Transplantation Proceedings
Volume 36, Issue 5 , Pages 1293-1296, June 2004

Pilot study of the optimum hematocrit for patients in the predialysis stage after renal transplantation

  • T Kawaguchi

      Affiliations

    • Department of Urology (T.K., K.S., M.H., T.T., H.Y.), Gunma University School of Medicine, Gunma, Japan
  • ,
  • T Moriyama

      Affiliations

    • Department of Internal Medicine and Therapeutics (T.M.), Osaka University Graduate School of Medicine, Osaka, Japan
    • Corresponding Author InformationAddress reprint requests to Dr Toshiki Moriyama, MD, PhD, Department of Medical Science II, School of Health and Sport Sciences, Osaka 560-0043, Japan
  • ,
  • K Suzuki

      Affiliations

    • Department of Urology (T.K., K.S., M.H., T.T., H.Y.), Gunma University School of Medicine, Gunma, Japan
  • ,
  • M Hatori

      Affiliations

    • Department of Urology (T.K., K.S., M.H., T.T., H.Y.), Gunma University School of Medicine, Gunma, Japan
  • ,
  • T Tanaka

      Affiliations

    • Department of Urology (T.K., K.S., M.H., T.T., H.Y.), Gunma University School of Medicine, Gunma, Japan
  • ,
  • S Takahara

      Affiliations

    • Department of Urology (S.T.), Osaka University Graduate School of Medicine, Osaka, Japan
  • ,
  • H Yamanaka

      Affiliations

    • Department of Urology (T.K., K.S., M.H., T.T., H.Y.), Gunma University School of Medicine, Gunma, Japan

Abstract 

Anemia is a common complication in patients with chronic kidney diseases including posttransplant patients. Guidelines for the treatment of anemia in chronic kidney disease published by NHF-K/DOQI recommend the target hemoglobin and hematocrit (Hb and Ht) levels to be in the 11 to 12 g/dL and 33% to 36% ranges, respectively, which are somewhat higher than those recommended in Japan (Ht = 30%). However, these guidelines were established mainly from the data on hemodialysis patients with only limited information available as to the impact of anemia control in posttransplant patients. The aim of the present study was to evaluate cardiac function and quality of life (QOL) when the Ht was raised to about 36% by administration of recombinant-human-erythropoietin (rHuEPO) to patients with mild impairment of renal function (s-Cre < 2.0 mg/dL) after renal transplantation. Twenty-five patients were analyzed for cardiac function, blood data, and QOL in a prospective study encompassing 8 months of rHuEPO treatment. Using a once weekly subcutaneous dose of 6000 IU of Epoetin-β, the Ht became 33% to 36% and Hb was 11 to 12 g/dL. Among the cardiac function tests, left ventricular end-diastolic diameter and left ventricular mass index decreased significantly. QOL did not show any significant changes after administration of rHuEPO. In conclusion, we demonstrated a potential benefit of using rHuEPO to maintain the Hb between 11 and 12 g/dL and the Ht between 33% and 36% in posttransplant patients with regard to the prevention of cardiovascular complications. Further study is required to establish the benefits of correcting anemia by rHuEPO on the outcome of posttransplant patients.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0041-1345(04)00521-4

doi:10.1016/j.transproceed.2004.04.089

Transplantation Proceedings
Volume 36, Issue 5 , Pages 1293-1296, June 2004