Capnogram and Fluid Responsiveness
NCT03788707 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL
Last updated 2021-07-28
Summary
Predicting fluid responsiveness in critically ill patients is of paramount importance. It can help define an adequate fluid balance. Overzealous fluid administration is poorly tolerated and has been associated with poor outcomes but so has insufficient administration. Currently available predictors of fluid responsiveness rely on invasive monitors and require patients to be on mechanical ventilation. It is thus important to develop non invasive novel methods to assess fluid responsiveness to provide an accurate management for a favorable outcome. We propose a readily available non-invasive method that relies on improvement of the ventilation perfusion mismatch as recorded by end tidal CO2.
Ventilation of physiologic dead space is part of a spectrum of mismatch between ventilation and perfusion of the lungs. The extent of pulmonary dead space varies depending on factors affecting pulmonary perfusion (e.g. pulmonary capillary hydrostatic pressure) and alveolar pressure (e.g. positive pressure ventilation). Compromised pulmonary capillary perfusion can lead to ventilation-perfusion mismatch in a patient with clear conductive airway and adequate alveolar oxygen pressure. Alveolar dead space results in decreased CO2 exchange that translates into lower levels of expired CO2.
Stroke volume of the right ventricle is a major determinant of the pulmonary capillary perfusion. Right ventricular cardiac output can be increased by passive lower limb elevation maneuver, which ultimately results in improvement of the ventilation to perfusion ratio. This effect leads to a higher participation of perfused (and ventilated) alveolar units in gas exchange and narrowing of the gradient between arterial and expired CO2 concentration. Performing a passive leg raising (PLR) maneuver leads to stroke volume enhancement in both healthy patients and in those experiencing hemodynamic instability. Responsiveness to PLR can be assessed by different methods including echocardiography and pulse pressure variation. Left ventricular cardiac output (LVCO) can be easily measured by transthoracic echo and be used as a surrogate of right ventricular preload changes. LVCO can thus be used to assess the fluid responsiveness of PLR and the effects of on end tidal CO2 that ensue.
We propose this study to test the hypothesis that expired CO2 is a reliable predictor of fluid responsiveness after performance of the PLR maneuver, based on the assumption that increasing right ventricular output causes a reduction of the ventilation to perfusion ratio, leading to increased levels of expired CO2. T
Conditions
- Healthy
- Blood Pressure
Interventions
- OTHER
-
Passive leg raising
After 30 seconds of lying flat, volunteers will have passive leg raising to 45 degrees. Expired CO2 will be measured via a face mask before and after leg raising.
Sponsors & Collaborators
-
Augusta University
lead OTHER
Study Design
- Allocation
- NA
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2019-05-01
- Primary Completion
- 2021-12-01
- Completion
- 2021-12-01
Countries
- United States
Study Locations
More Related Trials
-
Performance of Non-Invasive Monitors During ANH
NCT02179827 ·Status: WITHDRAWN
-
Fluid Responsiveness Evaluation in Sepsis-associated Hypotension
NCT02837731 ·Status: COMPLETED ·Phase: NA
-
Timing and Dose of Fluid Deresuscitation in Critically Ill Patients
NCT07275658 ·Status: RECRUITING
-
Transcutaneous pO2, Transcutaneous pCO2 and Central Venous SO2 Variations to Define Fluid Responsiveness
NCT01941472 ·Status: COMPLETED ·Phase: NA
-
Central Venous Pressure Change With Volume Challenge in Patients With Hemodynamic Instability
NCT01630577 ·Status: COMPLETED ·Phase: PHASE3
-
Hemodynamic Optimization By Non-Invasive Determination Of Cardiac Output In Critically Ill Patients
NCT01309724 ·Status: COMPLETED ·Phase: NA
-
Precision Resuscitation With Crystalloids in Sepsis
NCT06253585 ·Status: COMPLETED ·Phase: NA
-
Fluid Responsiveness Prediction During Prone Position
NCT05898269 ·Status: RECRUITING ·Phase: NA
-
Evaluation of the Variation of the Sub-pulmonary Velocity-time Integral to Predict Fluid Responsiveness
NCT07202637 ·Status: RECRUITING
-
Effect of Intermittent Pneumatic Compression Device of Lower Limbs in Oligohydramnios
NCT05474326 ·Status: UNKNOWN ·Phase: NA
-
Passive Leg Raise and Mini-fluid Challenge Effect on Various Cardiac Output Surrogates for Fluid Responsiveness
NCT06390423 ·Status: RECRUITING
-
A Simple Clinical Tool to Help Assess Patient Volume (Fluid) Status
NCT00599794 ·Status: COMPLETED
-
Changes in PPV Induced by PLR Test to Predict Fluid Responsiveness in ICU
NCT03225378 ·Status: COMPLETED
-
Comparison of 250 ml Versus 500 ml of Fluid Challenge
NCT03874923 ·Status: COMPLETED ·Phase: NA
-
Use of a Mini-fluid Bolus to Identify Fluid Responsiveness
NCT03058653 ·Status: WITHDRAWN ·Phase: NA
-
Hemodynamic Monitoring and Fluid Responsiveness in Venovenous Extracorporeal Membrane Oxygenation (VV ECMO) - "HemodynamECMOnitoring-VV Study"
NCT06593717 ·Status: RECRUITING ·Phase: NA
-
Physiological Effects of 38°C vs. 22°C Fluid Therapy in Critically Ill Patients
NCT04576806 ·Status: WITHDRAWN ·Phase: NA
-
The Fluid Translation of Research Into Practice Study
NCT02002013 ·Status: COMPLETED
-
Effect of Fluid Resuscitation and Microcirculation
NCT01369524 ·Status: COMPLETED
-
Fluid Challenges in Intensive Care
NCT01787071 ·Status: COMPLETED
-
Comparison of Different Protocols of Fluid Therapy in Severe Preeclamptic Patients Under Spinal Anesthesia
NCT03478618 ·Status: UNKNOWN ·Phase: EARLY_PHASE1
-
Non-invasive Fluid Management
NCT02892799 ·Status: UNKNOWN ·Phase: NA
-
Cardiac Responsiveness Assessment by CO2
NCT05430880 ·Status: UNKNOWN
-
Preventing Cardiovascular Collapse With Administration of Fluid Resuscitation During Induction and Intubation
NCT03787732 ·Status: COMPLETED ·Phase: PHASE4
-
Continuous Passive Paracentesis for Intra-abdominal Hypertension
NCT04322201 ·Status: UNKNOWN ·Phase: NA