HD performed the statistical analysis and helped in drafting the

HD performed the statistical analysis and helped in drafting the manuscript.AcknowledgementsWe thank Marie-Claude Gu��rin selleck kinase inhibitor for reviewing the manuscript. We received no financial support for conducting this study. This study was approved by the Institutional Review Board of Amiens University Hospital.
Fluid loading is a first-line therapy when hypovolaemia is suspected in patients with evidence of hypoperfusion, and it is commonly used in operating rooms and ICUs. The maintenance of adequate oxygen delivery and tissue perfusion is considered a primary goal in volume replacement [1] while avoiding fluid overload, which may lead to interstitial oedema [2].

Several studies have demonstrated the superiority of dynamic preload indices, such as pulse pressure variation (PPV) and stroke volume variation (SVV), rather than static indices for individualised evaluation of patients who are likely to benefit from an increase in preloading [3-5]. In addition, the use of SVV or PPV can reduce organ failure during individualised, goal-directed fluid optimisation [6,7].Although a fluid challenge should correct macrohaemodynamics (stroke volume (SV) and cardiac output (CO)), the ideal volume replacement strategy should also improve microcirculation perfusion and tissue oxygenation. Hypovolaemia during major surgery or sepsis leads to inadequate perfusion of the microcirculation and insufficient oxygen availability to meet tissue oxygen needs [8]. However, previous reports have suggested a mismatch between global haemodynamics and microcirculation and a potential independence of macrocirculation and microcirculation during fluid loading [9,10].

Thus, fluid administration may correct systemic haemodynamic variables but not regional and microcirculatory oxygenation and perfusion [11].Microcirculatory haemoglobin and oxygen availability can be measured by use of near-infrared spectroscopy (NIRS) [12], a noninvasive technique that can be performed at the bedside. In this method, the differential absorption of infrared light at two specific wavelengths (680 and 800 nm) by deoxyhaemoglobin is used to define the haemoglobin saturation level in vessels located in the tissue volume that is illuminated by the probe [13]. The dynamic response to tissue oxygen saturation (StO2), especially the StO2 recovery slope, during a standardised vascular occlusion test (VOT) is assumed to reflect the recruitment of microvessels in response to a local hypoxic stimulus [14].

Researchers in previous studies found that the StO2 recovery slope was a prognostic factor in septic patients [15] and was useful in evaluating the response to norepinephrine in severely hypotensive septic shock patients [16]. However, there is no information on the StO2 response during fluid resuscitation and in the presence of abnormal vascular reactivity in patients undergoing Cilengitide major surgery.

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