Treatment of hypophosphatemia in the intensive care unit: a review

Phosphorus is an essential element for all living cells, with different functions (Table 1) [1]. The phosphate balance is a complex interplay between phosphate uptake and phosphate excretion (Figure 1). Normal values of the total serum phosphate level are 0.80 to 1.45 mmol/L (2.5 to 4.5 mg/dl).

Hypophosphatemia can be caused by three different mechanisms [1, 2]: decreased intestinal absorption, increased renal excretion, or internal redistribution of inorganic phosphate (Figure 1). In most patients with severe hypophosphatemia, both depletion of total body phosphorus stores and redistribution of phosphate to the intracellular space are found. Decreased intestinal absorption of phosphate rarely causes hypophosphatemia, as a low-phosphate diet increases renal reabsorption and enhances intestinal uptake of phosphate. Still, malnutrition, diarrhea, and nasogastric suction are common features in critically ill patients.

Redistribution across the cell membrane is the most common cause of hypophosphatemia in ICU patients and can be caused by multiple clinical conditions [1, 3]: respiratory alkalosis-induced increase of intracellular pH causes phosphate to enter the cell by stimulating glycolysis [4]; administration of glucose and insulin also stimulates carbohydrate metabolism, during which phosphate is transported into the cells along with glucose; high serum levels of catecholamines such as epinephrine and norepinephrine, whether endogenous or exogenous, cause a decrease in serum phosphate [5]; cellular uptake of phosphate is increased under certain specific conditions such as the hungry-bone syndrome, and diseases with rapid cell proliferation such as acute leukemia; renal excretion of phosphate is increased by metabolic acidosis, and by many drugs, including diuretics, glucocorticoids [6], aminoglycosides, antiretroviral drugs, and anticancer drugs.

Serum phosphate levels are inversely correlated to levels of the inflammatory cytokines interleukin-6 and tumor necrosis factor-α [7]. The exact mechanism is unclear: renal phosphate excretion is very low in patients receiving interleukin therapy for cancer [8], suggesting that high interleukin levels cause internal redistribution of phosphate; hypophosphatemia may be caused by increased phosphate utilization by immune cells. Hypophosphatemia can be found in patients with severe infections, such as sepsis. Especially patients with Gram-negative bacteremia may develop hypophosphatemia [9]. Hypophosphatemia correlates to severity of illness and can even be used as a prognostic parameter in sepsis patients [10]. Infection with Legionella species is particularly associated with hypophosphatemia [11].

Hypophosphatemia often develops in the postoperative phase [12‐15]. Multiple causal factors may be present, such as respiratory alkalosis, administration of insulin, and the use of diuretics. This is particularly true for major surgery, such as cardiac surgery and abdominal aortic surgery. The role of cardiopulmonary bypass is not clear. After major hepatic surgery, hypophosphatemia is extremely frequent. Reported mechanisms involve both shifts of phosphate into hepatocytes [16] and renal phosphate wasting [17]. Hypophosphatemia is reported to be more frequently encountered in trauma patients [18]. Renal phosphate handling is altered in trauma patients, resulting in inadequately increased urinary phosphate excretion. Hypophosphatemia is even more frequent in burn-wound victims, where phosphate is lost through the skin [19, 20]. In patients with head trauma, induction of polyuresis may be an aggravating factor [21].

In patients with malnutrition, a so-called refeeding syndrome may develop when they receive (par-)enteral feeding, a syndrome characterized by multiple metabolic abnormalities including depletion of total body phosphorus stores and redistribution of phosphate to the intracellular compartment, which may result in severe hypophosphatemia [22].

Hypothermia induces polyuresis and is associated with hypophosphatemia as well [23]. The use of (continuous) renal replacement therapy may lead to hypophosphatemia when low-phosphate replacement solution and dialysate are used. Patients who require high-flux dialysis for intoxications are especially at risk. Addition of potassium phosphate to dialysate and replacement fluids safely prevents the development of hypophosphatemia [24].

Finally, patients with diabetic ketoacidosis commonly present with hypophosphatemia due to increased urinary phosphate excretion. Phosphate levels generally decrease further during treatment because of intracellular shifting along with glucose and potassium [25].

