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Safety and efficacy of a single total dose infusion (1020 mg) of ferumoxytol
PURPOSE: Iron deficiency anemia (IDA) is the most common type of anemia. A single dose infusion of intravenous (IV) iron is a convenient treatment option. Ferumoxytol is an IV formulation of iron that is typically given in two doses of 510 mg each. Utilizing a single dose of 1020 mg over 15 min has...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047823/ https://www.ncbi.nlm.nih.gov/pubmed/33912328 http://dx.doi.org/10.1177/20406207211006022 |
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author | Khan, Harris May, Paige Kuo, Elim Pai, Preetika Boles, Katherine McGee, Ashley Dang, Tanaka Schmit, Jessica |
author_facet | Khan, Harris May, Paige Kuo, Elim Pai, Preetika Boles, Katherine McGee, Ashley Dang, Tanaka Schmit, Jessica |
author_sort | Khan, Harris |
collection | PubMed |
description | PURPOSE: Iron deficiency anemia (IDA) is the most common type of anemia. A single dose infusion of intravenous (IV) iron is a convenient treatment option. Ferumoxytol is an IV formulation of iron that is typically given in two doses of 510 mg each. Utilizing a single dose of 1020 mg over 15 min has previously been described as safe and effective. In July 2018, we began to administer a single 1020 mg dose of ferumoxytol to patients needing IV iron replacement at the North Florida/South Georgia Veterans Health System. To evaluate the impact of this change, a utilization review was conducted. METHODS: Outcomes of all patients who received ferumoxytol injections in the 6 months prior to and after the dosing strategy change were analyzed. A total of 140 patients, who received 270 separate IV ferumoxytol infusions, were included in the analysis. RESULTS: No significant difference in safety was observed, with one infusion reaction occurring in each group (p = 1.00). Efficacy also appeared equivalent with no significant difference between the change in hemoglobin for those who received a single 1020 mg dose versus those who received two 510 mg doses (p = 0.764). As expected, those who received a single total dose infusion of 1020 mg had less clinic utilization (p < 0.0001). CONCLUSION: In summary, ferumoxytol administered as a 1020 mg single dose infusion was more convenient and should be considered a safe and effective treatment option for IDA. |
format | Online Article Text |
id | pubmed-8047823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-80478232021-04-27 Safety and efficacy of a single total dose infusion (1020 mg) of ferumoxytol Khan, Harris May, Paige Kuo, Elim Pai, Preetika Boles, Katherine McGee, Ashley Dang, Tanaka Schmit, Jessica Ther Adv Hematol Original Research PURPOSE: Iron deficiency anemia (IDA) is the most common type of anemia. A single dose infusion of intravenous (IV) iron is a convenient treatment option. Ferumoxytol is an IV formulation of iron that is typically given in two doses of 510 mg each. Utilizing a single dose of 1020 mg over 15 min has previously been described as safe and effective. In July 2018, we began to administer a single 1020 mg dose of ferumoxytol to patients needing IV iron replacement at the North Florida/South Georgia Veterans Health System. To evaluate the impact of this change, a utilization review was conducted. METHODS: Outcomes of all patients who received ferumoxytol injections in the 6 months prior to and after the dosing strategy change were analyzed. A total of 140 patients, who received 270 separate IV ferumoxytol infusions, were included in the analysis. RESULTS: No significant difference in safety was observed, with one infusion reaction occurring in each group (p = 1.00). Efficacy also appeared equivalent with no significant difference between the change in hemoglobin for those who received a single 1020 mg dose versus those who received two 510 mg doses (p = 0.764). As expected, those who received a single total dose infusion of 1020 mg had less clinic utilization (p < 0.0001). CONCLUSION: In summary, ferumoxytol administered as a 1020 mg single dose infusion was more convenient and should be considered a safe and effective treatment option for IDA. SAGE Publications 2021-04-12 /pmc/articles/PMC8047823/ /pubmed/33912328 http://dx.doi.org/10.1177/20406207211006022 Text en © The Author(s), 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Khan, Harris May, Paige Kuo, Elim Pai, Preetika Boles, Katherine McGee, Ashley Dang, Tanaka Schmit, Jessica Safety and efficacy of a single total dose infusion (1020 mg) of ferumoxytol |
title | Safety and efficacy of a single total dose infusion (1020 mg) of ferumoxytol |
title_full | Safety and efficacy of a single total dose infusion (1020 mg) of ferumoxytol |
title_fullStr | Safety and efficacy of a single total dose infusion (1020 mg) of ferumoxytol |
title_full_unstemmed | Safety and efficacy of a single total dose infusion (1020 mg) of ferumoxytol |
title_short | Safety and efficacy of a single total dose infusion (1020 mg) of ferumoxytol |
title_sort | safety and efficacy of a single total dose infusion (1020 mg) of ferumoxytol |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047823/ https://www.ncbi.nlm.nih.gov/pubmed/33912328 http://dx.doi.org/10.1177/20406207211006022 |
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