Excerpt
Besides the variables described in the review, clearly several other hemodynamic and perfusional parameters may be used to guide fluid resuscitation during sepsis. We agree that the markers of skin perfusion are among these end points. Markers such as capillary refill time and gradient temperatures have been described as indicators of inadequate tissue perfusion in circulatory shock (4) and after initial resuscitation (5). Nevertheless, to our knowledge, no prospective randomized large study has been reported that evaluated these variables as end points for fluid resuscitation in early stages of severe sepsis/septic shock. Skin perfusion parameters may be subject to biases such as room temperature and derangements in thermoregulatory response (like in anesthetized patients) and even distributive shock may intervene in skin temperature and capillary refill time (4). Vincent et al. (6) described that a cardiac index less than 1.8 L/min−1 m−2 was associated with a decrease in toe ambient temperature gradient of 5°C and that the increase in this gradient precedes the augmentation in skin oxygen partial pressure during recovery. A similar correlation, however, was not found in septic shock patients (6).
Recently, new devices such as capillary microscopy, laser Doppler flowmetry, and sidestream dark field were incorporated to research in intensive care. These techniques allowed the evaluation of microcirculation in "real time" and demonstrated that even when macrohemodynamic variables and global parameters of perfusion are "normalized," regional microcirculation dysfunction could persist and lead to irreversible tissue damage. However, microcirculatory imaging is still investigational in humans and has not been incorporated into routine practice. In addition, important issues related to the limitations of these technologies in "real life" are the limited number of human microcirculatory studies; the visualization only of body surface microcirculation, which might not reflect vital organs microcirculatory dysfunction; the complex interpretation of microcirculatory imaging data; and the difficulty in depicting a parallel to the clinical sepsis stages (7).
An intact microcirculatory network is a critical intermediary between the cardiovascular system and tissue oxygenation. Once microcirculation serves as the bridge between macrocirculation and tissue oxygenation, by tracking the response of variables related to tissue perfusion such as acid-base parameters, lactate, and venous oxygen saturation, we are indirectly evaluating the effectiveness of tissue perfusion (8).