASA II-III
• Those with normal renal function

Exclusion criteria

• Patients in renal insufficiency
• Patients with perioperative renal, ureter & bladder invasion
• Patients in whom perioperative urine monitoring cannot be performed
• Patients undergoing HIPEC
• Patients with missing data

Trial design

Primary purpose: Health Services Research

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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180 participants in 3 patient groups

Conventional fluid therapy

Experimental group

Description:

Patients who received conventional fluid therapy

Treatment:

Diagnostic Test: Akut kidnet injury(AKI)

Non invaziv goal directed therapy

Experimental group

Description:

Patients who received non invaziv goal directed therapy

Treatment:

Diagnostic Test: Akut kidnet injury(AKI)

Minimal invaziv goal directed therapy

Experimental group

Description:

Patients who received minimal invaziv goal directed therapy

Treatment:

Diagnostic Test: Akut kidnet injury(AKI)