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Roxadustat for treatment of erythropoietin-hyporesponsive anemia in a hemodialysis patient: A case report
BACKGROUND: Hyporesponsiveness to erythropoiesis-stimulating agents (ESAs) is a prevalent problem in patients with chronic kidney disease. It is associated with increased morbidity and mortality in patients who undergo dialysis. A significant proportion of patients do not respond to iron supplementa...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7723725/ https://www.ncbi.nlm.nih.gov/pubmed/33344604 http://dx.doi.org/10.12998/wjcc.v8.i23.6048 |
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author | Yu, Wei-Hong Li, Xie-Jia Yuan, Fang |
author_facet | Yu, Wei-Hong Li, Xie-Jia Yuan, Fang |
author_sort | Yu, Wei-Hong |
collection | PubMed |
description | BACKGROUND: Hyporesponsiveness to erythropoiesis-stimulating agents (ESAs) is a prevalent problem in patients with chronic kidney disease. It is associated with increased morbidity and mortality in patients who undergo dialysis. A significant proportion of patients do not respond to iron supplementation and conventional ESAs. We report a case of severe ESA hyporesponsiveness-related anemia that was successfully treated with oral roxadustat. CASE SUMMARY: A 59-year-old Chinese woman had high blood glucose for 25 years, maintenance hemodialysis for 7 years, and recurrent dizziness and fatigue for more than 2 years. Laboratory tests showed severe anemia (hemoglobin level of 54 g/L), though bone marrow biopsy, fluorescence in situ hybridization, and hemolysis tests were within normal ranges. We initially administered first-line therapies and other adjuvant treatments, such as blood transfusions, ESAs, and adequate dialysis, but the patient did not respond as anticipated. Her erythropoietin-resistant anemia was probably not only due to chronic renal insufficiency. The patient received the hypoxia-inducible factor prolyl hydroxylase inhibitor roxadustat (100 mg, three times weekly). After 12 wk of treatment, the patient’s hemoglobin increased significantly, and her symptoms were alleviated. During the follow-up period, adverse drug reactions were controllable and tolerable. CONCLUSION: Oral roxadustat is effective and tolerable for the treatment of ESA hypores-ponsiveness-related anemia in patients undergoing hemodialysis. |
format | Online Article Text |
id | pubmed-7723725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-77237252020-12-18 Roxadustat for treatment of erythropoietin-hyporesponsive anemia in a hemodialysis patient: A case report Yu, Wei-Hong Li, Xie-Jia Yuan, Fang World J Clin Cases Case Report BACKGROUND: Hyporesponsiveness to erythropoiesis-stimulating agents (ESAs) is a prevalent problem in patients with chronic kidney disease. It is associated with increased morbidity and mortality in patients who undergo dialysis. A significant proportion of patients do not respond to iron supplementation and conventional ESAs. We report a case of severe ESA hyporesponsiveness-related anemia that was successfully treated with oral roxadustat. CASE SUMMARY: A 59-year-old Chinese woman had high blood glucose for 25 years, maintenance hemodialysis for 7 years, and recurrent dizziness and fatigue for more than 2 years. Laboratory tests showed severe anemia (hemoglobin level of 54 g/L), though bone marrow biopsy, fluorescence in situ hybridization, and hemolysis tests were within normal ranges. We initially administered first-line therapies and other adjuvant treatments, such as blood transfusions, ESAs, and adequate dialysis, but the patient did not respond as anticipated. Her erythropoietin-resistant anemia was probably not only due to chronic renal insufficiency. The patient received the hypoxia-inducible factor prolyl hydroxylase inhibitor roxadustat (100 mg, three times weekly). After 12 wk of treatment, the patient’s hemoglobin increased significantly, and her symptoms were alleviated. During the follow-up period, adverse drug reactions were controllable and tolerable. CONCLUSION: Oral roxadustat is effective and tolerable for the treatment of ESA hypores-ponsiveness-related anemia in patients undergoing hemodialysis. Baishideng Publishing Group Inc 2020-12-06 2020-12-06 /pmc/articles/PMC7723725/ /pubmed/33344604 http://dx.doi.org/10.12998/wjcc.v8.i23.6048 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Yu, Wei-Hong Li, Xie-Jia Yuan, Fang Roxadustat for treatment of erythropoietin-hyporesponsive anemia in a hemodialysis patient: A case report |
title | Roxadustat for treatment of erythropoietin-hyporesponsive anemia in a hemodialysis patient: A case report |
title_full | Roxadustat for treatment of erythropoietin-hyporesponsive anemia in a hemodialysis patient: A case report |
title_fullStr | Roxadustat for treatment of erythropoietin-hyporesponsive anemia in a hemodialysis patient: A case report |
title_full_unstemmed | Roxadustat for treatment of erythropoietin-hyporesponsive anemia in a hemodialysis patient: A case report |
title_short | Roxadustat for treatment of erythropoietin-hyporesponsive anemia in a hemodialysis patient: A case report |
title_sort | roxadustat for treatment of erythropoietin-hyporesponsive anemia in a hemodialysis patient: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7723725/ https://www.ncbi.nlm.nih.gov/pubmed/33344604 http://dx.doi.org/10.12998/wjcc.v8.i23.6048 |
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