Serum bilirubin levels and mortality after myeloablative allogeneic hematopoietic cell transplantation

被引:44
作者
Gooley, TA
Rajvanshi, P
Schoch, HG
McDonald, GB
机构
[1] Fred Hutchinson Canc Res Ctr, Gastroenterol Hepatol Sect, Div Clin Res, Seattle, WA 98109 USA
[2] Fred Hutchinson Canc Res Ctr, Sect Clin Stat, Div Clin Res, Seattle, WA 98109 USA
[3] Univ Washington, Sch Med, Seattle, WA 98195 USA
关键词
D O I
10.1002/hep.20529
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Many patients who undergo hematopoietic cell transplantation experience liver injury. We examined the association of serum bilirubin levels with nonrelapse mortality by day +200, testing the hypothesis that the duration of jaundice up to a given point in time provides more prognostic information than either the maximum bilirubin value or the value at that point in time. We studied 1,419 consecutive patients transplanted from allogeneic donors. Total serum bilirubin values up to day +100, death, or relapse were retrieved - along with nonrelapse mortality by day +200 as an outcome measure - using Cox regression models with each bilirubin measure modeled as a time-dependent covariate. The bilirubin value at a particular point in time provided the best fit to the model for mortality. With bilirubin at a point in time modeled as an 8th-degree polynomial, an increase in bilirubin from I to 3 mg/dL is associated with a mortality hazard ratio of 6.42. An increase from 4 to 6 mg/dL yields a hazard ratio of 2.05, and an increase from 10 to 12 mg/dL yields a hazard ratio of 1.17. Among patients who were deeply jaundiced, survival was related to the absence of multiorgan failure and to higher platelet counts. In conclusion, the value of total serum bilirubin at a particular point in time after transplant carries more informative prognostic information than does the maximum or average value up to that point in time. The increase in mortality for a given increase in bilirubin value is larger when the starting value is lower.
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页码:345 / 352
页数:8
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共 48 条
  • [41] Hepatitis C virus infection and bone marrow transplantation: A cohort study with 10-year follow-up
    Strasser, SI
    Myerson, D
    Spurgeon, CL
    Sullivan, KM
    Storer, B
    Schoch, HG
    Kim, S
    Flowers, MED
    McDonald, GB
    [J]. HEPATOLOGY, 1999, 29 (06) : 1893 - 1899
  • [42] Chronic graft-versus-host disease of the liver: Presentation as an acute hepatitis
    Strasser, SI
    Shulman, HM
    Flowers, ME
    Reddy, K
    Margolis, DA
    Prumbaum, M
    Seropian, SE
    McDonald, GB
    [J]. HEPATOLOGY, 2000, 32 (06) : 1265 - 1271
  • [43] STRASSER SI, 2003, SCHIFFS DIS LIVER, P1636
  • [44] Mesenteric vasoconstriction triggers nitric oxide overproduction in the superior mesenteric artery of portal hypertensive rats
    Tsai, MH
    Iwakiri, Y
    Cadelina, G
    Sessa, WC
    Groszmann, RJ
    [J]. GASTROENTEROLOGY, 2003, 125 (05) : 1452 - 1461
  • [45] The effect of prophylactic fluconazole on the clinical spectrum of fungal diseases in bone marrow transplant recipients with special attention to hepatic candidiasis - An autopsy study of 355 patients
    van Burik, JAH
    Leisenring, W
    Myerson, D
    Hackman, RC
    Shulman, HM
    Sale, GE
    Bowden, RA
    McDonald, GB
    [J]. MEDICINE, 1998, 77 (04) : 246 - 254
  • [46] Bacterial translocation up-regulates GTP-cyclohydrolase I in mesenteric vasculature of cirrhotic rats
    Wiest, R
    Cadelina, G
    Milstien, S
    McCuskey, RS
    Garcia-Tsao, G
    Groszmann, RJ
    [J]. HEPATOLOGY, 2003, 38 (06) : 1508 - 1515
  • [47] The paradox of nitric oxide in cirrhosis and portal hypertension: Too much, not enough
    Wiest, R
    Groszmann, RJ
    [J]. HEPATOLOGY, 2002, 35 (02) : 478 - 491
  • [48] ACUTE-RENAL-FAILURE IN THE SETTING OF BONE-MARROW TRANSPLANTATION
    ZAGER, RA
    MADIAS, NE
    HARRINGTON, JT
    SINGH, A
    PERRONE, R
    KING, A
    LAFAYETTE, R
    NATOV, SN
    [J]. KIDNEY INTERNATIONAL, 1994, 46 (05) : 1443 - 1458