Central Venous Pressure Change With Volume Challenge in Patients With Hemodynamic Instability

Phase 3

Completed

• Conditions: Acute Circulatory Failure
• Interventions: Other: volume expansion using modified gelatin

• Registration Number: NCT01630577
• Lead Sponsor: University of Monastir

Brief Summary

We conducted this study to assess the value of early change in central venous pressure (CVP) in predicting fluid responsiveness in mechanically ventilated patients.

Detailed Description

In patients with shock a primary goal of treatment is to restore and maintain organ perfusion, for which an adequate cardiac preload is required. Apart from the situations in which hypovolemia is evident and a favourable response to fluid administration will be seen, clinical and biological parameters often fail to predict hypovolemia. Inappropriate use of volume expansion carries out the risk of generating volume overload and pulmonary oedema. Consequently, reliable predictors of fluid responsiveness are needed especially in the early phase of cardiocirculatory deterioration. In the clinical setting, different static and dynamic indices have been shown to be useful indicators of cardiac preload. Central venous pressure (CVP) is widely used to measure right ventricular preload in patients requiring invasive hemodynamic monitoring. However, the use of the CVP is much criticized because CVP poorly predicts cardiac preload and volume status. However several decades ago, Weil and Henning proposed the fluid challenge technique, based on the 2-5 rule using CVP. There is a method for guiding volume repletion based on measurements of the patient's response to fluid load. This method has not been validated in the prediction of fluid responsiveness. We therefore conducted a prospective study that in all patients we measured CVP change and stroke volume variation (SVV) after administration of fluids. Patients were classified as fluid responders when their SVV is \>10% after volume expansion and non-responders if SVV is ≤10%.

Study Timeline

• Study Start: 2012-01
• Study First Submitted: 2012-06-21
• Study First Submitted QC: 2012-06-26
• Study First Posted: 2012-06-28
• Primary Completion: 2013-04
• Study Completion: 2013-05
• Status Verified: 2016-05
• Last Update Submitted: 2016-05-04
• Last Update Posted: 2016-05-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

• mechanically ventilated patients
• acute circulatory failure defined by the need of vasopressive drugs (dopamine >5µg/kg/per minute or norepinephrine) with signs of tissue hypoperfusion (e.g., altered mental state, mottled skin, urine output below 0.5 ml per kilogram of body weight per hour during at least 2 h).
• admission serum lactate level more than 2.5mmol/L

Exclusion Criteria

• severe hypoxemia defined as a ratio of arterial oxygen pressure to fraction of inspired oxygen [PaO2/FiO2] < 100 mmHg

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
responder to fluid challenge	volume expansion using modified gelatin	fluid challenge

Primary Outcome Measures

Name	Time	Method
fluid challange responsiveness	within 20 minutes of fluid challenge	change of Stroke volume variation (SVV) by more than 10%

Trial Locations

Locations (2)

Emergency Department FB University Hospital; 🇹🇳 Monastir, Tunisia

CHU Fattouma Bourguiba; 🇹🇳 Monastir, Tunisia