Response to Varying the Rate of Administration of a Fluid Challenge

NCT ID: NCT03300323

Last Updated: 2017-10-03

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-10-31
• Study Completion Date: 2018-02-28

Brief Summary

Administration of intravenous fluids is a key step in the management of the post-operative patient. Fluid management has been identified as one area that can affect rates of post-operative complications and outcomes. It is important to give the right amount of fluid, enough to optimise cardiovascular function, but not so much that we flood the cells. To guide this, we use a fluid challenge, administration of a small amount of fluid to test the cardiovascular response. At present there is significant inter-user variability in the method of administration of a fluid challenge. To ensure accuracy and reliability in assessing the response to a fluid challenge, the optimal method of administration needs to be determined.

The aim of this study is to investigate the optimal rate to give a fluid challenge over. Patients will be randomised to receive a fluid challenge over either 5 or 20 minutes. Both of these rates are within the currently accepted range. All patients will receive a dose of 4ml/kg of intravenous fluid. Previous work has shown this to be the optimal dose to reliably stress the system.

Measurement of the mean pressure in the cardiovascular system (mean systemic filling pressure or Pmsf) during the administration of a fluid challenge will be used to assess which rate of administration effectively challenges the cardiovascular system. Pmsf is measured using a pneumatic tourniquet inflated for sixty seconds, above an arterial line. The invasive arterial pressure is observed to then determine Pmsf. Cardiac output will also be monitored during and after administration of the fluid challenge. Since the microcirculation may remain impaired despite stabilisation of the macrocirculation, we will also observe this at baseline, on completion of the fluid challenge, and at 5 minute intervals for 15 minutes. This is observed using a handheld camera placed under the tongue.

The hypothesis is that administration of a fluid challenge at a faster rate, over 5 minutes as opposed to 20 minutes, will be a more effective test of the cardiovascular response. An effective fluid challenge is defined as one that causes a significant rise in mean systemic filling pressure. As such, a higher proportion of responders will be seen in response to the faster rate of fluid challenge. A responder is defined by an increase in cardiac output or stroke volume of more than 10% from baseline in response to a fluid challenge.

Conditions

Peri-operative Fluid Management

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: SINGLE

Study Groups

IV Fluid challenge administration _5

4ml/kg intravenous fluid challenge administered over 5 minutes

Group Type: ACTIVE_COMPARATOR

IV fluid challenge administration

Intervention Type: DIAGNOSTIC_TEST

Administration of an intravenous fluid challenge to assess for fluid responsiveness

IV Fluid challenge administration 20

4ml/kg intravenous fluid challenge administered over 20 minutes

Group Type: ACTIVE_COMPARATOR

IV fluid challenge administration

Intervention Type: DIAGNOSTIC_TEST

Administration of an intravenous fluid challenge to assess for fluid responsiveness

Interventions

IV fluid challenge administration

Administration of an intravenous fluid challenge to assess for fluid responsiveness

Intervention Type: DIAGNOSTIC_TEST

Eligibility Criteria

Inclusion Criteria

• Elective surgical patients admitted post-operatively to the General and Cardiothoracic Intensive Care Unit, requiring optimization with fluid therapy, as per the current clinical indications.
• Adult patients, aged >18 years, who have given informed consent to participate in the study.

Exclusion Criteria

• Patients without capacity to consent for themselves
• Patients requiring aggressive fluid resuscitation due to life-threatening cardiovascular instability, such would not allow for period of observation for stability as defined in protocol.
• Pregnancy
• Possible contraindications to the use of the cardiac output monitoring device, or pathology known to affect accuracy of readings, including

• Extensive peripheral arterial occlusive disease in upper limbs
• Postoperative valvular insufficiency
• New onset arrhythmia
• Cardiac assist device
• Right ventricular failure, (formal pre-operative diagnosis)
• Severe left ventricular failure or diastolic dysfunction

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

St George's Healthcare NHS Trust

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Maurizio Cecconi

Role: STUDY_CHAIR

St George's University Hospital

Central Contacts

Victoria Bennett

Role: CONTACT

v.bennett1@nhs.net

02087250399

Maurizio Cecconi

Role: CONTACT

Other Identifiers

17.0092

Identifier Type: -

Identifier Source: org_study_id