Abstract
Background: Anaemia correction in patients with end-stage renal disease has been enhanced following the use of epoetin alfa or beta and there are a number of studies detailing its application. Dialysis centres are dealing with greater numbers of elderly patients and anaemia correction in these individuals may differ by virtue of co-existing comorbidity and their age.
Objective: The aim of this study was to examine the response of the elderly patients to anaemia correction using a locally devised anaemia correction protocol while receiving dialysis.
Methods: An incident, non-randomised, cohort observational study in a single centre was used to compare the correction of anaemia in a population of elderly (≥65 years of age) and young dialysis patients. All incident patients starting peritoneal dialysis and haemodialysis (HD) between January 1998 and December 2000 were selected and treated using a locally devised anaemia correction protocol and observed for at least 1 year. Anaemia correction following adjustments for factors such as age, comorbidity, dialysis type, dialysis access type and predialysis nephrological care was assessed.
Results: 198 patients commenced dialysis with 86 elderly patients (mean age ± SD 73.7 ± 4.9 years). The elderly patients had similar periods of predialysis nephrological care as the younger patients. Most patients received HD and required a tunnelled dialysis catheter (TC) as vascular access. Equivalent numbers of elderly patients received peritoneal dialysis. Comorbid scores were greater in the elderly and patient survival was dependent upon these comorbid factors. Following the strict use of TCs, patient survival was similar to those patients commencing HD with arterio-venous fistulae.
Anaemia correction in the elderly was similar to the younger patients, with a median haemoglobin of 11.3 g/dL. By 6 months of dialysis, most patients achieved the UK Renal Association anaemia correction standard (haemoglobin above10 g/dL). The elderly patients maintained significantly higher serum ferritin levels throughout (median 209 µg/L) and required less epoetin alfa or beta (median 91.6 units/kg/wk), indicating that functional iron deficiency in the elderly dialysis patients is less. Intravenous iron sucrose doses were similar in both age groups and iron overload (serum ferritin above 800 µg/L) had been avoided following the use of the intravenous iron protocol.
Conclusion: The study has noted that elderly patients responded to anaemia corrective therapies as well as the younger patients, despite greater levels of comorbidity while requiring less epoetin alfa or beta.
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References
Ansell D, Feest T. The fifth annual report: the UK renal registry, 2002. Renal Registry, editor. Bristol: Renal Registry, 2002
National Institutes of Health, National Institutes of Diabetes and Digestive and Kidney Diseases. USRDS 2002 annual data report [online]. Available from URL: http://www.usrds.org [Accessed 2004 Feb 2]
Australia and New Zealand Dialysis and Transplant Registry (ANZDATA). 25th Report of the Australia and New Zealand Dialysis and Transplant Registry (ANZDATA). Woodville (SA): ANZDATA; 2002 Jan 1
Moreno F, Aracil FJ, Perez R, et al. Controlled study on the improvement of quality of life in elderly hemodialysis patients after correcting end-stage renal disease-related anemia with erythropoietin. Am J Kid Dis 1996; 27(4): 548–56
Royal College of Physicians of London and the Renal Association, Standards Subcommittee of the Renal Association. Treatment of adult patients with renal failure: recommended standards and audit measures. 2nd ed. London: Royal College of Physicians of London and the Renal Association, 1997
Khan IH, Catto GR, Edward N, et al. Influence of coexisting disease on survival on renal-replacement therapy. Lancet 1993; 341(8842): 415–8
