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    0270-9139/85/0501-0079 02.00/0

    HEPATOLOGY

    Copyright 1985 by the American Association for the Study of Liver Diseases

    Vol. 5,No. ,pp. 79-84, 1985

    Printed in

    U.S A

    Test

    attern and Prognosis

    of

    Liver Function

    Abnormalities During Parenteral Nutrition in

    Inflammatory

    Bowel

    Disease

    JOSE . BENGOA,?TEPHEN

    .

    HANAUER, ICHAEL

    .

    SITRIN,

    ALFRED

    L. BAKER

    N D

    IRWIN . ROSENBERG

    Nutritio n Support Service and Liver Stu dy Unit Section of Gastroenterology Department of

    Medicine Th e University of Chicago Hosp itals and Clinics Chicago Illinois

    60637

    The pat tern of liver function

    test

    abnormalities was examined duri ng total parent era l nutrition

    (TPN), using both dextrose and fa t emulsions as caloric sources, in 92 patients with inflammatory

    bowel disease. Seventy-two patient s had completely normal tests before TPN while

    20

    had one

    or

    more abnormal liver function tests before TPN was started. Serum bilirubin levels were normal

    in

    all

    patients before TPN; w ithin 2 weeks

    on

    TPN, 25 of patient s had elevated bilirub in levels.

    Serum alkaline phosphatase rose to values above normal in 25 of patients with normal sta rti ng

    values but did not change in those with abnormal baseline liver function

    tests.

    Elevations of SGPT

    were characteristically more pronounced than were elevation of SGOT. After 2 weeks of TPN,

    mean serum SGOT rose from 15 to 26 IU per liter (p c 0.01) in patients with normal baseline

    values and from 28 to 50 IU per lit er in those with abnormal baseline values. Elevations of serum

    SGPT were most common, affecting 25 of patients with normal baseline. The mean SGPT value

    rose from 13 to 38 IU per

    liter

    (p < 0.01) at week of TPN. In patients with abnormal tests before

    TPN, the mean SGPT value rose from 45 to 102 IU per liter (p < 0.06). Liver biopsies performed

    in four patients with substantial elevations of aminotransferases revealed only minor nonspecific

    changes and no fatt y infiltration. Elevated liver function tests promptly re turn ed to baseline after

    TPN was discontinued, and progressive liver disease was not observed in any patient. Although

    abnormalities of liver function

    tests,

    particularly the aminotransferases,

    are

    common during

    balanced TP N in patients w ith inflammatory bowel disease, the favorable prognosis a nd benign

    histologic changes argue against th e need to discontinue TPN in the presence of such changes.

    Abnormalities of hepatic function and structure have

    been frequently recognized during total parenteral nutri-

    tion (TPN ) (1,3).Fatty infiltration of the liver has been

    observed mainly in patients receiving infusions with

    large amounts of dextrose as the only caloric source

    1,

    2). Cholestasis has been reported in other patients, par-

    ticularly premature infants (4-7). We have observed that

    patients with inflammatory bowel disease commonly

    show marked elevations of aminotransferase during bal-

    anced TPN in which both dextrose and fat emulsions

    are used as caloric sources. These patients, who often

    Received August

    5,

    1983; accepted Augu st 8, 1984.

    t Present address: Hdpital Cantonal Universitaire, Geneva

    121

    1,

    Switzerland.

    Th is work was supported in part by grants from the USPHS (NIH

    AM26678) Clinical Nutrition R esearch Unit, th e K raft Nu trition Fel-

    lowship (J. M. B.) an d the Beatrice Faculty Scholarship (M.

    D.

    S.).

    Address reprint requests to: Irwin H . Rosenberg,M.D.,he Univer-

    sity of Chicago, Department of Medicine, 950 East 59th Street,

    Box

    400, Chicago, Illinois 60637.

    have underlying hepatic abnormalities complicating their

    inflammatory bowel disease, may represent a patient

    group which is particularly susceptible to detrimental

    effects of TP N on the liver. The purpose of the present

    study was to examine hepatic complications during TPN

    in patients with Crohns disease and ulcerative colitis.

