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Clinical Trials/NCT02558166
NCT02558166CompletedNot Applicable

Relation Between the Renal Resistive Index and Markers of the Systemic Circulation, the Microcirculation, Fluid Status and of Renal Function.

Amsterdam UMC, location VUmc1 site in 1 country92 target enrollmentStarted: August 2015Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
92
Locations
1
Primary Endpoint
renal resistive index (RRI)

Study Overview

Brief Summary

This study consists of two substudies.

The first substudy:

'Renal resistive index in critically ill patients with cardiogenic and septic shock'

Design: cross-sectional observational

Aim of this project is:

  1. to determine whether critically ill patients with cardiogenic and septic shock have an elevated Renal Resistive Index and
  2. to determine whether Renal Resistive Index differs between cardiogenic/hypovolemic shock and shock due to sepsis/systemic inflammation (SIRS)
  3. to determine the relation between the (change in) renal vascular resistance and
  • Markers of the systemic - and the microcirculation
  • Fluid status as quantified by bioimpedance analysis
  • Concomitant renal function

The second substudy:

'Predictive value of the Renal Resistive Index on ICU admission and its course for the development of acute kidney injury in critically ill patients with cardiogenic and septic shock'

Design: longitudinal observational

The aim of this project is:

  1. to determine whether the renal resistance index on admission to the intensive care unit can predict the development of acute kidney injury (AKI) in critically ill patients with shock
  2. to investigate if the renal resistance index on admission to the intensive care unit is an independent predictor of the development of AKI or depends on the severity and duration of shock and other known risk factors of AKI such as comorbidity and use of nephrotoxic drugs

Aim of the large research project is to determine whether the Renal Resistive Index could become a monitoring tool for intervention studies aiming to prevent acute kidney injury or protect the kidney.

Detailed Description

Acute Kidney Injury (AKI) is a severe complication developing in intensive care patients as a result of hypovolemic, cardiogenic or septic shock. It is defined by an abrupt decrease in kidney function. It encompasses both direct injury to the kidney as well as acute impairment of function, including decreased glomerular filtration rate (GFR). Its prevention is crucial because AKI increases morbidity and mortality (1). Mechanisms comprise ischemia/reperfusion, oxidative stress, inflammation and toxicity (2).The common pathophysiological pathway includes endothelial damage to microvessels leading to impaired macro- and microvascular flow and this will aggravate ischemia (3).

Up to now, much controversy exists about

  • the changes in renal blood flow during different kinds of shock
  • the relation between renal blood flow, glomerular filtration rate and the development of AKI
  • the relation between renal blood flow and markers of the systemic and microcirculation

In this prospective observational study, three study measurement will be performed in two groups of critically ill patients (shock and no shock).

  1. The Renal Resistive Index (RRI) will be determined using Renal Doppler Ultrasound . The renal resistive index (RRI) is a sonographic index assessing resistance of the intrarenal arcuate or interlobar arteries and is used to assess renal arterial disease. It is measured as RRI = (peak systolic velocity - end diastolic velocity)/peak systolic velocity. The normal value is ≈ 0,60, with 0,70 being around the upper limits of normal.
  2. The sublingual microcirculation will be quantified using side stream dark field imaging (SDF)
  3. Fluid status will be determined by Bioelectrical impedance analysis (BIA) using the Akern device.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • First group (patients with shock):
  • Critically ill patients admitted to the intensive care unit (ICU) with cardiogenic shock or shock due to sepsis/SIRS or hemorrhage
  • Age > 18 years
  • Noradrenalin support
  • ICU admission < 24 hours
  • Signed informed consent
  • Second group (patients without shock):
  • Critically ill patients admitted to the intensive care unit (ICU) without shock, without vasopressor support and without fluid-dependent circulation
  • Age > 18 years
  • ICU admission < 24-h
  • Signed informed consent
  • In both groups, written consent will be obtained if and when the patients are awake and able to communicate ('deferred consent')

Exclusion Criteria

  • Severe pre-admission chronic renal insufficiency (eGFR < 30 ml/min)
  • Dialysis dependency
  • Renal transplantation

Outcomes

Primary Outcomes

renal resistive index (RRI)

Time Frame: 1 week

Secondary Outcomes

  • Creatine clearance (marker of GFR)(1 week)

Investigators

Sponsor
Amsterdam UMC, location VUmc
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

H.M. Oudemans-van Straaten, MD, PhD

Prof. Dr.

Amsterdam UMC, location VUmc

Study Sites (1)

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