The initial treatment of trauma and critically ill patients is aimed at securing the airway and establishing adequate breathing, followed by the correction of circulatory abnormalities ('ABC') 1. These basic principles underline the fact that optimization of oxygen delivery to the tissues is one of the cornerstones of critical care medicine, thus preventing cellular dysfunction and cellular death, and subsequent organ dysfunction. Disturbance of the delicate balance between oxygen delivery (DO₂) and oxygen consumption (VO₂) to the tissues can be defined as a state of shock. Impairment of DO₂ can be caused by severe anemia, hypoxia, or a low cardiac output. To preserve tissue DO₂ in several states of shock, especially to the heart and brain, many compensating physiological reserve mechanisms come into play. This leads to microvascular derecruitment in compliant vascular beds such as the skin and the splanchnic area, redirecting blood flow to more crucial body areas. During this process, systemic hemodynamics can be maintained at the expense of impaired microcirculatory perfusion. Nevertheless, if this microcirculatory state of hypoperfusion is not reversed in a timely manner, multiple organ failure can develop, with a high probability of death. This line of thought can be found in a recent general guideline for the treatment of patients with septic shock, in which infusion of volume is judged to be critical to basic care in these patients 2.

Systemic inflammatory response syndrome (SIRS) is seen after trauma, major surgery or hemorrhage. A similar phenomenon is seen in sepsis as a response to infection, and is still an important cause of death in critically ill patients. Both can progress to severe shock and multiple organ dysfunction syndrome (MODS) 3. This progression is currently thought to be due to an increased VO₂, a decreased peripheral vascular resistence and a maldistribution of tissue blood flow to preserve central blood volume. As a result, microcirculatory perfusion is shut down and is the final common pathway in shock. Especially in septic shock, alterations in metabolic pathways called 'cytopathic hypoxia' can lead to additional tissue damage 4. This review discusses briefly the importance of microcirculatory flow in the pathogenesis of sepsis and the progression to MODS.

The measurement of global hemodynamics reflects only a tiny part of whole-body circulatory blood flow. The microcirculation, with its huge endothelial surface, is in fact the largest 'organ' in the human body. We have come a long way since the disclosure of human bodily circulation by Harvey 5 and Malpighi 6. The number of publications concerning the microcirculation in humans is steadily increasing (Fig. 1). However, the microcirculation remains difficult to investigate. In clinical practice, microcirculatory perfusion is judged on aspects such as the color, capillary refill and temperature of the distal parts of the body (i.e. fingers, toes, earlobes and nose).

Perfusion of the microcirculation is regulated by an intricate interplay of many neuroendocrine, paracrine, and mechanosensory pathways 7. These mechanisms adapt to the balance between locoregional tissue oxygen transport and metabolic needs to ensure that supply matches demand. In sepsis, this process is severely compromised because of decreased deformability of red blood cells with inherent increased viscosity 8, an increased percentage of activated neutrophils with decreased deformability and increased aggregability due to the upregulation of adhesion molecules 9, activation of the clotting cascade with fibrin deposition and the formation of microthrombi 10, dysfunction of vascular autoregulatory mechanisms 11, and finally, the secondary enhanced perfusion of large arteriovenous shunts 12 (Fig. 2). These processes result in tissue dysoxia, either from impaired microcirculatory oxygen delivery and/or from mitochondrial dysfunction 413. Clinically this process is perceived as an oxygen extraction defect, a prominent feature of sepsis. A possible mechanism accounting for this phenomenon could be the shut-down of vulnerable microcirculatory units in the organ beds, promoting the shunting of oxygen transport from the arterial to the venous compartment leaving the microcirculation hypoxic 14. This might be an explanation for the different findings regarding locoregional tissue perfusion in shock (Fig. 3). In this so-called shunting theory of sepsis, correction of this condition should occur by recruitment of the shunted microcirculatory units. Applying strategies to 'open the microcirculation' by vasodilation would be expected to promote microcirculatory flow by increasing the driving pressure at the entrance of the microcirculation and/or decreasing the capillary afterload 15.