Jacobs C, Horl WH, Macdougall IC, et al. European best practice guidelines 5: target haemoglobin. Nephrol Dial Transplant 2000; 15Suppl. 4: 15–9
Kalantar-Zadeh K, Don B, Rodriguez R, et al. Serum ferritin is a marker of morbidity and mortality in hemodialysis patients. Am J Kidney Dis 2001; 37(3): 564–72
Foley RN, Parfrey PS, Morgan J, et al. Effect of hemoglobin levels in hemodialysis patients with asymptomatic cardiomyopathy. Kidney Int 2000; 58(3): 1325–35
Collins AJ, Ma JZ, Ebben J. Impact of hematocrit on morbidity and mortality. Semin Nephrol 2000; 20(4): 345–9
Besarab A, Bolton WK, Browne JK, et al. The effects of normal as compared with low hematocrit values in patients with cardiac disease who are receiving hemodialysis and epoetin [abstract]. N Engl J Med 1998; 339(9): 584
Furuland H, Linde T, Ahlmen J, et al. A randomized controlled trial of haemoglobin normalization with epoetin alfa in predialysis and dialysis patients. Nephrol Dial Transplant 2003; 18(2): 353–61
Jungers P, Massy ZA, Nguyen-Khoa T, et al. Longer duration of predialysis nephrological care is associated with improved long-term survival of dialysis patients. Nephrol Dial Transplant 2001; 16(12): 2357–64
Roderick P, Jones C, Drey N, et al. Late referral for end-stage renal disease: a region-wide survey in the south west of England. Nephrol Dial Transplant 2002; 17(7): 1252–9
Levin A. Consequences of late referral on patient outcomes. Nephrol Dial Transplant 2000; 15(90003): 8–13
Astor BC, Eustace JA, Powe NR, et al. Timing of nephrologist referral and arteriovenous access use: the CHOICE Study. Am J Kidney Dis 2001; 38(3): 494–501
Combe C, Pisoni RL, Port FK, et al. Dialysis outcomes and practice patterns study: data on the use of central venous catheters in chronic hemodialysis. Nephrologie 2001; 22(8): 379–84
Xue J, St Peter W, Ebben J, et al. Anemia treatment in the pre-ESRD period and associated mortality in elderly patients. Am J Kidney Dis 2002; 40(6): 1153–61
Jungers PY, Robino C, Choukroun G, et al. Incidence of anaemia, and use of epoetin therapy in pre-dialysis patients: a prospective study in 403 patients. Nephrol Dial Transplant 2002; 17(9): 1621–7
Macdougall IC. CREATE: new strategies for early anaemia management in renal insufficiency. CREATE Study Group. Nephrol Dial Transplant 2003; 18Suppl. 2: 13–6
McMahon LP, Mason K, Skinner SL, et al. Effects of haemoglobin normalization on quality of life and cardiovascular parameters in end-stage renal failure. Nephrol Dial Transplant 2000; 15(9): 1425–30
Weiss LG, Clyne N, Divino FJ, et al. The efficacy of once weekly compared with two or three times weekly subcutaneous epoetin beta: results from a randomized controlled multi-centre trial: Swedish Study Group. Nephrol Dial Transplant 2000; 15(12): 2014–9
Locatelli F, Baldamus CA, Villa G, et al. Once-weekly compared with three-times-weekly subcutaneous epoetin beta: results from a randomized, multicenter, therapeutic-equivalence study. Am J Kidney Dis 2002; 40(1): 119–25
Jones CH, Richardson D. Which EPO dose per week [letter]? Nephrol Dial Transplant 2002; 17(10): 1855
Macdougall IC. An overview of the efficacy and safety of novel erythropoiesis stimulating protein (NESP). Nephrol Dial Transplant 2001; 16Suppl. 3: 14–21
Locatelli F, Olivares J, Walker R, et al. Novel erythropoiesis stimulating protein for treatment of anemia in chronic renal insufficiency. Kidney Int 2001; 60(2): 741–7
Casadevall N, Nataf J, Viron B, et al. Pure red-cell aplasia and antierythropoietin antibodies in patients treated with recombinant erythropoietin. N Engl J Med 2002; 346(7): 469–75
Horl WH, Cavill I, Macdougall IC, et al. How to diagnose and correct iron deficiency during r-huEPO therapy: a consensus report. Nephrol Dial Transplant 1996; 11(2): 246–50
Macdougall IC. Poor response to erythropoietin: practical guidelines on investigation and management. Nephrol Dial Transplant 1995; 10(5): 607–14
Macdougall IC, Tucker B, Thompson J, et al. A randomized controlled study of iron supplementation in patients treated with erythropoietin. Kidney Int 1996; 50(5): 1694–9
