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Trendelenburg Maneuver Versus Passive Leg Raising Test for Fluid Responsiveness in High-Risk Surgical Patients

Not Applicable
Completed
Conditions
Trendelenburg Maneuver
Passive Leg Raising
High-Risk Surgical Patients
Interventions
Diagnostic Test: Trendelenburg maneuver (TM)
Diagnostic Test: Passive leg raising test
Registration Number
NCT06423833
Lead Sponsor
Tanta University
Brief Summary

The aim of this study is to evaluate whether Trendelenburg maneuver can be used to predict fluid responsiveness in high-risk surgical patients in intensive care unit as compared to Passive Leg Raising test.

Detailed Description

Passive Leg Raising test is a well validated dynamic method to predict fluid responsiveness with many advantages as it doesn't use fluid loading, its effect is reversible, and it doesn't rely on heart-lung interaction. However, it has many limitations as (has false negative effect in patients with intra-abdominal hypertension), also, it may not be suitable in some surgical patients.

Trendelenburg maneuver (TM) is often used to treat hemodynamic unstable patients when hypovolemia is suspected, through a mechanism similar to Passive Leg Raising test Yonis, et al reports that change in cardiac output during Trendelenburg maneuver is a reliable predictor of fluid responsiveness in patients with acute respiratory distress syndrome in prone position under protective ventilation. Another study reports that change in velocity time integral during trendelenburg maneuver predicts fluid responsiveness in cardiac surgical patients in operating rooms

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Aged ≥ 18 years old.

  • Criteria of high-risk surgical patients:

    1. Elderly ≥ 70 years old undergoing major surgery.
    2. Physical status ≥ 3 or more undergoing major surgery.
    3. Major intraoperative hemorrhage with Surgical Apgar Score (SAS 0-4).
    4. Emergency of upper abdominal surgery.
  • Criteria of hypoperfusion ≥ 2 or more the following:

    1. Mean arterial blood pressure < 65 mmHg.
    2. Urine output < 0.5 ml/Kg/hr.
    3. Capillary refilling time > 4 seconds.
    4. Blood lactate > 2 mmol/L.
    5. ScvO2 < 70%.
    6. CO2 gap > 6 mmHg.
  • Provided that:SpO2 ≥ 90% and Hb ≥ 7 g/dl.

Exclusion Criteria
  • Patients with body mass index > 35 kg/m2.
  • Pregnant female.
  • Contraindications to the Trendelenburg position or PLR test (major head trauma, intra-abdominal hypertension and gastric retention).
  • Poor echo window or unsatisfactory cardiac echogenicity (an inability to correctly align the Doppler beam to generate reliable velocity time integral measurements at the left ventricular outflow tract [LVOT]).

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Trendelenburg maneuverTrendelenburg maneuver (TM)The investigator will measure changes in velocity time integral (VTI) and stroke volume (SV) during Trendelenburg maneuver (TM) in high-risk surgical patients by trans-thoracic Doppler echo cardiography
Passive leg raising testPassive leg raising testThe investigator will measure changes in velocity time integral (VTI) and stroke volume (SV) during passive leg raising (PLR) test in high-risk surgical patients by trans-thoracic Doppler echo cardiography
Primary Outcome Measures
NameTimeMethod
The validity of Trendelenburg maneuverAt the end of Trendelenburg maneuver within 1 minute

Measurement of the validity of Trendelenburg maneuver to predict fluid responsiveness by measuring the percentage change in velocity time integral (VTI) by Doppler echocardiography in high risk-surgical patients.

Secondary Outcome Measures
NameTimeMethod
Correlation between the accuracy of the percentage change in velocity time integral (VTI) during Trendelenburg maneuver and passive leg raising test (PLR) testAt the end of Trendelenburg maneuver and passive leg raising test within 1 minute

Correlation between the accuracy of the percentage change in velocity time integral (VTI)during Trendelenburg maneuver and passive leg raising test will be measured.

Trial Locations

Locations (1)

Tanta University Hospitals

🇪🇬

Tanta, El-Gharbia, Egypt

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