Positive End-expiratory Pressure-induced Increase in Central Venous Pressure as a Predictor of Fluid Responsiveness in Robot-assisted Laparoscopic Surgery

Seoul National University

Status: Completed

Conditions: Urinary Bladder Neoplasm; Prostatic Neoplasm

Treatments: Procedure: Fluid loading of volulyte 300 ml

Study type: Interventional

Funder types: Other

Identifiers

NCT02977143

1609-101-793

Details and patient eligibility

About

In urologic robotic surgery with steep Trendelenburg position, maintenance of cardiac preload and cardiac output is important for clinical prognosis. Previous studies reported the positive end-expiratory pressure (PEEP)-induced increase in central venous pressure (CVP) could be a accurate predictor of fluid responsiveness in cardiac surgical patients. The authors attempt to evaluate the predictability of PEEP-induced increase in CVP as well as stroke volume variation in urologic robotic surgery with Steep Trendelenburg position.

Full description

In urologic robotic surgery with steep Trendelenburg position, maintenance of cardiac preload and cardiac output is important for clinical prognosis. As a preload index, the predictability of central venous pressure, pulse pressure variation and stroke volume variations may be impaired due to the impaired hemodynamics that result from the effect of increased abdominal pressure and decreased venous return. Previous studies reported the positive end-expiratory pressure (PEEP)-induced increase in central venous pressure (CVP) could be a accurate predictor of fluid responsiveness in cardiac surgical patients. Therefore, the authors attempt to evaluate the predictability of PEEP-induced increase in CVP as well as stroke volume variation in urologic robotic surgery with Steep Trendelenburg position.

Enrollment: 50 patients

Sex: Male

Ages: 20+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult patient undergoing robot-assisted laparoscopic radical prostatectomy or cystectomy.
• American Society of Anesthesiologist Physical Status Classification of 1, 2 or 3.

Exclusion criteria

• Medical history of arrhythmia or new-onset arrhythmia after anesthesia induction.
• Valvular or ischemic heart disease or left ventricular ejection fraction less than 40%.
• Any significant pulmonary disease or history of chronic obstructive pulmonary disease
• End-stage renal disease or preoperative creatinine > 1.4 mg/dl

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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50 participants in 1 patient group

Fluid responsiveness test

Experimental group

Description:

First, apply 10 cmH2O positive endexpiratory pressure (PEEP) and measure the increase in central venous pressure (CVP) as well as other preload indexes (central venous pressure, mean arterial pressure, stroke volume variation). Second, measure the increase in cardiac index after administration of volulyte 300 ml. If cardiac index increase more than 10%, fluid responsiveness is confirmed.

Treatment:

Procedure: Fluid loading of volulyte 300 ml