    MATERIALS AND METHODS

    PATIENTOPULATION

    We report a consecutive series of 92 patients with

    inflammatory bowel disease (43 males and 49 females)

    treated with bowel rest and TPN for 10 days or more by

    the Nutrition Support Service from July 1, 1979 to

    December 31, 1981. Sixty-nine patients had Crohns

    disease and 23 had ulcerative colitis as established by

    usual clinical and radiological findings and by histologic

    material in most patients. No patient had symptoms or

    physical findings which suggested the presence

    of

    liver

    disease. During TPN, all patients took nothing

    by

    mouth

    and almost all were on intravenous corticosteroids. Ex-

    79

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    80

    BENGOA

    Er AL. HEPATOLOGY

    cept for antibiotics in occasional patients, no other med-

    ications were prescribed.

    TPN

    TPN was administered through a central vein catheter

    and prescribed according to individual requirements fol-

    lowing a detailed clinical and nutritional evaluation. In

    all cases, the infusions included a combination of carbo-

    hydrate (dextrose, 15 to 25% )and lipid emulsions (Int ra-

    lipid lo , Cutter Laboratories, Inc., Berkeley, Calif.).

    Total calories infused ranged from 30 to

    55

    kcal per kg

    ideal body weight and the percent of calories supplied as

    lipid emulsion accounted for about one-fourth of nonpro-

    tein calories (range, 10 to

    45% ) .

    Crystalline amino acids

    in a 4.25% solution (Freeamine 11, McGaw Laboratories,

    Glendale, Calif. or Travasol, Travenol Laboratories, Inc.,

    Deerfield, Ill.) provided a dose of protein ranging from

    1.0 to 2.0 gm per kg ideal body weight. Electrolytes and

    minerals were included to meet appropriate require-

    ments. Vitamins were added in a standard multivitamin

    solution (MVI concentrate, USV Laboratories, Tucka-

    hoe, NY).

    A

    trace metal additive including manganese,

    copper, chromium and zinc was also used (IMS Ltd.,

    South El Monte, Calif.).

    LIVER UNCTIONESTS

    Routine serum chemistry values and liver function

    tests were obtained on all patients prior to TPN and

    thereafter once weekly until nutrition support was dis-

    continued. A commercial discrete sample analyzer (KDA,

    American Monitor, Indianapolis, Ind.) was used to de-

    termine total bilirubin, alkaline phosphatase, SGOT and

    SGPT. For data analysis, the patients were cansidered

    in two groups: (i)

    72

    patients with completely normal

    liver function tests before TP N, and (ii) 20 patients with

    one or more liver function tests elevated above the nor-

    mal established by the hospital clinical chemistry labo-

    ratory before TPN was administered.

    STATISTICALNALYSIS

    Statistical analysis was performed with the Student's

    paired t test, and

    p

    values less than 0.05 were considered

    significant.

    RESULTS

    There was no significant difference in demographic

    characteristics and parenteral nutrition prescription be-

    tween patients with normal baseline liver function tests

    and patients with one

    or

    several elevated baseline values

    (Table 1) . None of the patients developed symptoms or

    signs suggestive of liver disease such as hepatomegaly or

    right upper quandrant pain and tenderness during the

    period

    of

    TPN. The liver function test abnormalities

    which were observed during TPN did not correlate with

    differences in the administered dose of total calories,

    protein or lipid emulsion.

    TOTAL

    ILIRUBINFIGURE)

    All 92 patients had normal baseline total serum bili-

    rubin levels

    ( 4 . 2

    mg per dl). In the group with normal

    baseline liver function tests, total bilirubin values in-

    creased from a mean (& S.D.) of 0.40 rt 0.20 mg per dl

    before TPN to

    0.74 rt 0.91

    mg per dl after

    2

    weeks of

    TPN (p