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TSAT is a better predictor than ferritin of hemoglobin response to Epoetin alfa in US dialysis patients

Clinical guidelines recommend concurrent treatment of anemia in end-stage renal disease with erythropoiesis-stimulating agents (ESAs) and iron. However, there are mixed data about optimal iron supplementation. To help address this gap, the relationship between iron markers and hemoglobin (Hb) respon...

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Autores principales: Gaweda, Adam E, Bhat, Premila, Maglinte, Gregory A, Chang, Chun-Lan, Hill, Jerrold, Park, Grace S, Ashfaq, Akhtar, Gitlin, Matthew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232318/
https://www.ncbi.nlm.nih.gov/pubmed/23968235
http://dx.doi.org/10.1111/hdi.12078
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author Gaweda, Adam E
Bhat, Premila
Maglinte, Gregory A
Chang, Chun-Lan
Hill, Jerrold
Park, Grace S
Ashfaq, Akhtar
Gitlin, Matthew
author_facet Gaweda, Adam E
Bhat, Premila
Maglinte, Gregory A
Chang, Chun-Lan
Hill, Jerrold
Park, Grace S
Ashfaq, Akhtar
Gitlin, Matthew
author_sort Gaweda, Adam E
collection PubMed
description Clinical guidelines recommend concurrent treatment of anemia in end-stage renal disease with erythropoiesis-stimulating agents (ESAs) and iron. However, there are mixed data about optimal iron supplementation. To help address this gap, the relationship between iron markers and hemoglobin (Hb) response to ESA (Epoetin alfa) dose was examined. Electronic medical records of 1902 US chronic hemodialysis patients were analyzed over a 12-month period between June 2009 and June 2010. The analysis included patients who had at least one Hb value during each 4-week interval for four consecutive intervals (k − 2, k − 1, k, and k + 1; k is the index interval), received at least one ESA dose during intervals k − 1 or k, had at least one transferrin saturation (TSAT) value at interval k, and at least one ferritin value during intervals k − 2, k − 1, or k. Effect modification by TSAT and ferritin on Hb response was evaluated using the generalized estimating equations approach. Patients had a mean (standard deviation) age of 62 (15) years; 41% were Caucasian, 34% African American, 65% had hypertension, and 39% diabetes. Transferrin saturation, but not ferritin, had a statistically significant (P < 0.05) modifying effect on Hb response. Maximum Hb response was achieved when TSAT was 34%, with minimal incremental effect beyond these levels. Of the two standard clinical iron markers, TSAT should be used as the primary marker of the modifying effect of iron on Hb response to ESA. Long-term safety of iron use to improve Hb response to ESA warrants further study.
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spelling pubmed-42323182014-12-15 TSAT is a better predictor than ferritin of hemoglobin response to Epoetin alfa in US dialysis patients Gaweda, Adam E Bhat, Premila Maglinte, Gregory A Chang, Chun-Lan Hill, Jerrold Park, Grace S Ashfaq, Akhtar Gitlin, Matthew Hemodial Int Original Articles Clinical guidelines recommend concurrent treatment of anemia in end-stage renal disease with erythropoiesis-stimulating agents (ESAs) and iron. However, there are mixed data about optimal iron supplementation. To help address this gap, the relationship between iron markers and hemoglobin (Hb) response to ESA (Epoetin alfa) dose was examined. Electronic medical records of 1902 US chronic hemodialysis patients were analyzed over a 12-month period between June 2009 and June 2010. The analysis included patients who had at least one Hb value during each 4-week interval for four consecutive intervals (k − 2, k − 1, k, and k + 1; k is the index interval), received at least one ESA dose during intervals k − 1 or k, had at least one transferrin saturation (TSAT) value at interval k, and at least one ferritin value during intervals k − 2, k − 1, or k. Effect modification by TSAT and ferritin on Hb response was evaluated using the generalized estimating equations approach. Patients had a mean (standard deviation) age of 62 (15) years; 41% were Caucasian, 34% African American, 65% had hypertension, and 39% diabetes. Transferrin saturation, but not ferritin, had a statistically significant (P < 0.05) modifying effect on Hb response. Maximum Hb response was achieved when TSAT was 34%, with minimal incremental effect beyond these levels. Of the two standard clinical iron markers, TSAT should be used as the primary marker of the modifying effect of iron on Hb response to ESA. Long-term safety of iron use to improve Hb response to ESA warrants further study. BlackWell Publishing Ltd 2014-01 2013-08-22 /pmc/articles/PMC4232318/ /pubmed/23968235 http://dx.doi.org/10.1111/hdi.12078 Text en © 2013 The Authors. Hemodialysis International published by Wiley Periodicals, Inc. on behalf of International Society for Hemodialysis. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Gaweda, Adam E
Bhat, Premila
Maglinte, Gregory A
Chang, Chun-Lan
Hill, Jerrold
Park, Grace S
Ashfaq, Akhtar
Gitlin, Matthew
TSAT is a better predictor than ferritin of hemoglobin response to Epoetin alfa in US dialysis patients
title TSAT is a better predictor than ferritin of hemoglobin response to Epoetin alfa in US dialysis patients
title_full TSAT is a better predictor than ferritin of hemoglobin response to Epoetin alfa in US dialysis patients
title_fullStr TSAT is a better predictor than ferritin of hemoglobin response to Epoetin alfa in US dialysis patients
title_full_unstemmed TSAT is a better predictor than ferritin of hemoglobin response to Epoetin alfa in US dialysis patients
title_short TSAT is a better predictor than ferritin of hemoglobin response to Epoetin alfa in US dialysis patients
title_sort tsat is a better predictor than ferritin of hemoglobin response to epoetin alfa in us dialysis patients
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4232318/
https://www.ncbi.nlm.nih.gov/pubmed/23968235
http://dx.doi.org/10.1111/hdi.12078
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