Darbepoetin, effective treatment of anaemia in paediatric patients with chronic renal failure |
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Authors: | Jean-Luc André Georges Deschênes Bernard Boudailliez Françoise Broux Michel Fischbach Marie-France Gagnadoux Benjamin Horen Annie Lahoche-Manucci Marie-Alice Macher Bernard Roussel Michel Tsimaratos Chantal Loirat |
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Affiliation: | 1. Pediatric Nephrology Unit, H?pital d’Enfants, CHU de Nancy, Rue du Morvan, 54511, Vandoeuvre les Nancy, France 2. Pediatric Nephrology Unit, Assistance Publique-H?pitaux de Paris, H?pital Trousseau, 75012, Paris, France 3. Pediatric 1, H?pital Nord, CHU, 80030, Amiens, France 4. Pediatric Nephrology Unit-CHU, Hopital Charles Nicolle, 76031, Rouen, France 5. Pediatric 1, Hopital de Hautepierre-CHU, 67098, Strasbourg, France 6. Pediatric Nephrology Unit, Assistance Publique-H?pitaux de Paris, H?pital Necker-Enfants Malades, 75743, Paris, France 7. Pediatric Nephrology Unit, Hópital des Enfants-CHU, 31026, Toulouse, France 8. Pediatric Nephrology Unit, Hópital Jeanne de Flandre-CHU, 59037, Lille, France 9. Pediatric Nephrology Unit, Assistance Publique-H?pitaux de Paris, H?pital Robert Debré, 75019, Paris, France 10. Pediatric Nephrology Unit, American Memorial Hospital-CHU, 51092, Reims, France 11. Pediatric Nephrology Unit, Assistance Publique-H?pitaux de Marseille, H?pital de la Timone-Enfants, Marseille, France
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Abstract: | Darbepoetin alfa (DA) is a unique long-acting treatment for anaemia in patients with chronic renal failure (CRF). This study assessed the mean dose of DA to achieve and maintain haemoglobin (Hb) levels between 11 g/dl and 13 g/dl in CRF children aged 11 years to 18 years. This observational, prospective study was conducted in 39 patients treated with DA. Twenty-nine patients were switched from recombinant human erythropoietin (r-HuEPO), and ten patients were naive to r-HuEPO. Naive patients received initial doses of 0.45 μg/kg of DA. Switched patients received a dose adjusted to the prior dose of r-HuEPO (200 IU r-HuEPO:1 μg DA). Among the switched patients, 79.3% received dialysis. No naive patients underwent dialysis. Overall, 74% of patients showed increased Hb level, with a mean value of 11.6 ± 1.6 g/dl, using a mean DA dose of 0.63 ± 0.48 μg/kg per week, and 66.7% patients reached the target Hb level. Hb increased in naive patients from 9.5 (95% CI: 7.7, 11.4) to 11.7 (95% CI: 10.9, 12.6) g/dl and in switched patients from 11.1 (95% CI: 10.6, 11.5) to 11.5 (95% CI: 10.8, 12.2) g/dl). Higher doses of DA were needed in the “switched” than in the “naive” patients to maintain Hb levels over 11 g/dl, respectively 0.73 (95% CI: 0.54, 0.92) and 0.34 (95% CI: 0.16, 0.52) μg/kg per week. Our results indicate the doses of DA necessary to treat CRF patients aged 11 years to 18 years. DA was an effective treatment to stabilise CRF patients at extended dosing intervals. A prospective observational study, on behalf of the French Society for Pediatric Nephrology. Preliminary results of this study were published in part as an abstract and presented as a poster at the European Society of Pediatric Nephrology in Istanbul 11–13 September 2005 and at the ASN Renal Week in Philadelphia (Pennsylvania) 8–13 November 2005. |
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Keywords: | Darbepoetin alfa Paediatrics Chronic kidney disease Anaemia r-HuEPO Dialysis Haemoglobin Chronic renal failure |
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