A study of parenteral iron regimens in hemodialysis patients

被引:83
作者
Besarab, A [1 ]
Kaiser, JW [1 ]
Frinak, S [1 ]
机构
[1] Henry Ford Hosp, Dept Med, Div Nephrol & Hypertens, Detroit, MI 48202 USA
关键词
intravenous iron therapy; efficacy; kinetics;
D O I
10.1016/S0272-6386(99)70103-4
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
determine the most appropriate intervals for sampling iron parameters during intermittent need-based and continuous maintenance regimens and to quantify differences in efficacy between such regimens during long-term therapy. After a single course of 10 consecutive 100-mg iron doses administered to 14 patients on 16 occasions, transferrin saturation (TSAT) and ferritin were unreliable indices of iron status for the next 2 and 6 weeks, respectively. TSAT and ferritin levels at 1 week were virtually identical to those at 2 weeks after the administration of a single 50-mg or 1 OO-mg iron dextran dose to 16 other patients. Twelve patients on maintenance iron therapy (25 to 100 mg/wk; TSAT, 30% to 50%) had a statistically significant decrease in the amount of recombinant human erythropoietin (rHuEPO) needed to maintain hemoglobin (Hb) levels between 10 and 11 g/dL compared with 12 patients receiving intermittent need-based dosing, an effect that persisted from week 16 to week 72 of the study. Maintenance iron was feasible even in a third group of eight patients targeted to sustain an Hb level of 14 g/dL. In both iron maintenance groups, iron indices could be measured at weekly intervals, and ferritin levels did not progressively increase over time, Continuous maintenance iron dextran used to maintain TSATs of 30% to 50% significantly reduced rHuEPO requirements and resulted in no adverse side effects in chronic hemodialysis patients. After weekly maintenance 25- to 100-mg iron dextran doses, iron indices can be measured after 1 week; a delay of 2 weeks is not necessary. (C) 1999 by the National Kidney Foundation Inc.
引用
收藏
页码:21 / 28
页数:8
相关论文
共 29 条
  • [1] ALI M, 1982, LANCET, V1, P652
  • [2] The effects of normal as compared with low hematocrit values in patients with cardiac disease who are receiving hemodialysis and epoetin
    Besarab, A
    Bolton, WK
    Browne, JK
    Egrie, JC
    Nissenson, AR
    Okamoto, DM
    Schwab, SJ
    Goodkin, DA
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (09) : 584 - 590
  • [3] IRON OVERLOAD IN HEMODIALYSIS-PATIENTS INCREASES THE RISK OF BACTEREMIA - A PROSPECTIVE-STUDY
    BOELAERT, JR
    DANEELS, RF
    SCHURGERS, ML
    MATTHYS, EG
    GORDTS, BZ
    VANLANDUYT, HW
    [J]. NEPHROLOGY DIALYSIS TRANSPLANTATION, 1990, 5 (02) : 130 - 134
  • [4] Collins A., 1998, Journal of the American Society of Nephrology, V9, p204A
  • [5] Collins AJ, 1998, J AM SOC NEPHROL, V9, P2108
  • [6] TREATMENT OF THE ANEMIA OF PROGRESSIVE RENAL-FAILURE WITH RECOMBINANT HUMAN ERYTHROPOIETIN
    ESCHBACH, JW
    KELLY, MR
    HALEY, NR
    ABELS, RI
    ADAMSON, JW
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1989, 321 (03) : 158 - 163
  • [7] RECOMBINANT HUMAN ERYTHROPOIETIN - IMPLICATIONS FOR NEPHROLOGY
    ESCHBACH, JW
    ADAMSON, JW
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 1988, 11 (03) : 203 - 209
  • [8] CORRECTION OF THE ANEMIA OF END-STAGE RENAL-DISEASE WITH RECOMBINANT-HUMAN-ERYTHROPOIETIN - RESULTS OF A COMBINED PHASE-I AND PHASE-II CLINICAL-TRIAL
    ESCHBACH, JW
    EGRIE, JC
    DOWNING, MR
    BROWNE, JK
    ADAMSON, JW
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1987, 316 (02) : 73 - 78
  • [9] ESCHBACH JW, 1989, CONTRIB NEPHROL, V76, P160
  • [10] Fishbane S, 1996, J AM SOC NEPHROL, V7, P2654