Taylor JE, Peat N, Porter C, et al. Regular low-dose intravenous iron therapy improves response to erythropoietin in haemodialysis patients. Nephrol Dial Transplant 1996; 11(6): 1079–83
Fishbane S, Kowalski EA. The comparative safety of intravenous iron dextran, iron saccharate, and sodium ferric gluconate. Semin Dial 2000; 13(6): 381–4
Macdougall IC, Chandler G, Elston O, et al. Beneficial effects of adopting an aggressive intravenous iron policy in a hemodialysis unit. Am J Kidney Dis 1999; 34 (4 Suppl. 2): S40–6
Kletzmayr J, Horl WH. Iron overload and cardiovascular complications in dialysis patients. Nephrol Dial Transplant 2002; 17Suppl. 2: 25–9
Parkkinen J, von Bonsdorff L, Peltonen S, et al. Catalytically active iron and bacterial growth in serum of haemodialysis patients after i.v. iron-saccharate administration. Nephrol Dial Transplant 2000; 15(11): 1827–34
Patruta SI, Edlinger R, Sunder-Plassmann G, et al. Neutrophil impairment associated with iron therapy in hemodialysis patients with functional iron deficiency. J Am Soc Nephrol 1998; 9(4): 655–63
Drueke T, Witko-Sarsat V, Massy Z, et al. Iron therapy, advanced oxidation protein products, and carotid artery intimamedia thickness in end-stage renal disease. Circulation 2002; 106(17): 2212–7
Kaltwasser JP, Werner E, Becker H. Serum ferritin as a control parameter for oral iron therapy. Dtsch Med Wochenschr 1977; 102(32): 1150–5
Kaltwasser JP, Gottschalk R. Erythropoietin and iron. Kidney Int 1999; 69 Suppl.: 49–56
NKF-K/DOQI clinical practice guidelines for anemia of chronic kidney disease: update 2000 [online]. Available from URL: http://www.kidney.org/professionals/Kdoqi/index.cfm [Accessed 2004 Feb 13]
Macdougall IC. What is the most appropriate strategy to monitor functional iron deficiency in the dialysed patient on rhEPO therapy: merits of percentage hypochromic red cells as a marker of functional iron deficiency. Nephrol Dial Transplant 1998; 13(4): 847–9
Tessitore N, Solero GP, Lippi G, et al. The role of iron status markers in predicting response to intravenous iron in haemodialysis patients on maintenance erythropoietin. Nephrol Dial Transplant 2001; 16(7): 1416–23
Brugnara C. A hematologic “gold standard” for iron-deficient states? Clin Chem 2002; 48(7): 981–2
Jones CH, Richardson D, Ayers S, et al. Percentage hypochromic red cells and the response to intravenous iron therapy in anaemic haemodialysis patients. Nephrol Dial Transplant 1998; 13(11): 2873–6
Mast AE, Blinder MA, Lu Q, et al. Clinical utility of the reticulocyte hemoglobin content in the diagnosis of iron deficiency. Blood 2002; 99(4): 1489–91
Fishbane S, Galgano C, Langley Jr RC, et al. Reticulocyte hemoglobin content in the evaluation of iron status of hemodialysis patients. Kidney Int 1997; 52(1): 217–22
Acknowledgements
This is a paper discussing the practical issues in managing anaemia associated with chronic renal failure in elderly patients. This is an original piece of work conducted in a single centre and no conflicts of interest exist. The results of this paper have not been partially or completely published other than in abstract form.
I would like to thank all my colleagues and staff in the Renal Unit in New Cross Hospital, Wolverhampton, UK for all the support in collating information for this paper over the years. Additional thanks to Dr D. Leung whose comments and assistance were greatly appreciated in preparing this paper.
The authors have provided no information on sources of funding directly relevant to the content of this study.
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Nicholas, J.C.B. A Study of the Response of Elderly Patients with End-Stage Renal Disease to Epoetin Alfa or Beta. Drugs Aging 21, 187–201 (2004). https://doi.org/10.2165/00002512-200421030-00004
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DOI: https://doi.org/10.2165/00002512-200421030-00004