Indeed, in animal studies, these effects occur during hemorrhage and sepsis caused by microcirculatory shunting with associated tissue dysoxia 161718. Such microcirculatory shunting was reversed by vasodilation 14 and by improvement in regional flow in an animal sepsis model 19. In addition, oxygen extraction was improved 20 and microcirculatory shunting was reversed 21 by the use of nitric donors. To redirect microvascular flow, matters become more complicated if one realizes that sepsis causes heterogeneous effects in constriction and dilation in different organs and at different levels of the microcirculation 22. Although cardiac output is frequently increased in sepsis, high lactate levels and increased tonometric partial pressure of CO₂ (pCO₂) in tissues indicate at least regional tissue dysoxia. This has been termed oxygen extraction deficit in sepsis and has been well documented in different animal models of shock 232425. It is still a matter of debate whether it can be explained by pathologic flow heterogeneity due to dysfunctional autoregulatory mechanisms and microcirculatory dysfunction causing hypoxic pockets, or by mitochondrial dysfunction with associated impaired oxidative phosphorylation 4, or by a combination of both.

Especially in critical illness, function and dysfunction of the microcirculatory network are of utmost importance in the cause of disease and the development of organ failure. In sepsis, all three elements of the microvascular network are compromised, namely arteriolar hyporesponsiveness to vasocontrictors and vasodilators, a reduced number of perfused capillaries, and venular obstruction by the sequestration of activated neutrophils 22. However, an objective and reliable method of monitoring microcirculatory organ perfusion is still not available. 'Downstream' global derivatives of microcirculatory dysfunction such as lactate, tonometry, and mixed venous oxygen saturation (SvO₂), in addition to measurements of DO₂ and oxygen uptake VO₂, are used in daily intensive care clinical practice. But which parameters should be used to prevent further deterioration of organ function in a critically ill patient with septic shock? In this section we discuss the reasons for, and limitations of, several parameters that have been used to assess microcirculatory perfusion.

Lactate levels are thought to reflect anaerobic metabolism associated with tissue dysoxia and might predict a response to therapy and prognosis 26. The balance between lactate production due to global (shock, hypoxia), local (tissue ischemia), and cellular (mitochondrial dysfunction) factors on the one hand, and lactate clearance depending on metabolic liver function on the other hand, make the interpretation of lactate levels uncertain and difficult 27. SvO₂ can be measured with a pulmonary artery catheter and is thought to reflect the average oxygen saturation of all perfused microvascular beds. In sepsis, microcirculatory shunting can cause normal SvO₂ while severe local tissue dysoxia is present 14. Delayed therapy aimed at the normalization of SvO₂ failed to demonstrate a survival benefit 2829. Optimization of oxygen delivery might have been instituted too late in these studies, when irreversible cellular damage was already present. In addition, the frequent use of dobutamine to obtain preset goals of oxygen delivery might have affected the outcome, because dobutamine has been implicated in the impairment of hepatosplanchnic perfusion in sepsis 30. Nevertheless, besides ongoing discussions about the use of a pulmonary artery catheter in sepsis, the sole use of SvO₂ seems an inadequate parameter as a guideline for therapy in the restoration of local tissue oxygenation in septic shock patients. However, if an integrative approach is used in the early stage of treating critically ill patients, states of hypoperfusion are recognized earlier 31 and, if early treatment is started, can even improve survival 32. It is likely that the results of the Rivers study 32 are due largely to the prevention of irreversible cellular damage, in contrast to the earlier findings by Hayes and Gattinoni, who targeted high oxygen delivery levels during later phases of sepsis 2829.

An appealing alternative to the evaluation of tissue dysoxia might be regional intestinal capnography as introduced by Fiddian-Green and Baker 33. This method relies on the principle of CO₂ diffusion from the local anaerobic production site across tissue and cell membranes. Measurement of the difference between intestinal pCO₂ and arterial pCO₂ has been found to be better than that of pH_i alone, because arterial pCO₂ fluctuates in ventilated patients 34. In sepsis, the interpretation of tonometric results is affected by microcirculatory shunting. This complicates the clear establishment of impaired perfusion, because areas with reduced perfusion and CO₂ offloading are next to hypoxic regions 35. Recently, gastric intramucosal pCO₂ values were found to be well correlated with sublingual pCO₂ values 36. The baseline difference between sublingual pCO₂ and arterial pCO₂ values was a better predictor of survival than the change in lactate or SvO₂ 37. Further studies should demonstrate whether this parameter can be used in clinical management of patients with septic shock.

