Optimizing Fluid Status

Francisco Maduell56 enrolled

Overview

Title of study: Optimizing Fluid Status Study code: HD-IIT-01-E Study design: Prospective open design in study centre at two locations Applied medical device: Body Composition Monitor (BCM) for determination of fluid overload and dry weight Aim of the study: To improve the fluid status in chronic HD patients (measured as OH (overhydration) or TAFO (time averaged fluid overload)) based on BCM measurements. Up to now, the BCM was occasionally applied in both locations of the study centre. Study hypothesis: Regular measurement of fluid status (assessed by BCM) and display of dry weight (post-weight plan)will have significant consequences, namely a decrease of the: * time averaged fluid overload (TAFO), * proportion of patients with severe overhydration OH \> 2.5 L,or OH/ECW \> 15 %) * proportion of dehydrated patients (OH \< -1.0 L, or OH \< -7 %), * mean overhydration, * variance of overhydration, * time outside the reference range (-1.0L \< OH \< 2.5L). Devices used in this study: Dialysis machine 5008 equipped with Blood Pressure Monitor BPM, Blood Volume Monitor BVM, Blood Temperature Monitor BTM, and Online Clearance Monitor OCM ; Body Composition Monitor BCM ; Data management software / database system NephroLink Disposables used in this study: BVM blood lines and BCM electrodes Patients: 60 patients

Study Type

INTERVENTIONAL

Allocation

Masking

NONE

Enrollment

Conditions

Hypotension During Dialysis

Interventions

Prescription of post-dialytic weight based on BCM deviceOTHER

Prescription of post-dialytic weight target: On a weekly base, the patients are pre-dialytically measured by BCM (body composition monitor). The time average fluid overload (TAFO) determines the target range. TAFO is defined as the mean value of pre- and post-dialytic overhydration (TAFO = (OHpre+OHpost)/2). The target range is set asymmetrically around a TAFO of 0.8, from -1.0 L to +0.5, i.e. the TAFO target range will be from -0.2 L to 1.3 L. Prescription steps will be calculated weekly for all study patients. TAFO \< -0.2 L: Increase post-dialytic weight by Cw x 0.5 kg/week, TAFO between -0.2 to 1.3 L: No action, TAFO between 1.3 to 2.8 L Decrease post-dialytic weight by Cw x 0.5 kg/week, TAFO \> 2.8 L: Decrease post-dialytic weight by Cw x 1.0 kg/week.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Chronic renal failure stage V * Treatment thrice weekly with HD or on-line HDF for at least 6 months prior to inclusion * Ability to understand the nature and requirements of the study * Age: at least 18 years * Signed informed consent. Exclusion Criteria: * Interventional clinical study during the preceding 30 days or previous participation in the same study * Acute or chronic infection (HIV, Hepatitis B or C, ...) * Severe disease (malignant tumour, tuberculosis ...) * Usually single needle HD * Problems with shunt or high recirculation, * Severe intra-dialytic blood pressure instability in the last month * Instable angina pectoris * Major amputation at arm or leg, or a pacemaker.

Outcomes

Primary Outcomes

intra-individual difference in TAFO between study start and study end

Time frame: 3 months

Secondary Outcomes

Comparison between start and end of treatment will be performed for Pre-dialytic overhydration (OH)

Time frame: 3 months

Comparison between start and end of treatment will be performed for number of patients in target range (TAFO from -0.2 L to 1.3 L)

Time frame: 3 months

SF 36 total score and sub-scores as calculated according to official guidelines,

Time frame: 3 months

BNP

Time frame: 3 months

Blood pressure

Time frame: 3 months

laboratory parameters (sodium, calcium, potassium, chloride, haematocrit, haemoglobin, albumin, total protein, urea, creatinine, mean corpuscular volume, C-reactive protein, transferrin saturation, ferritin).

Time frame: 3 months

Change from Baseline in Medication at 12 weeks (erythropoetin, iron, blood pressure medication)

Time frame: 3 months

Change from baseline in intra-dialytic events (hypotension, cramps)

Time frame: 3 months

Change from baseline in Residual Renal Function

Baseline Residual renal function, measured as Kt/V residual, wil be compared with the Residual renal function at the end of 12 weeks.

Time frame: 3 months

Hospitalisation

Time frame: 3 months

Optimizing Fluid Status

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes

Secondary Outcomes