Fluids, Electrolytes, Acid-Base Disorders, and Nutrition Support
Adverse effects of overfeeding β Do not exceed 4β5 mg/kg/minute of glucose/carbohydrate in
exceed 1.3β1.5 x measured REE or 25β30 kcal/kg/day for most patients); do not exceed soybean
oil (SO)-ILE intake of 2.5 g/kg/day; most clinicians limit SO-ILE in critically ill patients to around
1 g/kg/day or less.
Hypercapnia: It was traditionally thought that excessive glucose intake alone was responsible for
hypercapnia observed during overfeeding. However, studies of acutely ill patients showed that
overfeeding (e.g., 1.3 x BEE) (Chest 1992;102:551-5). Because most institutions lack the ability to
measure energy expenditure, estimates are used. If the patient experiences hypercapnia without a
known cause, the nutrition therapy should be suspected and the caloric intake empirically decreased
(especially if the patient is having difficulty weaning from the ventilator).
Hyperglycemia: In a retrospective study of 102 patients receiving PN and who were not predisposed to
hyperglycemia, dextrose intakes in excess of 5 mg/kg/minute resulted in substantial hyperglycemia
Patients with stress-induced hyperglycemia or diabetes are even more susceptible to hyperglycemia
with EN or PN. This is one reason (of many) that critically ill patients who require PN should receive
PN via continuous infusion rather than cyclic infusion (i.e., over 12β14 hour/night), even if they
tolerated a cyclic infusion of PN prior to ICU admission (Nutr Clin Pract 2023;38:1263-72).
Fatty infiltration of the liver: May be because of overfeeding with fat or carbohydrate. Usually
presents as a cholestatic liver disease (increased gamma-glutamyl transferase (GGT), alkaline
phosphatase, and ultimately bilirubin) after at least 1 week to 10 days of overfeeding (Arch Surg
1978;113:504-8). May be transient or reversible or can progress to end-stage liver disease. Throughout
a few weeks, patients can appear jaundiced. Patients with critical illness and/or infections tend to
be more susceptible to hepatic steatosis compared with nonβcritically ill patients (possibly because
of an exaggerated inflammatory process). Although treatment with fish oil appears promising in
are limited. Usual treatment for adult patients with suspected PN-associated liver disease is first to
ensure that the patient is not being overfed. Although evidence is lacking, most nutrition support
clinicians would agree that if 100% SO-ILE is being used, consideration of an ILE formulation
with a lower percentage of SO is warranted (refer PN formulation section for description of ILE
formulations). Cyclic PN (when PN is infused over fewer hours per day) may be considered for
patients who are no longer critically ill. However, cyclic PN is typically not appropriate for critically
ill patients due to the high glucose infusion rate and large volumes of fluid (relative to time) required
for administration. Reinstituting EN as soon as possible (if possible) is of utmost importance.
Guideline recommendations