All parameters discussed are indirect and downstream from the pathological process in the microcirculatory network. Direct assessment of microcirculatory perfusion seems a superior and more direct approach and has been extensively studied in vivo by intravital microscopy (IVM) in animals. In humans, IVM studies are restricted to the eye, the skin and the nail fold owing to the size of the IVM equipment and the use of fluorescent dyes for contrast enhancement. IVM depends on trans- or epi-illumination and thus observations are limited to superficial layers of thin tissues only. By using fluorescent dyes a higher contrast is possible as well as labelling specific cells for visualization and quantification. Because of the potentially toxic effects of these dyes in humans, studies are mostly limited to animals 3839. We recently introduced 4041, validated 42, and clinically applied 43 a new method for observing the microcirculation in patients, called orthogonal polarization spectral (OPS) imaging (CYTOSCAN™; Cytometrics Inc., Philadelphia, PA), which creates high-contrast images without the use of fluorescent dyes. This technique is based on the reflection of light from the tissues. Contrast is obtained from the absorption of linearly polarized light by the haemoglobin in the blood. As a consequence, red blood cells in the microcirculation appear black on the white background of the surrounding tissue. For OPS imaging a 5 × objective (on-screen magnification of × 326) is used during measurements. Data are recorded on a digital video recorder for later analysis and displayed on a black and white monitor. Because the OPS machine is a small hand-held device (Fig. 4), it can be used at the bedside for humans in the visualization of unique in vivo images of the microcirculation 44. Although nailfold microcirculatory blood flow as established by OPS imaging correlates very well with IVM microvascular flow when analysed by specific video-analysis-software 42, this quantitative approach proved not to be usable with sublingual images owing to movement artefacts induced by tongue movements or respiration. A semi-quantitative approach was therefore used successfully to analyse changes in microcirculatory flow 4546.

Despite these shortcomings in the assessment of local tissue oxygenation, several studies have been performed aiming at recruitment of the tissue microcirculatory flow.

Data from several studies support the idea that the impairment of microcirculatory perfusion results in organ failure and increases the risk of death 1718224547484950. In this line of thought, restoring perfusion in disturbed microcirculatory networks might improve outcome. Indeed, survival was related to microcirculatory shutdown in rats that were bled and in which the blood volume was subsequently resuscitated, although whole-body hemodynamic parameters were comparable in survivors and non-survivors 51. Comparable findings have been reported in humans with septic shock. Bihari found that vasodilation might unmask a preexisting tissue oxygen debt. After increasing DO₂ with the vasodilator prostacyclin, all patients survived when the increase in DO₂ did not coincide with an increase in VO₂, whereas all patients died who showed increasing VO₂ 52. By recruitment of the microcirculation, oxygen might have become available to previously hypoxic tissues that had shut down. De Backer and colleagues 45 reported that sublingual microcirculatory perfusion was compromised to a greater extent in non-surviving than in surviving septic shock patients. We observed normal sublingual microcirculatory perfusion in a septic patient with hepatic failure who received high doses of norepinephrine (P Spronk, unpublished observation). Dubois recently reported a comparable observation in a septic patient treated with vasopressin 53, whereas others observed sublingual microcirculatory shutdown with the use of vasopressin (C Boerma, personal communication). Larger studies should demonstrate why these patients behave differently from those in previous reports. Nevertheless, De Backer and colleagues showed that microcirculatory perfusion improved over time in survivors, whereas the disturbance of perfusion in the microvessels of the non-survivors remained. In addition, they showed that sublingual microcirculatory perfusion abnormalities could be corrected by the topical application of acetylcholine, showing that the local endothelium was still responsive to nitric oxide (NO), whereas vasoplegia due to ongoing sepsis might be expected.

NO has been implicated as the major cause for hypotension, generated from endothelial cells through the expression of inducible NO synthase (NOS) 54, thus contributing to many of the manifestations of septic shock such as vasoplegia, diminished myocardial contractility, hepatic damage, and vascular and intestinal hyperpermeability. Others, however, found decreased NO production during sepsis 55, and, more recently, that NOS activity is diminished in mononuclear cells from sepsis patients 56. On the basis of the hypothesis that NO production is increased in sepsis, experiments in septic animal models were performed and indicated that hypotension could be prevented by inhibiting NOS. This led to clinical studies with several compounds capable of inhibiting NO synthesis. Early promising data showed increasing blood pressures and decreasing doses of vasopressors in septic shock patients treated with NOS inhibitors 57. However, a subsequent randomized controlled multicenter phase III trial was stopped when interim analysis showed increased mortality in the N^G-monomethyl-L-arginine group compared with placebo 58. Inhibition of NOS activity seems to result in an improvement in the general hemodynamic situation, but at the cost of increased mortality 59. Apparently, completely inhibiting vasodilation is not the proper answer to sepsis. A more specific approach by inhibiting only the inducible form of NOS might be an attractive alternative. Indeed, after the application of 1400 W (a synthetic blocker of inducible NOS) in a pig endotoxemia model, microvascular perfusion was restored by a redistribution within the gut wall and/or an amelioration of the cellular respiration 60.

