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Efficacy and safety of intravenous iron repletion in patients with heart failure: a systematic review and meta-analysis
INTRODUCTION: AFFIRM-AHF and IRONMAN demonstrated lower rates of the combined endpoint recurrent heart failure (HF) hospitalizations and cardiovascular death (CVD) using intravenous (IV) ferric carboxymaltose (FCM) and ferric derisomaltose (FDI), respectively in patients with HF and iron deficiency...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10116902/ https://www.ncbi.nlm.nih.gov/pubmed/37074386 http://dx.doi.org/10.1007/s00392-023-02207-2 |
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author | Vukadinović, Davor Abdin, Amr Emrich, Insa Schulze, P. Christian von Haehling, Stephan Böhm, Michael |
author_facet | Vukadinović, Davor Abdin, Amr Emrich, Insa Schulze, P. Christian von Haehling, Stephan Böhm, Michael |
author_sort | Vukadinović, Davor |
collection | PubMed |
description | INTRODUCTION: AFFIRM-AHF and IRONMAN demonstrated lower rates of the combined endpoint recurrent heart failure (HF) hospitalizations and cardiovascular death (CVD) using intravenous (IV) ferric carboxymaltose (FCM) and ferric derisomaltose (FDI), respectively in patients with HF and iron deficiency (ID) utilizing prespecified COVID-19 analyses. MATERIAL AND METHODS: We meta-analyzed efficacy, between trial heterogeneity and data robustness for the primary endpoint and CVD in AFFIRM-AHF and IRONMAN. As sensitivity analysis, we analyzed data from all eligible exploratory trials investigating FCM/FDI in HF. RESULTS: FCM/FDI reduced the primary endpoint (RR = 0.81, 95% CI 0.69–0.95, p = 0.01, I(2) = 0%), with the number needed to treat (NNT) being 7. Power was 73% and findings were robust with fragility index (FI) of 94 and fragility quotient (FQ) of 0.041. Effects of FCM/FDI were neutral concerning CVD (OR = 0.88, 95% CI 0.71–1.09, p = 0.24, I(2) = 0%). Power was 21% while findings were fragile with reverse FI of 14 and reversed FQ of 0.006. The sensitivity analysis from all eligible trials (n = 3258) confirmed positive effects of FCM/FDI on the primary endpoint (RR = 0.77, 95% CI 0.66–0.90, p = 0.0008, I(2) = 0%), with NNT being 6. Power was 91% while findings were robust (FI of 147 and FQ of 0.045). Effect on CVD was neutral (RR = 0.87, 95% CI 0.71–1.07, p = 0.18, I(2) = 0%). Power was 10% while findings were fragile (reverse FI of 7 and reverse FQ of 0.002). Rate of infections (OR = 0.85, 95% CI 0.71–1.02, p = 0.09, I(2) = 0%), vascular disorder (OR = 0.84, 95% CI 0.57–1.25, p = 0.34, I(2) = 0%) and general or injection-site related disorders (OR = 1.39, 95% CI 0.88–1.29, p = 0.16, I(2) = 30%) were comparable between groups. There was no relevant heterogeneity (I(2) > 50%) between the trials for any of the analyzed outcomes. CONCLUSIONS: Use of FCM/FDI is safe and reduces the composite of recurrent HF hospitalizations and CVD, while effects on CVD alone are based on available level of data indeterminate. Findings concerning composite outcomes exhibit a high level of robustness without heterogeneity between trials with FCM and FDI. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-10116902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-101169022023-04-20 Efficacy and safety of intravenous iron repletion in patients with heart failure: a systematic review and meta-analysis Vukadinović, Davor Abdin, Amr Emrich, Insa Schulze, P. Christian von Haehling, Stephan Böhm, Michael Clin Res Cardiol Original Paper INTRODUCTION: AFFIRM-AHF and IRONMAN demonstrated lower rates of the combined endpoint recurrent heart failure (HF) hospitalizations and cardiovascular death (CVD) using intravenous (IV) ferric carboxymaltose (FCM) and ferric derisomaltose (FDI), respectively in patients with HF and iron deficiency (ID) utilizing prespecified COVID-19 analyses. MATERIAL AND METHODS: We meta-analyzed efficacy, between trial heterogeneity and data robustness for the primary endpoint and CVD in AFFIRM-AHF and IRONMAN. As sensitivity analysis, we analyzed data from all eligible exploratory trials investigating FCM/FDI in HF. RESULTS: FCM/FDI reduced the primary endpoint (RR = 0.81, 95% CI 0.69–0.95, p = 0.01, I(2) = 0%), with the number needed to treat (NNT) being 7. Power was 73% and findings were robust with fragility index (FI) of 94 and fragility quotient (FQ) of 0.041. Effects of FCM/FDI were neutral concerning CVD (OR = 0.88, 95% CI 0.71–1.09, p = 0.24, I(2) = 0%). Power was 21% while findings were fragile with reverse FI of 14 and reversed FQ of 0.006. The sensitivity analysis from all eligible trials (n = 3258) confirmed positive effects of FCM/FDI on the primary endpoint (RR = 0.77, 95% CI 0.66–0.90, p = 0.0008, I(2) = 0%), with NNT being 6. Power was 91% while findings were robust (FI of 147 and FQ of 0.045). Effect on CVD was neutral (RR = 0.87, 95% CI 0.71–1.07, p = 0.18, I(2) = 0%). Power was 10% while findings were fragile (reverse FI of 7 and reverse FQ of 0.002). Rate of infections (OR = 0.85, 95% CI 0.71–1.02, p = 0.09, I(2) = 0%), vascular disorder (OR = 0.84, 95% CI 0.57–1.25, p = 0.34, I(2) = 0%) and general or injection-site related disorders (OR = 1.39, 95% CI 0.88–1.29, p = 0.16, I(2) = 30%) were comparable between groups. There was no relevant heterogeneity (I(2) > 50%) between the trials for any of the analyzed outcomes. CONCLUSIONS: Use of FCM/FDI is safe and reduces the composite of recurrent HF hospitalizations and CVD, while effects on CVD alone are based on available level of data indeterminate. Findings concerning composite outcomes exhibit a high level of robustness without heterogeneity between trials with FCM and FDI. GRAPHICAL ABSTRACT: [Image: see text] Springer Berlin Heidelberg 2023-04-19 2023 /pmc/articles/PMC10116902/ /pubmed/37074386 http://dx.doi.org/10.1007/s00392-023-02207-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 | Original Paper Vukadinović, Davor Abdin, Amr Emrich, Insa Schulze, P. Christian von Haehling, Stephan Böhm, Michael Efficacy and safety of intravenous iron repletion in patients with heart failure: a systematic review and meta-analysis |
title | Efficacy and safety of intravenous iron repletion in patients with heart failure: a systematic review and meta-analysis |
title_full | Efficacy and safety of intravenous iron repletion in patients with heart failure: a systematic review and meta-analysis |
title_fullStr | Efficacy and safety of intravenous iron repletion in patients with heart failure: a systematic review and meta-analysis |
title_full_unstemmed | Efficacy and safety of intravenous iron repletion in patients with heart failure: a systematic review and meta-analysis |
title_short | Efficacy and safety of intravenous iron repletion in patients with heart failure: a systematic review and meta-analysis |
title_sort | efficacy and safety of intravenous iron repletion in patients with heart failure: a systematic review and meta-analysis |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10116902/ https://www.ncbi.nlm.nih.gov/pubmed/37074386 http://dx.doi.org/10.1007/s00392-023-02207-2 |
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