Cardiac Output Clinical Trial
Official title:
Validation of a Novel, Minimally Invasive Ultrasound Indicator Dilution Technique for Measuring Cardiac Index in Critically Ill Children
A novel method to measure cardiac index based on ultrasound indicator dilution technology
(UIDT) has been developed by Transonic Systems Inc. (Ithaca, NY, USA). The method overcomes
many of the limitations that have plagued the existing techniques used to measure cardiac
index in critically ill children.
In the proposed investigation, the investigators hope to validate a novel application of an
existing technology in critically ill infants and children. The primary aim of this study is
to determine the accuracy of cardiac index measured by UIDT when compared to the
gold-standard Fick technique. The primary hypothesis is that the average of three
consecutive measurements of cardiac index by UIDT will be accurate when compared to the Fick
technique. Secondary aims will be to determine the precision of the measurement, the
feasibility of the technique with regards to time required and any complications
encountered. An exploratory secondary aim of this study is to determine whether central
blood volume (CBV) derived from indicator transit time (ITT) correlates with central venous
pressure (CVP) and echocardiography derived measures of preload.
n/a
Observational Model: Case-Only, Time Perspective: Prospective
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