Index
Module 3 • Clinical Pharmacology
Fluids, Electrolytes, Acid-Base & Nutrition
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Fluids, Electrolytes, Acid-Base & Nutrition
Ashley Hawthorne ~3 min read Module 3 of 20
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Fluids, Electrolytes, Acid-Base Disorders, and Nutrition Support

iv.

Biochemical evidence for EFAD (the β€œclassic definition” is an increased triene/tetraene

[eicosatrienoic acid/arachidonic acid] ratio greater than 0.2) occurs in 30%, 66%, 83%,

and 100% of patients after 1, 2, 3, and 4 weeks of fat-free β€œfull-calorie, continuous” PN

(Surgery 1978;84:271-7). Clinical signs and symptoms of EFAD (dry, scaly skin; hair loss;

poor wound healing) usually do not occur until about 2 weeks after biochemical evidence

in adults. Therefore, in most adults, the earliest appearance of EFAD is after about 3 weeks

of fat-free full-calorie continuous PN. Because the investigators initiated ILE soon after the

biochemical appearance of EFAD, only 2 of 32 patients developed clinical evidence suggestive

of EFAD. EFAD can occur much sooner for infants and children. Patients with obesity

receiving hypocaloric high-protein therapy can maintain normal plasma fatty acid profiles for

up to 5 weeks (J Nutr Biochem 1994;5:243-7). Cyclic PN has been suggested to mobilize lipid

from endogenous depots, but conclusive data are lacking and cyclic PN should be avoided in

critically ill patients, as previously discussed.

Serum triglyceride concentration should be monitored at least weekly and more often for those

with proven or suspected impaired triglyceride clearance (consider temporarily withholding

lipid emulsion when serum triglyceride approaches or exceeds 400 mg/dL) (Nutr Clin Pract

2020;35:769-82).

vi.

Predisposing conditions that may result in impaired clearance of triglycerides:

(a)Excessive lipid intake (propofol and clevidipine are 2 drugs commonly used in the ICU

setting that contain lipids within their preparation. Propofol is a 10% emulsion containing

1.1 kcal/mL, and clevidipine is a 20% emulsion containing 2 kcal/mL)

(b)Acute pancreatitis
(c)Uncontrolled diabetes
(d)Liver failure
(e)Kidney failure (decreased lipoprotein lipase activity, carnitine deficiency with long-term

hemodialysis patients)

(f)End-stage sepsis (multisystem organ failure)
(g)History of hyperlipidemia
(h)Obesity
(i)HIV (occurred even before current antiretroviral therapy) (Am J Med 1989;86:27-31)
(j)Pregnancy
(k)Small-for-gestational-age neonates (carnitine synthesis is maturational-dependent)

Electrolyte requirements (see the Fluids and Electrolytes section)

When initiating nutrition, particularly in patients with prolonged malnutrition and at

high nutrition risk, the occurrence of profound electrolyte abnormalities (hypokalemia,

hypomagnesemia, and hypophosphatemia) typically reflects refeeding syndrome. To prevent

refeeding syndrome, consider initiating nutrition at hypocaloric doses and titrating toward goal

over 1 to 3 days. If a patient experiences refeeding syndrome, recommendations are to slow the

rate of feeding and aggressively replete electrolytes according to guideline recommendations.

Vitamins

One full dose of multiple vitamins for infusion (i.e., 10 mL/day) should be included in every

bag of PN with few exceptions.

ii.

Conservative supplementation doses (i.e., higher than basal needs to replace losses) of certain

vitamins may be safely added to most PN admixtures (e.g. thiamine or folic acid).

iii.

Repletion doses of vitamins (i.e., to correct a known deficiency) should be provided separately

from the PN admixture because of numerous possible interactions affecting compatibility and

stability of the admixture (JPEN J Parenter Enteral Nutr 2022;46:273-99).

Trace minerals

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