Table 2 summarizes the reported incidence and prevalence of hypophosphatemia in surgical and medical ICU patients [7, 12, 14, 15, 17‐19, 21, 26‐30]. Hypophosphatemia is usually categorized as moderate (serum phosphate level of 0.32 to 0.65 mmol/L (1 to 2 mg/dl) or severe (<0.32 mmol/L (<1 mg/dl)). In the general hospital population, the prevalence of moderate hypophosphatemia ranges between 2.2 and 3.1% [31, 32], and the prevalence of severe hypophosphatemia is reported to be 0.2 to 0.4% [32‐34]. One study reports that 45% of all hospital hypophosphatemia cases occur in the ICU population [35]. Hypophosphatemia has a higher incidence in certain patient groups, such as patients with diabetic ketoacidosis, sepsis, and postoperative patients. Hypophosphatemia is found in as many as 34% of patients after elective cardiac surgery [12]. An extremely high incidence of hypophosphatemia is reported after major hepatic surgery, where almost all patients develop hypophosphatemia in the first postoperative week [17, 26]. In this group, serum phosphate levels decrease to a nadir within approximately 2 days and recover in the following days. This early nadir is also described after cardiac surgery and in patients with diabetic ketoacidosis and the refeeding syndrome. Trauma patients have a higher incidence of hypophosphatemia, especially patients with burn wounds [19] and head trauma [21]. Although the use of renal replacement therapy leads to hypophosphatemia, no epidemiologic reports were found.

Correction of hypophosphatemia, when encountered, is not reported in epidemiologic studies and the spontaneous course of serum phosphate levels without treatment is generally not addressed.

Serum phosphate levels do not accurately reflect total body phosphorus stores; hence the degree of hypophosphatemia does not always correlate to the presence of symptoms. Although most patients with hypophosphatemia do not develop symptoms, fatal complications have been described. A common mechanism in hypophosphatemia-caused complications is impaired energy metabolism, leading to cellular dysfunction in multiple organ systems. Symptoms are summarized in Table 3.

With the high prevalence of hypophosphatemia in critically ill patients, as well as their susceptibility to life-threatening symptoms, frequent laboratory monitoring is recommended, especially in previously mentioned high-risk groups. It is generally recommended to correct hypophosphatemia in hypophosphatemic patients with associated symptoms [2, 60]. However, no randomized controlled evidence indicates whether correction of hypophosphatemia in apparently asymptomatic patients leads to improved outcome. Taking this into account, the indication for -- and recommended frequency of -- laboratory monitoring and treatment remains debatable.

Correction of hypophosphatemia is possible via oral or intravenous routes. Intravenous administration of phosphate is not without complications, though. Phosphate may precipitate with calcium. Large intravenous doses of phosphate may result in hyperphosphatemia, hypomagnesemia, hypocalcemia, and hypotension. It is therefore necessary to know when intravenous therapy is indicated, and how much and how fast phosphate should be supplied. Intravenous therapy is generally recommended in symptomatic hypophosphatemia and phosphate levels <0.32 mmol/L. Multiple studies have evaluated the efficacy and safety of intravenous phosphate repletion regimens (Table 4) [61‐67]. These studies generally agree that aggressive phosphate supplementation is safe with phosphate doses up to 45 mmol with infusion rates up to 20 mmol per hour. Hyperkalemia is prevented by using sodium phosphate instead of potassium phosphate in patients with potassium levels >4 mmol/L.

Moderate hypophosphatemia can be treated with oral supplementation of phosphate. One should keep in mind that active vitamin D is required for intestinal absorption of phosphate. Typical oral supplementation amounts are three times the normal daily intake, with advised amounts of 2.5 to 3.5 g (80 to 110 mmol) per day, divided over two to three doses. Patients who receive feeding after a period of starvation are often phosphate depleted, so additional phosphate should be added to nutritional preparations. An additional preventive strategy is to build up the caloric intake slowly [22]. The total required amount of phosphate cannot be predicted by serum phosphate levels, as phosphate shifts between multiple body compartments.

Dipyridamole can decrease urinary phosphate loss [68]. Further research is needed to establish further the role of this drug in the treatment of hypophosphatemia in critically ill patients.