O ne to 25% of critically ill patients who are admitted to intensive care unit (ICU) develop acute renal failure (ARF), depending on the definition used (1). ARF has a significant impact on morbidity and represents an independent risk factor for mortality. The mortality rate for severe ARF exceeded 50% over the past three decades (2-6). The wide range of incidence in the literature depends on the lack of a reliable definition of the syndrome. On the basis of the most recent RIFLE classification (an acronym indicating Risk of renal dysfunction, Injury to the kidney, Failure of kidney function, Loss of kidney function, and ESRD) (7), ARF can be stratified for severity, and different outcomes depend on the degree of severity as assessed by the extent of GFR loss. Current management depends on the level of severity and includes optimization of hemodynamics and fluid status, avoidance of further renal insults, optimization of nutrition, and, when appropriate, the application of renal replacement therapy (RRT).Indications for RRT generally are clear for patients with the most severe of conditions (e.g., anuria with severe hyperkalemia in the setting of septic shock), whereas they can be a matter of controversy and require individualized assessment in less severe situations (e.g., polyuric ARF in a patient who has previous chronic renal dysfunction and is otherwise well 2 d after cardiac surgery). Optimal strategies to improve patient outcome in ARF may include optimization of delivered . This review focuses on RRT dose and its measurement and prescription in the ICU and on the current evidence concerning the relationship between RRT dose and outcome.
What Is RRT Dose, and How Is It Measured?The conventional view of RRT dose is that it is a measure of the quantity of blood purification achieved by means of extracorporeal techniques. As this broad concept is too difficult to measure and quantify, the operative view of RRT dose is that it is a measure of the quantity of a representative marker solute that is removed from a patient. This marker solute is taken to be reasonably representative of similar solutes, which require removal for blood purification to be considered adequate. This premise has several major flaws: the marker solute cannot and does not represent all of the solutes that accumulate in renal failure. Its kinetics and volume of distribution are also different from such solutes. Finally, its removal during RRT is not representative of the removal of other solutes. This is true for both end-stage renal failure and acute renal failure. However, a significant body of data in the end-stage renal failure literature (16 -21) suggests that, despite all of the above major limitations, single solute marker assessment of dose of dialysis seems to have a clinically meaningful relationship with patient outcome and, therefore, clinical utility. Nevertheless, the HEMO study, examining the effect of intermittent hemodialysis (IHD) doses, failed to confirm the intuition that "more dialysis (than recommended by current gui...