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Anemia warrants treatment to improve survival in patients with heart failure receiving sacubitril–valsartan

Angiotensin inhibition remains a cornerstone for pharmacologic management of heart failure (HF), despite being associated with decreased hemoglobin (Hb) levels. To investigate the effect of anemia and its treatment on patients with HF treated with sacubitril–valsartan (S/V), we conducted a retrospec...

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Autores principales: Yang, Tsun-Yu, Lee, Chii-Ming, Wang, Shih-Rong, Cheng, Yu-Yang, Weng, Shao-En, Hsu, Wan-Tseng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114364/
https://www.ncbi.nlm.nih.gov/pubmed/35581275
http://dx.doi.org/10.1038/s41598-022-11886-2
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author Yang, Tsun-Yu
Lee, Chii-Ming
Wang, Shih-Rong
Cheng, Yu-Yang
Weng, Shao-En
Hsu, Wan-Tseng
author_facet Yang, Tsun-Yu
Lee, Chii-Ming
Wang, Shih-Rong
Cheng, Yu-Yang
Weng, Shao-En
Hsu, Wan-Tseng
author_sort Yang, Tsun-Yu
collection PubMed
description Angiotensin inhibition remains a cornerstone for pharmacologic management of heart failure (HF), despite being associated with decreased hemoglobin (Hb) levels. To investigate the effect of anemia and its treatment on patients with HF treated with sacubitril–valsartan (S/V), we conducted a retrospective study involving patients with recorded left ventricular ejection fractions (LVEFs) of < 40% between January 2017 and December 2019. We identified 677 patients, 37.7% of whom received S/V. The median follow-up period was 868 days. Anemia was associated with significantly decreased survival, increased mortality rates, and higher all-cause hospitalizations in S/V-using patients. We further analyzed 236 patients with HF who had recorded renal function, LVEF, and Hb at the initiation of S/V therapy to identify Hb patterns after S/V therapy. Of these patients, 35.6% exhibited decreasing Hb 12 months after S/V initiation, which was associated with a lower survival rate. Among the patients who were not prescribed anemia medications, Hb of ≥ 12 (vs. < 12 g/dL) was associated with a higher survival rate; this association was absent among the patients undergoing anemia treatment. These results emphasize that consistent screening and treatment for anemia should be implemented to reduce the morbidity and mortality of patients with HF receiving S/V.
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spelling pubmed-91143642022-05-19 Anemia warrants treatment to improve survival in patients with heart failure receiving sacubitril–valsartan Yang, Tsun-Yu Lee, Chii-Ming Wang, Shih-Rong Cheng, Yu-Yang Weng, Shao-En Hsu, Wan-Tseng Sci Rep Article Angiotensin inhibition remains a cornerstone for pharmacologic management of heart failure (HF), despite being associated with decreased hemoglobin (Hb) levels. To investigate the effect of anemia and its treatment on patients with HF treated with sacubitril–valsartan (S/V), we conducted a retrospective study involving patients with recorded left ventricular ejection fractions (LVEFs) of < 40% between January 2017 and December 2019. We identified 677 patients, 37.7% of whom received S/V. The median follow-up period was 868 days. Anemia was associated with significantly decreased survival, increased mortality rates, and higher all-cause hospitalizations in S/V-using patients. We further analyzed 236 patients with HF who had recorded renal function, LVEF, and Hb at the initiation of S/V therapy to identify Hb patterns after S/V therapy. Of these patients, 35.6% exhibited decreasing Hb 12 months after S/V initiation, which was associated with a lower survival rate. Among the patients who were not prescribed anemia medications, Hb of ≥ 12 (vs. < 12 g/dL) was associated with a higher survival rate; this association was absent among the patients undergoing anemia treatment. These results emphasize that consistent screening and treatment for anemia should be implemented to reduce the morbidity and mortality of patients with HF receiving S/V. Nature Publishing Group UK 2022-05-17 /pmc/articles/PMC9114364/ /pubmed/35581275 http://dx.doi.org/10.1038/s41598-022-11886-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yang, Tsun-Yu
Lee, Chii-Ming
Wang, Shih-Rong
Cheng, Yu-Yang
Weng, Shao-En
Hsu, Wan-Tseng
Anemia warrants treatment to improve survival in patients with heart failure receiving sacubitril–valsartan
title Anemia warrants treatment to improve survival in patients with heart failure receiving sacubitril–valsartan
title_full Anemia warrants treatment to improve survival in patients with heart failure receiving sacubitril–valsartan
title_fullStr Anemia warrants treatment to improve survival in patients with heart failure receiving sacubitril–valsartan
title_full_unstemmed Anemia warrants treatment to improve survival in patients with heart failure receiving sacubitril–valsartan
title_short Anemia warrants treatment to improve survival in patients with heart failure receiving sacubitril–valsartan
title_sort anemia warrants treatment to improve survival in patients with heart failure receiving sacubitril–valsartan
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9114364/
https://www.ncbi.nlm.nih.gov/pubmed/35581275
http://dx.doi.org/10.1038/s41598-022-11886-2
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