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Monitoring of the fluid status of critically ill patients by bio-impedance vector analysis (BIVA): A before-and-after study

The use of bio-impedance vector analysis in the measurement of body water index in critically ill patients admitted to the intensive care unit: A before-and-after study

Status
Terminated
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615000130561
Acronym
Bio-Impendence Vector Analysis (BIVA) fluid status monitoring
Enrollment
87
Registered
2015-02-12
Start date
2014-08-02
Completion date
2015-02-20
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The monitoring of fluid status in critically ill patients is challenging. Fluid balance is often incorrect and does not take into account insensible fluid losses, which in febrile patients can add up to a litre or more/day. Weighing with beds equipped with electronic scales has been shown to be unreliable and inaccurate in ICU patients. Intravascular filling pressures are not reliably related to extravascular fluid accumulation. Oedema can only be detected once up to 4-5 litres of excess fluid have accumulated. These shortcomings in fluid assessment are particularly problematic in patients who stay in ICU for a longer period of time, where daily errors in assessment accrue to make estimates of fluid status particularly inaccurate. These technical problems are potentially clinically significance as fluid accumulation has been repeatedly identified as an independent risk factor for mortality in ICU patients. The development of novel bio-impedance vector analysis (BIVA) has recently been shown to provide a reliable, reproducible, robust, safe, and non-invasive assessment of hydration which can be performed at the bedside of critically ill patients by evaluating the bioelectrical impedance of the human body. This approach uses the administration of alternating (AC) microcurrents (microamperes) a low frequency (50kHz) with a standard four-electrode system. Such microcurrents are well below the sensation threshold for human beings. The resistance (R) and reactance (Xc) adjusted for height of the whole body provide information on the ability of the microcurrent to move from ankle electrodes and reach sensor wrist electrode. The relationship between resistance (dependent of body fluid volume) and reactance (dependent on the capacitance of membranes and tissue interfaces) allows the construction of a vector on an X-Y plot. This vector can be related to vectors obtained from >18,000 normal subjects which have been used to define reference values. These values identify states of low resistance and low reactance (fluid overload). Such individual vectors can then also be used to monitor changes in the fluid status of an individual. This approach has been applied to identify fluid overload in dialysis patients, cardiac failure patients, and, in pilot work, in critically ill patients. In this study, we propose to compare fluid management in mechanically ventilated patients expected to stay in ICU until the day after tomorrow treated with standard care during a period when clinicians are not informed of the bio-impedance measurement followed by a period in which they are informed of the measurement.

Interventions

Twice daily bio-impedance vector analysis monitoring commencing within the first 24 hours of admission in adult (aged 18 years or older) mechanically ventilated adult patients admitted to the intensive care unit. In the after period the patient's treating clinical care team will be informed of the finding of the assessment. For both patients both in the before and in the after period all other clinical decisions will be made as per the patient's treating clinical team.

Sponsors

Austin Health
Lead SponsorHospital

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Adult (aged 18 years or older) admitted to the intensive care unit 2. Currently receiving mechanical ventilation 3. Expected to stay in the intensive care unit until the day after tomorrow

Exclusion criteria

The following patients will be excluded from the trial 1. Patients on chronic dialysis 2. Patients admitted after cardiac surgery 3. Patients with a pacemaker 4. Patients with an implantable defibrillator 5. Pregnant patients 6. Patients with diaphragmatic pacing

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026