About this trial
Circulatory shock is characterized by tissue hypoxia. Although fluid resuscitation is an essential treatment in many forms of circulatory shock, its benefits are variable, and its administration carries a risk of potentially harmful fluid overload.
Assessment of fluid responsiveness generally relies on changes in cardiac output. However, the actual therapeutic objective is rather to improve tissue oxygen utilization, as reflected by oxygen consumption. Despite its physiological relevance, direct measurement of oxygen consumption remains complex and difficult to perform in routine clinical practice.
Capillary refill time is a simple, rapid, non-invasive, and readily available marker of peripheral perfusion. It is associated with outcomes in patients with circulatory shock, and a capillary refill time-guided therapeutic strategy may improve outcomes in patients with septic shock.
This study hypothesizes that changes in capillary refill time following fluid resuscitation may predict changes in oxygen consumption induced by fluid administration. If confirmed, capillary refill time and its changes could be incorporated into the criteria used to assess the indication for fluid resuscitation in patients with shock. They would also provide additional physiological information regarding the relationship between peripheral perfusion and oxygen consumption.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adult patient admitted to the intensive care unit within the previous 72 hours
Receiving invasive mechanical ventilation
For whom the clinician plans to perform a fluid challenge
No objection from the participant or a relative/legally authorized representative
Disqualifiers
Fraction of inspired oxygen greater than 60%
Administration of inhaled medications, including nitric oxide
Positive end-expiratory pressure greater than 15 cmH₂O
Excessive leaks in the ventilator circuit, defined as an expired volume less than 95% of the inspired volume
Trial population
Patients admitted to the ICU
Trial design
Cohort
Prospective
Treatments tested in this trial
Indirect calorimetry measurement
DeviceSetup of an indirect calorimetry measurement
Treatment groups
Trial outcomes
Primary outcomes
Assessment of the ability of fluid challenge-induced changes in capillary refill time to predict fluid challenge-induced changes in oxygen consumption
Area under the receiver operating characteristic curve of changes in capillary refill time for predicting a 15% increase in oxygen consumption during a fluid challenge
Sponsors and contacts
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