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Laboratory Monitoring of Parenteral Nutrition‐Associated Hepatic Dysfunction in Infants
Author(s) -
Vileisis Rita A.,
Inwood Richard J.,
Hunt Carl E.
Publication year - 1981
Publication title -
journal of parenteral and enteral nutrition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.935
H-Index - 98
eISSN - 1941-2444
pISSN - 0148-6071
DOI - 10.1177/014860718100500167
Subject(s) - bilirubin , alkaline phosphatase , cholestasis , hepatic dysfunction , transaminase , medicine , parenteral nutrition , gastroenterology , jaundice , direct bilirubin , serum bilirubin , alanine transaminase , endocrinology , chemistry , biochemistry , enzyme
Hepatic dysfunction associated with parenteral nutrition (PN) is a well recognized occurrence. In order to define the temporal inter‐relationships of direct bilirubin to other laboratory parameters, total and direct bilirubin, serum glutamic‐pyruvic transaminase (SGPT), serum glutamic‐oxaloacetic transaminase (SGOT), and alkaline phosphatase were measured prior to beginning PN and then weekly throughout the duration of PN in 60 consecutive neonates. Cholestatic jaundice (ChJ), defined as a direct bilirubin ≥2.0 mg/dl, developed in 11 (33%) of 33 infants receiving PN for at least 2 weeks. Direct bilirubin was the most sensitive and earliest indicator of ChJ. SGOT and SGPT values in the ChJ group were not statistically different from the non‐ChJ group until 2 weeks after the onset of cholestasis. Although there was a progressive increase in alkaline phosphatase during the course of PN, the increase was not greater in the ChJ group. In summary, direct bilirubin is the only laboratory indicator of hepatic status that need be determined serially in parenterally alimented infants. Although SGPT and SGOT may be helpful in characterizing hepatic dysfunction once ChJ has occurred, alkaline phosphatase levels do not reliably assess PN‐associated liver injury.