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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:
to determine whether critically ill patients with cardiogenic and septic shock have an elevated Renal Resistive Index and
to determine whether Renal Resistive Index differs between cardiogenic/hypovolemic shock and shock due to sepsis/systemic inflammation (SIRS)
to determine the relation between the (change in) renal vascular resistance and
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:
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.
Full 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
In this prospective observational study, three study measurement will be performed in two groups of critically ill patients (shock and no shock).
In addition, routinely measured markers of circulation, renal function and fluid balance will be collected for analysis.
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Inclusion criteria
First group (patients with shock):
Second group (patients without shock):
In both groups, written consent will be obtained if and when the patients are awake and able to communicate ('deferred consent')
Exclusion criteria
92 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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