Safety and efficacy of sodium ferric gluconate complex in patients with chronic kidney disease

被引:16
作者
Panesar, A
Agarwal, R
机构
[1] Indiana Univ, Sch Med, Indianapolis, IN 46202 USA
[2] Richard L Roudebush Vet Affairs Med Ctr, Indianapolis, IN 46202 USA
关键词
chronic kidney disease (CKD); anemia; iron deficiency; parenteral iron; time-to-event analysis; sodium ferric gluconate in sucrose (SFGC);
D O I
10.1053/ajkd.2002.36322
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
Background: We hypothesized that intravenous iron will improve hemoglobin (Hgb) concentrations in anemic patients with chronic kidney disease (CKD), and the response would be greater if the underlying erythropoietin deficiency also was treated. Methods: Charts of 58 CKD veterans (glomerular filtration rate<80 mL/min) administered at least 125 mg of sodium ferric gluconate complex in sucrose (SFGC) during a period of 1 year for the primary outcome of an increase in Hgb level by at least 0.5 g/dL were reviewed. Results: Mean Hgb level at baseline was 10.5 +/- 1.4 (SD) g/dL (105 +/- 14 g/L) in the 30 patients administered recombinant human erythropoietin (rHuEPO) plus SFGC and 10.1 +/- 1.3 g/dL (101 +/- 13 g/L) in the 28 patients administered SFGC alone (P=not significant). The primary event occurred in 83% of the rHuEPO-plus-SFGC group at 31 days compared with 60% at 62 days in the group administered SFGC alone (P=0.037, Cox F test). In patients administered SFGC alone, mean maximal Hgb level was 11.4 +/- 0.9 g/dL (114 +/- 9 g/L) in contrast to 12.4 +/- 1.7 g/dL (124 +/- 17 g/L) in the combination group, which remained significantly different even after adjustment for biologically important covariates (P=0.01, analysis of covariance). Of the 240 doses of SFGC administered for which infusion records were available, 237 doses were well tolerated; three hypotensive episodes occurred in 2 patients, which did not result in discontinuation of the drug in either case. Conclusion: Correction of anemia with parenteral iron alone suggests a high prevalence of iron deficiency in patients with CKD. Treatment of concomitant iron deficiency with SFGC was well tolerated in patients with CKD and appears to optimize management of anemia.
引用
收藏
页码:924 / 931
页数:8
相关论文
共 34 条
  • [1] AKMAL M, 1994, CLIN NEPHROL, V42, P198
  • [2] [Anonymous], 2001, Am J Kidney Dis, V37, pS182
  • [3] AUERBACH M, 1988, J LAB CLIN MED, V111, P566
  • [4] Parenteral iron use in the management of anemia in end-stage renal disease patients
    Bailie, GR
    Johnson, CA
    Mason, NA
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2000, 35 (01) : 1 - 12
  • [5] IRON METABOLISM IN PATIENTS WITH CHRONIC RENAL FAILURE
    BODDY, K
    LAWSON, DH
    LINTON, AL
    WILL, G
    [J]. CLINICAL SCIENCE, 1970, 39 (01) : 115 - &
  • [6] Intravenous iron sucrose: Establishing a safe dose
    Chandler, G
    Harchowal, J
    Macdougall, IC
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 38 (05) : 988 - 991
  • [7] Efficacy and safety of iron sucrose for iron deficiency in patients with dialysis-associated anemia: North American clinical trial
    Charytan, C
    Levin, N
    Al-Saloum, M
    Hafeez, T
    Gagnon, S
    Van Wyck, DB
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 37 (02) : 300 - 307
  • [8] Intravenous iron dextran treatment in predialysis patients with chronic renal failure
    Dahdah, K
    Patrie, JT
    Bolton, WK
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2000, 36 (04) : 775 - 782
  • [9] IRON-ABSORPTION IN EXPERIMENTAL UREMIA
    DELANO, BG
    MANIS, JG
    MANIS, T
    [J]. NEPHRON, 1977, 19 (01): : 26 - 31
  • [10] Drueke TB, 1997, CLIN NEPHROL, V48, P1