NO is an important vasodilator in the microcirculation during sepsis 61. Indeed, Ince and colleagues showed recently that NO donors were highly effective in correcting microcirculatory oxygenation after endotoxemia in a pig model of sepsis, with both mucosal and serosal microvascular PO₂ as well as intraluminal gastric pCO₂ being restored to baseline values 21. In addition, the glucose oxidation rate improves in septic patients after treatment with prostacyclin 62. Apparently, the microcirculation in sepsis fails to support adequate tissue oxygenation. Optimizing DO₂ can result in lower mortality rates, especially when therapy is started without delay 6364. Others, however, showed comparable mortality rates 29 or even a higher hospital mortality 65 in septic shock patients whose treatment sought to increase DO₂. In these studies, oxygen supply to the tissues was increased by manipulating macrohemodynamic endpoints such as cardiac output, hemoglobin, and central venous pressure and/or pulmonary artery wedge pressure. Radermacher and colleagues 66 treated septic shock patients with prostacyclin when no further increase in DO₂ could be obtained by volume resuscitation and dobutamine infusion. Gastric pH_i improved after starting prostacyclin, suggesting an increase in splanchnic blood flow.

These findings led us to propose that the addition of systemic NO to adequately volume resuscitated patients with septic shock results in an improvement of microcirculatory perfusion. In a small observational study in septic shock patients, we were indeed able to show an improvement in sublingual microcirculatory perfusion after the injection of 0.5 mg of nitroglycerin 46. The observation of capillary shutdown next to sustained flow in the larger vessels corroborates the shunting theory of sepsis. Upon the administration of nitroglycerin, microcirculatory flow increased not only in large microvessels but also in small microvessels. The latter finding argues against NO donation's inducing even more shunting flow. All patients except one, owing to late cerebral hemorrhage, were discharged from the hospital alive. This suggests that one can actively open up the microcirculatory network and keep it open by volume and vasodilator therapy. One might argue that oxygen consumption increases with a concurrent increase in DO₂ under nitrate administration 67. However, concentrations of nitrate/nitrite seem to be increased in septic shock patients anyway 68. We administered 1 mg/kg dexamethasone intravenously to all our patients at admission, which might well have attenuated the production of NO by inhibiting excessive activation of inducible NOS. With this background, a controlled opening strategy using NO donors might be a rational approach. Further studies should demonstrate whether this line of thought regarding therapy in sepsis can be guided by microcirculatory flow patterns and might result in a better outcome.

Therapy in shock should be aimed at the optimization of cardiac function, arterial hemoglobin saturation, and tissue perfusion. This will mean the correction of hypovolemia and the restoration of an evenly distributed microcirculatory flow and inadequate oxygen transport. How can the latter goals in particular be accomplished? Discussions about the role of vasodilators, particularly NO, in sepsis with microcirculatory disturbance will continue. Will the optimization of sublingual microcirculation become a novel resuscitation endpoint? Do we need to take mitochondrial function and tissue respiration into account 69? Or should we use an integrative approach incorporating both macrocirculatory and microcirculatory hemodynamic data, as proposed in Table 1? Several tools will become available for improving the assessment of regional oxygen demands in critical illness. This will create new challenges for the clinician to improve bedside critical care and optimization of microcirculatory perfusion, thus preventing the further deterioration of organ function and keeping the old principle of primum non nocere alive.

None declared.

DO₂ = oxygen delivery; IVM = intravital microscopy; MODS = multiple organ dysfunction syndrome; NO = nitric oxide; NOS = NO synthase; OPS = orthogonal polarization spectral; pCO₂ = partial pressure of CO₂; SIRS = systemic inflammatory response syndrome; SvO₂ = mixed venous oxygen saturation; VO₂ = oxygen consumption.